Aeon8800A User Manual

Aeon8800A Anesthesia Machine User Manual Statement
Statement
Beijing Aeonmed Co., Ltd. (Aeonmed for short) holds the copyrights to this manual, which is
non-public, published, and reserves the rights to keep it as a secure document. Refer to this
manual when operating, maintaining and repairing products only. Anyone other than Aeonmed
may not make it known to others.
Proprietary materials protected by the copyright law are included in this manual. Any section of it
cannot be reproduced, copied, or translated into other languages without any prior written
approval from Aeonmed who reserves the copyright.
Everything written in this manual is considered to be correct. Aeonmed is not legally responsible
for any mistakes printed within and any damages caused by incorrect installation and operation.
Aeonmed does not supply privileges endowed by the patent law to any other parties. Aeonmed is
not legally responsible for the results caused by patent law breaking and any rights of the third
party violating.
Refer to this manual before the product is used. The manual includes operating procedures which
must be performed with cautiously, operations that may result in non-normal working conditions
and the dangers which may damage equipment or cause bodily harm. Aeonmed is not
responsible for the security, reliability and function of the equipments in case that the dangers,
damages and non-normal phenomenon mentioned in this manual happen. Free repairs for these
malfunctions will not be provided by Aeonmed.
Aeonmed has the rights to replace any content in this manual without notice.
Manufacturer Responsibility:
Aeonmed is responsible for the security; reliability and function of the equipments when to
following conditions are adhered to:
 Installation, adjustments, mending and repairs must be performed by individuals authorized

by Aeonmed;
 Necessary electrical equipment and the working environment must be in accordance with the
national standards, professional standards and the requirements listed in this manual;
 Equipment must be used as instructed in the operating instructions.
i
CAUTION: This equipment is not for home use.
CAUTION: Malfunctioning equipment may become invalid and cause bodily injury if a
set of effective and approving repairing proposals cannot be submitted by
the institution which is responsible for using this equipment.
The paid theoretical framework diagram will be supplied according to customer requirements by
Aeonmed, plus calibrating method and other information to help the customer, under the
assistance of qualified technicians, repair the equipment parts where can be done by customer
himself based on the stipulation by Aeonmed.
Warranty:
Manufacturing techniques and materials:
For a period of one year from the date of original delivery, the components and assemblies of this
product is warranted to be free from defects manufacturing techniques and materials, provided
that the same is properly operated under the conditions of normal use and regular maintenance.
The warranty period for other parts is three months. Expendable parts are not included. Our
obligation under the above warranties is limited to repairing free of charge.
Free Obligations:
 Our obligation under the above warranties does not include the freight and other fees;
 Aeonmed is not responsible for any direct, indirect or final product broken and delay
which result from improper use, alteration by using the assemblies unratified and
maintenance by anyone other than Aeonmed;
 This warranty does not apply to the followings:
Improper use;
Machines without maintenance or machines broken;
The label of our original serial number or mark is removed or replaced;
Other manufacturers’ product.
ii
Safety, reliability and operating condition:
Aeonmed is not responsible for the safety, reliability and operating condition of this product in
case that:
 The assemblies are disassembled, extended and readjusted
 This product is not operated correctly in accordance with the manual instruction. The
power supply used or operating environment does not follow the requirements in this
manual.
Return
Follow the steps below in case that the product needs to be returned to Aeonmed:
1. Obtain the rights of return
Contact our customer service by informing them the number and type of the product. The number
is marked on the surface of the product. Return is unacceptable if the number cannot be identified.
Enclose a statement of the number, type and the reason of return as well.
2. Transportation charges
Transportation and insurance charges must be prepaid by the user for transporting the product to
Aeonmed for repairing. (Customers charges are added with regard to the products sold to
non-Chinese mainland users).
Device lifetime：8 years.
iii
Use Notice
Welcome to use our products.
To use this product correctly and effectively, the user must read this user manual carefully before
using this product.
When the user is using this product, this user manual must be understood totally and observe
strictly.
This product is only applied to the use this user manual described.
Only trained and professional service persons are allowed to repair and examine this product.
If there is any case happened in the process of use, please call us and intense service will be
provided.
If there is any change in product specification, another informs will not be given.
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Manufacturer(holder): Beijing Aeonmed Co., Ltd.
Manufacturer(holder) Room 405，Basement 1 to 4th Floor of 901 Unit, Building 9,

address: No.26 Outer Ring West Road, Fengtai District, Beijing 100070,
China
Facility: Beijing Aeonmed Co., Ltd.
Facility address: Room 405，Basement 1 to 4th Floor of 901 Unit, Building 9,

No.26 Outer Ring West Road, Fengtai District, Beijing 100070,
China
No.10 Chaobai Street, Yingbin Road West, Yanjiao

Development Zone, 065201, Langfang, Hebei, China
Service: Beijing Aeonmed Co., Ltd.
Service Address: No.10 Chaobai Street, Yingbin Road West, Yanjiao

Development Zone, 065201, Langfang, Hebei, China
Tel: +86-10-83681616
Fax: +86-10-63718989
Service Line: +86 800-810-8333
Website: http://www.aeonmed.com
E-mail: service@aeonmed.com
European Representative: Shanghai International Holding Corp. GmbH (Europe)
Address: Eiffestrasse 80, 20537 Hamburg Germany
Wechat Offical Account:
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Aeon8800A Anesthesia Machine User Manual CONTENTS
CONTENTS
1. Product Description .............................................................................................................................. 1-1
1.1. General Information ........................................................................................................................... 1-1

1.2. Symbols .............................................................................................................................................. 1-2
1.3. Abbreviations...................................................................................................................................... 1-6
1.4. Warnings and Cautions ....................................................................................................................... 1-8
2. Components ......................................................................................................................................... 2-1
2.1. Configuration ...................................................................................................................................... 2-1

2.2. Front View .......................................................................................................................................... 2-2
2.3. Side View ............................................................................................................................................ 2-6
2.4. Back View ........................................................................................................................................... 2-8
2.5. Breathing System .............................................................................................................................. 2-10
2.5.1. APL Valve ................................................................................................................................. 2-13
2.6. Vaporizer-VP300/VP500 --Optional .................................................................................................. 2-14
2.7. Anesthetic Gas Scavenging System-AP1000 --Optional.................................................................... 2-15
2.8. SUCTION --Optional .......................................................................................................................... 2-16
2.9. Electronic Flowmeter........................................................................................................................ 2-17
2.10. O2 flush ............................................................................................................................................. 2-18
3. User interface ....................................................................................................................................... 3-1
3.1. Main interface display layout ............................................................................................................. 3-3

3.1.1. The Interface layout without CO2or anesthesia gas monitoring................................................ 3-4
3.1.2. The Interface layout with only CO2 monitoring ......................................................................... 3-5
3.1.3. The Interface layout with CO2and anesthesia gas monitoring .................................................. 3-6
3.2. Information of the main interface ...................................................................................................... 3-7
3.2.1. Ventilation mode set and display area ...................................................................................... 3-7
3.2.2. Parameter set and display area ................................................................................................. 3-8
3.2.2.1. Parameter display .................................................................................................................................. 3-8
3.2.2.2. The button status when setting parameter ......................................................................................... 3-10
3.2.3. Alarm indication area ............................................................................................................... 3-11

3.2.4. Machine information area ....................................................................................................... 3-12
3.2.5. Waveform display area ............................................................................................................ 3-13
3.2.6. Patient message area ............................................................................................................... 3-14
3.2.7. Patient parameter monitoring area ......................................................................................... 3-15
3.2.8. Anesthesia gas monitoring area .............................................................................................. 3-15
3.2.9. Flowmeter area ........................................................................................................................ 3-16
vi
3.2.10. Message prompts area ............................................................................................................ 3-17

3.2.11. Shortcut key area ..................................................................................................................... 3-18
3.3. General menu layout ........................................................................................................................ 3-19
4. Pre-operative Preparation .................................................................................................................... 4-1
4.1. Initial Setup ......................................................................................................................................... 4-1

4.1.1. Connection of Tubes and Cables ................................................................................................ 4-1
4.1.2. Connection of Breathing Bag ..................................................................................................... 4-3
4.1.3. Connection of test plug .............................................................................................................. 4-4
4.1.4. Connection of O2 sensor ............................................................................................................ 4-5
4.1.5. Connection of the anesthetic gas/CO2 monitoring module (optional) ...................................... 4-7
4.1.5.1. Connection of the mainstream monitoring module .............................................................................. 4-7
4.1.5.2. Connection of the sidestream monitoring module ............................................................................... 4-9
4.1.6. AGSS Installation and Connection............................................................................................ 4-10

4.2. Pre-operative Test ............................................................................................................................ 4-12
4.2.1. Test before Operation ............................................................................................................. 4-12
4.2.1.1. System Check....................................................................................................................................... 4-13
4.2.1.2. Power Failure Alarm Test .................................................................................................................... 4-13
4.2.2. Pipeline Gas Supply Test .......................................................................................................... 4-14

4.2.3. Vaporizer Test .......................................................................................................................... 4-14
4.2.4. Alarm Test ................................................................................................................................ 4-15
5. Operating guide .................................................................................................................................... 5-1
5.1. Opening .............................................................................................................................................. 5-1

5.2. System Self–test ................................................................................................................................. 5-2
5.3. Automatic Leak Test ........................................................................................................................... 5-3
5.4. Manual Test ........................................................................................................................................ 5-7
5.5. Patient type setting .......................................................................................................................... 5-10
5.6. Ventilation mode setting .................................................................................................................. 5-12
5.6.1. Ventilation mode introduction ................................................................................................ 5-12
5.6.1.1. Manual Ventilation (Manual) .............................................................................................................. 5-12
5.6.1.2. Intermittent Positive Pressure Ventilation (IPPV) ............................................................................... 5-13
5.6.1.3. Pressure Control Ventilation (PCV) ...................................................................................................... 5-14
5.6.1.4. Synchronized Intermittent Mandatory Ventilation with Volume control (SIMV-VC) .......................... 5-15
5.6.1.5. Pressure Support Ventilation (PS) ....................................................................................................... 5-17
5.6.1.6. Pressure control ventilation with Volume Guaranteed (PCV-VG) --Optional ...................................... 5-18
5.6.1.7. Synchronous Intermittent Mandatory Ventilation with Pressure Control (SIMV-PC) --Optional ........ 5-20
5.6.2. Ventilation mode setting ......................................................................................................... 5-22
vii
5.6.3. Mode parameter setting .......................................................................................................... 5-23

5.7. Menu screens ................................................................................................................................... 5-24
5.7.1. Menu operating logic ............................................................................................................... 5-24
5.7.2. Alarm setting............................................................................................................................ 5-25
5.7.3. System setting .......................................................................................................................... 5-27
5.7.4. Calibration................................................................................................................................ 5-29
5.7.4.1. Oxygen sensor calibration ................................................................................................................... 5-29
5.7.4.2. CO2/Agents calibration ........................................................................................................................ 5-31
5.7.4.3. Touch screen calibration ..................................................................................................................... 5-32
5.7.5. Trend ........................................................................................................................................ 5-33

5.7.6. Check........................................................................................................................................ 5-34
5.7.6.1. Leak Test .............................................................................................................................................. 5-34
5.7.6.2. Compliance Test .................................................................................................................................. 5-36
5.7.7. Configuration ........................................................................................................................... 5-38

5.8. Shutdown ......................................................................................................................................... 5-40
6. Alarm and troubleshooting ................................................................................................................... 6-1
6.1. Brief introduction of alarm message .................................................................................................. 6-2

6.2. Alarm message ................................................................................................................................... 6-3
6.2.1. Alarm default value and setting range....................................................................................... 6-3
6.2.2. Technical alarm message table .................................................................................................. 6-4
6.2.3. Functional alarm message ......................................................................................................... 6-8
6.2.4. Self-test alarm .......................................................................................................................... 6-12
6.3. Failure diagnosis ............................................................................................................................... 6-14
7. Cleaning and Disinfection ..................................................................................................................... 7-1
7.1. Guideline ............................................................................................................................................ 7-3

7.2. User maintenance .............................................................................................................................. 7-4
7.3. Breathing system disassembly............................................................................................................ 7-5
7.4. Methods for cleaning and disinfecting ............................................................................................. 7-10
7.4.1. Cleaning and disinfecting for breathing system ...................................................................... 7-11
7.4.2. Cleaning and disinfecting for bellows ...................................................................................... 7-12
7.4.3. Cleaning and disinfecting for AGSS .......................................................................................... 7-12
8. Regular maintenance ............................................................................................................................ 8-1
8.1. General principle of maintenance ...................................................................................................... 8-2

8.2. Maintenance schedule ....................................................................................................................... 8-3
8.2.1. Appearance checklist ................................................................................................................. 8-3
viii
8.3. Replacement of replaceable parts ...................................................................................................... 8-4

8.4. Maintenance of O2 sensor .................................................................................................................. 8-5
8.4.1. Replacement of O2 sensor .......................................................................................................... 8-5
8.4.2. Main technical parameter of O2 sensor ..................................................................................... 8-5
8.5. Maintenance of fuse ........................................................................................................................... 8-7
8.6. Battery Maintenance .......................................................................................................................... 8-8
8.7. Consumptive components replacement ............................................................................................ 8-9
9. Technical Data ...................................................................................................................................... 9-1
9.1. Pneumatic Diagram ............................................................................................................................ 9-1

9.2. System technical data ......................................................................................................................... 9-4
9.3. Electrical diagraph .............................................................................................................................. 9-5
9.4. Physical data ....................................................................................................................................... 9-6
9.5. Environmental requirement ............................................................................................................... 9-7
9.5.1. IEC60601-1:2005 classification .................................................................................................. 9-8
9.6. Input and output ................................................................................................................................ 9-9
9.6.1. Electrical..................................................................................................................................... 9-9
9.6.2. Pneumatic ................................................................................................................................ 9-10
9.7. Breathing system technical data ...................................................................................................... 9-11
9.7.1. Compliance correction ............................................................................................................. 9-12
9.8. Anesthetic ventilator technical specifications .................................................................................. 9-13
9.8.1. Anesthetic ventilator performance.......................................................................................... 9-13
9.8.2. Ventilation parameter ............................................................................................................. 9-14
9.8.3. Gas dynamics ........................................................................................................................... 9-15
9.8.4. Monitor performance .............................................................................................................. 9-16
9.9. O2 sensor specification...................................................................................................................... 9-17
9.10. Gas monitoring module technical specifications .............................................................................. 9-18
9.10.1. MAC calculation of ISA gas analyzer ........................................................................................ 9-18
9.10.2. Gas data consideration ............................................................................................................ 9-19
9.10.3. Mainstream gas monitoring module ....................................................................................... 9-21
9.10.4. Sidetream gas monitoring module .......................................................................................... 9-28
9.10.4.1. System set-up ...................................................................................................................................... 9-29
9.10.4.2. Pre-use check ...................................................................................................................................... 9-29
9.10.4.3. Manitenance ....................................................................................................................................... 9-30
9.10.4.4. Zeroing................................................................................................................................................. 9-30
9.10.4.5. Alarms ................................................................................................................................................. 9-30
9.10.4.6. Cleaning ............................................................................................................................................... 9-31
ix
9.10.4.7. Warnings and Cautions........................................................................................................................ 9-31
9.11. EMC Guidelines................................................................................................................................. 9-40

9.12. Accessories List ................................................................................................................................. 9-45
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Aeon8800A Anesthesia Machine User Manual Product Description
1. Product Description
1.1. General Information
Aeon8800A Anesthesia Machine is a continuous flow anesthesia system which offers manual or
automatic ventilation, easily adjustable fresh gas delivery, anesthetic agent delivery, ventilation
monitoring, convenient ergonomics, and state-of-the-art safety systems.
In terms of theory of operation, Aeon8800A Anesthesia Machine, driven by pneumatics and

controlled by electricity, is a device used to administer to a patient continuously or intermittently, a
general inhalation anesthetic and to maintain a patient’s ventilation. The integrated breathing
system delivers the mixture of O2, N2O, AIR and anesthetic agents for patient breathing control,
while electrical control system functions as monitoring patient parameters.
Aeon8800A Anesthesia Machine is intended for use by licensed clinicians, for patients requiring
anesthesia within a hospital. This product is suitable for infants, children and adults.
1-1
1.2. Symbols
The following table provides descriptions of symbols that are used on the device and/or within this
manual.
Symbol Description Symbol
CAUTION！ Attention, consult accompanying documents./ Refer

to user manual.
Power switch on ON
Power switch off OFF
"ON" for a part of equipment
"OFF" for a part of equipment
Alternating Current (AC)
Direct Current (DC)
Dangerous Voltage
Earth (ground)
Protective earth (ground)
1-2
Equipotential
Date of manufacture
Manufacturer
Catalogue number
Serial number
Rotation in two directions
Rotate to adjust(increase counter-clockwise)
Lock
Unlock
Insp. flow
Exp. flow
1-3
O2 flush O2+
Breathing bag/manual ventilation
Fuse
Read the reading of the top floating-point
Draining valve operation guide
MANUAL/AUTO
Outer power supply has been connected
Recycle
This mark means that pneumatic and electric device rubbish is

not allowed to be dealt as unclassified city rubbish and should be
collected separately.
Battery charging condition
1-4
Alarm mute icon
Alarm icon
Interference many occur in the vicinity of equipment marked with

this symbol
Refer to product instructions
Authorized representative in the European community
This device complies with the requirements of Medical Device

Directive, 93/42/EEC.
Type B equipment
DEFIBRILLATION-PROOF TYPE BF APPLIED PART
Input, entrance
Electrostatic device(ESD) sensitivity
1-5
1.3. Abbreviations
Abbreviation Definition
A
AGSS Anesthetic gas scavenging system
APL Adjustable pressure limiting
B
BDU Basic data unit
C
C Compliance
CGO Common gas outlet
cmH2O Centimeters of Water
CO2 Carbon oxide
D
Des. Desflurane
E
EEPROM Electrically erasable programmable read only memory
Enf. Enflurane
ETCO2 End-expiratory CO2 concentration
F
FiO2 Fraction of Inspired Oxygen
Flow-t Flow-time wave
Flow Flow
Freq Frequency
FreqMIN Minimum Frequency in PS mode
G
GUI Graphic user interface
H
Hal. Halothane
I
I:E Ratio of Aspiratory time to Expiratory Time
INSCO2 Inspiratory CO2 concentration
Iso. Isoflurane
IPPV Intermittent positive pressure ventilation
L
L/min Liter per minute
L Liter
M
MAC Minimum Alveolar Concentration
Manual Manual ventilation
1-6
PMEAN Mean pressure

mL Mill Liter
MRI Magnetic resonance imaging
MV Minute volume
N
N2O Nitro oxide
O
O2 Oxygen
P
Paw Airway pressure
Paw-t Pressure-time wave
Pb Plum bum
PLAT Plat pressure
PCV Pressure Control Ventilation
PEEP Positive End Expiratory Pressure
PLIMIT Limit pressure
Pmax Maximum pressure
PMEAN Mean pressure
PPEAK Peak pressure
PS Pressure Support Ventilation
PTARGET Target Pressure
S
SIMV Synchronized Intermittent Mandatory Ventilation
Sev. Sevoflurane
T
TINSP Inspiratory Time
TP Inspiratory Pause Time
Trigger Flow trigger
TSLOPE Inspiratory Slope Time
V
VT Tidal volume
W
WDT Watch dog timer
ΔP Differential Pressure
1-7
1.4. Warnings and Cautions
Please read and adhere to all warnings, CAUTIONs and NOTICEs listed here and in the
appropriate areas throughout this manual.
WARNING: statement gives important information that, if ignored, could lead directly to
personal injury.
CAUTION: statement gives important information that, if ignored, could lead directly to
equipment damage and indirectly to personal injury.
WARNING: Aeon8800A must only be operated by trained, skilled medical staff.
WARNING: Aeon8800A Anesthesia Machine must and can only be serviced by
Aeonmed’s authorized service representatives.
WARNING: For a full understanding of the performance characteristics of this
equipment, the user should carefully read this manual before operating:
 All system connections.
 All WARNINGs and CAUTIONs.
 How to use the machine.
 How to test the machine.
WARNING: Do the following things before operating Aeon8800A:
 Finish all the tests listed in Pre-use Preparation.
 Test other systematic parts.
WARNING: Do not use the machine if any test failures. Contact Aeonmed’s authorized
service representative for maintaining the machine.
1-8
WARNING: Aeon8800A is not suitable for use in a magnetic resonance imaging （MRI）
environment.
WARNING: To avoid the risk of electric shock, this equipment must only be connected
to a supply main with protective earth.
WARNING: The highest attitude of Aeon8800A anesthesia machine is 3000m.
WARNING: The pipeline inlet pressure of Aeon8800A anesthesia machine must be

