BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    ARCOS INNER GUIDE TUBE; ARCOS OUTER GUIDE TUBE

    Reg #: 3010332206 · FEI: 3010332206 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BRADFORD TOOL GROUP
    Registration Number
    3010332206
    FEI Number
    3010332206
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1 Tong Street, Bradford, West Yorkshire
    City
    Bradford York
    Country
    GB

    Owner / Operator

    Firm Name
    Bradford Tool Group
    Operator Number
    10043332
    Address
    1 Tong Street, Bradford, West Yorkshire
    City
    Bradford
    State
    GB-BRD
    Postal Code
    BD4 9PW
    Country
    GB
    Correspondent
    Helen Senior

    US Agent

    Business Name
    Emergo by UL
    Contact Name
    Theresa Ramirez
    Address
    2500 Bee Caves Rd Ste 1 Ste 300
    City
    Austin
    State
    TX
    ZIP
    78746
    Country
    US
    Email
    [email protected]
    Phone
    512 2220262

    Products

    Device Name Product Code
    Device, Prosthesis Alignment IQO

    Proprietary Names

    ARCOS INNER GUIDE TUBE; ARCOS OUTER GUIDE TUBE

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)