BEUDAMED
    FDA Registration Active 🇲🇺 Mauritius

    LILMO Ltd

    Reg #: 3010872792 · FEI: 3010872792 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    4

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    Registration Details

    Registration Name
    LILMO Ltd
    Registration Number
    3010872792
    FEI Number
    3010872792
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Route Royale, Canton Bel Eau
    City
    PAMPLEMOUSSES
    Country
    MU

    Owner / Operator

    Firm Name
    Perouse Medical
    Operator Number
    10046668
    Address
    Batiment LW1 1 Route Des Troques
    City
    Chaponost
    State
    Auvergne-Rhone-Alpes
    Postal Code
    69630
    Country
    FR

    US Agent

    Business Name
    VYGON USA
    Contact Name
    Chris Steinke
    Address
    2750 Morris Road Suite A200
    City
    Lansdale
    State
    PA
    ZIP
    19446
    Country
    US
    Email
    [email protected]
    Phone
    603 7435988

    Products

    Device Name Product Code
    Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass DTL
    Syringe, Balloon Inflation MAV
    Set, Administration, Intravascular FPA
    Needle, Hypodermic, Single Lumen FMI

    Proprietary Names

    MyShell Lite Dolphin Inflation Device POLYPERF with injection site POLYPERF SAFE without injection site POLYPERF without injection site POLYPERF SAFE with injection site PPS PI® Pressure Injectable Safety Huber Needle

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)