InteliSwab™ COVID-19 Rapid Antigen Test (2 Tests)

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Testing Tool
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Product Overview

This is a OTC Test (Over the Counter). Over the Counter testing options are designed personal use in a non-clinical environment.  Each package comes with one or two tests (depending on the brand).

Meet InteliSwab, the COVID-19 rapid antigen test that makes self-testing remarkably simple. It’s so user-friendly, it can be used anytime and anywhere, and requires less than one minute of hands-on time. InteliSwab has received FDA Emergency Use Authorization* for self-testing. You do not need to ship samples to a lab or get a prescription from your healthcare provider. This easy-to-use self-test requires just 3 key steps: Swab, Swirl and See your result in 30 minutes. There is no assembly required. InteliSwab makes testing so easy, you’ll know you did it right.

InteliSwab COVID-19 Rapid Antigen Test, For results anytime and anywhere (2 Tests)

  • Detects active COVID-19 infection for both symptomatic and asymptomatic use
  • Shallow and gentle nasal swab (lower nostril)
  • 98% of untrained, unproctored users found InteliSwab™ easy to use
  • Requires less than one minute of hands-on time
  • No lab needed and no assembly required 
  • Get your results in 30 minutes
  • No difficult or confusing steps
  • No dropper bottle or number of drops required
  • No batteries or instruments needed
  • Designed in Bethlehem, Pennsylvania by OraSure Technologies, Inc.
  • Suitable for ages 15 and up
  • Bilingual instructions included in the test kit

Here's how the test works**:

  1. Swab:  Collect sample from nostrils with gentle, soft swab embedded in test device
  2. Swirl:  Stir test device in tube
  3. See:  Read your results after 30 minutes
  4. If negative, test again with 24-36 hours between tests

*This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA; This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and, This product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.