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: 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
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
