BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BLUE LINE CUFFED ORAL/NASAL ENDOTRACHEAL TUBE

    MDR report key: 1012549 · Received February 6, 2008

    Report

    Report Number
    1217052-2008-00006
    Event Type
    Malfunction
    Date Received
    February 6, 2008
    Date of Event
    January 10, 2008
    Report Date
    January 11, 2008
    Manufacturer
    SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V./SMITH MEDICAL
    Product Code
    BTR
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BLUE LINE CUFFED ORAL/NASAL ENDOTRACHEAL TUBE 73 BTR - TUBE, TRACHEAL WITH/WITHOUT CONNECTOR BTR SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V./SMITH MEDICAL * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *