BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8800

    MDR report key: 2030205 · Received March 7, 2011

    Report

    Report Number
    9617766-2011-00540
    Event Type
    Malfunction
    Date Received
    March 7, 2011
    Date of Event
    July 13, 2009
    Report Date
    March 7, 2011
    Manufacturer
    GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GY
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO CONCLUSION CAN BE DRAWN, AS REPAIR INFO IS UNAVAILABLE. HOWEVER, NO REPORTS OF PT OR STAFF INJURY WERE REPORTED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM CONTINUED TO BLOW FUSES. NO REPORT OF PT OR STAFF INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 8800 FLUOROSCOPIC XRAY JAA GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE) 8800

    Patients

    Seq Age Sex Outcome Treatment
    1