Zdrowie i gospodarka · 15/08/2025

FDA Revokes EUA for LumiraDx COVID-19 Diagnostic Device

The FDA has revoked the Emergency Use Authorization for the LumiraDx SARS CoV-2 RNA STAR Complete, a COVID-19 diagnostic device, following a request from the device's manufacturer, LumiraDx UK Ltd.

Source: Federal Register — Food and Drug AdministrationOpen original release →

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