BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2182207-1997-00059

    MDR report key: 98597 · Received June 13, 1997

    Report

    Report Number
    2182207-1997-00059
    Event Type
    Malfunction
    Date Received
    June 13, 1997
    Date of Event
    January 16, 1997
    Product Code
    GZB
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1