Celsis rapid microbial detection methods from Charles River
 

Status™ COVID-19/Flu A&B, rapid antigen immunoassay

Status COVID 19 Flu AB rapid antigen immunoassay

Principle: For the direct detection of SARS-CoV-2, Influenza Type A and Type B

Automation: NO

Approvals: FDA EUA

Suitability: Rapid Detection

Capital equipment required: NO

Description:

A rapid immunoassay for the simultaneous direct detection and differential diagnosis of SARS-CoV-2, Influenza Type A and Type B antigen from nasopharyngeal swab specimens. Flocked nasopharyngeal swab for superior specimen collection and patient comfort.


Key Points:

Sensitivity and Specificity

  • SARS-CoV-2 - Sensitivity 93.9%, Specificity 100%
  • Flu A - Sensitivity 91.4%, Specificity 95.7%
  • Flu B - Sensitivity 87.6%, Specificity 95.9%

Features and benefits:

  • Fast results:
    Visual read-out in 15 minutes, and no equipment needed!
  • FDA EUA
    Approved under FDA Emergency Use Authorization (EUA)
  • Swab included:
    Kit includes extraction buffer vials and flocked nasopharyngeal swabs for superior specimen collection and patient comfort.

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Areas:

    Clinical
Company contact details:

Hardy Diagnostics view full details
Santa Maria
United States

Website: Visit Website
Tel: +[1] 805-346-2766