BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6800

    MDR report key: 1880042 · Received October 13, 2010

    Report

    Report Number
    1720753-2010-03550
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 29, 2010
    Report Date
    October 13, 2010
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REP EVALUATED THE SYSTEM AND REPLACED THE HARD DRIVE, AND RELOADED SOFTWARE AND CALIBRATION FILES. SYSTEM OPERATES AS INTENDED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED MISMATCHED IMAGES. IMAGES DISPLAYED DO NOT CORRESPOND TO THE THUMBNAILS SELECTED. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 6800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 6800

    Patients

    Seq Age Sex Outcome Treatment
    1