BEUDAMED
    FDA Registration Active 🇵🇱 Poland

    Biovico sp. z o.o.

    Reg #: 3012479318 · FEI: 3012479318 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Biovico sp. z o.o.
    Registration Number
    3012479318
    FEI Number
    3012479318
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    7, Skandynawska Street
    City
    Wladyslawowo Pomorskie
    Country
    PL

    Owner / Operator

    Firm Name
    Biovico Sp. z o.o.
    Operator Number
    10060839
    Address
    Hutnicza 15B
    City
    Gdynia
    State
    Pomorskie
    Postal Code
    81-061
    Country
    PL

    US Agent

    Business Name
    Registrar Corp
    Contact Name
    David Lennarz
    Address
    144 Research Drive
    City
    Hampton
    State
    VA
    ZIP
    23666
    Country
    US
    Email
    [email protected]
    Phone
    757 2240177

    Products

    Device Name Product Code
    Dura Substitute GXQ

    Proprietary Names

    SyntheCel Dura Repair

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)