BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    AG-920RA Mulitgas Unit

    Reg #: 9611252 · FEI: 3002807720 · Expires 2025
    View on FDA
    Products
    8
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    8

    Registration Details

    Registration Name
    NIHON KOHDEN CORP.
    Registration Number
    9611252
    FEI Number
    3002807720
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    31-4 NISHIOCHIAI, 1-CHOME,
    City
    SHINJUKU-KU Tokyo
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K020046

    Owner / Operator

    Firm Name
    NIHON KOHDEN CORP.
    Operator Number
    8030227
    Address
    1-31-4 NISHIOCHIAI, SHINJUKU-KU
    City
    TOKYO
    State
    JP-13
    Postal Code
    161-8560
    Country
    JP

    US Agent

    Business Name
    NIHON KOHDEN AMERICA, LLC.
    Contact Name
    Charlemagne Chua
    Address
    15353 Barranca Pkwy, --
    City
    Irvine
    State
    CA
    ZIP
    92618
    Country
    US
    Email
    [email protected]
    Phone
    949 3303964

    Products

    Device Name Product Code
    Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.) CBS
    Analyzer, Gas, Isoflurane, Gaseous-Phase (Anesthetic Concentration) NHQ
    Analyzer, Gas, Sevoflurane, Gaseous-Phase (Anesthetic Concentration) NHP
    Analyzer, Gas, Oxygen, Gaseous-Phase CCL
    Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration) CBQ
    Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.) CBR
    Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase CCK
    Analyzer, Gas, Desflurane, Gaseous-Phase (Anesthetic Concentration) NHO

    Proprietary Names

    AG-920RA Mulitgas Unit AG-920RA

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility