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

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    Filters FDA Adverse Event ×

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·April 24, 2014

    CORE SUMEX DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·September 28, 2012

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 27, 2010

    PFNA-II BLADE L90 TAN

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·November 19, 2018