BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183456-1997-00001

    MDR report key: 98039 · Received June 6, 1997

    Report

    Report Number
    2183456-1997-00001
    Event Type
    Injury
    Date Received
    June 6, 1997
    Date of Event
    March 9, 1997
    Product Code
    GYC
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1