NEW ZEUS SARS-CoV-2 Antibody Tests
ZEUS SARS-CoV-2 IgG Test System:
Now with FDA Emergency Use Authorization (EUA)
Test with confidence. Test with ZEUS.
The ZEUS ELISA SARS-CoV-2 Antibody Test Systems are intended for qualitative detection of IgG antibody to the SARS-COV-2 virus in human serum and plasma.
Scalable to your laboratory needs!
This product is an in vitro diagnostic test system, requiring that the test be performed in a licensed clinical laboratory. Not for personal sale or use.
ZEUS ELISA SARS-CoV-2 Antibody Test Systems
What is COVID-19?
COVID-19 is an illness caused by a novel strain (SARS-CoV-2) of coronavirus which can spread from person to person. There are many types of coronavirus, the first being identified in the 1960s, but this particular strain is one which has not been previously detected. People with COVID-19 may exhibit a wide range of symptoms, from mild to severe illness.
What is SARS-CoV-2?
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the name of the virus that causes the COVID-19 disease.
ZEUS Scientific A company you can trust.
ZEUS Scientific is a trusted partner with over 40 years of in vitro diagnostic experience providing high quality diagnostic solutions. Our New Jersey based manufacturing facility:
- is FDA-inspected
- is fully certified and audited to ISO 13485 (2016)
- meets FDA Quality System Regulations (1996: 21 CFR § 820)
- meets IVD 98/79/EEC standards
We boast over 120 US FDA cleared devices. In these difficult times, you can count on us to apply our expertise and assist in the fight against COVID-19.
ZEUS Scientific is your first choice for high-performing, easy-to-use clinical diagnostic solutions that we manufacture and develop to ensure optimal efficiency, accurate diagnosis, and better patient care. US-based and family-owned, we offer an industry-leading menu of testing solutions developed with over 40 years of experience.
FDA EUA Disclaimer: This test has been authorized only for the presence of IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. This test has been authorized by FDA under an EUA for use by authorized laboratories. This test has not been FDA cleared or approved; This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.