BEUDAMED
    FDA Registration Active 🇨🇳 China

    Aneroid sphygmomanometer QL-20, QL-50, QL-201 (20A, 50A, 201C1)

    Reg #: 3031192529 · FEI: 3031192529 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Zhejiang LuDe Technology Development Co., Ltd.
    Registration Number
    3031192529
    FEI Number
    3031192529
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    NO. 298 Jichang North Road, Longwan District
    City
    Wenzhou Zhejiang
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K221857

    Owner / Operator

    Firm Name
    Zhejiang LuDe Technology Development Co., Ltd.
    Operator Number
    10090465
    Address
    NO. 298 Jichang North Road, Longwan District
    City
    Wenzhou
    State
    Zhejiang
    Postal Code
    325024
    Country
    CN
    Correspondent
    Iris Du

    Products

    Device Name Product Code
    Stethoscope, Manual LDE
    Blood Pressure Cuff DXQ

    Proprietary Names

    Aneroid sphygmomanometer QL-20, QL-50, QL-201 (20A, 50A, 201C1)

    Establishment Types

    Manufacture Medical Device