Active Anthrax Detect™ Plus Rapid Test
FDA Market Authorized for In Vitro Diagnostic Use – Rx ONLY
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.
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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