BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 873964 · Received July 2, 2007

    Report

    Report Number
    1720753-2007-02886
    Event Type
    Malfunction
    Date Received
    July 2, 2007
    Date of Event
    June 10, 2007
    Report Date
    July 2, 2007
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    GEHC SURGERY SERVICE PERSONNEL ORDERED PART 19-JUN-2007, CUSTOMER DOES NOT WANT SYSTEM REPAIRED UNTIL PARTS REQ PARTS FAN HAS BEEN DELIVERED AND INSTALLED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED UNIT WILL NOT GO UP, OR DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC 9800 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 YR