Mindray SynoVent E5 User manual

SynoVent E5 Ventilator
Operator’s Manual

I
© 2010-2014 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights Reserved.
For this Operator’s Manual, the issue date is April, 2014.

II
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called
Mindray) owns the intellectual property rights to this Mindray product and this manual. This
manual may refer to information protected by copyright or patents and does not convey any
license under the patent rights or copyright of Mindray, or of others.
Mindray intends to maintain the contents of this manual as confidential information.
Disclosure of the information in this manual in any manner whatsoever without the written
permission of Mindray is strictly forbidden. Release, amendment, reproduction, distribution,
rental, adaptation, translation or any other derivative work of this manual in any manner
whatsoever without the written permission of Mindray is strictly forbidden.
, , and SynoVent are the trademarks, registered or
otherwise, of Mindray in China and other countries. All other trademarks that appear in this
manual are used only for informational or editorial purposes. They are the property of their
respective owners.

III
Responsibility on the Manufacturer
Party
Contents of this manual are subject to change without prior notice.
All information contained in this manual is believed to be correct. Mindray shall not be liable
for errors contained herein or for incidental or consequential damages in connection with the
furnishing, performance, or use of this manual.
Mindray is responsible for the effects on safety, reliability and performance of this product,
only if:
all installation operations, expansions, changes, modifications and repairs of this product
are conducted by Mindray authorized personnel;
the electrical installation of the relevant room complies with the applicable national and
local requirements;and
the product is used in accordance with the instructions for use.
WARNING
It is important for the hospital or organization that employs this equipment to
carry out a reasonable service/maintenance plan. Neglect of this may result in
machine breakdown or personal injury.
NOTE
This equipment must be operated by skilled/trained clinical professionals.

IV
Warranty
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES,
EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR
FITNESS FOR ANY PARTICULAR PURPOSE.
Exemptions
Mindray's obligation or liability under this warranty does not include any transportation or
other charges or liability for direct, indirect or consequential damages or delay resulting from
the improper use or application of the product or the use of parts or accessories not approved
by Mindray or repairs by people other than Mindray authorized personnel.
This warranty shall not extend to:
Malfunction or damage caused by improper use or man-made failure.
Malfunction or damage caused by unstable or out-of-range power input.
Malfunction or damage caused by force majeure such as fire and earthquake.
Malfunction or damage caused by improper operation or repair by unqualified or
unauthorized service people.
Malfunction of the instrument or part whose serial number is not legible enough.
Others not caused by instrument or part itself.

V
Customer Service Department
EC-Representative: Shanghai International Holding Corp. GmbH(Europe)
Address: Eiffestraβe 80, 20537 Hamburg, GERMANY
Tel: [phone]
Fax: [phone]
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address: Mindray Building,Keji 12th Road South,High-tech industrial
park,Nanshan,Shenzhen 518057,P.R.China
Website: www.mindray.com
E-mail Address: [email protected]
Tel: [phone]
Fax: [phone]

VI
Preface
Manual Purpose
This manual contains the instructions necessary to operate the product safely and in
accordance with its function and intended use. Observance of this manual is a prerequisite for
proper product performance and correct operation and ensures patient and operator safety.
This manual is based on the maximum configuration and therefore some contents may not
apply to your product. If you have any question, please contact us.
This manual is an integral part of the product. It should always be kept close to the equipment
so that it can be obtained conveniently when needed.
Intended Audience
This manual is geared for clinical professionals who are expected to have a working
knowledge of medical procedures, practices and terminology as required for monitoring of
critically ill patients.
Illustrations
All illustrations in this manual serve as examples only. They may not necessarily reflect the
setup or data displayed on your ventillator.
Conventions
Italic text is used in this manual to quote the referenced chapters or sections.
[ ] is used to enclose screen texts.
→is used to indicate operational procedures.
Password
A password is required to access different modes within the ventilator machine.
User maintenance: 1234

