BEUDAMED
    FDA Adverse Event Other Summary report: N

    2921578-2007-00001

    MDR report key: 834537 · Received March 28, 2007

    Report

    Report Number
    2921578-2007-00001
    Event Type
    Other
    Date Received
    March 28, 2007
    Report Date
    March 5, 2007
    Product Code
    JEB
    Report Source
    Manufacturer report
    Reporter Location
    IA, US

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1