BEUDAMED
    5 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ROOT CANAL INSTRUMENT

    FDA Adverse Event
    Other ·MICRO-MEGA SA·Product code EKS·January 25, 2010

    DEVILBISS

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001

    UNKNOWN DEPUY STEM

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code KWA·February 20, 2013

    AMISTEM H FEMORAL STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWY·January 14, 2011

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·July 31, 2014