BEUDAMED
    FDA Registration Active 🇨🇳 China

    BIO PROTECH YANTAI INC

    Reg #: 3010805941 · FEI: 3010805941 · Expires 2026
    View on FDA
    Products
    12
    Proprietary Names
    17
    Establishment Types
    1
    Classifications
    12

    Registration Details

    Registration Name
    BIO PROTECH YANTAI INC
    Registration Number
    3010805941
    FEI Number
    3010805941
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    50 - 9, Beijingzhong Road, Development Zone
    City
    Yantai Shandong
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K100246

    Owner / Operator

    Firm Name
    BIO PROTECH, INC.
    Operator Number
    9048345
    Address
    151-3, Donghwagongdan-ro, Munmak-eup
    City
    Wonju-si
    State
    Gangwon
    Postal Code
    26365
    Country
    KR
    Correspondent
    Namhyun Cho

    US Agent

    Business Name
    BIO PROTECH USA INC.
    Contact Name
    Ikro Park
    Address
    13311 166th St Ste A
    City
    Cerritos
    State
    CA
    ZIP
    90703
    Country
    US
    Email
    [email protected]
    Phone
    909 4641464

    Products

    Device Name Product Code
    Interferential Current Therapy LIH
    Stimulator, Nerve, Transcutaneous, For Pain Relief GZJ
    Cable, Electrode IKD
    Electrode, Needle, Diagnostic Electromyograph IKT
    Electrode, Needle GXZ
    Stimulator, Muscle, Powered IPF
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Electrode, Cutaneous GXY
    Tubing/Tubing With Filter, Insufflation, Laparoscopic NKC
    Electrode, Electrocardiograph DRX
    Apparatus, Exhaust, Surgical FYD
    Tubing, Noninvasive GAZ

    Proprietary Names

    MAXIF Ultima5 CABLE, ELECTRODE PROEMG MAXEMS PROPENCIL PROPLATE MAXTENS PROTENS EvaQMax Laparo TELECTRODE Soft-Touch™ PROTAB PROEEG PRONEO EvaQMax Smoke Evacuation Tubing

    Establishment Types

    Manufacture Medical Device