Active Anthrax Detect™ Plus Rapid Test
FDA Market Authorized for In Vitro Diagnostic Use – Rx ONLY
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The Active Anthrax Detect™ Plus Rapid Test point-of-care diagnostic test for pulmonary anthrax is an in vitro immunochromatographic device for use as an aid in the diagnosis of inhalation anthrax.
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Resources
The first and only POC anthrax test available in the US via FDA’s De Novo classification
For use in point-of-care settings by military and healthcare professionals
PPA (Relative Sensitivity): >98%
NPA (Relative Specificity): 100%
For use with venous whole blood or serum
Fast results: 20 minutes
Room temperature: no refrigeration needed
Contains all reagents and controls to run 25 test specimens
Catalog No. | AAP-1 |
Format | ICT (cassette) |
Quantity/Kit | 25 tests |
Time to Result | 20 minutes |
Sample Type | Venous Whole Blood or Serum |
Storage | Room Temperature (15°C-30°C) |
Shelf Life | 24 months |
For more information, download instructions for use via the “Downloads” tab.
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