BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 29, 2017

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 29, 2014

    ADAPTER SLEEVE 11/13 +0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 20, 2013

    LUMBAR SCREW 6,7 X 40 MM + BALL RING

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code MNH·January 14, 2011