User's Manual
Page 10
WARNING Conductive parts of electrodes and associated connectors for
type BF or CF applied parts, including the NEUTRAL ELECTRODE,
should not contact any other conductive parts including earth
WARNING The stored data will not be affected. The measurement
accuracy will temporarily decrease during electrosurgery, but it will not
compromise the safety of patient and the equipment.
WARNING To avoid the risk of electric shock, this equipment must only be
connected to a supply mains with protective earth.
WARNING When using SpO2 function under the room temperature of 40
℃, SpO2,SpO2 test finger temperature will up to 43℃
Warning The performance of the AUTOMATED SPHYGMOMANOMETER
can be affected by extremes of temperature, humidity and altitude
Warning Connection to other equipment could result in previously
unidentified risks to patients, operators or third parties. Fukuda Denshi is
not responsible for the integrity of any installation or upgrade not
performed by authorized Fukuda Denshi service personnel. Contact an
authorized Fukuda Denshi service representative or other qualified service
personnel to ensure professional installation for safety and reliability
Warning Changes to other equipment could introduce new risks that
require additional analysis, changes including
- changes in network configuration
- connection of additional items
- disconnection of items
- update of equipment
Warning Devices connect to the system shall fulfill 60601-1 requirement
WARNING Please do not absolutely installation and operation of the
program other than Fukuda Denshi specified in the device. Normal
operation of this equipment cannot be guaranteed.
WARNING Please do not insert USB memory or other equipment while
operating this device. When an application or installation starts
automatically. Normal operation of this device can not be guaranteed
Caution Japan’s Law restricts this monitor to sale, distribution, or use by or
on the order of a physician or licensed healthcare professional.
Caution Electromagnetic interference risk. The monitor complies with
applicable domestic and international standards for electromagnetic
interference. These standards are intended to minimize medical
equipment electromagnetic interference. Although this monitor is not
expected to present problems to other compliant equipment or be affected
by other compliant devices, interference issues still may occur. As a
precaution, avoid using the monitor in close proximity to other equipment.
In the event that equipment interference is observed, relocate the
equipment as necessary or consult manufacturer’s direction for use.
Caution Use only a Class I (grounded) AC power supply cord for powering
this monitor.
Caution Do not use a long press of to power down the monitor when
it is functioning normally. You will lose patient data and configuration










