BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3003135857-2006-00032

    MDR report key: 727702 · Received June 1, 2006

    Report

    Report Number
    3003135857-2006-00032
    Event Type
    Malfunction
    Date Received
    June 1, 2006
    Product Code
    CBK
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE VENTILATOR WAS RECEIVED BY NEWPORT MEDICAL INSTRUMENTS INC ON 5/22/2006. IT WILL BE FORWARDED TO MFR/FLIGHT MEDICAL LTD. FOR FURTHER INVESTIGATION. A FAILURE ANALYSIS REPORT AND ACTION TAKEN IN RESOLVING TH IS ISSUE WILL BE SUBMITTED TO MEDWATCH PROGRAM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CBK

    Patients

    Seq Age Sex Outcome Treatment
    1