BEUDAMED
    FDA Registration Active 🇺🇸 United States

    KIT CAP/CTM HIV-1 v2 QUAL CE-IVD

    Reg #: 2243471 · FEI: 2243471 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ROCHE MOLECULAR SYSTEMS, INC.
    Registration Number
    2243471
    FEI Number
    2243471
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1080 US Highway 202 South
    City
    Branchburg
    State
    NJ
    ZIP
    08876
    Country
    US

    Owner / Operator

    Firm Name
    Roche Diagnostics Operations Inc.
    Operator Number
    9039767
    Address
    9115 Hague Road
    City
    Indianapolis
    State
    IN
    Postal Code
    46250
    Country
    US

    Products

    Device Name Product Code
    Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus MZP

    Proprietary Names

    KIT CAP/CTM HIV-1 v2 QUAL CE-IVD KIT CAP/CTM HCV v2 QUAL CE-IVD KIT COBAS 6800/8800 UTIL CHAN 96T CE-IVD KIT COBAS 6800/8800 HCV 96T CE-IVD KIT C58/68/8800 HIV1/HIV2 QUAL RMC IVD KIT COBAS 58/68/8800 CMV RMC IVD KIT COBAS 6800/8800 MPX RMC CE-IVD

    Establishment Types

    Manufacture Device in the United States for Export Only