BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test

    Reg #: 3012234563 · FEI: 3012234563 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CorDx, Inc.
    Registration Number
    3012234563
    FEI Number
    3012234563
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    9540 Waples St Unit C
    City
    San Diego
    State
    CA
    ZIP
    92121
    Country
    US

    Owner / Operator

    Firm Name
    CorDx
    Operator Number
    10050914
    Address
    9540 Waples St Unit C
    City
    San Diego
    State
    CA
    Postal Code
    92121
    Country
    US
    Correspondent
    Amber Wen

    Products

    Device Name Product Code
    Covid-19 Multi-Analyte Antigen Device QMN

    Proprietary Names

    CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility