BEUDAMED
    3 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    1020279-2014-00341

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·May 30, 2014

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 20, 2012

    TERUMO CDI 101 MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·September 17, 2010