BEUDAMED
    FDA Adverse Event Death Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 834343 · Received April 5, 2007

    Report

    Report Number
    MW1042443
    Event Type
    Death
    Date Received
    April 5, 2007
    Date of Event
    February 21, 2007
    Report Date
    April 2, 2007
    Manufacturer
    *
    Product Code
    NAJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    DEATH OCCURRED LESS THAN 24 HOURS AFTER BEING RELEASED FROM THE HOSPITAL WHICH WAS LESS THAN 24 HOURS POST-UAE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UTERINE ARTERY EMBOLIZATION * NAJ * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death