BEUDAMED
    FDA Adverse Event Other Summary report: N

    1223422-2006-00001

    MDR report key: 672773 · Received February 2, 2006

    Report

    Report Number
    1223422-2006-00001
    Event Type
    Other
    Date Received
    February 2, 2006
    Date of Event
    December 7, 2005
    Product Code
    GEI
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1