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disease for they may develop paral bleeding when this monitor is used to take the blood pressure measurement.
All the connecng cables and tubes of the applying parts should be kept away from the paent’s cervix to prevent
any possible suocaon of the paent.
To prevent the risk of the short circuit and to ensure the ECG signal quality, the device must be properly grounded.
The device should be considered an early warning device as a trend towards paent deoxygenaon is indicated,
blood samples should be analyzed by a laboratory CO-oximeter to completely understand the paent’s condion.
Although biocompability tests have been performed on all the applied parts, some exceponal allergic paents
may sll have anaphylaxis. Do NOT apply to those who have anaphylaxis.
Please peruse the relave content about the clinical restricons and contraindicaon.
It is recommended that the clinical operator regularly test device and accessories. And the visual and auditory
alarm signal can be checked by intenonally disconnect accessories or by seng it at Demo mode to simulate
alarm event.
Do not allow service or maintenance on the device while used in paent.
The operator can press alarm silence if sensors, probes, or modules are intenonally disconnected by the clinical
operator.
1.1.2 Cauons
All the parts of the monitor should NOT be replaced at will, substuon of a component dierent from that supplied
by the manufacturer might result in measurement error. If necessary, please use the components provided by the
manufacturer or those that are of the same model and standards as the accessories along with the monitor which
are provided by the same factory, otherwise, negave eects concerning safety and biocompability etc. may be
caused. No modicaon of this device is allowed.
The accessories which can be used repeatedly should have a thorough cleanness before it is used to another
paent. Please refer to the related chapter for maintenance method.
If the monitor falls o accidentally, please do NOT operate it before its safety and technical indexes have been
tested minutely and posive tesng results obtained.
Do not immerse the monitor or its accessories in liquid to clean.
The system might not meet its performance specicaons if stored or used outside the manufacturer’s specied
temperature and humidity ranges.
1.1.3 Notes
☞ All combinaons of equipment must be in compliance with the standard IEC 60601-1.
☞ Please do not posion the device so that it is dicult to connect the plug of the power cord.
☞ Aer the life cycle of the monitor and its accessories has been met, disposal should be accomplished following
naonal and/or local requirements.
☞ If the user requires more informaon such as circuit diagrams, parts list and product descripons, for repairs carried
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