BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Quest Diagnostics Collection Kit for COVID-19 (Individual & Activate)

    Reg #: 1930987 · FEI: 1930987 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LABONE, INC.
    Registration Number
    1930987
    FEI Number
    1930987
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    10101 Renner Blvd
    City
    LENEXA
    State
    KS
    ZIP
    66219
    Country
    US

    Owner / Operator

    Firm Name
    LABONE, LLC., d/b/a Quest Diagnostics
    Operator Number
    9004417
    Address
    10101 RENNER BLVD., --
    City
    Lenexa
    State
    KS
    Postal Code
    66219
    Country
    US
    Correspondent
    Lisa C Christo

    Products

    Device Name Product Code
    Covid-19 Test Home Collection Kit Devices QLW

    Proprietary Names

    Quest Diagnostics Collection Kit for COVID-19 (Individual & Activate) Quest Diagnostics Collection Kit for COVID-19 (Bulk) Quest Diagnostics Collection Kit for COVID-19 (Individual) Quest Diagnostics Collection Kit for COVID-19 (Bulk & Activate)

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility