BEUDAMED
    FDA Registration Active 🇨🇳 China

    ALL PURPOSE CUFF

    Reg #: 3006769302 · FEI: 3006769302 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD.
    Registration Number
    3006769302
    FEI Number
    3006769302
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    105 Huanguan South Road,Suite15, 2-3/F, Dahe Cummunity, GuanHu Subdistrict, LongHua District,
    City
    Shenzhen Guangdong
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K051904

    Owner / Operator

    Firm Name
    Suntech Medical Devices (Shenzhen) Co., Ltd,
    Operator Number
    10034244
    Address
    105 Huanguan South Road,Suite15,2-3/F, Dahe Community, Guanhu Sub-district, LongHua District
    City
    Shenzhen
    State
    Guangdong
    Postal Code
    518110
    Country
    CN

    US Agent

    Business Name
    SunTech Medical, Inc
    Contact Name
    Tonia Bryant
    Address
    5827 South Miami Blvd, Ste 100
    City
    Morrisville
    State
    NC
    ZIP
    27560
    Country
    US
    Email
    [email protected]
    Phone
    919 6542314

    Products

    Device Name Product Code
    Blood Pressure Cuff DXQ

    Proprietary Names

    ALL PURPOSE CUFF

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)