BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 545547 · Received September 17, 2004

    Report

    Report Number
    1018233-2004-00062
    Event Type
    Death
    Date Received
    September 17, 2004
    Date of Event
    July 26, 2004
    Manufacturer
    *
    Product Code
    KDH
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * KDH *

    Patients

    Seq Age Sex Outcome Treatment
    1 *