BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VIASYS

    MDR report key: 1041066 · Received April 22, 2008

    Report

    Report Number
    2021710-2008-00041
    Event Type
    Malfunction
    Date Received
    April 22, 2008
    Date of Event
    February 28, 2008
    Report Date
    April 21, 2008
    Manufacturer
    CARDINAL HEALTH 207, INC.
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VIASYS VOLUME VENTILATOR CBK CARDINAL HEALTH 207, INC. AVEA *

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR