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® is a registered trademark of Brainlab AG in Germany and/or the US.
- ExacTrac® is a registered trademark of Brainlab AG in Germany and/or the US.
Microsoft® and Windows® are registered trademarks of Microsoft Corporation in the United States and other countries.
Adobe® and Acrobat® are registered trademarks of Adobe Systems Inc. in the United States and other countries.
This product may be covered by one or more patents or pending patent applications. See https://www.brainlab.com/patent/ for more details.
Integrated Third-Party Software
- This software is based in part on the work of the Independent JPEG Group.
This product includes the Xerces C++ 3.1.1 software.
This product includes software developed by the Apache Software Foundation: http://www.apache.org/.
This product includes libtiff 4.0.4 beta, copyright © 1988 – 1997 Sam Leffler and copyright © 1991 – 1997 Silicon Graphics. For a full description of copyrights and license, see: http://www.simplesystems.org/libtiff.
- This software is based on the work of the Open JPEG Group. For licensing information, see: https://github.com/uclouvain/openjpeg/blob/master/LICENSE.
- This software is based in part on libjpeg-turbo. The full license and copyright notice can be found here: https://github.com/libjpeg-turbo/libjpeg-turbo/blob/master/LICENSE.md.
This product uses the XML2PDF Formatting Engine, which is the exclusive property of Altsoft bvba.
The CE label indicates that the Brainlab product complies with the essential requirements of European Council Directive 93/42/EEC, the Medical Device Directive (“MDD”).
RT Elements Spine SRS 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 occur related to this product to Brainlab and any relevant authorities.
Sales in the US
US federal law restricts this device to sale by or on the order of a physician.