Hcv Test Cards

HCV Rapid Test Antibodies (Uncut Sheet) Specimen: Whole Blood/Serum/Plasma Format:2.5mm 3.0mm 4.0mm Accuracy:99.6% Cut-off:2nCU/mL Sensitivity:99.8% Specificity:99.5% Package: in bulk or unit box package for your options Delivery date:7-10 days after receipt of the payment Pouch design: white pouch / netrual/ OEM design/CE Marked Payment:Westren Union,T/T

General Information One-Step HCV Rapid Test is to detect the antibodies to HCV in human serum, plasma or whole blood. Applied highly purified recombinant proteins : Core,NS3,NS4,NS5 Method; Double Antigens Sandwich Method, the 4th generation Rapid Tests Sensitivity : 100%, Specificity : 100% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min.

Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 94.3% Specificity: >98.9% Specimen: whole blood/serum/plasma .

HCV Rapid Hepatitis C Virus Test (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in whole blood, serum or plasma. It is for professional in vitro diagnostic use only

Malaria Antigen PF/PV Card Test

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Application For the detection of eye / nose / stool / rectal secretions or blood pathogens The most convenient and rapid diagnostic tool for canine distemper / canine parvovirus Feature High accuracy for monoclonal antibody capture target Good tools for antibody detection and disease diagnosis Easiest reagent to operate the test Quickly present the result Low testing cost Technical specification Technical Parameters for Rapid Canine Distemper Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: eye / nasal secretions or blood Interpretation of time: 10-15 minutes Sensitivity: 98% Specificity: 97% Shelf life: 24 months Storage temperature: 4-28 Packing: 10 Test/ box Technical Parameters for Rapid Feline Parvovirus Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: rectal / feces Interpretation of time: 10-15 minutes Sensitivity: 99% Specificity: 97% Shelf life: 24 months Storage temperature: 2-30 Packing: 10 Test / box

Rapid Influenza A + B Test Card Intended Use Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture. Contents of Kit Flu A + B Test Card 20 ea Sample Extraction Buffer 1 ea Extraction Tube 20 ea Nozzle With Filter 21 ea Sterilized Swab 20 ea Tube Stand 1 ea Instructions For Use 1 ea Storage And Stability Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial. Pre Cautions 1. For in vitro diagnostic use only. 2. Do not use after the expiration date. 3. The test device should remain in the sealed pouch until use. 4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test. 5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers. 6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation. 7. Visibly bloody samples should not be used for the testing. 25 tests/kit, 40 kits/carton

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.