LMDX - LumiraDx COVID-19 & Flu rapid antigen test secures CE marking
LumiraDx (NASDAQ:LMDX) announces that its SARS-CoV-2 & Flu A/B Antigen Test has achieved CE Marking. The microfluidic immunofluorescence assay can quickly verify potential infection for patients suspected of influenza and/or COVID-19. Existing respiratory tests on the LumiraDx Platform include the company's SARS-CoV-2 Antigen, SARS-CoV-2 Antibody and SARS-CoV-2 Antigen Pool tests which achieved CE Marking in August 2020, September 2020 and March 2021, respectively. Shipments of the LumiraDx SARS-CoV-2 & Flu A/B Antigen Test will begin shortly. Earlier this month, FDA reissued the emergency use authorization for LMDX's COVID-19 testing solution.
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LumiraDx COVID-19 & Flu rapid antigen test secures CE marking