This product is provided with a CE marking in accordance
with the regulations stated in Appendix II of the Directive
93/42/EEC of June 14
th
, 1993 concerning medical devices.
In accordance with Appendix IX of the Directive 93/42/
EEC, this device is assigned to class II b.
The CE marking applies only to medical devices which have been put on
the market according to the above-mentioned EC Directive.
Unauthorized changes to this product invalidate this declaration.
Whenever the hardware necessary to run the software is supplied, the
CE Mark is provided in accordance with, if applicable, Electro Magnetic
Compatibility Directive 2004/108/EC and / or Low-Voltage Directive
2006/95/EC.
Caution: Federal law restricts this device to sale by or on the order of a
physician (21 CFR 801.109(b)(1)).
This Operator Manual was originally written in English.
Legal Manufacturer
Siemens AG
Wittelsbacherplatz 2
DE-80333 Muenchen
Germany
Global Business Unit
Siemens AG
Medical Solutions
Medical Solutions Angiography &
Interventional X-ray Systems
Siemensstraße 1
DE-91301 Forchheim
Germany
Phone: +49 9191 18-0
www.siemens.com/healthcare
Global Siemens Headquarters
Siemens AG
Wittelsbacherplatz 2
80333 Muenchen
Germany
Global Siemens Healthcare
Headquarters
Siemens AG
Healthcare Sector
Henkestraße 127
91052 Erlangen
Germany
Phone: +49 9131 84-0
www.siemens.com/healthcare
Print No. AXA4-100.620.17.01.02 | © 09.2014, Siemens AG
www.siemens.com/healthcare