BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2221819-1996-00120

    MDR report key: 59873 · Received December 17, 1996

    Report

    Report Number
    2221819-1996-00120
    Event Type
    Malfunction
    Date Received
    December 17, 1996
    Date of Event
    September 5, 1996
    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