3-1
3 Installation
WARNING
z The installation of the monitor must be carried out by personnel authorized by us.
The software copyright of the monitor is solely owned by our company. Any action
to change, copy or exchange the software copyright by any organization or person
is regarded as copyright infringement and is not allowed.
z Accessory equipments connected to this patient monitor must be certified
according to the respective IEC standards (e.g. IEC 60950 for information
technology equipment and IEC 60601-1 for medical electrical equipment).
Furthermore all configurations shall comply with the valid version of the system
standard IEC 60601-1-1. Any person who connects additional equipment to the
signal input or signal output is responsible to ensure the system complies with the
requirements of the valid version of the system standard IEC 60601-1-1. If in
doubt, contact our company or customer service.
z If the monitor is connected to another electrical instrument and the instrument
specifications cannot tell whether the instrument combination is hazardous (e.g.
due to summation of leakage currents), you should consult us or experts in the
field to ensure the required safety of all instruments concerned.
NOTE
z The operations in this section are not all required. User-customized installation by
authorized personnel is provided.
3.1 Unpacking and Checking
Before unpacking, examine the packing case carefully for signs of damage. If any damage is
detected, contact the carrier or our company.
If the packing case is intact, open the package and remove the instrument and accessories
carefully. Check all materials against the packing list and check for any mechanical damage.
Contact our Customer Service Department in case of any problem.
NOTE
z Please save the packing case and packaging material for future transport and
storage.
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