Cat No : RK081-25. Ulta Covid-19 Ag test is a rapid Immunochromatographic assey for the qualitative detection of specific antigens to SAR-COV-2 present in human nasopharynx.
Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen.
Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2
10 µl of specimen: Serum, Plasma & Whole Blood
Long term storage of 24 months at 2 - 30 C
Complementary to RT-PCR Test
Can be performed without extra equipment
Cat No: 41FK10. Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection.
CAT No : RK055-25. STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx.
The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI.
Validated by ICMR & AIIMS
Sensitivity of 84.38 % & Specificity of 100%
Sample Type- Human Nasopharyngeal swab (No other sample recommended)
Results in 15-30 mins
Cat. No : 5513C. COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
ImmunoQuick Covid-19 IgM/IgG Test :
Covid-19 or commonly known as Coronavirus is a viral infection involving a patients upper respiratory tract. It is highly contagious and causes a severe lung infection which can be severely debilitating and sometimes fatal. Our test detects two types of antibodies to Covid-19 which appear from 2 to 21 days after infection. It is an invaluable test to diagnose people who have been sick for a few days or those who have recovered.
Salient Features of the Product
It is rapid immunoassay for qualitative detection of Covid-19 IgM and IgG antibodiesin
Human Serum or Plasma or Whole Blood.
Results available in 15 minutes.
Sensitivity :: >96%
Specificity :: >99%
No cross reactivity observed.
Can be stored at 4 to 30C
Stable for 24 months.
Pack size :: 25 tests.
Cat. No : F-NCOV-01G. STANDARD F COVID-19 Ag FIA is the fl uorescent immunoassay for the qualitative detection of specific nucleoprotein antigens to SARS-CoV-2 present in human nasopharynx. STANDARD F COVID-19 Ag FIA should be used with the STANDARD F Analyzers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection.
The iFinDx COVID-19 IgM/IgG is a rapid test kit for differential detection of specific IgM and IgG against COVID-19 in human serum, plasma and whole blood.
CAT No : 41FK51. The Panbio COVID-19 Antigen Self-Test is a single-use, in vitro (outside the body) visually read rapid immunoassay that uses a human nasal swab specimen for the qualitative detection of nucleocapsid protein SARS-CoV-2 antigen.
The test can determine if you have an active COVID-19 infection and you will know your test results in just 15 minutes
Only Proven High-Accuracy Self-Test in India
In clinical evaluations with self-test users, the Panbio COVID-19 Antigen Self-Test correctly identified 100% of negative samples and 95.2% of Positive Samples
Pregnancy had no impact on the performance of the test.
Genbody Influenza/ Covid - 19 Ag Triple,
Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy.
Production information:
1.Specimen: nasopharyngeal swab or Viral transport medium (VTM)
2.No Cross-reaction with 27 kinds of other respiratory viruses.
3.No interference with 23 kinds of interfering substances.
4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2.
5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
Product Details:
Brand : ABBOTT
ICMR Approved : Yes
Result Time (Rapid Kits) : 10-15 mins
Packaging Size: 1 T
CAT No : 41FK51
Certified CE certified
The Panbio COVID-19 Antigen Self-Test is a single-use, in vitro (outside the body) visually read rapid immunoassay that uses a human nasal swab specimen for the qualitative detection of nucleocapsid protein SARS-CoV-2 antigen.
The test can determine if you have an active COVID-19 infection and you will know your test results in just 15 minutes
Only Proven High-Accuracy Self-Test in India
In clinical evaluations with self-test users, the Panbio COVID-19 Antigen Self-Test correctly identified 100% of negative samples and 95.2% of Positive Samples
Pregnancy had no impact on the performance of the test.
Product Details:
Brand : Premier medicals
Result Time (Rapid Kits) : 15 min
Sample Type : Nasal Swab
Packaging Size : 25 Test Kits/Box
CAT No : SS03P25
Certified WHO Approved
Sure Status COVID-19 Antigen Card Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx
Product Details:
Number of Reactions(Preps)/Kit ; 2
Brand ; Genbody
Test Method : Antigen Test
Result Time (Rapid Kits) : 10-15 mins
Certified : CE certified
Cat. No : COVAG025-1
The GenBody COVID-19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) oranteriornasal (AN) swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first six days of symptom onset
LABROID BOD incubator is the most versatile and reliable low temperature incubator which is designed to maintain a constant temperature, necessary for Biological Oxygen Demand/Biochemical Oxygen Demand (BOD) determination.
LABROID Brand BOD incubators provide controlled temperature conditions for accelerated tests and are used to maintain temperature for test tissue culture growth, storage of bacterial cultures and incubation where high degree of constant temperature accuracy is required.
Construction: Double walled: Outer wall of Mild steel powder coated and inner chamber of Stainless steel 304.
Temperature Range: +5°C up to 60°C. (On Request Less than +5°C Available).
Accuracy: ± 0.5C. (On Request ±0. 2C)
Resolution: 0.1C
Sensor: PT 100
Door: Main Door with Magnetic gasket with lock and Key. (OPTIONAL SEE THROUGH GLASS DOOR -ON REQUEST)
Trays: Adjustable-Stainless Steel
Sub Doors: Inner Sub Doors Made of Acrylic
Fluorescent Lighting: Built-in lighting arrangement by low wattage lamp.
Power Supply: Single phase 230V, 50Hz, AC mains
LABROID Hot Air Oven are double walled insulation keeps the heat in and conserves energy, the inner layer being a poor conductor and outer layer being metallic.
Hot air ovens are electrical devices which use dry heat to sterilize, specifically designed to meet the challenging demands of various Laboratory for individual and specialized research applications.
Construction: Double walled: Outer wall of Mild steel powder coated or Stainless Steel and inner chamber of Stainlesssteel 304.
Temperature Range: +50C to 280°C. (On Request above 280°C)
Controller: Microprocessor based controller with LED Display, PID Digital Temperature Indicator cum Controller, with dual display of set Value and Process value for precise control of temperature.
Accuracy: ± 2 C
Resolution: 0.1 C
Door: Main Door with Rubber Gasket.
Trays: Adjustable-Stainless Steel.
Alarm: Audio / Visual Alarms for Temperature Deviations
Safety Features: Safety standby thermostat to cut off heater supply in case of overshoot of temperature.
Power Supply: Single phase 230V, 50Hz, AC mains.
WHO Approved, First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
100% - Specificity
100% - Sensitivity
Detects antibodies specific to Treponema pallidum
Rapid Result time within 20-25 Minutes
Storage at 4-30C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
HCG Urine Pregnancy Test measures the presence of the pregnancy hormone (HCG) in your urine for the early detection of pregnancy.
STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CTK Biotech's, CE Certified , the OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
Product Specification:-
Brand Name : CTK Biotech
Pkg Qty : 1
Number Of Items : 30
Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action
Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
CE certified, Qualitative detection of troponin in anticoagulated
(EDTA or heparin) venous whole blood
Reaction time: 15 min.
A positive result from a threshold (cut-off) of 100 ng/L
Storage at 2 to 8 C
Test can be used immediately after removal from the
refrigerator
Storage for 4 weeks at room temperature (15 to 25 C)
Roche TROP T sensitive rapid assay is available in 5
and 10 pack sizes
Content:
5 disposable test strips (individually sealed)
5 pipettes (150 L)
disposable labels
1 package insert
A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2)
Clear, dependable results in 15 minutes
Requires minimal training and no equipment
So easy it can be used at the lowest levels of health care service
Can use whole blood or serum/plasma
Collection can be by fingerstick or venipuncture
No refrigeration required
Storage conditions 2-30�°C
COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of
COVID-19 Chip-based Real Time PCR Test is a semi quantitative detection of RNA in human oropharyngeal and nasopharyngeal swab specimen and aids in detection and confirmation of infection and diagnosis of COVID-19. The test detects the E and Orf1a genes of the virus.
COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
Test Method (SARS-CoV-2) RT-PCR
Result Time (Rapid Kits) 30mins
The Viral/Pathogen Nucleic Acid Isolation Kit is designed to recover RNA and DNA from virus and gram-negative bacteria in samples such as blood, swabs, urine, and viral transport media (VTM). The kit utilizes magnetic-bead technology, ensuring reproducible recovery of high-quality nucleic acid compatible with a broad range of applications, including real-time PCR, digital PCR, and next-generation sequencing.
Abbott BinaxNOW S. pneumoniae Antigen Card provides accurate, rapid identification of S. pneumoniae antigen in patients with pneumococcal pneumonia and pneumococcal meningitis with an easy-to-use technology, aiding physicians in providing rapid, focused therapy.
Time to Result: 15 minutes
Performance data:
Urine Sensitivity/Specificity 86% / 94%
CSF Sensitivity/Specificity 97% / 99%
Ordering Information
Cat No. Description Specimen Pack size
710000 Streptococcus Urine, CSF 22 Tests
Pneumoniae Ag card
Cat No. 7D2543. By detecting early markers of Hepatitis B infection, the Alere Determineâ?¢ HBsAg helps to diagnose acute infection and confirm chronic infection - allowing healthcare professionals to initiate prompt and appropriate follow-up action for infected patients.
Rapid in-vitro qualitative ICT for detection of HBsAg
Sample Type: Serum/Plasma/Whole Blood
Sample Volume: 50�µL
Early marker of infection- helps in diagnosis
Facilitates appropriate follow-up of infected patients
Collection can be done by fingerprick or venipuncture
Clear, dependable results in 15 minutes
Quick Reference Card for the detection of HBsAg in
human serum/plasma or whole blood.
Cat. No: 03FK10CE. Sd bioline hiv 1/2 pack size: 1 x 30 test
one step rapid immunochromatrographic test for the detection of anti - hiv 1/2 in human serum, plasma or whole blood
CAT No : 11621947196.
Qualitative detection of troponin in anticoagulated
(EDTA or heparin) venous whole blood
Reaction time: 15 min.
Positive result from a threshold (cut-off) of 100 ng/L
Storage at 2 to 8C
Test can be used immediately after removal from the
Refrigerator
Storage for 4 weeks at room temperature (15 to 25 C)
Roche TROP T sensitive rapid assay is available in 5 and 10-pack sizes
Content:
5 disposable test strips (individually sealed)
5 pipettes (150L)
Disposable labels
1 package insert
Cat No : 05FK80I40. The SD BIOLINE Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.
Specomen: Whole blood
Time to result: 15 -30 minutes
Storage: 1-40 degree C for 24 months
Performance: Sensitivity: Pf-99.7%, Pv-95.5%
Specificity: 99.5 %
Optimal screening test for Plasmodium falciparum and Plasmodium vivax.
CAT No : 7D2343. A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2)
Clear, dependable results in 15 minutes
Requires minimal training and no equipment
So easy it can be used at the lowest levels of health care service
Can use whole blood or serum/plasma
Collection can be by fingerstick or venipuncture
No refrigeration required
Storage conditions 2-30C
Cat. No : 11FK45. SD BIOLINE Dengue Duo
(Dengue NS1 Ag + IgG/IgM)
The SD BIOLINE Dengue Duo kit is a rapid, an in-vitro immunochromatographic, one step assay designed to detect both dengue virus NS1 antigen and antibodies to Dengue virus (Dengue IgG/IgM) in human serum, plasma or whole blood. SD BIOLINE Dengue Duo rapid test contains two test devices (left side ; Dengue NS1 Ag test, right side ; Dengue IgG/IgM test). The SD BIOLINE Dengue Duo kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as RT-PCR, IgM / IgG ELISA or HI (Hemagglutination inhibition) test.
Detect Dengue Ag and Ab simultaneously at once.
Cover acute to convalescence stage
Performance: Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM)
Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM)
In primary infection with the dengue virus, IgG antibody appears a few days after IgM. In primary infections, IgG antibodies are produced at a lower level compared to IgM but will persist for many years after infection. In secondary infections, IgG response may rise quickly before or simultaneously with an IgM response and will become the predominant immunoglobulin isotype in secondary infections.
Cat No. 08FK50. SD BIOLINE TB Ag MPT64 Rapid is a rapid immune chromatographic identification test for the M. tuberculosis complex. M. tuberculosis has been known to secrete more than 33 different proteins. One of the predominant proteins, MPT64 was found in the culture fluid of only strains of the M. tuberculosis complex.
Rapid discrimination between the M. tuberculosis complex and MOTT bacilli
Identification of the M. tuberculosis complex in combination with culture systems
Sample: Colony, Condensation fluid(Solid cultures) or Liquid cultures
Interpretation time: 15minutes
Detection limit: 105CFU/ml.
Cat No.02FK10I30. SD BIOLINE HCV test is an immunochromatographic rapid visual test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood
Immobilized material: Recombinant HCV Core, NS3, NS4, NS5 Ag
Specimen Type: Serum, Plasma, Whole blood
Sample Volume: 10MuL
Shelf Life: 24months
Storage: 2-30oC
Performance: Sensitivity: 99.5% and Specificity: 98%
One Step Hepatitis C Virus Test.
The Alere SD BIOLINE Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood.
Optimal screening test for P.falciparum and other Plasmodium species
Ordering Information
Cat No. Description Type Pack size
05FK63I01 SD Malaria Device 1 Test
The MagMAX Viral/Pathogen Nucleic Acid Isolation Kit is designed to recover RNA and DNA from virus and gram-negative bacteria in samples such as blood, swabs, urine, and viral transport media (VTM). The kit utilizes MagMAX magnetic-bead technology, ensuring reproducible recovery of high-quality nucleic acid compatible with a broad range of applications, including real-time PCR, digital PCR, and next-generation sequencing.
Features of the MagMAX Viral/Pathogen Nucleic Acid Isolation Kit include:
Automation-ready protocols designed for the KingFisher Flex and KingFisher Duo Prime systems
Fast procedure allows for 96 samples to be processed in <30 minutes
Flexible protocol accommodates sample volume inputs from 200 µL to 2 mL of biofluids or transfer media
No need for carrier RNA
Elution volumes ranging from 50 to 100 µL
Cat No : 09N77-095. The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria.
CAT No : RCHM-02071. The CareStar COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.
CAT No : RK026-30. STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CAT No : RK025-40. One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood
Kit Contents:
Standard Q Malaria Pf/PV Ag cassette x 40
Specimen transfer device 3 microlitre x 40
Butter bottle 3m1 x 02
Instructions for use x 01
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and CAT Cat.No : RK025-40. Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity
Advantage:
Distinguish the infection between P.falciparum and P.vivax
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5�µl)
Room temperature storage.
Cat No : PI19FRC25. First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
100% - Specificity
100% - Sensitivity
Detects antibodies specific to Treponema pallidum
Rapid Result time within 20-25 Minutes
Storage at 4-30C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
CAT No : PI19FRC25. First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40C.
Specimen Type- Whole Blood.
CAT No : 09FIL10D. Filariasis Ag Test Kit Contents:
Test Device in a foil pouch with desiccant
Disposable dropper
Instruction for use
Cat No : 11FK50. Bioline DENGUE NS1 Ag TEST FOR EARLY CLINICAL PHASE OF DENGUE INFECTION
Bioline Dengue NS1 Ag rapid test is an in vitro immunochromatographic assay designed to detect Dengue virus NS1 antigen in human serum, plasma or whole blood.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Benefits:
Diagnosis of early acute dengue infection by detecting dengue NS1 antigen
Dengue NS1 antigen can be detected from 1 day after onset of fever
Specimen : Serum, plasma or whole blood (100�¼l)
Test result : 15~20 minutes
Specification:
Sensitivity 92.4%, Specificity 98.4%
Cat No :14FK10 Bioline* Rotavirus test is an immunochromatographic assay for the detection of Group A rotavirus in human fecal specimens. The test utilizes two kinds of antibody in a solid phase sandwitch immunochromatography to detect group specific proteins, including the major inner capsid protein, present in Group A rotaviruses.
â?¢ Early detection of rotavirus antigen group A all serotype
Shelf life and storage temperature: 18 months from the date of manufacturing at1-30 C
Performance: Sensitivity: 94 %, Specificity 98.3 % (vs. RT-PCR)
Cat No : ACKCRDPC3. Product Description : Acon Pregnancy Test Strip (HCG) is a one step pregnancy test kit containing test strip. The urine sample is to be collected in a clean, dry container and almost half test strip should be dropped inside the container. The first urine sample of the day is preferred. The pack insert should be thoroughly read before use. To know how to use and read test results. Acon pregnancy test strip detects pregnancy in just 5 minutes.
Features & Specifications : One Step Pregnancy Test Strip, Easy to Use, Quick Result in just 5 minutes, Pack of 3 Test Strips, For more info, please refer the product pack for usage instructions.
Product Details:
Number of Reactions(Preps)/Kit :30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK019-30
STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.
Easy to use, Easy to read and interpret
Discrimination between HIV-1 and HIV-2 antibodies
Room temperature storage
Performance
Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK013-10
One step, rapid, immunochromatographic test for the detection of IgM/IgG antibodies to four serotypes of dengue virus (DEN-1, DEN-2, DEN-3 and DEN-4) & Dengue virus NS1 antigen in human serum, plasma or whole blood.
Kit Contents:
Standard Q Dengue Ag Ab Duo cassette x 10
Specimen transfer device 10ml x 10
Butter bottle 4ml x 01
Instructions for use x 1
STANDARD Q Dengue Duo test is an immunochromatographic assay for the detection of NS1 antigen and Dengue virus-specific IgM and IgG antibodies in human serum, plasma and whole blood. By detecting the NS1 antigen, not only the initial infection can be detected, but also Dengue virus-specific IgM and IgG can be detected at the same time. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Product Details:
Number of Reactions(Preps)/Kit :20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15min
CAT No : RK012-20
One step, rapid, immunochromatographic test for the detection of Dengue IgMlIgG antibodies to four senatypes of dengue virus (DEN-I, DEN-2. DEN-3 and DEN-4) in human serum, plasma or whole blood.
Kit Contents:
Standard Q Dengue IgM IgG cassette x 20
Specimen transfer device 10ml x 20
Butter bottle 4ml x 01
Instructions for use x 1
STANDARD Q Dengue IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting IgM and IgG specific to Dengue virus, the primary and secondary Dengue virus infections can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Advantage:
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 �µl)
Product Details:
Number of Reactions(Preps)/Kit 40T
Brand ; SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15min
CAT No : RK025-40
One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood
Kit Contents:
Standard Q Malaria Pf/PV Ag cassette x 40
Specimen transfer device 3 microlitre x 40
Butter bottle 3m1 x 02
Instructions for use x 01
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity
Advantage:
Distinguish the infection between P.falciparum and P.vivax
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5aul)
Room temperature storage.
Product Details:
Number of Reactions(Preps)/Kit : 40T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK027-40
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium species antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium species, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Distinguish the infection between P.falciparum and others
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5aul)
Room temperature storage
Product Details:
Number of Reactions(Preps)/Kit: 30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10 min
Country of Origin : Made in India
CAT No : RK026-30
STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand ; SD Biosensor
ICMR Approved ; Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK029-20
STANDARD Q TSUTSUGAMUSHI IgM/IgG is a rapid,sensitive,qualitative Immunochromatographic assay for the detection of IgM/IgG antibodies against Orientia Tsutsugamushi in human serum,Plasma or whole blood specimen.it is an initial screening test and this test kit is for in vitro use only by professionals.
Differential detection of IgM & IgG Antibodies
Easy to use,Easy to interpret
Long term storage
Faster results with lesser specimen volume (10aul)
Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK024-20
STANDARD Q Chikungunya IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Chikungunya virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 aul)
Product Details:
Number of Reactions(Preps)/Kit : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : 09FIL10D
Filariasis Ag Test Kit Contents:
Test Device in a foil pouch with desiccant
Disposable dropper
Instruction for use
Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK018-30
STANDARD Q HCV Ab qualitatively analyzes antibodies specific to hepatitis C virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis C infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 98.9% (92/93) / Specificity : 100% (168/168)
Product Details:
Number of Reactions(Preps)/Kit : 50T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK022-50
"STANDARD QA Ultra-DotA HIV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect circulatingantibodies against HIV in human serum or plasma. The test is for invitro diagnostic use and is intended as an aid to early diagnosis ofHIV infection. This test is intended for professional use only as aninitial screening test."
Product Details:
Number of Reactions(Preps)/Kit : 50
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK023-50
STANDARD QA Ultra-DotA HCV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect antibodiesagainst HCV in human serum or plasma. This test is for in vitrodiagnostic use and intended as an aid to early diagnosis of HCVinfection in patient with clinical symptoms with HCV infection.The test provides an initial screening result only. More specificalternative diagnosis methods should be performed in order toobtain the confirmation of HCV infection.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/ control
Specimen volume : 75 Microliter
stored at ; 4 - 30 DegreeC
Cat No ; CFPC-44
T3
Assessing to diagnosis & to monitor thyroid diseases(T3)
This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement.
INTENDED USE :
ichroma T3 is a fluorescence Immunoassay (FIA) for the
quantitative determination of triiodothyronine (total T3) in
human serum/plasma. It is useful as an aid in management
and monitoring of determination of thyroid disorders.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the analyte in the sample binds to the
fluorescence labeled (FL) detection antibody in detection
buffer, to form the complex as sample mixture. This complex
is loaded to migrate onto the nitrocellulose matrix, where
the covalent couple of T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated,
resulting in less fluorescence signal.
MATERIALS SUPPLIED :
REF CFPC-44
Components of ichroma T3
Cartridge Box:
- Cartridge 25
- Detector tube 25
- Detector diluent 2
- ID chip 1
- Instruction for Use 1
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Specimen : Human serum/plasma/ control
Specimen volume : 75 microliter
stored at 4 - 30 DegreeC.
Cat No : CFPC-26
T4
Assessing to diagnosis & to monitor thyroid diseases(T4)
Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid.
INTENDED USE :
ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal.
MATERIALS SUPPLIED :
REF CFPC-26
Components of ichroma T4
Cartridge Box:
- Cartridges 25
- ID Chip 1
- Insert 1
- Detector tube (Granule) 25
- Detector diluent (5.5 mL) 1
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 T
Samples: human whole blood/serum /plasma
Specimen volume human whole blood/serum/ plasma
stored at 4-30 C
Cat. No. : CFPC-66
Human Chorionic Gonadotropin (�²-hCG)
Distinguish pregnancy and abnormal pregnancy
The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome.
INTENDED USE :
ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the
quantitative determination of -HCG in human whole blood/serum
/plasma. It is useful as an aid in management and monitoring of beta
human chorionic gonadotropin (hCG) level in human
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; Dried
antibodies in the detector tube, once diluted with the diluent, bind
with antigens in the sample to form antigen-antibody complexes.
These complexes then migrate through the nitrocellulose matrix and
are captured by another sets of immobilized antibodies on the test line.
The more antigens in the sample, the more antigen-antibody
complexes, which leads to a stronger fluorescence signal. This signal
then is interpreted by the reader to display the �²-HCG concentration in
the sample.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in the original
aluminum foil pouch) if stored at 4-30 C.
The detector, diluent and sample diluent are stable for 20 months
if stored at 2-8 C.
After the cartridge pouch is opened, the test should be
performed immediately.
