BEUDAMED
    5 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 1, 2021

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 6, 2014

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 15, 2010

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Death ·EV3 NEUROVASCULAR·Product code OUT·January 8, 2013

    M2A-MAGNUM MOD HD SZ 46MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 27, 2021