BEUDAMED
    9 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·October 18, 2016

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 20, 2025

    UNKNOWN DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSA·November 12, 2008

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 1, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 16, 2013

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·July 23, 2012

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MIH·October 31, 2022

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MIH·October 31, 2022