BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    cobas CT/NG Test, v2

    Reg #: 3003795116 · FEI: 3003795116 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    ROCHE DIAGNOSTICS INTERNATIONAL LTD.
    Registration Number
    3003795116
    FEI Number
    3003795116
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    FORRENSTRASSE 2
    City
    ROTKREUZ Zug
    Country
    CH

    Regulatory Submissions

    510(k) Number
    K132270

    Owner / Operator

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

    US Agent

    Business Name
    Roche Diagnostics Operations Inc
    Contact Name
    Brian Frazier
    Address
    9115 Hague Rd
    City
    Indianapolis
    State
    IN
    ZIP
    46256
    Country
    US
    Email
    [email protected]
    Phone
    317 5214603

    Products

    Device Name Product Code
    Dna Probe, Nucleic Acid Amplification, Chlamydia MKZ
    Real Time Nucleic Acid Amplification System OOI
    Dna-Reagents, Neisseria LSL

    Proprietary Names

    cobas CT/NG Test, v2 cobas z 480 Analyzer KIT COBAS PCR MEDIA UNI SWB 100 PKT IVD SW c4800 CT/NG AP V. 2.1 CD

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device