Mindray A9 Service Manual

1-12
1.1.3 Notes
NOTE
 Figures in this manual are provided for reference purposes only.
 Screens may differ based on the system configuration and selected parameters.
 Put the equipment in a location where you can easily see the screen and access the
operating controls.
 Keep this manual close to the equipment so that it can be obtained conveniently
when needed.
 The software was developed in compliance with IEC 60601-1.The possibility of
hazards arising from software errors is minimized.
 This manual describes all features and options. Your equipment may not have all
of them.
 The equipment is intended to be operated with its integral Breathing Pressure
monitoring in use.
 The equipment is intended to be operated with its integral Breathing Pressure
limiting devices in use.
 The equipment is intended to be operated with its integral Expiratory Volume
monitoring in use.
 The equipment is intended to be operated with its integral Breathing System
integrity Alarm System in use.
 The equipment is intended to be operated with its integral Continuous Pressure
Alarm in use.
 The equipment is intended to be operated with its integral O2 monitoring in use.
 An Anesthesia Vapor Delivery Device is to be used with an Anesthetic Agent
Monitor complying with ISO 80601-2-55. The connection of Patient Circuit and
Agent monitor should be made by a sample line.
 Continuously monitor the anesthetic agent concentration when using the anesthesia
system to ensure accurate output of the anesthetic agent.
 Check the liquid level of the anesthetic agent before and during all operations.
When the liquid level is below the warning line, more anesthetic agent needs to be
added. For the A8 anesthesia system, refer to the vaporizer Instructions For Use
for filling the vaporizer and other information. For the A9 anesthesia system, refer
to the Operator’s Manual for filling the vaporizer and other information.
 The system is designed to be equipped with an anesthetic vapor delivery device that
complies with ISO 80601-2-13.
 The battery supply of this equipment is not a user serviceable component. Only an
authorized service representative can replace the battery supply. If the system is
not used for a long time, contact a service representative to have the battery supply
disconnected. The disposal of battery should comply with local regulations. At the
end of the battery life, dispose of the battery supply in accordance with local
regulations.
 Areas designated for the servicing of oxygen equipment shall be clean, free of oil
and grease, and not be used for the repair of other equipment.
 Opening the cylinder valve quickly may cause unexpected pressure difference and
lead to potential fire or explosion hazard due to the oxygen pressure shock. Open

Mindray A9 Specifications

General

Brand	Mindray
Model	A9
Category	Medical Equipment
Language	English