Rapid Results

Influenza A/B (Flu A/B)/Respiratory Syncytial Virus (RSV)/Streptococcus A (Strep A) Antigen Combo Rapid Test

Simultaneous detection of Flu A/B, RSV, and Strep A antigens for quick respiratory infection diagnosis.

CE Certified
ISO 13485
Main image of Influenza A/B (Flu A/B)/Respiratory Syncytial Virus (RSV)/Streptococcus A (Strep A) Antigen Combo Rapid Test

Why Choose reOpenTest Infectious Disease Kits?

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

Comprehensive Detection

Detects Influenza A/B, RSV, and Strep A from a single nasopharyngeal swab.

Rapid Results

Provides results in just 10-15 minutes for timely clinical decisions.

Improved Patient Care

Facilitates appropriate treatment and infection control measures.

Product Overview

The Influenza A/B (Flu A/B)/Respiratory Syncytial Virus (RSV)/Streptococcus A (Strep A) Antigen Combo Rapid Test is an in vitro diagnostic test for the detection of influenza A and B viruses, respiratory syncytial virus (RSV), and Streptococcus A antigens from nasopharyngeal swab specimens. This test is designed for professional use and provides rapid results to aid in the diagnosis of respiratory infections.

Technical Specifications

Detection Target Influenza A, Influenza B, RSV, Streptococcus A antigens
Sample Type Nasopharyngeal swab
Methodology Immunochromatography
Detection Range Qualitative (Positive/Negative)
Reaction Time 10-15 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect a nasopharyngeal swab sample.
  2. Apply the sample to the test device.
  3. Read the results after 10-15 minutes.
  4. Interpret the results based on the appearance of control and test lines.

Result Interpretation

Positive Result
Positive: The presence of control and test lines indicates a positive result for one or more of the target antigens.
Negative Result
Negative: The presence of only the control line indicates a negative result.
Invalid Result
Invalid: If the control line does not appear, the test is invalid and should be repeated.

Frequently Asked Questions

It allows for rapid differentiation of common respiratory infections, enabling prompt treatment decisions and preventing unnecessary antibiotic use.

While rapid antigen tests are highly specific, they may have lower sensitivity compared to PCR. Confirm negative results with PCR if clinical suspicion is high.

Store the test kit at 2-30u00b0C (36-86u00b0F) and protect it from freezing. Do not use the test after the expiration date.

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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