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Product Details:
Usage/Application Hospital
shelf life 18 months
SD BIOLINE Syphilis 3.0 test is a solid phase immunochromatographic assay for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA) against Treponema pallidum (TP).

Specimen: Serum, Plasma, Whole Blood

Sample Volume: 10MuL Serum / Plasma and 20MuL Whole blood

Recombinant TP, 15kDa, 17kDa antigens used as captures and detectors

The optimal choice for mass screening program

No need preprocessing and equipments

Storage: Room temperature (2-30 degree C)

Performance: Sensitivity: 99.3% Specificity: 99.5%

One Step Syphilis Antibody Rapid test

Ordering Information

Cat No. Description Type Pack size

06FK10I50 SD Bioline Device 50 Tests

Syphilis 3.0

Product Details:
Usage/Application Hospital
Results 15 min
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

Ordering Information

Cat No. Description Type Pack size

08FK50 SD TB Ag MPT64 Device 25 Test

Product Details:
Usage/Application Hospital
Tests Kit Filarial antigen
Results 10 min
The BinaxNOW Filariasis is an in vitro immunodiagnostic test used to detect Wuchereria bancrofti antigen in whole blood, serum, or plasma. The test employs an antibody specific for W. bancrofti.

Accurate: Lymphatic filariasis does not always result in clinical symptoms so the most accurate way to diagnosis is using a blood test.

Simple: The BinaxNOW Filariasis card test does not require laboratory facilities.

Convenient: The test uses finger-prick blood taken at any time of the day without regard to nocturnicity of parasite. Traditionally testing was restricted to the hours of 10 pm and 2 am when the parasite appeared in the patientâ??s blood.

Flexible: The test detects filarial antigen in whole blood, serum or plasma.

Rapid: The test yields results in 10 minutes.

Product Details:
Usage/Application Hospital
Results 15-30 min
Specimen Whole Blood Test
Storage Room Temperature
shelf life 24 months
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

Product Details:
Usage/Application Hospital
Time To Result 15 Min
Method Rapid
Shelf Life 24
Temperature 1-40C
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

Ordering Information

Cat No. Description Type Pack size

05FK80I40 SD Malaria Device 40 Tests

GenBody COVID-19 Ag is an immunoassay kit for rapid and qualitative determination of SARS-CoV-2 infection from swab specimens.

The Antigen test takes approximately 15 minutes to produce a result and is 90% accurate.

Although this product is not always accepted for international travellers it is a very good indicator of infection and can be used as a pre-cursor for PCR Testing.

Subitem - Antigen RDT

Specification - Covid-19 Ag
Manufacturer:
Genbody

Unit - Kit (1 kit contains
25 tests)

Unit Price - $150.00 per kit

Serachem India Private Ltd. have been successfully able to develop a transport media for CORONA virus by deactivating it. This means, now we don't have to be at risk while transporting the samples for testing to lab. Also, at present, as per the laid guidelines of ICMR Corona Virus testing can only be done in Biosafe Level-III laboratories. Which are very limited in no. Reason for the same is due to high level of security required in handling the virus. But now when we use STM Viral Transport Medium and Total Nucleic Acid Preservation System provides a rapid and simple method for the collection, preservation and shipping of swab samples in place of VTM (Viral Transport Medium) handling of the virus will be very safe and tests can now be conducted by any testing lab without posing a spread risk. This breakthrough will help in stopping the possible outbreak inside testing labs and hospitals and prevent a bigger disaster.

Advantages of STM Viral Transport Medium:
1. No threat of exposure to live virus.
2. The Swab Preservative not only inactivates viruses but also prevents the growth of Gram-negative and Gram-positive bacteria and fungi allowing the resulting non-infectious samples to be handled and shipped safely.
3. The sample can be transported and preserved at room temperature for up to 3 days. (The sample does not get spoiled).
4. No need of having Biosafe Level -III safety norms in labs.
5. No chance of spreading of the virus in labs.
6. Safe for the institutions and their lab staff and medical staffs.
7. Testing facility can be increased exponentially.
8. More sample collection centres can be developed which will help in developing post outbreak strategies.
9. It has also been approved by ICMR.
10. Comes with two sterile Polyester Swabs with visible break point.
11. Price is almost same as VTM Kit.

Two separately packed sterile synthetic fibre NYLON swabs with break point.
10-15 ml volume screw-cap, leak-proof self-standing tubes containing 2-3 ml viral
transport medium (VTM)
Vial has labeling stickers
ï?? The pH is 7.3+ 0.3 and the osmolality in mOsm/Kg H20 500.00-600.00
The medium is stable at room temperature.
STM meets European CE-IVD / US-FDA approved. Approved by ICMR.

Simple COvid-19 Test for home use .

