BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3109509 · Received May 6, 2013

    Report

    Report Number
    1720753-2013-05729
    Event Type
    Malfunction
    Date Received
    May 6, 2013
    Date of Event
    April 26, 2013
    Report Date
    May 6, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SVC REP EVALUATED THE SYS AND REPLACED THE BATTERIES, RELUBRICATED THE CANDLESTICK CONNECTORS, AND PERFORMED A FILAMENT CALIBRATION. THE SYSTEM OPERATES AS INTENDED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SYS SHUT DOWN ON ITS OWN. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    195861 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1