Rapid Result

Influenza A (Flu A) Antigen Rapid Test

Detect Influenza A antigens quickly with our rapid test, aiding in prompt diagnosis and management of flu infections using nasal or nasopharyngeal swabs.

CE Certified
ISO 13485
Main image of Influenza A (Flu A) Antigen Rapid Test

Why Choose reOpenTest Infectious Disease Kits?

Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.

Rapid Detection

Results available within minutes for timely diagnosis.

Convenient Testing

Easy-to-use format for point-of-care settings.

Accurate Results

High sensitivity and specificity for reliable detection.

Product Overview

The Influenza A (Flu A) Antigen Rapid Test is an in-vitro diagnostic device for the rapid detection of influenza A virus antigens directly from nasal or nasopharyngeal swab specimens.

Technical Specifications

Detection Target Influenza A virus antigens
Sample Type Nasal or nasopharyngeal swab
Methodology Immunochromatography
Detection Range Positive/Negative
Reaction Time 10-15 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect nasal or nasopharyngeal swab sample.
  2. Mix the sample with the provided buffer.
  3. Apply the mixture to the test cassette.
  4. Read the results after 10-15 minutes.

Result Interpretation

Positive Result
Positive: The presence of both the control line (C) and test line (T) indicates a positive result for Influenza A.
Negative Result
Negative: The presence of only the control line (C) indicates a negative result.
Invalid Result
Invalid: If the control line (C) is not visible, the test is invalid and should be repeated.

Frequently Asked Questions

By providing rapid point-of-care results, the test enables early identification of infected individuals, facilitating prompt isolation and treatment measures to minimize influenza transmission.

Results are typically available within minutes, allowing for timely implementation of appropriate treatment strategies and infection control measures, thereby improving patient care outcomes.

Yes, the test's rapid turnaround time and ease of use make it well-suited for high-throughput testing environments, providing efficient and reliable detection of influenza A in diverse healthcare settings.

Technical Documents

Download product inserts and brochures for detailed information.

No technical documents are available at this time. Please check back soon.

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