BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Control Set for the BD ProbeTec Trichomonas vaginalis (TV) Qx Amplified DNA Assay

    Reg #: 1119779 · FEI: 1119779 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BECTON, DICKINSON & CO.
    Registration Number
    1119779
    FEI Number
    1119779
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    7 LOVETON CIR.
    City
    SPARKS
    State
    MD
    ZIP
    21152
    Country
    US

    Regulatory Submissions

    510(k) Number
    K130268

    Owner / Operator

    Firm Name
    Becton Dickinson and Company
    Operator Number
    9922032
    Address
    One Becton Drive
    City
    Franklin Lakes
    State
    NJ
    Postal Code
    07417
    Country
    US

    Products

    Device Name Product Code
    Trichomonas Vaginalis Nucleic Acid Amplification Test System OUY

    Proprietary Names

    Control Set for the BD ProbeTec Trichomonas vaginalis (TV) Qx Amplified DNA Assay Control Set for the BD ProbeTec Chlamydia trachomatis/Neisseria gonorrhoeae/Trichomonas vaginalis (CT/GC/TV) Qx BD ProbeTec Trichomonas vaginalis (TV) Qx Amplified DNA Assay Reagent Pack Amplified DNA Assays

    Establishment Types

    Manufacture Medical Device