MATERIALS SUPPLIED :
REF CFPC-66
Components of ichroma-HCG Plus
Cartridge Box:
- Cartridges 25
- ID Chip 1
- Instruction For Use 1
Buffer Box
For ichorma II
- Detectors (Capped with plastic lid) 25
- Diluent 1
For AFIAS-50
- Detectors (Sealed with aluminum foil) 25
- Diluent 1
Sample Diluent Box:
- Sample Diluent Tubes 25
Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human serum/plasma
Specimen volume : 150 Microliter
stored at 4 - 30 DegreeC.
Cat. No : CFPC-22
Thyroid Stimulating Hormone (TSH)
Diagnosing thyroid dysfunction
One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH).
INTENDED USE :
ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample.
MATERIALS SUPPLIED :
REF CFPC-77
Components of ichroma NT-proBNP
Cartridge Box:
- Cartridge 25
- ID Chip 1
- Instruction for Use 1
Buffer Box
For ichroma II
- Detector tube 25
- Detector diluent 1
For ichroma-50
- Detector tube 25
- Detector diluent 1
Product Details:
Brand : Boditech Med Incorporated
Size : 25 Test
Samples : Whole blood
Sample volume : 75 Microliter
Cat No : CFPC-38
Storage Temperature ; 4 - 30 DegreeC
HbA1c
Assessing the level of glycated hemoglobin in the blood
This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months.
INTENDED USE
ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. For in vitro diagnostic use only.
PRINCIPLE:
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : whole blood/serum/plasma
Sample volume : 75 Microliter
stored at 4 - 30 DegreeC
Cat No i CHROMA PSA-25
Prostate Specific Antigen (PSA)
Screening for the prostate cancer & monitoring the effects of the treatment
This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 Test
Samples : Serum/Plasma
Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin
Storage Temperature : 4 - 30 DegreeC
Cat No : CFPC-21
Progesterone
Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy
The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy.
PRINCIPLE :
The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.
Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0101C
Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 �¼mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 �¼mol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
Shelf life: 24 month
Individually sealed foil pouches containing:
One cassette device
One desiccant
5L capillary tubes
Sample diluent (REF SB-R0101, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/control
Specimen volume : 50 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-89
INTENDED USE :
ichroma AMH is a fluorescence Immunoassay (FIA) for the quantitative determination of AMH (Anti-m�¼llerian hormone) in human serum/plasma. It is useful as an aid in management and monitoring of premature ovarian insufficiency, menopause and ovarian reserve.For in vitro diagnostic use only.
COMPONENTS :
ichroma AMH consists of cartridges, detectors and diluent The cartridge contains the membrane called a test strip which has streptavidin at the test line and chicken IgY at the control line. All cartridges are individually sealed in an aluminum foil pouch containing a desiccant in a box The detector has 2 granules containing anti human AMH-fluorescence conjugate, anti-chicken IgY-fluorescence conjugate, anti-human AMH-biotin conjugate, bovine serum albumin (BSA) and sucrose as a stabilizer, MAB33 as a blocker in Tris-HCl buffer. All detectors are packed in a box The diluent contains bovine serum albumin and NaCl as a stabilizer, tween 20 and CA-630 as a surfactant and sodium azide as a preservative in phosphate buffered saline (PBS), and it is pre-dispensed in a vial. The diluent is packed in a box.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.More antigens in sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show human AMH concentration in the sample.
INTERPRETATION OF TEST RESULT :
The instrument for ichroma tests calculates the test result automatically and displays AMH concentration of the test sample in terms of ng/mL The working range: 0.02- 15 ng/mL
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 30 Microliter
Sample : human serum / plasma / control
Reaction Time ; 10 mins
Cat No : CFPC-32
Ferritin
Monitoring deficiency/excess of iron & inflammation
Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Too little ferritin can lead to anemia, while too much to liver disease, rheumatoid arthritis, other inflammatory conditions, or hyperthyroidism. The ferritin test measures the level of ferritin in the blood.
INTENDED USE :
ichromaâ?¢ Ferritin is a fluorescence Immunoassay (FIA) for the quantitative determination of Ferritin in human serum/plasma. It is useful as an aid for quantifying human ferritin.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigen in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by Instrument for ichrom tests to show ferritin concentration in sample.
MATERIALS SUPPLIED :
REF CFPC-32
Components of ichroma Ferritin
Cartridge Box:
- Cartridge 25
- Detector 25
- Detector Diluent 1
- ID Chip 1
- Instruction for Use 1
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample : whole blood (AFIAS), plasma, serum
Reaction Time : 15mins
Detection Range : ichroma(TM) (1 - 100 mIU/ml)
Cat No : CEPC-35
Follicle-stimulating Hormone (FSH)
Diagnosis of early menopause & ovarian degeneration and infertility
This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.
Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume ; 150 microliter
stored at 4-30 DegreeC
Cat No : CFPC-23-1
PCT
Assessing initial risk of bacterial infection and fatal sepsis
Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock.
INTENDED USE :
ichroma PCT is a fluorescence Immunoassay (FIA) for the quantitative determination of Procalcitonin (PCT) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.
The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PCT concentration in sample.
STORAGE AND STABILITY:
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.
MATERIALS SUPPLIED :
REF CFPC-23
Components of ichromaâ?¢ PCT Cartridge Box:
- Cartridges 10
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer tubes
- Detection Buffer Tubes 10
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 75 Microliter
Sample : human serum/plasma
Reaction Time : 15mins
Cat No : 13010
Luteinizing Hormone (LH)
Assessing and monitoring function of pituitary gland
This test helps evaluate pituitary function by quantifying luteinizing hormone in the blood, to diagnose pituitary gland disease, and to determine congenitally or acquired gonadotropin dysfunction.
INTENDED USE :
ichroma LH is a fluorescence Immunoassay (FIA) for the quantitative determination of Luteinizing hormone (LH) in human serum/plasma. It is useful as an aid in management and monitoring of determination of evaluating fertility issues, function of reproductive organs (ovaries or testicles), or detection of the ovulation.
For in vitro diagnostic use only.
PRINCIPLE:
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.
The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show LH concentration in sample.
MATERIALS SUPPLIED:
REF 13010
Components of ichroma LH Cartridge Box:
- Cartridges 25
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer Tubes
- Detection Buffer Tubes 25.
Product Details:
Number of Reactions(Preps)/Kit 30
Brand : CTK BioTech
Result Time (Rapid Kits) :20-25 Min
Sample Material :Serum / Plasma / Whole Blood
Cat. No : R0061c
The OnSite Dengue IgG/IgM 3.0 Combo Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM antiâ??dengue virus (DEN1, 2, 3 and 4) in human serum, plasma or whole blood.
Product Features:
Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 AUL Capillary tubes
Sample diluent (REF SB-R0061, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Specimen : human serum/plasma
Specimen volume : 50 Microliter
Cat. No. : CFPC-47
INTENDED USE :
ichromaâ?¢ Vitamin D is a fluorescence Immunoassay (FIA) for the quantitative determination of total 25(OH)D2/D3 level in human serum/plasma. It is useful as an aid in management and monitoring of regulating the concentration of calcium and phosphate in the bloodstream and promoting the healthy growth and remodeling of bone.For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method. In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of 25(OH)D3 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. The releasing buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. Opened detection buffer and releasing buffer are stable for 12 months at 2-8 C if kept capped in original container and free from contaminations. After the cartridge pouch is opened, the test should be performed immediately.
MATERIALS SUPPLIED :
REF CFPC-47Components of ichroma Vitamin D Cartridge Box:- Cartridges 25- Sample Mixing Tubes 25- ID Chip 1- Instruction For Use 1 Detection Buffer Vial (3 mL) 1 Releasing Buffer Vial (2 mL) 1
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human whole blood/serum/ plasma
Sample volume : 50 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-65
Troponin I (Tn-I) Plus
Early diagnosis of myocardial infarction with high sensitivity
Troponin I (Tn-I) Plus can diagnose myocardial infarction and myocardial necrosis at an early stage with high sensitivity by accessing Tn-I level in the blood, thus can help prevent progression to more severe cases.
INTENDED USE:
ichroma Tn-I Plus is a Fluorescence Immunoassay (FIA) for the quantitative determination of cardiac troponin-I (Tn-I) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of acute myocardial infarction (AMI).
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show Tn-I concentration in the sample.
MATERIALS SUPPLIED :
REF CFPC-65
Components of ichroma Tn-I Plus
Cartridge Box:
- Cartridge 25
- 50L Capillary tube 25
- ID chip 1
- Instruction for Use 1
Buffer Box
For ichorma II
- Detector (Capped with plastic lid) 25
- Diluent 1
For ichroma 50
- Detector (Sealed with aluminum foil) 25
- Diluent 1
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human whole blood/ serum/ plasma/control
Specimen volume : 10 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-77
NT-proBNP
Helping to diagnose heart diseases and evaluate the severity level
BNP and NTproBNP are peptides that are continuously produced in the heart. When the muscles in the left ventricle over-stretch as in heart failure, the secretion of these peptides into blood increases. One may utilize the level of NTproBNP in blood to assess the cardiac event and its severity. Both of BNP and NTproBNP can be used to show different aspects of the heart failure.
INTENDED USE:
ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample.
MATERIALS SUPPLIED :
REF CFPC-77
Components of ichroma NT-proBNP
Cartridge Box:
- Cartridge 25
- ID Chip 1
- Instruction for Use 1
Buffer Box
For ichroma
- Detector tube 25
- Detector diluent 1
For ichromaâ?¢-50
- Detector tube 25
- Detector diluent 1
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume : 5 Microliter
stored at 4-30 C
Cat No : CFPC-51
Anti-CCP Plus
Supporting to distinguish and diagnose rheumatoid arthritis
This test helps to diagnose and provide appropriate treatment for chronic systemic autoimmune diseases and rheumatism by quantifying Anti-CCP in the blood.
INTENDED USE :
ichroma Anti-CCP is a fluorescence Immunoassay (FIA) for the qualitative or semi-quantitative determination of human IgG autoantibodies to cyclic citrullinated peptides (CCP) in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of rheumatoid arthritis (RA) in combination with other clinical and laboratory findings.
For in vitro diagnostic use only.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.
PRINCIPLE :
A synthetic cyclic citrullinated peptide (CCP) is immobilized on a porous membrane. After a sample is added to the sample port, detection buffer, consisting of fluorescent conjugated polyclonal antibody to human IgG, is loaded to the buffer port. The more anti-CCP antibodies in sample forms the more the peptide antigen/anti-CCP antibodies complex and leads to stronger intensity of fluorescence signal on detector anti-human IgG, which is processed by instrument for ichroma tests to show anti-CCP level in sample.
MATERIALS SUPPLIED :
REF CFPC-51
Components of ichroma Anti-CCP Cartridge Box:
- Cartridges 25
- Sample collectors 25
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer Tubes
- Detection Buffer Tubes 25
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples: human whole blood/serum/ plasma
Specimen volume : 50 microliter
stored at 4 - 30 C
Cat No : CFPC-91
Total IgE
Assessing to diagnose acute allergic diseases
This test assesses IgE in blood to support diagnosing of acute allergic diseases.
INTENDED USE :
ichroma Total IgE is a fluorescence immunoassay (FIA) for the quantitative determination of total IgE in human whole blood/serum/ plasma. It is useful as an aid in diagnosis and management of allergic disease.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show total IgE concentration in the sample.
MATERIALS SUPPLIED :
REF CFPC-91
Components of ichroma Total IgE
Cartridge Box:
- Cartridge 25
- ID Chip 1
- Instruction for Use 1
Detection Buffer Box
- Detection Buffer 25
Product Details:
Brand : Boditech Med Incorporated
Size ; : 25 T
Samples : Human whole blood/plasma/control
Specimen volume : 10 Microliter
Storage : 4- 30 DegreeC
Cat No : CFPC-25
D-Dimer
Measuring D-dimer level in 12 mins
The presence of D-dimer in blood indicates that thrombin has been formed and fibrin generated from fibrinogen in vivo as a result of activation of the coagulation system. This test measures the level in the blood to help assess the thrombotic state.
INTENDED USE :
ichroma D-Dimer is a fluorescence Immunoassay (FIA) for the quantitative determination of D-Dimer in human whole blood/plasma. It is useful as an aid in management and monitoring of post therapeutic evaluation of thromboembolic disease patients.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show D-Dimer concentration in the sample.
MATERIALS SUPPLIED :
REF CFPC-25
Components of ichroma D-Dimer Cartridge Box:
- Cartridge 25
- ID chip 1
- Instruction for use 1 Box containing Detection Buffer tubes
- Detection buffer 25
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 75 Microliter
Sample : serum/plasma/control
Storage Temperature : 4-30 DegreeC.
Cat No : CFPC-27
Prolactin (PRL)
Assessing to diagnose hypothalamic impairments & pituitary disorders
This test helps select and diagnose mammary gland development, infertility treatment and pituitary diseases by quantifying blood PRL.
INTENDED USE :
ichroma PRL is a fluorescence Immunoassay (FIA) for the
quantitative determination of Prolactin (PRL) in human
serum/plasma. It is useful as an aid in management and
monitoring of hypothalamic-pituitary disorders.
For in vitro diagnostic use only.
PRINCIPLE:
The test uses a sandwich immunodetection method; the
detector antibody in buffer binds to antigen in sample,
forming antigen-antibody complexes, and migrates onto
nitrocellulose matrix to be captured by the other
immobilized-antibody on test strip.
The more antigen in sample forms the more antigenantibody
complex and leads to stronger intensity of
fluorescence signal on detector antibody, which is processed
by instrument for ichromaâ?¢ tests to show PRL concentration
in sample.
MATERIALS SUPPLIEED :
REF CFPC-27
Components of ichroma PRL
Cartridge Box:
- Cartridges 25
- ID Chip 1
- Instruction for Use 1
Detection Buffer Box:
- Detection Buffer tubes 25
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 10 Microliter
Sample : Human whole blood/serum/ plasma/control
Reaction Time : 3 mins
Cat No : ichroma CRP-25
CRP
Assessing to diagnose infection and inflammation
This test can help with proper prescription and treatment by quickly and accurately measuring CRP with a finger-tip blood.
INTENDED USE :
ichroma CRP is a fluorescence Immunoassay (FIA) for the quantitative determination of CRP in human whole blood/serum/ plasma. It is useful as an aid in management and monitoring of autoimmune diseases and infectious processes, such as rheumatoid arthritis.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show CRP concentration in the sample.
MATERIALS SUPPLIED :
REF i-CHROMA CRP-25
Components of ichrom CRP
Cartridge Box:
- Cartridge 25
- ID Chip 1
- Instruction for Use 1
- Sample Collector 25
Box containing Detection Buffer
- Detection buffer 25
Product Details:
Number of Reactions(Preps)/Kit 30 T
Brand SD Biosensor
ICMR Approved Yes
Result Time (Rapid Kits) 10 Min
Cat. No RK033-30
General Description:
STANDARD Q HIV/Syphilis Combo Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O, HIV 2 and Syphilis (Treponema pallidum) in human serum, plasma or whole blood. The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection for HIV or Syphilis infected patients, patients with signs and symptoms (HIV and Syphilis) and persons at risk. The test is able to quick screen the HIV/syphilis infection and gives the advantage of managing these two diseases at the same time.
Technical specifications:
Technology: Rapid chromatographic immunoassay.
Format: Test cassette, 25 tests.
Sample type: serum/plasma/venous whole blood specimen
Sample volume: Serum Plasma 10�µl/whole Blood 20 µl.
Sensitivity: HIV 100% & Syphilis 98.8%
Specificity: HIV 99.9%/syphilis 100%/
Time to result: Minimum of 15 minutes.
Product Details:
Number of Reactions(Preps)/Kit 25 Test
Brand SD Biosensor
Result Time (Rapid Kits) 15 Min
Cat. No 09LEP10D
STANDARD Q Leptospira IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Leptospira interrogans in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Advantage
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage of 2-40 / 36-104
Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl).
Product Details:
Brand J.Mithra
Test Kit Type: Dengue Test Kit (Rapid)
Sensitivity & Specificity High
Shelf Life: 30 months at 2-30 DegreeC
Pack Size: 10, 30 & 50 Tests
Cat. No IR028010
Intended Use : Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen and differential detection of IgM and IgG antibodies to Dengue virus in Human serum/plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue infection & presumptive diagnosis between primary and secondary Dengue infection.
Salient Features:
First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies.
Diagnosis of both Primary & Secondary Infection.
Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4).
Highly Sensitive & Highly Specific
Long shelf life: 30 months at 2-30 C.
Convenient pack sizes: 10 Tests, 30 Tests & 50 Tests.
Principle:Dengue Day 1 test kit consists of two devices: one device for detection of Dengue NS1 antigen and second device for the differential detection of Dengue IgM/IgG antibodies in Human serum/plasma. Dengue NS1 Antigen device contains two lines; (Control line) & T (Dengue NS1 Antigen test line). Test line is coated with anti-dengue NS1 Ag. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloidal conjugate making antigen antibodies complex. This complex migrates along the membrane to the test region and forms the visible pink line at as antibody-antigen-antibody gold colloid forms. Dengue IgM/IgG test device contains three lines; C (Control line), M (IgM test line) & G (IgG test line).IgM test line is coated with anti-human IgM and IgG test line is coated with anti-human IgG.When a sample is added to the device, IgG and IgM antibodies in the sample react with anti-human IgM or IgG antibodies coated on the membrane respectively. Colloidal gold complexes containing dengue 1-4 antigens is captured by the bound anti-dengue IgM or IgG on respective test bands located in the test window causing a pale to dark red band to form at the IgG or IgM region of the test device window.
The intensity of the test bands in the respective device will vary depending upon the amount of antigen /antibody present in the sample. The appearance of any pink/ red colour in a specific test region should be considered as positive for that particular antigen and/or antibody type (IgG or IgM). A red procedural control line should always develop in the test device window to indicate that the test has been performed properly
Dengue NS1 Ag :
Sensitivity 96% and Specificity 98%.
Dengue IgM/IgG Antibody test :
Sensitivity 95% and Specificity 97%.
Product Details:
Brand J.Mithra
Result Time (Rapid Kits) Within 20 Minutes
Test Kit Type Malaria Test Kit (Rapid)
Sensitivity & Specificity Excellent as per WHO Malaria RDTs Evaluation
Cat. No IR221050
Intended Use:Advantage MAL Card is a visual, rapid and sensitive immunoassay for the qualitative diagnosis of P.falciparum and other Plasmodium Species (P.vivax/ P.malariae/ P.ovale/ P.falciparum) based on pLDH antigen in human whole blood.
Salient Features:
Infection free- See through Device based on pLDH antigen Malaria parasite in whole blood
Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation.
Longer shelf life of 30 months at 4-30 C.
Easy to interpret Colour Bands
Results within 20 minutes.
Product Details:
Brand J.Mithra
Result Time (Rapid Kits) Within 3 Minutes
Test Kit Type HCV Test Kit (Rapid)
Sensitivity 100% WHO Evaluation
Specificity 98.9% WHO Evaluation
Cat. No HC020100
Intended Use:
The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma.
It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen
Salient Features:
Based on Flow Through Technology, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity.
Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device.
Detection of all the subtypes of HCV.
Results within 3 minutes.
In built quality control dot which validates the test.
100% Sensitivity & 98.9% Specificity as per WHO evaluation.
Shelf life : 24 months at 2-8C
Product Details:
Brand Abbott Afinion
Result Time (Rapid Kits) 15 min
Sample Type Blood
Country of Origin Made in India
Requires only 20 ml of specimen
Capillary tubes 20 ml
Immediate point of care HbA1c results for efficient monitoring of glycemic control.
The Afinion HbA1c assay is a test for quantitative determination of glycated hemoglobin (HbA1c) in human whole blood, used to monitor metabolic control in patients with diabetes. It provides the immediate test results you need for improved diabetic control, better patient outcomes, and enhanced clinic efficiencies.
SHORT ASSAY TIME IN 3 MINUTES
The CLIA-Waived Afinion HbA1c test gives you reliable, high quality results conveniently available when and where you need them.
TIMELY TREATMENT CHANGES
Diabetes can be treated and managed by healthful eating, regular physical activity, and medications to lower blood glucose levels. Lowering the HbA1c has been shown to reduce microvascular complications of diabetes and is also associated with long-term reduction in macrovascular disease.
LONG SHELF LIFE OF REAGENTS
Patient consultations can be carried out with confidence. The HbA1c Test Cartridge contains all reagents necessary for the measurement of glycated hemoglobin. The test has 3 months room temperature storage.
Product Details:
Material Hips
Usage/Application Clinical
Country of Origin Made in India
Sample Volume 2.5 microlitre
Brand Abbott
model number AFINION CRP
Assay time 3 to 4 minutes
Sample material Capillary blood,serum,plasma,or anticoagulated venous blood (EDTA or heparin)
Measuring range 5-200 mg/L (whole blood),5-160 mg/L (serum and plasma
Abbott AFINION CRP Rapid Vitro Diagnostic Test
Product Details:
Usage/Application Hospital
Country of Origin Made in India
The Afinion Lipid Panel test and the fully automated Afinion Analyzer, give you reliable results conveniently available when and where you need them. Patient consultations can be carried out with confidence.
Test for quantitative determination of Total Cholesterol, High-Density Lipoprotein (HDL) cholesterol, Low- Density Lipoprotein (LDL) cholesterol, Triglycerides (Trig), non-HDL and Chol/HDL ratio in whole blood, serum and plasma to be used in the diagnosis and treatment of lipid disorders.
BENEFITS:
Test for the quantitative determination of:
THE IMPORTANCE OF MEASURING A LIPID PANEL
Elevated cholesterol is one of the major risk factors for coronary heart disease, heart attack and stroke. As the blood cholesterol rises, so does the cardiovascular disease risk. Many patients such as those with metabolic syndrome have comorbid conditions such as high lipids and diabetes. And if other risk factors are present such as smoking, high blood pressure or diabetes, the risk increases even further.
Measuring a Lipid Panel/Cholesterol is recommended by NCEP (National Cholesterol Education Program) every five years in healthy adults, more regularly if you have other risk factors, in children and youths who are at an increased risk and to evaluate the success of lipid-lowering treatment.
See how POC diabetes testing significantly impacts patient care with better glycemic control, increased compliance, and improved office efficiencies. Read the presentation or download the PowerPoint for your own use.
Product Details:
Number of Reactions(Preps)/Kit : 100
Brand : Siemens
The Multistix 10 SG reagent strip is the reliable frontline test for detection of a broad range of conditions, from detecting urinary tract infections (UTI1) to diabetes and kidney disorders. Accurately gain a broader clinical insight into a patient's health.
Product Details:
Number of Reactions(Preps)/Kit : 96 wells
Brand : Abbott
Usage/Application : Hospital
Sample Material : Serum
CAT No : 11EK10
The Panbio Dengue IgM Capture ELISA is used to detect IgM antibodies to dengue antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Panbio. Dengue IgM Capture ELISA should be used in conjunction with other dengue serology.
Product Details:
Number of Reactions(Preps)/Kit ; 96 wells
Brand : Abbott
Test Type : Elisa
CAT No : E-LEP01M / E-LEP01M05
The Panbio Leptospira IgM ELISA is for the qualitative detection of IgM antibodies to leptospira in serum as an aid in the clinical laboratory diagnosis of patients with clinical symptoms consistent with leptospirosis.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Incubation Time: 60+60+60+5+10+1
Storage 2-8 C
Cat No : DDMS-1
The DENV DetectTM IgM Capture ELISA is for the qualitative detection of IgM antibodies to DENV recombinant antigens in serum for the presumptive clinical laboratory diagnosis of Dengue virus infection. The assay is intended for use only in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
1st Assay to Receive FDA Clearance.
