6
service.
4) The unit has previously been adjusted in the factory for optimum performance.
Do not attempt to adjust switches or any other things except those specified in this manual for
operation.
5) If you have experienced any trouble with the unit, switch it off immediately, and contact our
company or its authorized dealer for assistance.
6) Continuous cuff pressure due to connection tubing kinking can cause the blood flow interference
and resulting harmful injury to the patient.
7) Too frequent measurements can cause injury to the PATIENT due to blood flow interference.
8) The application of the CUFF over a wound can cause further injury.
9) The application of the CUFF and its pressurization on any limb where intravascular access or
therapy, or an arterio-venous (A-V) shunt, is present because of temporary interference to blood
flow and could result in injury to the patient;
10) CUFF and its pressurization on the arm on the side of a mastectomy should not be applied.
11) The pressurization of the CUFF can temporarily cause loss of function of simultaneously used
monitoring ME EQUIPMENT on the same limb;
12) It is necessary to check that operation of the automated sphygmomanometer does not result in
prolonged impairment of PATIENT blood circulation
13) If you plan to connect any device of other manufacturers electrically or mechanically to the unit,
contact our company or its authorized dealer for instructions before doing so.
When you connect computer or other system to the unit (RS-232C), the attached systems should
be those certified by IEC 950 or equivalent standards for data processing equipment.
Configurations shall comply with the system standard IEC 60601-1:2005.
Everybody who connects additional equipment to the signal input part or signal output part
configures a medical system standard IEC 60601-1:2005.
If in doubt, consult the A/S department of local distributor.
14) Avoid the following environments for storage;
- Where the ambient temperature falls -20°C or exceeds 60°C.
- Where the atmospheric pressure falls below 70kPa (700mbar) or exceeds 106kPa (1060mbar).
- Where the humidity is over 95% non-condensing.
- Where the unit is exposed to spray or splashing water.
- Where the unit is exposed to dust.
- Where the unit is exposed to water vapor.
- Where the unit is exposed to salty atmosphere.
- Where the unit is exposed to explosive gas.
- Where the unit is exposed to excessive shocks or vibrations.
- Where the angle of inclination of mounting surface exceeds 10 degrees.
- Where the AC power line voltage heavily fluctuates.
- Where the AC power line voltage changes heavily when this unit is in operation.
- Where the unit is exposed to direct sunlight.
15) This equipment has been tested and found to comply with the limits for medical devices to the
IEC 60601-1-2:2007. These limits are designed to provide reasonable protection against harmful
interference in a typical medical installation. This equipment generates, uses and can radiate
Summary of Contents for BP800
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