BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IODINE (I-125) SEEDS

    MDR report key: 2950114 · Received February 6, 2013

    Report

    Report Number
    2915056-2013-00002
    Event Type
    Injury
    Date Received
    February 6, 2013
    Date of Event
    January 1, 2009
    Manufacturer
    GE HEALTHCARE
    Product Code
    KXK
    PMA / PMN Number
    K914281
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    50690 IODINE (I-125) SEEDS RADIONUCLIDE BRACHYTHERAPY SOURCE KXK GE HEALTHCARE 6711

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Other