Performance thoroughly evaluated with clinically confirmed cases of dengue 1-4 serotypes.
Excellent positive and negative agreement with WHO reference panel (>90%).
Improves accuracy by monitoring background reactivity with a normal cell antigen.
Employs a simple, one step ratio method of interpretation.
CE Marked.
Product Details:
Number of Reactions(Preps)/Kit : 96wells
Brand : Abbott
Cat. No : 01PE10
The Panbio Dengue IgG Capture ELISA is used to detect elevated IgG antibodies to dengue virus (serotypes 1-4) in patients with secondary infection. This test is intended as an aid in the clinical laboratory diagnosis.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : Abbott
Cat. No : 01PE40
Panbio Dengue Early ELISA is a dengue NS1 antigen capture ELISA. It is used to detect NS1 antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Dengue Early ELISA should be used in conjunction with other dengue serological assays.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : Serum / Plasma
Storage : 2-8 C
Cat No : AE0315
The TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay for the qualitative detection of IgM anti- Chikungunya virus in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with Chikungunya viruses. Any reactive specimen with the TRUSTwell CHIK IgM Test must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay based on the principle of the indirect immunoassay technique for the detection of IgM anti- Chikungunya virus in human serum or plasma. The TRUSTwell CHIK IgM Test is composed of two key components: 1) Solid microwells pre-coated with recombinant CHIK antigen(s); 2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horse reddish peroxidase (HRP-anti-Human IgM conjugates). During the assay, the test specimen is first incubated with the coated microwells. IgM anti- Chikungunya virus, if present in the specimen, binds to the antigen coated on the microwell surface.
In the second incubation with the HRP-anti Human IgM conjugates, the IgM antiChikungunya antibody absorbed on the surface of microwell reacts to the conjugates, forming a complexed conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 336 specimens from susceptible subjects were tested by TRUSTwell CHIK IgM and by a commercial reference ELISA kits.
Relative Sensitivity: 91.3 %, (95 % CI: 73.2 % -97.6 %) Relative Specificity: 96.8 %, (95 % CI: 94.2 % -98.3 %) Overall Agreement: 96.4%, (95 % CI: 93.9 % -98.0 %).
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum / plasma
Storage : 2 - 8 C
Cat No : AE0710
INTENDED USE:
The TRUSTwell HBsAg ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of hepatitis B virus surface antigen (HBsAg) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HBV. Any reactive specimen with the TRUSTwell HBsAg ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
TRUSTwell HBsAg ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of antibody sandwich technique for the detection of HBsAg in human serum or plasma. The TRUSTwell HBsAg ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with monoclonal anti HBsAg antibody; 2) Liquid conjugates composed of polyclonal anti-HBsAg conjugated with horse radish peroxidase (HRP-HBsAb conjugates). During the assay, the test specimen and HRP-HBsAb conjugates are incubated simultaneously with the coated microwells. HBsAg, if present in the specimen, reacts to the anti-HBsAg antibody coated on the microwell surface as well as the HRPHBsAb conjugate, forming sandwich complex conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbance are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 1033 patient specimens from susceptible subjects were tested by the TRUSTwell HBsAg ELISA Kit.
Relative Sensitivity:100%,
Relative Specificity:99.78%,
Overall Agreement:99.81%
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum / plasma
Storage : 2-8 C
Cat No : AE0420
INTENDED USE:
The TRUSTwell HIV Ag-Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of HIV-1 P24 antigen, anti-HIV-1 including subtype O and anti-HIV-2 antibodies (including isotype IgG, IgM and IgA) in human serum or plasma. It is intended for professional use only as an aid in the early identification of infection with HIV-1 and HIV-2 viruses. Any reactive specimen with the TRUSTwell HIV Ag-Ab ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
The TRUSTwell HIV Ag-Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the double antibody/antigen sandwich technique for the detection of HIV-1 P24 antigen and various antibodies against HIV-1 and/or HIV-2 antigen in human serum or plasma. The TRUSTwell HIV Ag-Ab ELISA Kit is composed by two systems: 1) Solid microwells pre-coated with Recombinant HIV-1 and HIV-2 antigens and anti-P24 antibody 2) Liquid conjugates composed of a. Recombinant HIV-1 and HIV-2 antigens conjugated with horse radish peroxidase (HRP-HIV 1+2 conjugates) and avidin conjugated with HRP (HRP-avidin conjugates) b. Anti-P24 antibody conjugated with biotin (Biotinylated P24 Ab)
During the assay, the test specimen is first incubated with the coated microwells and followed by incubation with biotinylated P24 Ab. The anti-HIV-1 and anti-HIV-2 antibodies, if present in the specimen, bind to the antigens coated on the microwell surface. If P24 present in the specimen, binds to the anti-P24 antibody on the microwell surface and biotinylated P24 Ab in the solution. In the next incubation with the HRP-HIV 1+2 and HRP-avidin conjugates, the above bounded anti-HIV-1 and anti-HIV-2 antibodies and bounded P24 antigen reactive to the HRP conjugates, forming HRP-complex. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbance are read using a spectrophotometer at 450/620-690nm.
Clinical Performance:
A total of 1100 patient specimens from susceptible subjects were tested by the TRUSTwell HIV Ag-Ab ELISA Kit.
Relative Sensitivity: 100%,
Relative Specificity: 99.9%,
Overall Agreement: 99.9%.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum / plasma
Stroage : 2-8 C
Cat No : AE0410
INTENDED USE:
The TRUSTwell HIV 1+2 Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of anti-HIV-1 including subtype O and anti-HIV-2 antibodies (including isotype IgG, IgM and IgA) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HIV-1 and HIV-2 viruses. Any reactive specimen with the TRUSTwell HIV 1+2 Ab ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE :
TRUSTwell HIV 1+2 Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the double antigen-sandwich technique for the detection of the various antibodies against HIV-1 and/or HIV-2 in human serum or plasma. The TRUSTwell HIV 1+2 Ab ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with recombinant HIV-1 and HIV-2 antigens; 2) Liquid conjugates composed of recombinant HIV-1 and HIV-2 antigens conjugated with horse radish peroxidase (HIV 1+2 HRP conjugates). During the assay, the test specimen is first incubated with the coated microwells. The anti-HIV-1 and anti-HIV-2 antibodies, if present in the specimen, bind to the antigens coated on the microwell surface. In the second incubation with the HRP- HIV 1+2 conjugates, the anti-HIV-1 and antiHIV-1 antibodies absorbed on the surface of microwell react to the HRP-HIV 1+2 conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbance are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance :
A total of 1095 patient specimens from susceptible subjects were tested by the TRUSTwell HIV 1+2 Ab ELISA Kit.
Relative Sensitivity: 100% Relative Specificity: 99.9%, Overall Agreement: 99.9%
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum or plasma
Storage : 2-8 c
Cat No : AE0311
INTENDED USE :
The Dengue IgG ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of elevated anti-dengue viruses (DEN1, 2, 3, 4) IgG in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of active infection with dengue viruses, including secondary infection.
TEST PRINCIPLE:
The Dengue IgG ELISA Kit is a solid-phase enzyme-linked immunosorbent assay based on the principle of the capture immunoassay methodology for the detection of IgG anti-dengue virus in human serum or plasma. The Dengue IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with mouse monoclonal anti-human IgG antibody. 2) Conjugate composed of biotinylated dengue antigens and avidin HRP-conjugates. During the assay, the test specimen is first incubated in the coated microwell. IgG antidengue, if present in the specimen, binds to the anti-human IgG antibodies coated on the microwell surface, and any unbound specimen is then removed by a wash step. During a second incubation with Biotinylated dengue antigens, the IgG anti-dengue absorbed on the surface of microwell binds with dengue antigen, forming a complex. Unbound antigens are then removed by washing. After addition of Streptavidin HRP conjugate, it binds with biotinylated antigen and forming complex with HRP conjugate. After addition of the TMB substrate, the presence of the conjugate complex is shown by development of a blue color resulting from a reaction between the enzyme and substrate. This reaction is then quenched by addition of the Stop Solution, and the absorbance value for each microwell is determined using a spectrophotometer at 450/620-690 nm.
Accuracy of Detection :
A total of 262 patient specimens were collected from susceptible subjects and tested by Dengue IgG ELISA Kit and by a commercial leading brand EIA.
Relative Sensitivity: 95.2% (95% Confidence Interval = 83.8 - 99.4%)
Relative Specificity: 96.8% (95% Confidence Interval = 93.6 - 98.7%)
Overall agreement: 96.6% (95% Confidence Interval = 93.6 - 98.4%)
Product Details:
Number of Reactions(Preps)/Kit : 50
Brand : SD
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Sample Type : Oral & Nasal Swab
STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Product Details:
Number of Reactions(Preps)/Kit :96 Wells
Brand : InBios
Sample Material : Serum
Formet : Immunocapture
Incubation Time : 30+30+30+10
Cat. No : CHKG-C
CHIKjj Detect : IgG ELISA Kit
The CHIKjj DetectTM IgG ELISA is designed for the qualitative detection of IgG antibodies present in human serum targeting chikungunya virus E2/E1 proteins. This test is for the presumptive clinical laboratory diagnosis of chikungunya virus infection. This assay is intended for use only in patients with clinical symptoms consistent with chikungunya infection.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Key Features :
Developed using a novel technology1 that outperforms traditional antigen preparations, resulting in highly sensitive detection of recent and past CHIKV infection.
>90% Sensitivity and Specificity
DENV Detect and CHIKjj Detect can be run in parallel for differential diagnosis.
CE Marked
Ordering :
Cat No : CHKG-C
Formet : Immunocapture
Quantity : 96 wells/Plate
Incubation Time : 30 + 30 + 5 + 10 + 1
Sample Type : Serum
Storage : 2-8
Shelf Life : 12 months
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : Immunocapture
Incubation Time : 30+30+30+10
Cat No : CHKM-R
The CHIKjj Detect IgM ELISA is designed for the qualitative detection of IgM antibodies present in human serum targeting Chikungunya virus E2/E1 proteins. This test is not intended to screen blood or blood components. This test is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Key Features :
InBios chikungunya kits have been developed using a novel technology1 that outperforms traditional antigen preparations, resulting in highly sensitive detection of recent and past CHIKV infection.
Excellent results in CDC evaluation of commercially available chikungunya IgM assays.
Ordering:
Cat No CHKM-R
Formet Immunocapture
Quantity 96 wells/Plate
Incubation Time 30 + 30 + 5 + 10
Sample Type Serum
Storage 2-8
Shelf Life 12 months
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : Antigen Detection
Incubation Time : 60+30+20+1
Cat No : DNS1-1
The DENV DetectTM NS1 ELISA is for the early detection of Dengue virus (DENV) NS1 antigen in human serum. This test is for the presumptive clinical laboratory diagnosis of Dengue virus infection. This assay is intended for use in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever. Samples collected from patients within seven (7) days after the onset of clinical symptoms should be evaluated with this assay (day 0 â?? day 7). Negative results obtained with this test do not preclude the diagnosis of dengue and should not be used as the sole basis for treatment or other patient management decision. This assay is not FDA cleared or approved for testing blood or plasma donors.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
FDA Cleared & CE Marked
Early NS1 antigen detection (within first 7 days onset of symptoms)
Helps differentiate dengue from other flaviviruses that may cross react with dengue antibodies but not with the antigen
High Sensitivity & Specificity: 86.6% PPA & 97.8% NPA with prospectively collected positive and negative confirmed clinical specimens
Kit can be performed in parallel with InBiosâ?? FDA Cleared dengue IgM ELISA for presumptive diagnosis of acute or convalescent stage dengue virus.
Product Details:
Quantity/Kit : 96 wells/Plate
Format :Indirect
Brand : InBios
Incubation Time : 30 + 30 +10 + 1
Sample Type : Serum or dried blood spots
Cat No : FILA-1
he Filaria DetectTM IgG4 ELISA is for qualitative detection of specific IgG4 antibodies in specimens to highlyspecific antigen IWb123 target antigen expressed primarily in infective stage larvae (L3) of the lymphatic-dwelling parasite Wuchereria bancrofti (Wb). This product is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
For research purposes only.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : ELISA
Incubation Time : 30 + 30 + 5 + 10 + 1
Cat No : STMS-R
The Scrub Typhus Detect IgM ELISA for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA system for the detection of IgM antibodies in human serum to OT-derived recombinant antigen. This test is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Product Details:
Size 96 wells/Plate
Format Indirect
Incubation Time 30 + 30 + 5 + 10 + 1
Sample Type Serum
Storage 2-8 C
Cat No STGS-R
The Scrub Typhus Detectâ?¢ IgG ELISA test for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA assay system for the detection of IgG antibodies in human serum to OT-derived recombinant antigen. For research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Product Details:
Number of Reactions(Preps)/Kit ; 96 Wells
Brand : InBios
Format : Immunocapture
Specimen : Serum
Cat No : ZKM2-1
The ZIKV Detect 2.0 IgM Capture ELISA is intended for the qualitative detection of Zika virus IgM antibodies in human sera for the presumptive clinical laboratory diagnosis of Zika virus infection. The assay is intended for use only in patients with clinical signs and symptoms consistent with Zika virus infection, and/or CDC Zika virus epidemiological criteria (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). Assay results are for the presumptive detection of IgM antibodies to Zika virus (ZIKV). Positive results must be confirmed by following the latest CDC guidelines for the diagnosis of Zika virus infection.
Results of this test are intended to be used in conjunction with clinical observations, patient history, epidemiological information, and other laboratory evidence to make patient management decisions. Zika IgM levels are variable over the course of the infection and may be detectable near day four post onset of symptoms and persist up to approximately 12 weeks following initial infection.
Negative results may be seen in specimens collected before day four post onset of symptoms or after the window of detectable IgM closes, and therefore do not preclude the possibility of Zika virus infection, past or present.
1st Commercial serology kit to receive FDA Marketing Authorization
CE Marked
Differentiates Zika IgM positive patients from those infected with other flaviviruses such as West Nile or Dengue
Sensitivity: >90%
Specificity: >96%
Results in 4 hours
Tests up to 28 unknown specimens.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : Abbott
Product Type : Microplate
Sample : Serum
CAT. NO : 11EK50
The presence of circulating non-structural glycoprotein (NS1) indicates Viremia. If sufficient virus is present, NS1 can be detectable in a patientâ??s blood from day 0 to day 5 following disease onset. The detection of NS1 antigen is therefore useful as a test of early acute infection. â?¢ Early diagnosis of dengue infection High accuracy with all dengue serotypes (DEN1,2,3, and 4) Simple and easy to use: All necessary reagents included in the kit â?¢ Shelf life and storage temperature: 18 months from the date of manufacturing at 2-8 'C Performance: Sensitivity 93.3 % (87.4 - 96.6 %), Specificity 98.9 % (96.0 - 99.7 %)
Product Details:
Brand : CTK BIOTECH
Size : 96 Well
Specimen : Serum & Plasma
stored at 2 - 8 C
Cat No : E0100
The RecombiLISA HAV IgM ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of IgM anti-hepatitis A virus in human serum or plasma.
Product Features:
Utilizes IgM capture technique
Detects IgM anti-HAV in serum or plasma
Evaluated with BBI HAV serum conversion and HAV mixed titer performance panels
Useful for identifying acute HAV infections
Product Specification:
Microwells coated with anti-human IgM antibody
HAV IgM negative control
HAV IgM positive control
HRP-HAV conjugates
Wash buffer (30 x concentrate)
TMB substrate A
TMB substrate B
Stop solution
ELISA Working Sheet
Product insert
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample Material : Plasma/Serum
Storage : 2-8 C
Cat. No : E0105
INTENDED USE:
The RecombiLISA HEV IgM ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of anti-hepatitis E virus (HEV) IgM in human serum or plasma. It is intended for professional use only and to be used as an aid in the diagnosis of infection with HEV.
TEST PRINCIPLE:
The RecombiLISA HEV IgM ELISA is a solid-phase enzyme-linked immunosorbent assay based on the principle of the IgM capture technique for the detection of antiHEV IgM in human serum or plasma. The RecombiLISA HEV IgM ELISA is composed of two key components: 1) Solid microwells pre-coated with polyclonal anti-human IgM antibody 2) Liquid conjugate composed of HEV antigen conjugated with horseradish peroxidase (HRP-HEV Conjugate) During the assay, the test specimen is first incubated in the coated microwells. AntiHEV IgM, if present in the specimen, binds to the antibody coated on the microwell surface. Any unbound specimen is then removed by a wash step. During a second incubation with the HRP-HEV Conjugate, the anti-HEV IgM antibody is absorbed on the microwell surface which binds to the HRP-HEV Conjugate, forming a conjugate complex. Unbound conjugate is then removed by washing. After addition of the TMB substrate, the presence of conjugate complex is shown by development of a blue color resulting from a reaction between the enzyme and substrate. The reaction is then quenched by addition of the Stop Solution, and the absorbance value for each microwell is determined using a spectrophotometer at 450/620-690 nm.
Clinical Performance:
A total of 400 specimens from susceptible subjects were tested by the RecombiLISA HEV IgM ELISA and by a Chinese State Drug Administration (SFDA) licensed reference EIA.
Clinical Performance:
Relative Sensitivity: 100%, Relative Specificity: 100%, Overall Agreement: 100%.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample Material : Serum
Storage : 2-8 C
Cat. No : E1015
Total T3 ELISA CE
The Total Triiodothyronine (T3) ELISA is a solid-phase enzyme-linked immunosorbent assay based on the principle of the competitive ELISA technique for quantitative determination of Triiodothyronine in human serum.
The three main kit components are:
1) Solid microwells pre-coated with anti-T3
2) T3 Calibrators
3) Liquid T3 Enzyme Conjugate Mixture comprised of T3 labelled with horseradish peroxidase (T3-HRP)
Product Features:
Analytical Sensitivity: 173 ng/mL at 2-SD
Specificity: No cross-reactivity or interference with
d-Thyroxine 10 aµg/mL
d-Triiodothyronine 100 aµg/mL
Iodotyrosine 100 aµg/mL
Diiodotyrosine 100 aµg/mL
TBG 50 aµg/mL
Human Albumin 50 aµg/mL
Phenylbutazone 25 aµg/mL
Phenytoin 50 aµg/mL
ASA 500 aµg/mL
Acetaminophen 500 aµg/mL
Accuracy: correlation coefficient 0.99 with a reference method
Intra Assay Precision: CV a?¤ 7.5%
Inter Assay Precision: CV a?¤ 10.76%
Product Specification :
Anti-T3 Ab Coated Microwells
Total T3 Calibrators:
C1 (0 ng/mL)
C2 (0.5 ng/mL)
C3 (1.0 ng/mL)
C4 (2.0 ng/mL)
C5 (4.0 ng/mL)
C6 (8.0 ng/mL)
Total T3 Assay Control
Total T3 Enzyme Concentrate
Enzyme Buffer
Wash Buffer Concentrate
TMB Substrate
Stop Solution
Product Insert
Product Details:
Brand : Thermo Fisher
Model Name/Number : 7500 Fast
Usage/Application : Virus Test Especially Covid-19
Type : Real-Time PCR System
Feature : Simple Intuitive Software
Format : Convenient 96-Eell Format
Peak Block Ramp : 5.5 C/s
Run Time : 36 min
Dynamic Range : 9 Logs Of Linear Dynamic Range
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample ; Serum
Storage : 2-8 C
Cat No : E1030
The RecombiLISA TSH ELISA is a solid phase enzyme linked immunosorbent assay for the quantitative determination of the levels of Thyroid Stimulating Hormone (TSH) in human serum.
The RecombiLISA TSH ELISA is intended for professional use as an aid in the diagnosis of thyroid dysfunction. TSH values should not be the only factor in the determination of thyroid status, and all other available clinical and epidemiological information should be considered for an accurate diagnosis.
Recommended for use:
Any person presenting with signs or symptoms of hypo or hyperthyroidism
Any person presenting with an enlarged thyroid gland (goiter)
Pregnant women for first trimester screening
Any person requiring regular monitoring of treatment
Normally, thyroid function is first assessed by detection of TSH levels in the blood.
The monoclonal anti-TSH antibody coated on the surface of the microwells specifically recognizes the junction between the �± and �² subunits. The HRP-conjugated monoclonal anti-TSH antibody detects the �² subunit only.
Combining the measurement of TSH with the thyroid hormones (T3/T4) can provide more information for the determination of thyroid status.
Product Features :
Sensitivity: Detects TSH levels as low as 0.035 �µIU/mL
Specificity: No cross reactivity detected with related hormones: FSH, LH and hCG
Linearity: 1:128 dilution on 36 IU/mL sample
Precision: intra assay precision: CV 7.5%; inter assay precision: CV 8.0 %
Accuracy: R2= 0.986 against Roche TSH Chemiluminescence Immunoassay
Hook effect: No hook effect up to 8000 IU/mL
Interference: not affected by Hemoglobin 500mg/dL, Diltiazem 15uM, Bilirubin 20 mg/dL, Erythromycin 81.6uM, Triglycerides 3g/dL, Verapamil 4.4uM, HAMA 52.5ng/mL, T3 100ng/mL, RF 215IU/mL, T4 100ug/dL, Acetaminophen 1324uM
Calibration: Human TSH WHO 3rd International Standards (81/565 NIBSC)
Calibrators: 0, 0.5, 2.0, 5.0, 10, 20, 40 �µIU/mL in biological matrix
Shelf life: 18 months
Assay time: 80 minutes.
Product Specifications:
Anti-TSH Ab coated microwells
TSH standard S1
TSH standard S2
TSH standard S3
TSH standard S4
TSH standard S5
TSH standard S6
TSH standard S7
HRP-anti-TSH conjugates
TMB substrate
Wash buffer (30X concentrate)
Stop solution
ELISA working sheet
Product insert
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum or plasma
Storage : 2-8 C
Cat No : E0330
The RecombiLISA Leptospira IgM ELISA Kit is an indirect, solid phase enzyme-linked immunosorbent assay. The two main kit components are:
1) A 96 breakable well plate with the solid microwells pre-coated with L. interrogans antigen.
2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horseradish peroxidase (HRP-anti-human IgM conjugates).
This test is intended to be used for the qualitative detection of IgM anti-Leptospira interrogans (L. interrogans) in human serum or plasma. It is intended to be used by professionals as an aid in the diagnosis of acute infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers.
Recommended for use:
Any person presenting with clinical signs or symptoms consistent with acute infection with interrogansincluding: high fever, headache, chills, muscle aches, vomiting, jaundice, red eyes, abdominal pain, diarrhea, skin rash
After exposure to a known contaminated source
Product Features :
Sensitivity: 86.7%
Specificity: 96.8%
Cross Reactivity: No false positive results were observed on specimens from Dengue, Malaria, Typhi, ANA, HAMA, RF, HIV, HBsAg, HCV, Syphilis, pylori
Interference: No interference was seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 1.3 %;Heparin: 3,000 U/L; Creatinine: 5 mmol/L; Bilirubin: 10 mg/dL; EDTA: 3.4 �µmol/L
Shelf life: 12 months
Open vial stability: 8 weeks at 2-8 C, or until the expiration date
Kit Components :
Microwells coated with recombinant L. interrogans antigens
Lepto IgM positive control
Lepto IgM negative control
Sample diluent
HRP anti-human IgM conjugate
Wash buffer (30 x concentrate)
TMB substrate A
TMB substrate B
Stop solution
ELISA Working Sheet
Product insert
Product Details:
Number of Reactions(Preps)/Kit : 50T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Country of Origin : Made in India
STANDARD E Dengue NS1 Ag ELISA analyzes Dengue NS1 antigens in serum and plasma using enzyme linked immunosorbent assay.
Simple and easy to use: All necessary reagents included in the kit
Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)
Able to detect antigens in samples with high sensitivity and specificity
Performance
Sensitivity : 91.4% (181/198) / Specificity : 98.2% (221/225)
Product Details:
Brand : CTK BioTech
Samples : Serum
Storage : 2-8 C
Size : 96 Well
Cat. No. : E1025
The Total Thyroxine (T4) ELISA is a solid-phase enzyme-linked immunosorbent assay based on the principle of the competitive ELISA technique for quantitative determination of Thyroxine in human serum.
The three main kit components are:
1) Solid microwells pre-coated with anti-T4
2) T4 Calibrators
3) Liquid T4 Enzyme Conjugate Mixture comprised of T4 labelled with horseradish peroxidase (T4-HRP)
Product Freature:
Analytical Sensitivity: 176 aµg/dL at 2-SD
Specificity: No cross-reactivity or interference with
d-Thyroxine 10 aµg/mL
d-Triiodothyronine 100 aµg/mL
Iodotyrosine 100 aµg/mL
Diiodotyrosine 100 aµg/mL
TBG 50 aµg/mL
Human Albumin 50 aµg/mL
Phenylbutazone 25 aµg/mL
Phenytoin 50 aµg/mL
ASA 500 aµg/mL
Acetaminophen 500 aµg/mL
Accuracy: correlation coefficient 0.98 with a reference method
Intra Assay Precision: CV a?¤ 5.9%
Inter Assay Precision: CV a?¤ 7.6%
Product Specification :
Anti-T4 Ab Coated Microwells
Total T4 Calibrators:
C1 (0 ng/mL)
C2 (2.0 ng/mL)
C3 (5.0 ng/mL)
C4 (10.0 ng/mL)
C5 (15.0 ng/mL)
C6 (25.0 ng/mL)
Total T4 Assay Control
Total T4 Enzyme Concentrate
Enzyme Buffer
Wash Buffer Concentrate
TMB Substrate
Stop Solution
Product Insert
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Bran : CTK BioTech
Sample Material : serum or plasma
Storage : 2-8 C
Cat. No : AE0310
The Dengue IgM ELISA Kit is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of IgM anti-dengue viruses (DEN1, 2, 3, 4) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with dengue viruses.
TEST PRINCIPLE:
The Dengue IgM ELISA Kit is a solid-phase enzyme-linked immunosorbent assay based on the principle of the capture immunoassay methodology for the detection of IgM anti-dengue virus in human serum or plasma. The Dengue IgM ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with mouse monoclonal anti-human IgM antibody. 2) Conjugate working solution composed of dengue antigen and HRP-anti-dengue conjugates. During the assay, the test specimen is first incubated in the coated microwell. IgM antidengue, if present in the specimen, binds to the anti-human IgM antibodies coated on the microwell surface, and any unbound specimen is then removed by a wash step. During a second incubation with HRP-anti-dengue conjugate working solution, the IgM anti-dengue absorbed on the surface of microwell binds to the conjugate through dengue antigen, forming a conjugate complex. Unbound conjugates are then removed by washing. After addition of the TMB substrate, the presence of the conjugate complex is shown by development of a blue color resulting from a reaction between the enzyme and substrate. This reaction is then quenched by addition of the Stop Solution, and the absorbance value for each microwell is determined using a spectrophotometer at 450/620-690 nm.
Accuracy of Detection :
A total of 491 patient specimens were collected from susceptible subjects and tested by Dengue IgM ELISA Kit and by a commercial leading brand EIA.
Relative Sensitivity: 90.8% (95% Confidence Interval = 85.5 - 94.4%) Relative Specificity: 95.9% (93.1 - 97.7%) Overall Agreement: 94.1% (91.6 - 95.9%).
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum or plasma
Storage : 2 - 8 C
Cat No : AE0610
INTENDED USE:
The TRUSTwell Syphilis Ab kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of antibodies (IgG, IgM, IgA) against Treponema pallidum (Tp) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with Tp. Any reactive specimen with the TRUSTwell Syphilis Ab ELISA Test must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
The TRUSTwell Syphilis Ab ELISA Test is a solid phase enzyme linked immunosorbent assay based on the principle of the double antigen sandwich technique for the detection of antibodies to Tp in human serum or plasma. The TRUSTwell Syphilis Ab ELISA Test is composed of two key components: 1) Solid microwells pre-coated with recombinant Tp antigens; 2) Liquid conjugates composed of recombinant Tp antigens conjugated with horseradish peroxidase (HRP-Tp conjugates).
During the assay, the test specimen and HRP-Tp conjugates are incubated simultaneously with the coated microwells. Antibodies (IgG, IgM, or IgA) to Tp if present in the specimen, reacts to the Tp antigens coated on the microwell surface as well as the HRP-Tp conjugates, forming sandwich complex conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 1132 patient specimens from susceptible subjects were tested by the TRUSTwell Syphilis Ab ELISA Kit.
Relative Sensitivity:100%,
Relative Specificity:99.8%,
Overall Agreement:99.82%.
Product Details:
Number of Reactions(Preps)/Kit 96 Wells
Brand CTK BioTech
Sample serum or plasma
Storage 2 - 8 C
Cat No : AE0510
INTENDED USE:
The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of IgG to Hepatitis C virus (HCV) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HCV. Any reactive specimen with the TRUSTwell HCV IgG ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the indirect EIA technique for the detection of the IgG to HCV in human serum or plasma. The TRUSTwell HCV IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with recombinant HCV antigens; 2) Liquid conjugates composed of mouse anti-human IgG conjugated with horse radish peroxidase (HRP-anti Human IgG conjugates). During the assay, the test specimen is first incubated with the coated microwells. The IgG anti HCV, if present in the specimen, bind to the antigens coated on the microwell surface. In the second incubation with the HRP-anti-human IgG conjugates, the IgG antibodies absorbed on the surface of microwell react to the HRP-anti-human IgG conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 1108 patient specimens from susceptible subjects were tested by the TRUSTwell HCV IgG ELISA Kit.
Relative Sensitivity:100%,
Relative Specificity:99.81%,
Overall Agreement:99.82%.
Product Details:
Number of Reactions(Preps)/Kit 25T
Brand Abbott
Time To Result 15 Min
Result Time (Rapid Kits) 15 min
Sample Type Blood
Cat. No 05FK80
Bioline MALARIA Ag P.f/P.vTEST FOR PLASMODIUM FALCIPARUM AND PLASMODIUM VIVAX
The Bioline Malaria Ag P.f/P.v test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 (HRP-2) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.
BENEFITS
Differential diagnosis between Plasmodium falciparum and
Plasmodium vivax
Useful for the region where P.v and P.f are both dominant
Differentiate P.f mono infection from P.f/P.v co-infection
WHO prequalified
Specimen : Whole blood (5 l)
Time to result : 15 minutes (up to 30 minutes)
1-40C for 24 months
Performance:
P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5%
P.v (pLDH) : Sensitivity 95.5 %, Specificity 99.5%
Product Details:
Brand Abbott
Usage/Application Hospital
Results 30 min
Test Type Rapid Test
shelf life 24 months
Cat. No 05FK63I01
Bioline MALARIA Ag P.f/PanTEST FOR P.FALCIPARUM AND OTHER PLASMODIUM SPECIES
The Bioline Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 HRP2 antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood.
Benefits:
Distinguish P.f infection from other species (P.v, P.m or P.o)
Useful in regions where all malaria species are circulating
WHO prequalified
Specimen : Whole blood (5 l)
Time to result : 15 minutes (up to 30 minutes)
1-40C for 24 months
Performance:
- P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5 %
- Pan (pLDH) : Sensitivity 95.5 %, Specificity 99.5 %
Product Details:
Number of Reactions(Preps)/Kit 30T
Brand Abbott
ICMR Approved Yes
Result Time (Rapid Kits) 20Min
Self Time 24 months
Cat. No 03FK10CE
Bioline HIV 1/2 3.0HIV 1/2 ANTIBODY TEST
Bioline HIV 1/2 3.0 test is an immunochromatographic assay for the differential and qualitative detection of all isotypes (IgG, IgM, IgA) antibodies specific to HIV-1 including subtype O and HIV-2 simultaneously, in human serum, plasma or whole blood.
Benefits:
Highly sensitive even to IgM during early infection stage
Differentiated test result between HIV type I and II by clear band formation (3-lines)
Specimen : Serum, Plasma (10l), or Whole blood (20 l)
24 months at 1-30
Specification:
Sensitivity : 100%
Specificity : 99.8%
Product Details:
Number of Reactions(Preps)/Kit 10
Brand Abbott
Result Time (Rapid Kits) 15 mins
Results 15 - 20 min
Cat. No 11FK45
Bioline DENGUE DUO (DENGUE NS1 Ag + IgG/IgM)TEST FOR DENGUE INFECTION
The Bioline Dengue Duo kit is a rapid, in-vitro immunochromatographic assay designed to detect both dengue virus NS1 antigen and IgG/IgM antibodies against dengue virus in human serum, plasma or whole blood. Bioline Dengue Duo rapid test contains two test devices (left side; Dengue NS1 Ag test, right side; Dengue IgG/IgM test).
Benefits:
Simultaneous detection of Dengue Ag & Ab
Cover all clinical stages from acute phase to convalescence phase of infection
Fast test result : 15~20 min
Convenient storage condition : 1~30C
Specification:
Performance
- Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM)
- Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM)
Product Details:
Number of Reactions(Preps)/Kit 100T
Brand Abbott
Usage/Application Hospital
Result Time (Rapid Kits) 30 Min
Sample Type Blood
CAT No : 7D2343
DETERMINE HIV-1/2
Rapid HIV screening tested by billions and proven by practice. Determine HIV-1/2 test detects a wide variety of HIV subtypes (refer to IFU). This versatility helps healthcare workers across the world diagnose individual infection, monitor HIV prevalence, and enable fast linkage to care.
With its simple one-step procedure for serum/plasma or two-step procedure for whole blood, the Determine HIV-1/2 is quick and easy to use, delivering clear, dependable results in just 15 minutes.
PRODUCT INFORMATION
Method: Lateral flow
Time to results: 15 minutes
Storage conditions: 2-30C (36-86F)
Shelf-life: 18 months
Sample types: Serum/Plasma/Whole blood
SPECIFICITY
Overall 99.75%
Product Details:
Number of Reactions(Preps)/Kit 25T
Brand Premier
Result Time (Rapid Kits) 15 - 20
Certified WHO Aproved
CAT No : I20FRC25
First Response HIV 1+2 / Syphilis Combo Card Test is intended for use by healthcare professionals and trained user. It is a rapid, qualitative screening, in vitro diagnostic test for the detection of antibodies (IgG & IgM) specific to HIV (type 1 & 2) and Treponema pallidum in human serum, plasma or venous and capillary whole blood.
Sensitivity: 100%
Specificity: 100%
Storage at 4-30 C
Rapid Result time - 15 to 25 Minutes.
Detects antibodies specific to HIV and Syphilis.
Specimen Type Whole blood, Serum, Plasma
Shelf Life: 24 Months
Product Details:
Number of Reactions(Preps)/Kit 30 T
Brand Premier
Result Time (Rapid Kits) 15 min
CAT No; PI05FRC30
Certified WHO Aproved
First Response HIV 1-2.O Card Test (Ver. 2.0) is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative screening, in vitro diagnostic test for detection of antibodies specific to HIV-1 (including Group O) and HIV-2 in human serum, plasma or venous and capillary whole blood.
Product specifications :
Sensitivity: 100%
Specificity: 100%
Detects antibodies specific to HIV-1 (including Group O) and HIV-2.
Rapid Result time - 15 to 25 Minutes.
Storage at 4-30 C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 25 Min
Certified WHO Approved
CAT No; PI08FRC25
First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
100% - Specificity
100% - Sensitivity
Detects antibodies specific to Treponema pallidum
Rapid Result time within 20-25 Minutes
Storage at 4-30 C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
Product Details:
Number of Reactions(Preps)/Kit 30T
Brand Abbott
Usage/Application Hospital
Result Time (Rapid Kits) 15 mins
Cat. No 02FK10I30
Bioline HCVHEPATITIS C VIRUS TEST
When speed matters, choosing a highly sensitive rapid HCV test with a safe fingerstick procedure can make a difference.
In the global effort to eliminating viral hepatitis, fast detection in a wide range of settings and linkage to care are critical for achieving successful outcomes
Bioline HCV test is a immunochromatographic rapid test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood.
Specification:
Specimen :
- Serum, Plasma, Whole Blood (10 �¼l) for 02FK10, 02FK10CE, 02FK16, 02FK16CE, 02FK17, 02FK17CE, 02FK11
- Serum or Plasma (10 l) for 02FK12
Sensitivity :
- 99.3% (95% CI: 97.9 - 99.8%) for 02FK10CE, 02FK16CE, 02FK17CE
- 99.3% (95% CI: 96.1 - 99.9%) for 02FK10, 02FK16, 02FK17
- 100 % (97.6 - 100 %) for 02FK11, 02FK12
Specificity :
- 100% (95% CI: 99.7 - 100 %) for 02FK10CE, 02FK16CE, 02FK17CE
- 98.1% (95% CI: 94.5 - 99.4%) for 02FK10, 02FK16, 02FK17
- 99.4 % (98.7 - 99.7 %) for 02FK11, 02FK12
Shelf life: 24 months at 1-30C
Qualitative immunochromatographic assay
Recombinant HCV core, NS3, NS4, NS5 Ag used as capture materials
Product Details:
Brand Abon
No of test per kit 100
HCG Urine Pregnancy Test measures the presence of the pregnancy hormone (HCG) in your urine for the early detection of pregnancy.
Product Details:
Number of Reactions(Preps)/Kit 100
Brand Abbott
Usage/Application Hospital
By detecting early markers of Hepatitis B infection, the Alere Determine HBsAg helps to diagnose acute infection and confirm chronic infection - allowing healthcare professionals to initiate prompt and appropriate follow-up action for infected patients.
Rapid in-vitro qualitative ICT for detection of HBsAg
Sample Type: Serum/Plasma/Whole Blood
Sample Volume: 50µL
Early marker of infection- helps in diagnosis
Facilitates appropriate follow-up of infected patients
Collection can be done by fingerprick or venipuncture
Clear, dependable results in 15 minutes
Quick Reference Card for the detection of HBsAg in
human serum/plasma or whole blood
Ordering Information
Cat No. Description Type Pack size
7D2543 Alere Determine HBsAg Strip 100 Tests
Product Details:
Brand : Abbott
Package type : Microplate
Pack size : 96wells/Kit
Specimen : Serum
Description : Dengue IgM Capture ELISA
Cat.No. : 11EK20
Bioline DENGUE IgM CAPTURE ELISA
In primary infection with the dengue virus, IgM antibody becomes detectable about five days after disease onset, when circulating virus declines in the blood. IgM level rises quickly to peak at about 2 weeks and declines to undetectable levels after 2-3 months In secondary infections, IgM response is typically at a lower level compared to that in a primary infection. Early diagnosis of dengue infection (especially in primary dengue infection) High accuracy with all dengue serotypes (DEN1,2,3, and 4) Simple and easy to use: All necessary reagents included in the kit Shelf life and storage temperature: 18 months from the date of manufacturing at 2-8 C Included in the WHO Bulk Procurement Scheme Performance: Sensitivity 96.4 %, Specificity 98.9 % (vs. HAI test).
Product Details:
Brand ACON
Size 50 Test
Cat. No ACKCRDPC3
Product Description :
Acon Pregnancy Test Strip (HCG) is a one step pregnancy test kit containing test strip. The urine sample is to be collected in a clean, dry container and almost half test strip should be dropped inside the container. The first urine sample of the day is preferred. The pack insert should be thoroughly read before use. To know how to use and read test results. Acon pregnancy test strip detects pregnancy in just 5 minutes.
Features & Specifications :
One Step Pregnancy Test Strip
Easy to Use
Quick Result in just 5 minutes
Pack of 3 Test Strips
For more info, please refer the product pack for usage instructions
Product Details:
Number of Reactions(Preps)/Kit 20T
Brand Abbott
Result Time (Rapid Kits) 10 -20 min
Sample Material Fecal
Cat. No 14FK10
Bioline* Rotavirus test is an immunochromatographic assay for the detection of Group A rotavirus in human fecal specimens. The test utilizes two kinds of antibody in a solid phase sandwitch immunochromatography to detect group specific proteins, including the major inner capsid protein, present in Group A rotaviruses.
Early detection of rotavirus antigen group A all serotype
Shelf life and storage temperature: 18 months from the date of manufacturing at1-30 C
Performance: Sensitivity : 94 %, Specificity 98.3 % (vs. RT-PCR)
Product Details:
Number of Reactions(Preps)/Kit : 25T
Brand : Abbott
Usage/Application : Hospital
Results : 15 min
Sample type : Blood
Cat. No : 08FK50
Bioline TB Ag MPT64TEST TO DISCRIMINATE BETWEEN M. TUBERCULOSIS COMPLEX AND MOTT(NTM)
Bioline TB Ag MPT64 is a immunochromatographic identification test for the M. Tuberculosis complex. Biochemical, immunological and molecular biological characterization of Mycobacterium tuberculosis has led to the identification of several antigens which may be useful in the development of improved diagnostic methods in order to discriminate between the M. tuberculosis complex and mycobacteria other than M. tuberculosis (MOTT bacilli). M. tuberculosis has been known to secrete more than 33 different proteins. One of the predominant proteins, MPT64 was found in the culture fluid of only strains of the M. tuberculosis complex.
Performance
Sensitivity: 98.6 %, Specificity: 100 % (vs. Isolated culture method)
Simple, rapid assay using mouse monoclonal anti-MPT64
Rapid discrimination between the M. tuberculosis complex and other mycobacterium
Identification of the M. tuberculosis complex in combination with culture systems based on liquid media
Specimen : Solid cultures (colony, condensation fluid) or liquid cultures
Time to result : 15 minutes
1-30 C for 18 months
Product Details:
Number of Reactions(Preps)/Ki : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10-15 mins
CAT No : RK055-25
STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx.
The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI.
Validated by ICMR & AIIMS
Sensitivity of 84.38 % & Specificity of 100%
Sample Type- Human Nasopharyngeal swab (No other sample recommended)
Results in 15-30 mins
Product Details:
Brand ; Genbody
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Packaging Size : 25 Test Kits /Box
CAT No : COVAG025
GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
Product Details:
Number of Reactions(Preps)/Kit :96
Brand : Abbott
ICMR Approved ; Yes
Test Method : (SARS-CoV-2) RT-PCR
Cat. No : 09N77-095
The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria
Product Details:
Brand : SD Biosensor
Test Method : Antigen Test
Pack Type : 25
Cat. No : RK081-25
Product Details:
Number of Reactions(Preps)/Kit : 250 Rxns Per Box
Brand : HiMedia
Storage Temperature : 15 DegreeC to 25 DegreeC
Elution Volume : 50 to 80 microliter
Cat. No : MB615
Description
This kit carries out efficient extraction of viral RNA from wide range of viral strains like Dengue, Chikungunya and viral pathogen of animals. Sample is first lysed under the highly denaturing conditions provided by Buffer HRL to inactivate RNases and to
Used For
HiPur Viral RNA Miniprep Purification Kit can be used for isolation of viral RNA from a wide variety of viruses, but performance may vary depending on virus type
Product Details:
Number of Reactions(Preps)/Kit : 100 T
Brand : RADI
Storage Temperature : -25 C to -15 C
Sample Material : RNA extracted from Nasopharyngeal and/or Oropharyngeal swab
Target : S gene, RdRP gene
Cat. No : RV008
The RADI COVID-19 Detection Kit is intended for the presumptive qualitative detection of specific nucleic acid sequences from the genome of the SARS-CoV-2 S gene and RdRP gene from the upper respiratory specimens such as Nasopharyngeal swab, Oropharyngeal swab.
Product Details:
Brand : RADI
Storage Temperature : -25 to -15 C
Sample Material : Human Skin Lesion, Crust or swab
Cat. No : RV015
Detection : Probe Based
Target : FAM,HEX and Cy5 gene
RayBiotech Monkeypox Virus (MPXV) PCR Nucleic Acid Detection Kit is a real-time PCR assay for the detection of MPXV DNA in a liquid sample. It uses a fluorescent probe with specific primer sets to detect the J2R gene specific for the genome of MPXV.
Product Details:
Brand : TRIVITRON
Signal Signifies : Orthopox group, Monkeypox & Smallpox Virus
Test time : 1 hour
Compatible : Please visit Brochure
Storage : : - 20 between 2 C
Cat No : DVZ-30052 & DVZ-30053
Trivitron's Monkeypox Real-Time PCR kit is a multiplex RT-PCR Kit for the rapid qualitative in vitro detection of Monkeypox and Smallpox virus. The assay Kit can distinguish between smallpox and Monkeypox virus.
FEATURES
The kit is based upon Single Step RT-PCR, where both Reverse Transcription by Reverse Transcriptase and PCR by Taq Polymerase takes place in single tube.
Monkey Pox virus kit is developed using four colour fluorescence technology.
A signal from different channel signifies, presence of Orthopox group, Monkeypox & Smallpox virus respectively in the sample.
Assay validation through the additional human internal control gene.
Compatible with both dry swabs as well as sample swabs placed in VTM.
A total turnaround time of 1 hour
TECHNICAL SPECIFICATIONS
The kit has been validated on QuantStudio-5/3 and Bio-Rad CFX96, 384 and can also be used on applied Biosystems 7300/7500, Roche Diagnostics LightCycler 96/480, Qiagen Rotor-Gene Q, etc. (Instrument should be calibrated, maintained and used as per manufacturer recommendation).
Sample type: Swab samples collected from surface and/or exudate, roofs from more than one lesion, or lesion crusts.
Storage: -20 + 2 C
Product Details:
Number of Reactions(Preps)/Kit : 1000
Brand ; Thermofisher
Test Method : (SARS-CoV-2) RT-PCR
Sample Type : Nasal & Oral Swab
The Applied Biosystems TaqPath COVID-19 Combo Kit is a fast, highly sensitive multiplex diagnostic solution that contains the assays and controls needed for the real-time PCR detection of RNA from the SARS-CoV-2 virus.
Features of the newly developed multiplex diagnostic kit:
A complete workflow from viral RNA extraction from up to 94 specimens and genetic analysis using real-time PCR to diagnostic report generation in under 4 hours
Targeted specificity to 100% of currently available complete genomes for SARS-CoV-2
Assay targets spike (S) protein and nucleocapsid (N) protein regions having higher specificity and exhibiting lower risk for mutation
COVID-19 Interpretive Software, which automatically converts genetic analysis data into diagnosis, helping reduce risk of user interpretation error
The TaqPath COVID-19 Combo Kit consists of both the TaqPath RT-PCR COVID-19 Kit and the TaqPath COVID-19 Control Kit for simplified ordering. The kit can be used by clinical and public health laboratories to quickly evaluate up to 94 patient specimens in under 3 hours. The kit is approved for use with RNA extracted from nasopharyngeal swabs, nasopharyngeal aspirate (nasal aspirate), and bronchoalveolar lavage (BAL) from patients at risk of exposure to the SARS-CoV-2 virus or with signs and symptoms of COVID-19 (see product label for Intended Use Statement and product information). The TaqPath COVID-19 Combo Kit is a single, high-throughput (1,000 reactions) kit and is recommended for use with either the Applied Biosystems 7500 Fast Dx Real-Time PCR System or the 7500 Fast Real-Time PCR System (RUO version) and the associated Applied Biosystems COVID-19 Interpretive Software.
The TaqPath COVID-19 Combo Kit includes the following components:
TaqPath RT-PCR COVID-19 Kit
COVID-19 real-time PCR assay multiplexâ??multiplexed assays that contain three primer/probe sets specific to different SARS-CoV-2 genomic regions and primers/probes for bacteriophage MS2
MS2 phage controlâ??internal process control for nucleic acid extraction
TaqPath COVID-19 Controlâ??RNA control that contains targets specific to the SARS-CoV-2 genomic regions targeted by the assays
TaqPath COVID-19 Control Dilution Buffer dilution buffer for the IVT RNA control as defined in the IFU (information for use)
Product Details:
Number of Reactions(Preps)/Kit : 24 Test
Brand : Abbott
Result Time (Rapid Kits : 13 Min
Cat. No : 190-000
TECHNOLOGY ID NOW utilizes proven isothermal molecular technology in an intuitive platform, providing the fastest molecular results in the market.
EASE OF USE Simplifying the test process Designed for near-patient testing in a variety of environments* Assay kit contains necessary components for testing, including: 24 tests Swabs for sample collection Positive control swab Room-temperature storage eliminates need for refrigeration
Product Details:
Brand : SD Biosensor
Result Time (Rapid Kits) : 15-30 min
Packaging Size : 25 Test Kits/Box
CAT No : Q-NCOV-01G
STANDARD Q COVID-19 Antigen Test kit is chromatographic immunoassay for the qualitative detection of SARS CoV 2 nucleocapsid antigen present in human nasal sample.
Product Details:
Brand : Abbott
Model Name/Number : ID Now
Communication Interface : Bluetooth, USB
Scan time : 13 minutes
Usage : Molecular COVID-19 Test
Cat. No : NAT-000
ID NOW COVID-19SARS-COV-2 IN 13 MINUTES OR LESS*
The ID NOW platform combines the benefits of speed and accuracy for the fastest molecular results in the market.
The ID NOW COVID-19 test returns positive results in 13 minutes or less to enable immediate clinical decisions during the first patient visit.
The easy to use ID NOW platform is designed for near-patient, point-of-care use in a variety of healthcare settings.
Product Details:
Tidal Volume 0-2000ml
Brand Philips
Model Name/Number EV300
Respiratory Rate 0-90 BPM
Inspiratory/Expiratory (I:E) Ratio 9.9:1 to 1:9.9
Trilogy EV 300 Philips Trilogy Ventilator provides both invasive mechanical ventilation (IMV) and non-invasive ventilation (NIV) and a range of monitoring capabilities for patients at or above 2.5 kg. Therefore, patients can be treated with a single device throughout their hospital stay, regardless of changing conditions. Trilogy EV300 offers comprehensive, advanced NIV auto-titrating therapy modes include AVAPS-AE, and IMV is available with single- and dual-limb circuits.
A complete connected solution
Trilogy EV300 communicates: Transmits and translates data from the device to the hospital EPR via patient monitoring or middleware systems. Key features include:
Surveillance: The ability to remotely view ventilator settings, performance, and alarms from locations such as central monitoring stations.
Event review: The ability to look at changes in a patientâ??s condition and response to various therapies, alarms and other pertinent events.
Health Level 7 (HL7) interface: Used to export ventilator data to the patient chart and pull in patient demographics for patient identification.
Simplified workflow
Trilogy EV300 ventilators feature an easy-to-use 8-inch touchscreen and intuitive menu navigation. On-screen help and alarm guidance aid user proficiency making it easy for clinicians to feel confident.
Ultimate Portability
Trilogy EV300 has a 15-hour battery life* with an internal and detachable battery. Additionally, the hot swappable detachable battery provides uninterrupted power.
Easy to service
Trilogy EV300 only requires preventative maintenance once every year, and can be serviced and repaired onsite by biomedical engineers or Philips trained field engineers, reducing the device downtime and lifetime running costs.
Enhancing patient comfort
Designed to make breathing more comfortable, the Digital Auto-Trak setting provides an enhanced triggering response for patients with minimal respiratory effort while lessening the need for manual adjustments.
There are three types of Vacuum Unit. 1.600 ml , 2. 1000 ml and 2000 mi.
Sysmex 3-part XP 300 Differential Automated Hematology Analyzers
Product Details:
Automation Fully Automatic
Instrument Name Haematology Analyzer
Brand Sysmex
Differential Type 3-Part
Sample Volume Whole blood mode: 50 Microliter
Parameters Whole blood mode: 8 parameters with 3-part Differential WBC; RBC; HGB; HCT; MCV; MCH; MCHC; PLT;
Sysmex provides two 3-part WBC Differential automated hematology analyzers*. These systems are ideally suited for physician office laboratories, clinics and small hospitals that perform moderately complex testing. Built on reliable Sysmex technology, the 3-part differential analyzers feature simple operation, minimal maintenance and compact, space-saving designs.
With its simplified operation, the XP-300 is ideal for clinics, satellite laboratories and research testing. The XP-300 provides a CBC with 8 parameters, including a 3-part WBC Differential with an absolute neutrophil count (ANC).
Product Details:
Instrument Name Biochemistry Analyzer
Usage/Application Hospital
Brand abbott
Type SD Urometer 120 and 720
S.No Test Strip
1 SD Urocolor 10 - 100T
Urine Chemistry analyser
Based on reflectance photometer.
3.2 inch TFT color display having resolution(320*240 )
Auto calibration with power on.
Enhancing work efficiency by flexible options between quick & normal mode.
Enhancing user-convenience even for left hander by ergonomics design.
4~11 parameter testing available.
Maximum 300test/hr.
Memory- 100000 test results.
Easy to input multiple ID by key board, PC and barcode reader.
Interface: RS 232c and USB
LABROID Bacteriological incubator is used for the incubation of biological products under controlled conditions.
These units are designed to satisfy a wide array of needs of any Research Laboratory, Pharmaceutical Lab, Chemical Lab, Clinical Lab, Microbiological Determination, Pharmaceutical Stability Assays, Food Processing, QC etc for cultivation of bacteria and for facilitating biological test etc.
Construction: Double walled: Outer wall of Mild steel powder coated and inner chamber of Stainless steel 304.
Temperature Range: + 5�??C above ambient to 60�??C. (On Request Up to & 70�??C Available)
Accuracy: �?�± 0.5�??C. (On Request �?�±0. 2�??C)
Resolution: 0.1�??C
Door: Main Door with Magnetic gasket with lock and Key.
Trays: Adjustable-Stainless Steel.
Sub Doors:Inner Sub Doors Made of Acrylic
Power Supply: Single phase 230V, 50Hz, AC mains.
LABROID Laboratory refrigerators are used to cool samples or specimens for preservation. Where high Degree of Accuracy is required.
LABROID Laboratory Refrigerators provide an ideal cold storage environment for the preservation of vaccines, medicines, reagents, specimens etc. For consistent, reliable protection, storage & preservation of valuable medical products at a safe + 2 to +8 Deg C.
Construction: Double walled: Outer wall of Mild steel powder coated (OR) Stainless Steel and inner chamber of Stainlesssteel 304.
Controller: Microprocessor based controller with LED Display, PID Digital Temperature Indicator cum Controller, withdual display of set Value and Process value for precise control of temperature.
Temperature Range: Adjustable temperature range from 2Ã??C to 8Ã??C with an increment of 0.1Ã??C.
Accuracy: 0.5 C.
Resolution: 0. C
Fan: Air circulation provided to maintain temperature uniformity.
Door: Main Door with Magnetic gasket with lock and Key. (OPTIONAL SEE THROUGH GLASS DOOR -ON REQUEST)
Trays: Adjustable-Stainless Steel.
Power Supply: Single phase 230V, 50Hz, AC mains.
Construction- Outer Wall Mild Steel and Inner Stainless Steel or Fully Stainless Steel.
Hepa Filter Size- 610/915/1220/1830 x 610 x 75 (0.3 Micron)
Pre Filter- 500/600/800 x 400 x 50 mm (10 Micron)
Door- 5 mm Acrylic Foldable/Sliding Door
Illumination- 20/40 W LED Light- 1 No
UV Lamb- 15/30 W- 1 No
Power Socket- Yes- 1/2 No (230 V/5A)
Pressure Gauge- Yes
Power- Single Phase 230V/50 Hz
Noise Level- 70 db +/- 5 db
Construction: Outer Mild Steel Powder coated and Inner Stainless Steel or Fully Stainless Steel.
Main HEPA Filter Size - 610 x 450 x 75, 915 x 450 x 75, 1220 x 450 x 75, 1830 x 450 x 75 mm HEPA (0.3 Micron)- 1 No
Pre Filter Size â?? 600 x 120 x 50, 900 x 120 x 50, 1200 x 120 x 50, 1800 x 120 x 50 mm (10 Micron)- 1 No
Exhaust HEPA Filter- 610 x 450 x 75, 915 x 450 x 75, 1220 x 450 x 75, 1830 x 450 x 75 mm HEPA (0.3 Micron)- 1 No
Door- 5mm, Poly Carbonate Door
Gas Supply- Gas cock
Switch- 3 Pin Socket â?? 1 No (230V/20A)
Noise Level- 65 +/- 5 db
Power Supply- 230v AC, 50Hz
Light- 20 /40 W LED Fitting- 1 No
UV Light- 15/30 W â?? 1 No
Pressure Gauge - Yes
Duct- Your Scope (6 inch Dia)
S. No Code Description Size in Feet
1 SDPBSS2 Dynamic Pass Box 2 x 2 x 2 Feet
2 SDPBSS3 Dynamic Pass Box 3 x 2 x 2 Feet
3 SSPBSS2 Static Pass Box 2 x 2 x 2 Feet
4 SSPBSS3 Static Pass Box 3 x 2 x 2 Feet
Construction- Fully Stainless Steel or Outer Mild Steel and Inner Stainless Steel
Note- Customization also available
Product Details:
Model Name/Number : FS-114
Brand : Wondfo
Temperature Control : Provide better reaction condition
Convenient : easy to carry
Portable : Small in size 7800mAh built-in battery
Finecare FIA Meter Plus SEThe analyzer is intended for use by healthcare professionals to improve the way to diagnosing and monitoring various conditions, including COVID-19, diabetes, renal injury, cardiovascular disease, pregnancy, inflammation, tumor, etc
Thermofisher Quantstudio 5 Real Time PCR System, 96 wells
Product Details:
Model Name/Number QuantStudio 5
Includes Desktop
Brand Thermofisher
Sample Capacity/Format 96 wells
Volume Thermal Block Sample 0.2ml
Block Format Non-Interchangeable
Display Type Touch Screen
Smaller foot print 27x50x40 cm
CAT No : A28139
Features:
Proven OptiFlex technology (6 decoupled channels/21 filter combinations with white LED) for trusted results
User account management, locked workflow, and Pause features for greater control of experiment data
Built-in software features to support compliance with 21 CFR Part 11 guidelines
Secure cloud-based software provides increased accessibility and storage options
Simplified instrument software with interactive touchscreen for greater ease of use
The Applied Biosystems QuantStudio 5 Real-Time PCR System for Human Identification with tower computer is the latest addition to our human identification (HID) real-time PCR family of products. This instrument is designed for both new and experienced users who need a simple, reliable, and affordable real-time PCR system that doesnâ??t require compromise on performance or quality. When used with our latest advances in quantification chemistry and HID Real-Time PCR Analysis Software, this system offers a sensitive, robust solution for forensic DNA quantification. It also helps prepare laboratories for future quantification technologies. With maximum dye versatility, this HID solution offers accurate, trusted results in a small benchtop footprint
Quantstudio 3 Real Time Pcr System, 0.2 mL, 96 wells
Product Details:
Brand Thermofisher
Model Name/Number QuantStudio 3
Sample Capacity/Format 96 wells
Volume Thermal Block Sample 0.2 mL
Weight 25 kg
CAT No : A28137
Features:
Simplified instrument software with interactive touchscreen for greater ease of use
Proven OptiFlex technology (4 coupled channels with white LED) for trusted results
Secure cloud-based software option provides increased accessibility and storage options
User account management, locked workflow, and Pause features for greater control of experiments
Product Details:
Brand arkray
Model Name/Number A1c
Sample Mode Whole Blood
Measuring Principle Boronate affinity
Power Supply AC100 V-240 V +-10 % 50/60 Hz
Weight Instrument: 0.7 kg Printer: 0.5 kg
Dimensions (W x D x H) W 205 x D 135 x H95 mm
Detection method Fluorescence quenching
Specifications:
Samples Whole blood (capillary and venous blood)
Measured items HbA1c
Measurement principle Boronate affinity
Detection method Fluorescence quenching
Measurement range NGSP : 4-15
Throughput 4 minutes per sample
Sample volume 4 L(whole blood)
Imprecision CV < 3 % at 7 % A1c (NGSP)
Measurement conditions 18-30 , 20-80 relative humidity
Memory capacity 7000 test results
Printer Thermal printer, 58mm thermal paper (Optional)
External output USB Port
Power supply AC100 V-240 V ±10 % 50/60 Hz
External dimensions W 205 x D 135 x H95 mm
Weight Instrument: 0.7 kg Printer: 0.5 kg
Warm up time 5-20 mins dependent upon external temp conditions
Product Details:
Instrument Name Biochemistry Analyzer
Brand Abbott
Usage/Application Hospital
Automation Semi Automatic
Assays Thyroid, Cardiac, Diabetes
Cat. No 1116681
Weight 3.4 Kg
Brand Abbott
Size 20 cm x 19 cm x 33 cm
Display Color Touch Display
Connectivity Connectivity Solutions That Support Poct1-A
Maintenance No Maintenance Needed
S.No Code Pima CD4 Cartridge
1 1116795 Afinion 2 Test Kit - Hb1Ac
2 1116787 Afinion 2 Test Kit - CRP
3 1116781 Afinion 2 Test Kit - ACR
4 1116801 Afinion 2 Test Kit - Lipid Panel
Improve the way you diagnose, monitor and manage your patients
The Afinion 2 Analyzer is a compact, rapid, multi-assay analyzer that provides valuable near patient testing at the point-of-care.
With the Afinion System theres no need to send patients to the lab or spend time tracking down their results. That way you can keep your focus where it belongs on the patient.
Product Details:
Operation Mode Fully Automatic
Number Of Chambers 2
Sample Mode Whole Blood, Capillary
Test Time 20 Min
Power AC or Battery
Cat. No 260300003
S.No Pima CD4 Cartridge Code
1 Pima CD4 Cartridge (Qty 100) 260100100 (Worldwide)
2 Pima CD4 Cartridge (Qty 25) 260100025 (Worldwide)
The enumeration of absolute numbers of T-helper cells (commonly referred to as a CD4 count) has become an essential part of monitoring the course of immunosuppression caused by the Human Immunodeficiency Virus (HIV) and the initiation of Anti-Retroviral Therapy.
The Pima CD4 test gives you the ability to monitor patients while they are still in your care. Consisting of the Pima Analyser and Pima CD4 Cartridge, the Pimaâ?¢ CD4 test enables CD4 T-cell analysis at the point-of-care from a fingerstick or venous whole-blood sample in only 20 minutes, providing an effective and affordable tool in the management of HIV patients, specifically designed to serve the needs of the healthcare professional in the field, the laboratory or the office.
Product Details:
Brand BioRad
Sample Capacity/Format 96 wells
Dimensions (W x D x H) 26 x 47 x 23 cm (10 x 18 x 9'')
Display 5.7'' VGA color touch screen
Port 1 USB A
Cat. No. 1861096
Description
Use the T100 thermal cycler for fast and reliable PCR in a 96-well block format.
Save time programming with an intuitive touch screen
Optimize reactions quickly in a single run using thermal gradient technology
Manage and organize protocols easily using personalized folders
Save space with the small footprint
Product Details:
Brand Athenese-Dx
Model Name/Number ADX-410
Sample Capacity/Format 96 wells
Volume Thermal Block Sample 0.2 mL
Dimensions 355mm X 480mm X 485mm
Power consumption 900VA
The ALTA RT-96 is a Quantitative, real time PCR system which combined with easy to use software and optimized design features like highly sensitive optical system and uniform heating system provides precise and accurate results to your diagnostics and research demands.
Applied Biosystems SimpliAmp and MiniAmp Thermal Cycler
Product Details:
Brand Thermofisher
Sample Capacity/Format 96 wells
Volume Thermal Block Sample 0.2 mL
Cat. No A37835 and A24811
Voltage 100/240 V
No. of Programs >1000 protocols
MiniAmp Plus Thermal Cycler
Product Overview :
The Applied Biosystems MiniAmp Plus Thermal Cycler is a compact, accurate, and economical thermal cycler designed to fit your lab basic thermal cycling needs. Innovations like a responsive color touch-screen and VeriFlex Blocks temperature-control technology enable simple, accurate optimization. The MiniAmp Plus Thermal Cycler can be accessed through Thermo Fisher Connect, giving you the freedom to design and securely upload your methods from any mobile device or desktop computer.
Key features and benefits:
VeriFlex Blocks with three independent temperature zones for precise temperature control over your PCR optimization
5-inch intuitive color touch-screen for easy programming and training of new users
Small footprint With dimensions of 19 cm wide and 39 cm deep, you can fit the MiniAmp Thermal Cycler almost anywhere. And because its airflow is front to back, you can set multiple units side by side to save valuable bench space.
WiFi-enabled and accessible by Thermo Fisher Connect giving you the freedom to design and securely upload your methods from any mobile device or desktop computer
Applied Biosystems PCR plastics
Applied Biosystems PCR plastics have been designed and validated to work with our thermal cyclers for more than 25 years. Options for every format and throughput need are available to ensure consistent, precise results for any experiment. To find the best match please visit our Plastics Selection Guide.
SimpliAmp Thermal Cycler
Product Overview :
The SimpliAmp Thermal Cycler is a small, easy-to-use, and accurate thermal cycler that suits any lab's needs for everyday PCR. It is crafted with the reliable engineering and performance you have come to expect from Applied Biosystem instruments. It is elegantly designed to deliver quiet cycling, and features an innovative, safe heated lid and a large LCD color touch screen.
Key Features and Benefits:
VeriFlex blocks to optimize PCR temperature with precision the VeriFlex blocks provide 3 independent temperature zones, for precise temperature control over your PCR optimization.
8-inch color touch screen to help save time the large and responsive color touch screen simplifies instrument operations with an easy to read interface.
Truelab Quattro Real Time Quantitative Micro PCR Analyzer
Product Details:
Brand Truelab
Principle Patented real-time micro PCR
Optics Fluorescence, Three Wavelength
Speed 40 cycles of PCR/35 minutes
Size 248 mm x 185 mm x 112 mm
Cat. No. 623010001
Key Features
- Fully Automatic
- Three Wavelength System
- Performs 40-48 Tests in 8 Hours
- Completely Randomized Operation
- Runs on any Truenat Chip
- Portable
- Battery Operated
Product Details:
Instrument Name Haematology Analyzer
Usage/Application Laboratory
Brand Spinreact
Differential Type 5-Part
Number Of Parameters 34
Sample Mode Whole Blood
Display Digital
Sample Volume 20 Micro Litre
Storage 200000 Sample Results
No. Of Reagents Used 4
Power 250 VA
Weight 35 kg
Dimension 490x332x459 mm
Screen Size 10.4 inch
Voltage 100-240 V AC
Spincell 5compact Compact 5 Diff analyzer Compact 5 Diff analyzer Reticulocyte count Determination of reticulocytes Laser multi-dimensional cell classi cation Multi-dimensional laser classi cation Up to 60 samples per hour throughput Up to 60 samples per hour Supports both whole blood and capillary blood samples Analyze both blood samples total like blood cap
Automated Thermal Cycler (ATC), 384 Well, Laptop, 1-m Cable
Product Details:
Brand ThermoFisher
Block Configurations 384-well,0.02 mL block
Interface USB Wi-Fi,Ethernet
Thermal Range 4 DegreeC to 105 DegreeC
Capacity 1 x 384-well Full Skirted Plate
Cat No A33977
Applied BiosystemsAutomated Thermal Cycler (ATC), 384 well, laptop, 1-m cableCatalog number: A33977Related applications: PCR
SpecificationsWidth (Metric)17.9 cmDepth (Metric)31.7 cmHeight (Metric)13.3 cmWidth (English)7.1 in.Depth (English)12.5 in.Height (English)5.3 in.Voltage100/240 VWattage600 wBlock Configurations384-well, 0.02 mL blockMax. Ramp Rate2.8C/sec (Block), 1.6C/sec (Sample)Thermal Uniformity<0.5C (20 sec after reaching 95C)Thermal Accuracy ±0.25C (35C to 99.9 C)Thermal Range4 C to 105 C Warranty Limited WarrantyProduct TypeThermal CyclerIncludesDell E6540 RC laptop computer and 1m cableHigh-throughput CompatibilityDesigned for high-throughput robotic workflowsShipping ConditionApproved for shipment at Room Temperature or on Wet IceCapacity1 x 384-well Full Skirted PlateDisplay TypeNo DisplayInterfaceUSB Wi-Fi, EthernetFor Use With (Application)PCRWeight (Metric)6 kgWeight (English)13.2 lb.Reaction SpeedStandard
Contents & Storage ATC 384-well block module
ATC control module
Dell E6540 RC laptop computer
1-meter connection cable
CAT 5 ethernet cable
Product Details:
Brand HemoCue
Model Name/Number Hb 201 System
Sample Mode Whole Blood
Sample Volume 10 Microlitter
Measuring Time Within 60 Sec
Dimension 160x43x85 mm
HemoCue Hb 201+ SystemProviding lab accuracy and ease of use, the HemoCue 201+ System has become a standard in hemoglobin point-of-care testing.
Healthcare providers around the world rely on the immediate results so they can make the right decisions when they need them most right at the point of care.
Have confidence in your answers at the point of care
Precise factory calibration against the ICSH reference method
Patented microcuvette technology with excellent lot-to-lot reproducibility
Date and time storage for up to 600 results
Blood-based liquid controls available
Get easy access to lab-quality accuracy
Capillary, venous or arterial whole blood sample
Brief training with virtually no maintenance
Link result with patient ID for medical record integration
Printer interface
Product Details:
Brand arkray
Display Digital
Dimensions 124x81x36 mm
Memory 100 Tests
Method Dual wavelength reflectance method
Cat. No PU-4010
Reaction Time 1 min/test
Compact Urine Analyzer
PocketChem UA PU-4010
Palm-sized, fitting easily into a doctor's bag or uniform pocket.
In order to achieve the goals of "anytime", "anywhere" and "easy to handle", the printer can be separated from the "PocketChem" analyzer, leaving it with a weight of just 180g.
Multiple functions
Palm-sized meter driven by two batteries
Easy operation and daily maintenance
Highly reliable test results with Creatinine compensation
Product Details:
Brand Skyla
Instrument Clinical Chemistry Analyzer
Model No. D-66386
POC Clinical Chemistry Analyzer Provides the Best Solution for Point of Care Testing
The skyla HB1 Clinical Chemistry Analyzer provides clinical testing laboratories of medical facilities and clinics with an in-vitro clinical chemistry diagnostic tool that is compact, portable, and reports rapid results. The portable design of the clinical chemistry analyzer utilizes precision photometric measurement technology, combined with the single-use disposable reagent discs. The reagent disc contains a set of dry assay reagents that are used in the quantitative testing of various biomarkers in the blood sample.
Product Details:
Model Name/Number SE-1520
Brand arkray
Display Digital
Dimensions 225x135x138 mm
Sample Volume Range 22 Microlitter
Sample Whole Blood, Plasma, serum and urine
Electrolyte Analyzer with Ion-Selective Electrodes
SPOTCHEM EL SE-1520
SPOTCHEM EL is an electrolyte analysis system with capacity for total electrolyte analysis requirements in all fields.
Fast, accurate and simple electrolyte analysis of body fluids-essential in an emergency.
Whole blood, serum, plasma and urine can be measured with 22 ul
Two types of special twin-pipettes are available.
Easy calibration can be completed with magnetic card
Na, K, Cl are measured at the same time on the same E-Plate
Product Details:
Sample Volume 4 Micro L
Measuring Time In 5 minutes
Model No HbA1c 501
Dimensions (W x D x H) 198 x 217 x 136 mm
Power 9 V DC / 1.5 A
HemoCue HbA1c 501 System is a fast, easy and reliable point-of-care system for hemoglobin A1c tests. It is a fully automated HbA1c POC test that provides reliable results straight away for efficient diabetes care.
Stop sending samples to labs and waiting for results
Having to send blood samples to the lab and wait for the results to come back can be very frustrating. Not only is it time-consuming, it also delays the treatment of the diabetes patients. As a medical professional, you should be able to carry out tests fast and easy at the point of care, and provide your patients with reliable result straight away.
An automated system for testing HbA1c
HemoCue HbA1c 501 System is a fully automated point-of-care system for testing HbA1c. Hemoglobin A1c (HbA1c) is a glycated form of Hb that is tested primarily to identify the average amount of glucose (sugar) present in patients blood over the past three months. Blood sugar testing is an important part of the diabetes care and necessary for millions of diabetics.
Advantages of using our point-of-care system
Our HemoCue HbA1c 501 System brings many advantages into your work process. It provides a safe workflow for excellent patient care. Every step of the test is simplified to minimize human errors. Every element from size to the storing and handling of test cartridges is designed to be ideally suited for how you work. The system is easy to use, the tests are carried out quickly, and the results are exceptionally reliable. With our system, you will never have to doubt an answer at the point of care.
Onscreen instructions simplify every step of the process
Testing HbA1c with our system includes only a few simple steps. But to make it as easy as possible for you to carry out the tests, we provide you with clear online instructions animated on the screen. They describe exactly how you should do so that you never have to feel insecure about performing the tests.
Certified according to IFCC and NGSP to ensure quality
The HemoCue HbA1c 501 system is certified according to the International Federation of Clinical Chemistry & Laboratory Medicine (IFCC) and the National Glycohemoglobin Standardization Program (NGSP). It ensures that our system has a measuring range of 20-130 mmol/mol (IFCC) or 4.0-14.0% (NGSP) to ensure the quality of the tests.
Get the right answers at the right time every time
In the end, the result of the test is what decides the treatment of your patient. The test must not vary from time-to-time, on the contrary, it needs to be accurate every single time.
Product Details:
Brand HemoCue
Model Name/Number Albumin 201 system
Sample Mode Urine; Morning spot, overnight or 24 hr collection
Display Digital
Sample Volume 8 Microliter
Power AC adapter
Dimension 115x170x66 mm
HemoCue Albumin 201 SystemUsed for screening and monitoring of microalbuminuria and is ideal within diabetes care, hypertension treatment and as a possible marker for preeclampsia during pregnancy
The HemoCue Albumin 201 System is an easy, lab-accurate means of identifying microalbuminuria â?? long before any possible symptoms of renal or vascular complications may appear. HemoCue's patented microcuvette technology enables quantitative test results right at the point of care. You can make immediate treatment decisions, and give direct feedback to the patient.
Certainty in vital decisions
Lab-accurate results for screening, diagnosis and monitoring
Ability to monitor changes in albumin concentration in the very low range (5-20 mg/L)
Detection of low concentrations enables early treatment to delay the onset of future microvascular complications
Fast results with ease
Ease of use with minimal training Three simple steps
Test results in just 90 seconds
No need for lab confirmation due to quantitative results
Trusted and accepted methodology
Built on HemoCue's proven microcuvette technology
Factory calibrated system, ensures sustainable and reliable results
Product Details:
Brand HemoCue
Sample Mode Plasma, serum and aqueous solution
Display Digital
Sample Volume 20 Microlitter
Power AC Adapter or 4 AA batteries
Dimension 160x210x90 mm
HemoCue Plasma/Low Hb SystemMakes it possible to easily and accurately estimate hemolysis directly at the point of care
The degree of hemolysis is an essential indicator of the quality and integrity of blood products. The HemoCue Plasma/Low Hb System consists of a specially designed photometer and microcuvette for the quantitative determination of low levels of hemoglobin in plasma or serum specimens, aqueous solutions, or stored or banked erythrocytes.
Incorrect storage and insufficient deglycerolization of banked erythrocyte suspensions are typical situations where hemolysis of red cells can occur. In the laboratory, hemolysis is an important preanalytical factor that affects the accuracy and clinical utility of many test results. By assessing the degree of hemolysis before analysis, the sample can be accepted or rejected. Hemolysis is also a prime consideration in the context of perioperative or postoperative blood salvage where blood is processed by hemofiltration or by cell savers.
The HemoCue Plasma/Low Hb System makes it possible to easily and accurately estimate hemolysis directly at the point of care. You can count on HemoCue for the right solutions for all your needs.
Have confidence in your answers at the point of care
Replace subjective visual judgement
Precise factory calibration against the ICSH reference method
Patented microcuvette technology with excellent lot-to-lot reproducibility
Blood-based liquid controls available
Get easy access to lab-quality accuracy
Plasma, serum, aqueous solutions or stored erythrocyte suspensions
Simple to use, providing results within one minute
Portability enables testing anywhere
Brief training with virtually no maintenance
Product Details:
Brand HemoCue
Sample Mode Whole Blood
Display Digital
Dimensions 188x157x155 mm
Measuring Principle Imaging system characterizing white cells that are stained, identified and counted
Measuring Time Within 5 min
Power Supply AC adapter or batteries
HemoCue WBC SystemHemoCue WBC System brings you the unique benefit of determining total white blood cell counts right at the point of care. It based on HemoCues proven, reliable microcuvette technology. From assessment to treatment faster.
In just three minutes, you have results with the same precision and accuracy as those from a central laboratory. This will assist the physician in evaluating a patients condition, while the patient is still in the office.
Fitting seamlessly into a variety of clinical applications and even remote field clinics, the benefits are clear. Immediate WBC counts can mean the difference between waiting and taking action at the point of care helping you move from assessment to treatment within minutes rather than hours or days.
Answers right when you need them
Lab-accurate results in minutes
Faster treatment decisions and streamlined workflow
Easy to use by non-laboratory personnel after a brief training
Capillary or venous samples
Accuracy for confident decisions
Factory calibration with no further calibration needed
Unique software for internal QC
Blood-based liquid controls available
Product Details:
Instrument Name EPOC
Brand Siemens
The epoc Reader and Host2 Mobile Computer devices work together to bring you the right result at the right timeThe nearly instantaneous delivery of BGEM (blood gases, electrolytes, and metabolites) results at the bedside enables you to make immediate treatment decisions that may lead to improved patient outcomes Simply insert the Test Card into the epocReader and obtain a blood sample from the patientOnce fresh blood passes across the biosensors on the epoc Test Card, results are sent to the epoc Host2 Mobile ComputerWith the optional EDM System and LIS interface components, the test result is then wirelessly transmitted instantly over your existing Wi-Fi network to your EDM, LIS and EMR
Benefits
Auto-scans Test Card Barcode for simplified quality complianceIncorporates automated, integrated calibration and quality checks and fully portable; AC/rechargeable batteryDoes not require a committed blood sample for Test Card calibrationConnects wirelessly and integrates easily with your facility''s existing networkDelivers accurate, bedside results in about 3 minutesCritical result management with electronic documentationIntegrated 1D (2D-ready) Barcode ScannerEasy-to-use Operator/Patient/QC lockoutsCustomizable web-based epoc Host software and LIS/HIS/EMR connectionImprove documentation and results management
Specifications11 Analytes on 1 Test Card pH, pCO2, pO2, Na , K , Ca , Cl-, Glu, Hct, Lac, and CreaCalculated values cHCO3-, cTCO2, BE(ecf), BE(b), cSO2, cHgb, eGFR, eGFR-a, AGap, and AGapKRoom temperature test card storageCritical result reportingTest Card and patient ID bar codingTest with 92 L fresh whole bloodOperator / EQC lockoutsTransmit results securely in real time
Product Details:
Brand HemoCue
Model Name/Number Hb 301 System
Sample Mode Whole Blood
Measuring Principle 3 Sec
Power Supply AC adapter or 4 AA batteries
HemoCue Hb 301 SystemOptimized for anemia screening in primary care and blood donation settings
Optimized for anemia screening in primary care and blood donation settings, the HemoCue Hb 301 System is a simple and convenient solution. The HemoCue Hb 301 System provides quick, easy access to lab-quality results without compromising accuracy, even in demanding climates with high temperatures and humidity.
Have confidence in your answers at the point of care
Precise factory calibration against the ICSH reference method
Patented microcuvette technology with excellent lot-to-lot reproducibility
Robust testing within a wide range of temperatures and humidity
Blood-based liquid controls available
Get easy access to lab-quality accuracy
Capillary, venous or arterial whole blood sample
Brief training with virtually no maintenance
Link result with patient ID for medical record integration
Printer interface
Product Details:
Model Name/Number AFIAS-6
Brand Bio Technology Biotech
Throughput 36 tests / hour
Weight 15.1 Kg
Certified US FDA & CE
Analyzer 420 x 336 x 293 mm
AFIAS-6
Automated Immunoassay Analyzer with the all-in-one cartridge system
AFIAS-6 is a unique integrated (sample-to-answer) system featuring 6 parallel tests of differing parameters, fast turn-around and high sensitivity, rivaling those of the full-featured systems in commercial labs.
Product Details:
Instrument Name Blood Analyser
Automation Fully Automatic
Brand Abbott
Sample Mode Whole Blood
We are a top-notch supplier of Abbott i-STAT 300 Handheld Blood Analyzer.
Provide lab-quality results in minutes for faster patient care:
The easy-to-use Abbott i-STAT handheld operates with the advanced technology of single-use i-STAT test cartridges. Together, they create the i-STAT System a point of care (POC) system that provides lab-quality results in minutes and allows healthcare professionals to quickly respond to needs and conditions at the patient's side.
Benefits and features of the i-STAT System:
Simple to use: Only four steps required to get patient results in less time and at less cost
Faster results than benchtops: Studies have shown that the i-STAT System is significantly quicker than bench-top systems and the central lab
Patient-centered care: i-STAT enhances patient satisfaction by minimizing wait times and length of stay
Broad test menu: Single-use i-STAT test cartridges cover a large menu of commonly used tests in one platform
Streamlined information management: Data Management Software, Advanced Quality Features, and statutes help integrate test results into your facility's software
Additional Information:
Delivery Time: 1
Packaging Details: box
Product Details:
Form Cassette
Brand Abbott
Country of Origin Made in India
To perform a test with i-STAT single-use cartridges, 2 to 3 drops of blood are applied to a cartridge, which is then inserted into an i-STAT 1 or i-STAT Alinity blood analyser. Results are available in approximately 2 minutes for most tests. The i-STAT System allows clinicians to stay with the patient to perform diagnostic testing to help accelerate clinical decisions and time to treatment.
Product Details:
Brand arkray
Model Name/Number Hemo G
Battery Operation 2 X AAA 1.5V alkaline manganese batteries
Display LCD
Memory 500 Test Results
Pocketchem HemoGFeatures:
Compact handheld Hb testing device with calculated HCT
Just 7µl Blood required (Venous / Whole blood)
Special Micropipette to collect the right volume of blood sample
Results calibrated to cell counter
Easy 4 step process & result in just 5 seconds
Technical Specification:
POCKETCHEM HemoG meter
Battery operation 2 X AAA 1.5V alkaline manganese batteries
Number of measurements More than 1,000 measurements(with new batteries)
Method of measurement Optical method of the reflectance at 525 nm for determination of haemoglobin
Display LCD
Operation buttons 3 button (Power ON/OFF, Up and Down buttons)
Memory 500 test results
POCKETCHEM HemoG Strips
Measurementrange Hb: 5 ~25 g/dL
Repeatability of strip 1) 5.0 ~ 10.0 g/dL : Under SD ± 0.5 g/dL
2) 10.1 ~ 25.0 g/dL : Under CV 3%
Reference method HiCN and Met-Hb method
Type of sample Fresh capillary blood for self-testing & professional
Venous blood samples must be taken by a healthcare professional
Venous blood sample is used EDTA or Heparin anticoagulant tube
Blood sample volume 7 blood sample
Measurement time 5 seconds
Storage temperature 8~30
Measurement temperature 5~45 (41 - 113 )
Humidity: 10- 90 %RH
Product Details:
Brand Mission
Cat. No C111-3021
S.No Size Test Strips
1 50 Mission Mission Hb Hemoglobin Strips
System Details :
Features Specifications
Methodology Reflectance Photometry
Detection Principle Methemoglobin
Time to Results < 15 seconds
Memory 1,000 tests with date/time and ID number
Specimen Volume 10 µL
Specimen Type Capillary and Venous whole blood
Hb Measurement Range 4.5-25.6 g/dL
Hct Range 13-75%
Wavelengths 525 nm
PC Interface Mini USB Port
Calibration Automatic
Hb Within Run Precision 3%
Hb Total Precision CV 3%
Accuracy
Venous Blood: Y=0.9582X+0.5673, R2=0.992
Capillary Blood: Y=1.006X+0.026, R2=0.993
Operating Conditions 10 40 C (50 -104 F); 90 RH
Meter Storage Conditions 0-50 C (32-122 F); 90% RH
Strip Storage Conditions 2-30 C (36-86 F); 85% RH
Strip Shelf Life 2 years unopened canister; 3 months opened canister
Power Source 3 AAA Batteries or AC Adapter
Battery Life 2,700 tests or 360 hours
Automatic Shut Off 8 minutes
Meter Dimensions 127 58 25 mm (5.0 x 2.28 x 0.09 )
LCD Dimensions 39 37 mm (1.54 x 1.46 )
Product Details:
Brand : Seimens
The CLINITEK Status�®+ Analyzer features automatic checks (Auto-Checks*). The analyzer automatically checks each test strip for humidity exposure, common sample interferencesâ? and strip identification for Siemens test strips. Together, these provide improved clinical information.
Enhances confidence in clinical decisions with (Auto-Checks) performed on every test
Ensures consistent results interpretation with automatic timing and reading of every urine specimen
Ready for connectivity to data management solutions (DMS), via a simple upgrade kit
Offers a comprehensive point-of-care urinalysis menu for routine testing, detection of early kidney disease and hCG pregnancy testing
Product Details:
Brand : Abbott
Weight : 540g (incl. Reader pen and batteries)
Display Type : LCD, 2 x 16 Characters
Reader Pen ; : L:144 MM, D; 29.5 MM
Batteries Rechargeble Nimh Batteries Only, Size AA, 1.2 V, Recharge 8 - 18 Hours
S.No Code Cartridge
1 1116083 Nycocard HbA1c (24T)
The NycoCard READER II is a small battery powered instrument, designed to measure all NycoCard products. It consists of two units: the instrument box, which is the operational and calculating unit, and the Reader pen, which detects the signal.
Product Details:
Brand : SIEMENS
CAT No ; 2083
Quantity 25 Strips
CLINITEK Microalbumin 2 Strips provide albumin, creatinine and albumin-to-creatinine ratio results in one minute. The CLINITEK Microalbumin product is useful to test for microalbuminuria in patients with diabetes or hypertension in order to detect early kidney disease. The strips are used on the CLINITEK Status family of analysers.
Product Highlights:
Albumin, creatinine, and albumin-to-creatinine ratio results to help identify clinically relevant microalbuminuria
Increased sensitivity of albumin as recommended by ADA guidelines: sensitivity as low as 2.0 mg/dL
Results are corrected for varying urine concentrations when used on the CLINITEK Status urine analyzer, replacing the need for 24-hour urine collection and measurement.
Product Features
CLINITEK Microalbumin 2 Reagent Strips make it simple and easy to test patients with diabetes. Because testing for microalbuminuria can detect kidney disease in its early stages, physicians may begin intervention earlier than might otherwise have been possible. CLINITEK Microalbumin 2 Reagent Strips permit detection of elevated albumin sooner, more sensitively and more specifically than products designed for general protein testing.
Benefits
The CLINITEK Microalbumin 2 Reagent Strips provide semi-quantitative results with a hard-copy report on the CLINITEK Status family of analysers, making them ideal for point-of-care testing. Patient's urine sample sticks can be tested immediately during a physician, clinic or hospital visit, rather than sending them out and waiting for results.
The urine sample test strips are also convenient for testing random samples, eliminating the need to collect a timed sample.
Product Details:
Cat. No : 14-875
Brand : Abbott
S.No Code Cartridge
1 14-875 Cholestech LDX Analyzer
2 10-989 Cholestech LDX Test Kit - Lipid (10T)
CONFIDENCE IN RESULTS
Accurate, actionable results from the leader in point-of-care lipid testing.
The CLIA-waived Cholestech LDX Analyzer is engineered for confidence, providing accurate, actionable, and readily accessible results that have set the standard in point-of-care lipid profile, cholesterol, and glucose testing.
Product Details:
Usage/Application Laboratory
Brand J Mitra
Plate Format 96 well
Assays Performed ELISAs
User friendly to operate with Touch screen display.
Easily programmable for Qualitative and Quantitative tests.
Includes 4PL Method for Quantitative tests.
In-built thermal printer for printing test results
Storage Capacity: 1,000 patient data or 10,000 sample records.
CE MARKED
Product Details:
Usage/Application Laboratory
Brand J Mitra
Provided with 3wash bottles for switching off to3 different ELISA tests.
In built Incubator adjustable to required temperature (Ambient, 30�ºC& 37�ºC).
Provision for 2 ELISA PLATES (96T) incubation at a time
Inbuilt shaker provided for better washing
Accurate results due to cover lid as no Air Draft at the time of sample and Reagents incubation.
Provision of auto rinsing of tubes/probes & hence No cross contamination
CE MARKED
Product Details:
Brand Roche
Sample Capacity/Format 96 wells
The LightCycler 96 Instrument is a real-time PCR system for rapid cycling up to 96 samples. Applications include absolute and relative quantification, melting curve analysis, and endpoint genotyping. Precise LightCycler 96 Instrument thermal homogeneity and cycling speed produce accurate and reproducible results in a very short time.
The LightCycler 96 Instrument optical detection system flexibly detects sequence-dependent probes, such as hydrolysis probes and sequence-independent dyes (i.e., SYBR Green I). Multiplex and multicolor capabilities permit the use of up to four different fluorescent dyes. New innovative LightCycler 96 Application and Instrument Software creates a simple analysis workflow with easy import and export functions, email notifications after each run, online monitoring flexibility, and server-based network interfacing.
Features
Plate-based real-time PCR system with 96-well block
Temperature gradient (assay optimization)
Standalone system (integrated PC)
Touchscreen with separate instrument software (free to load on any PC)
Dynamic range of 10 log
Sensitivity of one copy
4-plex multicolor
Runtime of less than 1 hour
Applications: Absolute Quantification, Relative Quantification, Endpoint Genotyping, Melting Curve Analysis
Intuitive state-of-the-art software
PC analysis software can be loaded free of charge on any PC
Applied Biosystem ProFlex 3 x 32-well PCR System
Product Details:
Brand Thermo
Model Name/Number ProFlex
Sample Capacity/Format 3X32
Volume Thermal Block Sample 0.2 mL
The ProFlex 3x32-Well PCR System allows you to:
Run three experiments at once with the 3x32-well, 0.2-mL block
Interchange the 3x32-well block with another block type if your throughput needs change
Access the system remotely (and conveniently) through a mobile app
Program the instrument in seconds with a simple-to-use touchscreen interface
Simulate your old instrument with Thermal Simulation modes
Optimize your PCR quickly and efficiently with better-than-gradient VeriFlex blocks
Product Details:
Microtome Dimensions 477 mm x 620 mm x 295 mm
Dimension 477mm X 620mm x295mm
Weight Approx. 31 kg
Instrument : Microtomes
Brand : Leica BIOSYSTEM
Types : HistoCore BIOCUT, MULTICUT and AUTOCUT
The HistoCore Rotary Microtome line was designed with the user in mind. We are committed to providing consistent quality and enhanced efficiency, while maintaining a safe and healthy workplace
Learn more about our new microtomes:
HistoCore AUTOCUT
HistoCore MULTICUT
HistoCore BIOCUT
Product Details:
Brand Eppendorf
Color White
Model Name/Number C170i
Usage/Application Laboratory
Number Of Shelves 4
A CO2 incubator that also saves money and is produced to highest standards of quality? Let us introduce CellXpert a new family of Eppendorf CO2 incubators.
Flexibility for the future
Full control and easy documentation
Safety for your cells
Saves Money
Powerful contamination prevention
Product Details:
Brand HIMEDIA
Channels 2 & 4
Reaction Volumes 5-100 Microliter
Max. Ramping Rate 4 DegreeC/s
Footprint (DxWxH) cm 35.3 x 38.4 x 34.8
Product Code LA1024 & LA1023
Insta Q48 M Series - RT-PCR Detection System is the latest addition to HiMedia existing range of Real time & Semi Quantitative PCR Thermal Cyclers. Insta Q48 M machines are compact and user friendly, with a wireless experience for a human-computer interaction, offering a choice of 2 & 4 Detection channels for different customer requirements. The specially made Peltier by Ferrotec ensure better temperature accuracy, uniformity and machine stability. The advanced optical fiber technology along with bottom based detection ensures the accuracy and reliability for scientific research and clinical application. The Insta Q48 M machines have three different temperature controlled blocks for simultaneous amplification by three different user with different Denaturation and Annealing temperature requirements (Maximum range +6C)
Product Details:
Brand : Thermofisher
Model Name/Number : 3307CTS
Usage/Application : Laboratory
Capacity : 232
Thermo Scientific Forma Steri-Cult CO2 Incubators offer the ultimate protection for high-value cultures with every element of their design, from the ISO Class 5 HEPA filtration system to their easy cleaning processes and proven automated sterilization cycles. As the largest capacity stackable CO2 incubator in the market today, the CTS Series supports cell therapy needs from research to high volume production, providing the documentation critical to validation every step of the way.
