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Celltrion DIATRUSTPC DiaTrust COVID-19 Antigen Rapid Test - 25/bx

By Celltrion | Mfr#: DIATRUSTPC | Tiger#: TM111666



  • Rapid detection of SARS-CoV-2
  • Fast results in 15 minutes
  • Intended for Point of Care Testing of Symptomatic and Asymptomatic Patients
  • Authorized by the FDA under an EUA, pending FDA clearance / approval
  • Identifies with 93.33% sensitivity and 99.03% specificity
  • CLIA-waived
List Price: $550.00
You Save: $315.00 - 57%


Free Shipping (USA)
Ships Out Within: 3 - 5 Business Days
This product is only allowed to a Medical Professional
  • For Use Under The Emergency Use Authorization (EUA) Only
  • For In Vitro Diagnostic Use

Overview for Celltrion DIATRUSTPC DiaTrust COVID-19 Antigen Rapid Test - 25/bx

The Celltrion DiaTrust COVID-19 Antigen Rapid Test is a CLIA-waived lateral flow immunoassay test used by healthcare professionals, intended for point-of-care testing, for the direct and qualitative detection of Coronavirus (Sars-CoV-2) antigens collected through nasopharyngeal swabbing from patients. This rapid test can be used for individuals who are suspected of Covid-19, within the first seven days of the onset of symptoms, or in asymptomatic patients, when tested twice within three days, with at least 24 hours and no more than 48 hours interval between tests. 

Easy to Use & Reliable: The DiaTrust COVID-19 Antigen Rapid Test comes with specimen sampling swabs, extraction reagents, and test devices. Gathered nasal swab samples are mixed with the reagent immediately, making sure that enough specimen is well incorporated into the buffer solution, which is then dispensed (3 drops) into the sample well of the test device. Fast and precise results will be available within 15 minutes, which essentially boosts medical facilities’ capacity to conduct more in-patient rapid COVID-19 tests, resulting in faster identification of infectious individuals and contact tracing.

Quick and Accurate: Please take note that accurate results will be shown 15 minutes after applying the sample and should not exceed 20 minutes to avoid reading false positive or negative results. A solo colored horizontal mark on the "C" (control) area depicts that you have a negative result while a positive result shows two colored marks for the "C" and "T" (test) zones. Invalid results show no lines on the “C” zone. This rapid test can identify infection in patients with 93.33% sensitivity and 99.03% specificity.

FDA Disclaimer: This swab test kit is not FDA cleared or approved, but only authorized under an Emergency Use Authorization for point of care use. It is authorized for the rapid detection of proteins from SARS-CoV-2 and not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for the 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.