BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    28MM -4 LFIT V40 HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·April 30, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 10, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 29, 2010

    TAPERLOC 133 T1 PPS HO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·April 8, 2020

    TAPERLOC XR T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWZ·April 8, 2020

    TAPERLOC 133 MP TYPE1 PPS HO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWZ·April 8, 2020

    TAPERLOC 133 FP TYPE1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWL·April 8, 2020

    TAPERLOC 133 T1 PPS SO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·April 8, 2020