BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2183460-1996-00012

    MDR report key: 40143 · Received September 6, 1996

    Report

    Report Number
    2183460-1996-00012
    Event Type
    Malfunction
    Date Received
    September 6, 1996
    Date of Event
    January 10, 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 *