BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    Nipro Hydrophilic Guidewire

    Reg #: 9611446 · FEI: 3002807725 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    NIPRO MEDICAL INDUSTRIES LTD.
    Registration Number
    9611446
    FEI Number
    3002807725
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2-19-64, MATSUBARA
    City
    TATEBAYASHI-SHI Gunma
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K060034

    Owner / Operator

    Firm Name
    NIPRO CORPORATION
    Operator Number
    8030375
    Address
    3-26, Senriokashinmachi, Settsu,, --
    City
    Osaka
    State
    JP-27
    Postal Code
    566-8510
    Country
    JP
    Correspondent
    Nobuhiro Morimoto

    US Agent

    Business Name
    NIPRO MEDICAL CORPORATION
    Contact Name
    JESSICA OSWALD-MCLEOD
    Address
    3150 NW 107th Ave
    City
    Doral
    State
    FL
    ZIP
    33172
    Country
    US
    Email
    [email protected]
    Phone
    305 4326699

    Products

    Device Name Product Code
    Endoscopic Guidewire, Gastroenterology-Urology OCY

    Proprietary Names

    Nipro Hydrophilic Guidewire NIPRO HYDROPHILIC FOR UR

    Establishment Types

    Manufacture Medical Device