Product Details:
Brand Eppendorf
Model 1.5 C
Max. speed 3,000 rpm
Mixing orbit 3 mm
Temperature settings 1 C / 100 C
Interfaces USB interface
Eppendorf ThermoMixer C is for heating, cooling, and mixing almost any of your lab vessels. Reliable prevention of condensate formation in small vessels can be achieved with the heated lid Eppendorf ThermoTop (optional)
KingFisher Flex Purification System, King Fisher with 96 PCR Head
Product Details:
Format : 96-well Plate
Volume (Metric) Processing : 20 to 100 Microliter
Collection Efficiency of Particles : > 95%
Brand : ThermoFisher
Size : 680 x 600 x 380 mm
Cat. No : 5400610
Thermo Scientific KingFisher Flex Purification System, KingFisher with 96 PCR headCatalog number: 5400610Related applications: Automated Nucleic Acid Purification
Prepare samples efficiently from a variety of materials with the Thermo Scientific KingFisher Flex Purification System, which offers highly versatile, automated magnetic-particle processing for DNA/RNA, protein or cell purification from virtually any source. Using revolutionary magnetic particle separation technology, this system provides excellent reproduciblity and quality.
Specifications :
Volume (Metric) Processing : 20 to 100L
Plates per Deck : 24 or 96
Format : 96-well Plate
Capacity : 96 Samples
Description : KingFisher 96 plate, PCR plate
Collection Efficiency of Particles : > 95%
Display START / PAUSE / STOP / OK / TURNTABLE ROTATING CLOCKWISE / TURNTABLE ROTATING COUNTERCLOCKWISE / four cursor keys / LCD
For Use With (Application) Genomics and proteomics, target identification, veterinary assays, biomarker discovery, quality control, forensics
Heating Temperature From +5C above ambient temperature to +115C
Magnetic Rods 96 in one frame; Interchangeable magnet heads
Particle Size (Metric) ca. >1 m
Plate Type 24 or 96-well plates:;KingFisher 24 Deep Well plate (200 to 5000�µL);Microtiter 96 Deep Well plate (50 to 1000�µL);KingFisher 96 plate (20 to 200�µL);PCR plate (20 to 100�µL)
Depth (English) 23.6 in.
Depth (Metric) 60 cm
Height (English) 15 in.
Height (Metric) 38 cm
Weight (English) 62 lb.
Weight (Metric) 28kg
Width (English) 26.8 in.
Width (Metric) 68 cm
Unit Size Each
Product Details:
Wavelength Range 200-830 nm
Spectral Bandwidth 1 nm
Brand Eppendorf
Light source absorption Xenon flash lamp
Fluorometer excitation wavelength 470 nm, bandwidth: 25 nm
Fluorometer light source LED
Eppendorf BioSpectrometer basic shares its simplicity, flexibility and reliability. In addition to the Biophotometer D30, the Biospectrometer basic has freely selectable wavelengths from 200 830 nm (selectable in 1 nm increments). This allows the user to define the parameters of each assay, whether it be a scan, a single-wavelength measurement or a multi-wavelength measurement. The Eppendorf BioSpectrometer basic caters to more disciplines as the wavelengths are not pre-defined and allows for non-routine assays or new assays to be easily
Product Details:
Country of Origin Made in India
Brand ALTA
Alta Nucleic Acid Extractor utilizes the proven magnetic-particle technology to extract highly purifed nucleic acid from a wide range of sample types relevant for molecular diagnostics, genetic identity testing, forensic testing, biomedical research, and gene expression analysis. The combination of easy-to-use instruments, with pre-loaded protocols selection and magnetic particle-based sample preparation kits, filled with special reagent ensure rapid nucleic acid extraction and highly purified products.Unique remote controlAlta Nucleic Acid Extractor is an open system that can be easily operated through a 3.5 Touch screen combine with an unmatched remote control pad, no external computer is required. The pad connect the main unit via with, the Extractor app allows the operator to create, edit or delete the protocols. The protocols can also be easily shared between the main unit and pad, saving your stand-by time and improve your work eficiency.
Product Price: Rs 53,000 / Unit
Product Details:
Capacity(Litre per minute) 5 LPM
Brand Philips
Oxygen Concentration 93 +/- 3 %
Sound Level 45 (typical) dB
Weight (in kg) 14 kgs
Dimension 58.4 cm H x 38.1 cm W x 24.1 cm D (23" H x 15" W x 9.5" D)
Alarm Low Oxygen (82%) and Very Low Oxygen (70%)
I Deal In New Only
Input Voltage 120 +/- 10% VAC
Input Frequency 60 Hz
Until now, oxygen concentrators have been very similar - heavy, bulky, noisy, or requiring frequent maintenance. EverFlo from Respironics is a unique stationary concentrator that delivers what homecare providers want and patients deserve.
Features:
Lightweight for easy transport
The EverFlo Oxygen concentrator weighs in at only 31 pounds, reducing shipping and storage costs and risk of injury.
Compact design looks less like a medical machine
EverFlo's ergonomic design takes up less space and doesn't draw as much attention.
The Right Fit series focuses on patients' needs
EverFlo is part of the Right Fit, a complete portfolio of oxygen products and programs inspired by patients and built for business.
Low maintenance for reduced service costs
No homecare provider filter change for two years. Patients do not ever have to change filters.
Lower power consumption makes EverFlo patient-friendly
The system uses less electricity and produces less heat.
Humidifier Bottle Platform for extra flexibility
The platform is designed to be compatible with all bottle styles and features an easy-to-use velcro closure.
Recessed flow meter reduces accidental breakage
Recessed flow meter reduces accidental breakage
Oxygen purity indicator option for increased security
EverFlo is available with or without oxygen purity indicator. This OPI (Oxygen Percentage Indicator) ultrasonically measures oxygen output as a purity indication.
Product Details:
Model Name/Number 1025DS
Capacity(Litre per minute) 10 LPM
Brand DeVilbiss
Oxygen Concentration 96%
Warranty 3 years
Sound Level 40
Weight (in kg) 19 kg
Flow Single Flow
Product Type Stationary
Outlet Pressure 20.0 +/- 1.0 psi
Power Consumption 639 Watts
Dimensions 62.2 x 34.2 x 30.4 cm
Alarm Audible and visual high pressure, low/high flow, low oxygen, high gas temperature, power failure, Ox
Clear design for easy use
Lightweight and compact
Digital hour meter easy to read the top of the device
Convenient top and side hamdles for easy transport
Front label with clear visible LED's and easy to read
High performance
Capable of delivering yp to 96% purity from 2 lpm to 10 lpm
OSD sensor for continously monitoring oxygen levels
Can easily incorporate a comaptible transfill system, via the auxillary oxygen port and comaptible transfill caddy.
Reliable Safety features
Oxygen outlet incorporating a fire protection adpater
Tested in high temperature and high humidity for extended peroids of time
Alrams do not require a battery and indicate power failure, high gas temperature, high pressure, low and high flow, low oxygen and service required
Product Details:
Brand : ACON
Cat. No : OCP10s
S.No Code Size Test Strips
1 G133-111 50 On Call Plus Blood Glucose Test strips
2 G133-119 200 On Call Plus Blood Glucose Test strips
Designed By ACON Labs USA
For over 23 years, ACON Labs has led the way in making high-quality diagnostic and medical devices more affordable to people all around the world.
Headquartered in San Diego, California, the US office is the centre of strategic management, innovative research and development.
Beep Function
Early Detection of Hypoglycaemia
Post Surgery Sugar Monitoring
Monitoring Blood Sugar at Home
Monitoring Blood Sugar at Hospital
Accurate Results
Technology conceived and designed by ACON Labs USA ensures accurate reliable blood sugar tests recommended by Doctors for patients at home and hospitals.
Minimal Blood Sample Required
The On-Call Plus Technology is so sensitive only 0.4 Micro Litre of Blood Sample is required to process the blood sugar
Results
Quick Results in 10 Seconds.
On Call Plus Starter Kit
The Starter Kit has been designed for new users of Glucometer to ensure proper monitoring of blood sugar levels.
Hospitals
Clinics
Home Care
Elderly
Pregnant Women.
Product Details:
Type : 50 test/100 test
Brand : Roche
Product highlights
Helps to determine blood sugar level
Gives accurate and reliable results
Useful for both Type 1 and Type 2 Diabetes
Provides results in approximately 5 seconds
Proven Accuracy: The Accu-Chek Active strips help you to keep tabs on your diabetes regularly. It also fulfils ISO 15197:2013 standards of accuracy.
Clever functionality: Accu-Chek Active strip is a hassle-free product. The blood spreads across the strip and is automatically absorbed by it. The system then provides a fast and accurate result.
Easy-handling: A clear protective barrier runs along the entire length of the test strip to protect the strip, making it easy to use.
Blood volume: 1-2 �¼l
Visual double-check: To ensure accurate blood glucose measurement, Accu-Chek Active allows you to double-check the displayed result.
Out of meter dosing: Test strip outside the meter: approx. 08 seconds
Product Details:
Brand : Siemens
Product Type : Test Card
Cat. No : 10736515
10736515 Siemens EPOC BGEM BUN Test Cards, PKG/25 Tests
Siemens Healthineers Epocâ?¢ BGEM Test Card enables the epoc perform 13 different tests simultaneously on a single card
Description
Expansive test menu paired with accuracy and speed are critical to the Epocâ?¢
One test card with 13 analytes for improved inventory management and reduced waste.
Room-temperature storage.
Single use, with automatic calibration prior to analysis.
Error-free test panel recognition with bar-coded lot number and expiration.
Small sample size: Requires only 92 AUL blood sample.
Product Details:
Brand SD Biosensor
Specimen Whole blood
Specimen volume 1 mL
Storage temperature 2-25 C / 36-77 F
Cat. No 07TBF10C
Blood collection vacuum tube for diagnosis of latent tuberculosis infection
Intented Use
Blood collection vacuum tube which is used with STANDARD E TB-Feron ELISA for diagnosis of latent tuberculosis infection
Advantage
Specific detection of human IFN-I related to TB
Sensitive and specific IGRA test.
Product Details:
Brand SD Biosensor
Specimen Whole blood
Specimen volume 1 mL
Storage temperature 2-25 C / 36-77 F
Cat No 07TBF10C
Intented Use :
Blood collection vacuum tube which is used with STANDARD E TB-Feron ELISA for diagnosis of latent tuberculosis infection
Advantage:
Specific detection of human IFN-I³ related to TB
Sensitive and specific IGRA test
Product Details:
Display : 96-segment liquid crystal display (LCD)
Battery Life : approx. 1000 tests or approx. 1 year
Interface : USB (Micro B)
Memory Capacity : 00 test results with time and date, as well as 7, 14, 30 and 90 days averages
Brand:Roche
How to use Accu-Chek Active blood glucose meter
Testing your blood glucose is an essential part of managing diabetes. The Accu-Chek Active blood glucose meter can help to make it convenient by giving you fast, hassle-free, and accurate results in simple steps.
Product Details:
Automation : Semi Automatic
Brand : Sysmex
Model Name/Number : CA-104
Usage : coagulation system
Features & Benefits:
The Sysmex CA-104 analyser offers an economical, convenient, safe and secure, semi-automated coagulation analyser to standardise your essential haemostasis testing.
Economical
Utilises half-volume of plasma and reagent as compared to manual tilt-tube method.
Single cuvette testing.
Convenient
Simple operation.
Easy-to-use pre-programmed methods & on-screen prompts.
Automatic calculation of results.
Safe and secure
Built-in pre-incubation timer.
Auto-start and timing of measuring process.
Temperature controlled incubation block for reagents and samples.
Built-in thermal printer.
Calibration curves stored onboard.
Assay:
PT: Dade Innovin, Thromborel S
APTT: Dade Actin, Dade Actin FS, Dade Actin FSL, Pathromtin SL
Fibrinogen: Multifibren U
Thrombin Time: Test Thrombin, Thromboclotin
Factor Deficiency: Factor II, V, VII, VIII, IX, X, XI, XII
Specification:
Detection principles Clotting: turbodensitometric photo-optical measuring principle
Detection channel/method 4 LEDs with wavelength 870 nm for clotting assays
Parameters 1 simultaneous analysis parameter
Sampling Manual pipetting, auto-start function
Reagent holder 4 positions at 37�°C (1 with reagent mixer)
1 position at room temperature
Reference curves Manual input of reference curve (up to nine points)
Printer Built-in thermal printer
Dimensions (WxHxD)/weights 270 x 95 x 310 mm, 2.9 kg (without AC adaptor)
Cat. No : 601430050. Truenat COVID-19 Chip-based Real Time PCR Test is a semi quantitative detection of SARS CoV-2 RNA in human oropharyngeal and nasopharyngeal swab specimen and aids in detection and confirmation of SARS CoV-2 infection and diagnosis of COVID-19. The test detects the E and Orf1a genes of the virus.
Providing you the best range of Molbio Trueprep Auto Universal Cartridge Based Sample Prep Device, Molbio Trueprep AUTO Universal Cartridge Based Sample Prep Kit, Molbio Trueprep AUTO MTB Sample Pre Treatment Pack Kit, Molbio Trueprep AUTO Universal Sample Pre-treatment Pack and Molbio Trueprep AUTO Transport Medium for Swab Specimen Pack with effective & timely delivery.
The Acculaâ?¢ System from Thermo Fisher Scientific is a rapid diagnostic platform that combines the accuracy of RT-PCR with the simplicity, convenience, and procedural familiarity of traditional rapid immunoassays. The Acculaâ?¢ SARS-CoV-2 Test has received an Emergency Use Authorization (EUA) from the FDA for the detection of SARS-CoV-2 in Clinical Laboratory Improvement Amendments (CLIA) waived environments. Designed for use with the palm-sized Accula Dock, the Accula SARS-CoV-2 Test provides reliable, qualitative results in approximately 30 minutes
Pathodetect 2019- nCov Detectioin kit offer an in virto diagnostic real time PCR assay for qualitative detection of 2019 - Novel Coronavirus RNA in respiratory specimens and sera. The kit offer the universal detection of SARS- Like coronavirus and specific detection of 2019-nCOv.
Mylab Discovery solutions 2019-nCoV Detection Kit provides ready to use solution for detection of coronavirus using real time PCR technology. Detection is based on the amplification of a specific conserved RNA sequences of coronavirus and detection by Taqman probe-based chemistry. An Internal control is detected along with the coronavirus target controlling the extraction efficacy and possible PCR inhibition. The test is designed to use across wide range of PCR platforms. The recommended CDC protocol for coronavirus detection ensures that the kit leads to highly-specific and ultrasensitive results in short time.
KIT CONTENTS
Reagents for Nucleic acid extraction from respiratory/sera specimens
Reagents for Real time PCR
Inclusion of synthetic positive and negative controls
Cat No : RP10243X. Detection of COVID-19 specific target genes in a single tube- Reliable result with three target genes- Results within 1 hour and 50 minutes after extraction- Convenient work now on the automated MDx platform- Suitable for high-throughput- Providing whole process control for assay validity- Automated data interpretation with Seegene Viewer.
Cat No : 11NCo10. SD biosensor STANDARD M nCoV Real-Time Detection kit is used for identification and detectionof novel coronavirus (2019-nCoV) ORF1ab (RdRp) gene and E gene in humannasopharyngeal swab, oropharyngeal swab, and sputum specimens using reversetranscription (RT) real-time PCR. This kit is helpful for the auxiliary diagnosis of 2019novel coronavirus disease (COVID-19). The test results are for clinical referenceonly and cannot be used as a basis for confirming or excluding cases alone.
Product Details:
Brand : Applied Biosystems
Model Name/Number : QuantStudio 7 Flex
Sample Capacity/Format 48 wells
Volume Thermal Block Sample : 0.2 mL
No of Channel : 4
Features:
Increased application versatility through the accomodation of 4 different block types
Compatible with over 8 million TaqMan�® assays for gene expression, genetic variation, gene regulation, or protein expression experiments
The intelligent design of the QuantStudioâ?¢ platform combined with Applied Biosystem instrument reliability and accuracy
Easy-to-use software, responsive touch-screen, automation capabilities, and effortless block exchange without the need for any tools
CFX Opus 96 Real-Time PCR Instrument 0.2 mL, 96 Wells
Product Details:
Brand BioRad
Model Name/Number CFX Opus 96
Sample Capacity/Format 96 wells
Multiplex analysis Up to 5 targets per well
Dimensions (W x D x H), cm/in 33x56x36 / 13x22x14
Cat No 12011319
Description
CFX Opus is the newest real-time PCR system in our robust CFX Family. The CFX Opus 96 Real-Time PCR System can analyze 96 wells and offers a number of new features:
More uniform thermal performance
Expanded connectivity Wi-Fi, ethernet, and USB
Cloud connectivity: Operate CFX Opus on our BR.io cloud platform or with desktop CFX Maestro Software
Network storage drive access for excellent data management
Shuttle optical system yields consistent optical measurements across your sample plate
SpecificationsThermal CyclerMaximum ramp rate, C/sec5Average ramp rate, C/sec3.3Heating and cooling methodPeltierLid, C30 110 Temperature Range, C4 100Accuracy, C ±0.2 of programmed target at 90 C Uniformity, C ±0.3 well-to-well after 10 sec of arrival at targetGradientOperational range, C30 100Programmable span, C1 24Optical DetectionExcitation6 filtered LEDs Detection6 filtered photodiodes Range of excitation wavelengths, nm450 684 Range of emission wavelengths, nm510 730Sensitivity
Detects 1 copy of target sequence in human genomic DNADynamic range10 orders of magnitudeScan TimeAll channels, sec12
FAM/SYBR Green only, sec3SoftwareOperating systemWindows 10Multiplex analysisUp to 5 targets per wellSystemSample capacity, wells96
Sample size, µl150 (10 50 recommended)
Communication interface USB 2.0
Electrical approvalsIEC, CE Dimensions (W x D x H), cm/in33x56x36 / 13x22x14Weight, kg/lb22/48
ThermoFisher Scientific Accula System Rapid & Reliable RT-PCR Test for Corona in 30mins
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : Thermo
Test Method : (SARS-CoV-2) RT-PCR
Sample Type : Nasal Swab
Test Time 30 min
The Accula System from Thermo Fisher Scientific is a rapid diagnostic platform that combines the accuracy of RT-PCR with the simplicity, convenience, and procedural familiarity of traditional rapid immunoassays. The Acculaâ?¢ SARS-CoV-2 Test has received an Emergency Use Authorization (EUA) from the FDA for the detection of SARS-CoV-2 in Clinical Laboratory Improvement Amendments (CLIA) waived environments. Designed for use with the palm-sized Accula Dock, the Accula SARS-CoV-2 Test provides reliable, qualitative results in approximately 30 minutes
Hi-PCR Coronavirus (COVID-19) Multiplex Probe PCR Kit
Product Details:
Number of Reactions(Preps)/Kit : 100 Rxns Per Box
Brand : HIMEDIA
Storage Temperature : -10 to -20 C
Detection : Probe Based
Target : E, N and RdRp gene.
Cat No : MBPCR243
Description
A ready to use Rt-PCR Kit for Detection of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19). SARS-CoV-2 is a coronavirus, subgenus Sarbecovirus, 150-200nm in diameter with a genome size of about 30
Used For
A ready to use Rt-PCR Kit for Detection of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19).
Product Details:
Number of Reactions(Preps) per Kit : 100
Brand : Seegene
ICMR(Govt) Approved : Yes
Test Method : (SARS-CoV-2) RT-PCR
Test Time : 2 Hours
Cat. No : RP10243X
-Detection of COVID-19 specific target genes in a single tube- Reliable result with three target genes- Results within 1 hour and 50 minutes after extraction- Convenient work ow on the automated MDx platform- Suitable for high-throughput- Providing whole process control for assay validity- Automated data interpretation with Seegene Viewer
Additional Information:
Delivery Time: Immediate
First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40C.
Specimen Type- Whole Blood
CTK biotech, OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood. CE certified.
CTK Biotech's ,
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
WHO Approved,
First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen.
Sensitivity - 100%
Specificity - 100%
Rapid Result time within 20 - 30 Minutes.
Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum
Storage at 1 40C.
Specimen Type- Whole Blood
CTK Biotech's, OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
CTK BioTech's '
Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL,
Higher accuracy, sensitivity and specificity than the Guaiac Test,
No dietary restrictions,
Clear, easy-to-interpret result,
Individually sealed foil pouches containing:
One cassette test device,,
One desiccant,
Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011),
Patient ID stickers,
One package insert (instruction for use).
UNIQUE FEATURES:
EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch
HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy
FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds
BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results
USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 �µL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 µL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers 70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patient's visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 µL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use).
Cat No : COVAG025. GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
CAT No : Q-NCOV-01G. STANDARD Q COVID-19 Antigen Test kit is chromatographic immunoassay for the qualitative detection of SARS CoV 2 nucleocapsid antigen present in human nasal sample.
Cat. No : ICO-3000. iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Corona viruses are enveloped RNA viruses that are distributed broadly among humans, birds and other mammals, that cause respiratory, enteric, hepatic, and neurologic disease.
SPECIFICATIONS:
Whole blood/serum/plasma may be used for testing.
Results available in only 15 minutes.
Easy to use.
Result can be read visually.
No need for an analyser.
Cost effective method for assisting in screening COVID-19 disease.
Cat No : A28523. TaqPath 1-Step Multiplex Master Mix (No ROX) is a fast, single-tube, 4X RT-qPCR mix that provides for sensitive, reproducible detection of up to four different RNA/DNA targets in a single multiplex reaction. Particularly useful for diagnostics, virus detection, and high throughput gene expression workflows, the mix includes thermostable MMLV reverse transcriptase, dNTPs, UNG, and thermostable Fast DNA polymerase all in a single tube. TaqPath is manufactured under a strong ISO13485 quality management system and is designed to produce consistent product performance lot after lot.
This single-tube, 4X format facilitates easy reaction set upâ??just add user-supplied assay and sample (Figure 1). With reproducible performance even in the presence of inhibitors, coupled with stringent quality control to minimize lot-to-lot variation, TaqPath 1-Step Multiplex Master Mix (No ROX) is a superior choice for your multiplex diagnostic testing or development needs.
High sensitivity
To enable reproducible detection of low-titer pathogen and transcripts, TaqPath 1-Step Multiplex Master Mix (No ROX) has been optimized as a higher-concentration 4X master mix that allows you to input more sample into each reaction, increasing sensitivity even in low-volume reactions. Figure 1 shows the consistency of results obtained when detecting 10 copy inputs of RNA target.
Cat. No : 9901-NCOV-01G. Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2
The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.
This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment.
Cat. No : COVAG025-1.The GenBody COVID-19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) oranteriornasal (AN) swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first six days of symptom onset.
