BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 2040586 · Received March 22, 2011

    Report

    Report Number
    1720753-2011-02602
    Event Type
    Malfunction
    Date Received
    March 22, 2011
    Date of Event
    March 1, 2011
    Report Date
    March 22, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SVC REP PERFORMED AN ON SITE INVESTIGATION. THE LIFT MOTOR POWER SUPPLY WAS REPLACED AND THE COLLIMATOR WAS ADJUSTED. THE SYSTEM WAS TESTED AND OPERATES AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE UNIT WOULD NOT MOVE UP AND DOWN AND IRIS LEAVES APPEAR AT THE BEGINNING. NO PT INJURY WAS REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1