1
Table of Contents
1 Safety................................................................................................................................. 1-1
1.1 Safety Information .......................................................................................................... 1-1
1.1.1 Dangers .............................................................................................................. 1-2
1.1.2 Warnings............................................................................................................. 1-2
1.1.3 Cautions ............................................................................................................. 1-4
1.1.4 Notes .................................................................................................................. 1-6
1.2 Equipment Symbols ........................................................................................................ 1-7
2 The Basics ......................................................................................................................... 2-1
2.1 System Description ......................................................................................................... 2-1
2.1.1 Intended Use....................................................................................................... 2-1
2.1.2 Contraindications ............................................................................................... 2-1
2.1.3 Components ....................................................................................................... 2-1
2.2 Equipment Appearance ................................................................................................... 2-2
2.2.1 Front View.......................................................................................................... 2-2
2.2.2 Rear View........................................................................................................... 2-4
2.2.3 Air Compressor .................................................................................................. 2-5
3 Installations and Connections ......................................................................................... 3-1
3.1 Install the Display ........................................................................................................... 3-1
3.1.1 Install the Display onto the Ventilator................................................................ 3-1
3.1.2 Install the Display onto the Pendant................................................................... 3-2
3.2 Connect the Power Supply .............................................................................................. 3-4
3.2.1 Connect the System Power Supply .................................................................... 3-4
3.2.2 Connect the Main Unit Power Supply................................................................ 3-5
3.2.3 Connect the Compressor Power Supply............................................................. 3-6
3.3 Connect the Gas Supply .................................................................................................. 3-7
3.4 Install the Support Arm ................................................................................................... 3-8
3.5 Install the Water Traps................................................................................................... 3-10
3.6 Install the Breathing Hoses ............................................................................................3-11
3.7 Install the Humidifier .................................................................................................... 3-12
3.7.1 Install the Humidifier onto the Ventilator......................................................... 3-12
3.7.2 Install the Humidifier onto the Pendant ........................................................... 3-13
3.8 Install the Nebulizer ...................................................................................................... 3-15
3.9 Install the CO2 Module................................................................................................. 3-16
3.10 Install the O2 Sensor ................................................................................................... 3-17
4 User Interface ................................................................................................................... 4-1
4.1 Display Controls ............................................................................................................. 4-1
4.1.1 Display ............................................................................................................... 4-2
4.1.2 Fixed Hard Keys ................................................................................................ 4-4
4.2 Waveforms Screen........................................................................................................... 4-6

2
4.3 Spirometry Loops Screen................................................................................................ 4-7
4.4 Graphic Trend Screen...................................................................................................... 4-8
4.5 Tabular Trend Screen .................................................................................................... 4-10
4.6 Measured Values Screen.................................................................................................4-11
4.7 Freeze............................................................................................................................ 4-12
5 System Settings................................................................................................................. 5-1
5.1 Change Display Settings ................................................................................................. 5-1
5.1.1 Waveforms ......................................................................................................... 5-1
5.1.2 Spirometry Loops............................................................................................... 5-1
5.1.3 Measured Values ................................................................................................ 5-1
5.1.4 Colors ................................................................................................................. 5-2
5.2 Set Date and Time ........................................................................................................... 5-3
5.3 Change Language............................................................................................................ 5-3
5.4 Adjust Screen Brightness ................................................................................................ 5-3
5.5 Adjust Key Volume ......................................................................................................... 5-3
5.6 Set Unit ........................................................................................................................... 5-3
5.6.1 Set Weight Unit .................................................................................................. 5-3
5.6.2 Set Paw Unit....................................................................................................... 5-4
5.6.3 Set CO2 Unit...................................................................................................... 5-4
5.7 Turning on/off O2% Monitoring ..................................................................................... 5-4
5.8 Select Tinsp/I:E ............................................................................................................... 5-4
5.9 Set TV/f Source............................................................................................................... 5-4
5.10 Set Sigh ......................................................................................................................... 5-4
5.11 Set IP Address ............................................................................................................... 5-5
5.12 Manage Configurations................................................................................................. 5-5
5.12.1 Restore the Latest Configuration Automatically .............................................. 5-5
5.12.2 Set Power-on Default Configuration ................................................................ 5-5
5.12.3 Save as User Configuration.............................................................................. 5-6
5.12.4 Load Configuration Manually.......................................................................... 5-6
5.13 View System Information.............................................................................................. 5-6
5.13.1 Version Information.......................................................................................... 5-6
5.13.2 Configuration Information ............................................................................... 5-6
5.13.3 System Check Results ...................................................................................... 5-6
5.13.4 Maintenance Information ................................................................................. 5-6
5.14 Export............................................................................................................................ 5-7
5.14.1 Export Screen ................................................................................................... 5-7
5.14.2 Export Data ...................................................................................................... 5-7
6 Start Ventilation................................................................................................................ 6-1
6.1 Turn on the System ......................................................................................................... 6-1
6.2 Preoperative Test ............................................................................................................. 6-1
6.2.1 AC Power and Battery Power Source Switch Test ............................................. 6-1
6.2.2 Pipeline Tests...................................................................................................... 6-1
6.3 Power on Self-test ........................................................................................................... 6-2

