BEUDAMED
    FDA Registration Active 🇸🇪 Sweden

    Follicle Aspiration Set, Single Lumen Luer with Tubing

    Reg #: 3003995932 · FEI: 3003995932 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VITROLIFE SWEDEN AB
    Registration Number
    3003995932
    FEI Number
    3003995932
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Gustaf Werners Gata 2
    City
    Vastra Frolunda Vastra Gotaland
    Country
    SE

    Regulatory Submissions

    510(k) Number
    K161970

    Owner / Operator

    Firm Name
    VITROLIFE AB
    Operator Number
    9037178
    Address
    Gustaf Werners gata 2
    City
    Vastra Frolunda
    State
    Vastra Gotaland
    Postal Code
    SE-421 32
    Country
    SE
    Correspondent
    NINA - ARVIDSSON

    US Agent

    Business Name
    Vitrolife Inc.
    Contact Name
    Eli Soto
    Address
    3601 South Inca Street
    City
    Englewood
    State
    CO
    ZIP
    80110
    Country
    US
    Email
    [email protected]
    Phone
    303 8074272

    Products

    Device Name Product Code
    Needle, Assisted Reproduction MQE

    Proprietary Names

    Follicle Aspiration Set, Single Lumen Luer with Tubing Follicle Aspiration Set, Single Lumen, Luer Follicle Aspiration Set, Double Lumen Follicle Aspiration Set, Single Lumen

    Establishment Types

    Manufacture Medical Device