CAT No : SS03P25. Sure Status COVID-19 Antigen Card Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
Cat No : 195000. TheBinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Cat. No : RK033-30. General Description:
STANDARD Q HIV/Syphilis Combo Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O, HIV 2 and Syphilis (Treponema pallidum) in human serum, plasma or whole blood. The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection for HIV or Syphilis infected patients, patients with signs and symptoms (HIV and Syphilis) and persons at risk. The test is able to quick screen the HIV/syphilis infection and gives the advantage of managing these two diseases at the same time.
CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection Individually sealed foil pouches containing:
One cassette device
One desiccant
5 uL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK014-20
STANDARD Q Dengue NS 1 Ag qualitatively analyzes NS1 antigens specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting Dengue NS1 antigens, the initial infection status of Dengue virus can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Easy to use, Easy to read and interpret
Room temperature storage
Performance :
Sensitivity : 92.9% (184/198) / Specificity : 98.7% (222/225)
Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : CTK Biotech
Result Time (Rapid Kits) : 15 mins
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0160C
The OnSite Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description:
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
Product Specification:-
Brand Name : CTK Biotech
Pkg Qty : 1
Number Of Items : 30
Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action
Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK Biotech
Form : Cassette
Result Time (Rapid Kits) : 15 min
CAT No : R3002C
The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment.
Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : CTK Biotech
Result Time (Rapid Kits) ; 20mins
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0066C
The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood.
Product Details:
Number of Reactions(Preps)/Kit : 30
Brand : CTK Biotech
Result Time (Rapid Kits) : 20 mins
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0191C
The OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type : Rapid test
CAT No : R0063C
Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 auL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : AR0151C
Use of conserved antigens allows pan-filaria tests to be applicable
Simple procedure provides alternative to diagnosis by blood smear
Use serum, plasma or whole blood
No restrictions on time of day for sample collection
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (1 bottle, 5 mL)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 25T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type :Rapid Test
CAT No : R2011C
Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL
Higher accuracy, sensitivity and specificity than the Guaiac Test
No dietary restrictions
Clear, easy-to-interpret result
Individually sealed foil pouches containing:
One cassette test device
One desiccant
Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011)
Patient ID stickers
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit ; 25T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0192C
Clinical accuracy: 96.7% sensitivity, 93.8% specificity
Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens
Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis
Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid
Shelf life: 24 month
Individually sealed foil pouches containing:
One cassette device
One desiccant
Stool collection devices, each containing 2 mL extraction buffer
Plastic droppers for transferring watery stool
Package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits) :15 min
Sample Type :Blood
Test Type Rapid Test
CAT No : R0092C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patient's visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 Aul capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits): 15 min
Sample Type : Blood
Test Type Rapid Test
CAT No : R0090C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 aUL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit:10T
Brand : CTK BioTech
Result Time (Rapid Kits): 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0095C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 AUL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use).
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : CTK BioTech
Result Time (Rapid Kits) ; 15 min
Sample Type : Blood
Test Type Rapid Test
CAT No : R0162C
Detects the specific antigens from either S. typhi or S. paratyphi
Earlier detection results in faster treatment for disease eradication
Works with a variety of specimen types including: fecal, blood culture
Simple procedure minimizes operator error due to sample preparation
Test result within 15 minutes allows medical professionals to take immediate action
High level of reproducibility
Test kits can be used and stored at room temperature
Individually sealed foil pouches containing:
One cassette device
One desiccant
Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer (REF SB-R0162)
Sample diluent (REF SB-R0162-2, 5 mL/bottle)
Plastic droppers
Patient ID stickers
One package insert (instruction for use).
Product Details:
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits) : 20Min
Sample Material ; Serum / Plasma / Whole Blood
Cat. No : R0063c
The OnSite Dengue Ag rapid Test CE is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood.
The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus.
Any use or interpretation of this preliminary test result must also rely on other clinical findings and the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended for use:
Any person presenting with clinical signs or symptoms within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.
Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus.
As mild dengue fever symptoms can overlap with acute clinical manifestations of other arbovirus infections, such as Zika virus and chikungunya virus infections, correct diagnosis of dengue infection during early disease onset is critical for guiding clinical patient management.
Product Specification:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (REF SB-R0063, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit 30T
Brand CTK Biotech
Result Time (Rapid Kits) 20mins
Test Type Rapid Test
CAT No : R0234C
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
Product Details:
Brand RAPHA
CAT No : N116A
Size 50 T
Result Time 5 Min
UNIQUE FEATURES:
EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch
HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy
FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds
BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results
USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
Product Details:
Number of Reactions(Preps)/Kit 10 T
Brand CTK BioTech
Test Type Rapid test
Sample human serum, plasma, or whole blood
Test time 10 Min
Cat No : R0253C
The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood.
This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended for use:
Any person presenting with clinical signs or symptoms consistent with TORCH infection.
Women who are pregnant or who are planning to become pregnant
Individuals with a compromised immune system
The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection.
The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection.
The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2.
Product Specification :
Individually sealed foil pouches containing:
One cassette device
Two desiccants
Plastic droppers
Sample diluent (REF SB-R0253, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit 30 T
Brand CTK BioTech
Result Time (Rapid Kits) 10 Min
Sample Material Plasma/Serum
Test Type Rapid test
Cat. No R0310C
The OnSite RF Rapid Test is a lateral flow immunoassay for the qualitative detection of all subtypes of rheumatoid factor (RF) in human serum, plasma or whole blood at a sensitivity of 8 IU/ml.
Product Features :
Rapid test to make RF detection simpler and quicker than Latex
Detects RF levels as low as 8 IU/mL
Detects all RF isotypes including IgM, IgG, and IgA
Simple procedure minimizes risk of operator error â?? no sample preparation required.
The results are ready in 10 minutes, which increases diagnostic efficiency.
The least complicated RF test- can be performed in any setting by any health care provider with simple training
Rapid test format allows room temperature shipping and storage.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Capillary tubes (5 µL)
Sample Diluent ( REF SB-R0310, 5 mL/bottle )
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit 30T
Brand CTK BioTech
ICMR Approved Yes
Result Time (Rapid Kits) 20min
CAT No : AR5001C
Details :
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Detection buffer (tris-based buffered solution with preservatives)
Instructions for Use
Product Details:
Brand J.Mithra
Kit Type HIV Test Kit (Rapid) (Tri Dot)
Sensitivity 100% WHO Evaluation
Specificity 100% WHO Evaluation
Result Time Within 3 Minutes
Cat. No IR130100
Intended Use:The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG,IgM & IgA) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
Salient Features:
Rapid visual test ,based on Flow Through Technology.
Differential detection of HIV-1 & HIV-2.
Detection of group O & subtype C.
Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
100% sensitivity & 100% specificity as per WHO Evaluation.
Shelf life 24 months at 2-8C
Available in convenient pack sizes- 50 Tests and 100 Tests.
Results within 3 minutes.
No instrument required.
In built quality control dot.
Evaluations:
WHO Evaluation: Evaluation report from UNAIDS (WHO), CH-1211Geneva,Switzerland Aug 1999 the Sensitivity and Specificity of HIV TRI-DOT is 100 % .The panel used for evaluation of HIV TRI-DOT by Institute of Tropical Medicine, WHO Collaborating Centre in AIDS, Belgium also included HIV-O virus, which was found reactive with HIV TRI-DOT.
NIMHANS BANGALORE: Evaluation report from National HIV Reference Laboratories of Government of India , claiming Sensitivity and Specificity of HIV TRI-DOT to be 100 %.
CMC VELLORE: Evaluated by Department of Clinical Virology, Christian Medical College & Hospital, Vellore and published in JCM, vol. 38, Issue 2000,claiming 99.5% sensitivity and 99.9% specificity.
NARI PUNE: Evaluation Report from National AIDS Research Institute(NARI-Pune) claiming sensitivity & Specificity to be 100 %.
Approved by Drug Controller General of India( DCGI) for the usage in Blood Banks.
Product Details:
Brand J.Mithra
Test Kit Type HBsAg Test Kit (Rapid)
Detects All the 11 subtype of HBsAg
Sensitivity 100% by WHO Evaluation
Specificity 100% by PATH USA Evaluation
Cat. No HB010100
Intended Use : Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).
Salient Features:
Detects all the 11 subtype of HBsAg.
Antigen Sensitivity- 0.5 ng/ml.
No sample preparation required.
See through Device for easy result interpretation.
Shelf life-30 months at 2-30C.
WHO Evaluated with 100% Sensitivity.
Evaluations:
PATH USA: Sensitivity 100% and Specificity 100% .
DEPT. OF CLINICAL VIROLOGY, CMC VELLORE: Sensitivity 100% and Specificity 100%
Approved By Drug Controller General Of India( DCGI) For use In Blood Banks.
Product Details:
Usage/Application Hospital
Test for quantitative determination of albumin, creatinine and albumin/creatinine ratio (ACR) in human urine, used for early identification of renal disease in patients with diabetes and/or hypertension.
BENEFITSTIMELY TREATMENT CHANGES
The Afinion ACR (albumin, creatinine and albumin/creatinine ratio) detects microalbuminuria in human urine. Microalbuminuria is the first clinical sign of diabetic renal disease and cardiovascular disease. Simple testing for microalbuminuria is extremely efficient as an early indicator of renal failure.
SHORT ASSAY TIME IN 5 MINUTES
The Afinion ACR test gives you reliable results conveniently available when and where you need them.
Patient consultations can be carried out with confidence. The Afinion ACR Test Cartridge contains all reagents necessary for the measurement of albumin, creatinine and albumin/creatinine ratio.
Product Details:
Number of Reactions(Preps)/Kit : 96 wells
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 1hr 40 mins
STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Simple and easy to use - All necessary reagents included in the kit
Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)
Performance
Sensitivity : 97.4% (77/79) / Specificity : 96.6% (346/358)
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 -30 MIN
Certified WHO Aproved
CAT No; PI13FRC25
First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen.
Sensitivity - 100%
Specificity - 100%
Rapid Result time within 20 - 30 Minutes.
Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum
Storage at 1 40 C.
Specimen Type- Whole Blood
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 30 Min
Certified WHO Approved
CAT No; PI19FRC25
First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40 C.
Specimen Type- Whole Blood
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 30 Min
Certified WHO Aproved
CAT No; PI16FRC25
First Response Malaria Ag. pLDH/HRP2 Combo Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening test for detection of P.falciparum, P. vivax, P. ovale and P. malariae.
100% - Specificity
100% - Sensitivity
Rapid Result time within 20 - 30 Minutes.
Storage at 1 40 C.
Detects P.falciparum, P. vivax, P. ovale and P. malariae.
Specimen - Whole Blood
Product Details:
Number of Reactions(Preps)/Kit 22 Test
Brand Abbott
Usage/Application Hospital
Cat. No 710-000
Abbott BinaxNOW S. pneumoniae Antigen Card provides accurate, rapid identification of S. pneumoniae antigen in patients with pneumococcal pneumonia and pneumococcal meningitis with an easy-to-use technology, aiding physicians in providing rapid, focused therapy.
Time to Result: 15 minutes
Performance data:
Urine Sensitivity/Specificity 86% / 94%
CSF Sensitivity/Specificity 97% / 99%
Ordering Information
Cat No. Description Specimen Pack size
710000 Streptococcus Urine, CSF 22 Tests
Pneumoniae Ag card
Product Details:
Brand Roche
Result Time (Rapid Kits) 15 min
CAT No : 11621947196
Qualitative detection of troponin in anticoagulated
(EDTA or heparin) venous whole blood
Reaction time: 15 min.
Positive result from a threshold (cut-off) of 100 ng/L
Storage at 2 to 8 C
Test can be used immediately after removal from the
refrigerator
Storage for 4 weeks at room temperature (15 to 25 C)
Roche TROP T sensitive rapid assay is available in 5
and 10 pack sizes
Content:
5 disposable test strips (individually sealed)
5 pipettes (150 L)
disposable labels
1 package insert
Product Details:
Brand SD
Country of Origin Made in India
Specimen Serum
Shelf Life 24 Months
Temperature Storage 30 Degree Celsius
Sensitivity 97.6%
Specificity 98.0%
H.Pylori
Helicobacter pylori (H.pylori) is a spiral shaped bacterium and is found in the gastric mucous layer or adherent to epithelial lining of the stomach. H.pylori causes more than 90% of duodenal ulcers and up to 80% of gastric ulcers. Approximately two thirds of the world's population is infected with H.pylori. The immuno- chronomatographic techinques for the detection of antibodies specific to H.pylori has substantially resolved these problems.
General Information:
SD BIOLINE H.pylori test is a rapid test for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA etc) specific to Helicobacter pylori in human serum plasma or whole blood.
Detection of all isotype (IgG, IgM, IgA) antibodies against H.pylori
High Accuracy Sensitivity: 95.9%, Specificity: 89.6%
Specimen: Serum. Plasma, Whole blood
Material provided with this kit are as follows:
SD BIOLINE H.pylori test device multi-device
Assay diluent
Product Details:
Number of Reactions(Preps)/Kit 40
Brand Abon
Result Time (Rapid Kits) 15 mins
The Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Abbott
Result Time (Rapid Kits) 15-20 Min
Cat. No 11FK50
Biolineâ?¢ DENGUE NS1 AgTEST FOR EARLY CLINICAL PHASE OF DENGUE INFECTION
Bioline Dengue NS1 Ag rapid test is an in vitro immunochromatographic assay designed to detect Dengue virus NS1 antigen in human serum, plasma or whole blood.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Benefits:
Diagnosis of early acute dengue infection by detecting dengue NS1 antigen
Dengue NS1 antigen can be detected from 1 day after onset of fever
Specimen : Serum, plasma or whole blood (100l)
Test result : 15~20 minutes
Specification:
Sensitivity 92.4%, Specificity 98.4%
Product Details:
Number of Reactions(Preps)/Kit 100
Brand Alere
Usage/Application Hospital
Result Time (Rapid Kits) 15 mins
The irst and only FDA approved rapid point-of-care test that simultaneously andseparately detects HIV-1/2 antibodies and free HIV-1 p24 antigen on a single test strip.Determine Combo
Pack Size : 100 Test
Brand : 100 Test
Product Details:
Number of Reactions(Preps)/Kit 22T
Brand Abbott
Result Time (Rapid Kits) 15 Min
Cat. No 852-000
BinaxNOW Legionella Urinary Antigen Card is a rapid assay for the qualitative detection of Legionella pneumophila serogroup 1 antigen in urine samples from patients with symptoms of pneumonia. It is intended to aid in the presumptive diagnosis of Legionnaires disease caused by L. pneumophila serogroup 1 in conjunction with culture and other methods.
Sample Type: Urine
Time to Result: 15 minutes
Kit Size: 22 tests
Performance Data: Sensitivity/Specificity: 95%/95%
Product Details:
Brand Abbott
ICMR Approved Yes
Test Method Antigen Test
Result Time (Rapid Kits) 15 min
Packaging Size 25 Test Kits/Box
Cat. No 41FK10
Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection
Product Details:
Number of Reactions(Preps)/Kit ; 25
Brand : Cellex
Test Method : (SARS-CoV-2) IgM/IgG Rapid Antibody
Result Time (Rapid Kits) 30 minutes
Time To Result 15 mins
Cat. No : 5513C
COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
AbChek (SARS-CoV-2) IGM/IGG Corona Rapid Antibody Test Kit
Product Details:
Number of Reactions(Preps)/Kit : 50
Brand : AbChek
ICMR(Govt) Approved : Yes
Test Method : (SARS-CoV-2) IgM/IgG Rapid Antibody
Result Time (Rapid Kits) : 5-10 minutes
Sample Type : Blood
Type : Rapid Test Kit
Sensitivity : 98
Packaging Size : 50 Tests/ Box
Country of Origin : Made in India
Corona viruses are enveloped RNA viruses that are distributed broadly among humans, birds and other mammals, that cause respiratory, enteric, hepatic, and neurologic disease.
SPECIFICATIONS:
Whole blood/serum/plasma may be used for testing.
Results available in only 15 minutes.
Easy to use.
Result can be read visually.
No need for an analyser.
Cost effective method for assisting in screening COVID-19 disease.
Additional Information:
Item Code: RapidTestcov19
Production Capacity: 100000
Delivery Time: 10 days
Packaging Details: Carton Box
Product Details:
Number of Reactions(Preps)/Kit ; 2
Brand ; iHEALTH
Test Method : Antigen Test
Result Time (Rapid Kits) : 15mins
Sample Type : Nasal Swab
Cat. No : ICO-3000
iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Product Details:
Brand : Abbott
ICMR Approved ; Yes
Sample Type : Nasal Swab
Packaging Size : 25 Test Kits/Box
Cat. No: 195000
The BinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : Roche
ICMR Approved : Yes
Test Method : Antigen Test
Result Time (Rapid Kits) : 10-15 mins
Cat. No : 9901-NCOV-01G
Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2
The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.
This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment
Ethicon (W9922) Sutures Vicryl Rapide Und 4-0 19mm 3/8 R/C PS-2 75cm
Vicryl Rapide Sutures USP 2-0, 1/2 Circle Tapercut W9962
Material:Polyglactin910
Absorbable
Colour:Undyed
Braided
LABROID Deep Freezer is the most versatile and reliable Freezer which is designed to maintain a constant temperature.
Our freezers employ the Microprocessor based temperature control along with Digital display. Adjustable temperature range from -5Ã??C to -25Ã??C, -20Ã??C to -40Ã??C and -40Ã??C to -80Ã??C with an increment of 1Ã??C.
High efficiency insulation plus cabinet and door-mounted gaskets contribute to energy-efficient performance .Two types of Variants are available in the Deep Freezer they are Upright Freezer (Vertical Type) and Chest Freezer (Horizontal Type).
LABROID freezers are designed for storage of biological materials, blood banks, hospitals, epidemic prevention services, research institutes, and biotech storage applications etc. We provide Customizable extended warranties and preventivemaintenance plans.
Temperature Range: Adjustable temperature range from -5Ã??C to -25Ã??C, -20Ã??C to -40Ã??C and -40Ã??C to -80Ã??C with an increment of 1Ã??C.
Construction: Double wall, outer with M.S 18 swg (7 cycle process powder coat) & Inner tank with StainlessSteel (304/316).
Refrigerant: CFC Free (Eco Friendly).
Main Door: Main Door with durable magnetic rubber gasket and sealed with PPCP material.
Freeze Trays: Adjustable type with 3/4 Nos (Applicable for Vertical Freezer Only)
Freezer Sub Door: Independent compartments doors made of Arylic / Stainless Steel to minimize temperature loss while door opening.
Alarm:1) Audio-visual alarm for high/low temperature. 2) Power Failure Alarm 3) Door Ajar Alarm
Power: Works on 230 V AC single Phase 50Hz
Fully Automatic Semi-Auto Chemistry & Cogulation Analyser
Product Details:
Automation Semi Automatic
Brand ALTA
Dimension 400 x 300 x 160mm(L x W x H)
Display 7.0" TFT LCD with touch screen, 800*480 pixels
Power requirement Wide power supply AC100-240V, 50/60Hz
Cat No : ADX-220
Product Features:
Windows based, 7.0â?? inch true colour elegant display with touch screen
Large memory, over 300 programs and 2,00,000 test results
Inbuilt multifunctional incubator & blood coagulation function
Long Life Halogen lamp with auto sleep function
Powerful QC function: Levey Jennings plot with Westgard multirule
Supports USB, mouse, keyboard and barcode scanner for easy operation
Onboard thermal printer, supports external USB printers
Product Details:
Number of Reactions(Preps)/Kit : 100 VTM
Brand : Biopro
ICMR Approved : Yes
Sample Type : Nasal & Oral Swab
pH 7.3 + or - 0.2
Cat. No : Bp VTM 011
VIRAL TRANSPORT MEDIUM
SINGLE SWAB AND DOUBLE SWAB
NYLON OR POLYSTER SWABS AVAILABLE
15ML TUBE WITH 3ML VTM
MADE IN INDIA
ICMR APPROVED
The Ethicon W8707 Prolene 6-0 Blue Monofilament Suture is a high-quality surgical suture that is designed to provide excellent wound closure and healing.
W8304 Prolene (Prolene) 7/0, 60 cm, blue Col. Vize Black 9.3 mm x 2, 3/8
Brand: VICRYL
Ethicon Code: W9114
Suture Size: 3-0
Length: 75cm
Colour: Violet
Material/Composition: POLYGLACT" 910
Category: Ethicon Wound Closure
Quantity: 12
Absorbability: Absorbable
Absorption Rate: 56-70 Days
Directionality: Unidirectional
Needle Name: SH-2 PLUS
Needle Colour: Silver
Needle Length: 20mm
Strands Per Pack: 1
Needle Point Type: Taperpoint Plus
Ethicon PDS II Sutures USP 3-0, 1/2 Circle Round Body - W9116H
Product Code W9116H:
Needle Length: 20mm
Suture Length: 70 cm
Needle Description: 20mm, 1/2 Circle Round Body SH-2 Needle
ETHICON PDS II SUTURE VIOLET 70CM M2 W9124H [Pack of 36]
W8880T Prolene 3/0, 45 cm, blue Prime dir. 26 mm, 3/8
Sterile wax for bone hemostasis. Bone wax is a sterile mixture of bees wax, almond oil and salicylic acid and is used to control bleeding on bone surface in thoracic, orthopedic and oral surgery as well as neurosurgery. The wax achieves local hemostasis of bone by acting as a mechanical barrier.
Soft, kneadable and ready to use.
Used to control bleeding from bone surfaces. Creates local hemostasis of bone by acting as a mechanical barrier.
Sutures Absorbable W9024 150cm vicryl absorbable coated braided violet 3/0 pre-cut lengths Vicryl Ethicon
W8526-1/2 Circle Round Body MH-1 Double Needle, 2-0, PROLENE Blue Monofilament 90 cm
Ethicon Prolene Sutures USP 4-0, 1/2 Circle CC-25 Double Needle W8845
Needle Length: 26mm
Suture Length: 90 cm
Colour: Blue
Suture Type: Synthetic Monofilament
Absorption Profile: Non-absorbable
Suture Diameter: USP 4-0
Suture Material: Polypropylene
Needle Description: 26mm, 1/2 Circle CC-25 Double Needle
Tensile Strength: Indefinite Breaking Strength Retention
SKU: MP84361 Category: Ethicon Sutures Tags
PDS II suture 0, W9261T, CTX 150 cm loop purple
CAT No : STRUVTM01. Viral Tranport Medium (VTM) Kit:
50 Test Tubes
100 Swabs (Oral & Nasal)
Product Details:
Number of Reactions(Preps)/Kit : 25 Test
Brand : GenBody
Sample Type : Nasal Swab
Storage Temperature : -2 to - 30 C
Cat. No : CVIFG040-1
Genbody Influenza/ Covid - 19 Ag Triple,
Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy.
Production information:
1.Specimen: nasopharyngeal swab or Viral transport medium (VTM)
2.No Cross-reaction with 27 kinds of other respiratory viruses.
3.No interference with 23 kinds of interfering substances.
4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2.
5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
Product Details:
Brand : Strumed
Number of Pieces/Pack : 100
Kit Contains : Swab, Viral Transport Medium
Shelf Life : 1 year
Usage/Application : VTM
CAT No : STRUVTM01
Viral Tranport Medium (VTM) Kit:
50 Test Tubes
100 Swabs (Oral & Nasal)
