BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PEDIA ENDOTRACHEAL TUBE 2.5MM

    MDR report key: 1031941 · Received April 1, 2008

    Report

    Report Number
    2245270-2008-00001
    Event Type
    Injury
    Date Received
    April 1, 2008
    Date of Event
    March 11, 2008
    Report Date
    March 31, 2008
    Manufacturer
    VYGON SA
    Product Code
    BTR
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    NJ, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PEDIA ENDOTRACHEAL TUBE 2.5MM 2.5MM 12 FR ET TUBE BTR VYGON SA * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention