BEUDAMED
    FDA Adverse Event Death Summary report: N

    NONE

    MDR report key: 630569 · Received November 7, 2003

    Report

    Report Number
    6000095-2003-00003
    Event Type
    Death
    Date Received
    November 7, 2003
    Date of Event
    July 8, 2003
    Manufacturer
    VITATRON MEDICAL B.V.
    Product Code
    DTF
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE PERMANENT LEAD INTRODUCER DTF VITATRON MEDICAL B.V. VIK9S5 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 000 Death