BEUDAMED
    FDA Registration Active 🇺🇸 United States

    The Bouquet Speculum

    Reg #: 3012447313 · FEI: 3012447313 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Viospex
    Registration Number
    3012447313
    FEI Number
    3012447313
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7647 E. Windlawn Way
    City
    Parker
    State
    CO
    ZIP
    80134
    Country
    US

    Owner / Operator

    Firm Name
    Viospex
    Operator Number
    10051911
    Address
    7647 E. Windlawn Way
    City
    Parker
    State
    CO
    Postal Code
    80134
    Country
    US
    Correspondent
    Jean Bouquet

    Products

    Device Name Product Code
    Retractor, Vaginal HDL

    Proprietary Names

    The Bouquet Speculum

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility