BEUDAMED
    5 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KXA·May 8, 2014

    ULTHERA

    FDA Adverse Event
    Injury ·.·Product code GEI·October 18, 2012

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 21, 2007

    ELEKTA UNITY

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·September 12, 2025

    ELEKTA UNITY

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·June 4, 2025