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Celltrion DiaTrust™ COVID-19 Rapid Antigen At Home Test (2 Tests/Box)



Celltrion DiaTrust™ is an FDA EUA-authorized COVID-19 rapid antigen testing kit, giving you results in only 15 minutes. With 4 simple steps, the DiaTrust is a customer favorite. For use in individuals aged 14 years and older.

  • FDA EUA-AUTHORIZED HOME TEST (OTC): Celltrion DiaTrust COVID-19 Ag Home Test is an FDA EUA-authorized COVID-19 rapid antigen at-home testing kit. Test in the comfort of your own home, and get the knowledge you need, fast. Self-collected and adult-collected direct mid-turbinate swab samples.
  • RAPID RESULTS: The test gives you results in just 15 minutes and is authorized for at-home use without submitting sample collection to labs. Our home test is capable of detecting COVID-19.
  • TWO TESTS PER KIT: Each kit contains supplies for two tests: swabs, test devices, test tubes (extraction buffer), filter caps, and an Instructions for Use manual. Test yourself and a family member at the same time, or take two tests in a designated timeframe for travel, work, and more. Our products prioritize user comfort, utilizing flocks swabs with a softer tip that doesn’t irritate your nasal passages.
  • HANDY MOBILE APP: Celltrion SafeKey, our official companion app, walks through each step with easy-to-follow directions.

DiaTrust COVID-19 Ag Home Test IFU

DiaTrust COVID-19 Ag Home Test Fact Sheet for HCP

DiaTrust COVID-19 Ag Home Test Box Labels

DiaTrust COVID-19 Ag Home Test IFU for HCP

tests weight (lbs) measurements (in)
kit 2 0.20 8.75″ x 4.45″ x 1.5″
case 20 / 10 kits 3.00 10″ x 10″ x 10″
master case 120 / 60 kits / 6 cs 15.00 23″ x 18″ x 10″
pallet 2040 / 1020 kits / 17 mc 904 48″ x 40″ x 84″

This product 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, The emergency use of 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.


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