Description

The TOUCHBIO RSV + COVID19 + Flu Test is an innovative rapid antigen self-test kit designed to empower individuals with the ability to detect and differentiate between four common respiratory viruses: Respiratory Syncytial Virus (RSV), Influenza A, Influenza B, and SARS-CoV-2 (COVID-19). This comprehensive testing solution is ideal for use in the comfort of your home or any non-clinical setting, providing peace of mind when experiencing respiratory symptoms or following exposure to these viruses.

Key Features

• Ease of Use: The test utilizes an anterior nasal swab, making it simple and minimally invasive. Each kit includes all necessary components such as sterilized nasal swabs, extraction tubes with buffer solution, biohazard specimen bags, and a detailed instruction leaflet.

• Reliable Results: Employing a lateral flow immunoassay with a double-antibody sandwich method, the test delivers results swiftly within 15 to 20 minutes. Clear interpretation guidelines are provided, ensuring accurate reading of results.

• High Sensitivity and Specificity: The test boasts impressive sensitivity rates for all four viruses, with values exceeding 98%, and high specificity, ensuring trustworthy results.

Instructions for Use

1. Sample Collection: Gently collect a sample from both nostrils using the provided swab.
2. Sample Processing: Insert the swab into the extraction buffer tube and mix thoroughly.
3. Testing: Apply a few drops of the processed sample onto the test cassette.
4. Result Reading: Wait for 15–20 minutes before interpreting the results, following the clear instructions provided.

Storage and Shelf Life

• Storage Conditions: The kit should be stored at temperatures between 2–30°C and should not be frozen.
• Shelf Life: Each test has a shelf life of 24 months from the date of manufacture. It is important to use the test within one hour of opening the foil pouch and to avoid using it past the expiration date.

Regulatory Compliance

The TOUCHBIO test kit is CE marked and listed with the ARTG (Number: 408459), affirming its compliance with in vitro diagnostic standards. It includes internal procedural controls and requires no special training or equipment, making it accessible to all users.

Important Considerations

While the test provides valuable insights, results should be considered alongside symptoms and medical history. It is recommended to consult a healthcare professional if the test result is positive or if symptoms persist. The kit’s compact design and comprehensive instructions, including a video guide, enhance user experience, ensuring accurate and reliable testing at home.