Product Name: 
    HAV Hepatitis A virus IgM Test (Cassette)
    Instruction for use, pipette
    Principle of Test:
    Immunochromatographic assay





The HAV test is a rapid qualitative lateral flow test designed for the qualitative detection of hepatitis A infection (HAV).


1. Bring the pouched test device to room temperature (15-30℃) prior to testing. Do not open the pouch until ready to perform the assay.

2. Remove the test device from the sealed pouch. Lay it on a flat, clean and dry surface.

3. According to the proportion of 1:1000, add 4µl of specimen in the 4ml buffer bottle and shake well.

4. Then drop 2 drops (100µl ) of well mixed buffer into the sample well.

5. Read results within 10 minutes.


Positive: Two pink-colored lines appear in the result window, one in the test region (T) and another one in the control region (C). This indicates that the specimen contains detectable amount of HAV antibody.

Negative: Only one pink-colored line appears in the control region (C) of the result window. This indicates that there is no detectable HAV antibody in the serum specimen.

Invalid: If no line appears in the control region, the test result is invalid regardless of the presence or absence of the test line.

NOTE: Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for the control  line failure. Review the procedure and repeat the test with a new device. If problem persists, please contact your local distributor.