BEUDAMED
    FDA Registration Active 🇨🇳 China

    JDI ELECTRONICS FACTORY

    Reg #: 3003927385 · FEI: 3003927385 · Expires 2026
    View on FDA
    Products
    7
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    7

    Registration Details

    Registration Name
    JDI ELECTRONICS FACTORY
    Registration Number
    3003927385
    FEI Number
    3003927385
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Sima Industrial District, Sima Village, Chang Ping Town
    City
    Dongguan Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    Blue Ocean Innovation Limited
    Operator Number
    9054823
    Address
    Unit 50, 8/F Wah Lok Industrial Centre Phase 2 Blk F,, 31-35 Shan Mei Street.
    City
    FOTAN
    State
    HK-NOTA
    Postal Code
    --
    Country
    HK
    Correspondent
    SAM - LEE

    US Agent

    Business Name
    PETER TAM-ENGINEERING CONSULTANT
    Contact Name
    PETER TAM
    Address
    11217 Black Fire Opal Drive
    City
    Las Vegas
    State
    NV
    ZIP
    89138
    Country
    US
    Email
    [email protected]
    Phone
    949 4000888

    Products

    Device Name Product Code
    Respiratory Accessory Microbial Reduction Device. QXQ
    Set, Administration, Intravascular FPA
    Stimulator, Nerve, Electrical, Transcutaneous, For Migraine PCC
    Pump, Infusion FRN
    Immunoglobulin G (Igg) Infusion System PKP
    Disinfectant, Medical Devices LRJ
    Pump, Breast, Powered HGX

    Proprietary Names

    SoClean 3+ Bacterial Reduction Device IHS-needle set (#637) Cefaly #629 IHS Series CEFALY DUAL Enhanced CEFALY Connected and CeCe Migraine Management App

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)