BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    EX3242-3D (with 3D glasses H3G01 or H3G02)

    Reg #: 3000237660 · FEI: 3000237660 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    21
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    EIZO CORPORATION
    Registration Number
    3000237660
    FEI Number
    3000237660
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    153 SHIMOKASHIWANO
    City
    HAKUSAN Ishikawa
    Country
    JP

    Owner / Operator

    Firm Name
    EIZO Corporation
    Operator Number
    9085040
    Address
    153 Shimokashiwano
    City
    Hakusan
    State
    Ishikawa
    Postal Code
    924-8566
    Country
    JP

    US Agent

    Business Name
    EIZO Inc.
    Contact Name
    THOMAS WALETZKI
    Address
    5710 Warland DR
    City
    Cypress
    State
    CA
    ZIP
    90630
    Country
    US
    Email
    [email protected]
    Phone
    562 4315011

    Products

    Device Name Product Code
    Camera, Surgical And Accessories KQM

    Proprietary Names

    EX3242-3D (with 3D glasses H3G01 or H3G02) EX3140 CuratOR EX3220-3D (with 3D glasses H3G01 or H3G02) EX2620-3D (with 3D glasses H3G01 or H3G02) CuratOR EX2620-3D (with 3D glasses H3G01 or H3G02) EX3220-3D (with 3D glasses H3G01 or H3G02) CuratOR EX3140 EX2721 EX3141 CuratOR EX3220 CuratOR EX3241 CuratOR EX2721 CuratOR EX3141-3D (with 3D glasses H3G01 or H3G02) CuratOR EX2621 CuratOR EX2620 TM343 CuratOR EX3242-3D (with 3D glasses H3G01 or H3G02) TM344 CuratOR EX3242 TM351 (with 3D glasses H3G01 or H3G02) CuratOR EX2722

    Establishment Types

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