BEUDAMED
    5 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MODULAR HYBRID GLENOID POST¿REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2018

    MODULAR HYBRID GLENOID BASE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2018

    PFC SIGMARP STB TB IN 3 10.0

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) 9616671·Product code NJL·June 13, 2014

    UNKNOWN PRODUCT-RIGHT TRIATHLON KNEE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·October 13, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 12, 2012