BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3063578 · Received April 12, 2013

    Report

    Report Number
    1720753-2013-04915
    Event Type
    Malfunction
    Date Received
    April 12, 2013
    Date of Event
    April 4, 2013
    Report Date
    April 12, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM DISPLAYED A CHARGER FAILED ERROR AND WOULD NOT BOOT UP. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    158034 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1