Aeonmed VG70 PDF

Appendix 5:
Beijing Aeonmed Co., Ltd.

Content
1. Product Picture
2. Data Sheet
3. User Manual
4. EC Certificate
5. EC Declaration
Product Picture
VG70
TECHNICAL DATA
Patient type：Adult and pediatric patient
Ventilation modes： VCV(A/C)
PCV(A/C)
PRVC(optional)
SIMV(VCV)+PSV
SIMV(PCV)+PSV
SIMV(PRVC)+PSV
SPONT/CPAP+PSV
BIVENT/APRV+PSV(optional)
NIV/CPAP
NIV-T
NIV-S/T
Enhancements：
Apnea ventilation
Lung mechanic
Pressure and Flow trigger
Automatic Tube Compensation (ATC)
Smart suction
Manual breath
Insp/Exp hold
Waveform freeze
Nebulization
Non-invasive ventilation (NIV)
etCO2 measurement
Parameter settings
Ventilation frequency (f)VCV： 1-80/min （adult）
2-80/min （pediatric）
NIV Ventilation frequency (f)： 4-20/min （adult）

4-40/min （pediatric）
Inspiratory time (Ti)： 0.2-9 s （adult）
0.2-5 s （pediatric）
Tidal volume (VT)： 50-2000ml （adult）
20-300ml （pediatric）
Tpause： 0-4 s （adult）
0-2.5 s （pediatric）
Ventilation frequency (f)SIMV：1-40/min
Inspiratory pressure (Pinsp): 5-70 cmH2O
Psupp： 0-70 cmH2O
Psupp NIV： 0 to（50-PEEP ）cmH2O
PEEP: 0-35 cmH2O
PEEP in NIV： 2-20 cmH2O
CPAP in NIV： 2-20 cmH2O
Rise time (Slope)： 0-2 s
O2 concentration (FiO2)： 21%-100%
Trigger sensitivity: 0.5 to 20 L/min（Flow trigger）
-20 to 0 cmH2O （Pressure trigger）
Exp. sensitivity(% of peak flow)： 5%-80%
BIVENT
Thigh： 0.2-30 s
Tlow： 0.2-30 s
Phigh： 5-60 cmH2O
Plow： 0-35 cmH2O
Automatic Tube Compensation (ATC)
Inner tube diameter： 5-12mm （adult）
2.5-8mm（pediatric）
Tube type： Endotracheal tube ET
Tracheostomy tube Trach
Degree of compensation：0-100%
Measured values displayed
Airway pressure measurement：
Plateau pressure (Pplat)
Positive end-expiratory pressure (PEEP)
Peak inspiratory pressure (Ppeak)
Mean airway pressure (Pmean)
Min. airway pressure (Pmin)
Flow measurement：
Expiratory minute volume (MVe)
Spontaneous expiratory minute volume (MVespont)
Inspiratory tidal volume (VTi)
Expiratory tidal volume (VTe)

Frequency measurement:
Total respiratory frequency (ftotal)
Spontaneous respiratory frequency (fspont)
O2 measurement:
Inspiratory O2 concentration (FiO2)
CO2 measurement
End-expiratory CO2 concentration (etCO2)
Displayed calculated values
Compliance (C)
Resistance (R)
leakNIV
RSBI
WOB
Tispont
I:E
Vdaw
PEEPi
Tc
Elastance
Curve displays： Airway pressure (t) (Paw) -20 to 100 cmH2O
Flow (t) -180 to 180 L/min
Volume (t) 0 to 3000ml
CO2 (t) 0 to 80 cmH2O
Pressure-Volume loop
Pressure-Flow loop
Flow-Volume loop
Alarms
Expiratory minute volume (MVe) High / Low
Airway pressure (Paw) High / Low
Expiratory tidal volume (Vte) low
PEEP High / Low
Insp. O2 concentration (FiO2) High / Low
(automatic)
End - expiratory CO2 concentration (etCO2) High / Low
Respiratory rate (f) High
Apnea alarm time 10 to 60 seconds, Off
Inspiration duration High
Oxygen sensor failure Yes
O2 supply pressure Low
AC failure Yes
Low battery Yes
Limited battery capacity Yes
Occlusion Yes
CO2 sensor Error/Failure
Leakage out of range Yes
Fan block Yes
Performance data
Control principle:
Electronically driven and electronically controlled
Nebulization: 30min
Suction Oxygen enrichment: Before aspiration of sputum 3 min
Post aspiration of sputum 2min
Base flow： 5-25 L/min
Max flow： 180 L/min
Leakage compensating flow: 60L/min
Operating data
Main power connection： 100V-240V, 50/60Hz
Power consumption：
110-120VAC：2A,200VAC（Ventilator only）
10A（Ventilator plus Auxiliary Outlets）
220-240VAC：1A,200VAC （Ventilator only）

8A（Ventilator plus Auxiliary Outlets）
Gas supply：
O2 gauge pressure 280-600KPa
Language:
Chinese, English, Spanish, Polish, Turkish, Russian
Other languages can be customized.
Physical Specifications
Dimensions（W*D*H）：VG70 350mm*460mm*415mm
Cart 547mm*675mm*950mm
Weight： VG70 15kg
Cart 25kg
Diagonal screen size： 12"TFT color touch screen
Input / Output ports： 2 USB ports
Real-time VGA output
1 RJ 45 Ethernet connectors
Nurse call
CO2 port
Attention
Beijing Aeonmed Co., Ltd. (hereinafter referred to as "our company") holds the copyrights to
this non-public published manual, and reserves the rights to keep it as a secure document.
Refer to this manual when operating, maintaining and repairing products only. Only our
company may provide permission for the use of or copies of this document to others.
Proprietary materials protected by the copyright law are included in this manual. No section of
it may be duplicated, copied, or translated into other languages without prior written approval
from our company who reserves the copyright.
Everything written within this manual is considered to be correct, but it is not a substitute for
the exercise of professional judgment. Our company is not legally responsible for any mistakes
printed within and/or any damages caused by incorrect installation and operation of equipment.
Our company does not supply privileges endowed by the patent law to any other parties. Our
company is not legally responsible for the results caused by patent law breaking or any rights
of the third party violating.
Any user must read this article before using the products of our company. This article exposes
the operating steps that must be read carefully. Improper use might endanger equipment or
persons. The company will not undertake the responsibility for the safety, reliability and
performance if equipment is used improperly. The company will not offer complimentary
service for misused equipment.
Our company has the right to revise any content in this manual without notice; and has no
obligation to update either hardware or software of the equipment described herein to the user
or owner.
i
Warning for use
Welcome to use our products!
In order to use this product correctly and effectively, please read these operating instructions
carefully and completely before using the product for the first time.
When using the product, always proceed in accordance with the information provided in
these operating instructions on the basis of fully understanding the information in this
manual.
This product is only for intended use as described in these operating instructions.
Only specially trained service professionals are authorized to perform the installation and
service of this product.
For any situation in the use process, please contact with us. We will provide you with warm
service.
Product specifications are subject to change without notification.
Company name: Beijing Aeonmed Co., Ltd.

Registered address: 11B2, Fengtai Science Park, 100070 Beijing, PEOPLE‟S
REPUBLIC OF CHINA
Production address: 11B2, Fengtai Science Park, 100070 Beijing, PEOPLE‟S
REPUBLIC OF CHINA
No.10, Chaobai St., Yanjiao Development Zone, 065201 Sanhe,
Hebei Province, PEOPLE‟S REPUBLIC OF CHINA
After-sales service unit: Beijing Aeonmed Co., Ltd.
After-sales service Aeonmed Mansion, No. 4 Hangfeng Road, Science City, Fengtai
address: District, Beijing.
Zip code: 100070
Company phone: 010–83681616
Fax 010–63718989
Service hotline: 800-810-8333
Company website: http://www.aeonmed.com
European Shanghai International Holding Corp. GmbH (Europe)
Representative:
Address: Eiffestrasse 80, 20537 Hamburg Germany
ii
Table of Contents
1 Introduction ..................................................................................................................... 1-1

1.1 Manufacturer‟s Responsibility..................................................................................... 1-1
1.2 Operator‟s Responsibility for Patient Safety ............................................................. 1-1
1.3 Definitions ...................................................................................................................... 1-2
1.4 Warnings, Cautions and Notes ................................................................................... 1-2
1.4.1 Warnings ................................................................................................................ 1-2
1.4.2 Cautions ................................................................................................................. 1-4
1.4.3 Notes ...................................................................................................................... 1-6
1.5 Intended Use ................................................................................................................. 1-7
1.6 Indications for Use........................................................................................................ 1-7
1.7 Contraindication ............................................................................................................ 1-7
1.8 Abbreviations and Definitions ..................................................................................... 1-8
1.9 Frequently Used functions ........................................................................................ 1-10
1.10 Symbols ....................................................................................................................... 1-10
1.11 VG70 Ventilator Quick Start Guide .......................................................................... 1-11
2 System Overview ............................................................................................................ 2-1
2.1 Ventilator Components ................................................................................................ 2-1
2.2 User Interface Components ........................................................................................ 2-2
2.2.1 GUI Screen Front Panel ...................................................................................... 2-2
2.2.2 GUI Screen Side Panel ....................................................................................... 2-3
2.3 Main Control Unit .......................................................................................................... 2-4
2.3.1 Front Panel ............................................................................................................ 2-4
2.3.2 Rear Panel ............................................................................................................. 2-5
2.4 Cart ................................................................................................................................. 2-6
2.5 Humidifier....................................................................................................................... 2-6
2.6 Cylinder Kit .................................................................................................................... 2-6
3 CO2 Module ...................................................................................................................... 3-1
3.1 CO2 Module Intended Use ......................................................................................... 3-1
3.2 CO2 Module Specifications ......................................................................................... 3-1
3.2.1 General .................................................................................................................. 3-1
3.2.2 EMC ........................................................................................................................ 3-4
3.3 System Assembly Instruction ...................................................................................... 3-8
3.3.1 Set-up ..................................................................................................................... 3-8
3.3.2 Placement of IRMA Probe................................................................................. 3-10
3.4 Pre-use Check ............................................................................................................ 3-10
3.4.1 Zeroing Procedure.............................................................................................. 3-10
3.5 Alarms .......................................................................................................................... 3-11
3.6 Cleaning ....................................................................................................................... 3-11
3.7 Warnings ...................................................................................................................... 3-11
3.8 Cautions ....................................................................................................................... 3-13
3.9 Maintenance Information ........................................................................................... 3-13
iii
4 Setup................................................................................................................................. 4-1
4.1 Connect Power Supply ................................................................................................ 4-1
4.2 Connect Gas Source.................................................................................................... 4-1
4.3 Connect Accessories ................................................................................................... 4-2
4.3.1 Install Patient circuit ............................................................................................. 4-2
4.3.2 Install Humidifier (optional).................................................................................. 4-3
4.3.3 Install Patient Circuit Positioning Arm (optional) .............................................. 4-3
4.3.4 Install User Interface Screen .............................................................................. 4-4
4.3.5 Install Cylinder Kit (optional) ............................................................................... 4-4
5 Pre-use Test ..................................................................................................................... 5-1
5.1 When to carry out pre-use test ................................................................................... 5-1
5.2 Pre-use Test Procedure ............................................................................................... 5-1
6 Ventilator Operation ........................................................................................................ 6-1
6.1 Starting Up ..................................................................................................................... 6-1
6.2 Interface Layout ............................................................................................................ 6-4
6.2.1 Standby Interface Layout .................................................................................... 6-4
6.2.2 Ventilator Interface Layout .................................................................................. 6-8
6.3 Operation of Main Manu ............................................................................................ 6-14
6.3.1 Ventilation Mode ................................................................................................. 6-14
6.3.2 Alarm Limits ......................................................................................................... 6-21
6.3.3 Monitoring Data................................................................................................... 6-25
6.3.4 Lung Mechanics.................................................................................................. 6-25
6.3.5 Log ........................................................................................................................ 6-27
6.3.6 System ................................................................................................................. 6-30
6.4 Operation of Other Shortcut Keys ............................................................................ 6-47
6.4.1 Inspiratory Hold ................................................................................................... 6-48
6.4.2 Expiratory Hold ................................................................................................... 6-49
6.4.3 Nebulizer .............................................................................................................. 6-49
6.4.4 Manual.................................................................................................................. 6-50
6.4.5 Suction ................................................................................................................. 6-51
6.4.6 Print Screen ......................................................................................................... 6-52
6.4.7 Freeze .................................................................................................................. 6-52
6.4.8 Screen Lock......................................................................................................... 6-53
6.4.9 Alarm Limits ......................................................................................................... 6-55
6.5 Ventilation Parameter Set-up .................................................................................... 6-56
6.6 Turn off the Ventilator ................................................................................................. 6-58
7 Alarms and Troubleshooting ......................................................................................... 7-1
7.1 Alarms ............................................................................................................................ 7-1
7.2 Alarm Message Table .................................................................................................. 7-1
8 User Maintenance ........................................................................................................... 8-1
8.1 Cleaning and Disinfection ........................................................................................... 8-2
8.1.1 Cleaning and Disinfecting Agents/ Autoclaving ................................................ 8-2
8.1.2 Cleaning and Disinfection Methods ................................................................... 8-3
8.1.3 Cleaning and Disinfection of Components ....................................................... 8-3
8.2 Regular Maintenance ................................................................................................... 8-5
iv
8.2.1 Maintenance Principles ....................................................................................... 8-5
8.2.2 Periodic Maintenance Schedule ...................................................................... 8-5
8.2.3 Service Life of Product/Accessories .................................................................. 8-6
8.3 Maintenance in Operation and Transportation ......................................................... 8-7
8.3.1 Transportation ....................................................................................................... 8-7
8.3.2 Storage ................................................................................................................... 8-8
8.4 Consumables Replacement ........................................................................................ 8-8
8.4.1 Fuse Replacement ............................................................................................... 8-8
8.4.2 Battery Maintenance ............................................................................................ 8-9
8.4.3 Oxygen Sensor ................................................................................................... 8-11
8.4.4 Paramagnetic Oxygen Sensor (optional) ........................................................ 8-13
8.4.5 Diaphragm Replacement................................................................................... 8-15
8.4.6 One-way Diaphragm Replacement.................................................................. 8-16
8.4.7 Fan Filter Cotton Replacement ........................................................................ 8-17
8.4.8 Filter Element of Gas Inlet Replacement ........................................................ 8-18
8.4.9 Filter Replacement(Part No.:130003930) ....................................................... 8-19
8.5 Disposal ....................................................................................................................... 8-19
9 Warranty ........................................................................................................................... 9-1
9.1 Return............................................................................................................................. 9-1
10 Theory of Operation ...................................................................................................... 10-1
10.1 Ventilation Modes ....................................................................................................... 10-1
10.1.1 Assist/Control Ventilation .................................................................................. 10-1
10.1.2 Synchronized Intermittent Mandatory Ventilation .......................................... 10-4
10.1.3 Back-up Ventilation (Apnea Ventilation) ......................................................... 10-5
10.1.4 Spontaneous/CPAP Ventilation........................................................................ 10-6
10.1.5 BiLevel Ventilation (BIVENT) ............................................................................ 10-7
10.1.6 Non Invasive/Continuous Positive Airway Pressure ..................................... 10-8
10.1.7 NIV-T .................................................................................................................. 10-10
10.1.8 NIV-S/T .............................................................................................................. 10-10
11 VG70 Ventilator System Specifications .......................................................................11-1
11.1 System ......................................................................................................................... 11-1
11.1.1 General ................................................................................................................ 11-1
11.1.2 Operating Conditions ......................................................................................... 11-2
11.1.3 Non-operating Conditions.................................................................................. 11-2
11.1.4 Power Supply ...................................................................................................... 11-2
11.2 Ventilator ...................................................................................................................... 11-3
11.2.1 General ................................................................................................................ 11-3
11.2.2 Gas Supply .......................................................................................................... 11-4
11.2.3 Patient System Connectors .............................................................................. 11-4
11.2.4 User Interface...................................................................................................... 11-4
11.2.5 Acoustic Energy .................................................................................................. 11-4
11.3 Standard Conditions Specifications ......................................................................... 11-4
11.4 Inspiratory Channel .................................................................................................... 11-5
11.5 Expiratory Channel ..................................................................................................... 11-5
11.6 Monitoring .................................................................................................................... 11-6
v
11.7 Alarms .......................................................................................................................... 11-7
11.7.1 Allowed Alarm Settings ...................................................................................... 11-7
11.7.2 Alarms Miscellaneous ........................................................................................ 11-7
11.8 Ventilation Modes ....................................................................................................... 11-8
11.8.1 Controlled Ventilation ......................................................................................... 11-8
11.8.2 Supported Ventilation......................................................................................... 11-8
11.8.3 Combined Ventilation ......................................................................................... 11-8
11.9 Trend Function ............................................................................................................ 11-9
11.10 Log Function.............................................................................................................. 11-10
11.11 Shortcut Key Functions ........................................................................................... 11-10
11.12 Communication/Interface ........................................................................................ 11-11
11.12.1 Nurse Call Port.................................................................................................. 11-11
11.12.2 Ethernet Port ..................................................................................................... 11-11
11.12.3 RS-232 Port ....................................................................................................... 11-12
11.12.4 Nebulizer Output Port ...................................................................................... 11-12
11.13 Accessories ............................................................................................................... 11-12
11.14 Ventilating Parameters: Default Values and Allowed Settings (Standard
Configuration) ........................................................................................................................... 11-13
11.15 Delivery Accuracy ..................................................................................................... 11-16
12 Pneumatic Diagram....................................................................................................... 12-1
13 EMC................................................................................................................................. 13-1
vi
1 Introduction
1 Introduction
Review all information in this manual thoroughly before attempting to use the equipment.
This equipment must be used under the supervision of a physician.
1.1 Manufacturer’s Responsibility
Our company is responsible for the security; reliability and functions of the equipment, only
when the following requirements are strictly adhered to:
 Only individuals authorized by our company may perform installation, adjustments and
repairs.
 Necessary electrical equipment and the working environment must be in accordance with
the national standards, professional standards and the requirements listed in this manual.
 Equipment must be used as instructed in this manual.
CAUTION: This equipment is not for home use.
Our company will supply service information to help the customer, under the guidance of
qualified technicians, to repair the equipment.
1.2 Operator’s Responsibility for Patient Safety
The operator of this ventilator must recognize their full responsibility for choosing appropriate
ventilation settings to ensure proper ventilation and patient safety. The responsibility for the
selection of the appropriate level of patient monitoring depends solely on the equipment
operator.
All the monitoring information is for reference only; it should not be used as the sole basis for
therapeutic or diagnostic decisions.
Whenever a patient is connected to the ventilator, constant attention by qualified medical

personnel is required in order to provide immediate corrective action in case of a malfunction
and/or alarm occurrence.
The company will provide functional block diagram at the user's request for charge,
accompanied by explanation on calibration method and other information, so as to help users
let appropriate technical staff repair the equipment part that is allowed to be maintained by
user as stipulated.
1-1
1.3 Definitions
This manual uses three special indicators to convey information of a specific nature. They
include:
WARNING: Indicates a condition that can endanger the patient or the ventilator operator.
CAUTION: Indicates a condition that can damage the equipment.
Indicates points of particular emphasis that make operation of the ventilator

NOTE:
more efficient or convenient.
1.4 Warnings, Cautions and Notes
1.4.1 Warnings
WARNING: Do not use the system until you have read and understood this manual
including:
 All connections of the system

 All warnings and cautions
 Operation procedure of each and every component of the system
 Test procedure of each and every component of the system
WARNING: The Ventilator System is intended for use by authorized and trained medical
personnel only.
WARNING: The users must familiarize themselves with the operation and use of this
machine prior to first clinical use with a patient.
WARNING: To ensure proper servicing and avoid the possibility of physical injury, only
qualified personnel should attempt to service or make authorized modifications to the

ventilator.
WARNING: An authorized service engineer must first install the ventilator and run our
company‟s installation procedure, which includes calibration of various system components,

before you connect a patient to the ventilator.
1-2
1 Introduction
WARNING: If a fault is detected in the ventilator so that its life support functions are no
longer assured: start ventilation using an independent ventilation device (resuscitation bag)
without delay, if necessary with PEEP and/or increased inspiratory O2 concentration.
WARNING: Before activating any part of the ventilator, be sure to check the equipment for
proper operation and, if appropriate, run PUT (pre-use test) as described in this manual, see
section 5.
WARNING: The ventilator is not intended to be a comprehensive monitoring device and
does not activate alarms for all types of dangerous conditions for patients on life-support
equipment.
WARNING: Patients on life-support equipment must be appropriately monitored by
competent medical personnel and suitable monitoring devices at all times.
WARNING: An alternative source of ventilation, such as manual respiratory equipment,
should always be available when using the ventilator.
WARNING: Do not connect inspiratory or expiratory circuits to the exhaust port.
WARNING: Ensure that inspiratory and expiratory circuits are connected to the correct port
before operation of equipment.
WARNING: The expiratory gas pathway may become contaminated with body fluids or
expired gases during normal use, and the inspiratory gas pathway may become contaminated
during fault condition, such as occlusion, breath hoses disconnection.
WARNING: Disposable breathing hoses shall not be reused. Reuse of the single use
hoses can cause cross infection.
WARNING: Assure that hoses used have the appropriate resistance and compliance to
ensure proper therapy.
WARNING: Do not disconnect the cable between the Main Control Unit and the GUI
screen while Ventilator is operating.
WARNING: The ventilator must not be connected to any anti-static or electrically
conductive hoses, tubing or conduit

