Siemens MAGNETOM Skyra fit Operator's Manual page 131

Manufacturer's note:
This device bears a CE mark in accordance with the
provisions of Council Directive 93/42/EEC of June 14, 1993
concerning medical devices and the Council Directive
2011/65/EU of June 08, 2011 on the restriction of the use
of certain hazardous substances in electrical and electronic
equipment.
Global Business Unit
Siemens AG
Medical Solutions
Magnetic Resonance
Henkestr. 127
DE-91052 Erlangen
Germany
Phone: +49913184-0
www.siemens.com/healthcare
Global Siemens Headquarters
Siemens AG
Wittelsbacherplatz 2
80333 Muenchen
Germany
Print No. M6-04401.621.02.02.02 | © 2015, Siemens AG
www.siemens.com/healthcare
The CE marking applies only to medical devices which have
been put on the market according to the above-mentioned
EC Directives. Unauthorized changes to this product are
not covered by the CE mark and the related Declaration of
Conformity.
Please note: For products that are not legally manufactured
by Siemens but distributed, please refer to the Appendix of
this manual!
Global Siemens Healthcare
Headquarters
Siemens AG
Healthcare Sector
Henkestraße 127
91052 Erlangen
Germany
Phone: +49 9131 84-0
www.siemens.com/healthcare
Legal Manufacturer
Siemens AG
Wittelsbacherplatz 2
DE-80333 Muenchen
Germany