BEUDAMED
    FDA Adverse Event Summary report: N

    AIRLIFE

    MDR report key: 4120632 · Received September 4, 2014

    Report

    Report Number
    4120632
    Date Received
    September 4, 2014
    Date of Event
    August 27, 2014
    Report Date
    September 4, 2014
    Manufacturer
    CAREFUSION 211, INC..
    Product Code
    BZD
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    540902 AIRLIFE VENTILATOR, NON-CONTINUOUS (RESPIRATOR) BZD CAREFUSION 211, INC.. * CC14-A23

    Patients

    Seq Age Sex Outcome Treatment
    1 *