BEUDAMED
    FDA Registration Active 🇨🇳 China

    Diode Laser Therapy Device (DF-DIODE LASER-S1)

    Reg #: 3026294985 · FEI: 3026294985 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Weifang Dragonfly Electronic Technology Co., Ltd.
    Registration Number
    3026294985
    FEI Number
    3026294985
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    No. 5762 Dongfeng East Street, High-Tech Development Zone
    City
    Weifang Shandong
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K241547

    Owner / Operator

    Firm Name
    Weifang Dragonfly Electronic Technology Co., Ltd
    Operator Number
    10086847
    Address
    No. 5762 Dongfeng East Street, High-Tech Development Zone
    City
    Weifang
    State
    Shandong
    Postal Code
    261061
    Country
    CN
    Correspondent
    Ray Zhao

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX

    Proprietary Names

    Diode Laser Therapy Device (DF-DIODE LASER-S1)

    Establishment Types

    Manufacture Medical Device