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.
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.
Products with serial numbers between 27201 and 27534, 29101
and 29999, 32101 and 32999, 80401 and 81000, 85501 and
86554, 86557 and 86559, or 86562 and 86600 may contain non
RoHS complaint material.
Caution: Federal law restricts this device to sale by or on the
order of a physician, dentist, or veterinarian (21 CFR 801.109(b)
(1)).
The original language of this document is English.
EU Authorized Representative
Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
Siemens Healthineers
Headquarters
Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
Phone: +49 9131 84-0
siemens-healthineers.com
Legal Manufacturer
Siemens Shanghai Medical
Equipment Ltd.
278 Zhou Zhu Road
201318 Shanghai
P.R. China
Published by Siemens Shanghai Medical Equipment Ltd. / Print No. HC-C2-025.626.01.01.02 / © Siemens Shanghai Medical Equipment Ltd., 2019
Date of first issue: 2019-05
To Previous Page
Loading...
