BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2915056-1998-00003

    MDR report key: 194196 · Received October 22, 1998

    Report

    Report Number
    2915056-1998-00003
    Event Type
    Malfunction
    Date Received
    October 22, 1998
    Date of Event
    August 18, 1998
    Product Code
    KOD
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1