BEUDAMED
    FDA Adverse Event Other Summary report: N

    8600F0

    MDR report key: 697384 · Received April 7, 2006

    Report

    Report Number
    2183646-2006-00001
    Event Type
    Other
    Date Received
    April 7, 2006
    Report Date
    April 5, 2006
    Manufacturer
    NONIN MEDICAL, INC.
    Product Code
    DQA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    PULSE OXIMETER WAS PUSHED INTO A 3 TESLA MRI UNIT. THE PULSE OXIMETER WAS 7-8 FEET AWAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 8600F0 PULSE OXIMETER FOR MRI DQA NONIN MEDICAL, INC. 8600F0 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Other