BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GUIDANT CORP

    MDR report key: 432626 · Received December 10, 2002

    Report

    Report Number
    MW1026967
    Event Type
    Injury
    Date Received
    December 10, 2002
    Manufacturer
    *
    Product Code
    DXY
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    REPLACED LEADS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GUIDANT CORP PACEMAKER DXY * 1298 *
    2 GUIDANT CORP LEADS DTB * 4470 *
    3 GUIDANT CORP LEADS DTB * 4457 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Hospitalization| L