2 S a f e t y a n d Care
[ 1 ] I N S T R U C T I O N S F O R U S E 2 - 19
Siemens suggests that you request any person who performs maintenance,
or repairs, to provide you with a certificate showing:
The nature and extent of the work performed
Changes in rated performance
Changes in working ranges
Date of service
Name of person or firm performing the service
Signature of person performing the service
Technical documentation pertinent to the imaging system is available at an
additional charge. However, this does not in any way constitute an
authorization to conduct repairs or maintenance. Siemens refuses all
responsibility whatsoever for repairs that are performed without the express
written consent of the Siemens service department.
WARNING: Accessory equipment connected to the analog and digital
interfaces must be certified according to the respective EN and IEC standards
(for example, EN 60950 and IEC 60950 for data processing equipment and
EN 60601-1 and IEC 60601-1 for medical equipment). Furthermore, all
configurations shall comply with the system standards EN 60601-1-1 and
IEC 60601-1-1. Anyone who connects additional equipment to any signal input or
signal output ports configures a medical system and is therefore responsible
that the system complies with the requirements of the system standards
EN 60601-1-1 and IEC 60601-1-1. Siemens can only guarantee the performance
and safety of the devices listed in the System Reference. If in doubt, consult
Siemens service department or your local Siemens representative.
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