BEUDAMED
    3 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO, KG·Product code NVZ·February 15, 2013

    TOTAL ASR FEM IMP SIZE 45

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    UNKNOWN DEPUY SZ 3 8MM TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·August 1, 2014