BEUDAMED
    FDA Registration Active 🇨🇳 China

    Humidifier Non-direct patient interface (home-use)

    Reg #: 3020182147 · FEI: 3020182147 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    NINGBO AOXIANG ELECTRIC CO.,LTD
    Registration Number
    3020182147
    FEI Number
    3020182147
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    188 Shuntai Road,Jiaochuan, Zhenhai
    City
    Ningbo Zhejiang
    Country
    CN

    Owner / Operator

    Firm Name
    Ningbo Aoxiang Electric co.,ltd
    Operator Number
    10083947
    Address
    188 Shuntai Road,Jiaochuan, Zhenhai
    City
    Ningbo
    State
    Zhejiang
    Postal Code
    315207
    Country
    CN
    Correspondent
    Susie Su

    Products

    Device Name Product Code
    Humidifier, Non-Direct Patient Interface (Home-Use) KFZ

    Proprietary Names

    Humidifier Non-direct patient interface (home-use)

    Establishment Types

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