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Chapter1 Introduction
For an overall introduction to the monitor, please refer to
General Information.
For various messages displayed on the screen, please refer to
Screen Display.
For basic operating instructions, please refer to
Button Function
.
For allocation of interface sockets, please refer to
Interfaces.
For important facts to be noted during the battery recharging procedure, please refer to
Built-in Battery.
Warning
The Monitor is intended for clinical monitoring application with operation only granted to appropriate
medical staff.
The monitor can be used on only one patient at a time.
There could be hazard of electrical shock by opening the monitor casing. All servicing and future
upgrading to this equipment must be carried out by personnel trained and authorized by our company.
To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective
earth.
Possible explosion hazard if used in the presence of flammable anesthetics or other flammable substance in
combination with air, oxygen-enriched environments, or nitrous oxide.
You must verify if the device and accessories can function safely and normally before use.
You must customize the alarm setups according to individual patient situation and make sure that alarm
sound can be activated when alarm occurs.
Do not use cellular phone in the vicinity of this device. High level electromagnetic radiation emitted from
such devices may greatly affect the monitor performance.
Do not touch the patient, table, or the device during defibrillation.
Devices connected to the monitor shall form an equipotential system (protectively earthed).
When used with Electro-surgery equipment, you (doctor or nurse) must give top priority to the patient
safety.
Do not place the monitor or external power supply in any position that might cause it to fall on the patient.
Do not lift the monitor by the power supply cord or patient cable, use only the handle on the monitor.
Consult IEC60601-1-1 for system interconnection guidance. The specific requirements for system
interconnection are dependent upon the device connected to the monitor and the relative locations of each
device from the patient, and the relative location of the connected device to the medically used room
containing the monitor. In all circumstance the monitor must be connected to a grounded AC power supply.
The monitor is referred to as an IEC 601/F device in the summary of situations table contained in IEC
60601-1-1.
Dispose of the packaging material, observing the applicable waste control regulations and keeping it out of
children’s reach.
Grounding:Connect the monitor only to a three-wire, grounded, hospital-grade receptacle. The
three-conductor plug must be inserted into a properly wired three-wire receptacle; if a three-wire
receptacle is not available, a qualified electrician must install one in accordance with the governing
electrical code.
Do not under any circumstances remove the grounding conductor from the power plug.
Do not use extension cords or adapters of any type. The power cord and plug must be intact and
undamaged.
If there is any doubt about the integrity of the protective earth conductor arrangement, operate the
monitor on internal battery power until the AC power supply protective conductor is fully functional.
Note
The software was developed per IEC62304. The possibility of hazards arising from errors in the software
program is minimized.
Caution
The monitor's service life is 5 years.At the end of its service life, the product described in this manual, as
well as its accessories, must be disposed of in compliance with the guidelines regulation the disposal of such
