Hbsag Test Suppliers and Manufacturers

HBsAg Diagnostic test

Specification Strength/ Size Packing Size Packed In HBsAg Rapid Card Test 50 Tests 50 Box Pack

Hbsag rapid test antigen (uncut sheet) Specimen: whole blood/serum/plasma Format:2.5mm 3.0mm 4.0mm Accuracy:99.5% Cut-off:1.0ng/ml(whole blood), 2.5ng/ml(s/p) 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 HBsAg Rapid Test is to detect the Hepatitis B Virus Surface Antigen in serum, plasma or whole blood. Analytical sensitivity : 1ng/ml of HBsAg Sensitivity :100% , Specificity : 100% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min

HBsAg Rapid Test Cassette Uncut Sheet Specimen :WB/S/P Size :300*60mm One-Step HBsAg Rapid Test is to detect the Hepatitis B Virus Surface Antigen in serum, plasma or whole blood. Analytical sensitivity : 1ng/ml of HBsAg Sensitivity :100% , Specificity : 100% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min

Uncut Sheet HBsAg Rapid Test Package:30sheets/pouch Specimen:Whole blood/Serum/Plasma FOR THE QUALITATIVE ASSESSMENT OF HBsAg IN HUMAN SERUM, PLASMA OR WHOLE BLOOD INTENDED USE The HBsAg Rapid Test is a Chromatographic immunoassay (CIA) for direct qualitative detection of Hepatitis B type virus surface antigen (HBsAg) in human serum /plasma and whole blood. PRINCIPLE The HBsAg RST is a chromatographic immunoassay (CIA) for the detection of surface antigens of Hepatitis B in human serum/plasma and whole blood. Specific antibody against HBsAg is pre-coated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with anotherr specific antibody. If HBsAg is present, a pink colored band will develop on the membrane in proportion to the amount of HBsAg presented in the specimen. Absence of this pink colored band in the test region suggests a negative result. To serve as a procedural control, a pink colored band in the control region will always appear regardless the presence or absence of HBsAg. REAGENTS AND MATERIALS PROVIDED 1.One sealed pouched cassette with desiccant and a disposable pipette.. 2.Blood diluent in a dropper bottle. Store at 2-8°C. 3.One piece of operating instruction with 40 test pouches..

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

Hbsag rapid diagnostics test kits(CE & ISO)

Rapid HCG Pregnancy Test Card Intended Use HCG Pregnancy Urine Test is a chromatographic immunoassay for the early detection of human chrionic gonadotropin (HCG) in urine specimens. Contents of Kit HCG Pregnancy Test Card 25 ea Instructions For Use 1 ea Storage And Stability The kits should be stored at temperature 4-30ípC in the sealed pouch for the duration of the shelf life. Pre Cautions 1. For in vitro diagnostic use only. 2. Do not use after expiration date. 3. Test device should remain sealed until use. 25 tests/kit, 40 kits/carton

Rapid Malaria pf/pv Antigen Test Card Intended Use Malaria pf (HRP II) / pv (LDH) Antigen Test is for the rapid qualitative determination of Malaria P. falciparum specific histidine rich protein-2 (Pf HRP-2) and Malaria P. vivax specific lactate dehydrogenase (pvLDH) in human blood as an aid in the diagnosis of Malaria infection. Contents of Kit Malaria pf/pv Antigen Test Card 25 ea Malaria Sample Buffer 1 ea Instructions For Use 1 ea Storage And Stability The kit can be stored at room temperature or refrigerated (4-30ípC). The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date. Pre Cautions 1. For professional in vitro diagnostic use only. Do not use after expiration date. 2. Do not eat, drink or smoke in the area where the specimens or kits are handled. 3. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens. 4. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are being tested. 5. Humidity and temperature can adversely affect results. 25 tests/kit, 40 kits/carton