BEUDAMED
    3 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CERAMAX CERAMIC INSERT 36 X 52

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code MRA·June 10, 2014

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 10, 2012

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 23, 2015