BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2182207-2000-00068

    MDR report key: 266113 · Received February 24, 2000

    Report

    Report Number
    2182207-2000-00068
    Event Type
    Malfunction
    Date Received
    February 24, 2000
    Date of Event
    January 14, 2000
    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