BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 2914994 · Received December 20, 2012

    Report

    Report Number
    1720753-2012-10702
    Event Type
    Malfunction
    Date Received
    December 20, 2012
    Date of Event
    December 10, 2012
    Report Date
    December 20, 2012
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REP EVALUATED THE SYS AND REPLACED A WORKSTATION POWER SUPPLY. THE SYS OPERATES AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT, DURING AN EXAM, THE SYS DID NOT PRODUCE ANY IMAGES AND THEY HAD TO USE ANOTHER C-ARM TO FINISH THE CASE. THERE IS NO REPORT OF INJURY OR DEATH ASSOCIATED WITH THE EVENT DESCRIBED IN THIS COMPLAINT.

    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