BRIEF-Biomerieux Receives US FDA 510(K) Clearance And Ivdr CE Marking For Vitek Pro

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Nov 10 (Reuters) – Biomerieux SA: * RECEIVES U.S. FDA 510(K) CLEARANCE AND IVDR CE MARKING FOR VITEK PRO * COMMERCIAL LAUNCH OF SOLUTION IS PLANNED TO BEGIN IN Q1 OF 2027 * EXPECTS TO PROGRESSIVELY

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