BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ultra2 Genesys Variants Assay Components

    Reg #: 1931251 · FEI: 1931251 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Trinity Biotech (Primus Corporation dba Trinity Biotech)
    Registration Number
    1931251
    FEI Number
    1931251
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4231 E 75th Terrace
    City
    KANSAS CITY
    State
    MO
    ZIP
    64132
    Country
    US

    Owner / Operator

    Firm Name
    TRINITY BIOTECH, PLC
    Operator Number
    9025161
    Address
    2823 Girts Rd
    City
    Jamestown
    State
    NY
    Postal Code
    14701
    Country
    US

    Products

    Device Name Product Code
    Abnormal Hemoglobin Quantitation GKA

    Proprietary Names

    ultra2 Genesys Variants Assay Components ultra2 Resolution Variants Assay Components ultra2 Resolution Variants Analyzer ultra2 Genesys Variants Analyzer

    Establishment Types

    Manufacture Device in the United States for Export Only