BEUDAMED
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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

    ELLIPSE DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 30, 2014

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE·Product code OUR·January 3, 2013

    ALARIS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·October 18, 2010