DON’T MISS A MOMENT.

Rapid results lead to accurate treatment options, onsite in about an hour.

In the time it takes to send samples to a lab, you can test for multiple pathogens onsite, with results in about an hour. The bioMérieux syndromic testing approach uses multiplex PCR technology to test for a comprehensive grouping of targets, giving you accurate results, quickly. Streamline your testing to quickly provide your patients the appropriate treatment with BIOFIRE.

*This product has not been FDA cleared or approved, but has been authorized for emergency use by FDA under an EUA for use by authorized laboratories; This product has been authorized only for the detection and differentiation of nucleic acid of SARS-CoV-2 from multiple respiratory viral and bacterial organisms; and, The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

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BIOFIRE® RESPIRATORY 2.1-EZ PANEL (EUA)*

For use with the BIOFIRE® FILMARRAY® 2.0 EZ configuration in CLIA-waived settings.

BIOFIRE® FILMARRAY® GASTROINTESTINAL PANEL**

For use in CLIA-moderate settings.

BIOFIRE® JOINT INFECTION PANEL†

For use in CLIA-moderate settings.