BEUDAMED
    5 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    10.0 MM FLIP CUTTER II

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·June 30, 2014

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBE·January 3, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 17, 2010

    GENERATOR PULSAR II

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code GEI·November 23, 2016

    GENERATOR PULSAR II

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code GEI·October 7, 2016