BEUDAMED
    FDA Registration Active 🇺🇸 United States

    800 Series Cordless Illumination System

    Reg #: 1316463 · FEI: 1316463 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    WELCH ALLYN, INC.
    Registration Number
    1316463
    FEI Number
    1316463
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    4341 STATE STREET RD.
    City
    Skaneateles Falls
    State
    NY
    ZIP
    13153
    Country
    US

    Owner / Operator

    Firm Name
    BAXTER HEALTHCARE CORPORATION
    Operator Number
    1417572
    Address
    One Baxter Parkway
    City
    Deerfield
    State
    IL
    Postal Code
    60015
    Country
    US
    Correspondent
    Maha Nolasco

    Products

    Device Name Product Code
    Speculum, Vaginal, Nonmetal HIB

    Proprietary Names

    800 Series Cordless Illumination System 790 Series Cordless Iluminator and wire Illuminator KleenSpec Disposable Vaginal Speculum and accessories Accessories Obstetric-gynecologic Specialized Manual Instrument - KleenSpec Single Use Vaginal Speculum

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device