BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 30, 2012

    TRUL FEM IMPACTOR HEAD LOCKING

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code JWH·August 6, 2021

    TRULIANT PIN PULLER SYRINGE STYLE

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code JWH·August 6, 2021

    EXACTECH

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code LXH·October 28, 2021