BEUDAMED
    FDA Adverse Event Other Summary report: N

    NOCTURNAL PULSE OXIMETRY

    MDR report key: 24873920 · Received April 14, 2026

    Report

    Report Number
    MW5186808
    Event Type
    Other
    Date Received
    April 14, 2026
    Manufacturer
    NONIN MEDICAL, INC.
    Product Code
    DQA
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NOCUTURNAL PULSE OX DID NOT CAPTURE OR RECORD SATURATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    285639 NOCTURNAL PULSE OXIMETRY OXIMETER DQA NONIN MEDICAL, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown