BEUDAMED
    FDA Adverse Event Other Summary report: N

    GENERAL ELECTRIC MR 750W

    MDR report key: 3057329 · Received April 8, 2013

    Report

    Report Number
    MW5029731
    Event Type
    Other
    Date Received
    April 8, 2013
    Date of Event
    February 19, 2013
    Report Date
    April 8, 2013
    Manufacturer
    GENERAL ELECTRIC MAGNETIC RESONANCE
    Product Code
    ORR
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT UNDERWENT MRI ON (B)(6) 2013. ON (B)(6) 2013, I WAS NOTIFIED THAT PT IS REPORTING CONTINUING TINNITUS AND EAR PAIN SINCE HIS MRI.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    144270 GENERAL ELECTRIC MR 750W MRI ORR GENERAL ELECTRIC MAGNETIC RESONANCE

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR