Siemens ACUSON AcuNav 8F Gebrauchsanleitung Seite 34

July 2016 (0716) Release
©2004-2016 Siemens Medical Solutions USA, Inc.
All Rights Reserved.
AcuNav, ACUSON, ACUSON AcuNav, ACUSON Aspen,
ACUSON CV70, ACUSON Cypress, ACUSON P50,
ACUSON S Family, ACUSON S1000, ACUSON S2000,
ACUSON S3000, ACUSON SC2000, ACUSON Sequoia,
ACUSON X300, ACUSON X700, SwiftLink, and Vector are
trademarks of Siemens Medical Solutions USA, Inc.
All other product names are references to third-party products and
are trademarks or registered trademarks of their respective
companies. Siemens includes references to third-party products in
the user documentation for informational purposes only. Siemens
does not endorse third-party products referenced in the user
documentation. Siemens does not assume responsibility for the
performance of third-party products.
Siemens reserves the right to change its products and services at
any time. In addition, this manual is subject to change without
notice.
Legal Manufacturer
Siemens Medical Solutions USA, Inc.
Ultrasound
685 East Middlefield Road
Mountain View, CA 94043
U.S.A.
Phone: +1-888-826-9702
siemens.com/healthcare
10030119-ABS-001-12-12
CE Declaration
The ACUSON AcuNav 10F ultrasound catheter and
ACUSON AcuNav 8F ultrasound catheter are provided with
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
Siemens Healthcare Headquarters
Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
Phone: +49 9131 84-0
siemens.com/healthcare
34/34 10030119-12