BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    COVEACHEK COVID-19 IgG/IgM Rapid Test Cassette; COVID-19 IgG/IgM Rapid Test Device

    Reg #: 3014730829 · FEI: 3014730829 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VERIFY DIAGNOSTICS
    Registration Number
    3014730829
    FEI Number
    3014730829
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    D-122 Commerce Park Dr
    City
    Barrie Ontario
    Country
    CA

    Owner / Operator

    Firm Name
    Verify Diagnostics Inc.
    Operator Number
    10067091
    Address
    D-122 Commerce Park Dr
    City
    Barrie
    State
    Ontario
    Postal Code
    L4N 8W8
    Country
    CA

    US Agent

    Business Name
    Verify Diagnostics
    Contact Name
    Nancy Zwiep
    Address
    1000-5718 Westheimer Rd. Houston
    City
    Houston
    State
    TX
    ZIP
    77057
    Country
    US
    Email
    [email protected]
    Phone
    346 4061306

    Products

    Device Name Product Code
    Reagent, Coronavirus Serological QKO

    Proprietary Names

    COVEACHEK COVID-19 IgG/IgM Rapid Test Cassette; COVID-19 IgG/IgM Rapid Test Device 2019-nCoV lgG/lgM Rapid Test REAGENT, CORONAVIRUS SEROLOGICAL

    Establishment Types

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