Zeiss OPMI PROergo S7, Инструкция по эксплуатации

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Version 11.0
G-30-1435-en
Page 257
S7 / OPMI PROergo Device data
System enhancements
The device S7 / OPMI PROergo can be extended with the accessories offered
by ZEISS (see ordering data/accessories) to form an already tested system. This
device combination has been approved by ZEISS.
CAUTION As per IEC 60601-1-1 and IEC 60601-1, Section 16.2, this system's power
outlet is a multiple electrical outlet intended for use with an ME system.
Connecting electrical devices not approved by ZEISS can lead to a reduced
level of safety on the ME system.
• When configuring your ME system (using the power output socket),
make sure to comply with the requirements of IEC 60601-1, Section 16,
as well as the following measures:
– Do not place multiple electrical outlets on the floor.
– Do not connect any additional multiple electrical outlets.
– Only connect compatible components to the system.
– Do not exceed the max permissible electrical load of multiple
electrical outlets.
– Use multiple electrical outlets only for components of the system.
NOTE Connect accessories
Any additional equipment connected to medical electrical devices must
demonstrably comply with the applicable standards and directives
(e.g. IEC 60950 for data processing equipment).
Furthermore, all configurations must comply with the standards for medical
systems (see IEC 60601-1, section 16; in some countries IEC 60601-1-1 may
still be valid).
Anyone who connects auxiliary equipment to medical electrical devices is
a system configurer, and as such, is responsible for ensuring that the system
complies with the applicable system standards.
Please note that local legislation takes priority over the requirements set out
in the above-mentioned standards. If you have any questions, please contact
ZEISS Service or your local dealer.