BEUDAMED
    3 results · 14ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013

    UNIVERSAL DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code HXX·March 13, 2008

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·July 7, 2023