BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDTRONIC

    MDR report key: 343780 · Received June 26, 2000

    Report

    Report Number
    343780
    Event Type
    Other
    Date Received
    June 26, 2000
    Date of Event
    April 7, 2000
    Report Date
    June 2, 2000
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    LWS
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDTRONIC IMPLANTABLE DEFIBRILLATOR LWS MEDTRONIC, INC. 7271 *

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Other