BEUDAMED
    FDA Adverse Event Other Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 1811941 · Received August 18, 2010

    Report

    Report Number
    MW5017143
    Event Type
    Other
    Date Received
    August 18, 2010
    Date of Event
    May 25, 2010
    Report Date
    August 18, 2010
    Product Code
    MKN
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CONTINUOUS PAIN FOR 2.5 MONTHS WHICH WAS WHEN THE UAE WAS PERFORMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UTERINE ARTERY EMBOLIZATION NONE MKN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other