BEUDAMED
    FDA Registration Active 🇭🇰 Hong Kong

    Viospex

    Reg #: 3010367874 · FEI: 3010367874 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    TRICORBRAUN HONGKONG CORPORATION LIMITED
    Registration Number
    3010367874
    FEI Number
    3010367874
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Room 2202, 22/F., 168 Sai Yeung Choi Street,, Mongkok, Kowloon, Hong Kong
    City
    Hongkong
    Country
    HK

    Owner / Operator

    Firm Name
    TRICORBRAUN HONGKONG CORPORATION LIMITED
    Operator Number
    10043568
    Address
    RM109, 11/F. Hip Sang Building,, 107-115 Hennessy Rd, Wanchai
    City
    Hongkong
    State
    HK-NOTA
    Postal Code
    999077
    Country
    HK
    Correspondent
    Hector Liang

    US Agent

    Business Name
    TricorBraun, Inc.
    Contact Name
    Karen Schnabel
    Address
    6 CityPlace Drive, Suite 1000
    City
    Saint Louis
    State
    MO
    ZIP
    63141
    Country
    US
    Email
    [email protected]
    Phone
    562 4836609

    Products

    Device Name Product Code
    Retractor, Vaginal HDL

    Proprietary Names

    Viospex

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device