BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 1012292 · Received March 7, 2008

    Report

    Report Number
    2020550-2008-00005
    Event Type
    Other
    Date Received
    March 7, 2008
    Date of Event
    February 5, 2008
    Report Date
    March 6, 2008
    Manufacturer
    D & R PRODUCTS CO
    Product Code
    HTT
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ DISPOSABLE BURR HTT D & R PRODUCTS CO 28205HCS 22875

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Other