Directions for use

Allow the test, specimen and extraction buffer to equilibrate to room temperature (15-30℃) prior to testing. 1. Remove the test cassette from the sealed foil pouch and use it within one hour. Best results will be obtained if the assay is performed immediately after opening the foil pouch. 2. Tear off the aluminium foil on the extraction buffer tube. 3. Place the swab specimen in the extraction buffer tube. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the extraction buffer tube body to release the antigen in the swab. 4. Slightly lift the nasal swab then break the swab on the “break point” position. Leave the swab head in the sample collection vial and dispose of swab handle in accordance with your biohazard waste disposal protocol. 5. Fit the dropper tip on top of the extraction buffer tube. Place the test cassette on a clean and flat surface. Do not move the test cassette during the test. Hold the dropper vertically and transfer 3 drops of the sample solution (approx.80μL) to both sample wells and then start the timer. 7. Read the result at 10 minutes. Do not interpret the result after 20 minutes

Results: Positive

A coloured line appears in the Control region (C) and coloured line(s) appears in the Test region (T, A and/or B). A positive result in the SARS-CoV-2 region indicates that SARS-CoV-2 was detected in the specimen, a positive result in the Influenza A region indicates that Influenza A antigen was detected in the specimen, a positive result in the Influenza B region indicates that Influenza B antigen was detected in the specimen. *NOTE: The shade of the coloured lines(s) in the Test region (T, A and/or B) may vary. The result should be considered positive whenever there is even a faint line

Results: Negative

One coloured line appears in the control line region (C). No line appears in the test line region (T, A and B). A negative result indicates that SARS-CoV-2, Influenza A&B antigens are not present in the specimen, or is present below the detectable level of the test.

Results: Invalid

Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

About Coronavirus (COVID-19)

COVID-19 is an infectious disease that can affect your airways and lungs, caused by the most recently discovered coronavirus.

The most common symptoms associated with COVID-19 are fever, tiredness and a dry cough. However, symptoms can take up to 14 days to appear, so it is difficult to know if someone has been infected ahead of these conditions appearing. In the meantime, infected people can spread the virus unknowingly. For this reason, rapid testing is used as an accurate and cost-effective way to quickly and efficiently detect both symptomatic and asymptomatic cases and help suppress the spread of the virus.

About Influenza A&B

Influenza (commonly known as 'flu') is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease easily transmitted through coughing and sneezing of aerosolised droplets containing live virus.

Influenza outbreaks occur each year during the winter months. Type A viruses are typically more prevalent than type B viruses and are associated with most serious influenza epidemics, while type B infections are usually milder.

How many tests are in a box?

There are 25 tests in a box

Test Cassettes
Extraction Buffer Tubes
Sterile swabs
Workstation
IFU

SARS-CoV-2 & Influenza A/B Antigen Combined Rapid Test Cassette

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