BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2124979-1999-00013

    MDR report key: 251757 · Received November 23, 1999

    Report

    Report Number
    2124979-1999-00013
    Event Type
    Malfunction
    Date Received
    November 23, 1999
    Date of Event
    September 21, 1999
    Product Code
    HGG
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1