BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MITEK VAPR S90 4MM 90 DEGREE SUCTION ELECTRODE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEI·June 27, 2014

    SCREW UNKNOWN

    FDA Adverse Event
    Malfunction ·THEKEN SPINE·Product code KWP·October 29, 2010

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 7, 2013