BEUDAMED
    FDA Registration Active 🇺🇸 United States

    QuantiVirus™ SARS-COV-2 Test Kit

    Reg #: 3011918542 · FEI: 3011918542 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    DiaCarta, Inc.
    Registration Number
    3011918542
    FEI Number
    3011918542
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4385 HOPYARD RD, SUITE 100
    City
    Pleasanton
    State
    CA
    ZIP
    94588
    Country
    US

    Owner / Operator

    Firm Name
    DiaCarta, Inc.
    Operator Number
    10072142
    Address
    4385 HOPYARD RD, SUITE 100
    City
    Pleasanton
    State
    CA
    Postal Code
    94588
    Country
    US

    Products

    Device Name Product Code
    Reagents, 2019-Novel Coronavirus Nucleic Acid QJR

    Proprietary Names

    QuantiVirus™ SARS-COV-2 Test Kit QuantiVirus™ SARS-CoV-2 Multiplex Test Kit

    Establishment Types

    Manufacture Medical Device