BEUDAMED
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    Filters FDA Adverse Event ×

    EOPA ARTERIAL CANNULA

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code DWF·June 12, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWQ·October 7, 2010

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·December 12, 2012