BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 594835 · Received April 15, 2005

    Report

    Report Number
    9680515-2005-00004
    Event Type
    Death
    Date Received
    April 15, 2005
    Date of Event
    August 18, 2004
    Manufacturer
    TONTARRA MEDIZINTECHNIK GMBH
    Product Code
    HTX
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * HTX TONTARRA MEDIZINTECHNIK GMBH * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *