Zeiss S100/OPMI pico, Instructions For Use Manual

Page: 251 / 278

Version 7.0
G-30-1781-en
Page 251
S100 / OPMI pico System Data
System upgrades
The device S100 / OPMI pico can be extended with the accessories offered by
ZEISS (see ordering data/accessories) to form an already tested system. This
system combination has been approved by ZEISS.
Additional devices that are connected to electronic medical devices must
comply with the relevant standards and guidelines
(for example IEC 60950 for data processing devices).
Furthermore, any configurations must comply with normative requirements
for electronic medical devices (see IEC 60601-1:2005, chapter 16; in some
countries IEC 60601-1-1:2000 may still be valid).
The one who is connecting additional devices to electronic medical devices
acts as system configurer and is responsible for the system complying with the
normative requirements for electronic medical devices.
Please note that local legislation takes priority over the above-mentioned nor-
mative requirements. If you have any questions, please contact your local
dealer or ZEISS Service.
Ordering data
Operate the device only with accessories included in the scope of delivery and
recommended by ZEISS. The contact partners in charge of your country are
listed on the Internet on the following website:
www.zeiss.com/med
For authorized ZEISS partners, the contractual product configurations, acces-
sories and spare parts apply.
Please contact your authorized ZEISS partner for more information.
Illumination
Description Order number
Halogen lamp, 12 V, 100 W, 380079-9040-000