1-3
WARNING: Adding attachments or other components or sub-assemblies to the ventilator
breathing system can change the pressure gradient across the ventilator breathing system and
that such changes to the ventilation breathing system can affect the ventilator performance.
WARNING: Expiratory module is heated; use caution to avoid burns.
WARNING: Use caution when handling flammable or fragile components.
WARNING: Do not place containers of liquids (such as humidifier water reservoirs) on top
of or above ventilator. Liquids getting into the ventilator can cause equipment malfunction with
the risk of patient injury.
WARNING: To avoid risk of electric shock, this equipment must only be connected to a
supply mains with protective earth.
1.4.2 Cautions
CAUTION: The breathing circuit must not be installed whenever the powers up and
whenever a pre-use test is performed.
CAUTION: If the system test fails, do not use the system. Attempt to troubleshoot and fix
the failure. If you are unable to fix the device, ask an authorized service representative to
repair the device.
CAUTION: Check the ventilator periodically as outlined in this manual; do not use if
defective. Immediately replace parts that are broken, missing, obviously worn, distorted, or
contaminated.
CAUTION: Do not put ventilator into service until the patient setup is complete.
CAUTION: Measurements can be affected by mobile and RF communications equipment.
CAUTION: Do not use oxygen hoses that are worn, frayed, or contaminated by
combustible materials such as grease or oils. Textiles, oils, and other combustibles are easily
ignited and burn with great intensity in air enriched with oxygen.
1-4
1 Introduction
CAUTION: Follow your hospital infection control guidelines for handling infectious material.
Our company recognizes that cleaning, sterilization, sanitation, and disinfection practices vary
widely among health care institutions. It is not possible for our company to specify or require
specific practices that will meet all needs, or to be responsible for the effectiveness of cleaning,
sterilization, and other practices carried out in the patient care setting.
CAUTION: Equipment not suitable for use in the presence of a Flammable Anesthetic
mixture with Air or with Oxygen or Nitrous Oxide.
CAUTION: To avoid an electrical shock hazard while servicing the ventilator, be sure to
remove all power to the ventilator by disconnecting the power source and turning off all
ventilator power switches.
CAUTION: To avoid a fire hazard, keep matches, lighted cigarettes, and all other sources
of ignition (e.g., flammable anesthetics and/or heaters) away from the ventilator and oxygen
hoses.
CAUTION: In case of fire or a burning odor, immediately disconnect the ventilator from the
oxygen supply, facility power and backup power source.
CAUTION: During operation, do not block: Speaker Holes, Exhaust Port, Air Inlet or
Cooling Fan.
CAUTION: Do not use the Ventilator in a MRI environment.
CAUTION: The ventilator shall not be used in a hyperbaric chamber.
CAUTION: The ventilator shall not be used with helium or mixtures with helium.
CAUTION: Tip over hazard; use care when moving ventilator mounted to cart as device
could tip over leading to injury or damage of equipment.
CAUTION: Do not use sharp objects to make selections on the LCD touch screen or panel.
CAUTION: Do not connect a VGA or USB interface while the system is in service
CAUTION: The Network interface connection is for authorized service only.
1-5
CAUTION: Batteries should be removed if equipment will not be in service for more than 6
months. See Section 8.5 for battery replacement guidance.
CAUTION: Do not immerse the oxygen sensor or the connector in any type of liquid.
CAUTION: When ventilator is exposed to conditions outside the specified operating
environment, allow 24 hours in normal environment before using.
CAUTION: Storage environment: -20℃~+60℃ and ≤95%RH.
CAUTION: Operating environment: 5℃~40℃ and 5%RH~95%RH.
CAUTION: Do not connect items that are not specified as part of the system.
CAUTION: The auxiliary outlet is only for the recommended humidifier; do not connect to
any other equipment or an additional multiple socket outlets.
CAUTION: When using a humidifier, user should frequently check the water trap and look
for water in the hose. If water is found in the hose, this water should be removed. Also, it is
important the water trap is positioned in a way such that it is lower than the patient tubes.
CAUTION: Connecting electrical equipment to auxiliary outlet effectively leads to creating
a medical equipment system, and can result in a reduced level of safety, make sure the ME
SYSTEM comply with requirements of IEC 60601-1:2005. The user who connects is
responsible for the standard for the requirements applicable to the medical equipment system.
1.4.3 Notes
NOTE: The user of this product shall have sole responsibility for any ventilator malfunction
due to operation or maintenance performed by anyone not trained by our company.
NOTE: Usage of a filter on the expiratory side will increase the resistance of the patient
circuit.
NOTE: In non-invasive (NIV) ventilation, the exhaled volume of the patient can differ from
the measured exhaled volume due to leaks around the mask
1-6
1 Introduction
NOTE: Do not sterilize or immerse the Mainstream CO2 Adapter in any fluids. See Section
3 for proper use of Mainstream CO2 Adapter.
NOTE: All parts of the ventilator system are suitable for use within the patient environment.
NOTE: All gas volume, flow, and leakage specifications in this manual are expressed at
STPD (standard temperature and pressure dry), except when specified with another condition.
1.5 Intended Use
The VG70 Ventilator System is intended to provide continuous ventilation treatment to patients
and monitoring of patients with respiratory failure or respiratory insufficiency, requiring
respiratory support.
1.6 Indications for Use
The VG70 Critical Care Ventilator is an electronically controlled, electronically powered

machine, which is used in ICU for the critical care, in Respiratory Department or Emergency
Department for the rescue and therapy of the patient with respiratory insufficiency, and in other
departments for providing respiratory support for the patient.
The Critical Care Ventilator should only be used by:
• Professional health care providers;
• Technicians that have received training in the use of this system.
The Critical Care Ventilator is applicable for the patient weighing at least 3 kg (7 lbs.), who
require the following types of ventilatory support: Positive Pressure Ventilation, delivered
invasively (by ET or Tracheotomy tube) or non-invasively (by mask) via Assist/Control, SIMV,
CPAP and other modes of ventilation.
The Critical Care Ventilator is intended for use in hospital and hospital-type facilities. It may be
used during intra-hospital transport provided that electrical power is supplied.
1.7 Contraindication
WARNING: The Ventilator is not intended for use in areas with risk of explosion. Do not
operate the ventilator in the presence of flammable anesthetics.
1-7
WARNING: The Ventilator is not designed for use in an MRI environment. Do not use the
Ventilator near an MRI machine; injury or equipment damage could result.
WARNING: To avoid risk of electric shock, this equipment must only be connected to a
mains supply with protective earth. A “hospital grade” cord must be used and connected to a
“hospital grade” electrical outlet.
NOTE: See Section 1.4 (Warnings, Cautions and Notes) for all enviromental warnings.
1.8 Abbreviations and Definitions
(S) Means Set Value
(M) Means Measured Value
CPAP Continuous Positive Airway Pressure (S)
f Breath rate (frequency) in bpm, i.e. ventilation times per minute (S)
fspont Patient‟s spontaneous respiratory frequency ( M)
ftotal Total breath rate, i.e. the sum of breath rate f and spontaneous breath rate
fspont (M)
O2 Inspiratory O2 concentration (S & M)
I:E The ratio of Inspiration to Expiration (M)
MV Expiratory minute volume (M)
MVspont Spontaneously breathed minute volume (M)
MVleak Leakage minute volume (M)
Paw Patient airway pressure (M)
PEEP Positive End-Expiratory Pressure, which can improve the patient‟s

oxygenation (S & M)
PEEPi Intrinsic Positive End-Expiratory Pressure (M)
Pinsp Upper pressure level in PCV mode (S)
Pmean Mean airway pressure. This value is updated at the end of the last respiratory
cycle, hence, is a continuous average (M)
1-8
1 Introduction
Ppeak Airway pressure peak value during one ventilatory cycle (M)
Pplat End-inspiratory airway pressure (M)
Pmin Minimum airway pressure (M)
Psens Pressure sensitivity (S)
Psupp Pressure support (S)
Phigh Upper pressure level in BIVENT and APRV (S)
Plow Lower pressure level in BIVENT and APRV (S)
Timax Maximum inspiratory time (S)
Tinsp Inspiratory Time (S)
Tpause Inspiratory Pause Time, to increase the inspiratory time to improve the
patient‟s oxygenation (S)
Trigger by flow rate (S)
VT Tidal volume of mechanical ventilation (S)
Vte Expiratory tidal volume (M)
Vti Inspiratory tidal volume (M)
Esens Expiratory trigger sensitivity (S)
ETCO2 End-expiratory CO2 concentration (M)
WOB Work of breathing (M)
Tc Time constant (M)
Leak% Leakage percentage (M)
Cdyn Dynamic compliance (M)
Cstatic Static compliance (M)
Rinsp Inspiratory resistance (M)
Rexp Expiratory resistance (M)
Elastic Elastic resistance (M)
IP21 Solid particle protection level 2; Liquid ingress protection level 1
1-9
1.9 Frequently Used functions
(1) Power On / Off Switch

(2) Connect patient hoses and gas supply
(3) Pre-Use Test
(4) Settings
(5) Start Ventilation/Standby
(6) Monitoring data
(7) Alarm, Event/Alarm log
(8) Calibration
(9) Cleaning and disinfection
(10) Breathing Circuit Components
(11) System interconnections for gas supply
(12) Humidifier and system interconnections
(13) Nebulizer and system interconnections
1.10 Symbols
Instead of illustrations, symbols may be utilized. Not all of these symbols may necessarily
appear on the equipment or in this User manual. The symbols include:
On (Power) Protection Class Type B
Off (Power) Protection Class Type BF
Follow operating instructions Warning & Caution
Protective earth ground Dangerous voltage
EQUIPOTENTIAL connection loudspeaker
Lock Manufacturer
Unlock Date of production
1-10
1 Introduction
Inspiratory hold Serial Number
Nebulization Expiratory hold
Intelligent increase of oxygen Manual inspiration
Standby Waveform freeze
AC power int. Internal Battery
USB device Refer to documentation
Prompt message Already online
Flow trigger Pressure trigger
Adult Manual trigger
NIV modes Child
Main Menu Invasive modes
Neonate Alarm Silence Key
Do not reuse Disposal of Waste
1.11 VG70 Ventilator Quick Start Guide
Review all information in the Operator‟s Manual before attempting to use this equipment.
1. Connect Power Supply
Connect to AC Power Source, DC Power Source or Utilize Battery

1-11
2. Connect Gas Source
3. Power on Ventilator
Switch Ventilator on by turning to:
4. Technical Test
5. Pre-use Test
1-12
1 Introduction
6. Select New Patient
7. Prepare Patient Circuit
8. Connect CO2 Module (optional)
9. Connect IRMA Airway Adapter (optional)
1-13
10. Set Appropriate Ventilation Settings
1-14
2 System Overview
2 System Overview
2.1 Ventilator Components
The Critical Care Ventilator System consists of two required Components: a Main Control Unit
and a Graphical User Interface (GUI). Optional Components available for the Critical Care
Ventilator system are: Cart, Battery Backup Assembly, Patient Circuit Positioning Arm, Patient
Circuit Assemblies and CO2 module, etc.
Figure 2-1 VG70 profile
1 Main Control Unit 2 Humidifier 3 Patient Circuit
4 Water Trap 5 Nebulizer Tube 6 Y-piece
7 Test Lung 8 Mask 9 Connector
Patient Circuit
10 Nebulizer Connector 11
Positioning Arm
The GUI controls ventilator settings: Settings can be selected and adjusted by using a finger
on the screen and/or the encoder knob. The GUI verifies that all combinations of settings are
obtainable and will notify the user of any setting limitations.
2-1
Breathing parameters are continuously measured by transducers and controlled by a feedback
system in the Breathing Delivery Unit. The ventilator responds to a difference between the
actual measured value of a parameter and the preset or calculated value by adjusting gas
delivery to achieve the target value.
2.2 User Interface Components
2.2.1 GUI Screen Front Panel
Figure 2-2 GUI screen front panel
1. Alarm Lamp
2. Touch Screen
3. Encoder Knob
4. Alarm Silence Hard Key
The Alarm silence hard key enables the user to silence alarms for 2 minutes. Pressing a
location on the GUI screen will either bring up a sub-menu or will highlight a ventilator
parameter or shortcut key. Rotating the encoder knob when the ventilator parameter is
selected allows the user to scroll through the available range.
2-2
2 System Overview
2.2.2 GUI Screen Side Panel
Figure 2-3 GUI screen side panel
1. Main cable: This cable connects the GUI screen and the main control unit.
CAUTION: Do not disconnect this cable when the ventilator is operating.
2. VGA interface: For connection of a VGA display which will display the same information as
the GUI screen. Display resolution of 1024*768, 60Hz is suggested.
CAUTION: Do not connect VGA interface when the system is in use on a patient.
3. USB interface: Only external storage devices of low power consumption are permissible for
this USB interface.
CAUTION: Do not connect to the USB interface when the system is in service.
4. Network Interface: For connection to external equipment such as electronic health record.
Refer to section 11.12, Communication/interface for additional information..
CAUTION: Do not connect Network Interface; only the qualified personnel can use it.
2-3
2.3 Main Control Unit
The main control unit is responsible for control of the ventilator. It has interfaces on the front
and rear panels including pneumatic and electronic interfaces.
2.3.1 Front Panel
Figure 2-4 Front panel
1. Expiratory module: To remove the Expiratory module: Press the latch (5) on the right part
of front cover (i.e. unlock it) and then take out the Expiratory module. After cleaning or high
level disinfection, insert the module in the proper position until the locking latch returns to the
locked state.
NOTE: Use caution when inserting the expiratory module to avoid leakage. A system leak
test must be done before the machine is put into patient use.
CAUTION: Expiratory module is heated to prevent water condensation, use caution due to
high temperature.
2. Exhaust port: Patient expiratory gas is released through this port to room air.
2-4
2 System Overview
CAUTION: Do not block this port.
CAUTION: Do not connect inspiratory or expiratory limb circuit to this port.
3. Expiratory port
CAUTION: Do not connect inspiratory limb circuit to this port.
4. Water trap cup: Collect condensed water to prevent it from going into expiratory valve.
5. Expiratory module latch: A latch that is used to lock or unlock the expiratory module.
WARNING: Do not operate this latch or remove the Expiratory module while the Ventilator
is in use on a patient.
6. Nebulizer output port: For nebulizer device connection.
7. Oxygen sensor cover
8. Inspiratory port: Delivers gas from the ventilator to the patient inspiratory limb hose.
CAUTION: Do not connect expiratory limb circuit to this port.
2.3.2 Rear Panel
Figure 2-5 Rear panel

2-5
1 Battery Cover 2 CO2 Module Connector 3 Nurse Call Connector
4 Air Inlet 5 Low-flow Oxygen Inlet 6 Hyperbaric Oxygen Inlet
7 Cooling Fan 8 DC Power Fuse 9 DC Power Input Port
10 Equipotential Terminal 11 Power Supply Socket 12 Power Supply Switch
CAUTION: The Equipotential Terminal is used to connect various parts of the equipment or
of a medical equipment system to the same potential. When connected, it shall comply with the
IEC 60601-1.
WARNING: Never block the ports of the exhaust cooling fan and the air inlet! Clean the
filter regularly! Ventilator should not be covered or positioned in such a way that that the
operation or performance of the Ventilator is adversely affected (e.g. positioned next to a
curtain that blocks the flow of cooling air, thereby causing the ventilator to overheat).
WARNING: Use caution when handling flammable and/or damageable components. Call
for authorized service support when necessary.
CAUTION: CO2 Module Connector is only for the specified CO2 Module, and cannot be
connected with other serial ports.
2.4 Cart
An optional cart may be used to mount the Ventilator. It applies to placing and moving the
Ventilator. The cart includes an auxiliary AC panel.
2.5 Humidifier
An optional Humidifier, like the Fisher & Paykel MR850, or similar product, should be used with
the Ventilator. Our company may supply humidifiers in your area – talk with our company‟s
Sales Representative if you need more information.
2.6 Cylinder Kit
An optional Gas Cylinder Mounting Kit is available that holds 2 US E cylinders (O2).
2-6
3 CO2 Module
3 CO2 Module
3.1 CO2 Module Intended Use
The mainstream CO2 module is intended to be connected to the Ventilator for display of real
time and derived monitoring data of CO2.
The mainstream CO2 module is intended to be connected to a patient breathing circuit for
monitoring of inspired/expired gases during recovery and respiratory care. It may be used in
the operating room, the intensive care unit, patient room and emergency medicine settings for
adult and pediatric patients.
The CO2 module is not intended to be used as the only means of monitoring a patient. It must
always be used in combination with alternate monitoring systems.
3.2 CO2 Module Specifications
3.2.1 General
Description Extremely compact infared mainstream CO2 probe.
Dimensions (WxDxH) 38 x 37 x 34 mm (1.49” x 1.45” x 1.34”)
Cable Length 2.50 m ±0.02 m
Weight < 25 g (cable excluded)
Operating temperature 0 to 40°C / 32 to 104°F
Storage and transportation temperature -40 to75°C, -40 to 167°F
Operating humidity 10 to 95% RH, non-condensing
Storage and Transportation humidity 5 to 100% RH, condensing1)
525 to 1200 hPa (525 hPa corresponding to an

Operating atmospheric pressure
altitude of 4572 m / 15000 feet)
Storage and transportation pressure 500 to 1200 hPa
Withstands repeated 1.8 m drops on a hard surface.

Mechanical strength
Complies with requirements for road ambulances
3-1
according to EN1789:2007 (clause 6.4) and
requirements for shock and vibration according to
EN ISO 80601-2-55 (clause 201.15.3.5.101).
Surface temperature (at ambient temp.

Max 41°C / 106°F
23°C)
Disposable adult/pediatric:
Adds less than 6 ml dead space;
Pressure drop less than 0.3 cmH2O @ 30 LPM.
Airway adapters
Disposable infant:
Adds less than 1 ml dead space;
Pressure drop less than 1.3 cmH2O @ 10 LPM.
NOTE 1: After being in a condensing atmosphere, the unit shall be stored for more than 24
hours in an environment equivalent to the operating humidity. The humidity range 50 ~ 100%
is valid within the temperature range of -40 to 40°C only.
Gas analyzer
Probe 2-9 channel NDIR type gas analyzer measuring at 4 to 10

µm. Pressure, temperature and full spectral interference
correction.
Calibration Zeroing recommended when changing Airway adapter.
Warm-up time Full accuracy within 10 seconds
Rise time (@ 10 l/min) ≤ 90 ms
Total system response < 3 second

time
Accuracy specifications – during standard conditions
Range 1)
Gas CO2 (%) Accuracy
CO2 0 – 15 ±(0.2 vol% + 2% of reading)

15 – 25 Unspecified
NOTE 1: Gas concentration reported in units of volume percent.
3-2
3 CO2 Module
Accuracy specifications – during all conditions1)
Gas Accuracy
CO2 ±(0.3 vol% + 4% of reading)
NOTE 1: The accuracy specification is valid for the operating temperature and humidity
conditions specified, except for interference specified in the table “Interfering gas and vapor
effects” below.
Interfering gas and vapor effects
Gas or vapor Gas level CO2
N2O 3) 60 vol% – 1)
HAL 3) 4 vol% – 1)
ENF, ISO, SEV 3) 5 vol% +8% of reading 2)
DES 3) 15 vol% +12% of readin2)
Xe (Xenon) 3) 80 vol% -10% of reading 2)
He (Helium) 3) 50 vol% -6% of reading 2)
Metered dose inhaler propellants

3) Not for use with metered dose inhaler propellants
C2H5OH (Ethanol) 3) 0.3 vol% – 1)
C3H7OH (Isopropanol) 3) 0.5 vol% – 1)
CH3COCH3 (Acetone) 3) 1 vol% – 1)
CH4 (Methane) 3) 3 vol% – 1)
CO (Carbon monoxide) 4) 1 vol% – 1)
NO (Nitrogen monoxide)4) 0.02 vol% – 1)
O2 4) 100 vol% – 1)
NOTE 1: Negligible interference, effect included in the specification “Accuracy, all
conditions” above.
NOTE 2: 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
3-3
vol% CO2 and 50 vol%. Helium, the measured CO2 concentration will typically be (1-0.06) * 5.0
vol% = 4.7 vol % CO2.
NOTE 3: According to the ISO 80601-2-55 standard.
NOTE 4: In addition to the ISO 80601-2-55 standard.
CAUTION: The presence of oxygen can cause some interference in the CO2 measurement.
This is known as spectral broadening, and must be compensated. The Ventilator performs the
O2 compensation automatically for IRMA CO2. Use valid O2 sensor, mount O2 sensor and
connect cable to ventilator correctly, maintain regularly. Otherwise etCO2 accuracy may be
affected.
CAUTION: The presence of nitrous oxide can cause some interference in the CO2
measurement. This is known as spectral broadening. The ventilator is not intended for use with
nitrous oxide gas, and there is no compensation performed. Therefore, if nitrous oxide gas is
used with the ventilator, the etCO2 accuracy will be affected.
3.2.2 EMC
Guidance and PHASEIN’s declaration – electromagnetic emissions – for IRMA probe
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
The IRMA probe uses RF energy only for its

internal function. Therefore, its RF emissions
RF emissions CISPR 11 Group 1
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions CISPR 11 Class B

The IRMA probe is suitable for use in all
Harmonic emissions IEC
Not applicable establishments including domestic and those
61000-3-2
directly connected to the public low-voltage
Voltage fluctuations/ power supply network that supplies buildings
flicker emissions IEC Not applicable used for domestic purposes.
61000-3-3
3-4
3 CO2 Module
Guidance and PHASEIN’s declaration – electromagnetic immunity – for IRMA probe
IEC 60601 test Compliance Electromagnetic environment –

