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Igg Igm T Antibody Rapid Test Kit Suppliers In North America
4 companies found
based inSan Diego, CALIFORNIA (USA)
For over 23 years, ACON has led the way in making high quality diagnostic and medical devices more affordable to people all around the world. Headquartered in San Diego, California, the US office is the center of strategic management, ...
The SARS-CoV-2 IgG and IgM EIA Test Kits are qualitative enzyme immunoassays for the detection of IgG or IgM antibodies to SARS-CoV-2 in human serum or ...
based in, ONTARIO (CANADA)
Labex Canada Inc. was established as a federally registered company in 2011 in Halifax, Nova Scotia, Canada. In 2015 a new facility was opened in Newmarket, Ontario, Canada. Since the beginning the company has been active in import/export/marketing ...
Coronaviruses belong to a large family of potentially harmful RNA viruses. In humans, they are known to be involved mainly in respiratory infections ranging from the common colds to more severe diseases such as Middle East Respiratory Syndrome ...
based inJamnagar, INDIA
Spark Mobile Diagnostics was conceived with a multi-year research inspired by the technology revolution bought by development of paper-based affordable diagnostics. We believe that mobile phone penetration across the globe provides a tremendous ...
Spark Diagnostics is pleased to introduce a Rapid Whole Blood Test for COVID-19IgG / IgM: Cov-CHECK. The test is designed for the rapid qualitative detection of IgG and IgM antibodies to the 2019 novel Coronavirus (2019-nCoV,SARS-CoV-2) in ...
based inSan Diego, CA 92126 USA, CALIFORNIA (USA)
America Diagnostics, Inc. is a California company that develops and produces IVD devices and diagnostics raw materials. The quality of AmeriDx products is guaranteed by its quality management system. All the products are manufactured in a clean ...
This product is for in vitro diagnostic use, following guidance from the FDA for Emergency Use Authorizations of tests submitted for approval on March 16, 2020. This test has not been reviewed by the FDA and results from antibody testing should not ...