BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AIRWAY KIT GUEDEL SIZES 0-5 - SEEGAK

    Reg #: 3020460367 · FEI: 3020460367 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BOUND TREE MEDICAL, LLC
    Registration Number
    3020460367
    FEI Number
    3020460367
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2911 S GREAT SW PARKWAY, SUITE 200B
    City
    Grand Prairie
    State
    TX
    ZIP
    75052
    Country
    US

    Owner / Operator

    Firm Name
    BEMS Holdings, LLC
    Operator Number
    9003409
    Address
    5000 BRADENTON AVE, --
    City
    Dublin
    State
    OH
    Postal Code
    43017
    Country
    US
    Correspondent
    DARRELL HUGHES

    Products

    Device Name Product Code
    Airway, Oropharyngeal, Anesthesiology CAE

    Proprietary Names

    AIRWAY KIT GUEDEL SIZES 0-5 - SEEGAK Curaplex Air-Q sp3G BLS Kit Size 4 with Suction Cath, Connector, ET Tube Holder, and Lube Jelly - 670275-KIT Curaplex Air-Q sp3G Kit Size 4 with NG Tube and Lube Jelly - 670281-KIT

    Establishment Types

    Manufacture Medical Device