Qualitative rapid test for the detection of IgM/IgG antibodies against Hepatitis A virus in serum or plasma | 3001140 BIO-HAV IgG/IgM

Qualitative rapid test for the detection of IgM/IgG antibodies against Hepatitis A virus in serum or plasma | 3001140 BIO-HAV IgG/IgM

The HAV One-Step Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM and IgG antibodies to hepatitis A virus (HAV) in human blood, serum or plasma.

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Qualitative rapid test for the detection of IgM/IgG antibodies against Hepatitis A virus in serum or plasma | 3001140 BIO-HAV IgG/IgM

The HAV One-Step Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM and IgG antibodies to hepatitis A virus (HAV) in human blood, serum or plasma. It is designed to be used as a screening test and as an aid in the diagnosis of HAV infection. Any specimen that reacts with the HAV IgM/IgG rapid test should be confirmed with alternative methods and clinical history.

Weight100 kg
Dimensions10x10x10 cm
Description quick testsHepatitis A IgG/IgM
Sample Quick TestsSerum/Plasma
Presentation of quick tests25 cassettes
Filter 2024LIVER INFECTIOUS

Test time and temperature

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Assessment of BIO-HAV results in cassette

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For in vitro diagnostic use.

  1. You must read and understand the instructions completely before taking the test. Errors in following the instructions can cause inaccuracy in the results.
  2. Do not open the foil sachet until you are ready to test.
  3. Do not use expired equipment.
  4. Bring all reagents to room temperature (15-30ºC) before use.
  5. Do not use components from any other kit as a substitute for any component in this kit.
  6. Do not use hemolyzed blood for the test.
  7. Wear protective clothing and disposable gloves while using reagents and samples. Wash your hands thoroughly after testing.
  8. Users of this test should follow CDC universal precautions to prevent the transmission of HIV, HBV, and other bloodborne pathogens.
  9. Do not smoke, drink, or eat in areas where samples or reagents are handled.
  10. Treat all materials and samples as potentially infectious agents.
  11. Results should be read 15 minutes after applying the specimens to the test; readings after 15 minutes may give erroneous results.
  12. Do not perform the test in rooms with strong air flow, in front of a fan or strong air conditioning.

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