3
6.4 System Check.................................................................................................................. 6-2
6.5 Select Patient................................................................................................................... 6-3
6.6 Ventilation Type .............................................................................................................. 6-4
6.6.1 Invasive Ventilation............................................................................................ 6-4
6.6.2 NIV (non-invasive ventilation) .......................................................................... 6-5
6.6.3 Set Ventilation Type ........................................................................................... 6-5
6.7 Ventilation Mode............................................................................................................. 6-6
6.7.1 Ventilation Mode and Parameter Setup .............................................................. 6-6
6.7.2 Apnea Ventilation ............................................................................................... 6-7
6.7.3 IntelliCycle......................................................................................................... 6-8
6.7.4 V-A/C ................................................................................................................. 6-8
6.7.5 P-A/C ............................................................................................................... 6-10
6.7.6 CPAP/PSV.........................................................................................................6-11
6.7.7 V-SIMV and P-SIMV....................................................................................... 6-13
6.7.8 PRVC................................................................................................................ 6-16
6.7.9 DuoLevel.......................................................................................................... 6-18
6.7.10 APRV.............................................................................................................. 6-19
6.8 Change Alarm Limits .................................................................................................... 6-20
6.9 Ventilate the Patient....................................................................................................... 6-20
6.10 Ventilation Parameters Monitoring ............................................................................. 6-21
6.11 Enter Standby .............................................................................................................. 6-23
6.12 Turn the System off..................................................................................................... 6-23
7 CO2 Monitoring ............................................................................................................... 7-1
7.1 Introduction..................................................................................................................... 7-1
7.2 Prepare to Measure CO2 ................................................................................................. 7-2
7.3 Make CO2 Settings ......................................................................................................... 7-3
7.3.1 Set Working Mode.............................................................................................. 7-4
7.3.2 Set Pump Rate.................................................................................................... 7-4
7.3.3 Set Unit .............................................................................................................. 7-4
7.3.4 Set Humidity Compensation .............................................................................. 7-5
7.3.5 Restore Defaults................................................................................................. 7-5
7.3.6 Set CO2 Waveform ............................................................................................ 7-5
7.4 Measurement Limitations................................................................................................ 7-5
7.5 Troubleshooting .............................................................................................................. 7-6
7.6 Zero the Sensor ............................................................................................................... 7-6
7.7 Calibrate the Sensor ........................................................................................................ 7-6
8 Special Functions.............................................................................................................. 8-1
8.1 Manual Breath................................................................................................................. 8-1
8.2 Expiration Hold............................................................................................................... 8-1
8.3 Inspiration Hold .............................................................................................................. 8-2
8.4 Nebulizer......................................................................................................................... 8-2
8.5 O2↑................................................................................................................................ 8-3
8.6 Suction ............................................................................................................................ 8-3

4
8.7 P0.1 ................................................................................................................................. 8-4
8.8 NIF .................................................................................................................................. 8-4
8.9 PEEPi .............................................................................................................................. 8-5
8.10 P-V Tool ........................................................................................................................ 8-5
9 Alarms ............................................................................................................................... 9-1
9.1 Introduction..................................................................................................................... 9-1
9.2 Alarm Categories............................................................................................................. 9-1
9.3 Alarm Levels ................................................................................................................... 9-2
9.4 Alarm Indicators.............................................................................................................. 9-2
9.4.1 Alarm Lamp ....................................................................................................... 9-2
9.4.2 Audible Alarm Tones.......................................................................................... 9-3
9.4.3 Alarm Message................................................................................................... 9-3
9.4.4 Flashing Alarm Numeric .................................................................................... 9-3
9.4.5 Alarm Status Symbol.......................................................................................... 9-4
9.5 Set Alarm Volume ........................................................................................................... 9-4
9.6 Set Alarm Limits ............................................................................................................. 9-4
9.7 Set Apnea Time ............................................................................................................... 9-5
9.8 Alarm Silence.................................................................................................................. 9-5
9.8.1 How to Set Alarm Silence .................................................................................. 9-5
9.8.2 How to Cancel Alarm Silence ............................................................................ 9-5
9.9 Alarm Reset..................................................................................................................... 9-6
9.10 Nurse Call ..................................................................................................................... 9-6
9.11 Alarm Test ..................................................................................................................... 9-7
9.11.1 Battery in Use Alarm........................................................................................ 9-7
9.11.2 Battery Depletion Alarm .................................................................................. 9-7
9.11.3 Paw Too High Alarm........................................................................................ 9-8
9.11.4 TV Not Achieved Alarm................................................................................... 9-8
9.11.5 MV Too Low Alarm ......................................................................................... 9-8
9.11.6 O2 Supply Pressure Low Alarm....................................................................... 9-8
9.11.7 Air Supply Pressure Low Alarm....................................................................... 9-9
9.11.8 Airway Obstructed Alarm................................................................................. 9-9
9.11.9 FiO2 Too High Alarm....................................................................................... 9-9
9.11.10 FiO2 Too Low Alarm ..................................................................................... 9-9
9.11.11 EtCO2 Too High Alarm.................................................................................. 9-9
9.11.12 EtCO2 Too Low Alarm ................................................................................ 9-10
9.12 Alarm Logbook ........................................................................................................... 9-10
9.13 When an Alarm Occurs ................................................................................................9-11
10 Cleaning and Disinfection............................................................................................ 10-1
10.1 Methods for Cleaning and Disinfection ...................................................................... 10-2
10.2 Disassemble the Ventilator’s Cleanable Parts ............................................................. 10-4
10.2.1 Expiration Valve Assembly ............................................................................ 10-4
10.2.2 Expiration Valve Flow Sensor........................................................................ 10-5
10.2.3 Water Trap ...................................................................................................... 10-6

5
10.2.4 Breathing Hoses ............................................................................................. 10-7
10.2.5 Nebulizer ........................................................................................................ 10-8
10.2.6 Humidifier ...................................................................................................... 10-9
10.2.7 O2 Sensor..................................................................................................... 10-12
11 Maintenance...................................................................................................................11-1
11.1 Repair Policy................................................................................................................11-1
11.2 Maintenance Schedule..................................................................................................11-2
11.3 Pressure and Flow Zeroing...........................................................................................11-3
11.4 Flow Sensor Calibration...............................................................................................11-4
11.5 O2 Concentration Calibration ......................................................................................11-5
11.6 CO2 Module Calibration..............................................................................................11-6
11.7 Touch Screen Calibration .............................................................................................11-7
11.8 Battery Maintenance ....................................................................................................11-7
11.8.1 Battery Use Guidance......................................................................................11-8
11.8.2 Battery Performance Conditioning..................................................................11-9
11.8.3 Battery Performance Checking........................................................................11-9
11.8.4 Battery Recycling..........................................................................................11-10
11.9 Electrical Safety Inspection........................................................................................11-10
11.9.1 Auxiliary Electrical Outlet Test .....................................................................11-10
11.9.2 Electrical Safety Inspection Test ...................................................................11-11
11.10 Water Build-up in the Flow Sensor ..........................................................................11-12
11.10.1 Prevent Water Build-up ...............................................................................11-12
11.10.2 Clear Water Build-up...................................................................................11-12
12 Accessories .................................................................................................................... 12-1
A Theory of Operation....................................................................................................... A-1
A.1 Pneumatic System ......................................................................................................... A-1
A.2 Electrical System........................................................................................................... A-6
B Product Specifications.....................................................................................................B-1
B.1 Safety Specifications ......................................................................................................B-1
B.2 Environmental Specifications.........................................................................................B-2
B.3 Power Requirements.......................................................................................................B-2
B.4 Physical Specifications...................................................................................................B-3
B.5 Pneumatic System Specifications...................................................................................B-4
B.6 Ventilator Specifications.................................................................................................B-5
B.7 V
entilator Accuracy ........................................................................................................B-7
B.8 Alarms ............................................................................................................................B-9
B.9 Special Functions .........................................................................................................B-10
B.10 CO2Module Specifications ........................................................................................B-11
B.11 Compressor Specifications .........................................................................................B-12
B.12 O2Sensor Specifications ............................................................................................B-12

