Appendix A Technical Description
Instructions for Use A - 43
CE Declaration
This product is provided with a CE marking in accordance with the regulations stated in Council
Directive 93/42/EEC of June 14, 1993 concerning Medical Devices. The CE marking only
applies to medical devices that have been put on the market according to the above referenced
Council Directive.
Unauthorized changes to this product are not covered by the CE marking and the related
Declaration of Conformity.
EU Authorized Representative
Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
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