BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2023988-1997-00002

    MDR report key: 72555 · Received February 27, 1997

    Report

    Report Number
    2023988-1997-00002
    Event Type
    Injury
    Date Received
    February 27, 1997
    Date of Event
    January 2, 1997
    Product Code
    GWM
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1