(RTTNews) - LumiraDx Ltd. (LMDX), a diagnostics company, announced Friday that its rapid COVID-19 antigen assay, LumiraDx SARS-CoV-2 Ag Test has successfully received the Emergency Use Listing or EUL ...
ABBOTT PARK, Ill., Nov. 3, 2010 /PRNewswire/ -- Abbott today announced it has received a 2010 Chicago Innovation Award for its ARCHITECT HIV Ag/Ab Combo assay, the first test approved in the United ...
In a recent retrospective cross-sectional study posted to The Lancet* preprint server, researchers assessed rapid antigen (Ag) tests for identifying severe acute respiratory syndrome coronavirus-2 ...
SUWON, South Korea--(BUSINESS WIRE)--SD Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed ...
JURUPA VALLEY, Calif.--(BUSINESS WIRE)--GenBody America, LLC, the U.S. affiliate of GenBody, Inc., a South Korean manufacturer of rapid diagnostic tests and reagents for point-of-care applications for ...
The World Health Organization (WHO) said on December 24, 2025, that it has prequalified two rapid antigen diagnostic tests (Ag-RDTs) for SARS-CoV-2, the virus that causes COVID-19. According to WHO, ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results