BEUDAMED
    FDA Adverse Event Summary report: N

    LIGHT SPEED

    MDR report key: 1203630 · Received September 25, 2008

    Report

    Report Number
    1203630
    Date Received
    September 25, 2008
    Date of Event
    March 30, 2008
    Report Date
    September 19, 2008
    Manufacturer
    GE MEDICAL SYSTEMS, LLC
    Product Code
    JAK
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    CT SCANNER TABLE WOULD RAISE BUT IT WOULD NOT LOWER. TECHNICAL SUPPORT WAS ABLE TO ASSIST IN LOWERING THE TABLE BUT THE TABLE WOULD NOT ADVANCE INTO THE BORE OF THE CT SCANNER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIGHT SPEED CT X-RAY SYSTEM JAK GE MEDICAL SYSTEMS, LLC 2366438 *

    Patients

    Seq Age Sex Outcome Treatment
    1 9 YR