280-600kPa.
WARNING: Breathing tube, mask, SUCTION filter and so on, adapter of mainstream
CO2 module, water trap of sidestream CO2 module etc. are disposable
accessories. Before using check the pipeline to ensure the disposal
subassembly is out of using .Check the tube which will be used before use
and avoid reusing.
WARNING: When the suction flow is insufficient, the suction port filter should be
checked or replaced.
WARNING: Do not use anti-static and/or electric breathing tubes or masks; otherwise,
they will be flammable near high frequent surgery equipment.
WARNING: Do not incline the machine at the angle of more than 10 degree.
WARNING: Perform the pre-use checkout before operating Aeon8800A.
WARNING: Remove all equipments on the top cover before moving the machine. Use
the handle on the machine to move the machine.
WARNING: Ensure that the machine does not incline when it is upgrading,
downgrading, turning around or getting across a threshold. Do not push

the machine across pipelines, lines or any barrier on the ground.
1-9
WARNING: Remove all the equipments attached at the flank of the machine before
transportation, otherwise, incline of the machine will lead to personnel

damage.
WARNING: Apply the castor brakes when the anesthesia machine is in use.
WARNING: Do not put the item over 25 kg on the top board of Aeon8800A anesthesia
machine.
WARNING: Do not put the item over 12 kg on the work table of Aeon8800A anesthesia
machine.
WARNING: The whole width of machine should be less than 0.8m when hanging some
stuff.
WARNING: In order to protect patients and users from electrical hazards, it is
imperative that all systems consisting of electrical medical devices and

other electrical devices, such as but not limited to PCs, printers, etc., be
mounted exclusively by trained personnel.
WARNING: The medical gas pipeline system malfunction could cause one or more
devices connected to the system stopping their operation; this is not
applicable to the anesthetic machine that only uses cylinders for gas
supply.
WARNING: The parts of machine in contact with gas to be inhaled by patients don’t
contain phthalates, which are known to be carcinogenic, mutagenic or toxic
to reproduction.
WARNING: Possible explosion hazard. Do not operate machine near flammable
anesthetic agents or other flammable substances. Do not use flammable

anesthetic agents (i.e., either or cyclopropane).
1-10
WARNING: Only non-flammable anesthetics such as desflurane, sevoflurane,
enflurane and isoflurane, which are compatible to other gas are allowed to
use in anesthetic system.
WARNING: Possible fire hazard. Fuses (i.e., additional sockets) must only be replaced
by fuses of the same type and with the same rating.
WARNING: Possible electric shock hazard. The machine may only be opened by
Aeonmed qualified or Aeonmed authorized service engineer.
WARNING: Electric shock and fire hazard. Do not clean the machine while it is on and
/or plugged in.
WARNING: Disconnect the power plug from the mains supply before removing the rear
panels or servicing the machine.
WARNING: Independent means of ventilation (e.g. a self-inflating manually powered
resuscitator with mask) must be available whenever the machine is in use.
WARNING: Malfunction of the central gas supply system may cause more than one or
even all devices connected to it to stop their operation simultaneously.
WARNING: Use a cleaning and sterilizing schedule that confirms to your institution’s
sterilization and risk-management policies.
 Refer to the material safety data as applicable.
 Refer to the operation and maintenance manuals of all sterilizing equipment.
 A damaged oxygen sensor may lead to leakage of its highly caustic contents
that contain potassium chloride. Wear safety gloves and safety eye glasses
per manufacturer’s recommendations.
 Do not inhale fumes that may result from any sterilization process.
1-11
WARNING: Use extreme care while handling the absorbent as it is a caustic irritant.
WARNING: Use care in lifting and manipulating vaporizers during the mounting
process as their weight may be greater than expected, based on their size
and shape.
WARNING: All gas supplies should be of medical grade.
WARNING: To avoid endangering a patient, do not perform testing or maintenance
when the machine is in use.
WARNING: All gas volume, flow and leakage specifications have been tested under
STPD, except those associated with the Anesthetic Breathing System,
which be tested under BTPS.
WARNING: After the device replacement is finished, all calibrations must be done
again and only the service engineer is allowed to do this.
WARNING: If the anesthetic machine is equipped with Anesthetic Gas Delivery System,
Monitoring Equipment, Alarm System and Production Device, no matter

the machine is supplied by separate device or system assembly, the
anesthetic machine checklist must be provided.
WARNING: The medical device connected to the anesthesia system must conform to
IEC 60601-1:2005 and IEC 60601-1-2:2007
CAUTION: For your safety and that of your patients, strictly follow this user manual.
CAUTION: Perform the tests specified on the Pre-use Preparation and, in case of a fault,
do not operate the machine until the fault has been corrected.
CAUTION: Before starting the machine, users must be familiar with the information
contained in the User Manual.
1-12
CAUTION: If the machine does not function as described, it must be examined and
repaired as necessary by authorized service representative before being

returned to use.
CAUTION: Handle the machine with care to prevent damage or functional faults.
CAUTION: Ensure that the gas supply of the machine always complies with the
technical specifications.
CAUTION: Before clinical use, the machine must be correctly calibrated and the
respective tests must be performed, as described in the User Manual.
CAUTION: After servicing, all calibrations must be performed again and only the
professional service engineer can do this.
WARNING: The USB interface of Aeon8800A anesthesia machine isn’t suitable for
connecting with external devices such as mobile phones, tablet computers

and so on.
CAUTION: The anesthesia system conforms to ISO 80601-2-13:2011.
CAUTION: The anesthesia ventilator used together with anesthesia system conforms
to ISO 80601-2-13:2011.
CAUTION: The anesthesia system is used together with the following monitoring
device, alarm system and protection device:
• Conform to the pressure measurement of ISO 80601-2-13:2011;
• Pressure limit device in conformity with ISO 80601-2-13:2011;
• Conform to the exhale output monitor of ISO 80601-2-13:2011;
• Conform to the respiratory system with alarm system of ISO 80601-2-13:2011;
• Conform to the O2, CO2, and anesthetic gas monitor of ISO 80601-2-55:2011.
1-13
1-14
Aeon8800A Anesthesia Machine User Manual Components
2. Components
2.1. Configuration
Touch screen
E-Flowmeter
Auxiliary network power
Auxiliary flowmeter
Top light
3 drawers (a key for all three drawers)
Auxiliary drive gas output
Heater function
Configuration
Battery
Breathing system (supporting high-temperature sterilization)
SUCTION (Negative pressure suction device)
Liquid collecting bottle
Vaporizer(VP300/VP500)
External lamp
YOKE
AGSS (Anesthetic Gas Scavenging System)
CO2/anesthesia gas monitoring module(mainstream and sidestream)
2-1
2.2. Front View
1
16
15
2 14
13
3
12
4 11
10
5
9
6 8
Fig. 2-1 Aeon8800A Front View
No. Name No. Name
1 Display screen 9 Push-and-pull Handle
2 Knob 10 Auxiliary Work Table
3 Auxiliary O2 flowmeter 11 Cylinder Gauge
4 Electrical flowmeter 12 Power Switch
5 Breathing System 13 Gas Supply Gauge
6 O2 flush 14 Vaporizer Manifold
7 Caster (with brake) 15 Spotlight
8 Drawers Assembly 16 Top light
2-2
Functional description of components is as follows.
NO. Item Description Figure
Under any ventilation mode,

Auxiliary O2 STANDBY mode or power off
3 flowmeter status, it can provide pure
oxygen at the maximum of
15L/min.
Counterclockwise rotation of
flowmeter rotary knob increases
the flow; clockwise rotation of
flowmeter rotary knob decreases
the flow.
When flow meter is connected
with gas supply, rotate O2 or Air
knob, the digital screen displays
Electrical
4 data; there is O2 or Air flowing
flowmeter
out.
When O2 flow≥0.25L/min, turn
N2O knob, there is N2O flowing
out；
When O2≥0.5L/min, increase
of N2O flow is controlled by O2

flow, the increase ratio of O2 and
N2O is approximate to 1:3.
It locates on the front of the
machine. It can provide oxygen
from 35L/min to 75L/min to
breathing system and breathing
bag.
CAUTION: When central

6 O2 flush
gas supply or backup cylinder
is connected, pressuring O2
flush will deliver oxygen to
breathing system and
breathing bag, even the
machine is powered off.
2-3
Castor Push down to lock

7
(with brake) Lift to release
The handle is under the auxiliary
Auxiliary Work work table.

10
Table Pull the handle to open the
auxiliary work table.
Cylinder gauges can measure

Cylinder
11 the pressure from N2O, AIR and
Gauges
O2 respectively.
Set power switch to ―ON‖ to let

gas flow in and open anesthetic
system.
12 Power Switch
Set power switch to ―OFF‖ and
close anesthetic system to
prevent gas flowing in.
Gas supply Measure gauge gas supply

13 gauge pressure of N2O, AIR, O2 flowing
by airway.
2-4
WARNING: When
15 Spotlight adjusting the external lamp,
don’t touch the lamp surface
for 1s.
Rocker Switch: Press the LOW

or HIGH side, the switch is turn
on.
16 Top light
The LOW side means low light
and the HIGH side means high
light.
2-5
2.3. Side View
Fig. 2-2 Aeon8800A Side View
No. Name No. Name

1 SUCTION (Optional) 6 Absorber canister assembly
2 Auxiliary O2 port 7 Breathing system heater cable
socket
3 Auxiliary O2 output port 8 Drive gas interface
4 O2 sensor socket 9 AGSS (Optional)
5 Common gas outlet（C•G•O） 10 Caster
2-6
When the range of inlet gas pressure is

280 kPa—600kPa, the flow of drive gas
output is more than 90L/min.
Auxiliary O2 output
3 WARNING: The requirement flow
port
of the device connected to the
auxiliary drive gas outlet interface
cannot exceed 90L/min.
It functions as the linkage between

Common Gas
5 mainframe and breathing system and
Outlet（C•G•O）
delivers fresh gas to breathing system.
There are 3 interfaces: integrating

sampling tube port, heating gas cable
7 interface and drive gas interface
Outlet module
8 respectively. By connection of 3
interfaces, the breathing system can
connect with the main machine.
2-7
2.4. Back View
Fig. 2-3 Aeon8800A Back View
NO. Name NO. Name

1 Gas inlet module 5 Caster
2 Power cable 6 Potential equalization connector
3 YOKE 7 Auxiliary mains outlet socket
4 Battery 8 Fuse
2-8
WARNING: The
connection of electrical
equipment to the auxiliary
mains outlet socket may
Auxiliary mains reduce the system safety
7.
outlet socket level; therefore the
electrical equipment
connected to the auxiliary
mains outlet socket must
conform to the IEC
60601-1.
The Aeon8800A anesthesia

machine has two types fuse:
8 Fuse
T2AH 250VAC, F10AH
250VAC.
2-9
2.5. Breathing System
CAUTION: Breathing system used with Aeon8800A complies with ISO 80601-2-13:2011:
2011.
Breathing system is mainly used to store fresh gas including anesthetic gas, oxygen, and absorb
waste gas. It directly connects to airway to support patient’s respiration.
Fig.2-4 Breathing System
Number Name Number Name

1 Expiration Valve 8 Inspiratory Ports
2 Bag Arm 9 Y-Piece Seal
3 APL 10 PAW Gauge
4 Expiratory Ports 11 Inspiratory Valve
5 Hook equipment 12 O2 Sensor Plug
6 CO2 Absorber Canisters 13 Bellows Assembly （ including
bellow）
7 CO2 Absorber Canisters Release 14
bellows dome
Handle
2-10
It guarantees the single direction of gas flow in

1 Exp. valve
breathing system.
6 CO2
Absorber
It is used to absorb CO2 patient having exhaled.
Canisters
PAW It can measure airway pressure through

10
gauge breathing system.
It guarantees the single direction of gas flow in

11 Insp. valve
breathing system.
O2 sensor plug is used to seal the inspiratory

check valve if O2 sensor is not installed on the
check valve. O2 sensor can be used to measure
O2 Sensor the O2 concentration of fresh gas.

12 Plug Oxygen sensor is a consumable part, users
should note the validity of the sensor, and use it
according to standard operation. Please refer to
the 4.1.3.
The bellow is made of neoprene, more attention

should be given when use.
NOTE: The graduation marks of bellows

13 Bellows dome are from 300 to 1500. These marks are
for qualitative purposes only. Tidal volume
(VT) should be read exclusively from the
display of the user interface.
2-11
NOTE:
1. Description of inspiratory/expiratory valve:
Inspiratory and expiratory valve guarantee the single direction of gas flow in the breathing system.
When the anesthesia machine is working normally:
In the inspiratory phase, the inspiratory valve is acting and the expiratory valve is at rest; In the
expiratory phase, expiratory valve is acting and the inspiratory valve is at rest.
2. Applied Part of Aeon8800A anesthesia machine is the part between mask and Y-piece.
2-12
2.5.1.APL Valve
WARNING: Keep all inlets/cables away from the APL valve, and do not put lines/
cables underneath the APL valve in order to adjust the APL valve
smoothly.
CAUTION: The APL valve is automatically excluded from the breathing system
whenever an automatic ventilation mode is selected.
APL valve has two functions; one is that it limits the maximum pressure during manual ventilation;
the other is that the airway pressure can be exhausted quickly by lifting the APL valve.
The APL valve has a labeled knob for selecting between 0cmH2O to 70cmH2O and for indicating
approximate pressure settings. Click sound will be heard when adjusting the APL valve. In manual
mode, the APL valve knob can be rotated to change the pressure threshold at which gas will flow
through the pressure threshold at which gas will flow through the valve and into AGSS. Clockwise
rotation of the APL valve knob increases the pressure threshold, and counterclockwise rotation of
the APL valve knob decreases the pressure threshold. Lifting the top of the APL valve knob will
temporarily relieve pressure. The leakage from the anesthetic breathing in all operational modes
when tested at pressure of 3.0kPa (30cmH2O) is 40ml.
Fig. 2-5 APL Valve
2-13
2.6. Vaporizer-VP300/VP500 --Optional

The vaporizer delivers anesthetic agent of accurate concentration to breathing system. Anesthetic
agent of accurate concentration will be acquired by adjusting control knob on the vaporizer. It has
temperature compensation, flow compensation and pressure compensation. The vaporizer
cannot be used for patient with respiration because of the strong interior resistance. The vaporizer
can only use one specific anesthetic agent which can be identified by the label.
Fig.2-6 Vaporizer
NO. Name NO. Name

1 Canister Body 6 Anesthetic tag
2 Interlock bolt 7 Screw cap
3 lock lever 8 Liquid level indicator
4 control dial 9 Drain valve
5 Release button 10 Drain hole
WARNING: Only dry gas of medical degree can be used on the vaporizer. Any improper
operation of the vaporizer will bring damage to patient.
WARNING: The vaporizer should be placed vertically at the vaporizer mounting

manifold. Turn the vaporizer to OFF when it is not used.
CAUTION: The vaporizer used with Aeon8800A Anesthesia Machine complies with ISO
80601-2-13:2011.
CAUTION: For more operating and maintaining information of the vaporizer, refer to
User Manual.
2-14
2.7. Anesthetic Gas Scavenging System-AP1000 --Optional

Anesthetic gas scavenging system absorbs waste gas exhausted from breathing system and
delivers it to processing system.
Fig.2-7 Anesthetic Gas Scavenging System-AP1000
Number Name Number Name

1 window 5 floater
2 U-bracket 6 Patient inlet
3 canister 7 Pressure release port
4 Flow control knob
WARNING: Do not block the pressure relieve hole on top of the gas tank when using
AGSS.
CAUTION: The anesthetic gas scavenging system used with Aeon8800A Anesthetic
Machine complies with ISO 80601-2-13:2011.
CAUTION: If the AGSS used together with anesthesia system is produced by other
manufacturer, make sure that the AGSS conforms to ISO 80601-2-13:2011.
CAUTION: For more operating and maintaining information of AGSS, refer to AP1000
User Manual.
2-15
2.8. SUCTION --Optional
An optional suction device is available to remove secretions, blood or other semi-liquid fluid from
the patient’s respiratory tract.
Before performing suction, adjust the negative pressure on the Suction device to an appropriate
value. When using the Suction device, connect the gas inlet to the Aeon8800A auxiliary gas
supply port. If the Suction device is connected with other gas supplies, the pressure of gas supply
should be less than 0.4MPa.
If suction flow is insufficient, check the suction port filter.
Figure 2-8 Negative pressure suction device
No. Name No. Name
1 Negative pressure control switch 4 Overfill protection device
2 Negative pressure indicator 5 Negative pressure connector
3 Negative pressure control 6 Positive pressure input port
CAUTION: The negative pressure suction device used together with anesthesia system
conforms to EN ISO 10079-3.
CAUTION: For more information about operation and maintenance of the negative
pressure suction device, please refer to the Instruction for Use provided
with the negative pressure suction device.
2-16
2.9. Electronic Flowmeter
Figure 2-9 Electronic Flowmeter
As shown in Figure 2-19 the mechanical device used to adjust flow control. The flow setting is
displayed to the left of the adjustment knob and also below the corresponding flow tube on the
display. The Total Flow Tube will display the sum of O2, N2O, and air flow. The flow controller is
equipped with a control valve for the ratio of O2 and N2O, so as to ensure that the O2 concentration
is no less than 21% when the user is using O2 and N2O at the same time. With no O2 supply
pressure, N2O is cut off. The effective range of the flow controller is 0~15L/min and the accuracy
is ±10%. When the value is out of the range, the flowmeter readings are for reference only.
2-17
2.10. O2 flush
Figure 2-10
As shown in Figure2-10, by pressing the button, high flow of 35L/min--50L/min can be provided to
fresh gas outlet. When ―O2+‖ is pressed, between 35 L/min and 50 L/min of O2 flow will be
delivered to the Breathing System. Flush is available at all times when the machine is connected
to a Central Gas Supply System or Back-up Cylinder.
2-18
Aeon8800A Anesthesia Machine User Manual User interface
3. User interface
The panel of the anesthetic machine is composed of user interface, function keys and a knob. As
shown in figure 3-1.
3
2
Figure 3-1 User interface
No Name Description
1 Touch screen Touch screen.
The user interface can display real-time pressure and flow
waveforms, respiratory loop, monitoring data, Electronic Flowmeter
settings and anesthesia System and provides both sound and visual
alarms to assist the user.
2 Knob The user can set the parameter values by rotating the knob and
confirm set values by pressing the knob. Rotating the knob clockwise
increases values and rotating the knob counter-clockwise decreases
values.
3 MANUAL/ In Standby mode, first press MANUAL/AUTO knob, the system switch
AUTO to Manual mode, then secondly switch to IPPV mode.
In automatic mode, first press MANUAL/AUTO knob, the system
switch to Manual mode, then secondly switch to the original mode.
When entering or exiting the Manual mode, the user information area
displays according to the original model.
3-1
CAUTION: The required circumstance of the monitoring of the breathing system as

follows:
 Circumstance temperature: 25℃;
 Gas temperature: 25℃;
 Gas tidal: 30%;
 Gas: O2.
CAUTION: The anesthesia ventilator which is used with the anesthetic system complies
with ISO 80601-2-13:2011.
1 2 3
Figure 3-2 Rear panel
No. Name Description

WARNING: The USB interface of the anesthesia machine
1 USB interface isn’t suitable for connecting with external devices such as mobile
phones, tablet computers and so on.
RS-232/VGA For connection of a VGA display which will display the same
2
interface information as the GUI screen.
3 Network interface Only the qualified personnel can use it.
3-2
3.1. Main interface display layout
The user interface is divided into eleven areas, see Figure 3-3.
Figure 3-3 User interface areas
NO Name NO. Name

1 Anesthetic gas monitoring area 7 Shortcut key area
2 Flowmeter area 8 Machine information area
3 Ventilation mode set area 9 Patient message area
4 Parameter set and display area 10 Waveform display area
5 Prompt message area 11 Alarm indication area
6 Patient parameter monitoring area 12 Ventilation mode display area
3-3
3.1.1.The Interface layout without CO2or anesthesia gas monitoring
Figure3-4 Main interface display layout 1
3-4
3.1.2.The Interface layout with only CO2 monitoring
3-5
3.1.3.The Interface layout with CO2and anesthesia gas monitoring
3-6
3.2. Information of the main interface
3.2.1.Ventilation mode set and display area
3.2.1.1 Ventilation mode display
Name description
Ventilation mode display: ventilation mode area shows current ventilation mode. The mode setup
menu will be open by clicking the ventilation mode area via touch screen.
3.2.1.2 There are five states for the mode buttons as shown below:
Name description Diagram
The normal mode - without any operation to the mode button.
Focusing state - when rotating the knob to the purpose mode, the
corresponding button will display this state.
White state - means the current mode that is selected.
Pending state-this state is displayed when switching modes.
White focus state - this state has been selected and then rotate knob
through the button.
3-7
3.2.2.Parameter set and display area
3.2.2.1. Parameter display
Name description and Diagram
Parameter setting area is located at the bottom of the screen, with green/blue background and
round white buttons, which are applied for real-time respiratory parameter adjustment, including
six setting buttons.
3-8
The ventilation parameters of all models are arranged from left to right, as shown in
the chart below:
Parameter Parameter Parameter Parameter Parameter Parameter

Model
1 2 3 4 5 6
Patient Blank Blank Blank Blank Blank

Standby
type
IPPV VT Freq. I:E TP PEEP PMAX
PCV PTARGET Freq. I:E PEEP TSLOPE Blank
VT Freq. TINSP PEEP Trigger More

SIMV-VC
TP △P TSLOPE PMAX Blank Back
PS △P FreqMIN TSLOPE PEEP Trigger TSLOPE
Ptarget Freq. TINSP Tslope PEEP More
SIMV-PC
(Optional) ΔP Trigger Blank Blank Blank Back
PCV-VG VT Freq. I:E Tslope PEEP Pmax
(Optional)
ALARM
Manual Blank Blank Blank Blank Blank
on/off
3-9
3.2.2.2. The button status when setting parameter
There are three display statuses in the process of parameter

setting:
1.The first status displays when no operation has been performed to

the button;
2.The second status displays when the button has been selected by
the rotation of the knob;
3. The third status displays when the button has been pressed.
3-10
3.2.3.Alarm indication area
Alarm indication: when an alarm appears, an alarm bell icon shows in the warning area. For a
senior-level alarm, the alarm bell is red with white lettering. An intermediate-level alarm is yellow
with black lettering. A low-level alarm is blue-green with black lettering. At most, four alarms can
display on the screen at one time.
By pressing MUTE button, an ― ‖ shows on the alarm icon. Below the alarm bell a countdown
timer appears. The ― ‖ and countdown second display the same color as the alarm bell.
If there is an alarm, press alarm bell and the silence will keep for 120 seconds; press the key
again, and the silence is cancelled. If the alarm has a change but the silence less than 120s, the
silence will be cancelled.
The flickering frequency of higher priority alarm among all alarms indicates all alarms, alarm bell
and countdown seconds (if any). The alarm information text keeps own color respectively (if any).
3-11
3.2.4.Machine information area
Machine information area is at the top right-hand corner of the

screen. There are four icons in this area: Battery and AC Power
Indicator, USB Indicator, Time Indicator and Date Indicator.
Current date indicates at date display area, with format ―YYYY/MM/DD, MM/DD/YYYY or
DD/MM/YYYY‖.
Current time indicates at the time display area, with 12 hour or 24 hour format.
NOTE: Time and date format and value can be set in system setup menu.
Anesthesia machine should be able to automatically detect a USB device.
When the machine detects USB access, this icon shows. When the device is
unplugged or fails to detect USB, this icon does not show.
The description of these icons is as follows.
Power status includes AC power and backup battery state, which will be always
shown. When AC power is normal, the white plug icon shows consistently without
flashing. When net power is disconnected or fails, the white plug icon disappears.
Battery power 100%
Battery power 75%
Battery power 50%
Battery power 25%
Battery power low (≤10%)
Battery not connected
3-12
3.2.5.Waveform display area
Waveform display area is located in the center of the screen, including waveform and breathing
loop.
Waveform name Diagram
Pressure-time waveform (Paw-t)
Velocity-time waveform (Flow-t)
Tidal volume - time waveform (VT-t)
Carbon dioxide-time waveform
(CO2-t)
Breathing Loops
3-13
3.2.6.Patient message area
The patient message area is to the right of the alarm zone, and
to the left of the information area. In this area, there are two
icons: patient type and trigger type.
The description of these icons is as follows.
Patient type shows adult or child.
CAUTION: Patient type setting is conducted under standby

mode.
When patient triggers, the trigger logo will show in the patient
information area and disappear after 250ms. The background color
will restore the original color.
3-14
3.2.7.Patient parameter monitoring area
The patient parameter monitoring area is on the right side of

the screen. There are at most four groups of parameters:
pressure group, capacity group, oxygen concentration group
and carbon dioxide concentration group.
3.2.8.Anesthesia gas monitoring area
Gas monitoring parameter displays on the left side of the

screen, including three parameters: primary agent, nitrous oxide
(N2O) concentration, and exhale MAC value.
3-15
3.2.9. Flowmeter area
The electronic flow meter displays real-time N2O, air and O2 flow
values. Every flowmeter has 2 virtual flow tubes that display flow.
Each flow tube has the same icon, scale, structure and color (grey).
The units and numerical readings are displayed in white. The fill color
of virtual flow tubes is the same with gas icon color.
3-16
3.2.10. Message prompts area
Message prompt area is in the upper left corner of the parameter settings area. Message prompt
area is used to display critical information or to provide real-time help to the user.
3-17
3.2.11. Shortcut key area
The shortcut key area includes shortcuts to alarm settings, system settings, calibration, trend,
breathing loop, self test, configuration and main interface.
CAUTION: Shortcut keys are disabled during power up self test.
Alarm settings: when user presses alarm setting key, alarm menu
appears. If this button is pressed in open state, alarm setting menu
closes, and returns to main interface.
System settings: by pressing system setup key, the system setup

menu appears. If this menu is pressed in open state, system settings
menu disappears, and returns to main interface.
Calibration: by pressing calibration key, the calibration menu appears.

If this button is pressed in open state, calibration button disappears
and returns to main interface.
Trend: by pressing trend key, the trend menu appears. If this button is
pressed in open state, trend menu disappears and returns to main
interface.
Loops: by pressing Loops key, the loops menu appears. If this button is
pressed in open state, the functional menu disappears and returns to
main interface.
Check: user will repeat start-up self-check process, including leak

detection and system test. User only repeats self test in standby mode.
At this time the message will display "execution only in Standby mode
".
Configuration: by pressing configuration key, the user opens or closes
a menu that will cover the entire monitoring area. The shortcut key
exists only in standby mode. There is no configuration shortcut key in
other mode.
Main Interface: when normal key is pressed, all menus will be closed to
return to main interface.
3-18
3.3. General menu layout

The background of the overall menu is gray with the menu title shown centered, at the top of the
window. Below the menu title there are a number of tabs containing a variety of content within the
menu. In the top, right corner of the window is an " " button which closes the menu when
pressed. The menu elements include option key, button, label, indicative text and pictures, etc.
3-19
3-20
Aeon8800A Anesthesia Machine User Manual Pre-Operative Preparation
4. Pre-operative Preparation
4.1. Initial Setup
4.1.1.Connection of Tubes and Cables
First step
Connect one end of the sampling gas tube to
the breathing system integration bottom;
connect the other end of sampling gas tube to
outlet module.
Fig-4-1
Second step:
Connect CGO connection cable of the
breathing system with CGO interface in the left
of anesthetic machine.
Fig.4-2
Third step:
Connect one end of heating cable with the
interface below the breathing system; the other
end connected with interface marked ―Heater‖
in the outlet module.
Fig.4-3
4-1
Aeon8800A Anesthesia Machine User Manual Pre-operative Preparation
Fourth step:
Connect one end of drive gas tube with the
interface below the breathing system.
Fig.4-4
Fifth step:
Connect the other end of drive gas tube with
interface marked ―Ventilator‖ in the outlet
module.
Fig.4-5
4-2
4.1.2.Connection of Breathing Bag
Step 1:
Hold breathing bag to bag arm directly.
Fig.4-6
Second step:
Connect manual bag to manual bag arm with an
upper force.
Fig.4-7
4-3
4.1.3.Connection of test plug
First step:
Test plug is between inspiratory port and
expiratory port of the breathing system ―T‖ is
marked above the plug.
Fig.4-8
Second step:
Connect Y-piece to the Y-Piece seal.
Fig.4-9
4-4
4.1.4.Connection of O2 sensor
First step:
Pull out O2 cell plug from inspiratory valve cover
and then put O2 cell plug into the hole on the
bottom of breathing system integration.
Fig.4-10
Fig.4-11
Second step:
Connect the transparent joint which connects
O2 sensor by cable to the top port of O2 sensor.
Fig.4-12
Fig.4-13
4-5
Third step:
Connect O2 sensor with inspiratory valve cover.
Fig.4-14
Fourth step:
Connect the other end of O2 sensor connecting
cable to the port marked ―Oxygen‖ of the outlet
module.
Fig.4-15
4-6
4.1.5.Connection of the anesthetic gas/CO2 monitoring module

(optional)
CAUTION: The anesthetic gas/CO2 monitoring module has mainstream and sidestream.
The two types can’t be used at the same time.
CAUTION: The anesthetic gas/CO2 monitoring module conforms to ISO

80601-2-55:2011.
CAUTION: Please refer to the IRMA CO2/AX+ user guide, which is delivered together
with the IRMA CO2/AX+ sensor and include all the information about
operations and technical specifications of these two products.
4.1.5.1. Connection of the mainstream monitoring module
Step 1:
Snap the probe on top of the airway adapter. It
will click into place when properly seated.
Fig.4-16
Fig.4-17
4-7
Step 2: Connect the RS232 interface of the

adapter to the RS232 interface on the back of
the user interface.
Fig.4-18
Step 3:
CAUTION: After powering on the system,

a green LED indicates that the probe is
ready for use.
Fig.4-19
Connect the smaller end of the adapter to the
Y-piece connector.
Fig.4-20
Step 4:
Connect the other end of the adapter to the face
mask.
Fig.4-21
4-8
4.1.5.2. Connection of the sidestream monitoring module
Step 1:
Take out the sampling tube and elbow.
Sampling tube Elbow

Fig.4-22
Step 2:
Connect one end of the elbow to the Y-piece
Fig.4-23
Step 3:
Connect the other end of the elbow to the
breathing bag, or to patients through tube.
CAUTION: Use only Nomoline sampling
lines manufactured by MASIMO.
Fig.4-24
Step4:
Connect the other end of the elbow to the
sampling tube, and make a connection between
the sampling tube and the CO2 or anesthesia
gas water trap.
Fig.4-25
Step 5:
Connect the other end of the sampling tube to
the gas inlet of Aeon8800A.
Fig4-26
4-9
4.1.6.AGSS Installation and Connection
CAUTION: AP1000 cannot at an angle exceeding 5 degrees during normal

operation.
CAUTION: Make sure AP1000 installs at a place where operator can get a
clear view of it.
CAUTION: Connect AP1000 according to the practical situation if no GCX

rail is available on the anesthesia machine.
CAUTION: Make sure good connection in case of anesthesia gas leaks to

operating room.
Step 1: A wide slot at the left side of

anesthesia machine specially designed for
putting AGSS; put AGSS to U-bracket.
Fig.4-27
Step 2:
Hold AGSS with both hands ensuring the fixity
faces the wide slot. Slide AGSS horizontally to
rail till its limiting position.
Fig.4-28
4-10
Step 3:
Connect the two ends of screw thread to
EVAC port beneath breathing system and
AGSS respectively.
Fig.4-29
Step 4:
Connect exhaust pipeline to exhaust port of
AGSS, screw it clockwise tightly.
Fig.4-30
4-11
4.2. Pre-operative Test
WARNING: For a full understanding of the performance characteristics of this
equipment, the user should carefully read this manual before operating:
 All system connections.
 All WARNINGs and CAUTIONs.
 How to use the machine.
 How to test the machine.
WARNING: Do the following things before operating Aeon8800A:
 Finish all the tests listed in Pre-use Preparation.
 Test other systematic parts.
WARNING: Do not use the machine if any test failures. Contact Aeonmed’s authorized
service representative for maintaining the machine.
4.2.1.Test before Operation
Pre-use test should be performed under the following circumstances:
 Every day before used on the first patient.
 Before used on every patient.
 After maintenance or service.
4-12
4.2.1.1. System Check
WARNING: Make sure that the breathing system is in good connection and with no
damage.
1. Make sure the anesthesia machine has no damage.
2. Make sure all parts are correctly connected.
3. Make sure the breathing system is correctly connected and has no damage; the absorber
canister is fully filled with soda lime.
4. Make sure the vaporizer is well locked and is filled with adequate anesthetic agent.
5. Make sure the pipeline gas supply system is correctly connected and is at proper pressure.
6. Make sure backup equipments are available and functioning.
7. Make sure anesthetic agent and emergent medicine are available.
8. Make sure the castors are not loose and the forefront two castors are locked.
9. Make sure the anesthesia machine is connected to power socket and power indicator is light.
There is no power supply if power indicator does not light.
4.2.1.2. Power Failure Alarm Test
1. Turn on power switch; user interface is light, STANDBY interface displays after self-test is
finished.
2. After the anesthesia machine operates under STANDBY mode for five minutes, pull out
power cord
3. Make sure power failure alarm occurs (alarm bell sounds or user interface displays POWER
FAILUREURE message).
4. Reconnect power cord.
5. Make sure alarm is eliminated.
4-13
4.2.2.Pipeline Gas Supply Test
CAUTION: Operator should make sure gas supplies are correctly connected during
operation and there is no leak, wrong connection or damage in breathing

circuit. If something abnormal occurs, check the connections.
WARNING: The malfunction of the center gas supply system may cause one or even all
connection equipment connected with it stopping work.
1. Cut off pipeline gas supply. Perform the following steps if pipeline gauge does not read zero:
2. Connect O2 supply.
3. Set flow to the middle level.
4. Make sure N2O cylinder gauge reading restores to zero.
5. Cut off O2 supply.
6. Make sure O2 cylinder gauge reading restores to zero. Low gas source alarm occurs when O2
pressure is decreasing.
4.2.3.Vaporizer Test
CAUTION: For information of vaporizer’s function test, refer to VP300 User Manual.
 Make sure the vaporizer is steadily installed.
 Make sure the vaporizer is locked.
 Make sure only one vaporizer can be open at a time.
 Make sure the vaporizer is filled with adequate anesthetic agent.
4-14
4.2.4.Alarm Test
1. Connect a test lung to Y-piece.
2. Turn on power switch.
3. Set the following items:
Ventilation Mode IPPV
Ventilator Vt: 700mL

Freq: 20
I:E: 1:2
PAW-High: 40cmH2O
Anesthesia Machine All gas flow: OFF

Push O2 flush to inflate bellows.
4. Make sure:
 Initiate mechanical ventilation.
 No low gas source pressure alarm occurs.
 Ventilator displays correct values.
 Bellows moves up and down during mechanical ventilation.
5. Set O2 flow at 5L/min.
6. Make sure:
 End respiratory pressure is approximately between 2cmH2O to 3cmH2O.
 Ventilator displays correct values.
 Bellows moves up and down during mechanical ventilation.
7. Test O2 monitoring and alarm:
 Disassemble O2 sensor, make sure that O2 takes up 21% of room air according to
the test result.
 Set low O2 alarm to 50%, make sure low O2 alarm occurs.
 Set low O2 alarm to 21%, make sure low O2 alarm is eliminated.
 Assemble O2 sensor in breathing system.
 Set high O2 alarm to 50%.
 Push O2 flush button to inflate bellows.
 Make sure high O2 alarm is initiated.
4-15
 Set high O2 alarm to 100%, make sure high O2 alarm is eliminated.
 Put O2 sensor in pure oxygen; make sure that O2 takes up 100% according to the
test result.
8. Test low minute volume alarm:
 Return to alarm menu.
 Set low minute volume alarm limit to 16.0L/min.
 Make sure low minute volume alarm occurs.
 Return to alarm menu.
 Set low minute volume alarm limit to 10.0L/min, make sure low minute volume alarm
is eliminated.
9. Test high PAW alarm:
 Set high PAW below peak PAW.
 Make sure high PAW alarm occurs.
 Set high PAW alarm to 40cmH2O.
10. Test low PAW alarm:
 Disconnect test lung form breathing system.
 Other alarms occur, such as low minute volume alarm.
 Make sure low PAW alarm occurs.
11. Test continuous PAW alarm:
 Set control items:
APL valve: Adjust to the maximum value
Ventilation Mode: Manual
 Mechanical ventilation stops when the machine operates at Manual ventilation

mode.
 Block patient end and push O2 flush button.
 Make sure continuous PAW alarm occurs when continuous pressure is at 10cmH2O
for 15 seconds.
12. Turn off power switch.
4-16
Aeon8800A Anesthesia Machine User Manual Operating guide
5. Operating guide
5.1. Opening
WARNING: Make sure the assembly of patient breathing tube and controlling setting is
correct before ventilating.
1. Plug the power cord to an electrical outlet.

2. Connect the pipeline gas resource or cylinder gas resource (open the cylinder valve).
3. Close O2, N2O, Air flowmeter and the auxiliary O2 flowmeter.
4. Turn the switch to ―ON‖.
The user interface is lighted,

entering into the system self-test
interface.
Fig.5-1
5-1
5.2. System Self–test
Enter into the system self-test

interface after opening.
Fig.5-2
After the system self-test:
1) Select and confirm ―Continue‖, the
Automatic Test begins.
Fig.5-3
2) Select and confirms ―Skip‖, the
―Manual Test‖ interface appears.
Fig.5-4
5-2
5.3. Automatic Leak Test
After System Self Test, the

automatic Test begins.
Follow instructions on the user
interface.
1) Select ―Continue‖ to perform
Automatic Test.
2) Select ―Skip‖ to proceed to
Manual Test.
Fig.5-5
Select ―Continue‖, the system
enter into the Automatic Test
interface.
―Automatic Test…‖appears in the
user interface.
Fig.5-6
5-3
These situations may appear during the automatic test,

If these situations appear, please:
1. Do according to the prompt message on the user interface.
2. Select ―Continue‖ and press the knob ,the system begins to re-test, The interface displays
shown as above picture.
1. If the E-flowmeter isn’t closed,

the message ―Please close the
flowmeter‖ appears on the user
interface.

Automatic Test again.
Manual Test.
Fig.5-7
2. If the bellows is not full, the
message ―Push ―O2+‖ flush to
completely fill the Bellows‖
appears on the user interface.
Manual Test again.
Manual Test.
Fig.5-8
5-4
Automatic Test results

1. If the safety valve is valid and
the leakage is less than
100ml/min, the automatic test is
passed and then the system
proceeds to the Manual Test.
Fig.5-9
2. If the leakage is at the range of
100—400ml/min, the interface
shows as the picture on the right.
1) Select ―Retry‖ to perform the

2) Select ―Skip‖ to proceed to the
Manual Test, the automatic
ventilation is disabled.
Fig.5-10
3. If the leakage is more than
400ml/min, the interface shows as
the picture on the right.
1) Select ―Retry‖ to perform the

2) Select ―Skip‖ to proceed to the
Fig.5-11
5-5
4. Automatic Test failed
If the safety valve in the gas

module is disabled the automatic
test will fail, and the interface as
the picture on the right appears.
Select ―Continue‖ to perform

Fig.5-12
If the pressure sensor (Ambient

pressure sensor and Airway
pressure sensor) is disabled, the
automatic test will fail and the
prompt message will appear on the
user interface.
In the situation, only the manual

ventilation is available.
Fig.5-13
Select ―Manual‖ to enter into
Standby screen.
If the pressure rises during

automatic test, the test will fail and
the interface as the picture on the
right appears.
1) Select ―Retry‖ to do the

ventilation is disabled. Fig.5-14
5-6
5.4. Manual Test
1. If the automatic test is not done

before performing the manual test,
the user interface of manual test
will display as the picture on the
right.
Follow the instructions on the user

interface.
Select ―Skip‖, the system will enter

into normal interface.
Fig.5-15
2. If system enters into the Manual
Test when partial automatic test is
done, the user interface will display
as the picture on the right.
Press ―O2+‖ button according to the

instructions on the user interface
during 60s.

into normal interface.
Fig.5-16
5-7
Manual test results

1. If the PAW gauge value is bellow
20 cmH2O, the interface will display
as the picture on the right.
During the 60s count time proceed

the procedure according to the
instructions on the user interface.

into Standby interface.
Fig.5-17
2. If the manual test fails for three
times, the interface displays as the
picture on the right.

Fig.5-18
3. If the Y-piece port and manual
bag arm connector are not occluded,
the interface after test is shown as
the picture on the right.
During the 60s count time proceed

the procedures according to the
instructions on the user interface. Or
the system will enter into Standby
interface automatically after 60s.
Select ―Skip‖, the system will enter Fig.5-19

5-8
4. There is no operation of pushing

―O2+‖ to fulfill the bellows during the
first 60s count time after manual test
interface appears, the interface on
the right follows.

Fig.5-20
5.Manual test success
If the manual test succeeds, the
interface displays as shown on the
right.
The system will enter into Standby
mode automatically after 5s count
time.
Fig.5-21
5-9
5.5. Patient type setting
The patient type of the Aeon8800A anesthesia system has 2 type options: Child and Adult. The
user can select the needed.
CAUTION: Adult is the default patient type after starting system.
CAUTION: The changing of the patient type is only allowed in STANDBY mode
Adult is the default patient type after

starting system.
Fig.5-22
Press the knob to select the patient
type button in the bottom, left corner
of the screen. This button will show
yellow when selected.
Fig.5-23
5-10
Turn the knob to change the patient

type to ―Child‖.
Fig.5-24
Press the knob to confirm the setting.
Fig.5-25
5-11
5.6. Ventilation mode setting
5.6.1.Ventilation mode introduction
The system has seven ventilation modes:
Standard:
 Manual: Manual ventilation
 IPPV: Intermittent Positive Pressure Ventilation
 PCV: Pressure Controlled Ventilation
 SIMV-VC: Synchronized Intermittent Mandatory Ventilation Mandatory Ventilation with

Volume control
 PS: Pressure Support Ventilation
Optional:
 SIMV-PC: Synchronous Intermittent Mandatory Ventilation with Pressure Control
 PCV-VG: Pressure Control Ventilation with Volume Guaranteed
In addition, Standby mode is available. In Standby mode, mechanical ventilation cannot be

carried out and there are no ventilation waveforms or monitoring values.
5.6.1.1. Manual Ventilation (Manual)
In Manual mode, ventilation can be carried out by manual operation; there are ventilation
waveforms and monitoring values at present.
5-12
5.6.1.2. Intermittent Positive Pressure Ventilation (IPPV)
All the breathings are provided by the anesthesia machine, the patient cannot switch them by self.
The ventilation is managed by the predetermined ventilation volume, breathing frequency and
ratio of inspiratory time to expiratory time to keep the tidal volume stable, thereby assure the
stable MV.
Method: time switch and pressure switch.
IPPV mode setup parameters:
 Tidal volume (VT): 20-300mL (child), 20-1500mL (adult);
 Breathing frequency (Freq): 4-100bpm;
 Breathing ratio (I: E): 4:1-1:8;
 Inspiratory pause time (TP): OFF, 5-60%;
 Maximum pressure (Pmax): 10-70cmH2O;
 Positive End-Expiratory Pressure (PEEP): OFF, 3-30cmH2O.
Fig.5-26 Waveform of IPPV
5-13
5.6.1.3. Pressure Control Ventilation (PCV)
Ventilation is managed according to a set goal pressure. Ventilation capacity (and velocity) is
changed accordingly, and related to respiratory system compliance and airway resistance. Tidal
volume changes with pulmonary compliance and airway resistance. Flow is slow-moving wave.
Pulmonary alveoli are full at the beginning of inspiratory which is helpful for the gas exchange in
the lung.
PCV mode setup parameters: PTARGET, Freq, I: E, TSLOPE, and PEEP.
 Pressure control level (PTARGET): 5-70cmH2O;
 Pressure rising slope time (TSLOPE): 0-2s;
 Positive End-Expiratory Pressure (PEEP): OFF, 3-30cmH2O.
Fig.5-27 Waveform of PCV
5-14
5.6.1.4. Synchronized Intermittent Mandatory Ventilation with

Volume control (SIMV-VC)
SIMV is a ventilation mode which combines spontaneous breathing with control ventilation. Within
the trigger window, the patient can trigger the command positive pressure ventilation
synchronizing with the spontaneous breathing. Between the two command ventilation cycle, the
patient is allowed to breath spontaneously. The command breathing follows the presets volume.
By setting frequency and tidal volume to assure the minimum MV, cooperating with the patient’s
spontaneous breathing to reduce the rivalry between patient and machine and negative effect of
blood dynamics, and prevents the potential syndrome, such as air pressure injury and so on.
By changing the presets frequency to change the breathing support level, in other words, from
entire support to partial support, the machine can be used for long-term patient to retreat from
machine.
The Setup Parameters of SIMV Mode:
 Inspiratory Time (TINSP): 0.2-5s;
 Inspiratory pause time (TP): OFF, 5-60%;
 Positive End-Expiratory Pressure (PEEP): 3-30cmH2O.
 Flow Trigger (Trigger): 1-15L/min;
 Differential Pressure (△ P): 3-50cmH2O;
 Inspiratory Slope Time (TSLOPE): 0-2s;
 Maximum pressure (PMAX): 10-70cmH2O.
5-15
Fig.5-28 Waveform of SIMV-VC
5-16
5.6.1.5. Pressure Support Ventilation (PS)

PS belongs to a partial ventilation support model, and is an auxiliary mechanical ventilation mode
for patient trigger, pressure goal and flow switch. Patient triggers ventilation and control
respiratory frequency and tidal volume. When airway pressure reaches default pressure support
level and inhale velocity reduces to the level lower than threshold, inhale phase switches to
exhale phase. For appropriate setup level, there will be few human-machine confrontation, it will
effectively reduce work of breathing and increase the effectiveness of effort to breathe. Some
studies believe that 5-8 cmH2O PS can overcome the resistance of end tracheal tube and
breathing machine circuit, so PS can be used for machine withdrawal process. PS tidal volume is
determined by breathing system compliance and resistance.
PS ventilation mode setup parameters: △ P, FreqMIN, Trigger, PEEP, TSLOPE.
 Minimum frequency (FreqMIN): 2-60cmH2O;
 Triggering sensitivity (Trigger): 1-15L/min;
 •Positive End-Expiratory Pressure (PEEP): OFF, 3-30cmH2O;
 Inspiratory Slope Time (TSLOPE): 0-2s.
Fig.5-29 Waveform of PS
5-17
5.6.1.6. Pressure control ventilation with Volume Guaranteed

(PCV-VG) --Optional
In PCV-VG, breaths are controlled by the anesthesia machine (mandatory) and will be delivered
at a set rate and set volume (VT). Inspiratory pressure will be regulated to achieve the operator set
volume (Tidal Volume). The pressure range that the anesthesia machine will use is between the
PEEP + 2 cmH2O level on the low end and 5 cmH2O below Pmax on the high end. The inspiratory
pressure change between breaths is a maximum of +/- 3 cmH2O. PCV-VG begins by first
delivering a volume breath at the set tidal volume. The patient’s compliance is determined from
this volume breath and the inspiratory pressure level is then established for the next PCV-VG
breath. Inspiratory pressure from the last 3 breaths will be averaged to determine the pressure
needed to maintain the set tidal volume. Breath to breath inspiratory pressure change will be in
increments of 3 cmH2O up to PMAX - 5 cmH2O. When PMAX is reached the pressure is maintained
at the PMAX value until the end of inhalation. The inspiratory and expiratory valves will adjust to
maintain the PMAX value. When PMAX is reached, the next breath cycle will be normal PCV-VG
control and should not maintain PMAX.
PCV-VG ventilation mode setup parameters:
 Positive End-Expiratory Pressure (PEEP): OFF, 3-30cmH2O;
 Inspiratory Slope Time (TSLOPE): 0-2s;
 Maximum pressure (Pmax): 10-70cmH2O.
5-18
Fig.5-30 Waveform of PCV-VG
5-19
5.6.1.7. Synchronous Intermittent Mandatory Ventilation with

Pressure Control (SIMV-PC) --Optional
In SIMV - PC breaths will be controlled by the anesthesia machine (mandatory) or triggered by the
patient (spontaneous). When controlled by the anesthesia machine, breaths will be pressure
limited and time cycled, resulting in an operator set pressure (PTARGET) being delivered for an
operator set period (TINSP). The anesthesia machine delivers the mandatory breath in synchrony
with the patient’s inspiratory effort. If no inspiratory effort is detected, the anesthesia machine will
deliver a mandatory breath at the scheduled time. Mandatory breaths will be PCV-type breaths
with decelerating flow waveform. Between mandatory breaths the patient will be able to breathe
spontaneously. These breaths can be pressure supported. When PMAX is reached the pressure is
maintained at the PMAX value until the end of inhalation. The inspiratory and expiratory valves
should adjust to maintain the PMAX value.
SIMV-PC mode setup parameters:
 Target Pressure (PTARGET): 5-70cmH2O;
 Inspiratory Time (TINSP): 0.2-5s;
 Positive End-Expiratory Pressure (PEEP): OFF, 3-30cmH2O;
 Flow Trigger (Trigger): 1-15L/min;
 Inspiratory Slope Time (TSLOPE): 0-2s.
5-20
Fig.5-31 Waveform of SIMV-PC
5-21
5.6.2.Ventilation mode setting
The user can select the ventilation mode according to the patient’s actual situation.
CAUTION: When ventilation mode is switched, the contact time of preselected state and
confirmation state need to be more than 1s.
The ventilation mode menus locate on

the left corner of screen. Click on the
ventilation menu to select the
corresponding ventilation mode.
Fig.5-32
If you wish to choose PS mode, click
the PS mode button. The button will be
at pre-selection state.
NOTE:
When the ventilation mode button is at
pre-selection state, the corresponding
ventilation parameters that can be set
appear on the bottom of the screen.
Fig.5-33
Click the PS button again to confirm
your selection.
Fig.5-34
5-22
5.6.3.Mode parameter setting

If the patient type and ventilation mode have been selected, the system will display default
parameters according to the ventilation mode. The user could set the needed breathing parameter.
ΔP of PS mode is used below as an example of how this is done. These instructions also apply to
other modes and parameters.
Click the parameter button to be set,
for example ΔP. The ΔP button will be
at pre-selection state.
Fig.5-35
Turn the knob to adjust the wanted
parameter value.
Fig.5-36
Click on ΔP button again the setting.
Fig.5-37
5-23
5.7. Menu screens
CAUTION: The menu window covers the second and third waveform.
CAUTION: When selected, a short cut key will display the selected menu. When Normal
is selected the all menus will be removed.
Menu screens are used to access most

functions in the anesthesia machine. All
menus, except for the Normal menu,
open in specific menu windows. Each
menu opens or closes by touching the
screen or rotating the knob. Value
selection in the menu is accomplished
by touching the screen, rotating the
navigator knob and pressing the
navigator knob to confirm selection.
Fig.5-38
5.7.1.Menu operating logic
1. Open / close current menu by pressing the corresponding touch key.

2. An open menu can also be closed by clicking on the "X" key or ―Normal" key.
3. Press the "Alarm" key to open / close the alarm setting menu. Press once to open, and
press again to close.
4. When the mode is in "pre-selection" status, closing or switching to another menu will close
pre-selection state.
5. If parameters are being set and not confirmed, the unconfirmed set values will be lost and
the original set values will be restored if the user closes the current menu or switches to
another menu.
5-24
5.7.2.Alarm setting
The alarm settings can be opened by touching the Alarm shortcut key. The alarm setting menu
includes four sub-options: Vent, Gas, Agent, and Log. The default alarm sub-option on start-up is
Vent Alarm limits.
Vent:
At the left side of the vent menu,

there is a patient type icon, which
can be either adult or child, and
will match the patient icon at the
top of the interface.
In the middle of the vent menu, the Fig.5-39

low and high alarm limits of MV,
Pressure, and FreqMIN can be
set.
At the right side of the vent menu,

the alarm volume can be adjusted.
Gas:
The low and high alarm limits

of FiO2, etCO2 and FiCO2 can
be set.
Fig.5-40
Agent:
Alarm limits for Sevoflurane (SEV),

Desflurane (DES), Halothane (HAL),
Isoflurane (ISO), and Enflurane (ENF)
can be set.
Fig.5-41
5-25
Log:
All the alarm messages can be

viewed from the log menu.
Click on the alarm message
bar the detail information of
the corresponding alarm
Fig.5-42
appears on the screen.
Fig.5-43
5-26
5.7.3.System setting
System setting menu includes three sub-menus: Display, Info. and Setup. Display submenu is
default menu.
The display information on the

interface can be set in the display
menu.
Pressure: two options: Mean and Plat.
WAVE2: three sections including Flow,
CO2 and VT, which displays in WAVE 2
area.
WAVE 3: three options: Flow, CO2 and
VT, which displays in WAVE 3 area.
Touch Sound: two options: ON and Fig.5-44
OFF.
CO2 UNIT: two options: % or mmHg.
Gas Usage: the real-time monitoring
value of the agent and N2O.
The Info: menu includes the following

items.
Run Time: view machine power times,

total run time and last run time.
Gas Module: view the module type, the

software version, the hardware version
and S/N.
Fig.5-45
RT SensMon: the real-time monitoring value of the inspiratory valve flow sensor, the expiratory
flow sensor, the airway pressure sensor, the ambient pressure sensor, the oxygen sensor, the
oxygen supply pressure sensor, the air supply pressure sensor, the breathing system temperature
sensor, and the chassis temperature sensor.
EFM RT Sens Mon: view the real-time monitoring value of the oxygen flow meter sensor, the N2O
flow meter sensor, the air flow meter sensor, and the pressure sensor.
RT Vent Mon: view the real-time monitoring value of the inspiratory volume, the expiratory volume,
the system resistant, the system compliance, and the tube compliance.
SW Versions: the version of GUI, BDU, PSU, KBD, and EFM.
5-27
The Setup sub-menu includes the

follow items.
Language: have several types of

language, for example English,
Chinese and so on.
Data: three sections, including

MM/DD/YYYY, DD/MM/YYYY and
YYYY/MM/DD.
Fig.5-46
Time: two sections, 12 hour or 24 hour
format.
O2 Sensor: two sections, including
Enabled and Disabled.
Gas Module: two sections, including
Enabled and Disabled.
Demo: two sections, including OFF

and ON. Click on the OFF button, a
correlative screen appears, see the
right picture, enter the password
―2020‖ to open Demo mode.
Fig.5-47
5-28
5.7.4.Calibration
The Calibration menu includes Oxygen Sensor, CO2/Agents and Touchscreen.
5.7.4.1. Oxygen sensor calibration
CAUTION: Remove the oxygen sensor from the breathing system and expose the
sensor to room air for at least three minutes before proceeding.
Note: A plug is provided on a chain attached to the side of the breathing system for
plugging the O2 sensor port on the inspiratory valve during this operation.
CAUTION: The alarm “O2 Cal Due” will be displayed when the oxygen sensor has not
been calibrated for over 72 hours.
The oxygen sensor calibration

calibrates the oxygen sensor at 21%
oxygen concentration.
If the oxygen sensor is not connected,

the interface will display ―Oxygen
sensor is not connected‖.
Select ―Start‖ to calibrate.

Fig.5-48
Remove the oxygen sensor from the

breathing system and expose the
sensor to room air for at least three
minutes before proceeding.
Select ―Start‖ to proceed.
Fig.5-49
5-29
When the calibration is successful, the

interface will display ―Calibration
Successful‖ and the running bar will be
completely green.
On the calibration interface, there is a
voltage value (300~360mV). After
calibration, if the voltage value is lower
than 300mV, then the sensor should
be replaced; if the voltage value is
Fig.5-50
higher than 360mV, repeat calibration
a second time.
If the calibration fails, the interface will

display ―Calibration Failed‖ and the bar
will be completely red.
To perform the calibration again, press

the ―Repeat‖ button.
Fig.5-51
5-30
5.7.4.2. CO2/Agents calibration
The user can verify CO2 or anesthetic

gas in the air. If gas module is not
activated, the interface will display
―Please activate Gas Module first!‖, and
the status indicator is red.
Fig.5-52
If gas module is activated, select ―Start‖
to calibrate.
Fig.5-53
If the calibration successes, the
interface will display ―Calibration
Successful‖, the running bar’s color will
be green, and the status indicator will be
right.
Fig.5-54
If the calibration fails, the interface will
display ―Calibration Failed‖, the running
bar’s color will be red, and the status
indicator will be red.
Fig.5-55
5-31
5.7.4.3. Touch screen calibration
Click on ―TouchScreen‖ sum-menu, the

screen seen as the right picture appears.
Fig.5-56
Select "Start", then calibrate touch screen
according to the instruction.
There are three buttons on the screen,

choose one of them to perform the screen
calibration.
CAUTION: When calibrating the

touch screen, please click on the center
of the cursor.
Fig.5-57
5-32
5.7.5.Trend
When the trend shortcut is selected, the trend data can be viewed. The machine will record the
last 8 hours of trend data at intervals of 30 seconds.
The trend time will appear on the left side of the menu, and the trend data will appear on the right
side of the menu, including Ppeak, Pplat, Pmean, PEEP, Freq, Vt, MV, FiO2, etCO2, FiCO2, Agent1,
Agent2, N2O, MAC, FG-O2, FG-AIR and FG-N2O.
The first page includes data from 10

parameters, as shown in Figure.
Fig.5-58
The next page includes data from 7
parameters, as shown in Figure.
Fig.5-59
5-33
5.7.6.Check
In standby mode, when the ―Check‖ button is selected, the system test will be performed including
Leak test and Compliance Test.
CAUTION: Check can only be performed in standby mode.
5.7.6.1. Leak Test
After the ―Check‖ button is selected,

the interface is as shown in the
figure on the right.
Follow instructions on screen to
perform test
CAUTION: Leak Test can only

be performed in standby mode.
Fig.5-60
Select ―Start‖ to perform Leak Test

after completing the procedures on
the screen.
Fig.5-61
If the Leak Test is success, the
interface is shown as the picture on
the right.
Select ―Finish‖ to perform
Compliance Leak
Fig.5-62
5-34
If the Leak Test fails, the interface is

shown as the picture on the right.
Select ―Repeat‖ to perform the Leak
Test again.
Select ―Return‖ to enter into normal
interface.
Fig.5-63
5-35
5.7.6.2. Compliance Test
Select ―Compliance Test‖ sub-menu,

if the interface shown as the picture
on the right, select the ―Leak Test‖
sub-menu to perform leak test.
interface.
NOTE: Perform the Leak Test prior

to the Compliance Test when
starting the system test. Fig.5-64
If the Leak Test is performed first,

the interface as the picture shown on
the right appears after selecting
Compliance Test sub-menu.
Follow instructions on screen to

perform test
Fig.5-65
Select ―Start‖ to perform Compliance

Test after completing the procedures
on the screen.
Fig.5-66
5-36
If the Compliance Test is success,

the interface is shown as the picture
on the right.
Select ―Return‖ to finish the test.
Fig.5-67
If the Compliance Test fails, the

interface is shown as the picture on
the right.
Select ―Repeat‖ to perform the Leak
Test again.
interface.
Fig.5-68
5-37
5.7.7.Configuration
CAUTION: Configuration button is effective only in standby mode.
When the ―Configuration‖ button is

selected, the interface is as shown in
the figure on the right, including Vent
Defaults, Alarm Defaults and Service
mode.
Vent Defaults and Alarm Defaults are for

super user.
Service Mode is for service represent.
Fig.5-69
Enter password ―2020‖ and click on
― ‖, the interface shown as the picture
on the right.
If enter wrong password, click on ― ‖

to clear the entered number.
There are four ventilation modes in the

―Vent Defaults‖ tab, including IPPV,
PCV, SIMV and PS.
Fig.5-70
Select one ventilation mode, the
interface shown as the picture on the
right appears.
There are two sections in the menu, one
for adult and one for child. The user can
configure the default parameters for
each ventilation mode.
Settings entered will be used as the
default settings after unit power up.
Fig.5-71
"Load Factory Settings" button when
pressed , will change the default
settings to the factory defaults
5-38
Select the Alarm Defaults sub-menu,

the interface shown as the picture on
the right appears.
Fig.5-72
Enter password ―2020‖ and click on
― ‖, the interface shown as the picture
on the right appears
If enter wrong password, click on ― ‖

to clear the entered number.
There are four alarm limits in the ―Alarm

Defaults‖ tab, including Adult Vent
Alarm Limits, Child Vent Alarm Limits,
Gas Alarm Limits and Agent Alarm Fig.5-73
Limits.
Settings entered will be used as the

default settings after unit power up.
"Load Factory Settings" button when
pressed, will change the default settings
to the factory defaults.
―Service mode‖ tab is reserved for

service only.
Fig.5-74
5-39
5.8. Shutdown
The shutdown of the anesthesia system is as follows:
 Set the vaporizers to OFF;
 Turn OFF the gas supplies, until the gas in the system has gone out completely;
 Set all E-flowmeter settings to OFF;
 Set the auxiliary flowmeter to OFF;
 Turn the power switch to OFF to shut down the anesthesia system.
5-40
Aeon8800A Anesthesia Machine User Manual Alarm and troubleshooting
6. Alarm and troubleshooting
WARNING: Person without maintaining experience mustn’t mend the machine.
CAUTION: If alarm occurs, the patient’s safety must be protected firstly, then do
troubleshooting or necessary remedy.
CAUTION: Alarm presets will change with patient type automatically.
CAUTION: When several alarms occur at the same time, alarm message only displays
the front two in a sequence of “High” to “Low”.
CAUTION: When alarm silencing, the alarm bell has dashed “X” on itself. After
120s, the alarm bell renews to the old state; If the alarm is not dealt in time,
alarm continues.
CAUTION: If alarm occurs when the anesthetic machine works normally, visible and
audible signals will delay a certain time.
WARNING: Do not set alarm limit exceeding the extremes, otherwise, alarm system will
failure.
WARNING: A potential hazard can exist if different alarm presets are used for the same
or similar equipment in any single area, such as ICU or cardio tic operating
room.
WARNING: The operator should examine if the current alarm setting is suitable for every
patient.
WARNING: When power supply is interrupted, system will still renew the last alarm
settings when opening again.
6-1
6.1. Brief introduction of alarm message
The alarm states have 3 priorities: high, medium, low. High alarm needs to be dealt in time.
The sound pressure level of alarm signal is no less than 60dB.
The operator can judge if the alarm system is functional by visible and audible alarm message.
The distance that the operator can hear the alarm sound or distinguish the priority of alarm is 4
meters at least. And the distance to see the alarm message is not less than 1 meter at the front of
the machine.
The top area of the user interface displays alarm message, see figure 6-1.
Table 6-1 Alarm message
Table 6-1
Priority Definition Alarm Tone Mute Notice Message
Death or 10 alarm tones

Red background,‖!!!‖flickering,
High irreversible including 2hurry 120s
displaying frequency is 2Hz.
injury. alarm cycle is 8s.
Reversible 3 alarm tones, Yellow background,‖!!‖ flickering,

Medium 120s
injury. alarm cycle is 10s. displaying frequency is 0.5Hz.
Slight injury or 2 alarm tones, no Cyan background,‖!‖ flickering,

Low 120s
uncomfortable. repeat. long-term display.
6-2
6.2. Alarm message
The alarm method includes technical alarm and functional alarm; technical alarm includes startup
test list and alarm occurring during normal operation.
6.2.1.Alarm default value and setting range
High Low Setting range of high limit Setting range of

low limit
MV（Adult） 12 1 1～25 0～20
MV（Child） 6 1
PAW（Adult） 50 10 10～80 0～70
PAW（Child） 40 8
Freq（Adult） 18 --- 8～60 ---
Freq（Child） 30 ---
FiO2 100% 18% 21%～100% 18%～99%
Hal. 1.5 OFF 0.1%～8.4% OFF,0.1%～8.3%
Iso. 2.3 OFF 0.1%～8.4% OFF,
0.1%～8.3%
Enf. 3.4 OFF 0.1%～9.9% OFF,
0.1%～9.8%
Sev. 4.2 OFF 0.1%～9.9% OFF,
0.1%～9.8%
Des. 12.0 OFF 0.1%～21.9% OFF,
0.1%～21.8%
ETCO2 6.6% OFF 0.1%～9.9% OFF,
0.1%～9.8%
50mmHg OFF 1～75mmHg OFF,
1～74mmHg
INSCO2 0.7% --- 0.1～1.4% ---
5mmHg --- 1～10 ---

Other default items:
Manual Mode: Enabled
Alarm Volume: 2 tones
Patient type: Adult
6-3
6.2.2.Technical alarm message table
Table 6-2
Alarm Name Priority Cause Remedy
Low gas supply High Drive gas pressure is less Check pipeline gas supply and
pressure than 2.9psi±15% replace pipeline.
AC power Low AC power failure alarm Check connection, AC power

failure when AC power supply supply and fuse;
failure
Replace fuse when it is melt.
Low battery Medium No AC power and the Connect AC power supply

capacity battery voltage lower than immediately;
22V.
When the alarm appears, the
battery capacity can last 10
minutes.
Switch to the manual mode,
backup battery begins to supply
power and assure battery
capacity is full.
O2 sensor High Monitor O2 concentration Use exterior measurement

failure ＜ 10%,the alarm occurs system or replace O2 sensor.
immediately.
Monitor O2
concentration≥10%,
cancel the alarm
immediately.
When O2 sensor in the

system setting menu is
configured ―Disable‖, no
alarm occurs.
6-4
BDU High GUI receives and sends Switch to manual mode;

communication data from BDU unit failure
Call service Rep.
failure lasts for 2s
EFM High GUI receives and sends Switch to the manual mode
communication data from EFM unit failure
Call service Rep
lasts for 2s
failure
PSU High PSU send command to Switch to manual mode and call
communication GUI every 2secs, the service Rep.
failure alarm appears.
Gas module High When gas module Check cable connection or

communication communication is replace gas module
failure abnormal, if the cable is

interrupted, this abnormal
state will last 5s.
Gas module Low Pull out adapter probe in Call service Rep.
probe failure gas module for several
seconds.
CAUTION: If the gas
module communication
failures or interior error
in gas module, the alarm
message will not occur.
6-5
Interior error in Low Any case of software, Call service Rep.

gas module hardware, electric
―rotational speed‖ exceeds
limit, no factory calibration
or factory calibration
failure appears, the alarm
will occur.
CAUTION: If the gas

failures, the alarm
message will not occur.
Gas module High When any parameter of Call service Rep.

monitor the detected CO2, N2O, O2,
concentration anesthetic gas exceeds
exceed limit limit, the alarm message
appears.
CAUTION: If the gas
failures or interior error
in gas module or gas
module probe is
disabling, the alarm
message will not appear.
Keyboard Low No communication Switch to manual mode, Call

communication between GUI and service Rep.
failure keyboard lasts for 10s.
Paramagnetic High Paramagnetic O2 sensor is Call service Rep.

O2 sensor damaged.
failure
Paramagnetic High Paramagnetic O2 sensor is Call service Rep.

O2 sensor disconnected.
disconnection
6-6
Calibrate High Paramagnetic O2 sensor Power on the anesthesia

paramagnetic abnormal command. machine and recalibrate O2
O2 sensor and sensor. If paramagnetic O2
restart. sensor is still failure, call service
Rep.
6-7
6.2.3.Functional alarm message
Table 6-3

1. In MANUAL mode, airway
pressure>10cmH2O, and last more
than 15s,this alarm occurs;
2. In other mode, airway
1. Use manual
pressure>PEEP (+10cmH2O), and
Continuous high ventilation.
High last more than 15s,this alarm
airway pressure 2.Check patient’s
occurs;
expiratory passage；
3. In STANDBY mode, this alarm will
not appear;
4. In MANUAL mode, this alarm will
be closed.
1.Reset airway high
1. The current monitoring airway alarm limit;
Ppeak ≥Setting Ppeak; 2.Check if expiratory
High airway 2. There is no this alarm in STANDBY passage is blocked or
High
pressure mode; not;
3. Switch to MANUAL mode to close 3. If Vt setting is too big;
this alarm. 4.If the patient’ airway is
blocked.
1. Current monitoring airway
pressure≤-2cmH2O and lasts for
Negative
High more than 1s. Call service Rep.
pressure
2. Switch to MANUAL mode to close
this alarm.
1. Monitor tidal volume <10ml,or
2. Monitor average
pressure<1cmH2O, in MANUAL
mode, it is not determined, or Check whether the tube
APNEA High
3. Monitor average pressure equals is connected or not.
to 1cmH2O, and monitor
PEEP≤0cmH2O, in MANUAL
mode, it is not determined.
1. In MANUAL mode, current 1. Reset the airway
Low airway monitoring airway pressure is lower pressure lower alarm
Medium
pressure than pressure alarm lower limit.
limit>30s; 2. Check whether the
6-8
2. In other mode,Freq≥4; current tube is connected or not.

airway pressure is lower than
alarm low limit>15s,Freq<4,airway
pressure is lower than pressure
alarm low limit>30s;
3. There is no this alarm in STANDBY
mode.
Patient has no
APNEA backup
Medium In PS mode, FreqMIN trigger ventilator. spontaneous breathing
ventilation
Check the patient status.
1. Reduce alarm setting;
1. Current monitoring FiO2≤ Setting 2.Reduce air or N2O
Low FiO2limit. compensation value;
Low FiO2 High When O2 sensor configuration in the 3.Recalibrate O2
system menu is ―Disabled‖, this alarm sensor;
will not appear. 4.O2 battery is
exhausted;
1. Measured FiO2 value ≥ setting
1. Increase FiO2 alarm
value.
setting value.
High FiO2 Medium When O2 sensor configuration in
2. Recalibrate the O2
the system menu is ―Disabled‖, this
sensor.
alarm will not appear.
1.Increase high MV
1. Measured MV ≥ upper setting limit
alarm limit;
High MV Medium In MANUAL mode, this alarm could
2. Decrease the VT or the
be closed.
breathing frequency.
1.ReduceMV alarm
1. MV≤lower alarm limit
setting；
Low MV Medium In MANUAL mode, this alarm could
2.Check if there is leak in
be closed.
patient end；
1. MV ≥ High Freq setting 1.Check patient’s state
2. The patient has spontaneous and if there is
High Freq Medium breathing. spontaneous breathing;
3. This alarm only applied to PS 2. Increase the frequency
mode. upper alarm setting.
Expiratory CO2 concentration exceeds
High ETCO2 Increase breathing
Medium high limit and lasts at least 2
concentration frequency and VT.
continual breathes
ETCO2 concentration is lower than low
Low ETCO2 Decrease breathing
Medium alarm limit and lasts at least 2 continual
concentration frequency and VT.
breaths.
High INCO2 Medium CO2 in halation concentration> Upper 1. Replace the CO2
6-9
concentration alarm limit. absorbent.

2. Check the unilateral
character of In./Exp.
valve.
Detected PEEP exceeds PEEP setting
+5cmH2O for 2 breaths or 30s (choose
the minimum one between the two). Check if the exhaust port
High PEEP Medium
PEEP High alarm occurs. is blocked or not.
No this alarm in STANDBY and
MANUAL mode.
This alarm will not appear when in
Standby Mode.
High Insp. ISO. Inspiratory anesthetic agent

concentration>upper alarm setting
Decrease anesthetic
High Insp. ENF. High value for at least 2 respiratory cycle.
agent concentration
NOTE: This alarm will not appear
High Insp. SEV. when there is one or more gas module
alarm.
Inspiratory anesthetic agent

Low Insp. ISO. concentration<lower alarm value for at
Decrease anesthetic
least 2 respiratory cycle.
Low Insp. ENF. Medium agent concentration
NOTE: This alarm will not appear
lower alarm value.
Low Insp. SEV. when there is one or more gas module
alarm.
Use more than
one kind More than one kind anesthetic agent is Use only one kind
Medium
detected. anesthetic agent.
anesthetic agent
High fresh gas

Fresh gas flow rate>19 L/min, this Decrease fresh gas flow
flow rate Medium
alarm appears. rate
High gas supply

Measured O2 gas supply pressure is Decrease gas supply
pressure Low
over 800kPa, this alarm appears. pressure
No O2 sensor
calibration for 72 There is no calibration for O2 sensor for Recalibrate the O2
Low
72 hours. sensor.
hours
Bellows cannot Bellows cannot be full filled only in Push the ―O2+‖ button or
be full filled. High IPPV and SIMV-VC mode when adjust the flowmeter
ventilating. knob to increase flow.
6-10
There is no this alarm in the

CO2 Apnea STANDBY. Check the respiratory
High
There is on breathing action after at tube is connected or not.
least a completed breathing cycle.
Measured N2O concentration is above
High Insp. N2O 82% in the ventilation mode except
Increase O2 flow and
concentration High STANDBY, this alarm appears.
decrease N₂ O.
There is no this alarm in the
STANDBY.
6-11
6.2.4.Self-test alarm
Table 6-4
Alarm Name Probable Cause Remedy
O2 supply sensor failure O2supply sensor failure Replace the O2supply pressure
board.
Air supply sensor failure Air supply sensor failure Replace the Air supply pressure
board.
O2supplyfailure Disconnection of O2 supply Check the connection of
O2supply.
Air supply failure Disconnection of O2 supply Check the connection of Air
supply.
Please close flowmeter The flowmeter is open. Close the flowmeter.
O2flowmeter failure O2flowmeter is invalid. Replace the E-flowmeter
assembly.
Air flowmeter failure Air flowmeter is invalid. Replace the E-flowmeter
assembly.
N2Oflowmeter failure N2Oflowmeter is invalid. Replace the E-flowmeter
assembly.
EFM pressure sensor EFM pressure sensor is Replace the E-flowmeter
failure invalid. assembly.
PSU communication PSU send command to GUI Call service Rep.
failure every 2secs, the alarm
appears.
Breathing system heating Breathing system heating Call service Rep.
failure function is invalid.
Breathing system Breathing system temperature Call service Rep.
temperature sensor failure sensor is invalid.
EFPROM chip failure EFPROM cannot be read or Call service Rep.
written.
PAW sensor failure The data of the pressure Call service Rep.
sensor is incorrect.
Ambient pressure sensor The data of the ambient Call service Rep.
failure pressure sensor is incorrect.
PEEP valve failure Incorrect PEEP valve data Call service Rep.
6-12
Vent/Manual failure Incorrect valve state Call service Rep.

Flow sensor failure Incorrect sensor data, beyond Call service Rep.
the normal range.
SW version failure BDU, GUI, PSU software Call service Rep.
version is not the same with
the released one.
BDU Comm. failure GUI cannot receive and send All breathing functions fail, call
data from BDU unit for 0.5s. service Rep.
KBD Comm. failure No communication between All breathing functions fail, call
GUI and Keyboard. service Rep.
Inspiration valve failure Incorrect voltage of the The machine can continue to
inspiratory valve feedbacks work, but there is only manual
mode but automatic mode, the
monitor function is effective, call
service Rep.
Alarm speaker failure Alarm speaker is invalid The ventilation machine works
as normal, call service Rep.
AC power fail AC power fails Check AC power supply, check
the fuse and replace it when it is
melt.
O2sensor disconnect or O2 sensor fails or unconnected Replace O2 sensor or connect
failure O2 sensor.
EFM communication GUI receives and sends data Switch to the manual mode
failure from EFM unit failure lasts for Call service Rep
2s
Paramagnetic O2 sensor Paramagnetic O2 sensor is Call service Rep
failure (Optional) invalid
Solenoid Valve Call service Rep
(Paramagnetic O2 sensor
and gas module) failure
(Optional)
6-13
6.3. Failure diagnosis
Table 6-5
No. Message Cause Remedy
1. APL valve 1. The connection or setting 1.Check the installation and

failures of APL valve is incorrect. connection of APL valve；
2. Check whether the exhaust

port is blocked or not.
2. High breathing 1. Breathing system is too 1.Disconnect the breathing
system high. system heating cable and call
temperature service Rep.
3. Gas monitoring 1. Sample line is blocked or 1. Check sample line, water trap
has no unconnected. and Y-piece filter.
sampling signal
2. Replace if necessary.
4. Breathing 1.Incorrect connection of 1. Leakage from incorrect
system leakage pipeline or line connection of the breathing tubes.
2. Incorrect installation of
absorber canister.
3. Incorrect installation of Bellows

and Bellows cover,
4. Incorrect installation of O2
sensor or O2 sensor plug, or the
damage of O-ring of O2 sensor.
5. Incorrect installation of In./Exp.

valve cover.
6. Incorrect installation of airway

pressure gauge or the damage of
O-ring used with the pressure
gauge.
6-14
Aeon8800A Anesthesia Machine User Manual Cleaning and Disinfection
7. Cleaning and Disinfection
WARNING: Turn off Aeon8800A power switch before cleaning and disinfecting.
WARNING: Use a cleaning and sterilizing schedule that conforms to your institution’s
sterilization and risk-management policies.
 Refer to the material safety data policy of each agent.
 Refer to the operating and maintaining manual of all the sterilizing

equipments.
 Wear safety gloves and safety goggles.
 The O2 sensor may leak and burn (by Chlorine Potassium Oxide) if
damaged.
 Do not inhale fumes.
WARNING: Do not inhale any agents generated during cleaning and disinfecting.
CAUTION: User cleaning agent sparingly. Excess fluid could enter the machine,
causing damage.
CAUTION: Do not autoclave any parts of the machine unless specifically identified as
autoclave able in the User Manual. Clean the machine only as specified in
the User Manual.
CAUTION: To prevent system damage:
 Refer to the literature supplied by the manufacturer of the cleaning agent.
 Never use organic, halogenated or petroleum-based solvents, anesthetics,

glass cleaning agents, acetone or other irritant agents.
 Never use abrasive agents (i.e. steel wool or silver pool ish) to clean
components.
7-1
 Keep all liquid away from entering the equipment.
 Prevent liquid from entering the equipment.
 Do not immerse the bellows for more than 15 minutes as this may cause
expansion or accelerated aging.
 Only the components marked 134℃ are heat-resistant and

pressure-resistant parts that are capable of withstanding autoclave
sterilization.
 All cleaning solutions used must have a pH between 7.0 and 10.5.
CAUTION: Never use the oxygen sensor or its connector in any type of liquid.
CAUTION: Dispose of the oxygen sensor per the manufacturer’s specification.
CAUTION: Do not use acetic hydroperoxide or formaldehyde steaming.
CAUTION: Do not autoclave the APL valve.
CAUTION: The valve disc is fragile and must, therefore, be handled with care while
removing the valve cage from the valve assembly.
CAUTION: If moisture remains in the bellows after cleaning, it may become tacky.
CAUTION: Do not wash the inner surface of the connector.
CAUTION: Do not autoclave the oxygen sensor.
CAUTION: Prior to use after cleaning or disinfecting, power up the machine and follow
the on-screen prompts to perform the Leak Test and the Compliance Test.
CAUTION: The PAW gauge cannot withstand immersion or the heat and pressure of
autoclaving.
CAUTION: Peracetic acid and formaldehyde fumigation will damage external surfaces.
7-2
7.1. Guideline
Operator should have a better understanding of WARNINGS and CAUTIONS before cleaning
and disinfecting. Different methods will be used for different parts. Parts need to be completely
dried after cleaning and disinfecting.
After cleaning and disinfecting, the peruse calibration must be done before using after the
anesthesia machine is reinstalled, refer to ―Preoperative preparation‖ in Aeon8800A User Manual.
The recommended disinfection time of the machine is 100~300, according to the use condition
and sterilization time of anesthesia machine specifically.
ISO17664 conformity
Process of autoclave sterilization of the anesthetic breathing system conforms to ISO17664:2004.

The condition conforming to ISO17664:2004 is , use bacteria or virus filter to filter the flow that
exhaled by the patient and enters into the system and the flow which returns to the patient, so the
installation of the filter must be correct.
Cleaning Information
Cleaning is supposed to do before using the breathing system for the first time after installation.
If there is potential infective object in the breathing system, such as blood or secretion, please
clean it with disposable cloth and authorized sterilant instantly.
Only the components marked 134℃ are heat-resistant and pressure-resistant parts that are
capable of withstanding autoclave sterilization, all parts expect O2 sensor and PAW gauge can be
washed with moderate sterilant in the automatic washing machine.
O2sensor and PAW gauge can be only cleaned on surface, O2sensor, cannot be autoclave
sterilized and cleaned with automatic washing machine.
WARNING: Disinfection by ultraviolet light must be performed on the whole machine.
7-3
7.2. User maintenance
Foundational Action
maintenance
every day clean anesthetic machine’s surface
every week Ventilate for the system, open flow meter to make floating-point move in
order to flow meter pipe block or floating-point conglutination.
every month Leak test of bellow assembly; 100% O2 concentration calibration.
Cleanness and Check if assembly is damaged, replace or repair if necessary.
installation
According to actual Open drain valve to replace soda lime.
situation Pipeline replacement: User replaces breathing pipeline in time according
to actual situation to ensure normal running (no gas leak in breathing
pipeline‖) after breathing pipeline is used for a certain time.
7-4
7.3. Breathing system disassembly
WARNING: Wear latex gloves during disassembly in case that operator’s

hands get damaged.
Take C•G•O assembly from C•G•O.
Fig.7-1,7-2
Take the heater cable from the outlet module.
Fig.7-3,7-4
Take the heater cable from the heater port in
the breathing system.
Fig.7-5,7-6
7-5
Take the screwed pipe from the outlet module.
Fig.7-7,7-8
Take the screwed pipe from the breathing
system and store safely.
Fig.7-9,7-10
Take the integrated gas sampling pipe from the
outlet module.
Fig.7-11,7-12
One hand holds the bracket, the other hand
holds the other side of the breathing system,
and lift the breathing system vertically, take the
breathing system from the anesthesia machine.
Fig.7-13
7-6
Fig.7-14
Fig.7-15
Take PAW gauge from the breathing system
and store it safely.
Fig.7-16,7-17
7-7
Take O2 sensor from the inspiratory valve.
Fig.7-18,7-19
Turn the bellows counterclockwise and take it
from the breathing system.
Fig.7-20
Take the bellows and store safely.
Fig.7-21
7-8
As shown in the right figure, autoclave sterilizes

the disassembled breathing system.
Fig.7-22
7-9
7.4. Methods for cleaning and disinfecting
A: Wiping(Glutaraldehyde-based formulation of 2%; isopropyl alcohol at 70%～90%)
B: Washing Machine (Wet pasteurization at 70℃, 158℉, for 30 minutes after detergent cleaning)
C: Immersion (Glutaraldehyde-based formulations of 2%)
D: Autoclaving (Including steam r hot air at 134℃, 273℉). Use your manufacturer’s or your
facility’s recommendations.
Table 7-1
Part Name Method

A B C D
Workstation(Outside) √
Vaporizer √
Connection Cables And Wires √
Breathing Bag, Y-Fitting, T-Fitting √
Reusable Screw Tube √ √ √ √
Breathing System(After √ √ √ √
Disassembly）
Insp./Exp. Valve Disc √ √ √ √
Insp./Exp. Valve Bracket √ √ √ √
Insp./Exp. Valve Dome √ √ √ √
O-Ring √ √ √ √
APL Valve √ √ √ √
Paw Gauge √
O2 Sensor √
Flow Sensor Surface √
Flow Sampling Tube √
Flow Sampling Detector √ √ √
Absorber Canister √ √ √
Bellows Dome √ √ √
Bellows √ √ √
Bellows Gasket √ √ √ √
AGSS √ √ √ √
AGSS Transfer Tube √ √ √
7-10
7.4.1.Cleaning and disinfecting for breathing system
1. Breathing Circuit
After using on every patient, clean breathing circuit with 70%～90% alcohol, wash with clean
water and dry, or place it in autoclave staircase for sterilization.
2. Silicon screw tube and breathing bag
After using on every patient, clean silicon screw tube and breathing bag with clean water,
completely dry and put them in autoclave staircase for sterilization.
CAUTION: Do not use ultra-violet wave to sterilize silicon tube or breathing bag in case
of aging.
3. Absorber canister, breathing system tubes(not include single-use tube),bellows plate
Either vaporing or immersion disinfection can be used in practice; in case of immersion all
sterilized parts must be dried with the high pressure air or oxygen before reuse.
4. Insp./Exp. Valve
Dismount the cover of the inspiratory and expiratory valves by rotating it counter-clockwise, then
takes away the valve patch, clean valve seat and circle together. And clean cover of the
inspiratory and expiratory valves and valve patch with the gauze soaked with water soluble
sterilizing agent, after all parts cleaned and dried recover it in original integration. Then one must
check the leakage and the movement of the inspiration and expiration valves in accordance with
the required regulation and checking procedure. Please handle all parts with care preventing any
damage.
WARNING: Take care and do not damage or crash valve disc during cleaning.
7-11
7.4.2.Cleaning and disinfecting for bellows
WARNING: Never separate the diaphragm and the valve seat in a pressure-relief valve.
CAUTION: Do not immerse them more than 15 minutes to prevent inflation or aging.
CAUTION: Dry by hanging while fully spread. If moisture is left in the bellows, they may
become tacky.
1) Disassembling.
2) To prevent component damage, clean them lightly. Put the recommended non-enzyme mild
agent used for latex and plastic in hot water.
3) Rinse using clean hot water, and then dry.
4) Check the components if they are broken or damp, then perform the assembling and function
test.
5) Connect the bellow assembly, ventilator and breathing system.
6) Perform the preoperative check.
7.4.3.Cleaning and disinfecting for AGSS
CAUTION: For more cleaning and disinfecting information of AGSS, refer to AGSS
User Manual.
7-12
Aeon8800A Anesthesia Machine User Manual Regular maintenance
8. Regular maintenance
WARNING: To prevent fire:
 Please use admitted lubricant for anesthetic or O2 device.
 Do not use lubricant containing oil or lipin, because when O2

concentration reaches a certain degree, burning or explosion may
happen.
WARNING；Please observe disinfection control and safety regulation because the
devices having been used may contain blood and sap.
WARNING: Moving part and removable elements is in danger of jamming hands or
crush. More attention must be paid when moving or replacing system

parts.
WARNING: In the process of removing product, strike and quiver must be avoided.
WARNING: Exhausted and old instruments (such as battery and LCD screen) harmful
to environment must be treated according to present local regulations.
8-1
8.1. General principle of maintenance
This chapter provides message needed by Aeon8800A anesthetic machine in term maintenance.
Replace or adjust some components before doing some calibration or adjustment. If user uses
improper components such as improper specification causes malfunction, our company will not
take responsibility. Do not use malfunction device. Replacement and maintenance should be
finished by authorized service engineer or qualified, trained persons with repairmen experience.
After maintenance, the device should be tested and ensure its normal function and comply with
the manufacture’s regulation. Use components manufactured or sold by our company if
replacement is needed, then test and ensure device comply with the manufacture’s specification.
If service support is needed, please call local service engineer. In any case, the repairmen cost
will include the current price and reasonable personnel cost, but except repairmen items within
Aeonmed company’s warranty.
CAUTION: Person without repair experience about such device must not repair this
device.
8-2
8.2. Maintenance schedule
Table 8-1
Action After each repair Every 12 months Every 36 months

Check before use X X X
Check before operation √ X X
Check with eyes √ X X
Replace exhausted √ X X
component
Replace O2 sensor √ √ √
Replace/maintenance √ √ X
battery
Function test √ X X
CAUTION: According to this schedule to do maintenance timely and replace
corresponding parts.
CAUTION: The recommended repair time interval is 5 years. Breathing system,
vaporizer and parts are recommended to have a comprehensive test and

replacement every 5 year.
WARNING: The ineffective sodium lime has an obvious change in color when it’s
ineffective.
8.2.1.Appearance checklist
1. Assure the appearance of Aeon8800A no damage, the anesthesia machine can run
normally.
2. Assure absorbent canister install correctly and fill enough soda lime. Assure enough
anesthetic in vaporizer.
3. Assure the exhaust gas absorber pipe connected with APL valve no damage and dry
inside.
4. Assure O2, N2O, AIR, VAC and EVAC connection pipe no damage.
5. Assure O2, N2O, AIR, VAC and EVAC flexible pipe no damage (if they are be used).
6. Assure AC power cable no damage.
8-3
8.3. Replacement of replaceable parts
No. Replaceable part Every 6 Every 12 Every 36 Part Number

month month month
1. Replace O2sensor No Replace Replace 210001975
2. Replace O-ring in O2 No Replace Replace 304000101

sensor
3. Check /Replace No Check Replace 210002830
battery
4. Clean/Replace latex Clean Clean Replace 230000318
screwed pipe φ17
bellows assembly
U-type sealing ring
AGSS transmitted
pipe
valve sealing gasket
9. Check /Replace Check Replace Replace 304000096
O-ringφ9×1.8
（Pressure gauge）
10. Check /Replace Check Replace Replace 304000044
O-ring 14×2.65 （on
vaporizer mount）
CAUTION: The life-span of all components above is the result in normal circumstance
and work condition.
8-4
8.4. Maintenance of O2 sensor
WARNING: Exhausted and old O2 sensor must be treated according to the present
local regulation. Not burn or dispose the O2 sensor casually.
CAUTION: Calibration of O2 sensor please refers to Chapter 5.11.3.1.
8.4.1.Replacement of O2 sensor
Replacement steps of O2 sensor:
1. Pull out O2 sensor from inspiratory valve of breathing system.
2. Pull out O2 sensor cable connection port from O2 sensor.
3. Connect new O2 sensor to cable connection port and install it on inspiratory valve of
breathing system.
8.4.2.Main technical parameter of O2 sensor
CAUTION: Specific parameters refer to the latest published technical data by
manufacture.
O2 sensor can be used to detect partialO2 concentration of the anesthetic machine. O2sensor
belongs to consumptive products, so attentions should be paid to its useful-life.and use as the
characteristics and technical requirements provided by manufacture. Main technical requirements
of O2 sensor in Aeon8800A as follows:
8-5
Performance parameters:
Maximum input range of interface: 0mV－500mV DC
Interface form and definition: FCC-68 4 core telephone pin (RJ11-4), see the following figure.
Output: 9mV -13mV（210mBar O2）
Range: 0mBar -1500mBar O2
Signal: 100±1（100% O2）
Resolution: 1mBar O2
Expected use life-span: 1.5x106% O2 hour(in 20℃ circumstance); 0.8x106% O2hour（in

40℃circumstance）
Total response time: T90＜15s
ZERO signal(N2, +20℃): ＜200uV
Operation’s temperature range: -20℃～+50℃
Temperature compensation: within 0℃～40℃ is ±2%
Pressure range: 0.5Bar～2.0Bar
Relative humidity range: 0～99%（no condensation）
Long-term output excursion: ＜5%（in 100% O2 circumstance and use more than one year）
Crust Material: White ABS
N2O resistance: 100% N2O
8-6
Valid time: 13 months
Complied standard: EN12598/ISO7767
Suggested type and main characteristic parameters
8.5. Maintenance of fuse
ALARM: Disconnect AC power before fuse replacement, otherwise, it may cause injury
even death.
WARNING: When fuse replacement, fuse of the same type and size must be used,
otherwise, it can be harmful to the anesthetic machine.
CAUTION: Fuse belongs to damageable assembly, proper force must be used when
replacement.
CAUTION: Use screwdriver to swirl fuse and not use force largely and suddenly,
otherwise, it may cause fuse box broken.
Replacement steps:
Insert screwdriver into groove of the fuse box.
1. Rotate it about45°counterclockwise, and then pull out fuse holder.

2. Take the fuse.
3. Install new fuse.
4. Pull new fuse to the original position.
5. Rotate it for about45°with screwdriver clockwise to fix.
6. Connect AC power.
8-7
8.6. Battery Maintenance
CAUTION: Only service engineer authorized by our company can replace battery. If the
anesthetic machine is not used in a long time, please call service engineer
to cut power supply connection.
CAUTION: The exhausted and old battery must be treated according to present local
regulations.
 Battery configuration
DC24V, 4AH, 12V leadacid battery, 2 nodes inseries.
 CAUTIONs when use
Charging: when the AC power is connected, the system will charge the battery automatically,
the recommended charging time is no less than 8 hours.
Discharging: when the device uses battery to supply power, normally the work time is 120
minutes. When the battery’s electric capacity is insufficient, the device will display ―Low
power‖ alarm until power off. When the ―Low power‖ alarm occurs, the user should connect
AC power immediately and avoid the system closes (considering safety, manual startup
should be done to renew operation after the device closes automatically.)
Do not disassembly the battery causally and short battery connection line to avoid danger.
 Battery’s Preservation
If the battery is not used for a long time, it should be preserved after the battery is charged
fully.
When the preservation time exceeds 3 months, charge the battery at least every 3 months.
When preservation, humid and high temperature circumstances must be avoided.
Improper maintenance will cause battery broken, the battery should be replaced immediately
to avoid fluid leak erode device. Call manufacture when replace battery.
 Battery’ removal
Use screw driver to remove the screws of the back cover board, disconnect the battery
module with device to remove battery.
8-8
8.7. Consumptive components replacement
Since installation, consumptive components names and code in every time dimension as the table
in below:
Consumptive components 6 months 12months 48months
Check /replace bellows assembly needless Check Replacement

Check /replace U sealed circuit needless Check Replacement
Check/replace AGSS transmission
needless Check Replacement
tube(optional)
Replace O2 sensor Check Replacement Replacement
8-9
Aeon8800A Anesthesia Machine User Manual Technical Data
9. Technical Data
CAUTION: All technical specifications should be updated based on the real state of
Aeon8800A Anesthesia Machine; no notification will be made if any change

happens.
CAUTION: All display values are measured under dry environment and proper
pressure.
WARNING: Cylinder valve should be closed during pipeline gas supply, so that gas
shortage can be avoided due to exhausted gas supply or pipeline

problems.
9.1. Pneumatic Diagram
Pneumatic system plays the role of supplying O2, N2O, AIR and anesthetic agent to breathing
system, ensuring their pressures are within normal range respectively, so that normal operation of
anesthesia machine and patient’s safety can be guaranteed.
9-1
Fig.9-1 Aeon8800A Pneumatic Diagram（V1.0）
9-2
1 Inlet filter 21. Safety valve

2 Pressure gauge 22 PEEP valve
3 Check valve 23 Ambient pressure
4 N2O Pressure regulator 24 Flow sensor
5 AIR Pressure regulator 25 Airway pressure
6 O2 Pressure regulator 26 Sensor board
7 Pressure sensor 27 AGSS
8 Pressure regulator 28 Exhaust valve
9 Pressure regulator 29 Pressure reversing valve
10 Auxiliary breathing O2 30 Bellows
11 Auxiliary supply O2 31 Reversing valve
12 O2, N2O ratio valve 32 APL valve
13 E-flowmeter 33 Breathing bag
14 O2 flush valve 34 Flow sampling
15 Suction 35 Absorber container
16 Check valve 36 O2 sensor
17 Vaporizer mount 37 Insp. Check valve
18 Proportional solenoid valve 38 Exp. Check valve
19 Solenoid valve 39 Breathing system
20 Throttle
9-3
9.2. System technical data
CAUTION: All system gas supplies should be of medical degree.
Gas Supply
Table 9-1
Pipeline Gas O2, N2O, AIR

Pipeline Connection DISS-male, DISS-female, NIST（ISO 5359）.
Connectors for each of the gas cannot be interchanged.
Pipeline Input Pressure 280kPa -600kPa（2.8-6bar）
Flow Speed
Table 9-2
Gas Range Range

（thin flow tube）（thick flow tube）
O2 0.05 L-1L/min 1.1 L-10L/min
N2O 0.05 L-1L/min 1.1 L-10L/min
AIR 0.05 L-1L/min 1.1 L-12L/min
9-4
9.3. Electrical diagraph
Aeon8800A Anesthesia Machine can be divided into three parts: UI, drive control and circuit. UI
consists of computer system, auxiliary control circuit, power and etc, which mainly takes charge of
display, alarm, keyboard input and interface expansion. Drive control has BDU as its core.
Exterior sensor, signal processing, amplifier, power and battery are part of drive control which
mainly used for data acquisition and ventilation mode control. UI and drive control should be
connected by cables.
BDU PC104 LCD
Power Communication Inverter

AC/DC Ampilifer Interface and Power
DC/DC Management
SLA battery Encoder

RS232
Sensors and Valves : & x2
Ins/exp flow keypad
Flowmeter flow
airway/air/gas
pressure
Ins/exp/cmv valve
Top light
Back light
Heater
Fig.9-2 Electrical Diagraph
9-5
9.4. Physical data
CAUTION: All physical specifications are of approximate values; no CAUTION can be
made if any change happens.
CAUTION: Do not place Aeon8800A Anesthesia Machine in vibrant environment.
CAUTION: Do not put heavy stuff on the top panel or in the drawers.
Table 9-3
Dimensions: 1403mm(H)×695mm(W)×855mm(D)
Weight: 110kg±5kg（not include vaporizer and
System
backup cylinder）
Top Panel Load: 25kg
Castor 125mm, each front castor with brake
Drawer 142mm(H)×376.5mm(W)×438mm(D)
Display 15’ TFT LCD
Cylinder Gauge （ AIR, O2, Range: 0MPa -1MPa. Stepping: 0.05MPa
N2O） Accuracy: ±2.5% of full range
Range: -10 cmH2O - 100cmH2O. Stepping: 200Pa
PAW Gauge
Accuracy: ±2.5% of full range
Device Lifetime 8 years
9-6
9.5. Environmental requirement
CAUTION: The anesthesia machine should be stored in draught room where there is
no caustic gas and storing magnetic field.
Table 9-4
Temperature Operation: 10℃~40℃
Storage: -20℃ ~ 55℃
Transport -20℃ ~ 55℃
Relative Humidity Operation: Not more than 95%, non-condensing.
Storage: Not more than 95%, non-condensing.
Transport Not more than 95%, non-condensing.
Atmospheric pressure Operation: 70 kPa~106kPa
Storage: 70 kPa~106kPa
Transport 70 kPa~106kPa
Power AC100-240V,50Hz/60Hz
Highest Attitude 3000 m
9-7
9.5.1. IEC60601-1:2005 classification
Aeon8800A belongs to this class:
 Class I device
 B type applied part
 Common device/IP21
 Traveling device
 not use flammable anesthetic
 Continuous running
NOTE:
The applied Part of Aeon8800A anesthesia machine is the part between mask and Y-piece.
9-8
9.6. Input and output
NOTE:
1. When the anesthesia system stops transferring, the pipeline supplying pressure should
be 280KPa to 600KPa.
2. When main power fails, the system switches to battery power automatically, and all the
anesthesia machine components can work normally.
3. When main power and internal battery both fails, the gas output is not affected.
9.6.1.Electrical
WARNING: IEC60601-1is applicable to the connections between medical devices, and to
the connections between at least one medical device and one or more
non-electrical devices. Even if no functional connections between the single
devices, when using one auxiliary power outlet, they form a medical electrical
system. User must be aware of the risk of increased leakage current and
temperature and other increased risk may exist, when the device is connected
to the auxiliary socket-outlet.
WARNING: When earth wire has failure, if the device connects with auxiliary power supply,
it may cause patient current leakage exceeding the permitted range
WARNING: If the exterior protective grounded wire has questions during wiring, interior
power supply must be used for device running.
9-9
Table 9-5
Supply Voltage 100-240VAC, 50/60Hz
Maximum Input Current 8A
AC power fuse F10AH 250VAC, φ5X20（F）
Auxiliary AC power plug 4
Auxiliary AC power plug fuse T2AH 250VAC, φ5X20（F）
Maximum output valve of auxiliary 1.5A(single plug); 6A(in total)
AC power plug
Grounded resistance Small than 0.2Ω
USB interface
Table 9-6
Number of USB Interfaces Standard: 2
Drive Mode HOST interface, USB1.0/2.0 protocol
Power Supply 5 VDC±5%, 500 mA Max.
Interface Type USB A-type port
9.6.2.Pneumatic
Table 9-7
Pipeline supply O2, AIR, N2O

Pipeline connection DISS-male, DISS-female, NIST (ISO 5359)
All fittings used to connect O2, N2O and Air pipeline gas
supply are all ready.
APL valve 250kPa
Vaporizer connection 2 Selectable-tecmounts
Pressure display Color mark list
Pipeline inlet pressure 280kPa -600kPa
9-10
9.7. Breathing system technical data
Table 9-8
Flow compensation range: 1L-20L/min

Fresh gas compensation
Gases: O2, N2O, AIR, anesthetic agent
Absorbent 1500mL(for each absorber canister)
Connection CGO: ISO5356 connector（standard 22mm exterior diameter or
15mm interior diameter）
Breathing system leak These data ensures the continuous pressure is higher than the
anticipated pressure during mechanical ventilation.
Pressure: 3kPa, leak volume≤150ml/min
Breathings system Use a two-way sine wave test breathing system: Freq:20/min,
resistance Vt=1L,expiration. resistence≤0.6kPainspiration
resistence≤0.6kPa.
Breathing system with small patient resistance should be selected
in order to be accordance with standards.
APL valve resistance Flow speed:3L/min, flow resistance: 0.05kPa - 3kPa
Flow speed:30L/min, flow resistance: 0.1kPa - 0.5kPa
Connector leak （APL valve close）leak volume≤50ml/min
Check valve resistance In dry environment: ≤0.15kPa
Pressure generated from <0.14kPa
moist check valve
Pressure of opening moist <0.1kPa
check valve
System compliance 45mL/kPa (for standard breathing tube)
Interior capacity 7.6L±0.1L
O2 flush 25L-75L/min
O2 supply failure alarm <200kPa
O2 concentration Not less than 19%
Safety valve Openpressureis8.5kPa,theflowis5L/min.
9-11
9.7.1.Compliance correction
In all of software version, the anesthesia machine is able to carry out a compliance correction
which compensates for volume "lost" in hoses and in the breathing system.
The anesthesia machine determines the system compliance (hoses and breathing system) and
required later for compliance correction during the self test or standby leak test. The hose of
standard equipped compliance has a fixed value of 11mL/kPa.
The VT set is delivered during the first breath.
ΔP is calculated from end-expiratory pressure (P1) and end-inspiratory pressure (P2).
Csys: the system compliance.
Figure11-3 Pressure values
Having the system compliance (Csys) and ΔP, Anesthesia machine can calculate which volume
(ΔV) has been "consumed" by the system, or, in other words, which volume has not been
delivered to patient.
ΔV = Csys x ΔP
The anesthesia machine increases the volume to be delivered by the value ΔV.
VT corr = VT + ΔV
The anesthesia machine repeats this procedure during each breathing phase so that the V T
delivered to the patient gradually approaches the set VT. This procedure is completed as soon as
the plateau value stops changing (±0.5 cmH2O).The displayed flow and the resulting values (for
example, MV) are updated accordingly.
9-12
9.8. Anesthetic ventilator technical specifications
9.8.1.Anesthetic ventilator performance
Table 9-9
Maximum Inspiratory 80cmH2O

Pressure
Noise of the Whole Work normally(not including alarm), no more than 60dB(A)
Machine
Warm-up Time ≥5min
MV Max 30L/min
Inspiratory Flow Max 75L/min
Pressure Transmission 5 cmH2O-80cmH2O
Range
9-13
9.8.2.Ventilation parameter
Table 9-10
Item Range Steppin Default Value Remark

g
Vt 20mL-1500mL 10mL 120mL（Child）; 20mL-100mL, error is ±20mL;
500mL（Adult） 100mL-1500mL,error is ±20%
Freq. 4bpm -100bpm, 1bpm 20bpm（Child）; Error is ±1bpm or ±5%,

2bpm-60bpm(PS 12bpm（Adult） choose the maximum one
mode)
I:E 4:1-1:8 0.5 1:2 error is ±15%
TINSP 0.2s-5.0s 0.1sec 1sec（Child）; Have this function in SIMV
2sec（Adult） mode, error is ±10% or 0.1s,
choose the maximum one
PEEP OFF, 1cmH2 OFF When it is OFF, PEEP value
3cmH2O-30cmH2O O is 1cmH2O-3cmH2O; when
3cmH2O-30cmH2O, error is
±2cmH2O or ±15%, choose
the maximum one
FreqMIN 2bpm -60bpm 1bpm 4bpm（Child）; Have this function in PS mode
2bpm（Adult）
TP OFF, 5%-60% 5% 10% Have this function in IPPV,
SIMV-VC mode, error is ±30%
of the setting or ±0.05s,
Trigger 1L-15L/min 1L/min 2L/min(Child); Have this function in
3L/min(Adult) SIMV-VC, PS mode, error is
±20% or ±1.3L/min, choose
the maximum one
PTARGET 5cmH2O -70cmH2O 1cmH2 10cmH2O(Child Have this function in PCV
O ); 20cmH2O mode
（Adult）
ΔP 3cmH2O -50cmH2O 1cmH2 5cmH2O Have this function in

O SIMV-VC, PS mode, setting
range: 5cmH2O -70 cmH2O.
error is ±4 cmH2O or ±20%,
TSLOPE 0s -2s 0.1sec 0.5sec error is ±1s
9-14
PMAX 10cmH2O-70cmH2 1mH2O 40 cmH2O Have this function in IPPV,

O SIMV-VC, PCV-VG mode,
setting rage: ±3cmH2O or
±10%, choose the maximum
one
9.8.3.Gas dynamics
Table 9-11
Gas source Anesthetic system

Gas component O2
Rating supply pressure 400kPa
Inlet pressure range 280kPa ~ 600kPa
Flow valve range 5L ~75L/min
1
Output Pressure range: 08kPa ~ 8kPa；Flow range: 0L ~ 75L/min
Label 1: Within rated outlet pressure range and under double maximum rated inlet pressure condition.
Table 9-12
According to ISO8835-2, test under peak flow 60L/min, fresh gas 10L/min.
Item Standard Requirement Test Result

Expiratory resistance <0.6kPa 0.51
under manual condition
Inpiratory resistance <0.6kPa 0.39

under manual condition
Expiratory resistance <0.6kPa 0.57
under automatic condition
Inpiratory resistance <0.6kPa 0.22
under automatic condition
9-15
9.8.4.Monitor performance
Table 9-13
Item Range Stepping Accuracy
Vt 0mL - 3000mL 1mL 20-100mL, error is ±20mL;
100-3000mL, error is ±20%
Freq. 0bpm - 110bpm 1bpm 1bpm
PEAK -20cmH2O - 99cmH2O 1cmH2O ±5%, at least1cmH2O
MEAN -20cmH2O - 99cmH2O 1cmH2O ±5%, at least1cmH2O
PLAT -20cmH2O - 99cmH2O 1cmH2O ±5%, at least1cmH2O
FiO2 18％ - 100％ 1% Error is ±3 ％（ concentration
value）
C 0mL -100mL/cmH2O 1mL/cmH2 Error is 20% or 5mL/ cmH2O,
O choose the maximum one
PEEP -20cmH2O - 99cmH2O 1cmH2O 2cmH2O
PAW -20cmH2O -99cmH2O 1cmH2O Error is±3cmH2O or ±10%,
Battery 100%, 75%, 50%, 25%, 0%.
voltage When battery is used to supply power, this sign displays available remaining electric
state voltage.
display When the vehicle is connected with AC power, this sign means charging.
Pressure monitor range: 0cmH2O - 80cmH2O.According to different airway pressure,
gain the wave form displays is different.
0cmH2O ~ 10cmH2O, pressure axis gain: 5cmH2O
Paw-t
0cmH2O ~30cmH2O, pressure axis gain: 10cmH2O
wave form
0cmH2O ~80cmH2O, pressure axis gain: 20cmH2O
Time axis is a fixed range.（the axises of Flow-t, Paw-t is same.）:
When gas module is opened, 0s ~15s；Gas module is closed, 0s ~20s.
Display range of flow rate: -90L - 90L/min, gain: 45L/min. On time axis, the positive
Flow-t
axes stands for inspiratory direction; under the time axis, the negative axes stands
Wave form
for expiratory direction. Flow rate is 0L/min, which means no gas flow rate in airway.
CO2 display range is 0mmHg - 76mmHg, gain is 38mmHg. Time axis is a fixed
CO2 time
range.
wave form
When gas module is opened, 0s ~15s；Gas module is closed, 0s ~20s.
Horizontal abscissa displays Paw: fixed range: -20cmH2O~ 80cmH2O, gain is
P/V Loop 20cmH2O.
Vertical abscissa displays tidal Volume: fixed range is 0ml~ 1500ml, gain is 250ml.
Horizontal abscissa displays tidal Volume: -1400mL ~ 0mL, gain is700mL.
Vertical abscissa stands for Flow: fixed range: -90L - 90L/min, gain is 45L/min; The
F/V Loop
positive axes stands for aspiratory flow rate, the negative axes stands for expiratory
flow.
9-16
9.9. O2 sensor specification
Table 9-14
Response time No more than 15s.

Sensor type Chemical fuel battery
Antipated battery Normal operation period is 12 months.
life-span
O2 monitor monitors and displays O2concentration in the patient loop.
O2 sensor accessory includes one O2 sensor. This sensor can
produce a voltage proportional with O2partial pressure in its detected
surface and its metal electrode will exhaust gradually in the process
of oxidation.
O2 sensor is an electrochemical appliance (chemical battery).

O2diffuses into this device by penetrating a membrane to make the
metallic electrode oxidizing. In this process, electric current occurs,
Operating principle of which matches with partial pressure of oxygen displayed by electrode
O2 monitor sensor.
The sensor’s voltage is influenced by the temperature of monitoring

gas blender. The thermostat outside of the sensor can compensate
the temperature change in sensor.
O2 monitor uses signal to deal and analyze circuit, transforming the

sensor signal to corresponding oxygen percentage value.
The system displays this value and compares it with the saved alarm
extremes. If this value exceeds the extremes, the monitor will send
alarm.
9-17
9.10. Gas monitoring module technical specifications
The gas monitoring module is used to connect other medical devices, provide monitor data,
monitor and display CO2, N2O and 5 anaesthetic gases (halothane, isoflurane, enflurane,
sevoflurane, desflurane).
The gas monitoring module is connected to the patient’s breathing pipeline to monitor the
inspiratory and expiratory gas and can be applied to Adult/Child and Infant.
CAUTION: Gas monitoring module complies with ISO 80601-2-55:2011.
9.10.1. MAC calculation of ISA gas analyzer
Algorithms used in the host monitor to determine MAC values
Minimum alveolar concentration (MAC) is a standard for comparing the potency of inhalation
anesthetics. The MAC value represents the alveolar concentration of an anesthetic (at one
atmosphere) that, in 50 percent of a tested population, prevents gross muscular movement in
response to a painful, standardized stimulus.
If a mechanism to determine MAC values is implemented in the host device, the algorithms used
for this calculation must be adequately documented.
The MAC value may be calculated and displayed by using end-tidal (Et) gas concentrations
according to the following formula:
X(AA): HAL=0.77%, ENF=1.7%, ISO=1.15%, DES=6.65%, SEV=2.1%,N2O=105%
Note: Altitude, patient age and other individual factors are not considered in the
formula above.
9-18
9.10.2. Gas data consideration
Quantitative effects of humidity or condensate
The partial pressure and the volume percentage of CO2, N2O, O2 and anesthetic agents depend on the
amount of water vapor in the measured gas. The O2 measurement will be calibrated to show 20.8 vol%
at actual ambient temperature and humidity level, instead of showing actual partial pressure. 20.8 vol%
O2 corresponds to the actual O2 concentration in room air with 0.7vol% H2O concentration (at 1013 hPa
this equals for example 25°C and 23% RH). The measurement of CO2, N2O, and anesthetic agents (e.g.
all gases measured by the IR-bench) will always show the actual partial pressure at the current
humidity level.
In the alveoli of the patient, the breathing gas is saturated with water vapor at body temperature
(BTPS).
When the breathing gas is sampled, and passing the sampling line, the gas temperature will get close
to the ambient temperature before reaching the ISA sidestream gas analyzer. As the Nomoline
removed all condensed water, no water will reach the ISA gas analyzer. The relative humidity of the
sampled gas will be about 95%.
If CO2 values at BTPS are required, the following equation can be used:
Where:
EtCO2 = EtCO2 value sent from ISA [vol %]
Pamb = Ambient pressure sent from ISA [kPa]
3.8 = Typical partial pressure of water vapor condensed between patient circuit and ISA [kPa]
EtCO2(BTPS) = EtCO2 gas concentration at BTPS [vol%]
O2 is assumed to be room air calibrated at a humidity level of 0.7 vol% H2O.
Spectral broadening
The presence of oxygen and nitrous oxide can cause some interference in the CO2 measurement.
This is known as spectral broadening.
Nitrous oxide, N2O:
N2O compensation is not included in the system. Therefore, for the N2O broadening effect on CO2
measurement accuracy, please refer to the below table.
Displayed value if true

N2O concentration in gas mix Effect on gas reading
concentration is 5.0 vol% CO2
0 vol% 0% relative 5.3 vol%
30 vol% 5.17% relative 5.3 vol%
60 vol% 10.34 relative 5.5 vol%
82 vol% 14.14% relative 5.7 vol%
Oxygen, O2:
9-19
ISA sidestream analyzers capable of O2 measurements automatically compensates for spectral

broadening caused by oxygen.
For most applications, sufficient accuracy in CO2 measurement will be achieved by dividing the oxygen
concentration into three ranges: ―high‖, ―medium‖ and ―low‖. By using these ranges, along with the
SetO2 values in the table below, the maximal relative CO2 error will be limited to 1.2%.
O2 range Set O2 parameter

0-30 vol% 21
30-70 vol% 50
70-100 vol% 85
Gas measurement units
Gas concentration is reported in units of volume percent. The concentration is defined as:
The total pressure of the gas mixture is measured by a cuvette pressure sensor in the ISA gas
analyzer. For conversion to other units, the actual atmospheric pressure sent from the ISA
sidestream analyzer may be used, e.g.
CO2 in mmHg = (CO2 concentration) x (atm. pressure value in kPa from ISA) x (750 / 100).
Example: 5.0 vol% CO2 @ 101.3 kPa 0.05 x 101.3 x 750 / 100 = 38 mmHg
9-20
9.10.3. Mainstream gas monitoring module
Table 9-15
IRMA CO2 / AX+

Model
Interface type RS232,9600bps
Accessories Airway adapter, disposable.
Working principle of gas The gas module is a mainstream gas monitoring module, connecting to
module patient to monitor gas concentration of breath.
The gas module can be used for adults, children and infants.
The gas module uses infrared technology, which determines gas

concentrations by measuring different wavelengths according to
different absorption of gases to different ray.
9-21
Table 9-16
Basic Configuration
Description Extremely compact infrared mainstream multi-gas module.
Available in various parameter configurations.
Dimension(W×D×H) IRMA CO2/ AX+:
38×37×34mm(1.49″×1.45″× 1.34″)
Cable length 2.50m+/-0.1m
Weight <25g(except cable)
Operating temperature IRMA CO2: 0-40℃, 32-104℉
IRMA AX+: 10-40℃, 50-104℉
Storage and
transportation
IRMA CO2: -40-75℃, -40-167℉
temperature
IRMA AX+: -20-75℃, -4-167℉
Operating humidity <40hPa H2O(non-condensing)(95%RH at 30 degree celsius)
Storage and 5-100%RH, condensation1)

transportation humidity
Operating atmospheric 525-1200hPa(525 hPa corresponding to an altitude of

pressure 4572m/15000feet)
Storage and 500-1200hPa

transportation pressure
Mechanical strength Withstands Repeated 1.8m drops on a hard surface.
Complies with requirements for road ambulances according to

prEN1789 (clause 6.4) and requirements for shock and vibration
according to ISO 80601-2-55:2011 (clause 201.15.3.5.101,
9-22
transport).
Power supply IRMA CO2:
4.5-5.5VDC, Max 1.0W
(power on surge @ 5V less than 350mA during 200ms)
IRMA AX+:
4.5-5.5VDC, Max1.4W
(power on surge @ 5V less than 350mA during 200ms)
Surface temperature (at IRMA CO2:

ambient temperature
Max 39 degree C/102FIRMA AX+:
23℃)
Max 46 degree C/115F
Interface Modified RS-232 serial interface operating at 9600bps
Airway adapter Disposable adult/child:
Adds less than 6mL dead space;
Pressure drop less than 0.3cmH2O @ 30LPM.
Disposable infant:
Adds less than 1mL dead space;
Pressure drop less than 1.3cmH2O @ 10LPM.
NOTE 1: After being in a condensing atmosphere, this module shall be stored for more
than 24 hours in an environment equivalent to operating humidity.
The humidity range 50-100% is valid for the temperature range -40℃ - 40℃.
9-23
Table 9-17
Data Output
Fi and ET The newest breathing value (Fi and ET) is continually displayed after one
breath.
Gas monitor module CO2: CO2
Automatic agent IRMA AX+: Primary and secondary agent.

identification
Table 9-18
Gas Analyzer
Probe 2-9 channel NDIR type gas analyzer measuring at 4-10 μm. Pressure,
temperature and full spectral interference correction.
Warm-up Time IRMA CO2: <10 seconds (full accuracy)

IRMA AX+:<20 seconds (agent identification enabled and full
accuracy)
Rise time CO2≤90ms
(@10L/min)
N2O≤300ms
HAL, ISO, ENF, SEV, DES≤300ms
Agent identification <20s (Typically<10s)

time
Total system <1s

response time
9-24
Table 9-19
Accuracy specifications - standard conditions：The following accuracy specification is

valid for dry single gas at 22+/-5 degree C and 1013+/-40hPa.
Range1)
Gas CO2 AX+ Accuracy
CO2 0-15 0-15 ± (0.2vol%+2% of reading)
15-25 15-25 Unspecified
N2O -- 0-100 ± (2vol%+2% of reading)
HAL,ISO,ENF -- 0-8 ± (0.15vol%+5% of reading)
8-12
SEV -- 0-10 ± (0.15vol%+5% of reading)
10-15
DES -- 0-22 ± (0.15vol%+5% of reading)
22-25
NOTE 1: Gas concentration reported in units of volume percent.
Table 9-20
Accuracy specifications –all conditions1)
Gas Accuracy
CO2 ± (0.3vol%+4% of reading)
N2O ± (2vol%+5% of reading)
Agents2) ± (0.2vol%+10% of reading)
NOTE 1: The accuracy specification is valid for the operating temperature and humidity
conditions specified, except for interference specified in the table “Interfering

gas and vapor effects” below and the section "effect from water vapor partial
pressure on gas reading". The effect from water vapor partial pressure on gas
reading.
NOTE 2: The accuracy specification for IRMA AX+ is not valid if more than two agents
are present in the gas mixture.
9-25
Table 9-21
Interference gas and vapor effects
Gas or vapor Gas CO2 Agents N2O

level
IRMA CO2 IRMA AX+
N2O3) 60vol% --1) --1) --1) --1)
HAL3) 4vol% --1) --1) --1) --1)
ENF,ISO,SEV3) 5vol% +8% of reading2) --1) --1) --1)
DES3) 15vol% +12% of reading2) --1) --1) --1)
Xe (Xenon) 3) 80vol% -10% of reading2) --1) --1) --1)
Xe(Helium) 3) 50vol% -6% of reading2) --1) --1) --1)
Metered dose Not for use with metered dose inhaler propellants
inhaler propellants3)
C2H5OH(Ethanol) 3) 0.3vol% --1) --1) --1) --1)
C3H7OH(Isopropan 0.5vol% --1) --1) --1) --1)

ol) 3)
CH3COCH3(Aceton 1vol% --1) --1) --1) --1)

e) 3)
CH4(Methane) 3) 3vol% --1) --1) --1) --1)
CO(Carbon 1vol% --1) --1) --1) --1)

monoxide) 3)
NO(Nitrogen 0.02vol% --1) --1) --1) --1)

monoxide)3)
O23) 100vol% --1) --1) --1) --1)
NOTE 1: Negligible interference, effect included in the specification “Accuracy, all
conditions” above.
9-26
NOTE 2: Interference at indicated gas level. For example, 50vol% helium typically
decreases the CO2 readings by 6%. This means that if measuring on a

mixture containing 5.0vol% CO2 and 50vol% helium, the measured CO2
concentration will typically be (1-0.06)*5.0vol%=4.7vol% CO2.
NOTE 3: According to the ISO 80601-2-55:2011.
9-27
9.10.4. Sidetream gas monitoring module
Nomoline Family sampling lines
ISA samples gas from the respiratory circuit through the Nomoline Family sampling line at a rate
of 50sml/min, making measurements of CO2 possible for adult, pediatric and infant patients.
The Nomoline Family sampling lines incorporate a unique water separation (N2O Moisture)
section, which removes condensed water, The NOMO section is also fitted with a bacteria filter
that protects the gas analyzer from water intrusion and cross contamination.
As long as no sampling line is connected, the ISA gas analyzer remains in a low-power sleep
mode. Once the sampling line is connected, the ISA gas analyzer switches to measuring mode
and starts delivering gas data.
The Nomoline Family sampling lines are available in a wide variety of versions for both intubated
and spontaneously breathing patients and in both disposable and re-sposable configurations –
intubated patients can for instance be monitored using the disposable Nomoline Airway adapter
Set or a combination of the multiple patient use Nomoline Adapter and a disposable Nomoline
Extension / T-adapter. Spontaneously breathing patients could similarly be monitored using a
disposable Nomoline Nasal CO2 Nasal CO2 Cannula with Luer Connector.
The Nomoline Adapter may be used with other third party sampling line and canulas. Please
however note that the Nomoline Family or sampling line are designed for optimal performance
and measurement fidelity when used with the ISA gas analyzers. For instance, when connecting
to a respiratory circuit, the Masimo T-adapter provides a central gas sampling point thereby
minimizing the risk of sampling line occlusion
Note: Using sample tubes or cannulas with larger inner diameter than 1mm will increase ISA’s
total system response time.
For the Nomoline Family sampling line replacement, please call the service engineer authorized by our
company.
9-28
9.10.4.1. System set-up
To set up the medical backboard device for gas analysis, follow these steps:
1. Securely mount the ISA analyzer.
2. Connect the ISA analyzer interface cable to the medical backboard.
3. Connect a Nomoline Family sampling line to the ISA analyzer input connector.
4. Connect the gas sample exhaust port to a scavenging sys
5. Connect the gas sample exhaust port to a scavenging system or return the gas to the
patient circuit to prevent pollution of the operation room when N2O and/or anesthetic
agents are being used. Due to the risk of patient cross-infection, always use a bacteria
filter on the exhaust port side if sampled gas is intended to be re-breathed.
6. Power up the medical backboard.
7. A green LED indicates that the ISA analyzer is ready for use.
8. Perform a pre-use check as described in section 9.10.4.2.
Note: Returning the ISA’s exhaust gas to the patient circuit is not allowed in the USA.
9.10.4.2. Pre-use check
1. Before connecting the Nomoline Family sampling line to the breathing circuit, do the
following:
2. Connect the sampling line to the ISA gas inlet connector.
3. Check that the gas inlet connector is lit with a steady green light.
4. Breathe briefly into the sampling line and check that the medical backboard device
displays a valid CO2 waveform and valid values.
5. Occlude the sampling line with a fingertip and wait for 10 seconds.
6. Check that an occlusion alarm is displayed and that the gas inlet connector shows a
flashing red light.
7. Perform a tightness check of the patient circuit with the sampling line attached.
9-29
9.10.4.3. Manitenance
For the ISA analyzer maintenance, please call the service engineer authorized by our company.
9.10.4.4. Zeroing
The gas analyzer needs from time to time to establish a zero reference level for the gas
measurements and the flow.
ISA performs zeroing by switching the gas sampling from the respiratory circuit to ambient air. The
automatic zeroing is performed 1 to 3 times per day, and takes less than 3 seconds for ISA CO2
gas analyzers and less than 10 seconds for ISA Multigas analyzers.
During zeroing, if ISA’s exhaust gas returned to the patient circuit, the returned gas level will be
different from the gas level at the sampling site.
9.10.4.5. Alarms
See User Manual for the medical backboard device for a complete description of the alarm
handling related to the ISA sidestream gas analyzer.
ISA gas inlet connector status indicator
Indication Status
Steady green light ISA in operation and OK
Blinking green light Zeroing in progress
Steady blue light Anesthetic agent present
Steady red light ISA sensor error
Blinking red light Check sampling line
9-30
9.10.4.6. Cleaning
The ISA sidestream gas analyzers and the Nomoline Adapter may be cleaned using a cloth
moistened (not wet) with max 70% ethanol or isopropyl alcohol.
To prevent cleaning liquids and dust from entering the ISA gas analyzer throught its sampling gas
inlet connector, keep the Nomoline Family sampling line fitted while cleaning the analyzer.
Warning: Never sterilize or immerse the ISA sidestream gas analyzer in liquid.
9.10.4.7. Warnings and Cautions
Warning: The ISA sidestream gas analyzer is intended for use by authorized healthcare
professionals only.
Warning: Carefully route the sampling line to reduce the risk of patient entanglement or
strangulation.
Warning: Do not lift the ISA gas analyzer by the sampling line as it could disconnect
from the ISA, causing the ISA gas analyzer to fall on the patient.
Warning: Dispose Nomoline Family sampling lines in accordance with local regulations
for biohazardous waste.
Warning: Use only airway T-adapters with the sampling point in the center of the
adapter.
Warning: Do only sample lines intended for anesthetic agents if N2O and/or anesthetic
agents are being used.
Warning: Do not user T-adapter with infants, as this adds 7ml dead space to the patient
ciruit.
Warning: Do not use the ISA gas analyzer with metered-dose inhalers or nebulized
medications as this may clog the bacteria filter.
Warning: Since a successful zeroing requires the presence of ambient air(21% O2 and
0% CO2), ensure that the ISA is placed in a well ventilated place. Avoid
breathing near the ISA sidestream gas analyzer before or during the zeroing
procedure.
Warning: Never sterilize or immerse the ISA sidestream gas analyzer in liquid.
9-31
Warning: The ISA sidestream gas analyzer is intended only as an adjunct in patient
assessment. It must be used in conjunction with other assessments of
clinical signs and symptoms.
Warning: Measurements can be affected by mobile and portable RF communications

equipment. Make sure that the ISA sidestream gas analyzer is used in the
electromagnetic environment specified in this manual.
Warning: Replace the sampling line if the sampling line input connector starts flashing
red, or the medical backboard device displays a “Check sampling line”
message.
Warning: No modification of this equipment is allowed without authorization of the

manufacturer. If this equipment is modified, appropriate inspection and
testing must be conducted to ensure continued safe operation.
Warning: The ISA sidestream gas analyzer is not designed are not designed for MRI
environments.
Warning: During MRI scanning, ISA must be placed outside the MRI suite.
Warning: Use of high frequency electrosurgical equipment in the vicinity of the

