Cepheid Receives Emergency Use Authorization For SARS-CoV-2, Flu A, Flu B and RSV Combination Test

Cepheid today announced it has received Emergency Use Authorization (EUA) from the U.S. Food & Drug Administration (FDA) for Xpert® Xpress SARS-CoV-2/Flu/RSV , a rapid molecular diagnostic test for qualitative detection of the viruses causing COVID-19, Flu A, Flu B, and RSV infections from a single patient sample. The four-in-one test is designed for use on any of Cepheid’s over 26,000 GeneXpert® Systems placed worldwide, with results delivered in approximately 36 minutes.

URL: https://www.prnewswire.com/news-releases/cepheid-receives-emergency-use-authorization-for-sars-cov-2-flu-a-flu-b-and-rsv-combination-test-301139625.html?tc=eml_cleartime

1 Like