BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    GE DPX Bravo Bone Densitometer

    Reg #: 3036666444 · FEI: 3036666444 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    FUJITA CO., LTD.
    Registration Number
    3036666444
    FEI Number
    3036666444
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5-1-1 Koujimachi
    City
    Chiyoda-ku Tokyo
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K030962

    Owner / Operator

    Firm Name
    FUJITA CO., LTD.
    Operator Number
    10092556
    Address
    5-1-1 Koujimachi
    City
    Chiyoda-ku
    State
    Tokyo
    Postal Code
    1020083
    Country
    JP
    Correspondent
    Tetsuya Hara

    Products

    Device Name Product Code
    Densitometer, Bone KGI

    Proprietary Names

    GE DPX Bravo Bone Densitometer

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device