Immunity test
level level guidance
Floors should be wood, concrete or

Electrostatic
±6 kV contact ±6 kV contact ceramic tile. If floors are covered
discharge (ESD) IEC
±8 kV air ±8 kV air with synthetic material, the relative
61000-4-2
humidity should be at least 30 %.
±2 kV for power
Electrical fast Mains power quality should be that
supply lines
transient/burst IEC Not applicable of a typical commercial or hospital
±1 kV for
61000-4-4 environment.
input/output lines
±1 kV line(s) to
Mains power quality should be that
line(s)
Surge IEC 61000-4-5 Not applicable of a typical commercial or hospital
±2 kV line(s) to
environment.
earth
<5 % UT (>95 %
Mains power quality should be that
dip in UT) for 0.5
of a typical commercial or hospital
cycle
Voltage dips, short environment. If the user of the
interruptions and 40 % UT (60 % dip IRMA probe requires continued
voltage variations on in UT) for 5 cycles Not applicable operation during power mains
power supply input 70 % UT (30 % dip interruptions, it is recommended
lines IEC 61000-4-11 in UT) for 25 cycles that the IRMA probe is powered
from an uninterruptible power
<5 % UT (>95 %
supply or a battery.
dip in UT) for 5 sec
Power frequency Power frequency magnetic fields

(50/60 Hz) should be at levels characteristic of
3 A/m 3 A/m a typical location in a typical
magnetic field
commercial or hospital
IEC 61000-4-8 environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
3-5
Guidance and PHASEIN’s declaration – electromagnetic immunity – for IRMA probe
IEC 60601 test Electromagnetic environment –

Immunity test Compliance level
level guidance
Portable and mobile RF

communications equipment should
be used no closer to any part of the
IRMA probe, including cables, than
the recommended separation
distance calculated from the
equation applicable to the frequency
of the transmitter.
Recommended separation
distance
80 MHz to 800 MHz
800 MHz to 2.5 GHz
Conducted RF 3 Vrms where P is the maximum output

power rating of the transmitter in
IEC 61000-4-6 150 kHz to 80 MHz 10 Vrms
watts (W) according to the
transmitter manufacturer and d is
distance in meters (m).
Radiated RF 3 V/m 20 V/m Field strengths from fixed RF

transmitters, as determined by an
IEC 61000-4-3 80 MHz to 2.5 GHz
electromagnetic site survey, a
should be less than the compliance
level in each frequency range b
Interference may occur in the
vicinity of equipment marked with
the following symbol:
3-6
3 CO2 Module
NOTE 1: At 80 MHz and 800 MHz, 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.
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 the IRMA probe is used
exceeds the applicable RF compliance level above, the IRMA probe 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.
Recommended separation distances between portable and mobile RF communications

equipment and the IRMA probe
The IRMA probe is 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 portable and mobile
RF communications equipment (transmitters) and the IRMA probe as recommended below,
according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter [m]

Rated maximum
output power of 150 kHz to 80 MHz 800 MHz to 2.5 GHz
80 MHz to 800 MHz
transmitter [W]
0.01 0.035 0.018 0.035
0.1 0.11 0.057 0.11
1 1.00 0.18 1.00
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.
3-7
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
WARNING: 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.
3.3 System Assembly Instruction
3.3.1 Set-up
1. Plug the IRMA connector into the CO2 module connector on Ventilator rear panel 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.
3-8
3 CO2 Module
4. Connect IRMA/airway adapter 15 mm male connector to the breathing circuit Y-piece.
5. Connect the IRMA/airway adapter 15 mm female connector to the patient‟s endotracheal

tube.
Alternatively, connect a HME (Heat Moisture Exchanger) between the patient‟s endotracheal
tube and the IRMA probe. Placing a 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.
3-9
6. Unless the IRMA probe is protected with a HME always position the IRMA probe with the
status LED pointing upwards.
3.3.2 Placement of IRMA Probe
When connecting IRMA probe to an infant patient circuit it is important to avoid a direct contact
between the IRMA probe and the infant‟s body.
If, for whatever the reason, the IRMA probe is in direct contact with any parts of the infant‟s
body an insulation material shall be placed between the IRMA probe and the body.
WARNING: The IRMA probe is not intended to be in patient contact.
3.4 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.
3.4.1 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.
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
3-10
3 CO2 Module
adapter is of crucial importance for a successful Zeroing. If an “ZERO_REQ” alarm should

appear directly after a Zeroing procedure, the procedure must be repeated.
Always wait at least 10 seconds after changing the IRMA adapter before running the Pre-use
test to allow the CO2 sensor to warm up.
Zeroing needs to be performed only when an offset in gas values is observed, or when an
unspecified accuracy message is displayed.
3.5 Alarms
The IRMA probe LED status is as follows:
Steady green light System OK
Blinking green light Zeroing in progress
Steady red light Sensor error
Blinking red light Check adapter
Refer to Section 8, Alarms and Troubleshooting, for EtCO2 low and high signal alarms.
3.6 Cleaning
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.
CAUTION: The airway adapters are non-sterile devices. Do not autoclave the devices as
this will damage them.
CAUTION: Never sterilize or immerse the IRMA probe in liquid.
3.7 Warnings
WARNING: The IRMA probe is intended for use by authorized and trained medical
personnel only.
WARNING: The IRMA probe must not be used with flammable anesthetic agents.
3-11
WARNING: Disposable IRMA airway adapters shall not be reused. Reuse of the single use
adapter can cause cross infection.
WARNING: Used airway adapters shall be disposed of in accordance with local regulations
for medical waste.
WARNING: Do not use the IRMA Adult/Pediatric airway adapter with infants as the adapter
adds 6 mL dead space to the patient circuit
WARNING: Do not use the IRMA Infant airway adapter with adults as this may cause
excessive flow resistance.
WARNING: Measurements can be affected by mobile and RF communications equipment.
Assure that the IRMA probe is used in the electromagnetic environment specified in this
manual.
WARNING: 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.
WARNING: To keep secretions and moisture from pooling on the windows sensor port,
always position the IRMA probe in a vertical position with the LED pointing upwards.
3-12
3 CO2 Module
WARNING: 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.
WARNING: 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.
WARNING: Incorrect probe zeroing will result in false gas readings.
WARNING: Replace the adapter if rainout/condensation occurs inside the airway adapter
WARNING: Use only PHASEIN manufactured IRMA airway adapters.
WARNING: The IRMA probe is not intended to be in patient contact.
3.8 Cautions
CAUTION: Never sterilize or immerse the IRMA probe in liquid.
CAUTION: The IRMA airway adapters are non-sterile devices. Do not autoclave the
devices as this will damage them.
CAUTION: Do not apply tension to the probe cable.
CAUTION: Do not operate the IRMA probe outside the specified operating temperature
environment.
3.9 Maintenance Information
The IRMA probe is permanently calibrated at the factory and requires verification in regular
intervals using a service reference instrument.
WARNING: Never put ventilator into service until patient setup is completed.
Clinical safety has been a major consideration in design of the machine, but operator should
still be very cautious when operating the machine.
3-13
CAUTION: In case any measured value seems suspect, operator should first examine the
patient‟s vital signs using other means, and then check the ventilator.
3-14
4 Setup
4 Setup
This section describes the installation and preparation of the ventilator.
4.1 Connect Power Supply
The machine can work with one of 2 power supply sources: internal battery and AC power
supply. An icon on the right upper part of screen displays the supply being used. When
operating on battery, all functions except the expiratory port heater, the cooling fan and the
nebulizer are the same as under AC operation. The expiratory port heater, the cooling fan and
the nebulizer are disabled in battery operation to improve battery run time. If “low battery” is
displayed when the internal or extended battery is in use, the AC power supply must be
connected to charge the battery, otherwise the Ventilator may lose power.
Figure 4-1 Install power supply cable to AC inlet
After connecting the AC power supply, the AC power supply indicator will be shown indicating
the battery is being charged. A typical charge period is 3.5 hours. The power supply indicator
is lit yellow during periods of charging, and the light goes out when the battery is fully charged.
Remove AC Power supply cord from wall connection to disconnect ventilator from AC Mains.
4.2 Connect Gas Source
Hyperbaric Oxygen Inlet of the ventilator can be connected to multiple gas sources: bottled
oxygen and central supply O2. The gas source pressure must be between 280 ~ 600 kPa (41 ~
87 psi). Low pneumatic pressure will impair some functions of the ventilator.
4-1
For Low-flow Oxygen Inlet of the ventilator, the gas source pressure must be less than 600kPa,
and the flow is less than 15L/min.
There are diameter limits on the two inlets to prevent miss-connection.
Oxygen connected to the high pressure input ports of the ventilator will be used as Fresh Gas
and will be supplied to the patient.
4.3 Connect Accessories
4.3.1 Install Patient circuit
Figure 4-2
This figure shows the connection of patient circuit, including inspiratory port, water trap,
Inspiratory tube, Y-piece, breathing hoses and expiratory filter.
CAUTION: Assure patient hoses used have the appropriate resistance so that patient
receives proper therapy.
NOTE: When adding attachments or other components to the breathing system, the
breathing resistance may increase, or the monitoring pressure of the patient connect port is
higher than the actual pressure.
4-2
4 Setup
4.3.2 Install Humidifier (optional)
Figure 4-3
Install humidifier (1) into channel of mounting block (2).
4.3.3 Install Patient Circuit Positioning Arm (optional)
Figure 4-4
Install positioning arm (1) onto mounting block (2).
4-3
4.3.4 Install User Interface Screen
Figure 4-5
Connect User Interface (1) to the location (2).
4.3.5 Install Cylinder Kit (optional)
Figure 4-6
Install O2 cylinder (2) into the right side of holder (1). Secure cylinder using strap (3). Repeat
for the other O2 cylinder on the left side.
NOTE: The kit includes only the mounting brackets and attachments. User must supply the
Gas Cylinders with Gas Regulators and hoses compatible with the VG70 Gas Inlet
Connections and at the proper Pressure per VG70 Specifications.
4-4
5 Pre-use Test
5 Pre-use Test
5.1 When to carry out pre-use test
 Before use of the Ventilator on a new patient

 After patient hose or patient filter replacement
 After maintenance or repair
WARNING: Do not use the system until you have read and understood all the operation
and maintenance manuals of the components.
WARNING: If the system test fails, do not use the system. Attempt to troubleshoot and fix
the failure. If you are unable to fix the device, ask an authorized service representative to
repair the device.
CAUTION: The following measures should be taken to minimize risks in the ventilator
system.
5.2 Pre-use Test Procedure
After power on and technical test, the machine will enter the pre-use test following display of
the power-on page. Items included: Gas supply test, Leak test, Flow sensor test, Pressure
sensor test and Safety valve test in the power-on self-test: For details on testing, please refer
to Section 6.1.
There is also a “Pre-Use Test” key on Standby screen. There are more test items in the
“Pre-Use Test” page. Items included:
Test Items Remarks
Technical Test After each system has completed its initialization technical tests will
be performed, including: voltage checks at critical points in the
circuitry; data collection necessary for system operation; test of
communication between sub-systems; tests of measurement circuits
and valve control circuits.
AC/Battery test This test will verify whether the batteries can supply enough power to
operate the ventilator normally. Please follow instructions as
5-1
Test Items Remarks
displayed.
Gas supply test Test will proceed when hyperbaric oxygen is functional.
Oxygen sensor test. This test requires that oxygen supply is available. If oxygen source is
not available then a message “oxygen source is inadequate” and the
test cannot be carried out.
Leak test Internal leakage test.
Flow sensor test Flow sensors function and accuracy test.
Pressure sensor test Pressure sensors function and accuracy test.
Safety valve test Safety valve function and accuracy test.
Patient circuit test Circuit compliance value measurement.
CO2 Sensor test Performed if a CO2 module is detected. An Alert will be posted if the
test fails.
Below is a method for testing the function of the alarm system for conditions specified by
IEC60601-2-12. Alarm system tests are to be performed at the user‟s discretion.
Perform the following procedure to verify operation of the Low MVe and High Airway pressure
alarms:
1. Set the Power switch to ON.

2. Connect a breathing circuit and test lung to the ventilator.
3. Press Start Ventilation and ventilate with default settings except set O2 to 21%.
4. After 5 breaths, observe the MVe reading on the display.
5. Set the MVe low alarm limit to a value greater than the observed MVe reading.
6. Verify that a low level MVe low alarm is present on the 3rd breath.
7. Return the MVe low alarm limit to original setting.
8. After 5 breaths, observe the Ppeak reading on the display.
9. Set the PAW upper alarm limit to a value lower than the observed Ppeak reading.
10. Verify that a low level High Airway Pressure alarm is present after 1 breath and that a high
level High Airway Pressure alarm is present at the start of the 4th breath.
11. Return the PAW upper alarm limit to original setting.
12. Set the Power switch to OFF.
5-2
6 Ventilator Operation
WARNING: Never put ventilator into service until patient setup is completed.
Clinical safety has been a major consideration in design of the machine, but operator should
still be very cautious when operating the machine.
CAUTION: In case any measured value seems suspect, operator should first examine the
patient‟s vital signs using other means, and then check the ventilator.
6.1 Starting Up
Step 1: Connect to AC power supply
Connect power supply cable to power supply socket on the wall, and the AC power supply
indicator will be lit green.
Figure 6-1 Connect power supply
Step 2: Switching on
To switch ventilator on, actuate the power switch of ventilator from “ ” to “ ”. The
machine will then be turned on; initialization of the GUI Display, Main Control unit and other
systems will start, the power-on interface and then the company logo will be displayed.
6-1
Figure 6-2 Switching on
Step 3: Technical test
After each system has completed its initialization, technical test will be performed, including
voltages tests, data tests, communications tests, AD and DA converter tests, and valve control
tests. The ventilator is not operational during this period.
The technical test should be performed for 10 seconds then wait for all results to be sent to
GUI. If all tests pass, the technical test finished and continue to the pre-use test. If some test
fail or waiting timed out, the failure information shall be displayed on screen, the “Test” and
“Skip” button‟s state will change to enable. User can choose “Test” to do technical test again,
or choose “Skip” to skip technical test.
6-2
Figure 6-3 Technical test
Step 4: Pre-use test
After the unit has finished the technical test, it shall enter into the pre-use test routine.
Test Items include: Gas supply test, Leak test, Flow sensor test, Pressure sensor test and
Safety valve test. The pre-use test is an interactive test requiring the user to read and follow
screen prompts. See Figure 6-4 for sample screen. Along the bottom of the screen shall be 2
buttons: Test and Skip.
Test Items shall be performed one by one. If all tests pass, it shall enter Standby screen. If
some tests fail, the failed information shall be displayed on screen, the “Test” button‟s state
change to enable. Choose “Test” to do the test again, or choose “Skip” to enter Standby
screen.
6-3
Figure 6-4 Pre-use Screen
NOTE: The ventilator does not support patient ventilation during the pre-use, since the
Inspiratory valve is closed, and Expiratory valve is opened.
6.2 Interface Layout
After the Power-on self-check is finished or the “Skip” key has been clicked. Press the blue key
with the text “Start ventilation” ( ) to enter the currently selected ventilation mode and
the blue key will change to orange with text “standby” on it ( ). After pressing and
holding the standby key for 4 seconds, it will go back to “Start Ventilation” again.
6.2.1 Standby Interface Layout
In the standby interface (see Figure 6-5), the user can set the information of the new patient,
see the information of the previous patient, and do the pre-use test.
6-4
Figure 6-5
6.2.1.1 New Patient
a) Patient Settings
Step 1: Choose patient type (Adult or Child, default is adult)
Step 2: Ventilation type (Invasive or NIV, default is Invasive), Patient height (default is 150cm)
and Ventilation mode. See example in Figure 6-6.
NOTE: In the Ventilation Mode area, there is an “enter” key. Pressing the “Enter” key will
enter the Mode of main menu.
6-5
Figure 6-6
b) Patient Information
Click the Patient Information key to enter patient information for a new patient. In this page, the
user can enter the patient‟s name, Medical Record Number, Admission Date, Birth Date and
Height (cm). There is a small keyboard on the right side of the Patient Information. The format
of the admission date and birth date is YYYY/MM/DD, and the default date is the computer
date. In the lower right corner, there is “Clear” key to clear all the information. See the example
in Figure 6-7.
Figure 6-7
6.2.1.2 Previous Patient
For the Previous Patient key, the same content displays as for a new patient, except the
Patient Type and Vent Type appear on the Patient Settings page and the Patient information
cannot be changed, as shown in Figure 6-8.
6-6
Figure 6-8
6.2.1.3 Pre-use Test
Click the Pre-Use test key to enter the pre-use test page. There are ten tests that must be
done before the ventilator is connected to a patient: Technical test, AC/Battery Test, Gas
Supply Test, Oxygen Test, Leak Test, Flow Sensor Test, Pressure Sensor Test, Safety Valve
Test, Patient Circuit Test, and etCO2 Sensor Test. as shown in Figure 6-9.
There is a label with “√” at the front of each test item. Touch the test item can change the
selected state of it. At the bottom of items there is a label with “√” and text “Select All”, touch it
can select all test items.
NOTE: Before the ventilator is connected to a patient, we suggest that the user do all tests.
Figure 6-9
6-7
6.2.1.4Calibration
Click the calibration key to enter the calibration page, as shown in Figure 6-10. In this page,
the user can calibrate O2 sensor and flow sensor.
Figure 6-10
6.2.2 Ventilator Interface Layout
The ventilator interface can be divided into six parts: Parameter setup area, Short Cut keys
area, Patient Measured Parameters area, Patient Waveforms area, Information area and User
Message Prompts area, as shown in Figure 6-11.
6-8
Figure 6-11
Figure 6-12shows the actual operational screen layout of the ventilator.
Figure 6-12
6-9
6.2.2.1 Information Area
The Information area includes seven sections: Ventilation Mode, Alarm Messages, Network
and USB connection, Trigger, Patient Type and weight, AC and Battery indicators, and Time.
Figure 6-13
Ventilation Mode area: Displays the current mode of Ventilation.
Alarm Messages area: When there is no alarm message, this area is same background color
as other screen areas; when a technical or functional alarm occurs, the background color will
change to either red or yellow and text information will be displayed.
Network and USB connection indicator area: Displays the Network and USB connection
status.
AC and Battery indicators area: Displays the AC, internal battery and extended battery
connection status.
Trigger area: Displays the current ventilator trigger type. There are three trigger types:
Pressure Trigger, Flow Trigger, and Manual Trigger. If there is currently no trigger in use, the
trigger symbol will disappear.
CAUTION: If the trigger sensitivity is set too high, a self-triggering (auto-triggering)
condition may be reached. Triggering will then be initiated by the system and not by the patient.
This should always be avoided by decreasing the trigger sensitivity. This is also important
during transport as the movement of the body and the breathing system may lead to false
triggering.
Patient Type and weight area: Displays the current patient‟s type ( or )
and current patient‟s weight.
Time area: Displays the current time. There are two formats, 12-hour or 24-hour.
6-10
6.2.2.2 User Message Prompts Area
If no prompt message is displayed, this area will have the same background color as other
parts of the screen. If a prompt message is available, it will have a flashing bulb icon in front of
the relevant prompt message.
Figure 6-14
6.2.2.3 Patient Waveform Area
At center of the screen, the Patient Waveforms area is the main display area. In the default
state, this area will display three waveforms: Pressure waveform, Flow waveform and Volume
waveform. See the example in Figure 6-15.
Figure 6-15
6-11
6.2.2.4 Patient Measured Parameters Area
This area displays parts of the monitored patient parameters which are very important. When
in Standby mode, the monitoring values of all parameters will be displayed as “---”. The
background color for Parameters with alarm limits will change between black and red when a
high-level alarm occurs. The flash rate will be at 2 Hz ± 10 % and it will be synchronized with
the high-level alarm displayed in the Alarm Message Area. All the parameters can be changed
to other parameters by a sub menu which on the monitor. The parameters were separated into
3 groups, each group contain 2 parameters.
The parameters shall be divided into 3 groups: Group 1, 2 and 3. See example in Figure 6-16.
Figure 6-16
6.2.2.5 Ventilation Parameter Set-up Area
The ventilation parameter setup area is at the bottom of the screen. The breathing parameters
settings necessary for the current ventilation mode are displayed in this area. See the example
as shown in Figure 6-17. If the ventilation parameter setup items for the selected Ventilation
mode do not fit in this space, the “More Settings” key will allow the user to access and change
the other setup items.
6-12
Figure 6-17
6.2.2.6 Shortcut Keys Part
The ventilator has shortcut keys to access many ventilator operations, including Inspiratory
Hold, Expiratory Hold, Nebulizer, Manual breath delivery, Suction, Print screen, Freeze,
Screen Lock, Alarm Limits, Main Menu and Standby/Start Ventilation.
6-13
Figure 6-18
6.3 Operation of Main Manu
Click “Main Manu” of the shortcut key on the right side of the screen, the user can set Mode,
Alarm Limits, Monitoring Data, Lung Mechanic, Log, System. Specific operation is as follows.
6.3.1Ventilation Mode
6.3.1.1 Ventilation Mode Set-up
Step 1: Click in the shortcut keys area to enter the Main Menu, then click
to enter mode Setup interface, as shown in Figure 6-19.
6-14
Figure 6-19
Step 2: Click the mode you want, for example:
Click [VCV] to enter the [VCV] mode setup page. The [VCV] key will become yellow as shown
in Figure 6-20. The user can then set every parameter of VCV mode.
Figure 6-20
Step 3: Click [Accept], now VCV mode is set as the ventilation mode. See Figure 6-21.
6-15
Figure 6-21
NOTE: The setup procedures of other modes are similar to the one above.
WARNING: If “Accept” is not clicked, the screen will return to the main menu, and the last
setup changes made will have no effect.
6.3.1.2 Mode Descriptions
Backup ventilation mode is included for: SPONT/CPAP+PSV, SIMV (VCV) +PSV, SIMV (PCV)
+PSV, SIMV (PRVC) +PSV, and BIVENT+PSV. To setup the PSV mode, the user must set
Psupp setting to a value not equal to 0, then “+PSV” will be added to the bottom of the mode
name, as shown in Figure 6-22. Remember that mode changes are only in effect after Accept
is pressed, as shown in Figure 6-23.
Figure 6-22
6-16
Figure 6-23
The spontaneous ventilation modes include: SPONT/CPAP+PSV, SIMV (VCV) + PSV, SIMV
(PCV) + PSV, SIMV (PRVC) + PSV, and BIVENT + PSV. The backup ventilation mode will be
PCV.
There are two measures for recovery from apnea: patient triggering and operator resetting.
When setting the above ventilation modes, the operator should set the backup ventilation
mode. The default values and the range of the parameters are shown in the Table 6-1.
Table 6-1
Factory default
Setup range Adjustment
Parameter setup
step
Adult Child Adult Child
VCV, PCV, PRVC, VCV, PCV, PRVC,

