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Mindray Announces FDA 510(k) Clearance of Its A5 Anesthesia System
Date:2/23/2011

l designed with the most intuitive user interface in the business," said Thomas Barford, Vice President of Anesthesia Systems at Mindray North America. "We are confident that the A5 will be very competitive and well-received in the marketplace."

"The A5 is the first of our new series of anesthesia machines that bring advanced design features to the Mindray portfolio. By creating a highly differentiated product that includes more standard ventilation features, we are significantly expanding our ability to serve the US hospital market," said David Gibson, President, Mindray North America.

About MindrayWe are a leading developer, manufacturer and marketer of medical devices worldwide. We maintain global headquarters in Shenzhen, China, U.S. headquarters in Mahwah, New Jersey and multiple sales offices in major international markets. From our main manufacturing and engineering base in China and through our worldwide distribution network, we are able to supply internationally a broad range of products across three primary business segments, comprised of patient monitoring and life support products, in-vitro diagnostic products and medical imaging systems. For more information, please visit http://www.mindray.com.

Press Release A5 510(k) Clearance part number 0002-08-1394For investor and media inquiries, please contact:In the U.S.:   Hoki Luk   Western Bridge, LLC   Tel:   +1-646-808-9150   Email: hoki.luk@westernbridgegroup.comIn China:   Cathy Gao   Mindray Medical International Limited   Tel:   +86-755-2658-2620   Email: cathy.gao@mindray.com
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SOURCE Mindray Medical International Limited
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