BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    NIPRO VASCULAR CORPORATION Aichi Facility

    Reg #: 3030042169 · FEI: 3030042169 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    NIPRO VASCULAR CORPORATION Aichi Facility
    Registration Number
    3030042169
    FEI Number
    3030042169
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    1-176 Shiokusagaoka
    City
    Seto Aichi
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K243944

    Owner / Operator

    Firm Name
    NIPRO VASCULAR CORPORATION
    Operator Number
    10061300
    Address
    5F KDX Nagoya Sakae Building, 4-5-3 Sakae, Naka-ku
    City
    Nagoya
    State
    Aichi
    Postal Code
    4600008
    Country
    JP
    Correspondent
    Hirotaka Ishii

    Products

    Device Name Product Code
    Catheter, Percutaneous, Cutting/Scoring PNO

    Proprietary Names

    Aperta NSE PTA Balloon Dilatation Catheter

    Establishment Types

    Manufacture Medical Device