BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·April 14, 2017

    COPELAND SH HUM SZ4 STND PLUS

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·June 8, 2016

    UNKNOWN COPELAND HEMIARTHROPLASTY SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·October 21, 2016

    UNKNOWN COPELAND RESURFACING SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 16, 2017

    UNKNOWN COPELAND SHOULDER GLENOID COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·July 5, 2017

    DISTRACTION LOCK REMOVAL BAR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·April 10, 2013

    ENTRUST AT

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code LWS·April 12, 2011

    11 GAUGE AUTOPLEXTM SYSTEM WIT

    FDA Adverse Event
    Injury ·STRYKER PUERTO RICO·Product code JDZ·May 23, 2008

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD.·Product code LLZ·April 2, 2007