BEUDAMED
    FDA Registration Active 🇨🇳 China

    CT/NG/UU/UP Nucleic Acid Multiplex Detection Kit

    Reg #: 3026312356 · FEI: 3026312356 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SUZHOU TIANLONG BIOTECHNOLOGY CO., LTD.
    Registration Number
    3026312356
    FEI Number
    3026312356
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Building NE-33, Nanopolis, No.99 Jinjihu Avenue, Suzhou Industrial Park, China (Jiangsu) Pilot Free Trade Zone
    City
    Suzhou Jiangsu
    Country
    CN

    Owner / Operator

    Firm Name
    Suzhou TianLong Biotechnology Co., Ltd.
    Operator Number
    10086573
    Address
    Building NE-33, Nanopolis, No.99 Jinjihu Avenue, Suzhou Industrial Park, China (Jiangsu) Pilot Free Trade Zone
    City
    Suzhou
    State
    Jiangsu
    Postal Code
    215123
    Country
    CN
    Correspondent
    Yangyang Wu

    US Agent

    Business Name
    Regrek LLC
    Contact Name
    Leeyeo Kee
    Address
    19 Holly Cove Ln.
    City
    Dover
    State
    DE
    ZIP
    19901
    Country
    US
    Email
    [email protected]
    Phone
    302 6089028

    Products

    Device Name Product Code
    Kit, Identification, Neisseria Gonorrhoeae JSX

    Proprietary Names

    CT/NG/UU/UP Nucleic Acid Multiplex Detection Kit Neisseria Gonorrhoeae (NG) Nucleic Acid Detection Kit (Fluorescence PCR Method)

    Establishment Types

    Manufacture Medical Device