BEUDAMED
    FDA Adverse Event Other Summary report: N

    NEOTREND-L SENSOR

    MDR report key: 888669 · Received August 13, 2004

    Report

    Report Number
    9612233-2004-00022
    Event Type
    Other
    Date Received
    August 13, 2004
    Date of Event
    July 1, 2004
    Report Date
    July 19, 2004
    Manufacturer
    DIAMETRICS MEDICAL LIMITED
    Product Code
    CCL
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEOTREND-L SENSOR BLOOD GAS MONITORING SYSTEM CCL DIAMETRICS MEDICAL LIMITED N7004L 919

    Patients

    Seq Age Sex Outcome Treatment
    1 YR