The product is used in accordance with the instructions for use. The electrical installation of the relevant room complies with the applicable national and local requirements and Mindray is responsible for the effects on safety, reliability and performance of this product, only if: Īll installation operations, expansions, changes, modifications and repairs of this product are conducted by Mindray authorized personnel and Mindray shall not be liable for errors contained herein nor for incidental or consequential damages in connection with the furnishing, performance, or use of this manual. Manufacturer’s Responsibility All information contained in this manual is believed to be correct. Contents of this manual are subject to changes without prior notice. They are the property of their respective owners. All other trademarks that appear in this manual are used only for editorial purposes without the intention of improperly using them. Owned by Mindray in China and other countries. Release, amendment, reproduction, distribution, rental, adaption and translation of this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden.Īre the registered trademarks or trademarks Disclosure of the information in this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. Mindray intends to maintain the contents of this manual as confidential information. This manual may refer to information protected by copyrights or patents and does not convey any license under the patent rights of Mindray, nor the rights of others. (hereinafter called Mindray) owns the intellectual property rights to this product and this manual. Intellectual Property Statement SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.

© Copyright 2008 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Contents of this manual are subject to change without prior notice. This revision number changes whenever the manual is updated due to software or technical specification change. Revision History This manual has a revision number. The product complies with the requirement of standard EN 6 “Electromagnetic Compatibility – Medical Electrical Equipment”. The product is in radio-interference protection class A in accordance with EN55011.

The product bears CE mark indicating its conformity with the provisions of the Council Directive 93/42/EEC concerning medical devices and fulfils the essential requirements of Annex I of this directive.

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