BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDTRONIC

    MDR report key: 5402259 · Received October 14, 2003

    Report

    Report Number
    5402259
    Event Type
    Other
    Date Received
    October 14, 2003
    Date of Event
    September 15, 2003
    Report Date
    October 14, 2003
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    DTB
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    2

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDTRONIC PACEMAKER DTB MEDTRONIC, INC. 7231 CX

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR