BEUDAMED
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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 21, 2014

    MITEK VAPR VUE GENERATOR

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEI·September 26, 2012

    UNKNOWN DEPUY 52X28MM 10D LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·July 15, 2010