Preparations for use
OPMI Lumera
®
i on floor stand
Version 9.2
Page 64
G-30-1720-en
Medical electrical
systems
Any additional equipment you connect to medical electrical devices
must demonstrably comply with the applicable standards and directives
(e.g. IEC 60950-1 for data processing equipment).
In addition, all configurations must meet the standard requirements for
medical electrical systems (see IEC 60601-1).
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
normative requirements. If you have any questions, contact your local dealer
or ZEISS Service.
WARNING
Risk of serious injury from unauthorized modification!
You must not modify this device without the permission of the manufacturer.
The manufacturer is not liable for damage caused by unauthorized persons
tampering with the system.
Unauthorized modifications of the device may result in severe, irreversible
injuries to users and/or patients.
•
If you modify the device after consultation with the manufacturer, you
must conduct the appropriate inspections and tests to ensure that it can
still be used safely.
R502
NOTICE
Loss of warranty
The manufacturer is not liable for damage caused by unauthorized persons
tampering with the system. Furthermore, this will forfeit any rights to claims
under the warranty.
Содержание OPMI Lumera i on floor stand
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