BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1043582-1999-00001

    MDR report key: 228481 · Received June 23, 1999

    Report

    Report Number
    1043582-1999-00001
    Event Type
    Injury
    Date Received
    June 23, 1999
    Date of Event
    May 13, 1999
    Product Code
    GCY
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1