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  • COVID-19: Endemic Disease
  • Products
    • ASSURE-100 Home Tests
    • ASSURE-100 POC Tests
    • Buy ASSURE-100 Tests
  • News & Updates
  • Contact Us
  • BUY TESTS
Navigating the ‘Quad-demic’: Identifying COVID-19, Flu, RSV, and Norovirus Infections

Navigating the ‘Quad-demic’: Identifying COVID-19, Flu, RSV, and Norovirus Infections

by Oceanit | Feb 21, 2025 | General, National News

Navigating the ‘Quad-demic’: Identifying COVID-19, Flu, RSV, and Norovirus Infections As of February 2025, the United States is experiencing a ‘quad-demic,’ with concurrent surges in COVID-19, influenza, respiratory syncytial virus (RSV), and norovirus cases....
Understanding the XEC COVID-19 Variant in February 2025

Understanding the XEC COVID-19 Variant in February 2025

by Oceanit | Feb 13, 2025 | Education, General

Understanding the XEC COVID-19 Variant in February 2025 As of February 2025, the global health community continues to monitor the evolving landscape of COVID-19, with particular attention to emerging variants such as XEC. Understanding the characteristics of the XEC...
COVID-19 in February 2025: Updated Symptoms, Testing Recommendations, and Treatment Options

COVID-19 in February 2025: Updated Symptoms, Testing Recommendations, and Treatment Options

by Oceanit | Feb 5, 2025 | Education, Government

COVID-19 in February 2025: Updated Symptoms, Testing Recommendations, and Treatment Options As of February 2025, COVID-19 continues to impact communities worldwide. Staying updated on the latest symptoms, testing guidance, and treatment options is essential for...

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Copyright 2025 Oceanit Foundry LLC. The ASSURE-100 Rapid COVID-19 Test has not been FDA cleared or approved, but has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product 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 Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb- 3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
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