SIMV (VCV, PCV, SIMV (VCV, PCV,
PRVC) , BIVENT, PRVC) , BIVENT,
Mode PCV PCV -
SPONT/CPAP, SPONT/CPAP,
NIV/CPAP, NIV-T, NIV/CPAP, NIV-T,
NIV-S/T NIV-S/T
5mL for
under
100mL(incl.),
VT(mL) 400 80 50-2000 20-300 10mL for
over 100mL,
50mL over
1000mL
6-17
Factory default
Parameter setup
step
f(bpm) 15 30 1-80 1-80 1
f(SIMV)(bpm) 4 20 1-40 1-40 1
f(NIV-T) (bpm) 15 30 4~20 4~40 1
PEEP/Plow(cmH2
5 5 0-35 0-35 1
O)
CPAP(cmH2O) 5 5 2-20 2-20 1
O2 40% 40% 21%-100% 21%-100% 1%
Pinsp(cmH2O) in
20 10 5-(70-PEEP) 5-(70-PEEP) 1
invasive modes
Pinsp(cmH2O) in
20 10 5-(50-PEEP) 5-(50-PEEP) 1
NIV-T
Tp(s) 0 0 0-4 0-2.5 0.1
Tslope(s) 0.1 0.1 0-2 0-2 0.1
Trigger mode , , --
(cmH2O) -3 -3 -20-0 -20-0 1
( LPM) 2 2 0.5-20 0.5-20 0.5
TInsp(s) 1 0.6 0.2-9 0.2-5 0.1
I:E 1:2 1:2 1:10~4:1 1:10~4:1 0.5
Psupp (cmH2O) in
0 0 0-(70-PEEP) 0-(70-PEEP) 1
invasive modes
Psupp (cmH2O) in
0 0 0-(50-PEEP) 0-(50-PEEP) 1
NIV-S/T
Phigh(cmH2O) 15 15 5-60 5-60 1
Plow(cmH2O) 5 5 0-35 0-35 1
Thigh(s) 1 0.6 0.2-30 0.2-30 0.1
Tlow(s) 3 1.4 0.2-30 0.2-30 0.1
Esens 25% 25% 5%-80% 5%-80% 1%
High Spont Insp 1.99 + (1.99 + 0.4 sec to 0.4 sec to

0.1
Time (0.02x (0.02x (1.99 + (0.02 x (1.99 + (0.02 x
6-18
Factory default
Parameter setup
step
IBW)) IBW)) IBW)) sec IBW)) sec

sec) or sec) or
5 sec if 5 sec if
no IBW no IBW
Patient height(cm) 150 100 60-260 30-140 2
TC OFF OFF ON, OFF ON, OFF --
Compliance
ON ON ON, OFF ON, OFF --
compensation
Pipe diameter
7.5 5.0 5-12 2.5-8 0.5
(mm)
All modes in the mode menu include trigger type selection: pressure or flow. User can also set
the value for Psens or Vsens after choosing the trigger type. See Figure 6-24.
Figure 6-24
Tube compensation (TC) will be available only in pressure modes (PCV, SIMV (PCV),
SPONT/CPAP and BIVENT). Select tube compensation “On” and the “On” key will become
yellow as an acknowledgement, as shown in Figure 6-25.
6-19
Figure 6-25
Select the tube type in this interface: ET (Endotracheal Tube) or TT (Tracheotomy Tube), and
the selected one will become yellow as shown in Figure 6-25.
Tube inside diameter (mm) and Tube compensation amount (%) may be modified after being
clicked. Click “Accept” to store the new value.
When tube compensation is enabled, a message will be presented on the bottom of screen:
TC ON, as shown in Figure 6-26. Also a tube icon will display in the information area, see
Figure 6-27.
Figure 6 -26
Figure 6-27
Tube inside diameter ranges are: 5 to 12mm for adult, 2 to 5-8mm for child; increment: 0.5mm
for both adult and child.
6-20
Since the flow trigger is the default trigger mode, “pressure” is displayed on the trigger type
menu. SIMV‟s input interface is different from that of the other modes. The SIMV setup
interface is shown in Figure 6-28, and the other modes in Figure 6-29.
Figure 6-28
Figure 6-29
After the “pressure” trigger mode is selected, the Psens key can be adjusted and the Vsens key
will become gray.
6.3.2Alarm Limits
Click “Alarm Limits” in the “main menu” to enter the “Alarm Limits” menu interface, as shown in
Figure 6-30.
6-21
Figure 6-30
The Alarm Limits setting includes:
Paw: high and low limits of patient airway pressure (unit: cmH2O)
MVe: high and low limits of minute volume (unit: L)
Vte: low limit of tidal volume for Expiratory (unit: mL)
PEEP: high and low limits of positive pressure at expiratory end (unit: cmH2O)
Tapnea: apnea duration (unit: second)
fspont: high limits of rate of spontaneous breaths (unit: breath per minute)
etCO2: high and low limits of CO2 concentration at the end of Expiration (unit: mmHg)
The limit setup ranges are shown in the following table:
High limit of flow volume per minute 1 to 60L, OFF, 0.1step, default 30Lo
OFF, 0.1 to 40L, 0.1 step, default 1L for adult and 0.5L
Low limit of flow volume per minute
for child.
5 to 400mL for child, 5 to 4000mL for adult. Step: 5mL

Low limit of tidal volume for<100mL (incl.), 10mL for >100mL. Default: 250mL for
adult and 50mL for child.
Not less than PEEP+5 or PEEP+PCV (PSV)(Phigh)+5;

High limit of airway pressure
5 to 80 cmH2O, step 1 cmH2O, default 40cmH2O.
Low limit of airway pressure OFF, 1 to 60 cmH2O, step 1 cmH2O, default 5 cmH2O.
high limit of PEEP in Invasive

1 to 35 cmH2O, OFF, step 1 cmH2O, default 10 cmH2O.
Ventilation
Low limit of PEEP in Invasive OFF, 1 to 35 cmH2O, step 1 cmH2O, default OFF.
6-22
Ventilation
high limit of PEEP in NIV 1 to 20 cmH2O, OFF, step 1 cmH2O, default OFF.
Low limit of PEEP in NIV OFF, 1 to 20 cmH2O, step 1 cmH2O, default OFF.
High limit of apnea duration 10 to 60s, OFF, step 1s, default 20s.
High limit of spontaneous breath rate 10 to 80BPM, OFF. Default: OFF.
0.1%～13.3% (1mmHg～100mmHg or 0.1kPa～

High limit of etCO2
13.3kPa), default 6.5% (49mmHg or 6.5kPa).
OFF, 0.1%～13.2% (OFF, 1mmHg～99mmHg or OFF,

Low limit of etCO2
0.1kPa～13.2kPa), default 4.0% (30mmHg or 4.0kPa).
CAUTION: Do not set alarm limit parameter to extreme values that can render the alarm
system useless.
NOTE: The “default” values are manufacturer-configured alarm presets, user-configured
alarm presets can be made different from the manufacturer-configured alarm presets in
[Configurations] menu.
WARNING: A potential 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.
WARNING: When selecting “New patient”, confirm all alarm limits parameters are
appropriate prior to use on each patient
NOTE: To set alarm parameter to “OFF”, set the data display to the lowest or highest value.
Press the encoder knob, turn encoder knob one more click and confirm by pressing encoder
knob once more.
NOTE: All alarm limit setting parameters are retained during power interruption and can be
restored when power returns.

Alarm volume can be adjusted to 5 levels: 20%, 40%, 60%, 80%, 100%. The default volume is
20%.
NOTE: If [Alarm volume] requires adjustment, the procedure is as follows (the same
procedure is used for other alarm parameter setup):
Step 1: Click “Alarm volume” when the key‟s background color becomes yellow, then you can
adjust the level of alarm volume, as shown in Figure 6-31.
6-23
Figure 6-31
Step 2: Turn the encoder knob left or right to adjust the alarm volume, press the encoder knob
to confirm when proper value is reached. Background color will return to its original color, as
shown in Figure 6-32.
Figure 6-32
CAUTION: If the encoder knob is not pressed at the end, the system will go back to the
original value after 10 seconds, i.e. the new setting will have no effect.
CAUTION: In the case of an alarm during operation, the following cases may have
occurred:
1) Improper breathing parameter setting or alarm limit setting;
2) Leakage in patient circuit; turn off the machine first and then check. In case of no
resolution, contact service representative.
3) Problems with patient;
4) Power supply failure or ventilator failure.
In case there is not sufficient gas volume given to the patient, disconnect the ventilator from
the patient, use artificial respiration or other emergency devices for the patient. Check the
machine thoroughly.
6-24
6.3.3Monitoring Data
Click “Monitoring data” on main menu to enter “Monitoring data” interface. The parameters are
listed in four columns in this interface, as shown in Figure 6-33. All parameters will be also
shown in the main interface.
Figure 6-33
6.3.4Lung Mechanics
Click “Lung Mechanics” on “main menu” to enter “Lung Mechanics” page. On this page, you
can select the test items on the left (from the top down): Rinsp, C static and PEEPi. The results
of last test for the six parameters are listed on the right, as shown in Figure 6-34.
6-25
Figure 6-34
Step 1:
Click “Rinsp” to enter the test menu. The basic information is displayed in the middle of the
screen, which includes the result of last and current inspiratory Resistance measurement. The
result with date and time of last measurement is on the left, and the result of current
measurement with time and date is on the right, as shown in Figure 6-35. If the measurement
is not started, the results are “--”.
Figure 6-35
6-26
Step 2:
When the measurement is completed, current measured values with date and time will be
present. “Start” key appears again for another measurement.
NOTE: The test procedures of parameter C static and PEEPi are similar to “Rinsp”.
6.3.5Log
Click “Log” on “main menu” to enter log menu. There are two keys on the left of the page:
Event/Alarm and trend, as shown in Figure 6-36.
Figure 6-36
Step 1:
Click “Event/Alarm” on log menu to enter the submenu, as shown in Figure 6-37.
Figure 6-37
6-27
The middle area of this page is the message area. It can store up to 1000 messages, including
event messages and alarm messages. All messages will be listed in time sequence. The top is
the latest event or alarm message, and the bottom is the oldest. Use the scroll bar to check all
the messages. An asterisk (*) in front of an alarm message indicates that alarm message was
not displayed in the alarm message area. As shown in Figure 6-38. The event/alarm log
records all alarms and most actions.
Figure 6-38
Below is the message area of the Settings area resulting from highlighting an alarm. All
settings will be given here, as shown in Figure 6-39.
Figure 6-39
NOTE: Alarm/Event Log data is retained during a power interruption and can be viewed
when power returns.
Step 2:
Click “Trend” to enter trend interface. There are two trend types: graphical trend and tabular
trend, See Figure 6-40 & Figure 6-41.The default is graphical trend. Choose the tabular trend
to get more information.
In “Graphical Trend”, the first page displayed is trend map of pressure-related parameters,
including Ppeak, Pplat, PEEP, with timeline within 72h. See Figure 6-40.
6-28
Figure 6-40
Each graph shall have parameter as a title, the units of the parameter and range scale. Six
time bases shall be 1, 3, 6, 12, 24, and 72.The displayed parameter for each Trend graph shall
be selected from a pop-up menu that will give the user 8 parameters to choose from. The 8
parameter choices in the pop-up menu shall be configured in the Systems tab. “Zoom In” and
“Zoom Out” keys shall be available so that there is better resolution of the Graphs. “Left Arrow”
and “Right Arrow” keys shall be available to move a measuring line to the left or right. The
measured value shall be displayed to the right of the parameter label on the right side of each
graph. “Zoom In” shall decrease the time base. “Zoom Out” shall increase the time base. A
Tabular trend key shall be available for the user to select.
Figure 6-41
NOTE: The X-axis is timeline for all trend maps and Y-axis is the corresponding parameter
units.
The waveform on trend map is refreshed from left to right, with latest data on the very left.
Y-axis is set for full scale range display.
6-29
6.3.6System
Click “System” key to enter the System interface, as shown in Figure 6-42.
Figure 6-42
There are four keys on the left of the page: Settings, configurations, machine information and
service.
6.3.6.1 Settings
Click “settings” to enter the settings interface, as shown in Figure 6-43.
Figure 6-43
6-30
You can set the Gas standard, time and date, unit setting, and compliance compensation in
this page,
(1) Gas standard
There are two Gas Standard options available to the user: BTPS (Body Temperature and
Pressure Saturated) and ATP (Ambient Temperature and Pressure). When selected, the key
background color shall be yellow. The default is BTPS and it is chosen with a dot.
(2) Compliance compensation: ON or OFF.
(3) Dead space compensation: ON or OFF.
(4) Unit setting
Pressure unit: Two options: cmH2O and hPa. When a unit is selected, all pressure units are
converted to this unit, such as pressure unit in parameter setting area and parameter monitor
area. Default: cmH2O.
Weight unit: Two options: kg and lb. When a unit is selected, all body weight units are
converted to this unit. Default: kg
CO2 unit: Three options: mmHg, kPa and %. When a unit is selected, all CO2 units are
converted to this unit. Default: mmHg.
(5) Time and date
Date format: YYYY/MM/DD; Time format: 24hours.
When the date/time format is modified, all date/time areas on the screen will be modified
simultaneously. Modify date by clicking directly the numerical value at electronic calendar.
6.3.6.2Configurations
Click “Configurations” key to enter the configuration interface, as shown in Figure 6-44.
There are three choices in this page: Graphic Trend, Screen Brightness and Site configuration.
6-31
Figure 6-44
6.3.6.2.1 Graphic Trend
Click “Graphic Trend” to the “Graphic Trend” interface, as shown in Figure 6-45.
Figure 6-45
On this page, the Patient Measured Parameters can be set. All graphic trends recorded are
chosen from this screen. Trend 1-4 are the maps on the first page, and trend 5-8 are the maps
on the second page. Below the 8 parameter, there is a monitoring parameter list, including 18
parameters. The Trend 1-8 can be changed according to the need from the parameter list.
When a new parameter is chosen, the parameter on the main screen will be replaced at the
same time.
6-32
6.3.6.2.2 Screen Brightness
Click “Screen Brightness” to enter this page, and click the screen to choose day or night. As
shown in Figure 6-46. Day is the default.
Figure 6-46
6.3.6.2.3 Site Configuration
Step 1
Click “Site Configuration” to enter this page. Set a 4 digit numeric password in the dialog box to
have protected access to set Configuration. As shown in Figure 6-47.
Figure 6-47
6-33
Step 2
After entering the password correctly, configure the sub menu: As shown in Figure 6-48.
1) Ventilation;
2) Alarms;
3) TC;
4) Monitoring;
5) Others;
6) Network;
7) Load/Save.
Figure 6-48
(1) Ventilation
a. Settings
Click “Ventilation” key, the background color will change to yellow and the default page
“settings” will be displayed, as shown in Figure 6-48. User can configure this page for 1) Vent
Type, 2) Ventilation Mode, 3) Patient Type, 4) Start-Up value for Vt based on weight?, and 5)
Inspiratory time. Touching the key to choose the relative setting will remove the previously
selected configuration. Only one choice shall be selected per setting. A selection shall also be
provided to enable the user to restore the initial settings to factory defaults. Pressing the
“Restore” key shall immediately restore all displayed choices to their factory default.
I. Vent type: Invasive or NIV (Non-Invasive), the factory default is Invasive.
II. Ventilation Mode: VCV, PCV, PRVC, SIMV (VCV), SIMV (PCV), SIMV (PRVC), BIVENT,
and SPONT/CPAP for invasive mode, and for NIV are NIV/CPAP, NIV-T and NIV-S/T.
The factory default is PCV for Invasive mode and NIV/CPAP for NIV mode.
III. Patient Type: Adult or Child. The factory default is Adult.
IV. Start-up value for Vt based on weight? : Yes or No. The factory default is No.
6-34
V. Height: Adult or Child. The default for adult is 150cm and for child is 100cm.
VI. Inspiratory time: Tinsp or I:E. The factory default is Tinsp.
After setting all the values needed, press the “Save” key, otherwise all the settings are lost.
Another key “Restore” is under the “Save” key, pressing it restores all displayed choices to
their factory default.
b. Parameters
Selecting “Parameters” key, will display a parameters configuration page. This includes the
adult and child initial parameter settings. The user can configure for 1)Vt, 2) f, 3) Tinsp, 4)
Pinsp, 5) Tslope, 6) PEEP, and 7) Psupp 8) O2. As shown in Figure 6-49.
Figure 6-49
Each setting key represents a location that the user can select. Touching the key will change
the background color of the key, indicating that it has been chosen and can be changed by
rotating the encoder knob left or right to adjust the value. When the selection reaches its
maximum or minimum allowable setting, further rotation shall result in the minimum or
maximum value displayed continuously. Pressing the key or the encoder knob again confirms
the change.
NOTE: Touching any other keys (or touchable area), will deselect the change and the
parameter will be restored to the original setting. The background color will return to normal if
the encoder knob is not pressed within 10 seconds
After setting all the values needed, the user will press the “Save” key. Pressing the “Restore”
key restores all displayed settings to their factory default.
About the range of the parameters setting, please refer to Table 6-1.
(2) Alarms
6-35
Click the Alarms key to enter the alarms configuration page. There are two pages and six
configurable alarms on this screen: 1) Paw, 2) etCO2, 3) f spont, 4) PEEP, 5) Tapnea, 6) MVe.
See Figure 6-50.
Figure 6-50
Each setting key represents a location that the user can select. Touching the key to choose or
change the value, enter the upper and lower limits needed for each alarm, then press the Save
key to confirm. There are three configurable alarms available for the user in the second page:
1) MVe, 2) Vte. You can change the alarm limits based on whether the patient is an adult or
child, then press the Save key to save the new alarm limits.
Also there is a Restore key under the Save key. Pressing the Restore key restores all
displayed settings to their factory default. As shown in Figure 6-51.
Figure 6-51
6-36
(3) TC
Click the TC (Tube Compensation) key to enter the TC configuration page. In this page, you
can configure for 1) Tube Compensation, 2) Tube Type, 3) Compensation %,4) Diameter Adult
and 5) Diameter Child, as shown in Figure 6-52.
Figure 6-52
1) Tube compensation: ON or OFF, the factory default is OFF
2) Tube Type: ET or TT, the factory default is ET.
3) Compensation %, including Diameter Adult or Diameter Child. The range for Compensation
is 0 to 100 in 1% increments and the factory default is 0. Diameter Adult range is 5.0 to 12.0
mm and the default is 7.5 mm. Diameter Child range is 2.5 to 8.0 mm and the default is 5.0
mm.
After finishing all the settings, the user shall press the Save key. Pressing the Restore key
restores all displayed settings to their factory default.
(4) Monitoring
Click the Monitoring key to enter the Monitoring configuration page. On this page, you can
configure whether the monitoring is ON or OFF, as shown in Figure 6-53.
6-37
Figure 6-53
(5) Others
Click the “Other” key to enter the others configuration page. On this page, you can choose the
oxygen supply type, either HPO or LPO. The factory default shall be HPO. As shown in Figure
6-54.
When the Oxygen Supply Type is LPO, the ventilator should:
 Cancel the O2 high/low concentration alarm and low Oxygen Supply Pressure alarm.•
 O2 parameter adjustment shall be disabled.
 The nebulizer, suction, O2 sensor calibration functions shall be invalid.
 No Oxygen Supply Pressure monitor and calibration.
 When performing Pre Use Test, skip Gas supply test and Oxygen sensor test.
Figure 6-54
6-38
(6) Network
Ventilator data is shared by NetWork. As shown in Figure 6-55.
Figure 6-55
(7) Load/Save
Click the “Load/Save” key to enter the Load/Save configuration page. On this page, the load
button shall be load the user configuration to the machine, and the save button shall be save
the current configuration to the file which you saved.•As shown in Figure 6-56.
Figure 6-56
6-39
6.3.6.3 Service
Click “Service” to enter the “Service” page. On this page, the user needs to enter the password,
as shown in Figure 6-57.
Figure 6-57
Input the correct password to enter, There are six choices on this page: Calibration,
Event/alarm log, Machine Information, Language, Test Page, Update and Optional. The
default page is Calibration. See Figure 6-58.
Figure 6-58
6-40
6.3.6.3.1 Calibration
The calibration choices include: Pressure Sensor Calibration, Flow Sensor Calibration, O2
Sensor Calibration, CO2 Sensor Calibration, Inspiratory valve Calibration, Expiratory Valve
Calibration, Atmospheric Sensor Calibration, Touch Screen Calibration, Leak Test and Breath
Circuit test, as shown in Figure 6-59.
(1) Pressure Sensor Calibration: Click “Pressure Sensor” to enter the calibration interface.
A message is displayed: “This step is to zero the pressure sensor. Please remove the
breathing circuit from the ventilator before calibration.” A legend is displayed as well, as shown
in Figure 6-59.
Figure 6-59
Click “Start” to start pressure sensor calibration. A progress bar and a message “Calibration in
progress, please wait” will be displayed as shown in Figure 6-60. After calibration, the result
will appear: Calibration succeeded or Calibration failed. If failed, restart the calibration.
NOTE: During this period no other operation can be performed. Clicking other areas will
have no response.
6-41
Figure 6-60
(2) Flow Sensor Calibration: Click “Flow Sensor” to enter the interface. A message is
displayed: “This step is to calibrate the flow sensor. Please connect the insp. Port and Exp.
Port directly with a tube” as shown in Figure 6-61.
Figure 6-61
Click the “Start” button to start flow sensor calibration, the remaining procedure is the same as
the pressure sensor calibration.
(3) O2 Sensor Calibration: Click “O2 Sensor” to enter the interface. A message displayed:
“Please verify that the oxygen source are connected correctly. Verify that the gas inlet
pressure is within specification.” A legend will also be shown. There are two keys below the
legend: “Start 21%” and “Start 100%”. Choose the needed one and click, as shown in Figure
6-62. The remaining procedure is the same as described above.
6-42
Figure 6-62
(4) CO2 sensor Calibration: Click “CO2 Sensor” to enter the interface, as shown in Figure
6-63. A message displayed: “Disconnect the CO2 sensor with the adapter from breathing
circuit and ensure it is in ambient air. Wait 1 minute for warm up after the unit is powered on or
after installing an airway adapter. Press “Zero” when the State-Area turns green”. Please
follow the prompt message to calibrate.
Figure 6-63
(5) Inspiratory Valve Calibration: Click “Inspiratory Valve” to enter the interface. A message
displayed: “This step is to calibrate the inspiratory valve. Please connect the Insp. Port and
Exp. Port directly with a tube”, as shown in Figure 6-64.
Click the “Start” button to start inspiratory valve calibration, the remaining procedure is the
same as the pressure sensor calibration.
6-43
Figure 6-64
(6) Expiratory Valve Calibration: Click “Expiratory Valve” to enter the interface. A message
displayed: “This step is to calibrate the expiratory valve. Please connect patient circut and test
lung before calibration”, as shown in Figure 6-65.
Click the “Start” button to start expiratory valve calibration, the remaining procedure is the
same as the pressure sensor calibration.
Figure 6-65
(7) Touch Screen Calibration: Click “Touch screen” to enter the calibration interface. A
message is displayed: “This step is to calibrate the touch screen. The ventilator‟s screen will
disappear during the calibration. Please follow the instruction in the calibration program.” as
CAUTION: Please calibrate the touch screen periodically or when it works abnormally.
6-44
Figure 6-66
Click the “Start” key to start, the remaining procedure is as described in steps above.
(8) Leakage Test Calibration: Click “Leakage Test” to enter the test interface. A message is
displayed: “This step is to test the internal leakage of ventilator. Please connect the Insp. Port
and Exp. Port directly with a tube”, as shown in Figure 6-67.
Figure 6-67
Click “Start” to start the leakage test. A progress bar and a message “Test in progress, please
wait” will be displayed as shown in Figure 6-68. After test, the result will appear: Test
succeeded or Test failed. If failed, restart the test.
6-45
Figure 6-68
(9) Breath Circuit Test Calibration: Click “Breath Circuit Test” to enter the test interface. A
message is displayed: “This step is to test the compliance and leakage of breathing circuit.
Please connect the patient circuit to the T-piece, and plug up the patient end of the T-piece”,
as shown in Figure 6-69.
Before starting the test, ensure the patient circuit has been connected to the T-piece and the
patient end of the T-piece has been plugged up. Click the “Start” button to start the breath
circuit test, the remaining procedure is the same as the leakage test.
Figure 6-69
6-46
6.3.6.3.2 Event/Alarm Log
See Section 6.3.5 for detailed description.
6.3.6.3.3 Machine Information
Click the “Machine information” key to enter the Machine information page, this area includes
the following information, as shown in Figure 6-70.
1. Software Version:
a. UI
b. BDU
c. Power Supply
2. Runtime Hours
3. O2 Source Pressure
4. Atmospheric Pressure
Figure 6-70
6.3.6.3.4 Language
Click the Language button to enter the language screen. English and other languages are
available for the user to choose.
6.4 Operation of Other Shortcut Keys
The ventilator has 11 shortcut keys: Inspiratory Hold, Expiratory Hold, Nebulizer, Manual,
Suction, Print Screen, Freeze, Screen Lock, Alarm limits, Main Menu and Start
6-47
Ventilation/Standby. The shortcut keys are located on the right side of the screen, see Figure
6-71.
6.4.1 Inspiratory Hold
Inspiratory hold is available within the period of mandatory ventilation and in all modes except
full spontaneous breath modes as SPONT/CPAP+PSV, NIV/CPAP.
Press the Inspiratory Hold key during the Inspiratory phase. The operation becomes active
when a message stating “Inspiratory Hold” appears with a countdown timer. Keep pressing the
Inspiratory Hold key. The expiratory phase will not start until the key is released or after 30
seconds, whichever comes first. If the button is not released after 30 seconds, the system will
go to Expiratory state automatically and display a message “Inspiratory hold interrupted!”, as
Figure 6-71
6-48
Figure 6-72
6.4.2 Expiratory Hold
Expiratory hold is available in all modes. In Expiratory phase, press the Expiratory hold button
and the expiratory operation will become active when a message “Expiratory Hold” appears
with a countdown timer. The ventilator will stay in the expiratory phase and not transition to the
inspiratory phase until either 1) the key is released or 2) 30 seconds have elapsed.
When selected during the expiratory phase, the ventilator will stay in the expiratory phase and
not transfer to the inspiratory phase until either 1) the key is released and the current
expiratory phase is completed or 2) 30 seconds have elapsed.
Pressing the Expiratory Hold key for more than 30 seconds will cause a message to be
displayed. See example in Figure 6-73. Only one expiratory hold will be produced per key
press. When Inspiratory hold key is released or if the key is not released after 30 seconds, the
key background will revert to normal.
Figure 6-73
6.4.3 Nebulizer
The nebulizer function is available in all ventilation modes. Press the Nebulizer key turning the
key background color to yellow. Meanwhile, a low level alarm “Nebulizer On” is displayed and
the message “Nebulizer On, MM min SS s” with countdown timer is displayed in the message
area, as shown in Figure 6-74.
Figure 6-74
Nebulizer flow may be provided by high-pressure O2, and the flow rate is 6L/min±1L/min. To
ensure the delivery of tidal volume, the nebulizer is switched off when inspiratory flow rate is
less than 15L/min.
The nebulizer will start as inspiratory starts, and the nebulizer will last for the whole inspiratory
cycle. When Ventilation mode changes or if the flow is less than 15 L/min, the nebulizer
6-49
operation will be interrupted and a medium level alarm “Nebulizer Interrupted” will replace
“Nebulizer On” alarm and the countdown timer will stop.
CAUTION: During nebulization, please install the filter in front of the expiration valve to
prevent the nebulization drug from damaging the expiration flow sensor; inspect, clean and
replace the filter regularly.
The nebulizer operation will be cancelled by touching the nebulizer key for longer than 3
seconds in all ventilation modes. The user has two options to clear the “Nebulizer Interrupted”
alarm:
1) Remove the source of the shutdown and press the Nebulizer key to restart the Nebulizer
operation. Low level alarm “Nebulizer On” will replace “Nebulizer Interrupted” alarm and the
message countdown timer will continue or;
2) Acknowledge the alarm by pressing the Alarm Silence key. Nebulizer operation is cancelled
and the “Nebulizer Interrupt” alarm is cleared. Pressing the Nebulizer key during a “Nebulizer
Interrupted” condition without removing the source of the shutdown will result in the Nebulizer
not restarting.
CAUTION: The ventilator accuracy can be affected by the gas added by use of a nebulizer.
NOTE: Nebulizer function is not suggested when breath rate is less than 12, to ensure tidal
volume delivery.
NOTE: To ensure the flow volume accuracy, the nebulizer function is disabled if the flow
rate of the delivered breath is less than 15 LPM.
CAUTION: Nebulizer use is not available in noninvasive (NIV) modes.
6.4.4 Manual
Manual Trigger is available in all ventilation modes. Press the manual trigger key to initiate a
manual breath control as follows, as shown in Figure 6-75.
For VCV, PRVC, SIMV (VCV): set Vt and Tinsp, to control ventilation.
For BIVENT: set P high and Plow, to control ventilation switchover.
For PCV, SIMV (PCV): Set Pinsp, to control ventilation.
For modes or breath phase with PSV, set P supp, to control ventilation.
Manual trigger is also available during backup ventilation period. When initiated during backup
mode, the ventilator will remain in backup mode.
6-50
Figure 6-75 Figure 6-76
6.4.5 Suction
Suction support is available in ventilation modes. Pressing Suction button will turn the button
color to yellow signifying the start of Suction support as shown in Figure 6-76.
If the system detects that the circuit is disconnected, ventilation will be interrupted. During
sputum aspiration, all physiological alarms will be off and audio alarms will be suspended.
The Ventilator will provide a low flow rate when the circuit is disconnected in order to detect
reconnection of circuit. When pressing the suction support key, a message will be displayed in
the message prompt area, as shown in Figure 6-77.
Figure 6-77
The process of Suction support is performed in 3 phases as follows:
• Before aspiration of sputum – 3 minutes of increased oxygen concentration in preparation of

airway disconnection;
6-51
• Suction Phase - Airway disconnection for suction.
• Post aspiration of sputum – 2 minutes of increased oxygen concentration after reconnection

of the airway.
6.4.6 Print Screen
Print Screen shortcut soft key is between the Suction and the Freeze shortcut soft keys, as
shown in Figure 6-78. Print Screen is available after machine boot up is finished.
Figure 6-78
The Print Screen function is intended to be used with a USB Memory device attached to the
back of the monitor. With a memory device attached when the Print Screen shortcut softkey is
pressed, the system saves a copy of the screen into a JPG file and stores it on the USB device.
Each subsequent press of the Print Screen shortcut softkey will create a new JPG file with a
unique filename. If the memory stick is full, a message will be displayed stating this.
If the Print Screen shortcut soft key is pressed without a USB memory device connected, the
JPG file is saved until a USB memory device is inserted. One and only one screen capture is
saved when there is no memory device attached to the monitor.
6.4.7Freeze
Press “Freeze” key and the current real-time waveforms and loops freeze simultaneously in
the main screen when waveform drawing is completed. See example in Figure 6-79. Turing
6-52
the encoder knob moves the cursor over each point of the waveform and the corresponding
measured value is displayed. Pressing Freeze again will restart the waveform and any
information displayed during waveform freeze will disappear, and the Freeze key color returns
to normal. Waveform Freeze will automatically end 3 minutes after touching the freeze key.
Figure 6-79
6.4.8 Screen Lock
Press the “Screen Lock” button, displaying a message in the message prompt area. Press and
hold Screen Lock for 3 seconds to lock the screen, as shown in Figure 6-80. 3 seconds later,
the background color of Screen lock key will turn to yellow and all keys on the touch screen are
locked. Instead of the pre-message, a new message is displayed in the message prompt area
“Screen Locked. Press Screen Lock for 3 seconds to unlock the screen as shown in Figure
6-81.
6-53
Figure 6-80
Figure 6-81
6-54
Holding for 3 seconds, the screen lock is cleared, the background color of Screen Lock key
turns to normal and a message ”Screen Unlocked” is displayed in message prompt area as
Figure 6-82
6.4.9 Alarm Limits
Press the “Alarm limits” button to enter the alarm limits page in the main menu, as shown in
Figure 6-83. For detail information and operation refer to Section 6.3.2.
Figure 6-83
6-55
6.5 Ventilation Parameter Set-up
NOTE: If ventilation parameter setup keys are not visible along bottom of screen, close the
main menu by pressing Main Menu key. See ventilation parameter setup in the main screen as
Figure 6-84
Press the parameter key, turning it yellow. Rotate the encoder knob left or right to modify the
parameter value. Press the parameter key again or press the encoder knob to confirm the
modified value. If any other area on the screen is touched before confirmation, the new
parameter selection is canceled and the previous value will be displayed. As shown in Figure
6-85.
6-56
Figure 6-85
When ventilation mode is changed, the values of the parameter keys displayed will change to
correspond to the new ventilation mode.
CAUTION: If the encoder knob is not pressed for confirmation, the previous value will be
displayed.
The following conditions should be noticed in parameter setting:
a) In order to make parameter setting more safe and reasonable, interlock mode is used for
tidal volume VTI, ventilator rate and inspiratory time TI setting. In case any one of the three
parameters cannot be adjusted to required value within limits, modify the other two first.
b) Pressure parameter setting is subject to high pressure limit.
c) PSUPP and PINSP are relative pressure to PEEP.
6-57
6.6 Turn off the Ventilator
(1) Disconnect the breathing hoses from the patient.
(2) Return back to Standby by pressing the Standby key for more than 3 seconds.
(3) Turn off the power switch
(4) Disconnect the gas supply.
(5) Disconnect the power cord from the power supply
NOTE: Detachable power cord is a means to isolate circuits electrically from AC supply on
all poles simultaneously.
6-58
7 Alarms and Troubleshooting
WARNING: Only authorized person is permitted to perform maintenance.
7.1 Alarms
CAUTION: In case of alarm, monitor and support the patient first, then carry out
troubleshooting later.
An alarm message will appear in alarm information area and alarm indicator will light up. The
different colors of alarm in alarm area indicate different priority levels: red is high level (!!!, red
indicator flash), yellow is medium (!!, yellow indicator flash) or low level (!, yellow indicator
constantly lit).
The operator may be positioned anywhere around the unit to view the alarm light. The alarm
light is visible from a distance of 3 meters. To observe the alarm messages the operator
position must be in front of the display and within a distance of 1 meter.
7.2 Alarm Message Table
CAUTION: Monitor and support the patient first in case of alarm and perform
troubleshooting later.
CAUTION: Operation instructions are not included in the table.
CAUTION: Except for the normal alarm settings, other default alarm settings are changed
only by changing the control program and restricted access to changing or to the storage of
changes.
CAUTION: If alarm occurs, protect patient safety first, and then go to diagnose fault or
service it necessarily.
WARNING: Never leave patient unattended when alarm silence is activated.
7-1
NOTE: In the table below, L means low level, M means medium level, and H means high
lever; for the same level, the bigger the alarm number, the higher the alarm level, such as L2
level is higher than L1 level.
Alarm
Priority Type Cause Remedy
Message
Airway Pressure exceeds the

setting limit within one Airway pressure is
ventilation. lower than the
High Airway When the airway pressure alarm limit for
L1 Physiological
Pressure exceeds the setting value, the three consecutive
inspiratory phase changes into cycles or at most
the expiratory phase within 200 15sec.
ms and the pressure shall be
reduced below PEEP level.
The measured
The measured minute volume
minute volume
leak MVLEAK is higher than the
leak MVLEAK is in
minute volume measured on the
Leakage L2 Physiological normal range for 3
expiration path for 3 consecutive
consecutive
ventilation cycles or for 10
breaths or for 10
seconds.
seconds.
Low Oxygen Oxygen source is lower than Oxygen supply is

L3 Physiological
Supply 160kPa O2 is set to 21%. above 160kPa.
Pressure
When no battery
is supplied or
battery is invalid,
the power fault
alarm is of
During ventilator operation, high-priority and
when an AC power failure occurs lasts for longer
and there is no battery power, than 120s.
AC Failure L4 Technical the power board will alarm for When battery is
120 seconds minimum. When supplied,
powered from batteries, an “AC produces a
Failure” alarm would occur. low-level alarm
and gives the
prompt message
of “AC power
faulty” alarm.
Alarm cancellation
condition:
Restoration of AC.
7-2
Alarm
Message
Nebulizer
operation is
Nebulizer On L5 Physiological Start Nebulizer operation
completed or
Interrupted.
During ventilator operation,

when an AC power failure occurs
and there is the int. battery
power, an “Int. Battery
Calibrate the int.
Int. Battery Calibration required” alarm
battery. Then
Calibration L6.1 Technical occurs.
restart the
required When the ventilator starts
ventilator.
running and there is the int.
battery power, an “Int. Battery
Calibration required” alarm
occurs.
During ventilator operation,

when an AC power failure occurs
and there is the opt. battery
power, an “Opt. Battery
Calibrate the opt.
Opt. Battery Calibration required” alarm
battery. Then
Calibration L6.2 Technical occurs.
restart the
required When the ventilator starts
ventilator.
running and there is the opt.
battery power, an “Opt. Battery
Calibration required” alarm
occurs.
Expiratory hold
Expiratory Hold
L7 Physiological Start Expiratory holding operation is
Interrupted
completed.
Inspiratory holding
Inspiratory Hold
L8 Physiological Start the inspiratory holding operation is
Interrupted
completed.
When “Limited
Under the battery operation, the Battery Capacity”
Low Battery M1 Technical remaining battery run time is less alarm appears or
than 30min. AC power supply
starts.
7-3
Alarm
Message
Respiration Rate
Respiration Rate has exceeded
High is less than the
the set limit for four consecutive
Respiration M2 Physiological set limit for four
ventilation cycles or continuously
Rate consecutive
for 20sec.
ventilation cycles.
Measure signals
of the sensor
Oxygen Sensor Checked during pre-inspection
M3 Physiological through
Failure before use.
equipment
inspection.
Oxygen
concentration is
Oxygen concentration exceeds lower than the
High Oxygen
M4 Physiological the preset oxygen concentration preset oxygen
Concentration
+6% continuously for 30sec. concentration+
6% for 30sec
continuously.
Oxygen
concentration is
Oxygen concentration is lower higher than the
Low Oxygen than the preset oxygen preset oxygen
M5 Physiological
Concentration concentration -6% or lower than concentration- 6%
18% continuously for 30sec. or higher than
18% for 30sec
continuously.
Minute Volume
High Expiratory Minute Volume exceeds the set
M6 Physiological lower than the set
Minute Volume limit, after 1min of ventilation
limit for 15sec.
Minute Volume
Low Expiratory Minute Volume is lower than the
M7 Physiological higher than the
Minute Volume set limit within 1min.
set limit for 15sec.
7-4
Alarm
Message
Inspiratory period
NIV – inspiration duration is normal under
exceeds Tispont setting for three NIV mode.
times in succession
Maximum Within the
Inspiratory M8 Physiological Invasive - inspiration duration specified
Time exceeds 5 seconds for adult and condition for two
2 seconds for child for three consecutive PSV
times in succession ventilation under
invasive mode.
Nebulizer
operation
continued or
Nebulizer Nebulizer operation has been
M13 Physiological alarm is
Interrupted interrupted by mode changes.
acknowledged by
pressing Alarm
Silence key.
Inspiratory Tidal
Inspiratory Tidal Volume Volume is lower
Low Inspiratory
M14 Physiological exceeds the upper limit for one than the alarm
Tidal Volume
ventilation. limit for one
ventilation.
Under the battery operation, the

Limited Battery AC power supply
H1 Technical remaining battery run time is less
Capacity starts.
than 10min.
Cycle AC Power-if
alarm occurs
again stop using
Internal Error H2.1 Technical Internal computing error Ventilator, note
code displayed
and call for
Service.
Cycle power. If
Communication Failure detected in BDU the alarm occurs
H2.2 Technical
Error BDU communications. multiple times, call
for Service.
7-5
Alarm
Message
Cycle power. If
Communication Failure detected in PS the alarm occurs
H2.3 Technical
Error PS communications. multiple times, call
for Service.
S/W Mismatch System detects software

H2.4 Technical Call Service.
Error versions are incorrect.
Exp. Valve System detects expiratory valve

H2.5 Technical Call Service.
Heater Failure heater fails.
Remove any
obstructions.
System detects cooling fan Cycle Power. If
Fan Blocked H2.6 Technical
failure the alarm occurs
again, call
Service.
Check to make
sure inspiratory
and expiratory
circuits have no
Internal hardware failure
BDU Failure H2.7 Technical obstruction. Retry
detected.
power-up tests.
If this alarm
persists, Call
Service.
Airway pressure is
Airway pressure has exceeded
Continuous lower than
PEEP+15cmH2O continuously
Airway H3 Physiological PEEP+15cmH2O
for 15sec. Expiratory valve is
Pressure continuously for
opened for gas release.
5sec.
Airway pressure
exceeds the alarm
Airway Pressure is lower than
High Airway limit for three
H4 Physiological the set limit within three
Pressure consecutive
consecutive ventilation cycles.
cycles or at most
15sec.
7-6
Alarm
Message
Refer to Chapter
No ventilation cycles within the
Apnea H5 Physiological 11.1.3 for Apnea
apnea period.
resetting details.
Expiratory Tidal
Volume is higher
Expiratory Tidal Volume is lower than the setting
Low Expiratory than the setting value for three value for three
H6 Physiological
Tidal Volume consecutive ventilation cycles or consecutive
continuously for 30s. ventilation cycles
or continuously for
30s.
PEEP is lower
than the alarm
PEEP measurement is higher
limit for three
High PEEP H7 Physiological than the alarm limit for three
consecutive
cycles or at most
15sec.
Circuit Ventilating circuit is Re-connect

H8 Physiological
Disconnect disconnected. patient circuit.
Occlusion is
Occlusion H9 Physiological Ventilating circuit is occluded.
removed.
Leak is within
NIV Mode only- Leak exceeds 75% of the
Leakage out of
H10 Physiological 75% of the maximum volume maximum volume
range
compensation capacity. compensation
capacity.
Airway pressure is
Airway pressure is lower than higher than the
Low Airway the set limit for three consecutive alarm limit for
H11 Physiological
Pressure ventilation cycles. three consecutive
ventilation cycles
or at most 15 sec.
Low Oxygen Oxygen supply is lower than Oxygen supply is

Supply H12 Physiological
160kPa. above 160kPa.
Pressure
7-7
Alarm
Message
PEEP is higher
than the alarm
PEEP measurement is lower
limit for three
Low PEEP H13 Physiological than the alarm limit for three
consecutive
cycles or at most
15sec.
The CO2 module is not detected Redetect or

CO2 Accuracy
H14 Physiological during the probation period or replace the CO2
Error
the CO2 module fails. module.
Reconnect the
CO2 Adapter. If
CO2 Adapter
H15 Physiological Detected by CO2 Sensor. alarm occurs
Failure
again, replace the
CO2 Adapter.
Check the cable

The communication between the
CO2 sensor between the CO2
H16 Physiological CO2 module and the host
Comm. Failure module and the
instrument fails.
host instrument.
Reconnect the
CO2 sensor. If
CO2 Sensor
H17 Physiological Detected by CO2 Sensor. alarm occurs
Error
again, replace the
CO2 sensor.
Increase EtCO2 or
EtCO2 is lower than the setting
Low EtCO2 H18 Physiological reduce the setting
value.
value.
Reduce EtCO2 or
EtCO2 is higher than the setting
High EtCO2 H19 Physiological increase the
value.
setting value.
7-8
8 User Maintenance
8 User Maintenance
WARNING: Only authorized person is permitted to perform maintenance.
WARNING: Our company recognizes that cleaning, disinfection, and sterilization practices
vary widely among medical institutions. It is not possible to specify or require specific practices
that will meet all needs, or to be responsible for the effectiveness of cleaning, sterilization, and
other practices carried out in the patient care setting.
WARNING: Use a cleaning and disinfection schedule that conforms to your institution‟s
disinfection and risk-management policies:
 Refer to the material safety data as applicable.

