BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2183460-1996-00008

    MDR report key: 45669 · Received September 20, 1996

    Report

    Report Number
    2183460-1996-00008
    Event Type
    Malfunction
    Date Received
    September 20, 1996
    Date of Event
    July 11, 1996
    Product Code
    LWS
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *