BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8800

    MDR report key: 2850497 · Received November 27, 2012

    Report

    Report Number
    1720753-2012-09722
    Event Type
    Malfunction
    Date Received
    November 27, 2012
    Date of Event
    November 5, 2012
    Report Date
    November 27, 2012
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REPRESENTATIVE EVALUATED THE SYSTEM AND FOUND THE FOOTSWITCH WAS CAUSING THE PROBLEM AND NEEDED TO BE REPLACED. NO FURTHER REPAIR INFORMATION IS AVAILABLE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM WOULD NOT COMPLETE BOOT UP. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 8800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 8800

    Patients

    Seq Age Sex Outcome Treatment
    1