BEUDAMED
    FDA Registration Active 🇺🇸 United States

    THE ASCENCIODX MOLECULAR DETECTOR AND THE ASCENCIODX COVID-19 TEST

    Reg #: 3026000572 · FEI: 3026000572 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    ANAVASI DIAGNOSTICS, INC
    Registration Number
    3026000572
    FEI Number
    3026000572
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    15305 NE 95th Street
    City
    Redmond
    State
    WA
    ZIP
    98052
    Country
    US

    Owner / Operator

    Firm Name
    Anavasi Diagnostics, Inc
    Operator Number
    10088905
    Address
    15305 NE 95th Street
    City
    Redmond
    State
    WA
    Postal Code
    98052
    Country
    US

    Products

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

    Proprietary Names

    THE ASCENCIODX MOLECULAR DETECTOR AND THE ASCENCIODX COVID-19 TEST

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device