CE ISO Saliva Antigen Test Cassette

Short Description:


Used For CE ISO Saliva Antigen Test Cassette
Specimen Saliva
Certification CE/ISO13485
MOQ 1000 test kits
Delivery time 1 week after Get payment
Packing 1 test kits/Packing box,5 test kits/Packing box,20 test kits/Packing box
Test Data Over 95% Sensitivity and Specificity
Shelf Life 2 years
Production Capacity 1 Million/Week
Payment T/T, Western Union, Paypal


Product Detail

Product Tags


SARS-CoV-2 Antigen Rapid Test (COVID-19 Ag)——is a rapid test for the qualitative detection of antigens to the nove coronavirus SARS-CoV-2 in sputum.



- For in vitro diagnostic use only. Do not use after expiration date.

- The Test strip should remain in the sealed pouch until use.

- Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout

the procedure and follow the standard procedures for proper disposal of specimens.

- The used Test Strip should be discarded according to national, state and local regulations.

- Humidity and temperature can adversely affect results.



- Positive (+): Two coloured lines appear. One coloured line should always appear in the control line region (C) and another line should be in the T line region.

*NOTE: The intensity of the colour in the test line regions may vary depending on the concentration of SARS-CoV-2 present in the specimen. Therefore, any shade of

colour in the test line region should be considered positiveand recorded as such.

- Negative (-): One coloured line appears in the control line region (C). No line appears in the T line region.

- Invalid: Control line fails to appear. Insufficient specimen volume or incorrect proce dural techniques are the most likely reasons for control line failure. Review the

procedure and repeat the test witha new test.

If the problem persists, discontinue using the test kit immediately and contact your local distributor.

This self-test is a one-time in-vitro test for laypersons in a private environment.

A POSITIVE result must be confirmed by a laboratory test. To do so, please contact your doctor or go toa screening centre.

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