Ads 2

Product Information
Product name：ADS II Anesthesia Machine
Lifetime: 5 years
CE Mark
The product is marked with CE, as it conforms to European Council Directive for Medical
Devices (93/42/EEC), and meets basic requirements of appendix I in the directive.
This product is TypeⅠ,Class B radio jamming protective equipment that complies with the
EN55011. It meets the requirements of EN60601-1-2 standard “Medical electrical
equipment-Electromagnetic compatibility”.
User’s Responsibility
Please check the product and accessories firstly when you receive the product, make sure
it conform to the contract. If any damage of the package or the product is found before or
after you open the packing case, please contact the local office or the franchiser
immediately.
Users must perform the installation, operation, maintenance and carry out regular
inspection according to the instruction described in the manual. Replace the components
immediately if any damage, loss, distortion or contamination is found. Stop use when
I
malfunction occurs. Please contact the after service department of the Company for
repairing and replacing. Any change of the product is verboten without agreement of the
Company. Users must accept responsibility for any malfunction which results from
non-compliance with the servicing requirements detailed in this manual.
Preface
Description
This manual describes the intended use, function, installation, operation and maintenance
of the product. Please read and understand the contents carefully before use to ensure the
proper performance and patient safety. When you begin using the anesthesia machine, we
deem that you have read the manual carefully.
In order to use the equipment accurately, effectively and avoid the accident, please read
the manual carefully and comply with it strictly, especially pay attention to the “Warning”,
“Caution” and “Note”.
The optional features may not be completely included in the manual, if you have any
questions, please contact the Company.
Please read this manual carefully and keep within reach of the device.
Illustration
The illustration in the manual is only for reference. Some settings and data may not be
consistent with the real display, and please refer to the real product.
Conventions
 Bold Italic: The quoted section.
 【Character】：The character string on the user interface or on the control panel.
II
Content
PRODUCT INFORMATION .................................................................................................................. I
CE MARK................................................................................................................................................. I
USER’S RESPONSIBILITY ................................................................................................................... I
PREFACE ................................................................................................................................................II
CONTENT ............................................................................................................................................. III
CHAPTER 1 SAFETY INFORMATION ................................................................................................ 1
1.1 WARNING ................................................................................................................................... 2

1.2 CAUTION .................................................................................................................................... 7
CHAPTER 2 EQUIPMENT DESCRIPTION ...................................................................................... 10
2.1 BRIEF INTRODUCTION .............................................................................................................. 10

2.1.1 Intended use ...................................................................................................................... 10
2.1.2 Main feature ....................................................................................................................... 11
2.2 SYSTEM OVERVIEW................................................................................................................... 12
2.2.1 External pipeline connection diagram ............................................................................ 12
2.2.2 Front view diagramⅠ ....................................................................................................... 13
2.2.3 Front view diagram II ....................................................................................................... 14
2.2.4 Rear view ........................................................................................................................... 15
2.3 POWER SUPPLY ......................................................................................................................... 15
2.4 BATTERY .................................................................................................................................. 16
2.5 GAS SUPPLY .............................................................................................................................. 18
2.6 SYSTEM SWITCH ....................................................................................................................... 19
2.7 FLOWMETER ............................................................................................................................. 19
2.8 OXYGEN FLUSH BUTTON........................................................................................................... 20
2.9 PATIENT ABSORBER AND BELLOWS ASSEMBLY .......................................................................... 20
2.10 ANAESTHETIC GAS SCAVENGING SYSTEM (AGSS) （OPTIONAL） ........................................ 21
2.11 VAPORIZER ............................................................................................................................... 23
2.12 ANESTHESIA VENTILATOR ......................................................................................................... 23
2.12.1 Display ............................................................................................................................ 24
2.12.2 Membrane button.......................................................................................................... 25
2.12.3 User interface ................................................................................................................ 27
2.12.3.1 Power-up interface ......................................................................................................................... 27
2.12.3.2 manual mode leakage test .............................................................................................................. 28
2.12.3.3 Vent mode leakage test and compliance test................................................................................... 29
2.12.3.4 O2 sensor calibration...................................................................................................................... 30
2.12.3.5 Start-up interface ............................................................................................................................ 31
2.12.3.6 Standby interface ............................................................................................................................ 32
2.12.3.7 Main interface ................................................................................................................................ 32
III
2.12.3.8 Function interface........................................................................................................................... 35
2.12.4 Ventilation mode ........................................................................................................... 38
2.12.4.1 Manual ventilation mode ........................................................................................................... 38
2.12.4.2 Mechanical ventilation mode ..................................................................................................... 39
2.12.5 Compliance compensation .................................................................................................... 44
2.12.6 Fresh mixed gas compensation ............................................................................................. 44
2.12.7 Alarm system ..................................................................................................................... 44
2.12.7.1 General Description ....................................................................................................................... 44
2.12.7.2 Alarm limit setting.......................................................................................................................... 46
2.12.7.3 Alarm silence.................................................................................................................................. 47
CHAPTER 3 INSTALLATION AND CONNECTION ........................................................................ 48
3.1 POWER SUPPLY INTERFACE ....................................................................................................... 48

3.2 CONNECTING THE GAS SUPPLY ................................................................................................. 48
3.3 INSTALLING / REPLACING THE GAS CYLINDER （OPTIONAL） ................................................. 49
3.4 INSTALLING THE ABSORBER ...................................................................................................... 50
3.5 INSTALLING THE FOLDING BAG AND BELLOWS HOUSING ........................................................... 51
3.6 INSTALLING THE MICRO MANOMETER ....................................................................................... 51
3.7 INSTALLING THE OXYGEN BATTERY .......................................................................................... 52
3.8 INSTALLING THE CO2 CANISTER ............................................................................................... 53
3.8.1 Canned absorbent ............................................................................................................... 53
3.8.2 Installing the canister .......................................................................................................... 54
3.8.3 Replacing the absorbent .................................................................................................... 55
3.9 INSTALLING THE BREATHING HOSE AND THE Y CONNECTOR ..................................................... 56
3.10 INSTALLING THE MANUAL BREATHING BAG .............................................................................. 57
3.11 INSTALLING THE VAPORIZER ..................................................................................................... 57
3.11.1 Installing the vaporizer ...................................................................................................... 58
3.11.2 Adding the anesthetic ....................................................................................................... 59
3.11.3 Discharging the anesthetic ............................................................................................... 59
3.12 INSTALLING AGSS(OPTIONAL) ................................................................................................. 60
3.12.1 Installation .......................................................................................................................... 60
3.12.2 Connection ......................................................................................................................... 60
3.12.3 Checking before usage .................................................................................................... 60
3.12.4 Usage .................................................................................................................................. 60
CHAPTER 4 PRE-USE CHECK ......................................................................................................... 62
CHAPTER 5 OPERATION AND SETTING ....................................................................................... 64
5.1 TOUCH KEY .............................................................................................................................. 64

5.2 START-UP ................................................................................................................................. 64
5.3 PATIENT SETTING ..................................................................................................................... 65
5.4 STANDBY.................................................................................................................................. 66
5.5 VENTILATION SETTING ............................................................................................................. 67
5.6 ALARM SETTING ....................................................................................................................... 68
5.7 SYSTEM SETTING ...................................................................................................................... 69
IV
5.8 SYSTEM SHUT OFF .................................................................................................................... 73
CHAPTER 6 PHASEIN CO2 ANALYZER AND SPO2 MODULE(OPTIONAL) ............................ 75
6.1 PHASEIN CO2 ANALYZER ................................................................................................................. 75

6.1.1Summarize ................................................................................................................................ 75
6.1.2 System assembly instruction .................................................................................................... 77
6.1.3 Pre-use check .......................................................................................................................... 79
6.1.4 Zeroing procedure ................................................................................................................... 79
6.1.5 Alarms ..................................................................................................................................... 80
6.2 SPO2 MODULE ................................................................................................................................. 80
6.2.1 Introduction ............................................................................................................................. 80
6.2.2 Connecting and operating ....................................................................................................... 81
CHAPTER 7 MAINTENANCE ............................................................................................................. 83
7.1 MAINTENANCE SCHEDULE ........................................................................................................ 85

7.2 CLEANING AND DISINFECTION .................................................................................................. 85
7.3 MAINTENANCE OF THE ANESTHESIA MACHINE SURFACE .......................................................... 87
7.4 MAINTENANCE OF THE RESPIRATION SYSTEM .......................................................................... 88
7.4.1 Breathing tube and manual bag ................................................................................. 89
7.4.2 Bellows assembly ......................................................................................................... 89
7.4.3 Micro manometer and canister ................................................................................... 89
7.4.4 Pop-off valve assembly ................................................................................................ 90
7.4.5 Gas block and bellows cover ...................................................................................... 90
7.4.6 BYPASS assembly ....................................................................................................... 91
7.4.7 Absorber upper cover and APL .................................................................................. 91
7.4.8 Heat plant and the Bag/Ventilator and non-return valve assembly ....................... 92
7.4.9 Oxygen battery .............................................................................................................. 92
7.4.10 Expiratory and inspiratory connector and flow sensor ............................................ 93
7.5 IRMA PROBE............................................................................................................................ 94
CHAPTER 8 CONFIGURATION LIST ............................................................................................... 95
APPENDIX A WORKING PRINCIPLE .............................................................................................. 96
A.1 ELECTRICAL SCHEMATIC ................................................................................................................ 96
APPENDIX B PRODUCT SPECIFICATION ..................................................................................... 97
B.1 SAFETY SPECIFICATION .................................................................................................................. 97

B.2 ENVIRONMENT SPECIFICATION ....................................................................................................... 98
B.3 POWER SUPPLY SPECIFICATION ....................................................................................................... 98
B.4 GAS SUPPLY SPECIFICATION ........................................................................................................... 99
B.5 SYSTEM SPECIFICATION .................................................................................................................. 99
B.6 PARAMETER SPECIFICATION ......................................................................................................... 101
B.6.1 Specification of setting parameter .................................................................................. 101
B.6.2 Specification of monitoring parameter ........................................................................... 102
B.6.3 Specification of alarm parameters .................................................................................. 103
B.7HARDWARE SPECIFICATION ........................................................................................................... 103
V
B.8 PHASEIN CO2 ANALYZER（OPTIONAL） ................................................................................... 105
B.9 INTERFERING GAS AND VAPOUR EFFECT ....................................................................................... 105
B.10 ELECTROMAGNETIC COMPATIBILITY (EMC) .............................................................................. 106
APPENDIX C ALARM ..................................................................................................................... 111
APPENDIX D SYMBOL AND GLOSSARY .................................................................................... 113
D.1 GLOSSARY.................................................................................................................................... 113

D.2 EQUIPMENT SYMBOL .................................................................................................................... 114
D.3 PACKAGING SYMBOL .................................................................................................................... 116
APPENDIX E DEFAULT SETTING .................................................................................................. 117
E.1 PATIENT INFORMATION .................................................................................................................. 117

E.2 DEFAULT SETTING ......................................................................................................................... 117
E.3 ALARM DEFAULT SETTING ............................................................................................................. 118
APPENDIX F REFERENCE .............................................................................................................. 119
VI
ADS II ANESTHESIA MACHINE
Chapter 1 Safety Information

The safety information described in this chapter explains the unsafe conditions that may
occur if not performed correctly according to the manual. Please review all the warning,
caution and Note prior to operating the anesthesia machine.
This chapter contains important safety information of the anesthesia machine, and some
other safety information throughout each chapter of the manual. Please read and
understand all the safety information before use to avoid security risks.
The ponderance of the safety requirement has no relation with the list order.
Warning:
Identify conditions or practices that could result in serious adverse reactions or potential
safety hazards.
Caution:
Identify conditions or practices that could result in damage to the anesthesia machine or
other equipment.
Note：
Identify supplemental information to help you better understand how the ventilator works.
Page 1 of 117
1.1 Warning
Warning:
Preparing warning：
 Before using the device, please ensure that all the connections of the pipelines are
accurate and reliable, not twisted, knotted, pressed or blocked.
 The auxiliary mains socket-outlet of this equipment can only be used for the specified
facilities; otherwise it may result in safety risks.
 Before using the equipment please make sure that the balanced terminal of the
potential has been connected to the spot grounded point, otherwise, unpredictable
risks may occur.
 This equipment can only be operated by the qualified personnel, please make sure the
operators have corresponding qualifications before using.
 Only the specified and with protective earthing power supply can be used. If you have
any questions about the installation of the external line, the equipment must be
operated by the internal power supply.
 The inflammable anesthetic agent such as aether and cyclopropane can not be used.
Only the anesthetic agent that according with the requirements about the
non-flammable anesthetic described in the appendix DD of the IEC-60601-2-13 can
be used in this anesthetic system.
 This equipment can only be used in the specified environment, should not be used in
the inflammable or explosive environment, magnetism resonance imaging (MRI)
environment, or in the environment with other strong electromagnetism interfere.
 Only those conform to the latest IEC-601-1 standard accessories and auxiliary
equipment can be connected to this anesthesia machine. If peripheral equipment such
as computer、monitor、humidifier has been connected to the anaesthetic ventilator , the
whole system should meet the IEC-601-1 standard.
 Do not use flammable agent in the patient absorber.
 The container with water should not be placed on the equipment in order to prevent
Page 2 of 117
Warning:
liquid entering the equipment and lead to malfunction.
 The equipment will produce some castoff such as the sodium- calcareousness, the
one-off parts or the damageable parts which will lead to serious pollute or cross
infection if discarded randomly, and should be managed and disposed according to
the relative regulations.
 Before operating please ensure that all the separate facilities that work with this
anesthesia machine such as the anesthesia gas monitoring apparatus and the
anesthesia gas purifying apparatus are in good condition.
 Before operating please ensure that the gas supply needed by the equipment is in
good condition, the malfunction may make the equipment unable to work if connected
to the central air feeding system.
 A malfunction of the central gas supply system may cause more than one or even all
devices connected to it to stop their operation simultaneously.
Operating warning：
 Once the abnormal alarms occur or it cannot start-up normally during the startup
process, please stop using the equipment and contact the maintaining personnel
immediately.
 Do not open the outer casing of the equipment so as to avoid electric shock.
 Do not touch the power supply so as to avoid electric shock.
 The volume of the alarm sound should be kept at an appropriate level ,and it should
not disturb others or be ignored because of the inaudible volume.
 This equipment should only be used with the recommended accessories and
materials, otherwise unpredictable risks may occur.
 The machine must not be used if any of the alarm, monitoring device are not
functioning correctly.
 When worked with the high frequency electrical surgical equipment, should avoid
mechanical damages to this equipment or its components that caused by the electrical
surgical equipment.
Page 3 of 117
Warning:
 Those medical equipments that worked together with this anesthesia machine should
also conform to the corresponding safety requirements.
 Do not use the antistatic or conductive mask or breathing tubes.
 Additional equipment placed on the top shelf must be securely attached. Take care
when moving a fully loaded machine, particularly when negotiating ramps. Check that
hoses or power leads are not trailing on the floor.
 The exhausted gas should be discharged through the exhaust outlet and cannot be
discharged to the room, do not block the outlet.
 Do not replace the canister during the ventilation period, otherwise there may exist
risks.
 Prevent the absorbent turning dry; please replace the absorbent timely if it becomes
dry.
 The vent of the PEEP will discharge little air and oxygen continuously, so do not block
the vent, otherwise the anesthesia machine cannot work.
 During operation please ensure there is no testing plug or other foreign body in the
absorber.
 The expiratory valve of the anesthesia machine is with constantly open design, when
power failure or abnormal occurs, the valve is open and connected to the atmosphere
through the AGSS to ensure patient can breath freely. During use, please do not block
the AGSS to avoid suffocate the patient.
 If one or more devices are connected to the auxiliary mains socket-outlet, it will lead to
the increase of the leakage current risks, the leakage current should be checked
termly.
 Before using any additional electrical equipment powered by the auxiliary sockets on
the machine, check that the additional equipment is correctly wired and is earthed
through its plug. A missing or defective protective earth conductor may increase earth
leakage currents to the patient to values exceeding the allowable limits, resulting in
ventricular fibrillation, or interference with the pumping action of the heart.
Page 4 of 117
Warning:
 Remember to do a circuit leak test after reinstalling the CO2 canister.
 When installing the oxygen sensor, please check if the sealed ring is in good condition,
replace a new oxygen sensor if the sealed ring is damaged or there is no sealed ring.
Maintenance Warning:
 Please clean and disinfect the parts that have been repeatedly used and contacted
with the patient according to the ways that recommended in the user manual every
time before use.
 Please shut off the equipment and the power supply while cleaning.
 While cleaning the parts of the equipment, users must be away from the equipment.
 While cleaning the outer casing, please make sure that no liquid enters into the
controlling components, and it cannot be connected to the AC power supply until the
parts have turned dry after cleaned.
 Cooling the equipment for at least half an hour before disassembling it.
 While disassembling the outer casing of the equipment, the supply must be cut off and
should only be operated by experienced personnel.
 Please dispose the wrapper according to the local regulations or the hospital waste
disposal system.
 Do not throw the batteries or the oxygen sensors to the fire so as to avoid exploder.
 The exhausted batteries should be replaced or discarded according to the local
regulations and should not be disposed in a normal way.
 The oxygen sensor and the flow sensor should not be dipped in the liquid or disposed
by high temperature and high pressure.
 The immersion time in hot water of the bellows components should be not more than
15 min, to prevent dissolving or aging.
 The heating accessories of the flow sensor are electriferous, so that it should be
cleaned with a soft cloth soaked in alcohol and should not be disinfected by way of
dipping in the liquid.
 Do not use lube that contains oil or lipid.
Page 5 of 117
Warning:
 The moving parts and the knock-down parts may lead to pinched or crushed
dangerous, please pay more attention when moving or replacing the parts of the
system.
 Do not implement the calibration process when the system is connected to the patient.
 Please use the accessories provided by the Company in order to avoid the value
incorrect or the equipment failure.
 The one-off accessories can be used only once, repeated use may lead to
performance degradation or cross-infection.
 If there appear any problems about the accessory’s wrapping or the accessories, do
not use accessories.
Page 6 of 117
1.2 Caution
Caution:
Preparation Caution:
 Please double-check the power cord before connected to the city electricity, make
sure it has no damage, scratch or other factors which will lead to the inside conductor
exposed issues.
 When the equipment or the accessories are about to exceed the limit time, they should
be disposed according to the local regulations or the hospital systems.
 The electromagnetic fields may affect the performance of this device, so the other
facilities used around this must meet the corresponding EMC requirements.
 This equipment complies with the electromagnetic compatibility regulations of the IEC
60601-1-2 standard. If the interfering grade exceeds the limit grade, it may lead to the
stop of the mechanical ventilation.
 Please install or transport the equipment appropriately to avoid falling, hitting, serious
vibrating or other outside forcing damages.
 The anesthetic gas delivering device that used together with the anesthesia system
must comply with the ISO 8835-4:2004 or ISO-8835-4 requirements.
 This equipment should be used together with the anesthesia gas monitoring
apparatus that comply with the ISO 11196:1996 requirements.
 Any of the anesthesia ventilation systems that used together with the anesthetic
vapour delivery system should meet the requirements of the ISO 8835-2:1999
 The anesthesia ventilator that used together with the anesthesia system must comply
with the requirements of the ISO 8835-5:2005.
 The product itself Is not equipped with an anesthetic gas scavenging transfer or
receiving system that used together with the anesthesia system, if need additional
equipped, please use the anesthetic gas scavenging apparatus that accorded with the
ISO 8835-3:1997 requirements to connect to the AGSS port.
 The measuring conditions shown in this user manual are the ambient temperature and
Page 7 of 117
Caution:
the ambient temperature and pressure saturated (ATPS) conditions.
 The pressure in the medical gas pipeline keeps the original unchanged when the
anesthetic system stops delivering gas.
 When the pressure of the gas supply inlet is at twice the maximum rated inlet
pressure, the pipeline will not rupture or cause any security risk. But it is
recommended to keep the pressure in the specified range.
Operation Caution
 In order to prolong the battery life, please use the battery at least once per month, and
charge or discharge it fully.
 Please open the device and check the battery if not been used for a period of time to
avoid the battery malfunctions.
 The battery life lies on the frequency and time of used. The lithium battery life is about
3 years if maintenance and used in a proper way.
 Please pay attention to the position of the gas pipeline so as to avoid falling off.
 Please make sure that the power supply cable exposed outside the equipment is not
twisted to the patients, operators, other personnel or objects (including tubes),
otherwise, dangers may occur.
 When installing the breathing tube, please hold the joints on the two ends of the tube
in order to avoid damages of the tube.
 This equipment can use three kinds of anesthetic agents: the enflurane, the isoflurane
and the sevoflurane, only one anesthetic can be used at a time.
 This equipment may bring interference to other products.
 Do not use this equipment if it not passed the test before using, please contact the
after service department of the Company.
Maintenance Caution:
 Please use the methods recommended in this manual to clean or disinfect this
equipment.
 Take care when transporting,moving or disassembling the equipment to avoid
Page 8 of 117
Caution:
damages to the personnel.
 Do not use the abrasive detergents (such as the steel wool, silver polish or detergent).
 The display should be cleaned with a dry, soft and lint-free cloth; it should not be
cleaned by liquid.
 Please contact the repairing personnel or the Company if the calibration of the
equipment failed many times.
 Please use the parts that produced or sold by the Company to replace the damaged
parts. And have a test after replacing to ensure that the equipment accorded with the
specifications and requirements of the manufacturer.
Page 9 of 117
ADS II
Chapter 2 Equipment Description

2.1 Brief Introduction
2.1.1 Intended use

D/C series is a pneumatic controlled anesthesia machine which is used to manage and
control the respiration and anesthesia of the single patient during the anesthesia
operation, it is suitable for both adult and pediatric (the weight is above 5Kg). This
anesthesia machine can provide controlled concentrations and flows of anaesthesia
gases into a patient breathing system, (The concentration of oxygen is no less than 21%)
and also provide the respiratory support.
D/C series anesthesia machine is intended to use only in the operating rooms and
emergency rooms, not suitable for other places, and it can only be operated by the
professional anesthetist.
The anesthesia machine has two models: D serie and C serie, the differences of their
configurations are shown as below:
Configuration D serie C serie
s /Models
Gas supply O2,N2O / O2,N2O,Air O2,N2O
LCD 10.1″LCD 8″LCD
Touch screen Optional NO
Manual ,VCV, Manual ,VCV,PCV

Ventilation
PCV,SIMV(V)+PS,SIMV(P)+PS,SPO SIMV(V)+PS,SIMV(P)+PS,SPO
modes
NT NT
CO2 module Optional NO
SpO2 module Optional NO
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Warning:
 This equipment should be operated by the professional anesthetist or under the
guidance of the professional anesthetist. Personnel not authorized or trained can not
carry out any operations.
 The clinical environment of this equipment is operating rooms and emergency rooms.
2.1.2 Main feature
This anesthesia machine consists of the anesthetic-ventilator, patient absorber, CO2
canister, vaporizer assembly, flow meter assembly and gas connecting tubes.
This anesthesia machine has following functions and features:
1. Optional touch screen to select setting parameters and functional buttons easily and
conveniently.
2. Automatical leakage compensation and compliance compensation.
3. Make tidal volume compensation according to altitude.
4. Electronic adjustable PEEP;
5. Various monitoring parameters and graphs displaying.
6. Clear and differentiable auditory and visual alarms.
7. With a top lighting system, and a separately controlled small lamp on the top of the
machine.
8. Storing and reviewing the alarm events, recording the wrong status functions.
9. Optional high pressure cylinder.
10. With auxiliary oxygen configuration, the passive AGSS functions;
11. With the function of connecting to the monitor.
12. With the function of connecting to the tower crane.
Page 11 of 117
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2.2 System overview
Caution：
 Illustrations in this chapter are only for reference, due to the different configurations,
the illustrations may be not entirely consistent to the product.
2.2.1 External pipeline connection diagram
1. Trolley 2. Mask 3. Manual bag
4. Patient absorber 5. Gas supply inlet pipeline 6. Power jack
7. Host
Page 12 of 117
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2.2.2 Front view diagramⅠ
1. Caster brake plate 2. CO2 canister 3. Manual bag
4. APL valve 5. Oxygen flush button 6. Backup cylinder manometer
7. System switch 8. Gas supply manometer 9. Auxiliary oxygen flowmeter
10. Auxiliary oxygen connector 11. Bellows housing 12. CO2 Socket
13. Bag/Ventilator switch 14. Airway manometer 15. Expiratory non-return valve
16. Inspiratory non-return valve 17. Expiratory hose interface 18. Inspiratory hose interface
19. Oxygen sensor connector
Page 13 of 117
ADS II
2.2.3 Front view diagram II
1. Vaporizer 2. Battery 3. User screen
4. Anesthesia ventilator control panel 5. Electronic flowmeter 6. Electronic flowmeter display module
7. Flowmeter controlling knob 8. Single tube flowmeter 9. Circuit locking switch
10. Backup cylinder
Page 14 of 117
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2.2.4 Rear view
1. Auxiliary mains socket-outlet 2. Network interface 3. Gas supply interface
4. AGSS（Anesthesia gas scavenging system）vent
2.3 Power supply
1. AC Power supply: 100～240VAC，50/60Hz；
2. Auxiliary mains power supply: 100～240 VAC, 50/60Hz, 1.5A×3；
3. Fuse specification：T10AL/250V；
4. When AC power is connected, the AC indicator will be light; when AC power is
disconnected, the light will be off.
Page 15 of 117
ADS II
1.Equipotential earthing pole 2. Filter 3 .T2AL/250 fuse
4. Auxiliary mains socket-outlet 5. Communication interface 6. Network interface
7. RS232 Interface
Warning:
 If one or more devices are connected to the auxiliary mains socket-outlet, it will lead
to the increasing of the leakage current risks, the leakage current should be checked
termly.
2.4 Battery
The anesthesia machine is equipped with built-in rechargeable lithium battery to ensure
that the anesthesia machine can still work when the power supply is cut off. When the
anesthesia machine is connected to the AC power and switched on, the battery is
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ADS II
charging if not already full charged. When the power supply is cut off, the system will
automatically switch to the battery power supply, simultaneously, it will generate an AC
power supply failure alarm to prompt users, and will not lead to interruption of the
anaesthesia ventilator work.
The fill amount of the battery icon on the screen indicates the amount of battery power
remaining.
- The battery is working normally; the solid part indicates the battery capacity.
- Low battery capacity, it needs to be charged.
- The battery is exhausted and needs to be charged immediately.
- No battery.
When the battery power is low, the anesthesia machine will generate a medium alarm,
and the alarm message 【low battery capacity！

！】displays in the alarm area, it indicates
greater than 10 minutes of battery power remaining; when the battery is exhausted, there
will be a high level alarm, and the alarm message 【the battery is exhausted！！】displays
in the alarm area, it means greater than 3 minutes of battery power remaining, then the
anesthesia machine must be connected to the AC power supply.
Caution:
 The battery can not be replaced by users, if need, contact with the authorized
equipment maintenance personnel or the after service department of our company.
 The exhausted battery should be replaced or discarded according to the local
regulations.
Page 17 of 117
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2.5 Gas supply
There are three kinds of gas input: oxygen, air and N2O. They can be connected to the
central gas supply system, and the required rated pressure range is 0.28～0.6Mpa,there
is a filter, manometer and a non-return valve installed in each pipeline of the gas. The
machine can also be connected to the O2 and N2O cylinder, the pressure inside the full O2
cylinder is about 15.0Mpa and it is about 8.0Mpa inside the full N2O cylinder, there is a
filter, a manometer, a pressure valve and a non-return valve installed in each cylinder, if
the output pressure of the cylinder exceeds 0.6Mpa, it will be regulated to 0.28～0.6Mpa
by adjusting the pressure valve. And there is a pressure-relief valve connected to each of
the gas supply, which is as a security role to prevent high pressure of the gas supply, the
releasing pressure is 758kPa（110psi), when the pressure is above 758Kpa, it begins to
release the pressure, the pipeline will not rupture or cause any security risk. But it is
recommended to keep the pressure within the specified range.
The curve below displays the output pressure after the gas supply passes though the
pressure-relief valve.
The gas supply is mainly used as below:
1） The oxygen is the power source of the anesthetic ventilator;
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2） Proving fresh gas for the patient.
2.6 System switch
There is a system switch designed in order to achieve the functions of opening and cutting
off the anesthesia circuit freash gas and the system circuit at the same time. When the
system switch is turned on, users can adjust the gas flow by adjusting the electronic
flowmeter to make the fresh gas pass through the ACGO into the circuit, at the same time,
the system is connected to the power supply and begins to run according to the pre-set
state; when the system switch is turned off, the gas through the flowmeter is cut off, there
is no fresh gas output, the system is disconnected to the power supply, and the
anesthesia machine can not be operated, but can be operated manually.
Turn the system switch to the position: the system is turned on.
Turn the system switch to the position: the system is turned off.
2.7 Flowmeter
The flowmeter displays the flow of the gas :O2，N2O and Air. Their flow can be read
directly. The unit is: L/min.
The user can adjust gases flow by the controlling knob, turn the flowmeter controlling knob
counterclockwise to increase the flow and clockwise to decrease.
 O2 and N2O knobs consist of a linkage device.( O2、N2O linkage device)；
 While counterclockwise rotation of N2O knob, and N2O flow is increased to a
certain extent, O2 knob would be rotated together with N2O knob, and the O2 flow
would be increased, such a system could ensure the O2 concentration in the
fresh gas over than 21%
 While clockwise rotation of O2 knob, and O2 flow is decreased to a certain extent,
N2O knob would be rotated together with N2O knob, and the N2O flow would be
decreased, such a system could ensure the O2 concentration in the fresh gas
over than 21%.
There is a round float inside of the flowmeter, and the central plane scale of float is
indicates the current flow. See the graphic below:
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2.8 Oxygen flush button

The oxygen flush supply is provided by the oxygen supply separately, it passes through
the oxygen flush button and the gas resistance then enters the patient absorber. oxygen
flow will rush into the gas path when the oxygen flush button is pushed, and the gas path
is cut off when the button is released. The gas resistance is to reduce the impact of the
rapid oxygen flow on the patient and regulate the flow rate to the range of 25～75L/min.
2.9 Patient absorber and bellows assembly

In this anesthesia machine, the patient absorber is integrated with the bellows assembly.
The patient absorber is used in conjunction with the anesthesia machine as a part of the
closed respiratory system, connected with the appropriate respiratory pipeline, gas
reservoir bag and patient port, and absorbs CO2. According to the different gas flow set by
the anesthetist, the expiratory gas can completely or partially circulate and enter the
inspiratory port, achieve the closed、semi-closed ventilation.
The patient absorber and the bellows integrated system is connected to the anesthesia
machine by connecting the interface board on its side with the interface boartd on the side
of the host, after installed, lock the system by the locking device on the left front of the
anesthesia machine to prevent loosing or falling off and lead to gas leakage.
There is a Sodium lime canister at the bottom of the patient absorber, which is used to
absorb the exhalant CO2 and prevent the intraoperative excessive CO2 retentate which
may lead to hypercapnia. If you need to replace the sodium lime in use, remove the
sodium lime canister and the gas path will be closed automatically, it will not affect the
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ventilation or use, but it is not recommended to undergo surgery using the anesthesia
machine in the case of the sodium lime canister absent and the sodium lime disabled.
The inspiratory non-return valve,inspiratory flow sensor and the expiratory non-return
valve,expiratory flow sensor are there installed respectively on the inspiratory limb and the
expiratory limb of the patient absorber, which are used to monitor the inspiratory and
expiratory flow rate,the airway pressure as well as achieve the gas circulating circuit.
The system is integrated with an oxygen sensor, it is connected to the anaesthesia
ventilator through the cable, then displays the inspiratory oxygen concentration on the
user screen. It is accorded with the ISO 7767 standard.
There is also a micro-manometer installed above the patient absorber, it will display the
airway pressure, the display range is : -20～+100cmH2O.
The APL valve above the patient absorber is used to restrict the pressure during the
manual ventilation mode, the design range is 2～70cmH2O, when extruding the bag
manually, if the pressure exceeds the limited value, the gas will be vented from the valve
vent, and the exhausted gases are collected to the AGSS outlet and vented.
The system is integrated with the Bag/Ventilator switch valve, achieving the following
functions:
a) Spontaneous respiration or manual ventilation in manual mode.
b) Using the anesthesia machine to ventilate in mechanical ventilation mode.
2.10 Anaesthetic Gas Scavenging System (AGSS)

（Optional）
The device is used in the operation room of hospital, and it is the system for collection and
delivery of exhausted gas from anesthesia machine to the hospital exhaust centralized
disposal system. This is the solution to avoid the pollution of anesthetic exhausted gas in
the operation room. The device is well-structured, simply-operated, safe and reliable.
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AGSS consists of the exhaust port, float pump, float, cylinder, and inlet port.
AGSS has two models: 200A and 200B, there is difference between 200A and 200B, 200A
cylinder with the metal material and 200B with the plastic material.
Anesthetic Gas Scavenging System (AGSS)(Top, Front, and Right Views)：
1. Exhaust port: it is a specified screw thread connecting port matched with the
specified corrugation hose which connects to the hospital’s waste gas disposal
system.
2. Float pump: it is a transparent and plastic pump used for observing float” s
position, and marked the minimum scale line on the surface.
3. Float: it is a plastic disc that indicates AGSS’s intake flow.
4. Inlet port: it is the inner cone port (30mm) that complies with the standard of
YY1040.1-2003 and with a transfer hose connects to the anesthetic machine” s
exhaust gases outlet.
5. Cylinder: it is hollow cylinder that collects exhaust gases from the breathing
system.
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2.11 Vaporizer
The vaporizer transmits the anesthetic to the patient respiratory system to anesthetize the
patient. Different anesthetic should be used with the corresponding vaporizer; otherwise it
will result in inaccurate output concentration.
The D/C series series anesthesia machine adopts the imported PENLON vaporizer. The
enflurane, isoflurane and sevoflurane are optional. The anesthesia machine is equipped
with one vaporizer seating, and it can also support two vaporizer seatings. When installing
two vaporizers, it will only output one kind of anesthetic agent at the same time.
The vaporizer used in this anesthesia machine should be accorded with the standard
ISO8835-4.
For the particular operation of the vaporizer please refer to the user manual provided by
the vaporizer manufacturer.
2.12 Anesthesia ventilator

The anaesthesia ventilator is an auto-controlling equipment which replaces the traditional
manual ventilation, which adopts the pneumatic electronically controlling to achieve
different modes and parameters changes of the driving gas, and provides the monitoring
of the corresponding physiological and ventilation parameters as well as the auditory and
visual alarms for the abnormal events.
In order to control the flow of the driving gas accurately, accurate pressure-regulating
valve is used to adjust the driving gas supply pressure to 0.2Mpa, and then solenoid
proportional valve is used to achieve the different flow rate adjustment through electrical
controlling. The output gas passes through the machinery over-pressure valve and the
bellows to achieve the automatical ventilation for the patients. The over-pressure valve is
to guarantee the pressure of the driving gas circuit less than the safe pressure, and its
release pressure is designed to be 10.8kPa (110cmH2O). The expiratory valve is closed
when inspirating, and during expirating, the gas inside the bellows passes through the
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valve( the path is Ф18mm to the bellows interface andФ15mm to the PEEP valve gas
path interface) and enters the AGSS vent , to reduce the exhaust emission pollutions to
the operating environment.
In order to prevent the exceeding high pressure in the gas path which may bring dangers
to the patient or equipment, the anaesthesia ventilator monitors the pressure and flow
value of inspiratory and expiratory gas, and emits the auditory and visual alarms for the
abnormal events, besides the design of the over-pressure valve to ensure the driving gas
not exceed the safe pressure.
2.12.1 Display
The anesthesia machine adopts the colour TFT LCD, which can display various
parameters and graphics clearly. The diagram below contains the main interface of the
anesthesia machine. For the information of the other interfaces, please refer to section
2.11.3 User interface.
D serie:
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C serie:
2.12.2 Membrane button
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1. Alarm indicator light:
No practical function. Response to the anesthetic ventilator alarms, the light is red for the
high priority alarms and yellow for the medium and low priority alarms. （please refer to
5.6 Alarm settings for more information）
2. Alarm Silence：
1) The key is disabled when no alarm occurs.
2) When alarm sounds, push the key to mute the alarm, the duration is 100 seconds, the
alarm silence icon and the 100 seconds count down will display on the top right
corner of the interface.
3) Push the key again to resume the alarm sound.
3. Alarm Setting：
Push the key to access the alarm settings menu.
4. Ventilation Setting:
Push the key to access the ventilation modes and parameters setting interface.
5. System Setting:
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Push the key to access the system settings interface.
6. Start/Standby:
Push the key to access the Start/Standby interface.
7. Navigation wheel:
1) Turn: to switch among the membrane buttons or the function options; turn it clockwise
to increase the parameter value, or anticlockwise to decrease the parameter value.
2) Push it down to confirm settings.
8. Battery indicator light:
1) The full battery power capacity: green;
2) The insufficient battery power capacity: orange.
3) Battery is not fitted or battery failure: OFF.
9. AC power indictor:
1) The indicator light is on: the anesthesia machine is connected to the AC power;
2) The indicator light is off: the anesthesia machine is disconnected to the AC power.
10. Parameters setting key:
According to different ventilation modes, the parameters setting keys are corresponding to
different parameters.
2.12.3 User interface
Caution：
 The user interface may be different due to the different configurations, please take
the material object as valid.
2.12.3.1 Power-up interface
Power-up interface is the first interface display on the screen when the anesthetic
ventilator is turn on；
The self-testing items include power (10V, 5V, 12V, -12V), inspiratory valve, expiratory
valve, sensors （pressure sensor , flow sensor）and installing absorber.
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The message in self-test process shows " Please wait, the system is staring self-testing
Go to the test interface, when testing itself is successful
The message shows "Unit failure", when testing itself is failure, and system stop testing in
the Power-up interface. The system restarts until the failure is solved
2.12.3.2 manual mode leakage test
After the finish of self-testing, the system enters the manual mode leakage test, as
shown below:
Manual mode leakage test is focus on the checking of below points:
1. The leakage value of system in the manual mode;
2. APL valve.
Preparation for manual mode leakage test:
1. Set the Bag/Vent switch to Bag；
2. After install the Manual Bag and occlude the patient Y-piece in it；
3. Adjust APL valve to approximately 30cmH2O；
4. Shut off ACGO；
5. Shut off all the fresh gas controlling valve
6. Push O2+ until Paw gauge value is between 25 cmH2O to 35 cmH2O；
7. After reading of pressure gauge reach setting range ,take stock of the reading of
pressure gauge and the pressure waveform on the interface.If the pressure value
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decreases less than 5 cmH2O within 15 seconds, then it passes the test. Otherwise
it don’t
Remark: Choose 【Bypass】keyboard, the system go to “Start-up”.
2.12.3.3 Vent mode leakage test and compliance test
After manual mode leakage test, select【Continue】, then the system enter Vent mode
leakage test and compliance test, as shown below:
The test is focus on below points:
1. Test the system leakage value;
2. Check O2 valve and PPEP valve;
3. Check the compliance of circuit.
Preparations for Vent mode leakage test and compliance test:
1. Set the Bag/Vent switch to Vent.
2. Occlude the patient Y-piece
3. Press O2+ to fill the bellows.
4. Shut off all the fresh gas controlling valve
After preparation of self-test, press【Start】 and navigation wheel, the system begins
self-testing.
a) If the system passes test, the interface displays the information of 【Test
passed】; 【Leakage value】;【Compliance value】.
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b) If the test fails, the interface displays the message such as 【Test failed】;
【Leakage value】; 【Insufficient gas in the folding bag】;【Please shut off fresh
gas】.
Remark: Choose 【Bypass】keyboard, the system go to “Start-up”.
Warning：
 Small amount of leakage does not affect the function of this equipment; please
consider whether to continue using this equipment.
 If you feel leakage is serious, please contact the after service dept. of the Company.
2.12.3.4 O2 sensor calibration
After enter Vent mode leakage test and compliance test, select【Continue】, then the
system enter O2 sensor calibration , as shown below:
O2 sensor calibration is focus on the checking of below points
1. 21% O2 sensor calibration;
2. 100% O2 sensor calibration
Operate “Start 21% O2 sensor calibration” and “Start 100% O2 sensor calibration”,
according to the procedure of suggestive O2 concentration calibration in interface.
Note：
 100% O2 sensor calibration must be carried out after 21% O2 sensor calibration.
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 It is unnecessary to perform the O2 sensor calibration if O2 sensor is not fitted or not
used.
 Please perform the O2 sensor calibration if the measured O2 has obvious error or
after replacing O2 sensor.
2.12.3.5 Start-up interface
The anesthesia machine goes into "Start-up" interface, after it detects itself and
testing is passed, shown as below:
In the start-up interface, users can perform the following operations:
- Patient category (adult and pediatric) switch;
- The amendment of patient age;
- The amendment of Patient weight;
- Ventilation mode modification;
- Startup to enter working mode；
- Reset all setting parameters to default values.
Caution:
 For more information about the operation , please refer to chapter 5 “operations and
settings”
 In the start-up interface, buttons are invalid, except for【Alarm Silence】.
 In the start-up interface, the alarm function is normal if technical alarm occurs.
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2.12.3.6 Standby interface
When the standby mode is selected, the anaesthesia ventilator will enter the standby
mode, shown as below:
2.12.3.7 Main interface
The main interface displays when the anesthesia machine works, it displays the setting
parameters, measured parameters, each type of information and operation function, the
main interface of D serie and C serie anesthesia machines are different, shown as below:
D serie:
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C serie:
1. Mode information display area:
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1) Display the current ventilation mode;
2) Display the current patient category;
3) Display the CPAP icon;
2. Alarm information display area:
Display the current alarm information.
3. Status information display area:
1) Display the battery power status;
2) Display the alarm silence icon;
3) Display the menu button (C serie).
4. Function keys area:
There are 5 function keys for D serie:
1) Ventilation Setting;
2) Measured Values;
3) Alarm Settings;
4) System Setting;
5) System Log.
There are 6 function keys for C serie:
1) Ventilation Setting;
2) Measured Values;
3) Alarm Settings;
4) System Setting;
5) System Log;
6) Exit Menu.
In main interface, the focus is default on the menu button , push the navigation
wheel, the function keys area will display.
Different function keys can perform different function interfaces, please refer to section
2.12.3.8 Function interface for more information.
5. System time display area:
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Display the system date and time.
6. Waveform display area:
According to different configuration of models and different settings by users, it will display
the waveform or Loop.
7. Measured parameter area:
Display the current measuring parameter of the patient.
When PEEP is set to be OFF,the monitored parameters are not display in the areas of
Monitored values.
8. Ventilation modes setting area:
Except using the membrane button 【Ventilation settings】, users can set the relative
ventilation parameter of the current ventilation mode in the main interface directly, the
gray touch key means the parameter has nothing to do with the current ventilation mode
and cannot be adjusted.
2.12.3.8 Function interface
The function interface is the interface when the membrane button is pushed; it contains
the detailed settings and operation of certain functions. Take D serie for example, the
function interfaces are described as below:
1. Ventilation setting
The ventilation setting interface is shown as below:
In the Modes setting interface, users can perform the following operations:
- Selecting the ventilation mode;
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- Setting the relative parameters in each ventilation mode;
- Enable or disable “Cardio Pulmonary Bypass” in manual mode.
- Setting Altitude；（If the absolute pressure sensor is installed in the pneumatic control
board, this setting would not be displayed.）
Note：
 The design of the D/C series anesthesia machine makes the parameters setting
correspond with the current ventilation mode, in other words, when you select a
ventilation mode, the interface will only display the parameters related to the current
ventilation mode.
2. Measured value
The measured value interface is shown as below:
There is no user action in the measured value interface. It mainly displays the current
ventilation mode and the related setting parameters and measured value information.
- Real-time monitoring of ventilation parameters；
- 【R】-- real-time monitoring of gas resistance while setting breath holding time；
- 【C】-- real-time monitoring of dynamic compliance；
3. Alarm setting
The alarm setting view is shown as below:
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Users can set the alarm limit in this interface. The current measured value is between the
upper limit and the lower limit of the alarm value.
If no CO2 modules and SPO2 module are connected to the system, the alarm setting
interface will not display CO2 and SPO2 alarm limit settings.
4. System setting
The system setting interface is shown as below:
In the system setting interface, users can perform the following operations:
- Setting the current date and time;
- Setting the alarm volume;
- Setting the system language;
- Setting the waveform configuration of the interface;
- Setting the parameter area of the interface;
- information display；
- Compensation setting;
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- The super mode is non-user function, and it is used by trained engineers of the
Company to calibrate, upgrade and perform some other technical operations.
5. System Log
The system log interface is shown as below:
There is no user action in the system log interface. It mainly displays the operation
information that the user have performed and the alarm information during operation. Use
the Navigation wheel to view more content.
Note：
 The anesthesia machine can store up to the latest 500 logs for your view.
2.12.4 Ventilation mode
2.12.4.1 Manual ventilation mode
1. Switch the manual/mechanical controlling switch to manual position, the

“Manual” will be displayed in the ventilation modes display area.
2. Turn the controlling knob of the APL valve to adjust the pressure in the patient
absorber to an appropriate range.
In manual mode, the user can adjust peak pressure of the patient circuit and gas volume
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of the breathing bag by APL valve, when the pressure of the patient circuit exceeds the
limited value, APL valve will open to release superfluous gas.
Caution：
◆ In the manual ventilation mode, all the setting parameters are disabled.
2.12.4.2 Mechanical ventilation mode
Caution：
 The default mechanical ventilation mode of the D/C series anesthesia machine is
【VCV】mode. Users can set other mechanical ventilation modes in the modes
setting interface.
2.12.4.2.1 VCV mode
1. Principle description
VCV (volume control ventilation) mode is a basic completely mechanical ventilation mode.
Preset the tidal volume【VT】, breathing frequency 【f】and the expiratory and inspiratory
rate 【I:E】. When the inspiration begins, the gas flow will enter the lung at a constant
speed and it will reach the preset tidal volume within the preset inspiratory time and then
expire.
In 【VCV】mode, users can set the 【TIP:TI 】(inspiration hold) to improve the gas
distribution conditions in the patient’s lung; and set the 【PEEP】(positive end-expiration
pressure) to improve the vent of CO2 in end-expiration and increase oxygen in the
breathing process.
When the peek pressure exceeds【Plimit】,the system will release the pressure and give an
alarm.
2. Selecting the VCV mode
1) Push【Ventilation Settings】 key, the modes setting interface will display;
2) Push the modes option frame and select【VCV】 mode in the drop-down menu;
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3) When 【VCV】 mode is selected, the mode information display area will display
“VCV”.
3. Parameter need to be set
In VCV mode, following parameters need to be set:
-【VT】
-【f】
-【I:E】
-【TIP :TI】
-【PEEP】
-【Plimit】
2.12.4.2.2 Sigh function（Optional）
In volume control mode, the user can set sigh by ventilation mode interface
（range:OFF,10~100）, the extra volume will be increase by 50% above the tidal volume
set by the user(1.5xset volume) in the next inspiration cycle of the sigh setting value.
Note that sigh function is canceled when the unit is powered off.
2. Selecting Sigh
1) Push the 【Ventilation Settings】 key, the modes setting interface will display;
Set the 【Sigh】parameter in the modes setting interface (only volume control mode);
2.12.4.2.3 PCV mode
PCV (pressure control ventilation) mode is a basic completely mechanical ventilation
mode. Preset the airway pressure 【Pinsp】,breathing frequency【f】and expiratory and
inspiratory rate 【I:E】. When the inspiration begins, the gas flow will enter the patient’s
lung quickly, when it reaches the preset pressure level, it will reduce the flow rate through
the response system, and at the same time it will keep the airway pressure at the preset
pressure value till the end of the inspiratory and then expire.
In the 【PCV】mode, users can also set the 【PEEP】(positive end-expiratory pressure).
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2. Selecting the PCV mode
1) Push【Ventilation Settings】 key, the modes setting interface will display;
2) Push modes option frame and select【PCV】 mode in the drop-down menu;
3) When【PCV】 mode is selected, the mode information display area will display” PCV”.
In PCV mode, following parameters need to be set:
-【Pinsp】
-【f】
-【I:E】
-【PEEP】
2.12.4.2.4 SIMV(V)+PS mode
SIMV(V)+PS mode is a mixed ventilation mode; it is the SIMV (synchronized intermittent
mandatory ventilation) mode under the volume controlling.
In SIMV mode, the independent breathing frequency and the tidal volume is controlled by
the patient, and a synchronous control is activated at a certain interval of time; if the
trigger level (flow trigger) is met in the waiting trigger window, the anesthetic-ventilator will
provide a synchronized volume control ventilation for the patient; if the trigger level is not
achieved in the trigger window, at the end of the trigger window, the anesthetic-ventilator
will give a volume control ventilation.
2. Selecting the SIMV(V)+PS mode
2) Push the modes option frame and select the 【SIMV(V)+PS】 mode in the drop-down
menu;
3) When the 【SIMV(V)+PS】 mode is selected, the mode information display area will
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display” SIMV(V)+PS”.
In SIMV(V)+PS mode, the following parameters need to be set::
-【f】
-【FTRIG】
-【VT】
-【TI】
-【PEEP】
-【Plimit】
-【Psupp】
2.12.4.2.5 SIMV(P)+PS mode
The SIMV(P)+PS mode is a mixed ventilation mode; it is the SIMV (synchronized
intermittent mandatory ventilation) mode under the pressure controlling.
In SIMV mode, the independent breathing frequency and tidal volume are controlled by
the patient, and a synchronous control is activated at a certain interval of time; if the
trigger level (flow trigger) is met in the waiting trigger window, the anaesthesia ventilator
will provide a synchronized pressure control ventilation for the patient; if the trigger level is
not achieved in the trigger window, at the end of the trigger window, the anaesthesia
ventilator will give a pressure control ventilation.
2. Selecting the SIMV(P)+PS mode
2) Push the modes option frame and select the 【SIMV(P)+PS】 mode in the
drop-down menu;
3) When the 【SIMV(P)+PS】 mode is selected, the information display area will
display【SIMV(P)+PS】.
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In【SIMV(P)+PS】mode, following parameters need to be set:
- 【Pinsp】
- 【f】
- 【FTRIG】
- 【TI】
- 【PEEP】
- 【Psupp】
2.12.4.2.6 SPONT mode（Optional）
1. principle description
SPONT (spontaneous ventilation mode). In the SPONT mode, the patients will control the
breathing rhythm themselves, when the triggered level is met, the ventilator will support
with the pre-set inspiratory pressure; keep the pressure till the inspiratory flow decreased
to the pre-set value and then enter the expiration phase.
2. Selecting the SPONT mode
2) Push the modes option frame and select the 【SPONT】 mode in the drop-down
menu;
3) When the 【SPONT】 mode is selected, the information display area will display
【SPONT】.
In the【SPONT】mode, the following parameters need to be set:
- 【VT】
- 【f】
- 【Ti】
- 【Psupp】
- 【PEEP】
- 【Plimit】
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- 【Sigh】
- 【FTRIG】
Users can set the backup ventilation in the SPONT mode, providing the mandatory
ventilation when the patient is asphyxial.
2.12.5 Compliance compensation
The anesthesia machine affords compliance compensation for resolving the pipeline
compliance loss in breathe system. The compliance compensation operates according to
the system testing the compliance data from the tidal volume.
Cautions: The system compensates from a set of default compliance data, when it is not
system testing.
2.12.6 Fresh mixed gas compensation
The fresh mixed gas compensation purpose is to make up for the lack of tidal volume,
which is caused by changing 3 kinds of gas flowmeter (O2, N2O,Air), and makes the
concrete tidal volume and setting one equal.
2.12.7 Alarm system
2.12.7.1 General Description

The D serie/C anesthesia machine is designed with a perfect alarm system to help insure
patient safety. The D/C series anesthesia machine can signal 3 types of alarms according
to different potential risks during the alarm activated: High Priority, Medium Priority and
Low Priority.
When alarm occurs, it will remind the user by the alarm indicator light, alarm sound and
alarm messages, different types of alarms have different alarm information.
The alarm signals and conditions are grouped into physiological alarm conditions and
technical alarm conditions.
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1) Physiological alarms: the monitored gas parameters or the patient physiological
parameters exceed the specified range.
2) Technical alarms: Due to the improper operations or the malfunctions of the technical
or the equipment, the machine cannot monitor exactly.
According to the different risks when alarm activated, the alarms are grouped into: High
Priority, Medium Priority and Low Priority alarm.
1) High priority: when the high priority alarm occurs, it may endanger the patient’s safety
or the equipment cannot work normally, users must stop operating to dealing with the
malfunction.
2) Medium Priority: when the medium priority alarm occurs, it may endanger the
patient’s safety if lasting a long time, or some reasonable settings, users should
adjust the parameters to clear the malfunction.
3) Low priority: when the low priority alarm occurs, it will not endanger the patient’s
safety, there may be some reasonable settings or some unimportant malfunction,
users could adjust the setting parameters properly or clear up the malfunction when
complete operating the equipment.
When alarm occurs, the anesthesia machine will remind users by the following
auditory and visual signals.
1) High priority：
- Alarm indicator light:：red flashes;
- Alarm sound:du- du - du -- du - du ---- du - du - du - du - du；
- Alarm message：red background , and displays” ！

！！”behind the alarm message;
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2) Medium priority：
- Alarm indicator light:：yellow flashes;
- Alarm sound：du - du - du ----- du - du - du；
- Alarm message: yellow background, and displays” ！！ ”behind the alarm
message;
3) Low priority：
- Alarm indicator light:：yellow, static, not flashes
- Alarm sound：du-----du；
- Alarm message：yellow background, and displays” ！”behind the alarm message;
Caution：
 When different priorities of alarms occur simultaneously, only the alarm with highest
priority will display.
2.12.7.2 Alarm limit setting

Refer to 5.6 alarm setting. push【Alarm Setting】membrane button to enter the alarm
setting interface and set the alarm limit value.
Warning：
 A HAZARD can exist if different ALARM PRESETS are used for the same or similar
equipment in any single area, e.g. an intensive care unit or cardiac operating theatre.
Caution：
 Please always pay attention to the alarm limit parameter and make sure it is set at a
proper and reasonable level to avoid inaccurate alarms.
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2.12.7.3 Alarm silence

When alarm occurs, push 【Alarm silence】membrane button, the alarm sound wil be
muted, meanwhile, the alarm silence icon and alarm silence 100 seconds count
down will display on the top right area of the interface.
The alarm silence status lasts for 100 seconds, 100 seconds later, the alarm silence will
be disabled and the alarm sound resumes.
In the alarm silence status, push【Alarm silence】membrane button again to resume the
alarm sound.
Caution:
 In alarm silence status, except for the alarm sound, the other alarm functions are
working normally.
 In alarm silence status, if new alarms occur, the alarm silence will be disabled and
alarm sound will be activated according to the latest alarm.
 【Alarm silence】membrane button is invalid if no alarm occurs.
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Chapter 3 Installation and connection
Warning:
 Always ensure that there is no toxicity in the gas supply hose or the absorber, will not
cause allergic reactions in the patient's body, and will not react with the anesthetic to
produce dangerous substance.
 When the absorbent becomes dry, continuous using may cause dangerous to the
patient. Appropriate preventive measures should be taken to prevent the absorbent in
the vaporizer not becoming dry.
 Before using please make sure that the locking organs have been locked or it may
lead to unpredictable dangerous.
 Do not use anti-static or conductive mask or breathing hose.
 The installation of the equipment should be accomplished by the engineers appointed
by the manufacturer.
 This equipment has an exhaust emission vent, users should pay more attention to the
disposal of the vented residual gases.
 The operating environment and the power supply of this equipment must comply with
the requirements of the B.2environment specifications and B.3power supply
specifications.
3.1 Power supply interface
Warning：
 The facilities that connected to the power outlet will lead to increasing of the leakage
current, so the leakage current should be tested regularly.
3.2 Connecting the gas supply
The anesthesia machine provides three kinds of gas supply inlet: O2,N2O and Air.
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The following graphic indicates that the tubes of the three air source are connected
correctly.
Warning：
 Only the medical gas supply can be used. Other types of gas supply may contain
water, oil or other contaminations.
3.3 Installing / replacing the gas cylinder （Optional）
The procedure of installing / replacing the gas cylinders is as below:
1. Turn the handle of the gas cylinder clockwise, close the valve of the cylinder that to
be replaced, unscrew the T-handle anticlockwise;
2. Release the T-handle fully, break apart the door and remove the gas cylinder.
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3. Do not place any objects that may be damaged easily due to the releasing of high
pressure gas in front of the new cylinder outlet.
4. Open the gas cylinder valve quickly, eliminate the dust on the outlet of the cylinder;
5. Make the cylinder position align with the indexing pin;
6. Close the door and tighten the T-handle;
7. Test the gas cylinder.
Warning：
 During the process of pipeline gas supplying, do not let the backup cylinder valve
open. Otherwise, when the gas supplying of the pipeline goes wrong, the gas of the
cylinder may be exhausted and lead to the inadequate supply of reserves.
3.4 Installing the absorber
Put absorber inwards along with the lead rail, as followed figures. While it clicks, that
means it is all right.
Note: make sure the lock is open before installation. And lock it after installation.
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3.5 Installing the folding bag and bellows housing

1. Cover the bellows base with the folding bag; make sure the bottom of the folding bag
can be nested tightly to the bellows base. The graphic is as below;
2. Put the side that printed a scale of the bellows face to the front of the anesthesia
machine, note that the four block spaces should be pointed at the corresponding four
gaps of the patient absorber;
3. Slightly push it down, and turn the bellows housing clockwise until you cannot turn it:
Caution:
 Please make sure that the sealed ring inside the bellows cover can not be turned over
or extruded transmutative.
3.6 Installing the micro manometer

As shown below, firstly, press and hold the button in the direction of arrow, and then hold
the micro manometer and insert its head into the jack, when installation is completed,
adjust its surface to the front of the anesthesia machine.
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Caution：
 Before installing or removing the micro manometer, always press the button first so
as not to damage the micro manometer.
3.7 Installing the oxygen battery

Revolve the battery at the oxygen battery mounting hole clockwise. Hold the crystal head
of the connecting line and inset it at the jack of the oxygen battery:
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3.8 Installing the CO2 canister

3.8.1 Canned absorbent
The structural graphic of the canister is as below:
canister
Guiding
shelf
Guiding
tube
Filter plate
1. Spill the used absorbent from the canister to the specified position, take out the filter
plate and the guiding shelf,clean away the dust and then put them back.(for the first
time please implement the step2 directly);
2. Defilade the top of the guiding shelf with a plastic lid or other objects to avoid dust
enter the guiding tube, dump the sodium lime (1) slowly to the CO2 canister to the
specified position of the graphic below:
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1
Shielding
cover
Sodium lime
filling line
3. Clean away the dust on the wall of the canister with paper or special cloth.
3.8.2 Installing the canister

1. Hold the bottom of the canister, push it upward to be directed at the screw thread and
align with silk-screen direction indicated by arrow.
Silk-screen direction
indicated by arrow
2. Rotate it counterclockwise, it shown as below:
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3. Rotate the canister anticlockwise until it is turned to limit position block of BYPASS
base, the following figure is shown as the installed canister.
Enlarge figure for

limit position block
Caution：
 Please check whether the installation of the canister is in place or not after
installation.
 It is recommended to keep your hands clean and dry when installing the canister.
 Please do circuit leakage detection after reinstalling the canister.
3.8.3 Replacing the absorbent
The steps for replacing the absorbent is the same as the steps described in 3.8.1 Canned
absorbent.
Caution：
 The commonly used absorbent are two types: sodium lime and barium lime, it is
recommended to use the sodium lime as absorbent.
 Before installing the canister, please check the color of the absorbent to decide
whether you need to replace the absorbent.
 The changes of the absorbent color are just shown in general. Please use the CO2
monitor to decide whether you should replace the absorbent.
 Please discard the absorbent if the color is changed. If placed a few hours, it may
restore its original color and lead to misusage.
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 Appropriate defensive measures should be taken to ensure the absorbent not turn
dry. Please cut off the gas supply when complete using the system. When the
absorbent turns dry, if contacting with the anesthetic, it will emit carbon monoxide
(CO) which will bring hazards to patients. Therefore, please replace the absorbent in
time for the patients’ safety.
 In order to ensure the humidity of the sodium lime and avoid the emitting of CO,
please pay attention to the following:
 Reduce the flow of fresh gas in the sealed circuit.
 Replace the sodium lime every week at least.
 Record the replacing date of sodium lime.
 Avoid gases flow through the sodium lime when the machine not being used.
 Uses can add sodium lime temporarily in urgent conditions.
 During surgery or complete a case, please check the color of the absorbent and take
corresponding measures. For the detail information about the color change of the
absorbent, please refer to the instructions on the packaging of the absorbent.
3.9 Installing the breathing hose and the Y connector
Caution：
 When installing the breathing hose, please grab the two ends of the hose to avoid
damages to the hose.
1. Connect the two separate ends of the two breathing hoses to the expiratory
connector and the inspiratory connector of the patinet absorber;
2. Connect the other end of the two breathing hoses to the two parallet intefaces of the
Y connector:
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Caution：
 For the one-off accessories, the Y connector has been connected with the breathing
hose, so cancel this step.
3.10 Installing the manual breathing bag
Put the manual bag forcibly to the manual bag connector (marked”1” in the graphic
below):
3.11 Installing the vaporizer
Warning：
 If the anesthesia machine and the vaporizer do not match, their performance will
decrease. Please use the vaporizer that matches the anesthesia machine.
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Caution：
 For the detailed description of the installation and operation of the vaporizer, please
refer to the manual of the corresponding vaporizer.
 When installing the vaporizer, make sure the vaporizer is locked well; otherwise it
may lead to leakage.
3.11.1 Installing the vaporizer
1. Hang the vaporizer to the fixing socket of the anesthesia machine;
2. Rotate the locking pole and push it, fix the vaporizer to the fixing socket;
3. Make sure the top of the vaporizer is in parallel, otherwise it should be removed and
installed again;
4. When re-installing the vaporizer, users should lift each of the vaporizer upward to let it
fall off the fixing socket instead of pulling it forward, be careful not to let the vaporizer
rotate on the fixing socket;
5. When the vaporizer is lifted off the fixing socket, install it again and carry out the steps
1 to 3.
6. Try to open more than one vaporizers.
Test each possible combination. If the user tries to open more than one vaporizers at one
time, these vaporizers should be removed and installed again, then complete the steps 1
to 6.
A:Locking pole； B: Interlock bolt； C: Tighten hook;
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3.11.2 Adding the anesthetic
1. Check the controlling knob A and set it to Zero; check and tighten the screw C;
2. Unscrew the screw cap B;
3. Pour the anesthetic liquid slowly to the vaporizer. During the process of pouring the
liquid, please pay attention to the height of the liquid inside the vaporizer, when it
reaches the maximum level, stop pouring the liquid;
4. Tighten the screw cap B, but not overly.
Caution：
 The maximum level of the anesthetic in the vaporizer is 250mL; and the minimum
level is 35mL.
3.11.3 Discharging the anesthetic
1. Check the controlling knob A and set it to Zero;
2. Unscrew the screw cap B;
3. Place a bottle marked with the name of the corresponding anesthetic under the
vaporizer, put the mouth of the bottle at the tundish that under the discharging pipe,
loosen the screw C, ensure the anesthetic flow into the bottle. Make sure the
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anesthetic flow into the bottle.
3.12 Installing AGSS(optional)
3.12.1 Installation
Hang or fix AGSS tank to on the side of the machine and ensure that AGSS”s outlet port
is upward and vertical. There is a certain space in AGSS tank so as to be good for air
movement.
3.12.2 Connection
1. AGSS inlet port used with the specified transfer hose which connects to the
anesthetic machine” s exhaust gases outlet. The one end of the corrugated hose with
30mm connects onto AGSS inlet port, and the other end connects onto anesthetic
machine” s exhaust gases outlet.
2. AGSS exhaust port used with the specified transfer hose and connector connects to
the hospital’s waste gases scavenging system, and tightens with nut.
3.12.3 Checking before usage
Please check following items in steps before using machine:
1. Checking the negative pressure of waste gas processing system is enough or not.
Observe AGSS system buoy, if it is on the minimum scale, it means the negative
pressure is normal, and can work, but if the negative pressure is not enough, the
AGSS system can not work.
2. Checking the air inlet is jammed or not which is under the AGSS system cup. If it is
jammed, Use it till need clear the blockage.
3.12.4 Usage
After connection and check, AGSS system could be used normally.
Check the following items at any time during using.
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1. Check if float can rise and exceed the minimum scale line.
2. Check if cylinder’s inlet ports on the underneath are blocked.
3. Check if inlet and exhaust hoses are smooth.
If occurs the above malfunction, it must be solved immediately, otherwise AGSS will not
be used normally.
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Chapter 4 Pre-use check

Before using this equipment, please read the user manual and understand the operation
and maintenance of each part of the equipment, and make sure it meets following
requirements:
1. The using environment should meet the relative requirements of the Appendix B;
2. The equipment is in good condition and no damages.
3. All the components are connected correctly.
4. The respiratory system is connected accurately with no damage.
5. The gas supplying system is connected accurately, the pressure is normal;
6. All the emergency equipment is in ready and in good condition.
7. All the equipment that used for the maintenance of the pipeline and the intubatton of
the windpipe are available and in good condition.
8. Make sure there is no loose phenomenon on the truckle and the brake has been
locked and the anesthesia machine cannot be moved.
9. Connect the power cord to the AC power outlet, switch on the AC power supply, the
AC power indicator and the battery indicator will light, if not, that means the system
has no electricity.
10. The gas supply connection test:
1) Connect the O2,N2O and Air source ( please refer to the section 3.2 Connecting the
gas supply).
2) Connect the power supply and switch on the system.
3) View O2, N2O and Air manometers, make sure the reading of the each manometer is
in the range of 280~600kPa.
4) Cutoff the gas supply and discharge the gas in the pipeline, view the manometers
and make sure the readings zero.
5) Check if waste gas disposal system’s negative pressure is enough, and observe
AGSS’s float, if the float can rise and exceed the minimum scale line, it means the
negative pressure system is normal, otherwise the negative pressure is deficiency
and AGSS system could not be used normally.
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6) Check that cylinder’s inlet ports are blocked or not; if any blockage, please dispose
blockage existed before using.
Warnings：
 Please always do a pre-use check before the anesthesia machine is connected to the
patient.
 Please connect the power cord to a protective grounded power outlet in order to
avoid electric shock.
 If any functional failures detected, and the failures persist, the anesthesia machine
cannot be connected to the patient.
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Chapter 5 Operation and setting
5.1 Touch key
The touch keys will display different colors to indicate different status:
1. The blue key pad indicates the normal status; you can push it to operate. For
example:
2. The yellow key pad indicates the active status: the key is selected, and can be
operated directly. For example:
3. The dark blue key pad indicates the selected status; the parameter cannot be
adjusted currently. For example:
4. The gray key pad indicates the invalid status, the key is disabled, and the
parameter cannot be adjusted currently. For example:
5.2 Start-up
1. Connect the power cable to the power outlet; make sure the power supply works
normally.
2. Turn on the system switch in front of the main unit.
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Warning：
 If abnormal alarms occur when the system starts up, please discontinue operation
and contact the authorized repaired personnel or the after service department of the
Company.
 Only the specified, protective grounded power supply can be used in this equipment.
5.3 Patient setting
1. According to the patient’s weight and age, the patient category is divided into two types:
-【adult】；
-【pediatric】；
Different patient categories decide different parameter setting and operation. In start-up
interface, user can set or change the patient categories.
1) In start-up interface, push the 【adult】or【pediatric】to select the patient category.
2) Push the navigation wheel to confirm the selection.
1. Patient age setting:
The user could set the patient age in the start-up interface. The system calculates
corresponding MAC value based on the different ages when there is anesthetic agents in
machine.
Patient age range: 1-100 years old.
1) Click patient age, the area would turn to be yellow.
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2) Adjust the patient age through navigation wheel.
3) Press navigation wheel, the area turn to be light blue.
2. Weight setting:
User can set the patient’s weight in Start-up interface. The anesthesia machine calculates
the referenced tidal volume value in the volume ventilation mode according to different
weight of the patient.
For different patient categories, the setting ranges of the weight are different:
- adult：20-150kg；
- Pediatric：5-20kg；
1) Push the patient’s weight area, the area turns light yellow.
2) Adjust the weight value by turning the navigation wheel.
3) Push the navigation wheel to confirm the setting, the area turns dark blue.
5.4 Standby
User can select the standby mode if need.
Enter the standby mode:
1) Push【Start/Standby】key.
2) Push【Standby】touch key in the pop-up window.
3) Push the navigation wheel to enter the standby mode.
In the standby mode, push【default】touch key, then push the navigation wheel to
confirm, this returns all setting parameters to default values.
Exit the standby mode:
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1) In the standby mode, push【start】touch key.
1) push the navigation wheel to exit standby mode to the main menu.
5.5 Ventilation setting
Modes and parameters setting:

1) In ventilation status, push【Ventilation Setting】key.
2) Push 【Mode】 option frame and select the ventilation mode in the drop-down menu.
3) Push the ventilation parameter that you need to set, turn the navigation wheel to
adjust the value and push the navigation wheel to confirm the setting.
4) Push【Exit】touch key to exit the current page.
Cardio pulmonary bypass
Cardio bypass mode could be started in the manual mode, and it is used for special
equipment that replaces the work of patient's heart and lungs for blood circulation and
gas exchange.
When Cardio pulmonary bypass is set, the following alarms will be disabled:
Apnea alarm;
Tidal volume low alarm;
Minute volume low alarm;
CO2 (EtCO2 and FiCO2) low alarms;
Frequency low alarm;
Paw low alarm.
When the mechanical ventilation is turned back on, Cardiac pulmonary bypass returns to
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“Disable”, and alarms become active.
Atitude
Altitude setting range:100~5000 meter;
If the absolute pressure sensor is installed in the pneumatic control board, the system
could make tidal volume compensation automatically, otherwise, the tidal volume
compensation has to be realized by altitude setting.
5.6 Alarm setting
Users can use the alarm setting function to adjust the alarm parameters for the needs of
monitoring and protecting the patients.
For the detail alarm parameters and setting range, please refer to the Appendix B.6.3
1) Push the upper limit or the lower limit parameter value, the frame turns yellow.
2) Turn the navigation wheel to adjust the value.
3) Push the navigation wheel to confirm the setting.
4) Push【default】touch key, all the parameter value will resume to the system default
value.
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5.7 System setting
1. Common settings
Users can set the date/time, alarm volume and language of the system.
1) Push the parameter value that you desire to set, the frame turns yellow.
2) Turn the navigation wheel to adjust the value and push the navigation wheel to
confirm the setting.
2. View settings
Users can configure the waveform displayed on the interface; the system can display
three waveforms simultaneously.
1） The first waveform options:
- Airway Pressure(Paw);
2） The second waveform options：
- Flow;
- Volume
3） The third waveform options：
- SpO2; （Optional）
- CO2; （Optional）
- Volume;
- Airway pressure(Paw);
- Flow
4）The display format options：
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- Normal;
- Wave+Loop
If you select 【wave】, the interface will only display the waveform, if you select
【wave+Loop】, the Loop will display on the right side of the interface, the Loop contains
the following types:
- Flow-Pressure (F-P);
- Pressure-Volume (P-V);
5）Parameter area
- electronic flowmeter;
- SPO2;
- Measured values;
After the option is selected, it will be displayed in the Monitored Parameters Area in
the Main Interface.
3. Special settings
1）information
The system version, gas controller version, display control version, gas flowmeter version,
gas module version and SPO2 module version,SN are in this interface.
2) Super mode
Push 【Super Mode】key to access the super mode interface.
functions of the super mode are only for trained engineers of the Company to calibrate or
upgrade the system, and a password is required.
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3) Compensation Setting
O2 and N2O compensation settings
The presence of oxygen and nitrous oxide can cause some interference in the CO2
measurement. So they should be compensated.
Setting the O2compensation：
The O2 compensation is performed automatically for IRMA probes with the oxygen sensor
fitted. When using an IRMA without an oxygen sensor, i.e. when oxygen measurement is
performed by the host equipment, the current oxygen concentration should be transmitted
to the IRMA probe or the analyzer using the SetO2 command.
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
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these ranges, the maximal relative CO2 error will be limited to 1.2%.
Set O2 range:
0-30 vol%;
30-70 vol%;
70-100 vol%.
Setting the N2Ocompensation:
The N2O is measured and automatically compensated for all IRMA probes except for in
IRMA CO2.
When using the IRMA CO2, the current N2O concentration should be transmitted to the
ISA gas analyzer or the Probe using the SetN2O command.
For most applications, sufficient accuracy in CO2 measurement will be achieved by setting
N2O to one standard concentration used always with N2O in use, as recommendation
span 30-70 vol% N2O. when N2O is not in use, set N2O range 0-30 vol%.
By using this range, the maximum CO2 error with N2O compensation on (30-70%) will be
limited to 3.2% relative.
Set N2O range:
- 0-30 vol%;
- 30-70 vol%;
Set-mode
For normal use, the ISA sensor has three operating modes: Self test, Sleep,
Measurement.
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Self test:
The sensor performs a self test and does not respond to commands from the host.
Sleep Mode：
Low-power standby state. The host can communicate with the sensor, but all functions are
disabled.
Measurement Mode:
The sensor is measuring gas concentrations.
SetApnea:
The apnea setting range is from 20 to 60 seconds.
Normal Zeroing:
For all IRMA mainstream multigas analyzers, they need to establish a zeroing every time
after replacing the adapter or you have any doubts about the accuracy of the measured
values.
Push【Normal Zeroing】touch area, the analyzer will begin normal zeroing.
Unit:
Three units can be selected:
- %;
- kPa;
- mmHg.
5.8 System shut off
When you have completed using the system, please shut off of the system as the
following procedure:
1) Disconnect the pipeline that connected to the patient;
2) Turn off the system switch;
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3) Shut off the AC power supply;
4) Clean the surface of the equipment if need.
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Chapter 6 PHASEIN CO2 analyzer and

SPO2 module(optional)
6.1 Phasein CO2 analyzer
6.1.1Summarize
The D serie anesthesia machine adopts the PHASEIN CO2 mainstream probe to measure
the CO2 concentration.
It is intended to be connected to a patient breathing circuit for monitoring of
inspired/expired gases during anesthesia, recovery and respiratory care. It may be used
in the operating suit, intensive care unit, patient room and emergency medicine settings
for adult, pediatric and infant patients.
It is not intended to be used as the only means of monitoring a patient. It shall always be
used in combination with other vital signs monitoring devices and / or professional human
judgments of patient condition. The IRMA probe is intended to be used by trained and
authorized health care professionals only.
Warning：
 The IRMA probe is intended for use by authorized and trained medical personnel
only.
 The IRMA probe must not be used with flammable anesthetic agents.
 Disposable IRMA airway adapters shall not be reused. Reuse of the single use
adapter can cause cross infection.
 Used airway adapters shall be disposed of in accordance with local regulations for
medical waste.
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 Use only PHASEIN manufactured oxygen sensor cells. Depleted oxygen sensors
shall be disposed of in accordance with local regulations for batteries.
 Do not use the IRMA Adult/Pediatric airway adapter with infants as the adapter adds
6 ml dead space to the patient circuit.
 Do not use the IRMA infant airway adapter with adults as this may cause excessive
flow resistance.
 IRMA probe is not designed for MRI environments.
 Measurements can be affected by mobile and RF communications equipment. It
should be assured that the IRMA probe is used in the electromagnetic environment
specified in this manual.
 Do not place the IRMA airway adapter between the endotracheal tube and an elbow
as this may allow patient secretions to block the adapter windows and result in
incorrect operation.
 To keep secretions and moisture from pooling on the windows or oxygen sensor port,
always position the IRMA probe in a vertical position with the LED pointing upwards.
 Do not use the IRMA airway adapter with metered dose inhalers or nebulized
medications as this may affect the light transmission of the airway adapter windows.
 Do not try to open the oxygen sensor assembly. The oxygen sensor is a disposable
product and contains a caustic electrolyte and lead.
 The IRMA probe is intended only as an adjunct in patient assessment. It must be
used in conjunction with other assessments of clinical signs and symptoms.
 The IRMA probe is not intended to be in patient contact.
Caution：
 Never sterilize or immerse the IRMA probe in liquid.
 The IRMA oxygen sensor cell and IRMA airway adapters are non-sterile devices. Do
not autoclave the devices as this will damage them.
 Do not apply tension to the probe cable.
 Do not operate the IRMA probe outside the specified operating temperature
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environment.
 Do not leave depleted oxygen sensors mounted in the IRMA probe, even if the probe
is not in use.
6.1.2 System assembly instruction
Please follow the procedures below:
1. Plug the IRMA connector into the IRMA input of host device and switch the power on.
2. Snap the IRMA probe on top of the IRMA airway adapter. It will click into place when
properly seated.
3. A green LED indicates that the IRMA probe is ready for use.
4. Connect IRMA / airway adapter 15 mm male connector to the breathing circuit
Y-piece.
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5. Connect the IRMA / airway adapter 15mm female connector to the patient’s
endotracheal tube.
Alternatively, connect an HME (Heat Moisture Exchanger) between the patient’s
endotracheal tube and the IRMA probe. Placing an HME in front of the IRMA probe
protects the airway adapter from secretions and effects of water vapor and eliminates the
need of changing the adapter. It allows free positioning of the IRMA probe as well.
6. Unless the IRMA probe is protected with an HME always position the IRMA probe
with the status LED pointing upwards.
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Warning：
 The IRMA probe is not intended to be in patient contact.
6.1.3 Pre-use check
Always verify gas readings and waveforms on the monitor before connecting the airway
adapter to the patient circuit.
Perform the tightness check of the patient circuit with the IRMA probe snapped on the
IRMA airway adapter.
6.1.4 Zeroing procedure
Warning：
 Incorrect probe Zeroing will result in false gas readings.
In order to secure high precision of the IRMA probe measurements the following zeroing
recommendations should be followed.
Zeroing is performed by snapping a new IRMA airway adapter onto the IRMA probe,
without connecting the airway adapter to the patient circuit, and then using the host
instrument to transmit a Zero reference command to the IRMA probe.
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Special care should be taken to avoid breathing near the airway adapter before or during
the Zeroing procedure. The presence of ambient air (21% O2 and 0% CO2) in the IRMA
airway adapter is of crucial importance for a successful Zeroing.
Always perform a pre-use check after zeroing the probe.
Zeroing needs to be performed ONLY when an offset in gas values is observed, or when
an unspecified accuracy message is displayed.
Allow 10 seconds for warm up of the IRMA CO2 probe after power on and after changing
the IRMA airway adapter before proceeding with the Zeroing Procedure. The green LED
on the probe will be blinking for approximately 5 seconds while zeroing is in progress.
6.1.5 Alarms
The description of the status LED situated on the IRMA probe is as below:
Steady green light System OK

Blinking green light Zeroing in progress
Blinking red light Check adapter
6.2 SPO2 module
6.2.1 Introduction
The detecting of SpO2 adopts Pulse Oximetry. That is a method of the durative and
untraumatic detecting HbO2 saturation (functional saturation). The process is that the light
from the emitter to the receiver across patient’s part of body like finger or ear. The quantity
of penetrable light is dependent on numerous factors, the much of light is constant. But
the arterial blood changes regularly with time, because it is pulsant. The module can get
HbO2 saturation, By means of detecting the receiving light in patient pulse time, moreover
can receive “volume drawing” waveform and pulse rate
Warning:
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 If there are carboxyhaemoglobin, methemoglobin or attenuant chemical medicine,
the SpO2 value occurs error probably.
 Need to clean the SpO2 probe before used.
 Don’t put the SpO2 probe and blood pressure bond on one arm together, because
that affects the SpO2 saturation reading.
 Environment light, movement, EMI, ornaments, hemoglobin dysfunction, blood
coloration and so on can cause interference probably.
 The SpO2 detecting has no preventing defibrillation function, and don’t use with the
defibrillation equipment. That can cause interference probably.
 Clip one patient’s part no more than 2 hours, for the skin needs to get some air.
 The probe sensor should avoid shinning from troubled light in the process of
detecting SpO2.
 Please choose the type SpO2 probe to the needs of the sick before used, otherwise
the SpO2 value occurs error probably.
 Check the sensor before used, if the sensor packing or itself is damaged, don’t use.
 Don’t make the cable and sensor cable twisting together.
◆ Don’t put together the SpO2 probe on the arm which has conduit or injection syringe.
6.2.2 Connecting and operating
Detecting steps:
The SpO2 module works using probe clamping down the adult’s finger or infant’s palm or
foot. Refer to the below steps:
1) Switch on the power.
2) put the SpO2 probe on the patient’s right place.
3) Connect the SpO2 probe cable and interface.
Be shown in the following figure.
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Put the finger in the probe
Warning:
 Check the using status and skin every 2 hours in a long continuous detecting
process.
 Check the position of probe periodically in a long continuous detecting process, avoid
moving to cause error probably.
Attention:
 Choose right SpO2 probe to detect.
 Put the SpO2 probe cable on the hand, and make sure the nail face on the light from
lamp-house.
 If the detecting part can not face on the probe, that maybe cause error, even don’t
search the pulse and don’t detect, and now need to locate again.
 Move the detecting part can cause error probably, should make the patient quiet and
replace detecting part, to minimize this impact.
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Chapter 7 Maintenance
Warning：
 Please comply with the appropriate safety precautions.
 Please read all the operation and maintenance instructions of the disinfection devices
carefully.
 Please wear the safety gloves and glasses, the damages to the oxygen sensor may
result in leakage and lead to fire (contains potassium hydroxide).
 After every disassembled cleaning or reinstallation, it can be used regularly only after
the pre-use check in chapter 4.
 In order to prevent the leakage of the patient absorber system, during disassembling
and re-installing process, please pay attention to avoid damages to the components
and make sure the correctness of the installation, especially note the installation of
the seal ring; during the process of cleaning and disinfecting, please make sure the
way to clean and disinfect is applicable and correct.
 The used devices may be polluted by blood or body fluid, please apply to the
disinfection controlling and safety regulations.
 The moveable parts and removable components may have pinching or crunching
dangers, please pay more attention to those parts when moving or replacing the
system components.
 Do not use the devices with malfunctions, the machine should be maintained、
dismantled or operated only by the qualified personnel.
 After repairing, the equipment should be tested to ensure the normal function of the
equipment.
 Everyone should realize that some parts of the anesthetic-ventilator may be in danger
of infection when dismantled and cleaned.
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Caution：
 In order to prevent damages, if you have any problem about the cleanser, please see
the data provided by the manufacturer.
 Don no use abrasive cleanser. (like steel wool, silver polish or detergent)
 Place the liquids far away from the electronic components.
 Do not let liquid penetrate into the equipment.
 The soaking time of the synthetic rubber can not exceed 15 minutes, or it will lead to
expansion or accelerated aging.
 Those personnel who don’t have the experiences of repairing such equipment should
not carry out the maintenance
 Use parts produced or sold by our company to replace those broken ones, and have
a test after replacement to assure that they correspond with the specification
requirements of the manufacturer.
 Certain parts of this equipment should not be disposed in a normal way.
 All the disposable (one –off) parts should be disposed in a safe and environmental
way according to the hospital regulations.
 When taking any parts from the anesthesia machine, you should abide by the
hospital rules and regulations about taking and disposing infectiousness materials.
Because the way of cleaning, sterilizing in the Medical institutions is very different
from the practice. Therefore the Company can not satisfy all the special needs and
can not be responsible for cleaning, sterilizing or other hygienic measure taken by the
hospital during therapeutic process. We suggest that you use the effective methods
already proven in this user manual, specific equipment and steps. Other methods
may be just as effectively, but we do not guaranteed unless the Company provides
written authorization.
 We suggest that when cleaning or sterilizing, you should use drinking water at least
or more healthful water, otherwise, the result may be affected.
 Cleaning is the most important step in cleaning and sterilizing process. If you clean
the instrument improperly, it would be impossible to sterilize or high temperature
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sterilize effectively. Eliminating most of bacterium and filth by cleaning is significant
guarantee for achieving the best sterilization.
 The instrument should be cleaned and sterilized immediately after using if possible.
Filth like saliva or blood should not remain in the instrument and turn dry.
 If you need service or support, please contact with the after service department of the
Company.
7.1 Maintenance schedule

Maintenance
Maintenance
Frequency
Every patient Reusable breathing tube, manual bag, patient absorber.
Every day The anesthesia machine surface, the alarm system testing
The Pop-off valve components, BYPASS components, bellows
Every half year
components, flow sensor, batteries.
Every year The oxygen battery, vaporizer.
When cleaning
Check the parts good or not, if necessary change or repair it
and installing
Perform based on Reusable breathing tube, manual bag, patient absorber, bellows
requirement components, flow sensor.
7.2 Cleaning and disinfection
Components marked with are pressure-resistant and heat-resistant
components, like metal、glass can be disinfected with the high-temperature and
high-pressure steam, the recommended temperature is 134ºC. Use the high-pressure
steam boiler to increase the steam pressure, and the temperature is also increased to
make the bacterial albumen solidify rapidly. This method is rapid and credible. If kept in
the conditions of 1.05 kg/cm2 steam pressure and 121ºC temperature for 15 to 20 minutes,
all bacilluse and most of the sporangium will be killed. These kinds of components can
also be cleaned manually or by machines. Scrub the components of the patient system
(except the oxygen sensor) by mild detergent of which the PH value is less than 10 and
make them dry.
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Warning：
 Do not use the talc、zinc stearate, calcium carbonate, corn flour or the similar
materials to avoid conglutination. These materials may enter the patient’s lung or air
channel, causing stimulation or damages.
 Do not soak the oxygen sensor in the liquid or dispose it by high-temperature and
high pressure.
 Check if the parts have damages, replace them if necessary.
Each component on the absorber of the anesthesia machine can be cleaned and
disinfected. The methods of cleaning and disinfecting for different components are
different. Users should select the appropriate method according to the actual circs to
clean and disinfect each component of the absorber in the anesthesia machine to prevent
cross -infection of the patients while using the anesthesia machine.
AGSS is a corollary equipment of the anesthetic machine that must be cleaned and
serviced synchronously.
The methods of cleaning and disinfecting described in the form below are recommended
by our company.
The
medium The high level disinfection
Components
disinfection
A* B* C*
The breathing hose and
√
Y-connector
The flow sensor √
The bellows assembly √
Pop-off valve components √ √
Bag/Ventilator switch √ √
assembly
APL valve assembly √ √
The inspiratory and √
expiratory non-return
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valve assembly
oxygen battery √
The canister assembly √
The inspiratory and √ √
expiratory assembly
The patient absorber √ √
The reusable manual bag √ √
A*： Clean with a cloth that soaked in the mild cleanser and dry it by using a lint-free cloth;
B*：Wash it with clean water firstly, and then soak it in the water and the cleanser solution
(the recommended temperature is 40°C) for about 3 minutes, finally, clean up with clean
water and wipe it with 70% medical alcohol;
C*：The high-temperature and high-pressure steam sterilization (the maximum
temperature is 134°C).
7.3 Maintenance of the anesthesia machine surface
1. Use a wet cloth that has been soaked in the mild cleanser solution (such as the 70%
medical alcohol) to wipe the surface of the anesthesia machine;
2. After finish clean of the surface, using dry, Lint-free clothe to wipe the residual
detergent.
Warning：
 If liquid dip into the controlling components, it will damage the equipments or induce
people in danger, in the process of cleaning the surface, please make sure there is
no liquid dip into the controlling components, and disconnect the equipment and the
AC power. Reconnect the equipment to the AC power after all the parts that have
been cleaned are dry.
Caution：
 The screen must be cleaned by the cloth that is dry, soft and lint-free, can not be
cleaned by liquid.
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7.4 Maintenance of the respiration system
In order to clean and disinfect the respiration system, firstly dismantle the parts that can
be cleaned and disinfected. These parts are shown as below:
1. Bellows assembly 2. Bellows seating assembly
3. Pop-off valve 4. Gas block
5. BYPASS adapter block 6. Canister assembly
7. The upper cover main parts of the 8. Heat plate (including the Bag/Ventilator
absorber(including the APL) and non-return valve)
9. The lower cover main parts of the 10. Oxygen battery
absorber(including the manual bag
connector)
11. Flow sensor 12. Inspiratory and expiratory connector
assembly
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7.4.1 Breathing tube and manual bag
1. Disassembling:
1） Pull out all the breathing tubes that connected to the patients.
2） Remove the manual bag and place it with the tubes to the specified position for
disinfecting and depositing.
2. Cleaning and disinfection: please refer to 7.2 Cleaning and disinfection.
Caution：
 When disassembling breathing hoses, please grab the two ends of the hose to
prevent damages to the hose.
7.4.2 Bellows assembly
1. Disassembling: please refer to 3.5 Installing the folding bag and bellows housing,.
The method of disassembling is contrary to the method of installing.
7.4.3 Micro manometer and canister
1. Disassembling: please refer to 3.6 Installing the micro manometer. The method of
disassembling is contrary to the method of installing.
Warning：
 The absorbent is strong corrosive substance which can irritate the eyes、skins and
the respiration system badly. If touches the skins carelessly, please flush with clean
water for at least 15 minutes. If the irritating substance still remains after cleaning,
please seek for the doctor’s help.
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Cautions：
 The manometer of the absorber airway can not be disinfected, please take and place
it gently during the disassembling and installing process, cannot hit it violently.
 When disinfection of each component is completed, inset the manometer to its
original place separately, and a sound will be heard.
7.4.4 Pop-off valve assembly
1. Disassembling:
1） Open the absorber lock, and remove the patient absorber;
2） Unscrew the four screws 1 by hands or tools, take out the base 2 and the Pop-off
assembly 3, the diagram is shown as below:
1 1
2
3
1 1
Caution：
 The damages of the Pop-off valve may lead to the gas leakage or serious
malfunction, therefore, please be careful to maintenance it.
7.4.5 Gas block and bellows cover
1. Disassembling:
1） Unscrew the four screws 1 and the six screws 6 , take out the upper cover of the
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bellows assembly 2 and the lower cover 4;
2） Take out the gas block 5 from the heat plate. The diagram is shown as below:
1 1 3
2 3
4
1
1
3 5
3
1
1
3
3
7.4.6 BYPASS assembly
1. Disassembling: unscrew the four screws 1 by tools, and take out the BYPASS
assembly 2.
2 1
1
7.4.7 Absorber upper cover and APL
1. Disassembling: Unscrew the micro manometer 1 by a monkey wrench, and then take
out the nine screws 2. The diagram is shown as below:

5
2 3 2 2
2 2 2
4
2
1 2
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Pull the Bag/Ventilator handle 3 to the middle, and take out the upper cover 4 with the APL
assembly 5.
Caution：
 The APL assembly is fastened in the upper cover of the absorber; it can be
disinfected without being disassembled.
 If you need to disassemble it, please keep the dismantled parts to prevent loss.
7.4.8 Heat plant and the Bag/Ventilator and non-return valve
assembly
1. Disassembling: Remove the upper cover main unit, then you can easily take out the
heat plate 1 and the Bag/Ventilator assembly 2 (it is built in the heat plate, advise not
to dismantle it). Please see the diagram below:
2
1
3 3
Hold the non-return valve assembly 3 forcibly and pull out it upwards, then take out the
non-return valve.
7.4.9 Oxygen battery
1. Disassembling: please refer to 3.7 Installing the oxygen battery. The method of
disassembling is contrary to the method of installing.
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Warning:
 Do not soak the oxygen sensor to liquid or dispose it by high-temperature and high-
pressure.
 The vapor condensate on the surface of the oxygen battery will lead to failure of the
oxygen concentration measurement. Should take out the oxygen battery and clean
way the condensate on the surface and then install it to the absorber again.
7.4.10 Expiratory and inspiratory connector and flow sensor
1. Disassembling:
1） Unscrew the connector nut 1 anticlockwise by hand, hold the expiratory and
inspiratory connector 2 and pull them out with the nut 1 from the lower cover unit. The
diagram is shown as below:
1 1
2 2
2） Fasten the two button ears A of the flow sensor assembly 1, and pull out the flow
sensor slightly. Shown as below:
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1
A 1
A
7.5 IRMA probe
The IRMA probe can be cleaned using a cloth moistened with maximum 70% ethanol
or maximum 70% isopropyl alcohol.
Remove the disposable IRMA Airway Adapter prior to cleaning the IRMA probe.
Warning:
 Never sterilize or immerse the IRMA probe in liquid.
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Chapter 8 Configuration list
Warning：
 Please use accessories provided by the Company in order to avoid the inaccurate
data or equipment failure.
 The disposable accessories can be used only once, repeated using may lead to
performance degradation or cross-infection.
 If you discover that the accessories package or the accessories are damaged, do not
use the accessories.
The recommended accessories, damageable parts list:
No. Name Specification/Model

1 Oxygen battery MOX-4
2 Mask Adult/Pediatric
Adult
3 Manual bag
Pediatric（Optional）
The absorptivity is no less than
4 Sodium lime
25%
5 PHASEIN IRMA CO2 200101 (optional)
Caution：
 The accessories listed above are recommended by our company, we have no
responsibilities for the result if accessories of other specification are used.
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Appendix A Working Principle
A.1 Electrical schematic
NO. Isolation Name Isolation type Isolation description

1 A-f basic insulation Between parts of opposite polarity of the mains part.
2 A-a1 basic insulation Between mains part and the signal input/output
3 A-a1 basic insulation between the internal power supply and the grounded
protect enclosure
4 A-e double insulated between mains part and the signal input/output
5 A-a2 reinforced between mains part and the non-grounded protect
insulation enclosure
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Appendix B Product specification
B.1 Safety specification
According to USA's State Food and Drug Administration classification, this anesthesia
machine is Class III device.

ClassⅠ， Containing the internal power supply
Electric shock If you have any doubt about the integrality of the external protective
protection type grounding or the protective grounding cable, the device must be replaced
by: the internal power supply (batteries).
Electric shock
Type B
protection grade
Working mode Continuing working
Explosion protection Not providing the explosion protection (common device), do not use
grade flammable anesthetic agents.
Liquid protection grade Not providing the liquid protection (common device) －IPX0（IEC 529）.
The method of
The connection between the device and the patient is non-electrical
connecting the device
connection.
with the patient
Fixed devices: not including the anesthesia machine base and the truckle,
Moving grade including the fixed shelf;
Mobile devices: including the anesthesia machine base and truckle.
Use alcohol to clean the surface, some parts that contacted with the patient
should be dipped in the ethylene oxide, and some parts can resist to
Disinfecting method
the high temperature and high pressure steam and can be
disinfected.
After packed according to the designed method, the anesthesia machine
must meet the requirements of the test procedure 1A (requirements for
Transportation containerized cargo) of the ISTA (International Safe Transit Association).
The transporting carton must be marked with the allowable temperature、
humidity and the altitude conditions of storage.
frequency cycle range(Hz) 5~35~5
amplitude value(mm) 0.35
Frequency sweeping cycles frequency
Vibration test 15
(time)
frequency sweeping speed ≤1 octave/minute
working state Non-working state
2
acceleration (m/s ) 50
Collision test pulse duration(ms) 11±2
collision frequency (time) 1000±10
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pulse repetition frequency(Hz) 1.0~1.7

pulse waveform half sine wave
working state non-working state
Falling test Meet the requirements of IEC 60601-1, clause:21.6 (rough handling)
Meet the requirements of IEC 60601-1, clause:44.3, and the requirements
Spilled and exudates
of the non-protective devices (IPX0) in IEC 529.
Surface temperature Meet the requirements of clause:42.1,42.2 and 42.3 in IEC 60601-1
Mechanical stability Meet the requirements of the clause 24.1 in IEC 60601-1.
Meet the requirements of the clause 56.3 in IEC 60601-1 and FDA
Incompatibility of the
Reviewer Guidance for Premarket Notification Submission November1993，
external connector
i2
Shell stiffness and Meet the requirements of clause: 21a, 16a and 21b in IEC 60601-1
strength Meet the requirements of clause 55 in UL 2601-1.
Thermal conditions
Meet the requirements of clause 52.5.5 in IEC 60601-1.
deteriorate
Leakage current Meet the requirements of clause 19 in IEC 60601-1/EN 60601-1
Dielectric strength Meet the requirements of clause 20 in IEC 60601-1/EN 60601-1
Grounding impedance Meet the requirements of Clause 18 in IEC 60601-1
Protective earthing Meet the requirements of Clause 58 in IEC 60601-1
B.2 Environment specification

Climate environment
Ⅱ using in the general environment
division
Mechanical environment Ⅱ The devices that is allowed to general vibration and impact in use,
division generally refers to the devices that are easy to move.
temperature -20℃～+55℃
Storage environment humidity 10%～93%，non-condensation
atmospheric pressure 50 kPa～106 kPa
temperature 10℃～40℃
Operating environment humidity 15%～95 %，non-condensation
atmospheric pressure 70 kPa～106 kPa
B.3 Power supply specification

Parameter Specification
External AC power supply
Input voltage 100～240 VAC
Input frequency 50/60Hz
Input power 8.5A
Auxiliary mains power 100～240 VAC , 50/60Hz , 1.5A×3
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Internal battery
Battery quantity 1
Rated battery voltage 18.5VDC
Battery capability 4 Ah
It can be used for at least 10 minutes after the first alarm for low power
Shutdown delay
capability (using the new and fully charged battery).
The shortest supplying 60 min (using the new and fully charged battery, the ambient temperature
time is 25ºC).
Charging time The battery should be charged continuously for at least 10 hours for the
first time, and about 5 hours in the future.
B.4 Gas supply specification

Parameters Specification
Oxygen supply(O2) 280 kPa~600 kPa，dry and clean
Nitrous oxide supply(N2O) 280 kPa~600 kPa，dry and clean
Air supply 280 kPa~600 kPa，dry and clean
Flow rate ＞100L/min
B.5 System specification

Technical parameter Specification
Host
Rapid oxygen supplying flow rate 25～75L/min
Supplementary oxygen Non-pressure compensation, flow rate: 0～15L/min
Gas system safety pressure Not above 12.5kPa
Noise of the complete device ≤60dB
Resistant pressure of the ventilation
≥1200kPa
pipeline
Leakage from the inlet to the flow
controlling valve ≤25mL/min
Leakage from the flow controlling Under the pressure of 3 kPa, the leakage is not more than 50
valve to the common gas outlet mL/min.
Under the pressure of 3 kPa, the leakage is not more than 150
Leakage of the absorber
mL/min.
Inspiratory impedance Not above 0.4 kPa
Expiratory impedance Not above 0.4 kPa
Anesthetic ventilator
Driving mode Pneumatic electronically control
Driving gas oxygen
Driving gas pressure 0.28～0.6 Mpa
Driving gas flow rate ≤120 L/min
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Ventilation mode PCV,VCV,SIMV(V)+PS, SIMV(P)+PS,SPONT,Manual

Pressure-time; flow-time; volume-time; CO2-time(optional);
Graph
pressure-volume loop; flow-volume loop
Inspiratory oxygen concentration, tidal volume, airway pressure, breathing
Alarms frequency, end-inspiratory CO2 concentration, minute ventilation, suffocation,
continuous high pressure alarm.
Alarm sound >65dB
100mL below is：±20mL；

Tidal volume
100mL above is：±20mL or 15% of the set value, take those
with the largest error
Breathing ±2bpm or ±10% of the set value, take those with the largest
frequency error
Positive
±2cmH2O or ±10% of the set value, take those with the
end-expiratory
largest error
pressure
Pressure control
largest error
Controlling ±2cmH2O or ±10% of the set value, take those with the
Pressure support
accuracy largest error
Pressure limit
largest error
±0.1s or ±5% of the set value, take those with the largest
Inspiratory time
error
Inspiratory holding
±10% of the set value
percent
Inspiratory and
±15% of the set value
expiratory rate
±1L/min or ±10% of the set value, take those with the largest
Flow trigger
error
System The losing gas capacity caused by the system compliance (gasbag mode): adult
compliance mode≤3 mL/cmH2O, Pediatric mode≤2 mL/cmH2O
Breathing
system Inspiratory resistance:≤0.4kPa, expiratory resistance:≤0.4kPa
resistance
Flowmeter
The oxygen、Nitrous oxide, air electrical flowmeter, 1～
Three kinds of gas supplies
10L/min (20℃)。
Anesthetic vaporizer
Two-station vaporizer mounting systems with interlock function.
three anesthetic vaporizer can be selected :enflurane, isoflurane, sevoflurane

Ambient working：15～35℃；storage：-20～50℃；transport（not exceed 7 days）：-40～
temperature 60℃
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Maximum capability：250 ml
Capability Minimum capability： 30 ml
Remnants capability：60±10 ml
Safely releasing pressure：38 kPa

Pressure
Working pressure：0～5kPa
0～2% vol, 0.2% vol
Scale 2～max, 0.5% vol
off status mark “0”.
B.6 Parameter specification
B.6.1 Specification of setting parameter
parameters Pediatric adult step Working mode
20～100：mL；
20 ～ 300mL (D
5mL;
serie) VCV
100 ～ 1000 ：
Tidal volume:VT 40 ～ 300mL (C 100～1500ml SIMV(V)+PS
10mL；
serie) SPONT
1000 ～ 1500 ：
50mL
PCV
Pinsp 5～70 cmH2O 5～70 cmH2O 1cmH2O
SIMV(P)+PS
f 4～60 bpm 4～60 bpm 1 bpm VCV,PCV
SIMV(V)+PS
SIMV frequency 1～40 bpm 1～40 bpm 1bpm SIMV(P)+PS
SPONT
I:E 3:1～1:6 3:1～1:6 0.5 PCV，VCV
D serie: D serie:
OFF ， 4 ～ 30 OFF ， 4 ～ 30
cmH2O cmH2O
PEEP C serie: C serie: 1cmH2O All modes
OFF ， 4 ～ 20 OFF ， 4 ～ 20
cmH2O cmH2O
Inspiration pause OFF，5%～50% OFF，5%～50% 2% VCV

SIMV(V)+PS
Inspiration time 0.1～10.0 s 0.1～10.0 s 0.1s SIMV(P)+PS
SPONT
SIMV(V)+PS
FTRIG 1～15 L/min 1～15 L/min 1 L/min SIMV(P)+PS
SPONT
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SIMV(V)+PS
Psupp 5～60 cmH2O 5～60 cmH2O 1cmH2O SIMV(P)+PS
SPONT
VCV
Plimit （PEEP+5）～100 （PEEP+5）～100 1cmH2O SIMV(V)+PS
SPONT
B.6.2 Specification of monitoring parameter
parameter range resolution

Inspiratory tidal volume 0～2000 mL 1mL
Expiratory tidal volume 0～2000 mL 1mL
Minute ventilation 0～60 L 0.1L
Spontaneous minute ventilation 0～60 L 0.1L
Breathing frequency 0～100bpm 1bpm
Spontaneous breathing 0～99 bpm 1bpm
Frequency
I:E 3:1～1:6 0.1
The average airway pressure 0～100cmH2O 1cmH2O
PEEP 0～70cmH2O 1cmH2O
Inspiration platform pressure 0～100cmH2O 1cmH2O
Airway peek pressure -12～100 cmH2O 1cmH2O
Minimum airway pressure 0～100 cmH2O 1cmH2O
Inspiratory oxygen concentration 21%～100% 1%
Airway resistance 0～200cmH2O/(L/S) 1 cmH2O/(L/S)
Compliance 0～200mL/cmH2O 1mL/cmH2O
End-expiratory CO2(optional) 0～99mmHg 1mmHg
Inspiratory CO2(optional) 0～99mmHg 1mmHg
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B.6.3 Specification of alarm parameters
Parameters Range Step

Upper-limit alarm of the airway
1～100cmH2O 1 cm H2O
pressure
Lower-limit alarm of the airway
0～99cmH2O 1 cm H2O
pressure
Upper-limit alarm of the oxygen
21～100% 1%
concentration
Lower-limit alarm of the oxygen
OFF，21～100% 1%
concentration
Upper-limit alarm of the tidal
40～1500mL，OFF
volume
10mL；
Lower-limit alarm of the tidal
20～1500mL
volume
Upper-limit alarm of the minute
1～40L，OFF 1L
ventilation
Lower-limit alarm of the minute
OFF, 1～40L 1L
ventilation
Upper-limit alarm of the breathing
1～60 bpm 1 bpm
frequency
Lower-limit alarm of the breathing
0～60bpm 1 bpm
frequency
Upper-limit alarm of the
1～99mmHg，OFF 1mmHg
end-expiratory CO2(optional)
Lower-limit alarm of the
0～99mmHg 1mmHg
end-expiratory CO2(optional)
Suffocation alarm 10～40s 5s
Lower-limit alarm of the
70～99% 1%
SPO2(optional)
When the airway pressure is continuous above （PEEP+15）
Continuous airway pressure
cmH2O for 15 seconds
Negative pressure alarm When the airway pressure is less than（-10）cmH2O。
Oxygen supplying malfunction When the oxygen supplying pressure is less than 0.28Mpa, The
alarm alarm sound is no less than 60dB.
The insufficient battery power The battery working time is 10 minutes after alarm
B.7Hardware specification
Parameter Specification
The whole equipment
Size 1575×840×725 mm （ H×W×D）
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Weight(net weight) About 85kg

The maximum load
capacity of the top 34 kg（75lb）
shelf
Display
Type Colour TFT LCD
Size 10.1inch (D serie), 8.0 inch (C serie)
Resolution 800×600 Pixels
LED indicate
Alarm indicator one （yellow, red. If the high priority alarms and medium priority alarms happen
light at the same time, only the red light flashes.）
AC power indicator One （the indicator light is green when connected to the AC power supply）
Batery indicator One （green: the battery is full；yellow：the battery is not full）
Audio indicating
Alarm sound, key tone, the alarm sound meets the requirements of ISO
Speaker
9703-2:1992 standard.
Buzzer It gives an alarm when the system is out of order.
Controlling
Knob One knob, it can be turned clockwise / anticlockwise and pressed down
11 keys:Alarm Silence,Alarm Settings, Ventilation Settings, System Settings,
keys
System Log, Start/Standby and six parameters setting keys.
Interface
Power supply One AC power interface and three assistant output power interface
Network One Ethernet interface
Equipotential One equipotential grounding terminal
Serial port One
PS2 interface One
Mobile devices
Trolleys Four trolleys，diameter:12.5 cm
Brake
Braking board On the two front truckles, with the function of braking when trodden.
Toolbox
Drawer 150×338×308 mm （Height×Width×Depth）
Breathing system
Bellows capacity About 1500 mL
Canister capacity 1.5L
Inspiratory/ACGO port: standard outside diameter 22 mm, inner diameter
15mm, cone-shaped connector; expiratory port: standard outside diameter 22
Connections
mm, inner diameter 15mm, cone-shaped connector; manual bag: outside
diameter 22 mm.
The absorber pressure under 3 kPa, then the leakage is not more than 150
Absorber leakage
mL/min
Respiration system Inspiratory impedance：not more than 0.6 kPa ; expiratory impedance：not more
Page 104 of 117

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resistance than 0.6 kPa。

Real time clock
Range Year 2000（00:00:00）～2099（23:59:59）
Accuracy ±1 minute/month（condition: 21±3º）
Display resolution One second
Power supply Independent power supply
B.8 PHASEIN CO2 analyzer（optional）

Parameter Specifications
Measuring mode Mainstream
Operating temperature 0-40℃/ 32-104 ℉
Storage and transpjoration

-40-75℃/ -40-167 ℉
temperature
Operating humidity 10-95% RH， non-condensing
Storage and transportation

5-100 % RH，condensing
humidity
Operating atmospheric 525-1200 hPa (525hPa corresponding to an altitude of 4572 m/1500
pressure feet)
Storage and transportation
500至1200 hPa
pressure
Total system response time ＜1 second
Accuracy Range Accuracy

specifications-during 0～15 ± （0.2 vol%+ 2% of reading）
standard conditions 15～25 Unspecified
Accuracy
specifications-during ± （0.3 vol%+ 4% of reading）
all conditions
B.9 Interfering gas and vapour effect

CO2
Gas
Gas or vapor IRMA IRMA Agent N2O
level
CO2 AX+/OR+
N2O 4) 60 vol% _1&2) _1&2) _1) _1)
HAL4) 4 vol% _1) _1) _1) _1)
5 vol% +8% of _1)
ENF, ISO, SEV4) 3) _1) _1)
reading
Xe (Xenon) 4) 80 vol% -10% of reading3) _1) _1)
He(Helium) 4) 50 vol% -6% of reading3) _1) _1)
Metered dose inhaler Not for use with metered dose inhaler propellants
Page 105 of 117

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propellants4)
C2H5OH (Ethanol) 4) 0.3 vol% _1) _1) _1)
C3H7OH (Isopropanol) 4) 0.5 vol% _1) _1) _1)
CH3COCH3(Acetone) 4) 1 vol% _1) _1) _1)
CH4 (Methane) 4) 3 vol% _1) _1) _1)
CO(Carbon monoxide)5) 1 vol% _1) _1) _1)
0.02
NO(Nitrogen monoxide) 5) _1) _1) _1)
vol%
100
O25) _2) _2) _1)
vol%
Note 1: Negligible interference, effect included in the specification “Accuracy, all
conditions” above.
Note 2: For probes not measuring N2O and / or O2 the concentrations shall be set from
host according to the instructions in section 5.7 System setting (SetN2O/SetO2)
Note 3: Interference at indicated gas level. For example, 50 vol% Helium typically
decreases the CO2 readings by 6%. This means that if measuring on a mixture containing
5.0 vol% CO2 and 50 vol% Helium, the actual measured CO2 concentration will typically
be (1-0.06)*5.0 vol%=4.7 vol% CO2
Note 4: According to the EN ISO 21647:2004 standard.
Note 5: In addition to the EN ISO 21647:2004 standard.
B.10 Electromagnetic compatibility (EMC)
Electromagnetic emission
The IRMA probe is intended for use in the electromagnetic environment specified below.
The customer or the user of the IRMA probe should assure that it is used in such an
environment.
Emissions test Compliance Electromagnetic environment-guidance
RF emissions Group 1 The IRMA probe uses RF energy only for its
CISPR 11 internal function. Therefore, Its RF emissions are
very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions Class B The IRMA probe is suitable for use in all
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CLSPR 11 establishments including domestic and those
Harmonic emissions N/A directly connected to the public low-voltage
IEC 61000-3-2 power supply network that supplies buildings
Voltage fluctuations/flicker N/A used for domestic purposes.
emissions IEC 61000-3-3
Electromagnetic immunity
The IRMA probe is intended for use in the electromagnetic environment specified below.
Customers or end users of ISA gas analyzers should assure that they are used in such an
environment.
Immunity test IEC 60601 Compliance Electromagnetic
test level level environment-guidance
Electrostatic discharge ±6 kV contact ±6 kV contact Floors should be wood, concrete or
(ESD) IEC 61000-4-2 ±8 kV air ±8 kV air ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%
Electrical fast ±2 kV for power N/A AC power quality should be that of a
transient/burst supply lines typical commercial or hospital
IEC 61000-4-4 ±1 kV for environment.
input/output lines
Surge IEC 61000-4-5 ±1 kV line(s) to N/A AC power quality should be that of a
line(s) typical commercial or hospital
±2 kV line(s) to environment.
earth
1
Voltage dips, short ＜5% UT N/A The power supply quality should be the
interruptions and ( ＞ 95% dip in same as in a typical commercial or
voltage variations on UT) for 0.5 cycle hospital environment. If the user of the
power supply input 40% UT (60% dip IRMA probe requires continued operation
lines IEC 61000-4-11 in UT) for 5 during power outages, the IRMA probe
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ADS II
cycles should be powered by an uninterruptible
70% UT (30% dip power supply or a battery.
in UT) for 25
cycles
＜5% UT
( ＞ 95% dip in
UT) for 5 Sec
Power frequency 3 A/m 3 A/m Power frequency magnetic fields should
(50/60Hz) magnetic be at levels characteristic of a typical
field IEC 61000-4-8 location in a typical commercial or hospital
environment.
Conducted RF IEC 3 Vrms 150kHz 10 Vrms Portable and mobile RF communications
61000-4-6 to 80 MHz 20 V/m equipment should be used no closer to
Radiated RF IEC 3 Vrms 80 MHz any part of the IRMA probe, including
61000-4-3 to 2.5 GHz cables, than the recommended separation
distance calculated from the equation
applicable to the frequency of the
transmitter.
Recommended separation distance:
d=0.35 P
d=0.18 P 80MHz to 800 MHz
d=0.35 P 800MHz to 2.5GHz
where P is the maximum output power
rating of the transmitter in watts(W)
according to the transmitter manufacturer
and d is the recommended separation
distance in meters (m).
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Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
a
survey, should be less than the
compliance level in each frequency
b
range. interference may occur in the
vicinity of equipment marked with the
following symbol.
Note1：At 80 MHz and 800 MHz, the higher frequency range applies.
Note2: These guideline may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.

a
Field strengths from fixed transmitters, such as base stations for radio(cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV
broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic
environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which ISA is used exceeds the
applicable RF compliance level above, ISA should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the IRMA probe.

b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10
V/m.
Separation distance to RF communications equipment

In this section the recommended separation distances between portable and mobile RF
communications equipment and the IRMA probe are specified.
ISA gas analyzers are intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the IRMA probe can
help prevent electromagnetic interference by maintaining a minimum distance between
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ADS II
portable and mobile RF communications equipment(transmitters) and the IRMA probe as
recommended below, according to the maximum output power of the communications
equipment.
Rated maximum Separation distance according to frequency of transmitter [m]
output power of 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
transmitter[W]
d=0.35 P d=0.18 P d=0.34 P
0.01 0.035 0.018 0.035
0.1 0.11 0.057 0.11
1 0.35 018 0.35
10 1.1 0.57 1.1
100 3.5 1.8 3.5
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters(m) can be estimated using the equation applicable to the
frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts(W) according to the transmitter manufacturer.
Note 1: At 80MHz and 800MHz, the separation distance for the higher frequency range
applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
Warning:
 Measurements can be affected by mobile and RF communications equipment. Make
sure that the IRMA probe is used in the electromagnetic environment specified in this
manual.
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Appendix C Alarm
This chapter lists some of the most important parameters and technical alarm information,
some information may not be listed.
Note that in this chapter:
- The “L” is the default alarm level: H for the high priority; M for the medium; L for
the low;
- For each of the alarm information, there lists the corresponding solutions. If the
problem persists after operated in accordance with the solutions, please
contact with the maintenance man.

Alarm
L Reasons and solution
information
High tidal The expiratory tidal volume exceeds the upper limit of the alarm settings.
M
volume Decrease the set tidal volume or increase the alarm upper limit
The expiratory tidal volume is less than the lower limit of the alarm
Low tidal
M settings.
volume
Increase the set tidal volume or decrease the alarm lower limit.
The minute ventilation volume exceeds the upper limit of the alarm
High minute settings.
M
ventilation Decrease the set tidal volume or the respiratory frequency or increase
the alarm upper limit.
The minute ventilation volume is less than the lower limit of the alarm
Low minute settings.
M
ventilation Increase the set tidal volume or the respiratory frequency or decrease
the alarm lower limit.
High breathing The ventilation frequency exceeds the upper limit of the alarm settings.
L
frequency Decrease the set respiratory frequency or increase the alarm upper limit.
The ventilation frequency is less than the lower limit of the alarm
Low breathing settings.
L
frequency Decrease the set respiratory frequency or decrease the alarm lower
limit.
High inspiratory The FiO2 exceeds the upper limit of the alarm settings.
oxygen M Decrease the oxygen volume of the fresh gas or increase the alarm
concentration upper limit.
Low inspiratory The is less than the lower limit of the alarm settings.
oxygen H Increase the oxygen volume of the fresh gas or decrease the alarm
concentration lower limit.
High airway The airway peek pressure exceeds the upper limit of the alarm settings.
H
pressure Check if the ventilation pipeline bent or plugged up, if the pipeline
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ADS II
connection is normal, the inspiratory pressure or the tidal volume should

be decreased or increase the alarm upper limit.
The airway pressure ( pressure waveform data) is less than the lower
limit of the alarm settings.
Low airway
H Check if the ventilation pipeline leak or fall off, if the pipeline connection
pressure
is normal, the inspiratory pressure or the tidal volume should be increase
or decrease the alarm lower limit.
High
end-expiratory M The measuring value is more or less than the upper or lower limit of the
CO2 alarm settings.
Low Check the patient’s physical conditions、make sure if the patient type
end-expiratory M and the set alarm limit applicable to the patient.
CO2
The patient absorber airway pressure has been above the （PEEP+15）
continuous high
H cmH2O more than 15 seconds.
airway pressure
Check if the pipeline bent, plugged up or disconnected.
Lower than the atmospheric pressure 10cmH2O.
Check if the patient is breathing spontaneously. Increase the fresh gas
Negative
H flow. Observe whether there is high speed flow passing through the
pressure alarm
residual gas purging system. If there is, check the negative pressure
releasing valve on the receiver.
In the Settings Tapnea time, no mechanical ventilation and manual
breathing;
Suffocation H
Increase the settings of the tidal volume and respiratory frequency or
begin manual ventilation.
The oxygen source pressure is low.
Low O2 supply H
Should use or replace the backup cylinder immediately.
The battery power is low.
The system is operable, please connect it to the AC power at once.
Low battery If the power supply is cutoff, please use manual ventilation to support
M
power the patient breath.
If the batteries can not be charged fully within 24 hours, please contact
with the specified maintenance men.
The battery power is too low, and the system will shut off within three
minutes.
Please connect it to the AC power at once.
Exhausted
H If the power supply is cutoff, please use manual ventilation to support
battery power
the patient breath.
If the batteries can not be charged fully within 24 hours, please contact
with the specified maintenance men.
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Appendix D Symbol and glossary
D.1 Glossary
Abbreviation Define
AA Anesthetic agent
AGSS Anesthesia Gas Scavenging System
ACGO Auxiliary Common Gas Outlet
APL Adjustable pressure-limiting valve
ENF Enflurane
ISO Isoflurane
SEV Sevoflurane
BPM Breaths per minute
BTPS body temperature and pressure，Saturated
ATPD Ambient temperature and pressure
Manual Manual ventilation
PCV Pressure control ventilation
PSV Pressure support ventilation
SIMV Synchronized intermittent mandatory ventilation
VCV Volume control ventilation
N2O N2O
O2 Oxygen
C Compliance （Cdyn）
Paw Airway pressure
TI Inspiratory time
PEEP Positive end-expiratory pressure
Pinsp Pressure control level of inspiration
Pmean Mean airway pressure
Ppeak Peak pressure
Pplat Plateau pressure
Pmin Minimum pressure
Plimit Limit pressure
f Frequency
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ADS II
InCO2 Inspiratory CO2
EtCO2 End-Tidal CO2
Psupp Pressure support level
R Resistance
FiO2 Fractional concentration of O2 in inspired gas
TIP:TI Percentage of inspiratory plateau time in inspiratory time
VT Tidal volume
I:E Inspiratory time:Expiratory time ratio
MV Minute ventilation
MVspn Spontaneously breathed minute volume
VTE Expired tidal volume
VTI Inspired tidal volume
D.2 Equipment symbol

Attention , see the
accompanying document (this High pressure warning
manual)
Alternating current Fuse
Battery Equipotential pole
Debug serial port Alarm settings
The device is switched on The device is switched off
Ventilation settings Start / Standby
System settings Oxygen flush button
Manual ventilation Manual bag
Lock Unlock
Earthing Oxygen sensor interface
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Network interface Flowmeter knob
Cylinder N2O supply connector
pipeline Air supply connector
Light O2 supply connector
Flowmeter backlight mechanical ventilation
The maximum pressure at the The maximum pressure at

oxygen cylinder inlet the N2O cylinder inlet
The maximum load

CO2 canister capacity of the monitor
arm
Oxygen cylinder
Vaporizer
manometer
N2O cylinder manometer AGSS vent
ClassⅠ ClassⅠequipment CE mark
TYPE B equipment Heating diaphragm label
Proper disposal of products
Page 115 of 117

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D.3 Packaging symbol
THIS WAY UP FRAGILE
KEEP AWAY FROM RAIN DO NOT STACK
KEEP AWAY FROM

DO NOT ROLL
SUNLIGHT
Caution:
 Due to the different configuration, some symbols may be not entirely consistent to the
equipment, please take the equipment as valid.
Page 116 of 117

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Appendix E Default setting

This chapter lists some of the most important default settings of the anesthesia machine.
Users can not change the factory settings, but can reset the anesthesia machine to the
default settings when necessary.
E.1 Patient information
Patient information Factory default setting
Patient type adult Pediatric
Weight 65kg 7.5 kg
E.2 Default setting
Factory default setting
Patient type adult Pediatric
Respiratory parameter settings
Inspiratory time（sec） 1.7 0.7
Tidal volume VT（mL） 460 50
Breathing frequency f（bpm） 14 30
Inspiratory pause TIP:TI(%) OFF OFF
I:E 1:2.0 1:2.0
PEEP（cmH2O） OFF OFF
Flow trigger FTRIG（L/min） 2 2
Pressure controlling level Pinsp （cmH2O） 20 15
Pressure supporting level Psupp （cmH2O） 20 15
Pressure limit Plimit（cmH2O） 40 20
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E.3 Alarm default setting
Alarm default setting
Tidal volume (mL) Upper limit: OFF, lower limit:300
Minute ventilation volume (L) Upper limit:20, Lower limit:3
Respiratory frequency (bpm) Upper limit: 40, Lower limit: 0
Inspiratory oxygen concentration(%) Upper limit: OFF, Lower limit: 21
Airway pressure (cmH2O) Upper limit: 40, Lower limit: 0
End expiratory CO2 (mmHg) Upper limit: 60, Lower limit: 30
The airway pressure is >（PEEP+15）cmH2O for

Continuous airway pressure (cmH2O)
15 seconds.
Suffocation (s) Upper limit: 20
Page 118 of 117

Appendix F Reference
EN 60601-1/IEC60601-1 Medical electrical equipment Part I: General requirements for
safety
IEC 60601-2-13:2003 Medical electrical equipment Part 2: Particular requirements for the
safety and essential performance of anaesthetic systems
ISO 8835-4:2004 Inhalational anaesthetic systems- Part 3: Anaesthetic vapour delivery
devices.
EN 740 Anaesthetic workstations and their modules - Particular requirements
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Product Information

Product name：ADS II Anesthesia Machine

Devices (93/42/EEC), and meets basic requirements of appendix I in the directive.

EN55011. It meets the requirements of EN60601-1-2 standard “Medical electrical

non-compliance with the servicing requirements detailed in this manual.

deem that you have read the manual carefully.

“Caution” and “Note”.

questions, please contact the Company.

 Bold Italic: The quoted section.

 【Character】：The character string on the user interface or on the control panel.

USER’S RESPONSIBILITY ................................................................................................................... I

CONTENT ............................................................................................................................................. III

CHAPTER 1 SAFETY INFORMATION ................................................................................................ 1

1.1 WARNING ................................................................................................................................... 2

CHAPTER 2 EQUIPMENT DESCRIPTION ...................................................................................... 10

2.1 BRIEF INTRODUCTION .............................................................................................................. 10

CHAPTER 3 INSTALLATION AND CONNECTION ........................................................................ 48

3.1 POWER SUPPLY INTERFACE ....................................................................................................... 48

CHAPTER 4 PRE-USE CHECK ......................................................................................................... 62

CHAPTER 5 OPERATION AND SETTING ....................................................................................... 64

5.1 TOUCH KEY .............................................................................................................................. 64

CHAPTER 6 PHASEIN CO2 ANALYZER AND SPO2 MODULE(OPTIONAL) ............................ 75

6.1 PHASEIN CO2 ANALYZER ................................................................................................................. 75

CHAPTER 7 MAINTENANCE ............................................................................................................. 83

7.1 MAINTENANCE SCHEDULE ........................................................................................................ 85

CHAPTER 8 CONFIGURATION LIST ............................................................................................... 95

APPENDIX A WORKING PRINCIPLE .............................................................................................. 96

A.1 ELECTRICAL SCHEMATIC ................................................................................................................ 96

APPENDIX B PRODUCT SPECIFICATION ..................................................................................... 97

B.1 SAFETY SPECIFICATION .................................................................................................................. 97

APPENDIX C ALARM ..................................................................................................................... 111

APPENDIX D SYMBOL AND GLOSSARY .................................................................................... 113

D.1 GLOSSARY.................................................................................................................................... 113

APPENDIX E DEFAULT SETTING .................................................................................................. 117

E.1 PATIENT INFORMATION .................................................................................................................. 117

APPENDIX F REFERENCE .............................................................................................................. 119

Chapter 1 Safety Information

caution and Note prior to operating the anesthesia machine.

accurate and reliable, not twisted, knotted, pressed or blocked.

facilities; otherwise it may result in safety risks.

risks may occur.

operators have corresponding qualifications before using.

operated by the internal power supply.

non-flammable anesthetic described in the appendix DD of the IEC-60601-2-13 can

be used in this anesthetic system.

the inflammable or explosive environment, magnetism resonance imaging (MRI)

environment, or in the environment with other strong electromagnetism interfere.

equipment can be connected to this anesthesia machine. If peripheral equipment such

as computer、monitor、humidifier has been connected to the anaesthetic ventilator , the

whole system should meet the IEC-601-1 standard.

 Do not use flammable agent in the patient absorber.

infection if discarded randomly, and should be managed and disposed according to

the relative regulations.

anesthesia gas purifying apparatus are in good condition.

to the central air feeding system.

devices connected to it to stop their operation simultaneously.

 Do not touch the power supply so as to avoid electric shock.

not disturb others or be ignored because of the inaudible volume.