BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    Thetis Medical Achilles Rupture Night Splint, Thetis Medical Achilles Rupture Trauma Splint

    Reg #: 3022381831 · FEI: 3022381831 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    THETIS MEDICAL LTD.
    Registration Number
    3022381831
    FEI Number
    3022381831
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    15 Leopold Street
    City
    Birmingham
    Country
    GB

    Owner / Operator

    Firm Name
    Thetis Medical Ltd.
    Operator Number
    10084925
    Address
    15 Leopold Street
    City
    Birmingham
    State
    GB-NOTA
    Postal Code
    B12 0UP
    Country
    GB

    US Agent

    Business Name
    Registrar Corp
    Contact Name
    David Lennarz
    Address
    144 Research Drive
    City
    Hampton
    State
    VA
    ZIP
    23666
    Country
    US
    Email
    [email protected]
    Phone
    757 2240177

    Products

    Device Name Product Code
    Splint, Extremity, Noninflatable, External, Sterile FYH

    Proprietary Names

    Thetis Medical Achilles Rupture Night Splint, Thetis Medical Achilles Rupture Trauma Splint

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device for Another Party (Contract Manufacturer)