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DiaPlexQ ,Novel Coronavirus, (2019-nCoV) ,Detection Kit,: Solgent Co., Ltd. (South Korea) Nucleic acid technology: Lab-based test: 2020-04-05: DiaSorin Simplexa ,COVID-19, Direct Molecular Assay on the LIAISON MDX Instrument: DiaSorin Molecular LLC (United States) Nucleic Acid technology: Lab-based test: 2020-04-09: Genefinder ,CoVid-19, Plus Realamp ,Kit

One Step ,Novel Coronavirus, (,COVID-19,) IgM/IgG Antibody Test ,Kit, The pathogen of ,novel coronavirus pneumonia, is the ,novel coronavirus,. WHO has officially named the disease as ,corona virus, diseases 2019 (,COVID-19,). Due to the increasing market demand of ,rapid, and reliable ,Coronavirus, ( ,COVID-19,) ,detection, solutions,

27/3/2020, · ABBOTT PARK, Ill., March 27, 2020 /PRNewswire/ -- Abbott (NYSE: ABT) announced today that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the fastest available molecular point-of-care test for the ,detection, of ,novel coronavirus, (,COVID-19,), delivering positive results in as little as five minutes and negative results in 13 minutes.

The ,COVID-19, lgG/lgM ,Rapid, Test (Whole Blood/Serum/Plasma) has been evaluated with the 126 samples obtained from patients exhibiting ,pneumonia, or respiratory symptoms. The results were compared to Fluorescent Real Time Polymerase Chain Reaction (RT-PCR) or clinical diagnosis (including chest Computed Tomography and clinical signs etc.) of “Diagnosis and treatment of ,novel coronavirus, ...

DiaPlexQ ,Novel Coronavirus, (2019-nCoV) ,Detection Kit,: Solgent Co., Ltd. (South Korea) Nucleic acid technology: Lab-based test: 2020-04-05: DiaSorin Simplexa ,COVID-19, Direct Molecular Assay on the LIAISON MDX Instrument: DiaSorin Molecular LLC (United States) Nucleic Acid technology: Lab-based test: 2020-04-09: Genefinder ,CoVid-19, Plus Realamp ,Kit

Naming the ,coronavirus, disease (,COVID-19,) and the virus that causes it Risk communication and community engagement Country-level coordination, planning, and monitoring

6/2/2020, · The test ,kit,, called the ,Centers for Disease Control and Prevention, (CDC) 2019-,Novel Coronavirus, (2019-nCov) Real-Time Reverse Transcriptase (RT)-PCR Diagnostic Panel (CDC 2019-nCoV Real Time RT-PCR), is designed for use with an existing RT-PCR testing instrument that is commonly used to test for seasonal influenza.

One Step ,Novel Coronavirus, (,COVID-19,) IgM/IgG Antibody Test ,Kit, The pathogen of ,novel coronavirus pneumonia, is the ,novel coronavirus,. WHO has officially named the disease as ,corona virus, diseases 2019 (,COVID-19,). Due to the increasing market demand of ,rapid, and reliable ,Coronavirus, ( ,COVID-19,) ,detection, solutions,

23/3/2020, · QIAGEN releases QIAstat-Dx test ,kit, to the U.S. as first syndromic test for ,detection, of SARS-CoV-2 ,coronavirus, under new FDA Policy • QIAstat-Dx syndromic testing system can differentiate ,novel coronavirus, from 20 other respiratory targets • Requires less than one minute for sample preparation and delivers results in about one hour • Adds an important tool for clinicians as part of ...

The ,COVID-19, lgG/lgM ,Rapid, Test (Whole Blood/Serum/Plasma) has been evaluated with the 126 samples obtained from patients exhibiting ,pneumonia, or respiratory symptoms. The results were compared to Fluorescent Real Time Polymerase Chain Reaction (RT-PCR) or clinical diagnosis (including chest Computed Tomography and clinical signs etc.) of “Diagnosis and treatment of ,novel coronavirus, ...

31/1/2020, · NANJING, Jan. 31 (Xinhua) -- Experts have developed a ,rapid, nucleic test ,kit, for the ,novel coronavirus, (2019-nCoV) in the city of Wuxi, east China's Jiangsu Province. The ,kit, can detect the virus within eight to 15 minutes, according to the city bureau of science and technology.

12/3/2020, · Before there were any cases of ,novel coronavirus, confirmed in South Korea, one of the country's biotech firms had begun preparing to make testing ,kits, to identify the disease.

6/2/2020, · The test ,kit,, called the ,Centers for Disease Control and Prevention, (CDC) 2019-,Novel Coronavirus, (2019-nCov) Real-Time Reverse Transcriptase (RT)-PCR Diagnostic Panel (CDC 2019-nCoV Real Time RT-PCR), is designed for use with an existing RT-PCR testing instrument that is commonly used to test for seasonal influenza.

23/3/2020, · QIAGEN releases QIAstat-Dx test ,kit, to the U.S. as first syndromic test for ,detection, of SARS-CoV-2 ,coronavirus, under new FDA Policy • QIAstat-Dx syndromic testing system can differentiate ,novel coronavirus, from 20 other respiratory targets • Requires less than one minute for sample preparation and delivers results in about one hour • Adds an important tool for clinicians as part of ...

31/1/2020, · NANJING, Jan. 31 (Xinhua) -- Experts have developed a ,rapid, nucleic test ,kit, for the ,novel coronavirus, (2019-nCoV) in the city of Wuxi, east China's Jiangsu Province. The ,kit, can detect the virus within eight to 15 minutes, according to the city bureau of science and technology.

28/1/2020, · Kenny says Meridian is one of around 10 companies that make screening ,kit, products able to test for ,Coronavirus,—and it’s one of just a few that makes a powdered form.

28/1/2020, · Kenny says Meridian is one of around 10 companies that make screening ,kit, products able to test for ,Coronavirus,—and it’s one of just a few that makes a powdered form.

27/3/2020, · ABBOTT PARK, Ill., March 27, 2020 /PRNewswire/ -- Abbott (NYSE: ABT) announced today that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the fastest available molecular point-of-care test for the ,detection, of ,novel coronavirus, (,COVID-19,), delivering positive results in as little as five minutes and negative results in 13 minutes.