BEUDAMED
    3 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEXGEN STEMMED TIBIAL BROACH IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HWA·November 11, 2010

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 23, 2013

    COREVALVE 29MM AORTIC VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code NPT·July 10, 2014