BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    Kitazato IUI Catheter with Stainless Steel Center Core Type, 10 cm, model number Type 1-v1

    Reg #: 9611680 · FEI: 3002807969 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    RADIA INDUSTRY CO., LTD.
    Registration Number
    9611680
    FEI Number
    3002807969
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    168 Ooyagi
    City
    Takasaki Gunma
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K112396

    Owner / Operator

    Firm Name
    Radia Industry Co., Ltd.
    Operator Number
    10042849
    Address
    168 Ooyagi
    City
    Takasaki
    State
    Gunma
    Postal Code
    370-0072
    Country
    JP
    Correspondent
    Masako Tomita

    US Agent

    Business Name
    Globizz Corp.
    Contact Name
    Takahiro Haruyama
    Address
    970 W. 190th St., Suite 200
    City
    Torrance
    State
    CA
    ZIP
    90502
    Country
    US
    Email
    [email protected]
    Phone
    310 5383860

    Products

    Device Name Product Code
    Catheter, Assisted Reproduction MQF

    Proprietary Names

    Kitazato IUI Catheter with Stainless Steel Center Core Type, 10 cm, model number Type 1-v1 Kitazato IUI Catheter without Stainless Steel Center Core Type, 7 cm, model number Type 2-v2 Kitazato IUI Catheter without Stainless Steel Center Core Type, 10 cm, model number Type 2-v1 Kitazato IUI Catheter with Stainless Steel Center Core Type, 7 cm, model number Type 1-v2

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)