ISA/medical backboard device may produce interference and cause incorrect
measurements.
Warning: Do not apply negative pressure to remove condensed water from the
Nomoline Family sampling line.
Warning: Too strong positive or negative pressure in the patient circuit might affect the
sample flow.
Warning: Strong scavenging suction pressure might affect the sample flow.
Warning: Exhaust gases should be returned to the patient circuit or to a scavenging

system.
Warning: Due to the risk of patient cross-infection, always use a bacteria filter on the
exhaust port side if sampled gas is intended to be re-breathed.
Warning: Do not place the ISA gas analyzer in any position that might cause it to fall on
the patient.
9-32
Warning: Do not re-use disposable single-patient use Nomoline Family sampling lines
due to the risk of cross contamination.
Warning: Do not sterilize or immerse Nomoline Family sampling lines in liquid.
Warning: Do not operate the ISA sidestream gas analyzer if the enclosure is damaged.
Warning: Do not use the Nomoline Airway Adapter Set Infant with adult/pediatric
patients.
Caution: The ISA analyzers should be securely mounted in order to avoid the risk of
damage to the ISA.
Caution: Do not operate the ISA sidestream gas analyzer outside the specified
operating environment.
(US Only) Caution: Federal law restricts this device to sale by or on the order of a physician. For
professional use. See instructions for use full prescribing information, including indications
contraindications, warnings, precautions and adverse events.
Table 9-22
ISA CO2 / AX+

Model
Interface type RS232, 9600bps
Accessories Sampling tube, CO2 or anesthetic gas Water trap, disposable.
Working principle of gas The gas module is a sidestream gas monitoring module, connecting to
module patient to monitor gas concentration of breath by electrical machine
inhaling trace gas.
The gas module can be used for adults, children and infants.
The gas module uses infrared technology, which determines gas

concentrations by measuring 10 different wavelengths according to
different absorption of gases to different ray.
9-33
Table 9-23
Basic Configuration
Description Ultra-compact, low-flow sidestream gas analyzers with integrated

pump, zeroing valve and flow controller.
Dimension(W×D×H) ISA CO2/ AX+:
23 mm×64 mm×39mm(0.9″×2.5″× 1.5″)
Weight 70g
Operating temperature ISA CO2: 0℃-50℃, 32℉-122℉
ISA AX+: 5℃-50℃, 41℉-122℉
Storage and -40℃-70℃,-40℉-158℉

transportation
temperature
Operating humidity ＜4kPa H2O(no condensation)
(95%RH at 30℃)
Storage and 5%-100%RH(condensation)1)

transportation humidity
(100%RH at 40℃)
Operating atmospheric 52.5kPa-120kPa(corresponding to a max altitude of

pressure 4572m/15000feet)
Storage and 20kPa-120kPa(corresponding to a max altitude of

transportation pressure 11760m/38700feet)
Ambient CO2 ≤800ppm
Mechanical strength ISA CO2:
Meets the shock and vibration requirements for transport of ISO

80601-2-55:2011 (clause 201.15.3.5.101) and EN
1789(clause6.3.4.2).
ISA AX+:
9-34
Meets the shock and vibration requirements for transport of ISO

80601-2-55:2011 (clause 201.15.3.5.101)
Power supply 4.5-5.5VDC,
ISA CO2: ＜1.4W(normal op.), ＜1.8W(peak @5VDC）
ISA AX+: ＜1.6W(normal op.), ＜2.0W(peak @5VDC）
Interface Modified RS-232 serial interface.
Software upgrade possible using the RS-232 serial interface.
Water handling Sampling line with proprietary water removal tubing.
Sampling lines 2 m±0.1m and 2 m±0.1m versions
Sampling flow rate 50 mL±10mL/min
NOTE 1: After condensation, the unit shall be stored for more than 24 hours in an
environment with relative moisture content below 95%RH (non-condensing).
Table 9-24
Data Output
Fi and ET ISA CO2: CO2
ISA AX+: CO2, N2O, primary and secondary agents(HAL, ENF, ISO,
SEV, DES)
Automatic agent ISA AX+: Primary and secondary agent.

identification
9-35
Table 9-25
Gas Analyzer
Sensor head 2-9 channel NDIR type gas analyzer measuring at 4μm -10μm.
Calibration When the detected value is offset;
When alarm occurs because ―gas module monitor concentration

exceeding the limits‖;
After replacing gas circuit adapter of gas monitor module.
Warm-up Time ISA CO2: <10s(concentrations reported and full accuracy)
ISA AX+: <20s(concentrations reported, automatic agent identification

enabled and full accuracy)
Rise time2 at 50 ISA CO2

ml/min sample flow
CO2 ≤200ms
ISA OR+/AX+
CO2 ≤300ms
N2O, O2, ENF, ISO, SEV, DES ≤400ms
HAL ≤500ms
Agent identification <20s (typically<10s)

time
Total system ISA CO2 < 3 seconds

response time
ISA OR+/AX+ CO2 < 4 seconds
（with 2m Nomoline Airway Adapter Set sampling line）
9-36
Table 9-26
The following accuracy specifications are valid for dry, single gases at 22±5℃ and 1013±40 hPa.
Accuracy specifications - standard conditions
Gas Range Accuracy
CO2 0%-15% ± (0.2vol%+2% of reading)
15%-25% Unspecified
N2O 0%-100% ± (2vol%+2% of reading)
HAL,ISO,ENF 0%-8 % ± (0.15vol%+5% of reading)
8%-25% Unspecified
SEV 0%-10% ± (0.15vol%+5% of reading) Unspecified
10%-25%
DES 0%-22% ± (0.15vol%+5% of reading) Unspecified
22%-25%
Table 9-27
Accuracy specifications – all conditions
Gas Accuracy
CO2 ± (0.3vol%+4% of reading)
N2O ± (2vol%+5% of reading)
Agents1) ± (0.2vol%+10% of reading)
NOTE 1: The accuracy specification is not valid if more than two agents are present in
the gas mixture. If more than two agents are present, an alarm will be set.
9-37
Table 9-28
Interference gas and vapor effects
Gas or vapor Gas CO2 Agents N2O

level
ISA CO2 ISA AX+
N2O4) 60vol% --2) --1) --1) --1)
HAL4) 4vol% --1) --1) --1) --1)
ENF,ISO,SEV4) 5vol% +8% of reading3) --1) --1) --1)
DES4) 15vol% +12% of reading3) --1) --1) --1)
Xe(Xenon) 4) 80vol% -10% of reading3) --1) --1) --1)
Xe(Helium) 4) 50vol% -6% of reading3) --1) --1) --1)
Metered dose Not for use with metered dose inhaler propellants
4)
inhaler propellants
C2H5OH(Ethanol) 4) 0.3vol% --1) --1) --1) --1)
C3H7OH(Isopropan 0.5vol% --1) --1) --1) --1)

ol) 4)
CH3COCH3(Aceton 1vol% --1) --1) --1) --1)

e) 4)
CH4(Methane) 4) 3vol% --1) --1) --1) --1)
CO(Carbon 1vol% --1) --1) --1) --1)

monoxide) 4)
NO(Nitrogen 0.02vol% --1) --1) --1) --1)

monoxide)4)
O24) 100vol% --1) --1) --1) --1)
NOTE 1: Negligible interference, effect included in the specification “Accuracy, all
conditions” above.
9-38
NOTE 2: Negligible interference with N2O/O2 concentrations correctly set, effect
included in the specification “Accuracy specifications- all conditions” above.
NOTE 3: Interference at indicated gas level. For example, 50vol% helium typically
decreases the CO2 readings by 6%. This means that if measuring on a mixture
containing 5.0vol% CO2 and 50vol% helium, the measured CO2 concentration
will typically be (1-0.06)*5.0vol%=4.7vol% CO2.
NOTE 4: According to the ISO 80601-2-55:2011.
9-39
9.11. EMC Guidelines
Below cables information are provided for EMC reference.
Max. cable length, Cable

Cable Number
Shielded/unshielded classification
AC cable 4.8m Unshielded 1 Set AC Power
Mainstream gas
2.4m Unshielded 1 Set DC Power
monitoring module cable
Sidestream gas
0.5m Unshielded 1 Set DC Power
monitoring module cable
Important information regarding Electro Magnetic Compatibility (EMC)
Aeon8800A needs special precautions regarding EMC and put into service according to the EMC
information provided in the user manual; Aeon8800A conforms to this IEC 60601-1-2:2014
standard for both immunity and emissions. Nevertheless, special precautions need to be
observed:
 Aeon8800A with Following ESSENTIAL PERFORMANCE is intended used in Professional

healthcare facility environment.
ESSENTIAL PERFORMANCE: IPPV mode Vt=500, other parameters by default, control is

correct.
 WARNING: Portable RF communications equipment (including peripherals such as antenna

cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of
the Aeon8800A, including cables specified by the manufacturer. Otherwise, degradation of
the performance of this equipment could result.‖
 The use of accessories, and cables other than those specified by AEONMED, with the
exception of accessories and cables sold by AEONMED of Aeon8800A as replacement parts
for internal components, may result in increased EMISSIONS or decreased IMMUNITY of the
Aeon8800A.
 WARNING: Use of this equipment Aeon8800A adjacent to or stacked with other equipment
should be avoided because it could result in improper operation.‖
9-40
EMI Compliance Table
Table 1 - Emission
Phenomenon Compliance Electromagnetic environment
CISPR 11
RF emissions Professional healthcare facility environment
Group 1, Class A
IEC 61000-3-2
Harmonic distortion Professional healthcare facility environment
Class A
Voltage fluctuations IEC 61000-3-3

Professional healthcare facility environment
and flicker Compliance
NOTE The EMISSIONS characteristics of this equipment make it suitable for use in industrial
areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which
CISPR 11 class B is normally required) this equipment might not offer adequate protection
to radio-frequency communication services. The user might need to take mitigation
measures, such as relocating or re-orienting the equipment.
EMS Compliance Table
Table 2 - Enclosure Port
Basic EMC Immunity test levels

Phenomenon
standard Professional healthcare facility environment
Electrostatic IEC 61000-4-2 ±8 kV contact
Discharge ±2kV, ±4kV, ±8kV, ±15kV air
3V/m
Radiated RF EM field IEC 61000-4-3
80MHz-2.7GHz
80% AM at 1kHz
Proximity fields from
RF wireless IEC 61000-4-3
Refer to table 3
communications
equipment
Rated power
30A/m
frequency magnetic IEC 61000-4-8
50Hz or 60Hz
fields
9-41
Table 3 – Proximity fields from RF wireless communications

equipment
Test frequency Band Immunity test levels

(MHz) (MHz) Professional healthcare facility environment
385 380-390 Pulse modulation 18Hz, 27V/m
450 430-470 FM, ±5kHz deviation, 1kHz sine, 28V/m
710
780
810
930
1720
1970
5240
5785
9-42
Table 4 – Input a.c. power Port

Immunity test levels
Basic EMC
Phenomenon
standard
Electrical fast ±2 kV
IEC 61000-4-4
transients/burst
100kHz repetition frequency
Surges
IEC 61000-4-5 ±0.5 kV, ±1 kV
Line-to-line
Surges
IEC 61000-4-5 ±0.5 kV, ±1 kV, ±2 kV
Line-to-ground
3V, 0.15MHz-80MHz
Conducted
disturbances induced IEC 61000-4-6 6V in ISM bands between 0.15MHz and 80MHz
by RF fields
80%AM at 1kHz
0% UT; 0.5 cycle
At 0º, 45º, 90º, 135º, 180º, 225º, 270ºand 315º
0% UT; 1 cycle
Voltage dips IEC 61000-4-11
and
70% UT; 25/30 cycles
Single phase: at 0º
Voltage interruptions IEC 61000-4-11 0% UT; 250/300 cycles
Table 5 – Signal input/output parts Port

Immunity test levels
Basic EMC
Phenomenon
standard
Electrical fast ±1 kV
IEC 61000-4-4
transients/burst
100kHz repetition frequency
3V, 0.15MHz-80MHz
Conducted
disturbances induced IEC 61000-4-6 6V in ISM bands between 0.15MHz and 80MHz
by RF fields
80%AM at 1kHz
9-43
9-44
9.12. Accessories List
NO. Part NO. Name Specification
1. 122000048 O2 Pipeline （white） M22×1.5 , Φ11.5 connecter
2. 122000049 N2O Pipeline（blue） M22×1.5 , Φ9.5 connecter
3. 122000050 Air Pipeline（black） M22×1.5 , Φ9 connecter
4. 122001476 Auxiliary O2 pipeline M14×1.5, Φ10 connecter
5. 122002613 Adult PVC Breathing Circuit package
6. 230000311 FACE MASK(PVC) XL(4#)
7. 230000312 Anesthesia Breathing Circuit ADULT
8. 230000075 Bag（3L） 3L
9. 230000076 Breathing Bag（2L） 2L
10. 121000065 Adult Silicon Breathing Circuit package
11. 230000538 Adult Silicon Hose package l=1000mm,Φ22
12. 230000163 Adult Silicon FACE MASK PN-0007AM(4#)
13. 230000113 Elbow Male and female cone Φ22
14. 230000101 Y Piece Φ22, Φ15cone
15. 130000798 Straight connector Φ22 male cone
16. 240000415 IRMA_CO2 module IRMA CO2
17. 240000414 IRMA_AX+ gas module IRMA_AX+
18. 210001975 O2 sensor MOX-4
19. 122000831 Wean PVC Breathing Circuit package
20. 240000028 Wean Anesthesia Breathing Circuit Wean
9-45
21. 122003285 Wean Silicon Breathing Circuit package
22. 230000066 FACE MASK ( PVC) HX.O11 M(2#)
23. 230000539 Wean Silicon Hose package l=1000mm,Φ15
9-46
This manual No.: 130014952
CE mark in this manual apply only to

product with CE mark.
Directive 93/42/EEC
concerning Medical Devices
Beijing Aeonmed Co., Ltd.
Tel: +8610-83681616
Fax: +8610-63718989
E-Mail: service@aeonmed.com
Website: http://www.aeonmed.com
Edition 00.01
March 2019

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Aeon8800A Anesthesia Machine User Manual Statement

 Installation, adjustments, mending and repairs must be performed by individuals authorized

CAUTION: This equipment is not for home use.

Manufacturing techniques and materials:

 This warranty does not apply to the followings:

Machines without maintenance or machines broken;

The label of our original serial number or mark is removed or replaced;

Other manufacturers’ product.

Safety, reliability and operating condition:

 The assemblies are disassembled, extended and readjusted

1. Obtain the rights of return

Device lifetime：8 years.

Welcome to use our products.

Manufacturer(holder): Beijing Aeonmed Co., Ltd.

Manufacturer(holder) Room 405，Basement 1 to 4th Floor of 901 Unit, Building 9,

Facility: Beijing Aeonmed Co., Ltd.

Facility address: Room 405，Basement 1 to 4th Floor of 901 Unit, Building 9,

No.10 Chaobai Street, Yingbin Road West, Yanjiao

Service: Beijing Aeonmed Co., Ltd.

Service Address: No.10 Chaobai Street, Yingbin Road West, Yanjiao

Service Line: +86 800-810-8333

European Representative: Shanghai International Holding Corp. GmbH (Europe)

Address: Eiffestrasse 80, 20537 Hamburg Germany

Wechat Offical Account:

1.1. General Information ........................................................................................................................... 1-1

2. Components ......................................................................................................................................... 2-1

2.1. Configuration ...................................................................................................................................... 2-1

3. User interface ....................................................................................................................................... 3-1

3.1. Main interface display layout ............................................................................................................. 3-3

3.2.2.2. The button status when setting parameter ......................................................................................... 3-10

3.2.3. Alarm indication area ............................................................................................................... 3-11

3.2.10. Message prompts area ............................................................................................................ 3-17

4. Pre-operative Preparation .................................................................................................................... 4-1

4.1. Initial Setup ......................................................................................................................................... 4-1

4.1.5.2. Connection of the sidestream monitoring module ............................................................................... 4-9

4.1.6. AGSS Installation and Connection............................................................................................ 4-10

4.2.1.2. Power Failure Alarm Test .................................................................................................................... 4-13

4.2.2. Pipeline Gas Supply Test .......................................................................................................... 4-14

5. Operating guide .................................................................................................................................... 5-1

5.1. Opening .............................................................................................................................................. 5-1

5.6.1.2. Intermittent Positive Pressure Ventilation (IPPV) ............................................................................... 5-13

5.6.1.3. Pressure Control Ventilation (PCV) ...................................................................................................... 5-14

5.6.1.5. Pressure Support Ventilation (PS) ....................................................................................................... 5-17

5.6.2. Ventilation mode setting ......................................................................................................... 5-22

5.6.3. Mode parameter setting .......................................................................................................... 5-23

5.7.4.2. CO2/Agents calibration ........................................................................................................................ 5-31

5.7.4.3. Touch screen calibration ..................................................................................................................... 5-32

5.7.5. Trend ........................................................................................................................................ 5-33

5.7.6.2. Compliance Test .................................................................................................................................. 5-36

5.7.7. Configuration ........................................................................................................................... 5-38

6. Alarm and troubleshooting ................................................................................................................... 6-1

6.1. Brief introduction of alarm message .................................................................................................. 6-2

7. Cleaning and Disinfection ..................................................................................................................... 7-1

7.1. Guideline ............................................................................................................................................ 7-3

8. Regular maintenance ............................................................................................................................ 8-1

8.1. General principle of maintenance ...................................................................................................... 8-2

8.3. Replacement of replaceable parts ...................................................................................................... 8-4

9. Technical Data ...................................................................................................................................... 9-1

9.1. Pneumatic Diagram ............................................................................................................................ 9-1

9.10.4.2. Pre-use check ...................................................................................................................................... 9-29

9.10.4.3. Manitenance ....................................................................................................................................... 9-30

9.10.4.4. Zeroing................................................................................................................................................. 9-30

9.10.4.5. Alarms ................................................................................................................................................. 9-30

9.10.4.6. Cleaning ............................................................................................................................................... 9-31