Global Point of Care
Clearview™ Influenza A/B is for detection of Influenza A and Influenza B virus antigens in specimens of nasopharyngeal swab, throat swab, nasopharyngeal aspirate and nose blow samples. This is a rapid immunochromatographic assay with results in just 8 minutes.
Not available for sale in the United States.
Minimal training required.
Contains all you need to perform a flu test. No additional accessory packs are required.
Clear results, simple interpretation.
Results available in just 8 minutes.
Provides accurate results and includes built-in controls.
Clearview™ Influenza A/B correlation with Virus Culture Method
*nasopharyngeal swab
Influenza A overall agreement 92.3%
Influenza B overall agreement 93.3%
| Clearview™ Influenza A/B IIN-501 | Code |
|---|---|
| IIN-501 | |
Registered under Act 737. MDA registration number: IVDC89477332018 (Clearview Exact Influenza A & B, IIN-501)
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