BEUDAMED
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    Filters FDA Adverse Event ×

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 18, 2014

    SCREW, UNKNOWN

    FDA Adverse Event
    Malfunction ·THEKEN SPINE·Product code KWQ·October 7, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 17, 2012