BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    VentStar Helix dual heated N Exten. Kit

    Reg #: 8022265 · FEI: 3002861325 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    GLOBALMED, INC.
    Registration Number
    8022265
    FEI Number
    3002861325
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    155 N. MURRAY ST.
    City
    TRENTON Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K222822

    Owner / Operator

    Firm Name
    Molded Devices, Inc.
    Operator Number
    10058611
    Address
    740 W Knox Road
    City
    Tempe
    State
    AZ
    Postal Code
    85284
    Country
    US

    US Agent

    Business Name
    Molded Devices, Inc., dba Aptyx
    Contact Name
    Samuel Brayton
    Address
    22 Hudson Falls Rd
    City
    S Glens Falls
    State
    NY
    ZIP
    12803
    Country
    US
    Email
    [email protected]
    Phone
    518 6360303

    Products

    Device Name Product Code
    Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer BZE

    Proprietary Names

    VentStar Helix dual heated N Exten. Kit VentStar Helix heated (N) Plus Double connector 11ID/15OD 20x

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)