BEUDAMED
    FDA Registration Active 🇨🇳 China

    CF1701-500A1-DB, CF1701-1000A1-DB, CF1701-1000C)

    Reg #: 3033842401 · FEI: 3033842401 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SHENZHEN GREATMADE TECH LIMITED
    Registration Number
    3033842401
    FEI Number
    3033842401
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    604-1, 6th Floor, Henghe International Building, No.1 Donghuan road, Jinglong Community,, Longhua Street, Longhua District
    City
    Shenzhen Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    Shenzhen Greatmade Tech limited
    Operator Number
    10091633
    Address
    604-1, 6th Floor, Henghe International Building, No.1 Donghuan road, Jinglong Community,, Longhua Street, Longhua District
    City
    Shenzhen
    State
    Guangdong
    Postal Code
    518000
    Country
    CN
    Correspondent
    Hanzhi Zhang

    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
    Infusor, Pressure, For I.V. Bags KZD

    Proprietary Names

    CF1701-500A1-DB, CF1701-1000A1-DB, CF1701-1000C) Pressure Infusion Bag (CF1701-500A, CF1701-500A1, CF1701-500A-BL, CF1701-500A1-BL, CF1701-1000A, CF1701-1000A1, CF1701-1000A-BL, CF1701-1000A1-BL, CF1701-3000A, CF1701-3000A1, CF1701-3000B, CF1701-500A1-TR, CF1701-500C,

    Establishment Types

    Manufacture Medical Device