Rapid Result

Influenza A/B (Flu A/B) Antigen Rapid Test Device (Swab)

Quickly detect Influenza A and B antigens with our rapid swab test for timely diagnosis and effective management of flu infections.

CE Certified
ISO 13485
Main image of Influenza A/B (Flu A/B) Antigen Rapid Test Device (Swab)

Why Choose reOpenTest Infectious Disease Kits?

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

Rapid Results

Provides results within minutes for quick clinical decisions.

Easy to Use

Simple procedure with minimal training required.

High Accuracy

High sensitivity and specificity for reliable results.

Product Overview

The Influenza A/B (Flu A/B) Antigen Rapid Test Device is an in vitro diagnostic test for the rapid, qualitative detection of influenza A and B viral antigens in nasal swab specimens. It aids in early diagnosis and management of influenza infections.

Technical Specifications

Detection Target Influenza A and B viral antigens
Sample Type Nasal 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 swab sample.
  2. Insert swab into the provided tube.
  3. Add buffer solution.
  4. Apply sample to the test device.
  5. Read results after 10-15 minutes.

Result Interpretation

Positive Result
Positive: The presence of both control (C) and test (T) lines indicates a positive result for Influenza A or B.
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

Our Influenza A/B Rapid Test demonstrates high sensitivity and specificity, providing reliable results comparable to PCR testing, enabling timely and informed clinical decisions.

Yes, our Influenza A/B Rapid Test is designed to specifically detect and differentiate between Influenza A and Influenza B viral antigens, providing accurate identification of the infecting subtype for effective patient management.

The Influenza A/B Antigen Rapid Test device has a shelf life of 24 months when stored at 2-30u00b0C, ensuring long-term usability and reliable performance in various 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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