BEUDAMED
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    Filters FDA Adverse Event ×

    3.0MM TI CANNULATED SCREW INSTRUMENT & IMPLANT SET

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FSM·June 12, 2014

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·December 12, 2012

    LAMITRODE TRIPOLE 8 SURGICAL LEAD

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·September 29, 2010