BEUDAMED
    FDA Adverse Event Death Summary report: N

    NONIN MODEL 8604-D-L PULSE OXIMETER

    MDR report key: 23467 · Received December 9, 1994

    Report

    Report Number
    36222-1994-09004
    Event Type
    Death
    Date Received
    December 9, 1994
    Date of Event
    October 17, 1994
    Report Date
    October 26, 1994
    Manufacturer
    NONIN MEDICAL
    Product Code
    KLK
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    MN, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    SEE REFERENCED REPORT # 36222-1994-9001. SAME EVENT DESCRIPTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONIN MODEL 8604-D-L PULSE OXIMETER OXIMETER KLK NONIN MEDICAL 8604D-L NA

    Patients

    Seq Age Sex Outcome Treatment
    1 8 MO Death