How to use the CLINITEST® Rapid COVID-19 Antigen Self-Test – for use in the USA Siemens Healthineers Humasis COVID-19 Ag Test uses monoclonal antibodies specific to COVID-19 antigens to detect COVID-19 specific antigens in human nasal swab and nasopharyngeal swab specimens. The test shows the same sensitivity and specificity for OMICRON and other virus variants. This means that the COVID-19 rapid test will only be used in the presence of medical professionals. DiaTrust was jointly developed by Celltrion and Humasis, a Korean R&D company. The test kit Evaluated RAT demonstrated satisfactory performance with more reliable results in younger patients. Humasis COVID-19 Ag RAT is potentially a valuable tool in areas where access to molecular methods is limited; however, RT-PCR remains a gold standard for SARS-CoV-2 detection. Lateral flow immunoassay. Sensitivity. 84.6%. Disposable. Yes. Includes. 40 cardboard, book-shaped hinged test cards with test strips, 1 x 7.5 mL extraction reagent bottle with reagent, 40 sterile nasal swabs, 1 positive control swab containing non-infectious recombinant SARS-CoV-2 nucleocapsid antigen, 1 negative control swab, 1 product insert In the context of COVID-19, the goal of screening by rapid antigen testing is to increase the detection of asymptomatic or presymptomatic infection and reduce onward transmission of SARS-CoV-2. Evaluations of rapid screening tests should be designed based on this goal. With this context and goal, test sensitivity of rapid antigen tests compared Carefully read instructions for using the STANDARD Q COVID-19 Ag Test. Check the test device and the desiccant pack in the foil pouch. Yellow Yellow: Valid Green: Invalid Green 30°C (86°F) 2°C (36°F) T C COVID-19 Ag Result window Specimen well STANDARD Q COVID-19 Ag Test TM Check the expiry date at the consistent with COVID-19. The LumiraDx SARS-CoV-2 Ag Test is intended for use by medical professionals or operators who are proficient in performing tests in point of care settings. rJOg.