QuickVue® At-Home COVID-19 Test, From

Fast. Easy. Ready When You Are. Keep your team safe at home and at the office with the QuickVue® At-Home COVID-19 Test. Developed by Quidel®, QuickVue has received FDA Emergency Use Authorization (EUA) and provides rapid results in the privacy of your home.

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QuickVue® At-Home COVID-19 Test
QuickVue® At-Home COVID-19 Test in Bulk
QuickVue® At-Home COVID-19 Test
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About Quidel® and QuickVue®

Quidel is a trusted innovator in the medical device industry for over 40 years and is a leading provider of rapid diagnostic testing solutions. The QuickVue test has FDA Emergency Use Authorization (EUA) and employs the same Quidel lateral flow technology used for decades by healthcare professionals. It is an at-home solution intended to detect antigens from SARS-CoV-2 from individuals with or without symptoms when tested twice over two or three days, and with at least 24 hours and no more than 36 hours between tests. This test is authorized for individuals aged 14 years and older, and individuals ranging in ages 2 to 14 must have the test administered by an adult.

Why QuickVue?

  • 2 Tests/Kit
  • Results in 10 minutes
  • Excellent performance, with positive results agreeing with PCR test 83.5%, and negative results agreeing with PCR test 99.2% of the time
  • Detects the virus that contain variants, such as Omicron and Delta
  • Utilizes trusted technology by used for decades by healthcare professionals
  • FDA Emergency Use Authorization (EUA)
  • Convenient at-tome test
  • Shelf life: 24 months and dispose after use
  • Store between 59-86°F / 15-30°C

How it Works

The test uses a gentle self-collection anterior nasal swab sample to determine a positive or negative COVID-19 result. Collecting a sample takes approximately 15 seconds and is an easy to follow, gentle process. The swab is swirled in a tube of reagent solution, then removed, before a test strip is inserted. After ten minutes, you can take the strip out of the tube and see your results. Before you begin the test, it’s important to first read and closely follow the detailed instructions included in the package.

QuickVue COVID-19 Test Kit

Materials supplied with the QuickVue® At-Home COVID-19 Test Kit

  • Swabs – individually wrapped sterile foam swabs
  • Test Strips – individually packaged, single-use strips
  • Pre-filled Tubes
  • Tube Holder
  • Instruction Sheet
  • Fact Sheet for Individuals

Frequently Asked Questions

How do you take a sample?

Self-collect your sample with swab from home following the instructions provided. Collecting a sample takes approximately 15 seconds and is an easy to follow, gentle process.

What happens if I receive a positive result?

If you receive a positive result you should remain in self-isolation, and inform your healthcare provider of your result. You should follow the guidance provided by the Centers for Disease Control and Prevention (CDC).

If you develop emergency warning signs for COVID-19, get medical attention immediately. Emergency warning signs include*:

  • Difficulty breathing or shortness of breath
  • Persistent pain or pressure in the chest
  • New confusion or inability to arouse
  • Bluish lips or face

*This list is not all inclusive. Please consult your medical provider for any other symptoms that are severe or concerning.

What does FDA authorized mean?

QuickVue™ At-Home COVID-19 Test has been issued an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for non-prescription home use, which provides consumers with the ability to test themselves from the comfort and safety of their homes.

When there is a critical situation impacting health and safety and there are no FDA-approved or cleared tests available, and other criteria are met, the FDA can make tests available under an emergency access mechanism called an Emergency Use Authorization (EUA). The EUA for this test is supported by the Secretary of Health and Human Service’s (HHS’s) declaration that circumstances exist to justify the emergency use of in vitro diagnostics for the detection and / or diagnosis of the virus that causes COVID-19.

What is the difference between PCR nasal swab and COVID-19 antigen test?

In general, antigen tests are very specific for COVID-19, but are not as sensitive as molecular PCR (polymerase chain reaction) tests. This means that there is a higher chance of false negatives than many molecular tests.

What is Serial Testing?

Serial testing is when a single person is tested for COVID-19 more than once. Because antigen tests are less sensitive than other COVID-19 tests and false results may occur, repeated testing may identify more individuals with COVID-19 infection than a single test. By repeating testing, it may be possible to more quickly identify cases of COVID-19 infection and reduce spread of infection. Additional testing with molecular COVID-19 test may be necessary, depending on your individual risk factors and test results.

How do I place a bulk order for my organization or institution?

For bulk order inquiries, please fill out the quote form on this page with as much detail as possible pertaining to your request.

Restrictions

  • Test authorized for use by persons age 2+
  • Test takers ages 2 through 14 must be accompanied by an adult during specimen collection

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