BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183460-1997-00090

    MDR report key: 110974 · Received August 4, 1997

    Report

    Report Number
    2183460-1997-00090
    Event Type
    Injury
    Date Received
    August 4, 1997
    Date of Event
    May 20, 1997
    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