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

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    Filters FDA Adverse Event ×

    OPMI LUMERA I

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG·Product code HRM·July 20, 2015

    DEPUY ASR FEM IMPLANT SZ 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·January 28, 2013

    COLLEAGUE PUMP CE ENGLISH VERSION

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 16, 2010