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

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    Filters FDA Adverse Event ×

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 18, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MED SYSTEMS GMBH·Product code JAA·December 22, 2010

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 17, 2014

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·November 29, 2017