BEUDAMED
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    Filters FDA Adverse Event ×

    ACTIVE FIXATION ENDOCARDIAL LEAD

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2008

    CXDI CCS NE VER.2.02.0.16

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·June 28, 2013

    PENUMBRA SYSTEM REPERFUSION CATHETER 054

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·August 18, 2011