BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    PROVIEW SELF-SEALING STERILIZATION POUCH

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INFANT WARMER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRAVIEW DM3 MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALUMINA CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LZO·June 12, 2014

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 7, 2015

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 9, 2010

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020