Influenza A (Flu A) Antigen Rapid Test
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Rapid detection of Influenza A antigen in nasal and nasopharyngeal swab samples.
A Foundation of Trust
Why Rapid Influenza A Testing?
Prompt identification of Influenza A allows for timely antiviral treatment, reducing the duration and severity of illness and preventing further spread of the virus.
Inside NomoFlow™: The Source of This Test's Superior Performance
The Influenza A Antigen Rapid Test demonstrates high clinical performance compared to RT-PCR.
Performance vs. RT-PCR
| Analyte | Sensitivity (PPA) | Specificity (NPA) | Overall Agreement |
|---|---|---|---|
| Influenza A Antigen | 94.5% (95% CI: 88.6-97.5%) | 98.8% (95% CI: 96.5-99.6%) | 97.2% |
Relevant studies and publications will be available here soon.
| Time to Result | 10 minutes |
|---|---|
| Sample Type | Nasal or Nasopharyngeal Swab |
| Kit Size | 25 Tests/Kit |
| Storage Conditions | 2-30u00b0C |
| Shelf Life | 24 months |
| Included Materials | Test Cassettes, Swabs, Extraction Buffer, Package Insert |
| Required Materials (Not Included) | Timer |
| Certifications | CE, ISO 13485 |
Collect Sample
Collect nasal or nasopharyngeal swab sample.
Prepare Sample
Mix the swab with the provided extraction buffer.
Apply Sample
Add the extracted sample to the test cassette.
Read Result
Read the test result after 10 minutes.
Product Information
- Catalog Number: VIR-FLAAG
- Product Name: Influenza A Antigen Rapid Test
Download the product insert and other relevant documents here.
Frequently Asked Questions
Direct answers regarding clinical performance, workflow, and logistics.
Have more specific technical or clinical questions?
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Integrate into a Complete Respiratory Workflow
This test is a key component of a broader strategy for managing respiratory outbreaks, optimizing resource allocation, and improving patient outcomes. See how it fits into a complete workflow solution.
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