BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LuMatic® CLIA Analyzer (Ref IN008)

    Reg #: 1036223 · FEI: 1036223 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    AWARENESS TECHNOLOGY, INC.
    Registration Number
    1036223
    FEI Number
    1036223
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1935 S.W. MARTIN HWY.
    City
    PALM CITY
    State
    FL
    ZIP
    34990
    Country
    US

    Owner / Operator

    Firm Name
    AWARENESS TECHNOLOGY, INC.
    Operator Number
    1036223
    Address
    1935 S.W. MARTIN HWY., --
    City
    Palm City
    State
    FL
    Postal Code
    34990
    Country
    US

    Products

    Device Name Product Code
    Analyzer, Chemistry (Photometric, Discrete), For Clinical Use JJE

    Proprietary Names

    LuMatic® CLIA Analyzer (Ref IN008) NeoLumax® CLIA Analyzer (Ref IN010) Autoplex® ELISA & CLIA Analyzer (Ref IN006) PrisMatic® ELISA Analyzer (Ref IN013) Autoplex® 2nd Generation ELISA & CLIA Analyzer (Ref IN006-2) NeoEldex® ELISA Analyzer (Ref IN009) Immunoassay Plate Washer (Ref IN002) Autoplex® 3rd Generation Dual Plate ELISA Analyzer (Ref IN006-3)

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)