BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183460-1996-00019

    MDR report key: 40580 · Received September 27, 1996

    Report

    Report Number
    2183460-1996-00019
    Event Type
    Injury
    Date Received
    September 27, 1996
    Date of Event
    June 21, 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