1-13
and close the cylinder valve slowly.
Changes in inlet pressure, outlet resistance, or ambient temperature may affect the
accuracy of flow values.
The power supplies, terminal units and pipeline systems can be supplied by one or
several different manufacturers.
Regional or national regulations that apply to manufacturers of medical equipment
can exist.
The product does not contain latex parts.
The operator should stay right in front of the equipment within four meters away
from the display to facilitate observation of the displayed information on the
equipment.
Some alarm settings on this equipment are not configurable by users.
The tidal volume and minute ventilation displayed on this equipment are measured
in BTPS conditions. The fresh gas flow is measured in STPD conditions.
For the method of connecting this equipment to an external monitor or other
devices, please see Anesthesia System Bracket Installation Instructions.
All the materials of this equipment exposed to gases are compatible with O2, air
and N2O.
To avoid abnormal gas supply, the anesthesia system has a 758 kPa (110 psi)
pressure relief valve installed at the gas supply inlet. When the gas supply pressure
is abnormally elevated, the pressure relief valve is turned on to ensure the proper
operation of the anesthesia system. When the pressure relief valve is on, the
anesthesia system and the O2 flush are both operating properly, and their P-F
(pressure/flow) characteristics are consistent with those under rated conditions.
The pressure at the high-pressure O2 outlet will be elevated to 758 kPa (110 psi),
and the maximum flow rate meets requirements in the specifications.
The defibrillation restoration time is 15 seconds unless otherwise stipulated.
Unauthorized servicing may void the remainder of the warranty. Check with the
factory or with a local authorized distributor to determine the warranty status of a
particular instrument.
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