BEUDAMED
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    Filters FDA Adverse Event ×

    GUIDE WIRE, SMOOTH-TIPPED, STERILE T2 HUMERUS Ø2,2X800 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·December 2, 2015

    GUIDE WIRE, BALL-TIPPED, STERILE T2 HUMERUS Ø2.5X800 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·December 2, 2015

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    RALON MEDICAL EQUIPMENT CO. LTD.·Product code ILS·June 3, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH. LTD./ HUNTINGTON·Product code HQL·November 16, 2012

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 23, 2010