Terumo CDI 550 Operator's Manual page 123

Blood parameter monitoring system
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In accordance with IEC 60601-1: Accessory equip-
ment connected to the analog and digital interfaces
must be certified according to the respective IEC stan-
dards (i.e. IEC 950 for data processing equipment and
IEC 60601-1 for medical equipment). Furthermore, all
configurations shall comply with the system standard
IEC 60601-1. Anyone who connects additional equip-
ment to the signal input port or signal output config-
ures a medical system, and is therefore responsible
that the system complies with the requirements of
IEC 60601-1. If in doubt, consult the technical service
department or your local representative.
Restrict use of IEC 950 certified data processing
equipment to those with covers that can only be re-
moved with the use of a tool.
When using IEC 950 compliant data processing
equipment do not simultaneously contact patient and
parts of data processing equipment that may be elec-
trically energized.
This system was tested with the following equipment
connected as a worst case scenario; 550AVHCT,
Sarns Centrifugal System, TLink Data Management
System and 540 Calibrator.
B-8
appendix b

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