BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K042172

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·September 2, 2022

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 9, 2013

    ADVANTAGE SERIES 26 OBS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 15, 2011

    INSIGNIA PLUS

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008