BEUDAMED
    FDA Registration Active 🇳🇱 Netherlands

    SAKURA FINETEK EUROPE B.V.

    Reg #: 9614585 · FEI: 3002689354 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    7
    Establishment Types
    2
    Classifications
    2

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    Registration Details

    Registration Name
    SAKURA FINETEK EUROPE B.V.
    Registration Number
    9614585
    FEI Number
    3002689354
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Flemingweg 10A
    City
    Alphen aan den Rijn Zuid-Holland
    Country
    NL

    Owner / Operator

    Firm Name
    Sakura Global Holding Company
    Operator Number
    8031662
    Address
    1750 W 214th St
    City
    Torrance
    State
    CA
    Postal Code
    90501
    Country
    US

    US Agent

    Business Name
    Sakura Finetek USA
    Contact Name
    Solmaz M. Shaida
    Address
    1750 West 214th Street
    City
    Torrance
    State
    CA
    ZIP
    90501
    Country
    US
    Email
    [email protected]
    Phone
    310 7835076

    Products

    Device Name Product Code
    Container, Specimen Mailer And Storage, Non-Sterile NNK
    Microtome, Rotary IDO

    Proprietary Names

    Histo-Tek® Biopsy Bags Tissue-Tek Lab Aid Filing Cabinet System Tissue-Tek Lab Aid Ultra II Cabinets Tissue-Tek® Biopsy Bags Accu-Cut® SRM™ 300 LT Accu-Cut® SRM™ 200 Tissue-Tek AutoSection

    Establishment Types

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