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Influenza and Flu Self Test Kit

Influenza and Flu Self Test Kit

£2.99 – £14.50

Our Flu test is a quick and accurate diagnostic tool designed to detect and differentiate influenza type A and type B antigens (commonly known as flu) in nasal swab specimens

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Our Flu test is a quick and accurate diagnostic tool designed to detect and differentiate influenza type A and type B antigens (commonly known as flu) in nasal swab specimens. It provides qualitative results, enabling swift identification of the specific influenza types present in the sample.

Influenza, commonly known as the flu, is a highly contagious viral infection that affects the respiratory tract. Each year, during the autumn months, influenza outbreaks pose a significant health risk to communities worldwide. The virus spreads through the air via aerosolized droplets, primarily transmitted when an infected person coughs or sneezes.

To empower you with a quick and reliable method for flu detection, we proudly present the Newfoundland Flu Home Test. This revolutionary home testing kit is designed for the qualitative and differential detection of influenza type A and type B antigens, providing you with timely insights into your health status from the comfort of your home.

How it Works: The Newfoundland Flu Home Test utilizes lateral flow immunoassay technology, a widely trusted method for rapid diagnostic testing. With a simple, user-friendly process, you can efficiently perform the test in the privacy of your home.

Pack Size

Single Test, Pack of Five (5)
Instructions

To gather and analyse your sample, follow these simple steps:

Preparation:

1. Wash or sanitize your hands thoroughly. Ensure they are dry before beginning the test.
2. Familiarise yourself with the instructions provided for the Flu Test.
3. Check the expiration date on the cassette foil pouch to ensure it is still valid.
4. Allow the test, specimen, and extraction buffer to reach room temperature (15-30°C) before proceeding with the test.
5. Open the pouch and place the cassette on a flat and clean surface. Verify the result window and specimen well on the cassette.

Test Procedure:

1. Carefully remove the aluminum foil from the top of the extraction buffer, being cautious not to spill any of its contents.
2. Insert the tube into the hole on the kit box or place the tube in the tube holder.
3. Open the swab packaging from the stick end. Caution: Avoid touching the absorbent tip of the swab with your hands.
4. Gently insert the entire absorbent tip of the swab head into one nostril, typically around 1.5 – 2.5 cm.
5. Rotate the swab five times, brushing against the inside of the nostril, and then remove the swab from the nostril.
6. Repeat steps 4 and 5 for the other nostril.
7. Insert the swab into the tube and swirl it for 30 seconds.
8. While squeezing the side of the tube, rotate the swab five times.
9. Remove the swab while continuing to squeeze the tube.
10. Firmly attach the dropper tip to the extraction buffer tube. Mix the contents thoroughly by swirling or flicking the bottom of the tube.
11. Gently squeeze the tube and dispense 4 drops of the solution into the specimen well.
12. Wait for the colored line(s) to appear. Read the result after 15 minutes. Do not interpret the result after 20 minutes.

Please follow these instructions carefully to ensure accurate and reliable test results.
Reading the Results

1. Negative Result:

– Only one coloured line appears in the control region (C).
– No coloured line is apparent in the test line regions (A or B).
– This indicates that no Influenza A or B antigen was detected in the sample.

2. Positive Result for Influenza A:

– Two distinct coloured lines appear: one in the control region (C) and another in the Influenza A region (A).
– A positive result in the Influenza A region indicates the presence of Influenza A antigen in the sample.

3. Positive Result for Influenza B:

– Two distinct coloured lines appear: one in the control region (C) and another in the Influenza B region (B).
– A positive result in the Influenza B region indicates the presence of Influenza B antigen in the sample.

4. Positive Result for both Influenza A and Influenza B:

– Three distinct coloured lines appear: one in the control region (C) and two in the Influenza A region (A) and Influenza B region (B).
– A positive result in both the Influenza A and Influenza B regions indicates the presence of Influenza A antigen and Influenza B antigen in the sample.

Note:

The intensity of the colour in the test line regions (A or B) may vary depending on the amount of Influenza A or B antigen present in the sample.

Any shade of colour in the test regions (A or B) should be considered positive.

5. Invalid Result:

– If the control line fails to appear, it indicates an invalid test.
– Possible reasons for control line failure include insufficient specimen volume or incorrect procedural techniques.
– In such cases, carefully review the procedure and repeat the test using a new test dipstick.
– If the problem persists, immediately discontinue using the test kit and contact your local distributor for assistance.

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