BEUDAMED
    FDA Registration Active 🇨🇳 China

    xp-39

    Reg #: 3011215096 · FEI: 3011215096 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    17
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    GUILIN YIKESHI Medical Device CO LTD
    Registration Number
    3011215096
    FEI Number
    3011215096
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    D-8, Guilin National High-tech Zone Information Industrial Park, Chaoyang Road, Qixing District
    City
    Guilin Guangxi
    Country
    CN

    Owner / Operator

    Firm Name
    Guilin Yikeshi Medical Instrument Co Ltd
    Operator Number
    10047368
    Address
    D-8, Guilin National High-tech Zone Information Industrial Park, Chaoyang Road, Qixing District
    City
    Guilin
    State
    Guangxi
    Postal Code
    541004
    Country
    CN
    Correspondent
    Ai Juan Yang

    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
    Plugger, Root Canal, Endodontic EKR

    Proprietary Names

    xp-39 xp-PRT xp-35C xp-GC2 xp-GD7 xp-35 xp-GS7 xp-34 xp-G7 xp-GN7 xp-NK7 xp-GM7 xp-GK7 xp-34s xp-35B xp-35A Obturation System

    Establishment Types

    Manufacture Medical Device