Clinitest Rapid COVID-19 Antigen Self-Test (EUA), 5 test/kit

Non-invasive and easy to use, the Siemens Clinitest Rapid COVID-19 Antigen Self-Test (EUA) is an effective lateral flow immunoassay test, used for prescription home use or point-of-care testing, to determine active covid-19 infection in a patient. An individual, with or without symptoms and aging from 2 years old and above, can easily be tested and get accurate results in just 15 minutes. Each kit has 5 individual tests and has a shelf life of up to 10 months.

Simple and Efficient: This COVID-19 Antigen Self Test was made to quickly detect Sars-CoV-2 nucleocapsid protein antigen in a person, following simple and easy steps. Using the included highly-absorbent nasal swab, the specimen can be obtained by brushing 5 times against the inner wall of both nostrils of a patient. You can effectively get a sample just by inserting the swab ½ to ¾ inches inside the nose since this test kit promotes optimal comfort for the user.

The specimen is then placed in the solution tube, thoroughly mixing the swab 6 times and leaving it for 1 minute, to make sure that all the samples collected are incorporated within the buffer solution. After removing the swab and sealing the tube with a tip, simply prepare the test cassette and put 4 drops in the sample well, and wait for 15 minutes. Fast and precise results can help individuals and healthcare professionals be aware of their condition, which can promote proper diagnosis and action.

Quick and Accurate Result: Results will automatically appear on the stick after a few minutes, and you can determine its meaning based on the result reference guide in the kit. A solo horizontal mark on the "C" (control) area depicts that you have a negative result. A positive result shows two marks for the "C" and "T" (test) zones. Invalid results show no lines on the stick or incomplete lines. Its sensitivity is 86.5 percent while specificity is 99.3 percent.

FDA Disclaimer: This swab test kit is not FDA cleared or approved, but only authorized under an Emergency Use Authorization for home use or 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. 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.

WARNING: This product can expose you to chemicals known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.