"PCB Testing.
Weight:30grams"

Covid Ab IgG/IgM Ab Whole blood test device
Sensitivity: 86.94%
Specificity: 99.31%
Accuracy: 93.36%
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Covid Antigen Ag swab rapid test card
Sensitivity: 96.17%
Specificity: >99.9%
Accuracy: 98.79%
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Covid Antigen Ag saliva rapid test card
Sensitivity: 97.1%
Specificity: >99.9%
Accuracy: 99.57%

Covid Antigen Ag swab rapid test card
Sensitivity: 96.17%
Specificity: >99.9%
Accuracy: 98.79%
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Covid Antigen Ag saliva rapid test card
Sensitivity: 97.1%
Specificity: >99.9%
Accuracy: 99.57%

COVID-19 Real Time RT-PCR Kit detects the novel corona virus, COVID-19 using one-step real-time RT-PCR in a single tube.
The target genes for the detection of the virus are Orf1 ab and N gene.
The kit includes primers and probe set targeting the human Rnase P gene that serves as an internal positive control for the real-time RT-PCR.
Ordering Info : 96 Tests/Kit (MOQ : 10 Kits)

BioFACT Viral RNA/DNA Prep Kit is designed to isolate viral RNA/DNA from virous samples such as serum, plasma, cell-culture media, cell free body fluids and tissue.
Highly purified viral RNA/DNA from Coronavirus(COVID-19), Adenovirus, Norovirus, Zikavirus, HCV, HIV and Yellow fiber virus can be isolated through the kit.

-Isolation of pure viral RNA/DNA from virus samples
-No carrier RNA required
-Glass fiber membrane column based
-Safety use : No phenol nor chloroform

-Quantitative PCR (qPCR, qRT-PCR)
-Pathogen detection
-Poly-A detection
-cDNA synthesis
-Microarray
-Northern blotting

COVID-19 Self Swab Test Kit is the first commercialized Black Gold Particle technology in the world (High Sensitivity & Specifity)
-It's made as User friendly Dual Color System (Control Line: Red, Test Line: Black)
-Rapid Test Time takes 5~8 Min.
-It's intended to use for detection of SARS-CoV2 antigen
-20 Tests / Kit (Box)
-Tester indicates Negative(C: Red), Positive(C: Red & T: Black) and Invalid(No "C")

This kit is called CTM(Clinical Virus Transport Medium).
CTM is intended for the collection and transport of clinical specimen containing Corona Virus and others.

Collected Samples by each Nasopharyngeal Swab and Oropharyngeal Swab can be preserved in One Virus Transport Medium(CTM) simultaneously.
-Nasopharyngeal Swab : Tilt the patient's head back slightly to straighten the passage from the front of the nose, and gently inset the swab along the base of the nose(not upwards) until it reaches the nasopharynx-gentle rotation of the swab for a few seconds may be helpful.
-Oropharyngeal Swab : Press the tongue and extract the secretion from the back wall of pharynx.

1. Product Overview
-EnSave is â??IMPROVER of COMBUSTION EFFICIENCY for INTERNAL COMBUSTION ENGINEâ?? operated by â??CATALYSTâ?? which is created from chemical reaction by rare earth element and precious metal such as platinum, lanthanum, &, etc.
-EnSaveâ??s Catalytic Action acts to Enhance the Combustion Efficiency of the engine by leading close to perfect combustion.
- As a result, EnSave realizes both â??FUEL SAVING and FUEMS SAVING - â??Double Effectâ?? at the same time, the Remarkable and Innovative Technology is under Patent Pending now.
2. Effectiveness
1) Improving Fuel Efficiency (5~20%): Save fuel cost & Profit-up
2) Engine Power up Higher Combustion Efficiency leads to Engine Power-up
3) Fumes Down: Makes Eco-friendly Green Car
4) Noise & Shaking Down: Driving Fatigue & Stress Down
5) Simple & Easy Installation: Just put EnSave into Air Cleaner Space, No A/S required

X-Perso Clean Protection Kit is ready to go. This is a product for everyone and a useful product. We are accepting new orders from Feb 2021 onwards.

MOQ - 1 million pieces

Monthly capacity 5 million pieces.

This kit consist of following:

a. 1 - 3Ply disposable mask.
b. 1 - Pair of Plastic disposable gloves.
c. 1 - Disinfectant Wipe
d. 1 - 2ML Hand Sanitiser
e. 1 - Facial wet wipe

All products inside the kit are FDA and CE compliant.

Payment terms - 50% advance payment for booking and remaining 50% at the time of supply.

Product Name: COVID-19 IgG/IgM TEST KIT(Colloidal Gold Method)
HS code: 3002.15
Packing: 40Kits/Box; 36Box/Carton(1440pcs/Carton);
Diluents: 2 bottles/Box.
Carton size: 56*43*40CM
Gross Weight: 15 KG/Carton.

1. Sample: Blood (Whole blood, Serum)
2. Measuring Time: 10~15 Minutes
3. Test Principle
- Identification of COVID 19 antibody in blood COVID 19 IgG / IgM Rapid Test (WB / Serum / Plasma in human blood) is a fast chromatographic immunoassay for qualitative analysis of IgG and IgM antibodies to COVID 19.
4. Characteristics
- Simplicity: No special equipment required and intuitive visual interpretation.
- Rapid: Fast sampling with blood at the tip of the finger, results in 10~15 minutes.
5. Main Use
- People with symptoms
- Suspicious with or without mil d symptoms patient.
- It is also used to test people in close contact with infected patients and those in quarantine.

The COVID-19 RT-PCR Peptide Nucleic Acid (PNA) KIT is a real-time reverse transcription (RT)-Polymerase chain reaction (PCR) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, anterior nasal swabs, midturbinate nasal swabs, bronchoalveolar lavage (BAL), and nasopharyngeal wash/aspirates or nasal aspirates collected from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests.

Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities.

Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.

The COVID-19 RT-PCR PNA KIT is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR PNA KIT is only for use under the Food and Drug Administrations Emergency Use Authorization.