6
C EMC ................................................................................................................................ C-1
D Alarm Messages.............................................................................................................. D-1
D.1 Physiological Alarm Messages...................................................................................... D-1
D.2 Technical Alarm Messages............................................................................................ D-2
E Factory Defaults ..............................................................................................................E-1
E.1 CO2 Module ................................................................................................................... E-1
E.2 Alarm .............................................................................................................................. E-1
E.3 Ventilation Mode ............................................................................................................ E-2
F Symbols and Abbreviations............................................................................................. F-1
F.1 Symbols........................................................................................................................... F-1
F.2 Abbreviations .................................................................................................................. F-3

1-1
1 Safety
1.1 Safety Information
DANGER
Indicates an imminent hazard that, if not avoided, will result in death or serious
injury.
WARNING
Indicates a potential hazard or unsafe practice that, if not avoided, could result in
death or serious injury.
CAUTION
Indicates a potential hazard or unsafe practice that, if not avoided, could result in
minor personal injury or product/property damage.
NOTE
Provides application tips or other useful information to ensure that you get the
most from your product.

1-2
1.1.1 Dangers
There are no dangers that refer to the product in general. Specific “Danger” statements may
be given in the respective sections of this manual.
1.1.2 Warnings
WARNING
The ventilator must only be operated and used by authorized medical personnel
well trained in the use of this product. It must be operated strictly following the
Operator’s Manual.
To avoid the risk of electric shock, this equipment must only be connected to
supply mains with protective earth.
The equipment must be connected to a properly installed power outlet with
protective earth contacts only. If the installation does not provide for a protective
earth conductor, disconnect it from the power line.
Use AC power source before the batteries are depleted.
To avoid explosion hazard, do not use the equipment in the presence of flammable
anesthetic agent, vapors or liquids.
Do not place the ventilator adjacent to any barrier, which can prevent cold air
from flowing, resulting in equipment overheat.
Do not open the equipment housings. All servicing and future upgrades must be
carried out by the personnel trained and authorized by us only.
Do not rely exclusively on the audible alarm system for patient monitoring.
Adjustment of alarm volume to a low level may result in a hazard to the patient.
Remember that alarm settings should be customized according to different patient
situations and always keeping the patient under close surveillance is the most
reliable way for safe patient monitoring.
The physiological parameters and alarm messages displayed on the screen of the
equipment are for doctor’s reference only and cannot be directly used as the basis
for clinical treatment.
Dispose of the package material, observing the applicable waste control regulations
and keeping it out of children’s reach.
All staff should be aware that disassembling or cleaning some parts of the
ventilator can cause risk of infection.
Maintenance mode should be used only when the equipment is not connected to a
patient.

