BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1031043 · Received April 17, 2008

    Report

    Report Number
    1720753-2008-20621
    Event Type
    Malfunction
    Date Received
    April 17, 2008
    Date of Event
    April 2, 2008
    Report Date
    April 11, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS, INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE SVC REP ORDERED REPLACEMENT PS3 POWER SUPPLY AND REPLACED THE PS3 POWER SUPPLY. HE VERIFIED VERTICAL LIFT OPERATION - SYS FUNCTIONING AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED ERRORS WITH THE VERTICAL COLUMN. THE SYS WOULD GO UP, BUT WOULD NOT GO DOWN. 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, INC NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1