Zeiss OPMI Lumera i, Instructions For Use Manual

Page: 60 / 184

Preparation for use OPMI Lumera i
Version 8.0
Page 60 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 requirements of the
above-mentioned standards. If you have any questions, contact your local
dealer or ZEISS Service.
WARNING Risk of serious injury due to unauthorized modification!
You must not modify this device without the permission of the manufacturer.
The manufacturer is not liable for damages caused by an unauthorized use
of the device.
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
have to carry out the appropriate inspections and tests to ensure that it
can still be used safely.
R502
NOTE Loss of warranty
The manufacturer is not liable for damages caused by an unauthorized use
of the device. Furthermore, such unauthorized modifications will render the
warranty and any claims under warranty invalid.