Rapid Results

Coronavirus (COVID-19)/Influenza A/B (Flu A/B)/Respiratory Syncytial Virus (RSV)/Adenovirus (Adeno)/Mycoplasma pneumoniae (M.P)/Streptococcus A (Strep A)/Chlamydia pneumoniae (C.P)/Human Metapneumovirus (HMPV)/Human Parainfluenza Virus 1/3/12 (HPIV 1/3/12) Antigen Combo Rapid Test

Simultaneous detection of 9 common respiratory pathogens from a single nasal swab.

CE Certified
ISO 13485
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Main image of Coronavirus (COVID-19)/Influenza A/B (Flu A/B)/Respiratory Syncytial Virus (RSV)/Adenovirus (Adeno)/Mycoplasma pneumoniae (M.P)/Streptococcus A (Strep A)/Chlamydia pneumoniae (C.P)/Human Metapneumovirus (HMPV)/Human Parainfluenza Virus 1/3/12 (HPIV 1/3/12) 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.

Extensive Detection

Detects 9 common respiratory pathogens.

Rapid Results

Provides results in minutes, facilitating quick clinical decisions.

Easy to Use

User-friendly format minimizes training requirements.

Product Overview

This multi-analyte rapid diagnostic test simultaneously detects antigens from nine common respiratory pathogens: Coronavirus (COVID-19), Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), Adenovirus, Mycoplasma pneumoniae, Streptococcus A, Chlamydia pneumoniae, and Human Parainfluenza Viruses 1, 3, and 12. This test is intended for professional use to aid in the rapid diagnosis of respiratory infections.

Technical Specifications

Detection Target COVID-19, Influenza A, Influenza B, RSV, Adenovirus, Mycoplasma pneumoniae, Streptococcus A, Chlamydia pneumoniae, HPIV 1/3/12 antigens
Sample Type Nasal swab
Methodology Immunochromatographic assay
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 nasal swab specimen.
  2. Add the extraction buffer into the extraction tube.
  3. Insert the swab into the extraction tube and rotate the swab vigorously for 15 seconds.
  4. Add 3 drops of the processed specimen to the sample well of the test device.
  5. Read the results at 10-15 minutes.

Result Interpretation

Positive Result
Positive: The presence of a colored line in both the test line region (T) and the control line region (C) indicates a positive result for the specific antigen.
Negative Result
Negative: The presence of a colored line only in the control line region (C) indicates a negative result.
Invalid Result
Invalid: If no colored line appears in the control line region (C), the test is invalid and should be repeated with a new device.

Frequently Asked Questions

This test detects Coronavirus (COVID-19), Influenza A/B, RSV, Adenovirus, Mycoplasma pneumoniae, Streptococcus A, Chlamydia pneumoniae, and Human Parainfluenza Viruses 1/3/12.

This comprehensive panel allows for rapid and accurate differentiation of multiple respiratory infections, leading to better patient management and infection control.

This assay is suitable for use in various clinical settings, from primary care offices to hospital emergency rooms.

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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