BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2221819-1998-00767

    MDR report key: 196713 · Received November 9, 1998

    Report

    Report Number
    2221819-1998-00767
    Event Type
    Malfunction
    Date Received
    November 9, 1998
    Date of Event
    September 29, 1998
    Product Code
    DSP
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1