 Refer to the operation and maintenance manuals of all disinfection equipment.
 Do not inhale fumes that may result from any disinfection process.
WARNING: Movable and removable parts may clamp or even crush your hand. Use
caution when moving or replacing system components.
CAUTION: The disposal of environmentally harmful devices (such as batteries and LCD
display) must be in accordance with local regulations.
WARNING: Do not use talc, zinc stearate, calcuim carbonate, corn starch or similar
material to prevent sticking of the bellows, as these materials may enter the patient‟s lungs or
airway, causing irritation or injury.
CAUTION: To prevent system damage:
 Refer to the literature supplied by the manufacturer of the cleaning agent.

 Never use organic, halogenated or petroleum-based solvents, anesthetic, glass cleaning
agents, acetone or other irritant agents.
 Never use abrasive agents (i.e. steel wool or silver polish) to clean components.
 Keep all liquids away from electronic components.
 Prevent liquid from entering the equipment.
 All cleaning solutions used must have a pH between 7.0 and 10.5.
8-1
CAUTION: Never immerse the oxygen sensor or its connector in any type of liquid.
 Dispose of the oxygen sensor per the manufacturer‟s specification.
CAUTION: Do not wash the inner surface of the oxygen sensor.
CAUTION: Prior to use after cleaning or disinfecting, power up the system as described in
section 6 and follow the on-screen Pre-Use test prompts to perform the Leak Test and Circuit
Compliance Test.
8.1 Cleaning and Disinfection
CAUTION: Before the first use clean, disinfect, and sterilize the ventilator.
Disposable components must be disposed in accordance with local regulations. Don‟t use
hard brushes or other sharp tools in cleaning to avoid damage to parts
8.1.1 Cleaning and Disinfecting Agents/ Autoclaving
Agent Classification
Detergent
• Mild dishwashing detergent
Detergent
• Soapy water with detergent ph between 7.0
and 10.5
• Isopropyl alcohol (70% solution) Intermediate level disinfectant
• Window cleaning solution (with isopropyl Intermediate level disinfectant

alcohol and ammonia)
• Sodium hypochloride- (bleach) in water

Intermediate level disinfectant
(10% solution)
Intermediate level disinfectant
• Hydrogen peroxide (3% solution)
• Gluteraldehyde 2% solution High level disinfectant
• Steam autoclaving up to a maximum High level disinfectant

temperature of 134°C (273°F).
8-2
8 User Maintenance
8.1.2 Cleaning and Disinfection Methods
Different parts of the ventilator have their respective cleaning and disinfection methods. The
following categories are defined for the parts noted in Table 8-1. The parts need to be cleaned,
disinfected and thoroughly dried before reassembly.
A: Wipe: If there is a potentially infectious substance on the breathing system, such as blood or
secretion, wipe away the substance with disposable cloth using proper disinfectant. Use a soft
cloth with a water-soluble detergent or disinfectant wipes.
B: Machine washing: Automatic washing with washer and disinfecting with disinfection
machine.
C: Immersion disinfection: Soak in glutaraldehyde-based formulations of 2%.
D: High temperature and pressure disinfection: At 121℃ for 20 minutes minimum, or at 134℃
for 8 minutes minimum. Follow the manufacturer‟s instructions for high level disinfection.
High-temperature disinfection does not have any cleaning effect. It should only be used on
components that have already been cleaned by hand or machine and then thoroughly dried.
Table 8-1
Cleaning and disinfection methods

Part name
A B C D
Ventilator exterior, including housing,
√
gas supply hoses and power cord
All components in Figure 8-3 √ √ √ √
CO2 sensor, other breathing circuit
Follow the manufacture‟s guidelines
parts or accessories
8.1.3 Cleaning and Disinfection of Components
8.1.3.1External Surfaces
Using a soft cloth with a water-soluble detergent or disinfectant wipes, clean the housing, gas
supply hoses and power cord.
8.1.3.2 Expiratory Module
(1) Disassembly
8-3
Figure 8-3
To remove the components from expiratory module:
a. Press the button(1 in Figure 8-1);
b. Pull out the expiratory valve core component (2 in Figure 8-1, Figure 8-2);
c. Remove the end cover(1 in Figure 8-3) and the gasket (2 in Figure 8-3);
d. Remove the scale board(3 in Figure 8-3)and the diaphragm(4 in Figure 8-3);
e. Rotate the expiratory connector (5 in Figure 8-3) clockwise;
f. Pull out one-way valve core(6 in Figure 8-3), rubber o-sealing ring(7 in Figure 8-3)
and one-way diaphragm(8 in Figure 8-3);
g. Rotate the water trap (9 in Figure 8-3), then pull it out.
(2) Cleaning
a. Wash each component using a mild detergent and water solution.
8-4
8 User Maintenance
b. Rinse with clean, hot water and allow to thoroughly dry.
(3) Disinfection
NOTE: Ensure that all the components have been cleaned before disinfecting.
Using the Gluteraldehyde disinfection solution, follow the manufacturer‟s instructions for high
level disinfection and rinsing of all components while adhering to facility policies and
procedures.
All the components can also be high temperature and pressure disinfected. Using an
autoclave, follow the manufacturer‟s instruction for high level disinfection of all the components
while adhering to facility procedures.
(4) Assembly
Reassemble the components in the reverse order.
After installation, please perform a pre-use test and verify all tests passed.
8.2 Regular Maintenance
8.2.1 Maintenance Principles
Do not use a faulty machine. Ask an authorized agent of our company to carry out all
necessary maintenance tasks. Test the machine after maintenance for normal operation.
Every parameter should meet requirement in specification.
In order to ensure the reliability of the machine, all maintenance and repair work should be
carried out by an authorized agent of our company.
CAUTION: Only authorized personnel are permitted to perform maintenance.
Use products of our company to replace damaged ones and test, ensuring all specifications
met.
Contact local service agent of our company in case support is needed. In all cases,
maintenance fee is the current component price plus reasonable labor cost, except for those
within guarantee period.
8.2.2 Periodic Maintenance Schedule
The schedule is designed based on the typical condition, that is to say, the least maintenance
times vs 2000h operating per year. In case the actual operating time is longer than 2000h per
year, the maintenance times should be more.
8-5
If necessary, our company can provide circuit diagram, service part list, calibration instructions
to assist authorized service personnel.
Minimum maintenance interval Task
Daily Drain water in gas supply inlet filter, check liquid in

expiratory module water trap (collected liquid volume
cannot be more than half of the bottle).
Weekly Calibrate oxygen sensor
1-3 month(s) Clean air filter Clean cooling fan filter on rear of machine.
Every year Calibrate flow sensor and pressure sensors;

Calibrate inspiratory valve and expiratory valve (if
necessary).
Every 6 months Charge and discharge the batteries once (Charge time: at
least 3.5h).
Every year or after a failed Replace the O2 sensor (actual life depends on temperature
calibration and O2 concentration)
After cleaning and installing Check components and replace or repair when necessary.
WARNING: If the Ventilator will not be in use for a period of more than 6 months, the
internal batteries must be disconnected or removed to prevent possible damage to the

equipment or risk to users or service personnel.
WARNING: The ventilator must not use, nor be connected to, any anti-static or electrically
conductive hoses and tubing.
8.2.3 Service Life of Product/Accessories
Service Life is defined as the time that the manufactured device can be expected to be
'serviceable' or supported by our company and the maximum time the device can be used
safely. Some items within the device may require maintenance, repair or replacement within
this time. Such items will be available from our company for the service life of the product. The
calculation of the service life begins at the installation of the product at the customer site. Our
company recommends for safe use that each device is replaced after its service life is
completed.
CAUTION: The service life of the following items is based on specified operating
conditions.
8-6
8 User Maintenance
Mask, patient breathing circuit Sterilize for 20 times at 121℃
Power supply cable, gas supply

8 years
pipe
Machine 8 years
500 cycles of full charge(The battery from

Battery
exhausted to full )
8.3 Maintenance in Operation and Transportation
The location of machine should be proper so that it cannot obstruct or be disturbed by medical
care personnel. Fix power supply cable well to avoid failure. Use caution not to touch
accidental keys on the panel, which may make tidal volume setting wrong.
During transportation of the ventilator, with or without a patient connected, make sure that the
following conditions are fulfilled:
 Gas cylinders are connected with a sufficient amount of gas and the Battery module is
functioning. Follow the hospital guidelines.
 Use the handles on the Mobile Cart. Transport the bed and the ventilator slowly, and
watch the patient connection carefully to see that no pulling or other movement occurs.
 Be careful not to tip the Mobile Cart when crossing an obstacle such as a doorstep.
8.3.1 Transportation
Use care when moving machine within hospital or clinical environment.
WARNING: If Control Unit of Ventilator is dropped or damaged during transportation,
equipment failure could result in patient injury.
WARNING: Tip over hazard – use care when moving Ventilator mounted to Cart as device
could tip over leading to injury or damage to the equipment and possible subsequent patient
injury.
User can carry packaged machine while riding in vehicle, plane and train. Impact, severe
shock and moisture should be avoided during transportation, with ambient temperature
-20°C~+60°C and relative humidity not more than 95%. In case transportation conditions do
not meet this requirement, put the machine in specified operating environment for at least 24h
before using.
8-7
8.3.2 Storage
CAUTION: Do not put ventilator into the shock environment.
CAUTION: Do not lay heavy items on the top of the ventilator.
The machine should be stored in a room with temperature -20°C to + 60°C and relative
humidity not more than 95% non-condensing, with ventilation and no corrosive gases.
WARNING: If the storage environment conditions don‟t agree, put the machine in specified
operating environment at least 24h before using.
CAUTION: The device should be stored at the room that is ventilated and in which no
corrosive gases exist.
CAUTION: When the storage conditions are beyond the requirements of operational
environment, and the storage state is transferred into operation state, the product only can be
used after being stored in environment for over 24 hours.
8.4 Consumables Replacement
8.4.1Fuse Replacement
WARNING：Before replacing fuse, first disconnect AC power. Otherwise, it will cause injury
or even death.
WARNING：When replacing fuse, make sure the new fuse is the same type and size as the
old one; otherwise, the ventilator will be damaged.
CAUTION: Fuse is a damageable part, which shall be replaced with moderate force and
speed.
1. AC Circuit Fuse
Fuse replacement steps:
• Insert screwdriver into the trench (2) of end of fuse box, see Figure 8-4.
• Pull out fuse holder (1).
• Remove the fuse (3).
• Load new fuse.
• Push the new fuse into the original position gently.
• Connect AC power, and then start the ventilator to test.
8-8
8 User Maintenance
Figure 8-4
2. DC Power Fuse
Fuse replacement steps:
• Insert screwdriver into the trench (1) of end of fuse box, see Figure 8-2.
• Pull out fuse holder (2).
• Remove the fuse (3).
• Load new fuse.
• Push the new fuse into the original position gently.
Figure 8-5
8.4.2Battery Maintenance
NOTE: One or more batteries must be used.
NOTE: Before the machine is put into patient use, the battery must be fully charged. If the
battery must not be fully charged and AC power supply fails, be careful about the battery
power.
8-9
• Battery specification
Battery module:
-- DC12V, 6.6AH, 14.4V lithium-ion battery

-- Typical charge time: 3.5 hours
-- Typical discharge time: 2 hour
When the main power supply voltage is too low or the main power supply fails, two backup
batteries (one is necessary, and one is optional) can protect the ventilator. When having a
power failure, the ventilator can switch to battery supply automatically, and can normally work
without pneumatic power supply failure. The two batteries are usually available for the
ventilator working for 4 hours.
• Precautions
Charge: When operating with AC power supply on, the system will maintain the battery
automatically. Charge time is less than 3.5 hours.
Discharge: The machine is operating on battery.
In case of low battery condition, an alarm message “Low battery” will appear, notifying the user
to restore AC power supply to charge, otherwise the batteries will be depleted and another
alarm “Limited Battery Capacity” will be displayed, and eventually the system will shut down
(for safety reason, manual power-on is required to start the machines again after an automatic
shutdown).
Before the machine is put into patient use, or disconnect AC power for the transport or other
purposes, check the battery power. If the battery is not fully charged, connect the ventilator to
AC power for at least 3.5h and recharge the battery until the power reaches 80%~100%.
• Battery storage
In case the battery is to be stored for a long time, charge it fully prior to storage.
To keep the battery power and prolong the battery life, please ensure that the ventilator is
connected to the main power. Charge the battery every six months, while the actual time
depends on the storage environment.
High humidity and high temperature environments should be avoided for storage.
• Battery replacement
Open the battery cover (See Figure 2-5), then remove the battery from its housing.
Same model battery with CE certification is suggested. Make sure AC power supply is
disconnected before replacing.
8-10
8 User Maintenance
CAUTION: An authorized service representative can replace the battery. If the battery is
not to be used for a long-time, please contact the service representative to disconnect the
battery. The waste battery should be disposed of in accordance with the local policies.
• Battery charging and calibration
Use the battery charger supplied by our company to charge or calibrate the battery. After
calibrating the battery, the ventilator can read the residual battery capacity accurately.
Please charge or calibrate the battery according to the instructions of the battery charger.
CAUTION: When „low battery‟ alarm occurs, charging should be done immediately.
Otherwise the Ventilator System could shut off automatically in several minutes.
8.4.3Oxygen Sensor
The oxygen sensor can be used to measure the local oxygen concentration when it is
connected to the ventilator or other equipments. The oxygen sensor is suitable for adult and
child.
8.4.3.1 Oxygen Sensor Replacement
Disassembly
Step 1: Open outward (1), and then remove the cover.
Figure 8-6
Step 2: Turn the oxygen sensor (3) anticlockwise, and then remove it.
8-11
Figure 8-7
Assembly
Inspect the oxygen sensor for damage and replace as necessary. Then reassemble the
oxygen sensor.
8.4.3.2 Oxygen Sensor Calibration
For oxygen sensor calibration, refer to section 6.8.3.1.
8.4.3.3 Technical Specifications of Oxygen Sensor
Measure range 0-1500 mBar O2

Measure accuracy <1%
Response time <15 s (air to 100% O2)
Operating temperature -20℃ ～ +50℃
Operating pressure 0.5 - 2.0 Bar
Operating humidity 0 - 99% RH non-condensing
Storage temperature 0℃ to 20℃
Drift <200 µV
Reproducibility ±1%
Type Chemical fuel cell
0.94 x 106% O2 hours at 20°C
Expect life time
0.6 x 106% O2 hours at 40°C
Total system response
<60s
time
The O2 monitor surveys and displays the O2 concentration in the
Working principle of O2 patient loop. The oxygen sensor component contains an oxygen
monitor sensor, which can produce the voltage proportional to the
oxygen partial pressure (concentration) on its detection surface.
8-12
8 User Maintenance
The oxygen sensor is an electrochemical device (chemical

battery). Oxygen expands in this device through a layer of film
and oxidizes the base metal electrode. The oxidation process
produces a current with an amplitude proportional to the oxygen
partial pressure indicated by the electrode sensor. The base
metal electrode is gradually exhausted during the oxidation
process.
The voltage of the sensor is influenced by the temperature of
the monitoring gas mixture. The surgical thermosensitive
resistor of the sensor automatically compensates temperature
change in the sensor.
The O2 monitor converts the sensor signal into the
corresponding oxygen percentage value by using signal
processing and circuit analysis. The system displays the value
and compares it with the stored alarm limit value. If the value
exceeds the threshold, the monitor will alarm.
NOTE: After being in a condensing atmosphere, the oxygen sensor shall be stored for
more than 24 hours in an environment equivalent to operating humidity.
8.4.3.4 Oxygen Sensor Maintenance
The oxygen sensor should be regularly calibrated. For the calibration interval, refer to section
8.2.2.
To improve the life time of the oxygen sensor, when the ventilator is not in use the oxygen
sensor should be avoided contact with the high-concentration oxygen.
The oxygen sensor is consumptive, and the period of valid is ordinarily 12 months. So the user
should pay attention to the valid of the oxygen sensor. When the oxygen sensor fails, please
contact the manufacturer.
The recommended oxygen sensor is produced by our company.
WARNING: Do not immerse oxygen sensor in liquid. Do not conduct autoclave or high
temperature fumigation on the oxygen sensor.
8.4.4Paramagnetic Oxygen Sensor (optional)

The paramagnetic oxygen sensor can be used to measure the local oxygen concentration
when it is connected to the ventilator or other equipment. The oxygen sensor is suitable for
adult and child.
8-13
8.4.4.1Paramagnetic Oxygen Sensor Calibration
For the paramagnetic oxygen sensor calibration, refer to section 6.3.6.3.1.
8.4.4.2Technical Specifications of Paramagnetic Oxygen Sensor
Performance
Technology Paramagnetic
Range 0-100% O2 (with over range -15% O2 to 200% O2)
Accuracy (Intrinsic Error) ＜± 0.2% O2
Linearity ＜± 0.2% O2
Repeatability ＜± 0.2% O2
Zero Drift ＜± 0.4% O2 in first 24 hours, then ＜± 0.2% O2 /week, then ＜±
0.2% O2 /month
Response Time (T10 8 to 20 seconds dependent on application and filter selection
–T90) (biological filter on request)
Outputs/Controls
Signal Output Digital UART or linear mV output (0.5mV or 10mV per % O2)
Physical
Weight 70g (2.47oz)
Dimensions Molex low profile connector: 33.5×30.0×46.1mm (1.32×1.18×1.81”)
Diffusion Port Aperture diameter: 15.5mm (0.61”)
Sample condition
Sample Gas Condition Clean dry gas, free of entrained oil, particulates ＜3μm,
non-condensing
Gas Exchange Diffusion
Ambient conditions
Operation Temperature 5℃ to 50℃ (41℉ to 122℉)
Storage Temperature -30℃ to 70℃ (-22℉ to 158℉)
Temperature Within a range of 0℃ to 50℃: Zero ＜± 0.5% O2 /10℃, Span: ＜
Coefficient ±0.5% O2 /10℃
Operating Pressure ±33kPag (±5psig)
Range
Ambient Humidity 0 to 95% non-condensing
External Power Supply 5V dc, 70mA nominal
Power Consumption 350mW
8-14
8 User Maintenance
8.4.5 Diaphragm Replacement
Diaphragm replacement method:
h. Press the button(1 in Figure 8-8);
i. Pull out the expiratory valve core component (2 in Figure 8-8);
j. Remove the safety valve cover (1 in Figure 8-9) and the gasket (2 in Figure 8-9);
k. Remove the scale board (3 in Figure 8-9) and the diaphragm (4 in Figure 8-9)；
l. Reassemble the above components in the reverse order.

Test: When the diaphragm and scale board are replaced, the inspiratory valve must be
calibrated.; Also, perform a pre-use test and verify all test pass.
8-15
8.4.6 One-way Diaphragm Replacement
Figure 8-10
The one-way diaphragm replacement method：
a. Remove the expiratory valve core component;
b. Remove the one-way valve core component (1);
c. Remove one-way diaphragm(2);
d. Reassemble the above components in the reverse order.
Test: When the one-way diaphragm has been replaced, the inspiratory valve must be
calibrated.
8-16
8 User Maintenance
8.4.7 Fan Filter Cotton Replacement
Figure 8-11
The replacement method of the fan filter cotton:
a. Remove the fan filter cotton cover(2)；
b. Remove the fan filter cotton(1);

c. Reassemble the above components in the reverse order.
8-17
8.4.8 Filter Element of Gas Inlet Replacement
Figure 8-12
Filter element of gas inlet replacement method:
a. Remove the filter cover(1)；
b. Remove the filter support sleeve(2);

c. Remove the filter element of gas inlet(3);
8-18
8 User Maintenance
8.4.9 Filter Replacement(Part No.:130003930)
Figure 8-13
The filter replacement method:
a. Remove the two screws (1) (Hexagon socket head cap screws M4×10)；
b. Remove the oxygen inlet connector(2);

c. Remove the filter(3);
8.5 Disposal
This product must not be disposed of with your other waste. Instead, it is your responsibility to
dispose of your waste equipment by handing it over to a designated collection point for the
recycling of waste electrical and electronic equipment, or by returning it to our company for
reprocessing. The separate collection and recycling of your waste equipment at the time of
disposal will help to conserve natural resources and ensure that it is recycled in a manner that
protects human health and the environment. For more information about where you can drop
off your waste equipment for recycling, please contact your local city office, your waste
disposal service, or your product distributor or retailer.
8-19
Correct Disposal of Batteries and O2 Sensors
WARNING: Treatment of batteries and O2 sensor:
 Follow all local regulations with respect to environmental protection when disposing of
batteries and O2 sensor. These products contain toxic compounds irrespective of physical
condition. They should be disposed of according to local waste management requirements
and environmental legislation. They should not be burned since they may give off toxic fumes.
 Do not throw into fire! Risk of explosion.
 Do not force open! Danger of bodily injury.
8-20
9 Warranty
9 Warranty
Manufacturing techniques and materials:
For a period of one year from the date of original delivery to the customer, the components and
assemblies of this product are warranted to be free from defects caused by manufacturing
techniques and materials, provided that the equipment is properly operated under conditions
of normal use and that the equipment is regularly maintained per requirements specified by
our company. The warranty period for other parts is three months. Consumable parts are not
included in this warranty. Our company‟s obligation under the above warranty is limited to
repairing the equipment free of charge.
Freedom from Obligations:
 Our company‟s obligation under the above warranties does not include freight and other
fees;
 Our company is not responsible for any direct or indirect product damage or delays which
result from improper use; alteration by using assemblies in an unapproved configuration;
and maintenance by anyone other than our company or our company‟s appointed
representatives;
 This warranty does not apply to the following situations:
• Improper use;
• Machines used without the proper maintenance or damaged;
• Our company original serial number label or mark is removed or replaced.
Security, reliability and operating condition:
Our company is not responsible for the security; reliability and operating condition of this
product in cases where:
 The assemblies are disassembled, extended and readjusted
 The product is not operated correctly in accordance with these User manual instructions.
 The AC power used or the operating environment does not follow the requirements in this
manual.
9.1 Return
Follow these steps in case the product must be returned to our company:
1. Obtain the rights of return (Return Material Authorization Number)

Contact our Customer Service and inform us of the part number and type of the product. The
part number is marked on the surface of the product. Return is not allowed if the number
cannot be identified. Receive an RMA number from our company and mark it on the exterior of
9-1
the product packaging. Enclose a statement of the product number, product type and also the
reason for return.
2. Transportation charges
Transportation and insurance charges must be prepaid by the user for transporting the product
to our company for repair.
9-2
10 Theory of Operation
10.1 Ventilation Modes
There are Invasive and non-invasive (NIV) ventilation modes in the ventilator. All the modes
are suitable for children and adults.
CAUTION: Nebulizer use is not available in noninvasive (NIV) modes.
Invasive ventilation modes include:
• Assist/Control ventilation (A/C) modes. These modes allow mandatory ventilation and
include VCV, PCV and PRVC.
• Synchronous Intermittent Mandatory Ventilation (SIMV) modes. These modes allow both
mandatory ventilation (including VCV, PCV and PRVC) and spontaneous ventilation (including
spontaneous ventilation and pressure support ventilation - PSV).
• Spontaneous/ Continuous Positive Airway Pressure ventilation (SPONT/CPAP) mode.
This mode only allows spontaneous ventilation.
• Bi Level ventilation (BIVENT) mode. This mode allows both mandatory ventilation
(switching between high level CPAP and low level CPAP) and spontaneous ventilation.
NIV modes, include:
• NIV/CPAP mode – CPAP mode in NIV.
• NIV-T mode – A/C (PCV) mode in NIV.
• NIV-S/T mode – SPONT mode in NIV.
10.1.1 Assist/Control Ventilation
In Assist/Control ventilation, breaths are controlled by the ventilator (mandatory) or triggered

by the patient (spontaneous) or triggered by the operator. When controlled by the ventilator,
Ventilator Initiated Mandatory (VIM) breaths are flow controlled and time cycled, thus
delivering an operator set volume (Tidal Volume) or pressure. Extra breaths, called Patient
Initiated Mandatory (PIM) breaths, shall be possible if the patient overcomes the pre-set trigger
level. PIM breaths are either pressure or flow triggered. If the trigger setting is adjusted so that
the patient cannot trigger the ventilator, all breaths shall be VIM breaths, including operator
triggered breaths.
1. Volume Control Ventilation:
10-1
In VCV, VIM breaths deliver the set volume (Tidal Volume - Vt).
Figure 10-1
Figure 10-2
10-2
2. PCV Pressure Controlled ventilation
In PCV, VIM breaths deliver the set Pressure (Pinsp) using a decelerating flow pattern.
Figure 10-3
3. Pressure Regulated Volume Control Ventilation
PRVC breaths will be delivered at a set rate and set volume (VT). The flow pattern resembles
PCV. Inspiratory pressure will be regulated in PRVC to achieve the operator set volume (Tidal
Volume). The first ventilation in PRVC will have a square flow waveform and each successive
ventilation will have a ramp flow (decelerating) waveform.
10-3
Figure 10-4
PRVC ventilation operation shall be as follows:
When PRVC is selected, a volume controlled test breath, to the set tidal volume, will be
delivered to the patient. The ventilator will set the target pressure for the first pressure control
breath to the end inspiratory pressure of the test breath.
The next ventilation and all subsequent breaths will be delivered as pressure control breaths.
The inspiratory pressure will be based on the dynamic compliance of the previous ventilation
and the set tidal volume. Inspiratory pressure will be adjusted automatically by the ventilator to
maintain the target tidal volume. The maximum step change between two consecutive breaths
shall be 3 centimeters of water pressure. The maximum tidal volume delivered in a single
ventilation shall be 1.5 times the Vt setting.
The test ventilation sequence shall be initiated when any of the following events occur:
Entering the Mode (PRVC) mode; Changing the set tidal volume while in PRVC; Delivered
tidal volume >= 1.5 times the set volume; Flow termination of the test ventilation; activation of
any of the following alarms - High Peak Pressure Alarm; Low Peak Pressure Alarm; Low PEEP
alarm; Patient Circuit Disconnect Alarm; I-Time Limit; I:E Limit.
10.1.2 Synchronized Intermittent Mandatory Ventilation
SIMV is a ventilation mode where the patient is allowed to breathe spontaneously and the
machine delivers VC mandatory breaths in synchrony with the patient‟s effort at the operator
set rate and volume (or pressure). This is accomplished by a combination of spontaneous and
mandatory windows that open and close. The type of ventilation delivered depends upon
10-4
whether the event during the window is patient initiated, operator initiated or time initiated.
Spontaneous breaths occurring between mandatory breaths can be pressure supported.
Synchronized breaths shall be either pressure or flow triggered. Back-up (Apnea) ventilation
shall be provided when there is no patient trigger, mandatory ventilation or manual ventilation
for a period that exceeds the apnea alarm setting. Backup Ventilation shall be available in
SIMV - See section on Backup Ventilation for details on these modes and settings.
SIMV ventilation cycle, PIM delivered within mandatory interval and

SIMV ventilation cycle, PIM not delivered within mandatory interval
Figure 10-5
1. SIMV (VCV)
In SIMV (VCV), mandatory ventilator breaths are volume controlled. Between the mandatory
breaths the patient can breathe spontaneously. These spontaneous breaths can be pressure
supported. Backup ventilation will be PCV.
2. SIMV (PCV)
In SIMV (PCV),mandatory ventilator breaths are pressure controlled. Between the mandatory
breaths the patient can breathe spontaneously. These spontaneous breaths can be pressure
supported. Backup ventilation will be PCV.
3. SIMV (PRVC)
In SIMV (PRVC), mandatory ventilator breaths are pressure-regulated volume controlled.

Between the mandatory breaths the patient can breathe spontaneously. These spontaneous
breaths can be pressure supported. Backup ventilation will be PCV.
10.1.3 Back-up Ventilation (Apnea Ventilation)
1. Transition into Back-up Ventilation
The current Ventilation mode shall transition to Back-up Ventilation - PCV when an apnea
occurs in SPONT/CPAP mode.
10-5
occurs in BIVENT mode.
occurs in NIV-S/T mode.
occurs in an SIMV mode.
2. Characteristics of Back-up Ventilation
Apnea ventilation settings include Pinsp, Tinsp or I:E.
3. Exiting Back-up Ventilation
Two methods to exit Back-up Ventilation shall be supported: trigger by patient or reset by
operator.
When in Back-up Ventilation and the patient triggers two consecutive breaths and also the
Expiratory Vt >= 0.5 x Inspiratory Vt for those two breaths, then the ventilator shall return to the
Ventilation mode and settings prior to the Apnea event.
When in Back-up Ventilation and the operator resets the Apnea Alarm and confirms the reset
by pressing the Encoder Knob, then the ventilator will return to the Ventilation mode and
settings prior to the Apnea event.
Mode transitions when exiting Back-up Ventilation shall occur only when an Expiratory has
been completed.
10.1.4 Spontaneous/CPAP Ventilation
In SPONT/CPAP Ventilation, the patient breathes spontaneously at a pressure level

determined by the PEEP setting. Spontaneous ventilation may also be assisted by the
ventilator at an operator set level of inspiratory pressure (Pressure Support). Inspiration is
initiated by the patient and terminated when the inspiratory flow falls below an operator set
percentage of the peak flow during this ventilation. During SPONT/CPAP, the patient
determines the respiratory rate, and the patient and ventilator determine the inspiratory time
and tidal volume. Ventilation detection shall be either pressure or flow triggered. PCV back-up
ventilation shall be provided when there is no patient trigger, for a period that exceeds the
apnea alarm setting. (See Section on Back-up ventilation for details)
10-6
Figure 10-6 Spontaneous /CPAP ventilation
10.1.5 BiLevel Ventilation (BIVENT)
In BIVENT, breaths shall be controlled by the ventilator (mandatory). Pressure controlled

breaths are provided by switching between a high and low airway pressure in an adjustable
time sequence. Spontaneous breaths can be pressure supported at the high and low pressure
levels. When the expiratory time (Tlow) is less than the inspiratory time (Thigh) the displayed
ventilation mode shall be Bi Vent APRV. PCV back-up ventilation shall be provided when there
is no patient trigger, mandatory ventilation or manual ventilation for a period that exceeds the
apnea alarm setting. (See Section on Back-up ventilation for details)
Figure 10-7 BIVENT

10-7
Figure 10-8 BIVENT APRV
10.1.6 Non Invasive/Continuous Positive Airway Pressure
NIV/CPAP is a spontaneous mode of operation and no ventilator controlled breaths are

provided. Throughout the ventilation cycle, an operator set pressure (CPAP) may be provided.
In NIV/CPAP, the ventilator controls the airway pressure as the preset PEEP value.
Figure 10-9
Illustration shows NIV/CPAP. Pressure shall rise according to the selected rise time, with
target pressure 1.5 cmH2O above PEEP to improve work of ventilating.
10-8
Figure 10-10
This illustration shows NIV/CPAP spontaneous breaths with Pressure Support
Figure 10-11
Pressure support will be terminated when:
10-9
• Inspiratory flow returns to zero during phase 1 of inspiration, (i.e. when the patient exhales
or fights the ventilator),
• Inspiratory flow in phase 2 of inspiration phase falls below a certain ratio (Esens) of the
maximum value previously supplied when compared to the peak inspiratory flow supplied
or
• Based on high Spont Inspiratory Time setting is exceeded
10.1.7 NIV-T
In NIV-T, breaths shall be controlled by the ventilator (mandatory) or shall be triggered by the
patient (spontaneous) or shall be triggered by the operator. When controlled by the ventilator,
breaths shall be pressure limited and time cycled, resulting in an operator set pressure (Pinsp)
being delivered for an operator set period (Tinsp). Extra breaths shall be possible if the patient
overcomes the pre-set trigger level or if the operator selects a manual ventilation. Patient
triggered breaths shall be flow triggered.
10.1.8 NIV-S/T
NIV-S/T is a spontaneous mode of operation and no ventilator controlled breaths are provided.
Throughout the ventilation cycle, spontaneouse ventilation may also be assisted by the
ventilator at an operator set of inspiratory pressure (Pressure Support). If the trigger time of the
patient exceeds the setting value of the apnea time, the mode will enter into back-up
ventilation.
NIV-S/Td is a spontaneous mode of operation and no ventilator controlled breaths are

provided. Throughout the ventilation cycle, an operator set pressure (CPAP) may be provided.
In NIV/CPAP, the ventilator controls the airway pressure as the preset PEEP value.
10-10
11 VG70 Ventilator System Specifications
WARNING: Do not operate the Ventilator outside specified operating ranges or patient
injury or equipment damage could result.
NOTE: To add a measure of safety, an electronic hardware watchdog timer monitors the
system operation at all times. In cases where the system software does not respond in a safe
time period, the watchdog timer will reset the system. This enables the system software to be
in control at all times.
11.1 System
11.1.1 General
This device complies with requirements of Medical Device Directive 93/42/EEC.
Standards
IEC 60601-1: The device classification is: Class I, Type B applied part (ventilator breathing
tube and mask), type BF applied part (CO2 module), ordinary enclosed equipment without
protection against ingress of liquids, continuous operation
ISO 80601-2-12
WARNING: Equipment not suitable for use in the presence of a Flammable Anesthetic
mixture with Air or with Oxygen or Nitrous Oxide.
Electromagnetic Compatibility (EMC)
According to IEC 60601-1-2
Patient Range (cm)
Adult: 60 – 260
Child: 30 – 140
11-1
NOTE：Leakage from VBS COMPLIANCE：
• 50 ml/min at 20 hPa for a VENTILATOR intended to provide DELIVERED VOLUME less

than 50 ml;
• 100 ml/min at 40 hPa for a VENTILATOR intended to provide DELIVERED VOLUME
between 300 ml and 50 ml;
• 200 ml/min at 50 hPa for a VENTILATOR intended to provide DELIVERED VOLUME
greater than 300 ml.
11.1.2 Operating Conditions
Operating Temperature Range: +5 to +40℃

Relative Humidity: 5 to 95% non-condensing
Atmospheric Pressure: 700 to 1060 hPa
Enclosure Protection Rating IP21 per IEC 60529
11.1.3 Non-operating Conditions
Storage Temperature Range: -20 to +60 C

Storage Relative Humidity: ≤95% non-condensing
Storage Atmospheric Pressure: 700 to 1060 hPa
11.1.4 Power Supply
Ventilator
Power Supply 100-240 +/- 10% VAC 50/60 Hz
DC Power 12-24 VDC
Two rechargeable lithium-ion battery modules, 14.4

V, 6.6 Ah each. Recharge time approximately 3.5
Battery Backup (Standard)
hours. Battery backup time of 120 minutes minimum
with only standard internal battery.
Maximum Power Consumption 200VA
AC Circuit Fuse UDA3.15
DC Power Fuse GDA012
11-2
Cart
115V 2A 60Hz
Socket 220V 1A 50Hz
Humidifier
230V 1A 50/60Hz
Output Fuse 250V H3.5A
115V 5A 60Hz
Ventilator 220V 5A 50Hz
230V 5A 50/60Hz
115V 8A 60Hz
Input 220V 8A 50Hz
230V 8A 50/60Hz
CAUTION: DC power conforms to IEC 60601-1.
CAUTION: The Power Supply should meet the above specifications.
WARNING: Connecting any equipment that has not been supplied as a part of the
ventilator system to the socket of the cart may generate the risk.
11.2 Ventilator
11.2.1 General
User Interface: 350 wide x 55 deep x 244 high (mm)

Dimensions Ventilation Delivery Unit: 322 wide x 375 deep x 366 high (mm)
System with Cart (optional): 547 wide x 675 deep x 950 high (mm)
Total: 40 kg
User Interface: 2.5 kg
Weight (Approximate)
Ventilation Delivery Unit: 12.5 kg
Cart: 25 kg
Trigger Method Flow and Pressure
Maximum limited pressure 80 cmH2O
Maximum working
80cmH2O
pressure
Warm-up time ≥20 min
The ventilator has the automatic atmospheric pressure

Pressure compensation
compensatory function.
11-3
11.2.2 Gas Supply
Supplied gases must be free of water, oil and particles.
Inlet Gas Pressure
O2: 280 kPa to 600 kPa (41 – 87 PSI)
Connection Standards Available
DISS, NIST
The maximum 10 s average input flow required by ventilator for O2 is 60.69 LPM at a pressure
of 280 kPa. For a 3 second average and at a pressure of 280kPa, the maximum averaged
transient input flow required by the Ventilator is 64.44 LPM for O2.
CAUTION: The ventilator is a high flow device and should only be connected to a pipeline
installation designed using a diversity factor that allows for the indicated high flow at a
specified number of terminal outlets, in order to avoid exceeding the pipeline design flow,
thereby minimizing the risk that the ventilator interferes with the operation of adjacent
equipment.
11.2.3 Patient System Connectors
Male 22 mm Conical Fittings in accordance with ISO 5356-1.
11.2.4 User Interface
Attach to the ventilation delivery unit, the head mast, or other mounting system.
11.2.5 Acoustic Energy
The A-weighted sound pressure level of the ventilator is 45 dB; the A-weighted sound power
level is 52 dB.
11.3 Standard Conditions Specifications
Error ranges in this document assume the following standard conditions:
 Ambient pressure: 101.3 kPa (1 atmosphere)

 Room temperature: 20℃
 Dry gases in patient system
 Inlet pressure: 345 kPa (50 PSI)
11-4
11.4 Inspiratory Channel
Pressure Drop
Maximum 5 cmH2O at a flow of 60 liters/min.
Rated Inspiratory Gas Pathway Resistance
Less or equal to 50 cmH2O/L/s
Compliance
Maximum 2 mL/cmH2O (With Fisher & Paykel MR 810 Humidifier and Patient Circuit of
reusable silica gel).
Gas Delivery System
Microprocessor controlled valves.
Gas Delivery Device
Flow Range:
Adult: 1 to 180 liters/min
Child: 0 to 60 liters/min
Maximum Pressure Setting: 70 cmH2O
NIV Max leakage compensation level
Adult: 60 lpm
Child: 30 lpm
11.5 Expiratory Channel
Pressure Drop (Resistance)
Maximum 5 cmH2O at a flow of 60 lpm.
Rated Expiratory Gas Pathway Resistance
Less or equal to 20 cmH2O/L/s
Compliance
Maximum 2 mL/cmH2O (With Fisher & Paykel MR 810 Humidifier and Patient Circuit of
reusable silica gel).
PEEP Regulation
Microprocessor controlled valve
11-5
PEEP Setting Range
0 ~ 35 cmH2O
Expiratory Flow Measurements
Range: 0 ~ 180 lpm.
Because of power failure or partial loss power, the ventilatory capacity is unnormal. When the
ventilator supplies 60L/min volume, for the expiratory valve the pressure drop is 0.18kPa in
inspiration, the pressure drop is 0.11kPa in expiration.
11.6 Monitoring
Inspiratory and Expiratory Minute Volume
Range: 0 ~ 60 lpm.
Accuracy: +/- 1 LPM or +/- 15% of measured value (whichever is greater)
Resolution: 0.1 lpm > 1 lpm, 0.001 lpm < 1 lpm
Inspiratory and Expiratory Tidal Volume
Range: 0 ~ 4000 mL
Adult Accuracy: +/- 25 ml or ±15% of the measured value (whichever is greater)
Child Accuracy: +/- 10 ml or ±10% of the measured value (whichever is greater)
Resolution: 1 mL
O2 Concentration
Range: 18 ~100%
Accuracy: +/- 3 vol. %
Resolution: 1%
Airway Pressure
Range: -20 to 80 cmH2O

Accuracy: ± (2 cmH2O + 4% of reading)
Resolution: 1 cmH2O
Measurement uncertainty
Volume: +/- 2% of reading or +/- 20 mL (whichever is greater)
Pressure: +/- 0.75% of reading or +/- 0.1 cmH2O (whichever is greater)
O2: +/- 1%
Airway Pressure and Flow Rate Waveform
Filtering of 5 samples is performed for smoothing.
11-6
11.7 Alarms
11.7.1 Allowed Alarm Settings
Airway Pressure (upper limit)
5 to 80 cmH2O
High Continuous Pressure
Set PEEP level + 15 cmH2O for at least 15 sec
O2 Concentration
Set value +/- 6 vol % or <= 18 vol %
Expired Minute Volume (Upper alarm limit)
1 ~ 60 liters/min; OFF
Expired Minute Volume (Lower alarm limit)
0.1 ~ 40 liters/min; OFF
Apnea Time
10 ~ 60 sec; OFF
Respiratory Frequency
10 ~ 80 bpm; OFF
Low End Expiratory Pressure
1 ~ 35 cmH2O; OFF
Or 1 ~ 20 cmH2O; OFF (NIV modes only)
End-Tidal CO2 (Upper alarm limit)
0.1% to 13.3% or 1 mmHg to 100 mmHg or 0.1 kPa to 13.3 kPa
End-Tidal CO2 (Lower alarm limit)
OFF, 0.1% to 13.2% or OFF, 1 mmHg to 99 mmHg or OFF, 0.1 kPa to13.2 kPa
11.7.2 Alarms Miscellaneous
Gas Supply
< 160 kPa (29 psi) +10% for 5 seconds or more
11-7
Alarm Silence/reset
Press this key to silence alarms for two minutes. This key also resets latched alarms.
Alarm Sound Pressure
The alarm sound pressure is above 60 dB at lowest volume setting at a distance of 1 meter
from the front of the ventilator.
11.8 Ventilation Modes
11.8.1 Controlled Ventilation
Pressure Control (PCV)
Pressure controlled ventilation
Volume Control (VCV)
Volume controlled ventilation
Pressure Regulated Volume Control (PRVC)
Pressure regulated volume controlled ventilation
Noninvasive Pressure Control (NIV-T)
Noninvasive pressure controlled ventilation
11.8.2 Supported Ventilation
SPONT/CPAP+PSV
Spontaneous continuous positive airway pressure ventilation with pressure supported

ventilation
NIV-S/T
Noninvasive pressure supported ventilation
11.8.3 Combined Ventilation
SIMV (PCV) + PSV
Synchronized intermittent mandatory ventilation based on pressure controlled ventilation with

pressure supported ventilation
11-8
SIMV (VCV) + PSV
Synchronized intermittent mandatory ventilation based on volume controlled ventilation with

pressure supported ventilation
SIMV (PRVC) + PSV
Synchronized intermittent mandatory ventilation based on pressure regulated volume

controlled ventilation with pressure supported ventilation at high and low pressure levels
BIVENT
Pressure controlled ventilation that allows the patient the opportunity of unrestricted
spontaneous ventilating with pressure support at high and low pressure levels
11.9 Trend Function
Peak Airway Pressure Ppeak
Plateau Airway Pressure Pplat
Mean Airway Pressure Pmean
End Expiratory Pressure PEEP
Minimum Airway Pressure Pmin
Inspiratory Tidal Volume Vti
Expiratory Tidal Volume Vte
Expiratory Minute Volume MVe
Spontaneous Minute Volume MVespont
Inspiratory/Expiratory Ratio I:E
Total Ventilating Frequency f total
Spontaneous Ventilating Frequency fspont
Oxygen Concentration O2
Expiratory Resistance Rexp
Dynamic Compliance Cdyn
Rapid - shallow ventilating index RSBI
Work of Ventilating WOB
Leak Leak NIV
11-9
11.10 Log Function
Alarm/Event Log
Alarms
Ventilator Settings
Shortcut key functions
Service Page
Technical alarms
Test results
Calibration results
Configuration log
11.11 Shortcut Key Functions
Insp. Hold
Inspiratory Hold
Exp. Hold
Expiratory Hold
Nebulizer
Start and stop the Nebulizer operation
Manual
Initiation of 1 ventilation in all ventilation modes except SPONT/CPAP
Suction
Initiate and terminate the suction support process.

Disconnection detection – Automatic
Reconnection detection – Automatic
Pre-oxygenation – Max.3 minutes
Active Suction phase – Max.2 minutes
Post-oxygenation – 2 minutes
Freeze
Freeze the current waveforms and loops, or unfreeze the Waveform display
Screen Lock
Lock or unlock the touch screen
11-10
Main Menu
Return to the main menu
11.12 Communication/Interface
11.12.1 Nurse Call Port
The Ventilator has a modular jack configured to interface with external systems and is wired for
normally open (N.O., close on alarm) signals. Contacts close on High priority alarms, loss of
AC power and Speaker failure.
Floating DC contact
Voltage: Max. 50V
Current: Max. 200mA
Pin assignment:
1 Normally open 2 Normally open 3 Normally open

4 Common pin 5 Common pin 6 Common pin
11.12.2 Ethernet Port
Ethernet Port per IEE 802.3 to enable the VG70 to connect to external equipment such as a
electronic health record.
CAUTION:
• connection of the VG70 to an equipment could result in previously unidentified risks to
patients, operators or third parties;
• the facility should identify, analyze, evaluate and control these risks
• subsequent changes to the Ethernet port could introduce new risks and require additional
analysis; and
• changes to the Ethernet Port include:
changes in Ethernet Port configuration;
connection of additional items to the Ethernet Port;
disconnecting items from the Ethernet Port;
update of equipment connected to the Ethernet Port;
update of equipment connected to the Ethernet Port.
11-11
11.12.3 RS-232 Port
Laptop-ready connection for user and service use in future software release.
11.12.4 Nebulizer Output Port
Output port for connection to nebulizer locates in the front of the ventilator. The whole
nebulizer lasts for 30 minutes.
11.13 Accessories
Mobile Cart
Weight: 25Kg
Dimensions: 547 wide x 675 deep x 950 high (mm)
Gas Cylinder Kit
Capacity is two cylinders max, US E cylinders
Humidifier
Fisher & Paykel MR850, MR810
Breath circuit
Fisher & Paykel reusable breathing circuit:
MV1006 (F&P) 900MR761 Adult Circuit Kit

MV1005 (F&P) 900MR742 Adult Single Limb Heated Circuit Kit
MV1007 (F&P) 900MR780 Adult Circuit Kit, Dual Heated 4 LPM
MV1008 (F&P) 900MR781 Infant Circuit Kit, Dual Heated 4 LPM
Other recommended breathing circuit:

Adult breathing circuit (Disposable): mask, headband, elbow,
122000761
breathing circuit etc. Produced by INSPIRED MEDICAL
Adult Breathing Circuit (silicone)-mask, headband, elbow,
122005487
breathing circuit etc. Produced by Liming Rubber
Pediatric Breathing Circuit-(silicone)-mask, headband, elbow,
122005490
breathing circuit etc. Produced by Liming Rubber
Adult breathing circuit (Disposable). Produced by INSPIRED
51005800
MEDICAL
Pediatric breathing circuit (Disposable). Produced by INSPIRED
51008400
MEDICAL
11-12
Oxygen Sensor: To be replaced every 2 years or as necessary. Part number: 210001975
CO2 Module
240000415 IRMA CO2 module

240000416 IRMA Adult airway adapter
240000417 IRMA Pediatric airway Adapter
11.14 Ventilating Parameters: Default Values and

Allowed Settings (Standard Configuration)
Factory Set Default Setting Range

Parameter
Child Adult Child Adult
ATC Tube
OFF OFF ON/OFF ON/OFF
Compensation
ATC Tube Type ET ET ET/Tracheotomy ET/Tracheotomy
ATC Tube
80 80 0 – 100 0 – 100
Compensation (%)
ATC Tube Diameter

5.0 7.5 2.5 – 8.0 5.0 – 12.0
(mm)
Backup Ventilation
Pressure above PEEP 10 20 5 – (70-PEEP) 5 – (70-PEEP)
(cmH2O)
Backup Ventilation
0.6 1.0 0.2 – 5 0.2 - 9
Tinsp (s)
Compliance
ON ON ON/OFF ON/OFF
Compensation
CPAP (cmH2O) in NIV 5 5 2 – 20 2 – 20
Expiratory Trigger
25 25 5 – 80 5 – 80
Sensitivity - Esens(%)
Flow Trigger – Vsens

2.0 2.0 0.5 – 20 0.5 – 20
(l/min)
Frequency - VCV bpm 30 15 1 – 80 1 – 80
Patient Height (cm) 100 150 30 – 140 60 – 260
I:E ratio 1:2 1:2 1:10 – 4:1 1:10 – 4:1
11-13
Parameter
Maximum inspiratory
60 180 --- ---
flow (liters/min)
Maximum permitted
pressure – safety valve 110 110 --- ---
(cmH2O)
Mode (in NIV) NIV/CPAP NIV/CPAP --- ---
Mode(in Invasive
PCV PCV --- ---
Ventilation)
Nebulizer OFF OFF ON/OFF ON/OFF
Nebulizer Time
30 30 --- ---
(minutes)
NIV Rate (bpm) 30 15 4 – 20 4 – 40
O2 Concentration (%) 40 40 21 – 100 21 – 100
PEEP (cmH2O) 5 5 0 – 35 0 – 35
PEEP in NIV (cmH2O) 5 5 2 – 20 2 – 20
Phigh(cmH2O) 15 15 5 – 60 5 – 60
Plow (cmH2O) 5 5 0 – 35 0 – 35
Press trig sensitivity

-3 -3 -20 – 0 -20 - 0
level (cmH2O)
Pressure level above

10 20 5 – (70-PEEP) 5 – (70-PEEP)
PEEP (cmH2O)
PS above PEEP
0 0 0 – (70-PEEP) 0 – (70-PEEP)
(cmH2O)
PS– BIVENT above

0 0 0 – (70-PEEP) 0 – (70-PEEP)
PEEP (cmH2O)
PS– NIV above PEEP

0 0 0 – (50-PEEP) 0 – (50-PEEP)
(cmH2O)
SIMV rate (bpm) 20 4 1 – 40 1 - 40
Thigh(s) 0.6 1.0 0.2 – 30 0.2 - 30
Tinsp(s) 0.6 1.0 0.2 – 5 0.2 – 9
Tidal Volume (mL) 80 400 20 – 300 50 – 2000
11-14

Parameter
Tlow (s) 1.4 3.0 0.2 – 30 0.2 – 30
Tpause (s) 0 0 0–4 0–4
Tslope(s) 0.1 0.1 0–2 0–2
Alarm Settings: Default Settings and Allowed Ranges

Alarm Limits
Airway Pressure, high limit (cmH2O) 40 40 5 - 100 5 - 100
Airway Pressure, low limit (cmH2O) 5 5 OFF, 1 - 60 OFF, 1 - 60
PEEP Low limit in Invasive

OFF OFF OFF, 1 – 35 OFF, 1 - 35
Ventilation(cmH2O)
PEEP Low limit in NIV (cmH2O) OFF OFF OFF, 1 – 20 OFF, 1 - 20
PEEP high limit in Invasive Ventilation

10 10 1 – 35, OFF 1 - 35, OFF
(cmH2O)
PEEP high limit in NIV (cmH2O) OFF OFF 1 – 20, OFF 1 - 20, OFF
OFF, 0.1 –
etCO2 low limit % 4.0 4.0 OFF, 0.1 – 13.2
13.2
etCO2 low limit mmHg 30 30 OFF, 1 - 99 OFF, 1 - 99
OFF, 0.1 –
etCO2 low limit kPa 4.0 4.0 OFF, 0.1 – 13.2
13.2
etCO2 high limit % 6.5 6.5 0.1 – 13.3 0.1 – 13.3
etCO2 high limit mmHg 49 49 1 - 100 1 - 100
etCO2 high limit kPa 6.5 6.5 0.1 – 13.3 0.1 – 13.3
Expired Minute Volume, low limit

0.5 1.0 OFF, 0.1 – 40 OFF, 0.1 – 40
(lpm)
Expired Minute Volume, high limit

30 30 1 – 60, OFF 1 – 60, OFF
(lpm)
Expired Tidal Volume, low limit (mL) 50 250 5 - 400 5 - 4000
Respiratory Frequency, Spontaneous,

OFF OFF 10 - 80, OFF 10 - 80, OFF
Upper limit (bpm)
11-15
Alarm Limits
Time, Apnea – until alarm (sec) 20 20 10 – 60, OFF 10 - 60, OFF
NOTE: Regarding occlusion detection and continuing pressure events:
Occlusion detection occurs in every ventilation mode. In the case that the Patient Airway
Pressure is positive for more than 15 seconds at an unexpected level, the system will treat this
continuing pressure event as an occlusion and behave accordingly.
NOTE: Regarding Nebulizer usage while on battery power:
The nebulizer function is disabled when the Ventilator is powered by either the internal or
external battery.
Ventilating Parameters: Default Values and Allowed Settings (Standard Configuration).
11.15 Delivery Accuracy
Airway Pressure
+/- 10% of settings or +/- 3 cmH2O (whichever is greater)
Tidal Volume
Adult Accuracy: +/- 10% of settings +/- 25 mL (whichever is greater)
Child Accuracy: +/- 10% of settings +/- 10 mL (whichever is greater)
O2 Concentration
+/- 5% full scale for all modes
21% to 90% rising time (at worst case): 3 min 22 s
PEEP
+/- 10% of settings or +/- 2 cmH2O (whichever is greater) for all modes
Measurement uncertainty
Volume: +/- 2% of reading or +/- 20 mL (whichever is greater)
Pressure: +/- 0.75% of reading or +/- 0.1 cmH2O (whichever is greater)
O2: +/- 1%
11-16
12 Pneumatic Diagram
12 Pneumatic Diagram
12-1
13 EMC
13 EMC
Electromagnetic Compatibility
Changing or reassembling this equipment without our company‟s authorization may cause
electromagnetic compatibility problems. Contact our company for assistance. Designing and
testing this equipment is in accordance with the following stipulations.
WARNING: Using cell phone or other radio radiant equipment near this product may cause
malfunction. Closely monitor the working condition of this equipment if there is any radio
radiant supply nearby.
Using other electrical equipment in this system or nearby may cause interference. Check if the
equipment works normally in these conditions before using on a patient.
Use caution of the following when the ventilator is connected:
Do not put any object which is not in accordance with EN 60601-1 in the 1.5M range of
patients.
A complete system current leaking test (according to EN 60601-1) must be performed after
any equipment is connected to these outlets.
If a portable all-purpose outlet is used as the alternating current supply, it must be in

accordance with EN 60601-1 and cannot be put on the floor. Using another portable
all-purpose outlet is not recommended.
Do not connect the non-medical equipment directly to the alternating current outlet on the wall.
Only the alternating current supply of the isolated transformer can be used. Otherwise, the
surface leaking current may exceed the range permitted by EN 60601-1 under the normal
conditions, and misoperation may cause injury to patients or operators.
WARNING: Do not use other power cords and if it is necessary, the selected cable must be
in accordance with IEC60601-1-2.
WARNING: The equipment should not be used adjacent to or stacked with other
equipment and if adjacent or stacked use is necessary, the equipment should be observed to
verify normal operation in configuration in which it will be used.
13-1
Guidance and manufacture’s declaration – electromagnetic emission for the Ventilator
The Ventilator is intended for use in the electromagnetic environment specified below. The
customer of the user of the Ventilator should assure that it is used in such an environment.
Emission test Compliance Electromagnetic environment – guidance
The Ventilator uses RF energy only for its

internal function. Therefore, its RF emissions
RF emissions CISPR 11 Group 1
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emission CISPR 11 Class A
The Ventilator is suitable for use in all

Harmonic emissions IEC
Class A establishments, including domestic and those
61000-3-2
directly connected to the public low-voltage
power supply network that supplies buildings
Voltage fluctuations/ used for domestic purposes.
flicker emissions IEC Complies
61000-3-3
Guidance and manufacture’s declaration – electromagnetic immunity for the Ventilator
customer or the user of the Ventilator should assure that it is used in such an environment.
Electromagnetic
Immunity test IEC 60601 test level Compliance level
environment- guidance
Floors should be wood,

concrete or ceramic tile. If
Electrostatic
±6 kV contact ±6 kV contact floors are covered with
discharge (ESD)
±8 kV air ±8 kV air synthetic material, the
IEC 61000-4-2
relative humidity should be
at least 30%.
±2 kV for power Mains power quality should

Electrical fast
supply lines ±2kV for power be that of a typical
transient/burst
±1 kV for input/output supply lines commercial or hospital
IEC 61000-4-4
lines environment.
Mains power quality should

±1 kV differential ±1 kV differential
Surge be that of a typical
mode ±2 kV common mode ±2 kV
IEC 61000-4-5 commercial or hospital
mode common mode
environment.
Voltage dips, short <5% UT (>95% dip in <5% UT (>95% dip Mains power quality should
13-2
13 EMC
interruptions and UT) for 0.5 cycle in UT) for 0.5 cycle
be that of a typical
voltage variations 40% UT (60% dip in 40% UT (60% dip in commercial or hospital
on power supply UT) for 5 cycles UT) for 5 cycles environment. If the user of
input lines 70% UT (30% dip in 70% UT (30% dip in the Ventilator requires
IEC 61000-4-11 UT) for 25 cycles UT) for 25 cycles continued operation during
power mains interruptions, it
<5% UT (>95% dip in <5% UT (>95% dip
is recommended that the
UT) for 5 sec in UT) for 5 sec
Ventilator be powered from
an uninterruptible power
supply or a battery.
Power frequency magnetic

Power frequency fields should be at levels
(50/60Hz) characteristic of a typical
3A/m 3A/m
magnetic field location in a typical
IEC 61000-4-8 commercial or hospital
environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacture’s declaration – electromagnetic immunity for the Ventilator
customer or the user of the Ventilator should assure that it is used in such an environment.
IEC 60601 Electromagnetic environment -

Immunity test
test level Compliance level guidance
Portable and mobile RF

communications equipment should
be used no closer to any part of the
Ventilator, including cables, than
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
Conducted RF 3 Vrms 150 kHz 3 V √
IEC 61000-4-6 to
√
80 MHz
outside ISM 10V
bands a
3Vrms 150 kHz √ 80 MHz to 800 MHz
13-3
Radiated RF to √ 800 MHz to 2.5 GHz
IEC 61000-4-3 80MHz in ISM 10 V/m Where P is the maximum output
banda power rating of the transmitter in
3 V/m 80 MHz watts (W) according to the
to 2.5 GHz transmitter manufacturer and d is
distance in metres (m). b
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey ,c
should be less than the compliance
level in each frequency range .d
Interference may occur in the
vicinity of equipment marked with
the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
a. The ISM (industrial, scientific and medical) bands between 150kHz and 80MHz are 6.765
MHz to 6.795 MHz; 13.553MHz to 13.567MHz; 26.957 MHz to 27.283 MHz; and 40.66
MHz to 40.70.
b. The compliance levels in the ISM frequency bands between 150 kHz and 80MHz and in the
frequency range 80MHz to 2.5GHz are intended to decrease the likelihood that
mobile/portable communications equipment could cause interference if it is inadvertently
brought into patient areas. For this reason, an additional factor of 10/3 is used in
calculating the recommended separation distance for transmitters in these frequency
ranges.
c. 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 the Ventilator is used
exceeds the applicable RF compliance level above, the Ventilator should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the Ventilator.
d. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
13-4
13 EMC
Recommended separation distances between portable and mobile RF communications

equipment and the Ventilator
The Ventilator is intended for use in an electromagnetic environment in which radiated RF

disturbances are controlled. The customer or the user of the Ventilator can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile
RF communications equipment (transmitters) and the Ventilator as recommended below,
according to the maximum output power of the communications equipment.
Rated Separation distance according to frequency of transmitter (m)

maximum 150 kHz to
output power 150 kHz to 80 MHz 80 MHz to 800 MHz to
80 MHz outside
of transmitter in ISM bands 800 MHz 2.5 GHz
ISM bands
(W) √ √ √
√
0.01 0.17 0.12 0.12 0.23
0.1 0.37 0.38 0.38 0.73
1 1.17 1.2 1.2 2.3
10 3.7 3.79 3.79 7.27
100 11.7 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in metres (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 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTE 2: The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz
are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and
40.66MHz to 40.70MHz.
NOTE 3: An additional factor of 10/3 is used in calculating the recommended separation
distance for transmitters in the ISM frequency bands between 150 kHz and 80 MHz and in the
frequency range 80 MHz to 2.5 GHz to decrease the likelihood that mobile/portable
communications equipment could cause interference if it is inadvertently brought into patient
areas.
13-5
This manual No.: 130013843
CE mark in this manual apply only to product

with CE mark.
Directive 93/42/EEC
concerning Medical Devices
Edition 01.01
Jan. 2017

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Appendix 5:

Beijing Aeonmed Co., Ltd.

Patient type：Adult and pediatric patient

Ventilation modes： VCV(A/C)

Pressure and Flow trigger

Automatic Tube Compensation (ATC)

Non-invasive ventilation (NIV)

Ventilation frequency (f)VCV： 1-80/min （adult）

NIV Ventilation frequency (f)： 4-20/min （adult）

Inspiratory time (Ti)： 0.2-9 s （adult）

Tidal volume (VT)： 50-2000ml （adult）

Tpause： 0-4 s （adult）

Ventilation frequency (f)SIMV：1-40/min

Inspiratory pressure (Pinsp): 5-70 cmH2O

Psupp： 0-70 cmH2O

Psupp NIV： 0 to（50-PEEP ）cmH2O

PEEP: 0-35 cmH2O

PEEP in NIV： 2-20 cmH2O

CPAP in NIV： 2-20 cmH2O

Rise time (Slope)： 0-2 s

O2 concentration (FiO2)： 21%-100%

Trigger sensitivity: 0.5 to 20 L/min（Flow trigger）

-20 to 0 cmH2O （Pressure trigger）

Exp. sensitivity(% of peak flow)： 5%-80%

Phigh： 5-60 cmH2O

Plow： 0-35 cmH2O

Automatic Tube Compensation (ATC)

Inner tube diameter： 5-12mm （adult）

Tube type： Endotracheal tube ET

Tracheostomy tube Trach

Measured values displayed

Airway pressure measurement：

Plateau pressure (Pplat)

Positive end-expiratory pressure (PEEP)

Peak inspiratory pressure (Ppeak)

Mean airway pressure (Pmean)

Min. airway pressure (Pmin)

Expiratory minute volume (MVe)

Spontaneous expiratory minute volume (MVespont)

Inspiratory tidal volume (VTi)

Expiratory tidal volume (VTe)

Total respiratory frequency (ftotal)

Spontaneous respiratory frequency (fspont)

Inspiratory O2 concentration (FiO2)

End-expiratory CO2 concentration (etCO2)

Displayed calculated values

Flow (t) -180 to 180 L/min

Volume (t) 0 to 3000ml

CO2 (t) 0 to 80 cmH2O

Expiratory minute volume (MVe) High / Low

Airway pressure (Paw) High / Low

Expiratory tidal volume (Vte) low

PEEP High / Low

Insp. O2 concentration (FiO2) High / Low

End - expiratory CO2 concentration (etCO2) High / Low

Respiratory rate (f) High