Chembio Ebola Virus Diagnostic Test Receives U.S. FDA Emergency Use Authorization
Chembio Diagnostics, Inc. (CEMI)
Last chembio diagnostics, inc. earnings: 3/12 04:07 pm
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Source: GlobeNewswire
MEDFORD, N.Y., Nov. 09, 2018 (GLOBE NEWSWIRE) -- Chembio Diagnostics, Inc. (Nasdaq: CEMI), a leading point-of-care ("POC") diagnostics company focused on infectious diseases, today announced the receipt of U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA) for its DPP® Ebola Antigen System for use with human capillary “fingerstick” whole blood, EDTA venous whole blood, and EDTA plasma. The DPP® Ebola Antigen System includes the DPP® Ebola Assay and DPP® Micro Reader. The DPP® Ebola Antigen System utilizes Chembio’s patented DPP® technology platform, which is the same proven technology used in the Company's FDA approved HIV antibody tests and FDA authorized DPP® Zika System. The test detects viral antigens and provides qualitative results in 15-20 minutes, when used with the hand-held, battery-operated DPP® Micro Reader to reduce the risk of human error during test interpretation. The test is authorized for the presumptive detection of Ebola virus (species Za
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