Aged 2 to 13 years should be tested by an adult. Gently insert the entire tip of the swab head into the child’s nostril (1⁄2 to 3⁄4 of an inch). With children, the maximum depth of insertion Intended for use as an additional, more specific test to confirm the presence of antibodies to HIV-1 and HIV-2 for specimens found to be repeatedly reactive by diagnostic screening procedures. 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. SPERA™ COVID -19 Ag Test . Instructions for Use . Rapid Test for the Detection of SARS -CoV-2 Antigen. For Use under the Emergency Use Authorization (EUA) only . For . in vitro. The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the uncertified COVID-19 test kit: 1. “ICHROMA COVID-19 AG” 2. “HUMASIS COVID-19 AG TEST ONE STEP COVID-19 AG TEST” The FDA verified through post-marketing surveillance that the abovementioned COVID-19 test kits are COVID-19 Ag Test ENG Please read the instruc ons carefully before use! Invalid If there is no colored line in the control region (C), the result is invalid. COVID-19 Ag COVID-19 Ag If no colored line appears in the test line (T) and a colored line is present on the control region (C), then the result is negative. Wr5mM. How to use the CLINITEST® Rapid COVID-19 Antigen Self-Test – for use in the USA Siemens Healthineers In one brand of the self-test kits found in the European Union’s common list of Covid-19 rapid antigen tests, for example, the instruction to users is to dispose of the used kit in household 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. The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the uncertified COVID-19 test kit: 1. “ICHROMA COVID-19 AG” 2. “HUMASIS COVID-19 AG TEST ONE STEP COVID-19 AG TEST” The FDA verified through post-marketing surveillance that the abovementioned COVID-19 test kits are Humasis COVID-19 Ag Test: 12/23/2022 individuals without symptoms or other epidemiological reasons to suspect COVID-19), the test is now authorized for use at least three times over five days Under the section ‘Interpreting Results’ it states that ‘C’ (which indicates a negative result) stands for Control Line and ‘T’ (which indicates an inconclusive result) stands for Test

humasis covid 19 ag test how to use