BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Lacrimal Light Probe Fiberoptic

    Reg #: 9680660 · FEI: 3002808473 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    WALSH MEDICAL DEVICES, INC.
    Registration Number
    9680660
    FEI Number
    3002808473
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1200 SOUTH SERVICE RD. WEST, UNIT 3
    City
    OAKVILLE Ontario
    Country
    CA

    Owner / Operator

    Firm Name
    WALSH MEDICAL DEVICES, INC.
    Operator Number
    9010481
    Address
    1200 SOUTH SERVICE RD. WEST, UNIT 3
    City
    OAKVILLE
    State
    Ontario
    Postal Code
    L6L 5T7
    Country
    CA

    US Agent

    Business Name
    JEDMED INSTRUMENT COMPANY
    Contact Name
    DUSTIN BIGGERSTAFF
    Address
    5416 Jedmed Ct
    City
    Saint Louis
    State
    MO
    ZIP
    63129
    Country
    US
    Email
    [email protected]
    Phone
    314 8453770

    Products

    Device Name Product Code
    Transilluminator, Battery-Powered HJN

    Proprietary Names

    Lacrimal Light Probe Fiberoptic

    Establishment Types

    Manufacture Medical Device