Version 7.1
G-30-1158-en
Page 11
KSK 150 FC
Safety Measures
System kit
Any additional equipment connected to medical electrical devices must de-
monstrably comply with the applicable standards and directives (e.g. IEC
60950-1:2005, mo Cor.:2006 + A1:2009, mo A1:2009/
Cor.:2012 + A2:2013, modified for data processing equipment).
Furthermore, any configurations must comply with normative requirements
for electronic medical devices (see IEC 60601-1-1:2000 or IEC 60601-1:2005
+ A1:2012, chapter 16).
Anyone connecting additional equipment to medical electrical devices is a
system configurer and as such is responsible for compliance of the system
with the normative requirements for medical electrical systems.
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.
Prerequisites for operation
Prior to the very first use
Our service representative or an expert authorized by us will install the system.
Please make sure that the following requirements continue to be met for fur-
ther operation:
The connecting components have been properly connected. The screw
connections have been firmly tightened.
All cables and connectors are in a perfect condition, i.e. they do not dis-
play any worn areas, kinks or other defects.
The voltage set on the system corresponds to the rated line voltage on the
site of installation.
Insert the power plug only into a socket that is fitted with a flawless
protective earth conductor.
The power cord being used is the one designed for use with this system.
Содержание KSK 150 FC
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