Global Point of Care
Bioline™ Influenza Ag A/B/A (H1N1) rapid test kit is a chromatographic immunoassay for the differential and qualitative detection of Influenza virus type A, type B and A (H1N1) antigens directly from nasal/throat/nasopharyngeal swab or nasal/nasopharyngeal aspirate specimens. This assay is intended for professional use and for in vitro diagnostic use only.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Differential detection of Influenza virus type A, type B and A (H1N1) antigen (4 lines)
Nasal swab, throat swab, nasopharyngeal swab or nasal/nasopharyngeal aspirate
Based on 2 clinical studies
Study Site 1 (759 specimens)
Study Site 2 (124 specimens)
|
Cat. No. |
Description. |
Type |
Pack size |
Specimen |
Validity |
|---|---|---|---|---|---|
|
19FK32 |
Influenza |
Strip |
25T/Kit |
Throat, Nasal, |
24M |
Registered under Act 737. MDA registration number: IVDC28690356118 (Bioline™ Influenza Ag A/B/A(H1N1); 19FK32)
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Not all products are available in all regions. Check with your local representative for availability in specific markets. For in vitro diagnostic use only. For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area.
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