BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Tenax Laser Resistant Endotracheal Tube TUBE, TRACHEAL (W/WO CONNECTOR)

    Reg #: 3011481350 · FEI: 3011481350 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    BD MEDICAL DEVELOPMENT
    Registration Number
    3011481350
    FEI Number
    3011481350
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1140 Millennium Dr
    City
    Crown Point
    State
    IN
    ZIP
    46307
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200761

    Owner / Operator

    Firm Name
    BD Medical Development
    Operator Number
    10092278
    Address
    1140 Millennium Drive
    City
    Crown Point
    State
    IN
    Postal Code
    46307
    Country
    US
    Correspondent
    Mary Depel

    Products

    Device Name Product Code
    Cuff, Tracheal Tube, Inflatable BSK
    Tube, Tracheal (W/Wo Connector) BTR

    Proprietary Names

    Tenax Laser Resistant Endotracheal Tube TUBE, TRACHEAL (W/WO CONNECTOR) Tenax Laser Resistant Endotracheal Tube CUFF, TRACHEAL TUBE, INFLATABLE

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)