BEUDAMED
    FDA Registration Active 🇨🇳 China

    ADC NINGBO CO., LTD.

    Reg #: 3010262192 · FEI: 3010262192 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    ADC NINGBO CO., LTD.
    Registration Number
    3010262192
    FEI Number
    3010262192
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Suite # 1406, #181, Zhongshan East Road
    City
    Ningbo Zhejiang
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K053006

    Owner / Operator

    Firm Name
    ADC Ningbo Co., Ltd.
    Operator Number
    10046012
    Address
    Suite # 1406, #181, Zhongshan East Road
    City
    Ningbo
    State
    Zhejiang
    Postal Code
    315000
    Country
    CN
    Correspondent
    Jackie Wu

    Products

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

    Establishment Types

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