BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6000008-1997-00030

    MDR report key: 68376 · Received February 13, 1997

    Report

    Report Number
    6000008-1997-00030
    Event Type
    Malfunction
    Date Received
    February 13, 1997
    Date of Event
    December 30, 1996
    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