BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 499886 · Received July 31, 2003

    Report

    Report Number
    1035617-2003-00003
    Event Type
    Malfunction
    Date Received
    July 31, 2003
    Date of Event
    June 4, 2003
    Manufacturer
    *
    Product Code
    ILZ
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *