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Coronavirus Disease 2019 (COVID 19) Emergency Use Authorizations for Medical Devices. On February 4, 2020, the Secretary of the Department of Health Cellex gets first EUA for rapid antibody test for COVID 19 The rapid antibody test for COVID 19 developed by the US diagnostic and biopharmaceutical company Cellex receives the first Emergency Use Authorization (EUA) approval for marketing from the US FDA, announced the company.. The test allows to obtain results within 15 20 minutes after a drop of the sample including serum, plasma, or whole blood is placed into a well on a small cartridge.Diagnostic Kits Suppliers, Manufacturers, Wholesalers and Covid 19 Coronavirus IgG / IgM antibody rapid test One boxcontains 25 sterile, individually packaged rapid tests, a special diluent and instructions for use in English. use1.Drip a drop of blood for the test. 2.Add 1 2 drops of sample diluent. 3.Wait until the colored line (s)

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