BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Alinity m STI Amplification Kit, Alinity m STI Control Kit

    Reg #: 3005248192 · FEI: 3005248192 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ABBOTT MOLECULAR, INC.
    Registration Number
    3005248192
    FEI Number
    3005248192
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1300 EAST TOUHY AVENUE
    City
    Des Plaines
    State
    IL
    ZIP
    60018
    Country
    US

    Owner / Operator

    Firm Name
    ABBOTT LABORATORIES
    Operator Number
    1415939
    Address
    100 ABBOTT PARK RD., D-03Q3, AP52-1
    City
    Abbott Park
    State
    IL
    Postal Code
    60064
    Country
    US

    Products

    Device Name Product Code
    Dna-Reagents, Neisseria LSL

    Proprietary Names

    Alinity m STI Amplification Kit, Alinity m STI Control Kit Alinity m STI Application Specification File Alinity m Multi-Collect Specimen Collection Kit List 09N19-010 Alinity m STI Application Specification File List 09N17-05A

    Establishment Types

    Manufacture Device in the United States for Export Only