Legal Information
Copyright
This guide contains proprietary information protected by copyright. No part of this guide may be reproduced or translated without express written permission of Brainlab.
Brainlab Trademarks
Brainlab® is a registered trademark of Brainlab AG in Germany and/or the US.
Buzz® is a registered trademark of Brainlab AG in Germany and/or the US.
Curve® is a registered trademark of Brainlab AG in Germany and/or the US.
iHelp® is a registered trademark of Brainlab AG in Germany and/or the US.
Non-Brainlab Trademarks
Intel® Xeon® and Intel® Core™ i7 are registered trademarks of Intel Cooperation or its subsidiaries in the US and/or other countries.
Novalis Tx™ is a trademark of Varian Medical Systems, Inc.
RayStation® is a registered trademark of RaySearch Laboratories AB.
Windows® is a registered trademark of Microsoft Corporation in the United States and other countries.
Patent Information
This product may be covered by one or more patents or pending patent applications. For details, see: www.brainlab.com/patent.
Integrated Third-Party Software
This software is based in part on the following work. The full license and copyright notice can be found at the links below:
-
Independent JPEG Group (https://github.com/uclouvain/openjpeg/blob/master/LICENSE)
- This product includes software developed by the Apache Software Foundation (http://www.apache.org). Copyright© 1999-2004 The Apache Software Foundation. All rights reserved.
- Open JPEG Group (https://github.com/uclouvain/openjpeg/blob/master/LICENSE).
CE Label
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The CE label shows that the Brainlab product complies with the essential requirements of Council Directive 93/42/EEC, the Medical Device Directive (“MDD”). RT Elements Adaptive Hybrid Surgery Analysis is a Class IIb product according to the rules established by the MDD. |
Report Incidents Related to This Product
You are required to report any serious incident that may have occurred related to this product to Brainlab, and if within Europe, to your corresponding national competent authority for medical devices.
Sales in US
US federal law restricts this device to sale by or on the order of a physician.