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

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    Filters FDA Adverse Event ×

    RX90-2 ARCOM HW/32MM LINER SZ 44

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·June 10, 2014

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·October 11, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012