BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    Newfoundland Menopause Self-test

    Reg #: 3031231787 · FEI: 3031231787 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    NEWFOUNDLAND DIAGNOSTICS
    Registration Number
    3031231787
    FEI Number
    3031231787
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3a Station Road
    City
    Amersham Buckinghamshire
    Country
    GB

    Owner / Operator

    Firm Name
    Newfoundland Diagnostics
    Operator Number
    10090412
    Address
    3a Station Road
    City
    Amersham
    State
    Buckinghamshire
    Postal Code
    HP7 0BQ
    Country
    GB
    Correspondent
    Ludovic Czartoryski Bruseth

    US Agent

    Business Name
    Dawa Medical LLC
    Contact Name
    Stephan Toupin
    Address
    7320 North West 12th Street Suite 103
    City
    Doral
    State
    FL
    ZIP
    33126
    Country
    US
    Email
    [email protected]
    Phone
    305 5999373

    Products

    Device Name Product Code
    Test, Follicle Stimulating Hormone (Fsh), Over The Counter NGA

    Proprietary Names

    Newfoundland Menopause Self-test

    Establishment Types

    Foreign Private Label Distributor Export Device to the United States But Perform No Other Operation on Device