BEUDAMED
    FDA Registration Active 🇧🇪 Belgium

    X-Lite

    Reg #: 8020160 · FEI: 6347 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    RUNLITE S.A.
    Registration Number
    8020160
    FEI Number
    6347
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    9 AVENUE DE LA COOPERATION, MICHEROUX
    City
    SOUMAGNE Liege
    Country
    BE

    Owner / Operator

    Firm Name
    RUNLITE SA
    Operator Number
    8020160
    Address
    9 AVENUE DE LA COOPERATION,, MICHEROUX
    City
    SOUMAGNE
    State
    BE-NOTA
    Postal Code
    4630
    Country
    BE
    Correspondent
    SEBASTIEN - HENDRIX

    US Agent

    Business Name
    Kinetec USA, Inc.
    Contact Name
    Lori Kalsow
    Address
    N174W21475 Alcan Drive
    City
    Jackson
    State
    WI
    ZIP
    53037
    Country
    US
    Email
    [email protected]
    Phone
    262 6771248 ext. 109

    Products

    Device Name Product Code
    Splint, Extremity, Noninflatable, External, Sterile FYH

    Proprietary Names

    X-Lite 3D-Lite

    Establishment Types

    Manufacture Medical Device