BEUDAMED
    FDA Registration Active 🇳🇱 Netherlands

    VitreQ Directional Laser Probe

    Reg #: 3012037425 · FEI: 3012037425 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    VITREQ BV
    Registration Number
    3012037425
    FEI Number
    3012037425
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Seggelant-Noord 2
    City
    Vierpolders Zuid-Holland
    Country
    NL

    Regulatory Submissions

    510(k) Number
    K182646

    Owner / Operator

    Firm Name
    VITREQ BV
    Operator Number
    10050448
    Address
    Seggelant-Noord 2
    City
    Vierpolders
    State
    Zuid-Holland
    Postal Code
    3237 MG
    Country
    NL

    US Agent

    Business Name
    Beaver-Visitec International Inc.
    Contact Name
    Silvana Brown
    Address
    500 Totten Pond Rd
    City
    Waltham
    State
    MA
    ZIP
    02451
    Country
    US
    Email
    [email protected]
    Phone
    952 7377242

    Products

    Device Name Product Code
    Laser, Ophthalmic HQF
    Endoilluminator MPA
    Photocoagulator And Accessories HQB

    Proprietary Names

    VitreQ Directional Laser Probe VitreQ Chandelier & Light Fibers

    Establishment Types

    Manufacture Medical Device