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Saringer Life Scienc - Communication Consultants GmbH

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Potential distributors and global partners should note that the Venowave has obtained its<br />

CE mark for use in Europe and is also approved for use in North America by the Federal<br />

Drug Administration (FDA) and Health Canada. Venowave production has met stringent<br />

ISO 13485 standards for design and manufacturing.<br />

At MEDICA 2011, <strong>Saringer</strong> <strong>Life</strong> <strong>Scienc</strong>es will be displaying and demonstrating the new<br />

improved Venowave along with its other products in Hall 4, Booth H40 as part of the<br />

Ontario, Canada Pavilion.<br />

-30-<br />

For further information, please contact: inga@saringer.com

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