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

By Reuters News

Nov 10 (Reuters) - Biomerieux SA BIOX.PA:

  • 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 EXPAND AVAILABILITY ACROSS OTHER REGIONS WORLDWIDE IN Q2 2027 TO REPLACE VITEK 2 AND VITEK XL SYSTEMS

Source text: [ID:]

Further company coverage: BIOX.PA

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