BEUDAMED
    FDA Registration Active 🇮🇹 Italy

    NOVA Lite ANCA Kit

    Reg #: 3012348571 · FEI: 3012348571 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    INSTRUMENTATION LABORATORY SPA
    Registration Number
    3012348571
    FEI Number
    3012348571
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Via Leonardo da Vinci, 36
    City
    Roncello Lombardy
    Country
    IT

    Regulatory Submissions

    510(k) Number
    K961340

    Owner / Operator

    Firm Name
    Instrumentation Laboratory SpA
    Operator Number
    10082968
    Address
    Viale Monza 338
    City
    Milan
    State
    Lombardy
    Postal Code
    20128
    Country
    IT
    Correspondent
    Natale Bova

    Products

    Device Name Product Code
    Test System, Antineutrophil Cytoplasmic Antibodies (Anca) MOB

    Proprietary Names

    NOVA Lite ANCA Kit Anti-neutrophil Cytoplasmic Autoantibody Reagents NOVA Lite ANCA (Ethanol Fixed) NOVA Lite ANCA NOVA Lite ANCA Substrate Slide Pack

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device