BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VITROS CA 125 II Range Verifier

    Reg #: 1319681 · FEI: 1000136573 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    10
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    ORTHO-CLINICAL DIAGNOSTICS, INC.
    Registration Number
    1319681
    FEI Number
    1000136573
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    100 Indigo Creek Dr
    City
    Rochester
    State
    NY
    ZIP
    14626
    Country
    US

    Owner / Operator

    Firm Name
    QuidelOrtho Corp.
    Operator Number
    2024674
    Address
    9975 Summers Ridge Road, --
    City
    San Diego
    State
    CA
    Postal Code
    92121
    Country
    US

    Products

    Device Name Product Code
    Single (Specified) Analyte Controls (Assayed And Unassayed) JJX

    Proprietary Names

    VITROS CA 125 II Range Verifier VITROS AFP Range Verifier VITROS Total PSA Range Verifier VITROS B12 Range Verifier VITROS Metabolism Controls VITROS CA 15-3 Range Verifier VITROS Folate Range Verifier VITROS Cortisol Range Verifier VITROS INTACT PTH Controls VITROS Immunodiagnostic Products Progesterone 2 Range Verifiers

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device