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International Growth Continues: Rhythmlink International, LLC Receives CE Marking & ISO 13485 Certification
Date:3/9/2010

owth of the company. This certification demonstrates to the markets in the European Union that Rhythmlink will provide products backed by a quality management system that reduces risk to patients," said Martin Barry, Rhythmlink International's regulatory affairs specialist.

As an electrode manufacturing company, within the medical devices industry, Rhythmlink International is bound by strict FDA regulations and regulatory requirements. Rhythmlink's quality management system has demonstrated the ability to provide medical devices and services that consistently achieve customer and regulatory requirements, thus receiving ISO 13485:2003 certification and ISO 13485:2003 + AC:2007 CE Markings.

Under European Directives and supported by European standards, Rhythmlink and its products are in full compliance with essential health and safety requirements. The CE Marking is Rhythmlink's declaration that all products meet the essential requirements of the European directives.

For more information about Rhythmlink's certifications, products and services, visit Rhythmlink.com.

About Rhythmlink International, LLC'/>"/>

SOURCE Rhythmlink International, LLC
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