Active Anthrax Detect™ Plus Rapid Test

FDA Market Authorized for In Vitro Diagnostic Use – Rx ONLY

The Active Anthrax Detect™ Plus Rapid Test.
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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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  • 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

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