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Omnyx is CE Marked under the European Union’s ‘In Vitro Diagnostics Directive’ for routine clinical use in the EU for VL4 and DPS and not any other products.
Omnyx is cleared by Health Canada for routine diagnostic use for VL4 and DPS and not any other products.
In the US, Omnyx products are for research only and not for use in diagnostic procedures.
US Patents 8,463,741 and 8,396,269
©2013 Omnyx, LLC – All rights reserved.
Omnyx, LLC reserves the right to make changes in specification and features shown herein, or discontinue the product described at any time without notice or obligation.
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