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Integrity Life Sciences Receives CE Mark and ISO Certifications for the Integrity Spinal Care System Medical Device
Date:7/12/2012

TAMPA, Fla., July 12, 2012 /PRNewswire-iReach/ -- Integrity Life Sciences announced today that on March 30th, 2012 TÜV SÜD Product Service GmbH of Munich, Germany issued to Integrity the CE Marking (Certificate of European Conformity) and compliance with these requirements is proved within a certified quality management system according to EN ISO 13485 (International Standards Organization). Integrity Life Sciences was granted by TUV SUD the CE Mark together with an ISO 13485 certificate representing a certified quality management system in compliance with the International Organization of Standardization's standard 13485:2003 / AC:2009. Together, the CE Mark and the ISO Certification serve as a virtual passport to the world as it is recognized beyond the stringent borders of Europe. This follows the European Union's "New Approach Directives" and is mandatory for all manufacturers. This legislation requires Integrity to clearly display CE Marking on its products and ensures legal responsibility that the Integrity Spinal Care System Medical Device conforms to the requirements of the directive and for applying CE Marking.

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CE Mark:

The letters "CE" are a well known accomplishment to most in the international medical community. Established by the EU, the term initially identified with the phrase "EC Mark" and it was officially replaced by "CE Marking" in the 1993 Directive 93/68/EEC. Today, the letters "CE" are the abbreviation of French phrase "Conformité Européene" which literally means "European Conformity". "CE Marking" is now used in all EU official documents. CE Marking on Integrity's products means that, as a manufacturer, Integrity is declaring that their product complies with the essential requirements of the relevant European health, safety and environmental protection legislation in accordance
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