BEUDAMED
    FDA Adverse Event Death Summary report: N

    NONIN MEDICAL INC.

    MDR report key: 2642925 · Received June 25, 2012

    Report

    Report Number
    2183646-2012-00001
    Event Type
    Death
    Date Received
    June 25, 2012
    Date of Event
    May 30, 2012
    Report Date
    June 25, 2012
    Manufacturer
    NONIN MEDICAL, INC.
    Product Code
    DQA
    PMA / PMN Number
    K080255
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    IT WAS ALLEGED THAT THE OXIMETER WOULD NOT GIVE READINGS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONIN MEDICAL INC. AVANT 7500 DQA NONIN MEDICAL, INC. 7500

    Patients

    Seq Age Sex Outcome Treatment
    1 Death NONE KNOWN