Know your COVID-19 status in minutes with our reliable, fast test and the NAVICA™ App
Social distancing, hand washing, vaccines, and mask wearing are best practices for minimizing the spread of COVID-19. Testing is another powerful tool to help you feel more confident about visiting your favorite places again.
The NAVICA App allows you to obtain a digitally encrypted NAVICA™ Pass if your COVID-19 test results are negative. The NAVICA Pass can be shown at facilities or events requiring a test result for entry.
Download the NAVICA app, then take an Abbott rapid COVID-19 test at a NAVICA-enabled testing site or at home. The tests use a simple nasal swab and provide results in 15 minutes.
Receive a notification when test results are available to view in the NAVICA app. A negative test result automatically generates an encrypted NAVICA Pass. If the test is positive, the participant is advised to contact their healthcare provider, quarantine and follow CDC guidelines.
Display a NAVICA Pass, similar to an airline boarding pass, at NAVICA-enabled environments such as office buildings and schools to verify a recent negative test for COVID-19.
NAVICA will display a digital NAVICA Pass via a QR code, similar to an airline boarding pass, for the NAVICA user who has received a negative result from a NAVICA-enabled test site. This allows organizations to verify negative test results, enabling people to move about with greater confidence, or see a positive test result and request that the person self-quarantine to avoid infecting others.
Getting a NAVICA pass is an easy 3-step process:
The BinaxNOW COVID-19 Ag Card is a rapid lateral flow antigen test administered by a healthcare professional or a trained operator. It tests for active infection using a direct nasal swab. It provides a positive or negative result in 15 minutes with no instrument required.
Our technical services team can be reached Monday to Friday 8AM to 8PM Eastern Standard Time at (800) 257-9525. Please have the following information available so we can best assist you: phone type, phone operating version, and app version.
Watch the video to learn more about the digitally-connected rapid test and mobile app.
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The BinaxNOW™ COVID-19 Ag Card EUA has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization for use by authorized laboratories. The test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
This website is governed by applicable U.S. laws and governmental regulations. The products and information contained herewith may not be accessible in all countries, and Abbott takes no responsibility for such information which may not comply with local country legal process, regulation, registration and usage. Not all products are available in all regions. Check with your local representative for availability in specific markets. For In Vitro Diagnostic Use Only. For the use of registered medical practitioners, hospitals and Laboratories only.
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