BEUDAMED
    3 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEPUY ASR FEM IMPLANT SZ 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·September 26, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 18, 2013

    APEX MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 16, 2010