BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SPRINT

    MDR report key: 1050038 · Received May 8, 2008

    Report

    Report Number
    2950456-2008-00003
    Event Type
    Injury
    Date Received
    May 8, 2008
    Manufacturer
    MEDTRONIC CARDIORHYTHM
    Product Code
    DTB
    Removal / Correction Number
    NI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SPRINT IMPLANTABLE TACHY LEAD DTB MEDTRONIC CARDIORHYTHM 6945 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention