BEUDAMED
    3 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·May 20, 2014

    UNKNOWN REJUVENATE HIP DEVICE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 23, 2012

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·August 31, 2010