BEUDAMED
    FDA Registration Active 🇫🇷 France

    FibroScan 230

    Reg #: 3012038665 · FEI: 3012038665 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    ECHOSENS CRETEIL
    Registration Number
    3012038665
    FEI Number
    3012038665
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5 Rue Jean Lemoine
    City
    Creteil Val-de-Marne
    Country
    FR

    Regulatory Submissions

    510(k) Number
    K212035

    Owner / Operator

    Firm Name
    Echosens
    Operator Number
    10043955
    Address
    6 rue Ferrus
    City
    Paris
    State
    FR-75
    Postal Code
    75014
    Country
    FR

    US Agent

    Business Name
    Echosens North America
    Contact Name
    Jon S. Gingrich
    Address
    1 Research Dr Ste 400b
    City
    Westborough
    State
    MA
    ZIP
    01581
    Country
    US
    Email
    [email protected]
    Phone
    508 6546565

    Products

    Device Name Product Code
    Transducer, Ultrasonic, Diagnostic ITX
    System, Imaging, Pulsed Echo, Ultrasonic IYO

    Proprietary Names

    FibroScan 230

    Establishment Types

    Manufacture Medical Device