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LumiraDx Limited: LumiraDx Announces FDA EUA Submission for
LumiraDx Limited: LumiraDx Announces FDA EUA Submission for
LumiraDx Limited: LumiraDx Announces FDA EUA Submission for its SARS-CoV-2 & Flu A/B Rapid Antigen Test
- Rapid microfluidic immunofluorescence assay for use with the LumiraDx Platform intended for the simultaneous detection and differentiation of SARS-CoV-2, Influenza A, and Influenza B viral
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