BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ BREATH ATOMIZER

    MDR report key: 3949875 · Received July 15, 2014

    Report

    Report Number
    MW5037336
    Event Type
    Malfunction
    Date Received
    July 15, 2014
    Date of Event
    July 13, 2014
    Report Date
    July 14, 2014
    Manufacturer
    NEPHRON PHARMACEUTICALS
    Product Code
    CCQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DEVICE CEASES OPERATION AFTER A FEW USES. IT IS UNNECESSARILY COMPLICATED. A SIMPLE NEBULIZER WOULD BE MORE USEFUL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    412929 EZ BREATH ATOMIZER ATOMIZER CCQ NEPHRON PHARMACEUTICALS EZ-100-MC 130601

    Patients

    Seq Age Sex Outcome Treatment
    1