Description

The Touch SARS-CoV-2 & Flu A/B Antigen RAT is an innovative rapid antigen test kit designed for convenient self-testing. It enables users to detect and differentiate between SARS-CoV-2, Influenza A, and Influenza B antigens using a simple nasal swab specimen.

Key Benefits

• Quick Results: Provides results within 15-20 minutes, allowing for timely decision-making.
• User-Friendly: No special training or equipment is required, making it accessible for home use.

Detection Capabilities

This test is particularly beneficial for individuals feeling unwell, exhibiting flu-like symptoms, or those who have been in contact with someone infected with these viruses. Its high sensitivity rates ensure reliable detection:

• SARS-CoV-2: 98.85%
• Influenza A: 98.12%
• Influenza B: 98.33%

Variant Detection

The test is capable of detecting SARS-CoV-2 variants, including Delta and Omicron, providing comprehensive coverage.

Result Interpretation

Interpreting the results is straightforward:

• Positive Results: Indicated by specific line patterns on the test device.
• Negative Results: Indicated by a single line in the control region (C).
• Invalid Results: Occur if no line appears in the control region (C).

Kit Contents

Each kit includes:

• 2 test devices
• 2 sterilized nasal swabs
• 2 extraction tubes
• 2 biohazard specimen bags
• Instructions for use

Usage Instructions

1. Collect a nasal swab specimen.
2. Mix the swab in the provided extraction buffer.
3. Apply the sample to the test device.
4. Wait 15-20 minutes for results.
5. Interpret results based on the visibility of lines in specific regions:
6. Control (C): Indicates the test is valid.
7. Test Lines (A, B, T): Indicate positive results for Influenza A, Influenza B, and SARS-CoV-2, respectively.

Storage and Shelf Life

• Shelf Life: 24 months
• Storage Conditions: Store at 2°C to 30°C. Ensure components are at room temperature before use.

Safe Disposal

Used test components should be disposed of in the provided biohazard bag and placed in household waste.

Additional Information

The test employs immunochromatography with a membrane strip precoated with antibodies specific to the nucleocapsid antigens of the viruses. Users are advised to follow public health guidance and consult a medical practitioner if symptoms persist despite a negative result.

Regulatory Compliance

This TGA-listed product is registered under ARTG Number 395591, ensuring compliance with relevant health regulations.