BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 997106 · Received January 12, 2008

    Report

    Report Number
    2027009-2008-00001
    Event Type
    Other
    Date Received
    January 12, 2008
    Manufacturer
    KARL STORZ IMAGING, INC.
    Product Code
    FWF
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FWF KARL STORZ IMAGING, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1