BEUDAMED
    FDA Registration Active 🇨🇳 China

    Diagnostic Kit for Immunoglobulin E(IgE) (Fluorescent Immunnochromatographic Assay)

    Reg #: 3027318375 · FEI: 3027318375 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Hangzhou Sightnovo Medical Technology Co., Ltd.
    Registration Number
    3027318375
    FEI Number
    3027318375
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    101M, Building 7, No. 22, Xinyan Road, Donghu Street, Linping District
    City
    Hangzhou City Zhejiang
    Country
    CN

    Owner / Operator

    Firm Name
    Hangzhou Sightnovo Medical Technology Co., Ltd.
    Operator Number
    10087607
    Address
    101M, Building 7, No. 22, Xinyan Road, Donghu Street, Linping District
    City
    Hangzhou City
    State
    Zhejiang
    Postal Code
    311100
    Country
    CN
    Correspondent
    Liping Sun

    US Agent

    Business Name
    UGK-LVM UNITED INC
    Contact Name
    Henry Henry
    Address
    6547 N Academy Blvd #2266
    City
    Colorado Springs
    State
    CO
    ZIP
    80918
    Country
    US
    Email
    [email protected]
    Phone
    323 5104660

    Products

    Device Name Product Code
    Reagents, Specific, Analyte MVU

    Proprietary Names

    Diagnostic Kit for Immunoglobulin E(IgE) (Fluorescent Immunnochromatographic Assay) Fibroblast Growth Factor2(FGF2) Angiopoietin-2(Ang-2) Diagnostic Kit for Interleukin 6(IL-6)(CLIA) Diagnostic Kit for Interleukin 6(IL-6) (Fluorescent Immunnochromatographic Assay)

    Establishment Types

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