BEUDAMED
    4 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DIACAM (510(K) K 901019)

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code KPS·March 13, 2001

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 5, 2014

    LCS ROT PATELLA LG+

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·January 8, 2013

    SIGMA 300 DR

    FDA Adverse Event
    Death ·MEDTRONIC S.A.·Product code DXY·November 17, 2010