1-3
WARNING
Positive pressure breathing may be accompanied by some side effects such as
barotrauma, hypoventilation, hyperventilation etc.
Using the ventilator in the vicinity of high-frequency electrosurgery units,
defibrillators or short-wave therapy equipment may impair correct functioning of
the ventilator and endanger the patient.
Do not use antistatic or conductive masks or breathing hoses. They can cause burns
if they are used near high frequency electrosurgical equipment.
Do not use the ventilator in a hyperbaric chamber to avoid potential fire hazard
due to an oxygen-enriched environment.
If the equipment internal monitoring system malfunctions, an alternative plan
must be available to ensure adequate level of monitoring. The operator of the
ventilator must be responsible for proper patient ventilation and safety under all
circumstances.
As required by the relevant rules and regulations, oxygen concentration should be
monitored when the equipment is used on the patient. If your ventilator is not
configured with such monitoring function or this function is turned off, use a
monitor which complies with the relevant international rules and regulations for
oxygen concentration monitoring.
When auxiliary electrical outlets are configured, the voltage and current
specifications of the devices connected to the electrical outlets must be within the
permissible ranges for those of the electrical outlets. When the protection
grounding is defective, connection of equipment to the auxiliary electrical outlet
may increase the patient leakage current to values exceeding the allowable limits.
When the auxiliary electrical outlet does not work normally, check if the
corresponding fuse is burned.
All analog or digital products connected to this system must be certified passing the
specified IEC standards (such as IEC 60950 for data processing equipment and
IEC 60601-1 for medical electrical equipment). All configurations shall comply
with the valid version of IEC 60601-1-1. The personnel who are responsible for
connecting the optional equipment to the I/O signal port shall be responsible for
medical system configuration and system compliance with IEC 60601-1-1 as well.
Do not touch the patient when connecting the peripheral equipment via the I/O
signal ports or replacing the oxygen cell to prevent patient leakage current from
exceeding the requirements specified by the standard.
This product must be operated by doctors, respiration therapist or other specially
trained and authorized personnel. Anyone unauthorized or untrained must not
perform any operation on it.
This equipment is not suitable for use in an MRI environment.

1-4
WARNING
When the ventilator input system fails or has faults, please contact us immediately
for specified personnel to service the ventilator.
Use the humidifiers with a CE mark or recommended by us only.
The ventilator cannot use He and O2 mixed gas.
Do not move the ventilator before removing the support arm from it, in order to
avoid the ventilator getting tilted during the movement.
Nebulization or humidification can increase the resistance of breathing system
filters and that you need to monitor the filter frequently for increased resistance
and blockage.
The ventilation accuracy can be affected by the gas added by use of a nebulizer.
The ventilator shall not be used with nitric oxide.
The ventilator shall not be used with helium or mixtures with Helium.
For non-invasive ventilation, the exhaled volume of the patient can differ from the
measured exhaled volume due to leaks around the mask.
Check if the alarm limit settings are appropriate before taking measurement.
The mains plug is used to isolate the ventilator circuits electrically from the
SUPPLY MAINS，not to position the ventilator so that it is difficult to operate the
plug.
No modification of this equipment is allowed.
Do not touch the patient when connecting the peripheral equipment via the I/O
signal ports or replacing the oxygen cell to prevent patient leakage current from
exceeding the requirements specified by the standard.
RJ45 port is used for software upgrades by the personnel trained and authorized
by us only. Do not connect it to other devices or internet.
1.1.3 Cautions
CAUTION
The ventilator must be inspected and serviced regularly by trained service
personnel.
To ensure patient safety, always prepare pulmotor for use.
Always have a special person attend and monitor the operation of the equipment
once the ventilator is connected to the patient.
During the operation of the ventilator, do not disassemble the expiration valve and
expiratory flow sensor, which, however, can be disassembled in standby mode.

1-5
CAUTION
To ensure patient safety, use only parts and accessories specified in this manual.
At the end of its service life, the equipment, as well as its accessories, must be
disposed of in compliance with the guidelines regulating the disposal of such
products.
Magnetic and electrical fields are capable of interfering with the proper
performance of the equipment. For this reason make sure that all external devices
operated in the vicinity of the equipment comply with the relevant EMC
requirements. Mobile phone, X-ray equipment or MRI devices are a possible
source of interference as they may emit higher levels of electromagnetic radiation.
This system operates correctly at the electrical interference levels identified in this
manual. Higher levels can cause nuisance alarms that may stop mechanical
ventilation. Pay attention to false alarms caused by high-intensity electrical fields.
Before connecting the equipment to the power line, check that the voltage and
frequency ratings of the power line are the same as those indicated on the
equipment’s label or specified in this manual.
Always install or carry the equipment properly to avoid damage caused by drop,
impact, strong vibration or other mechanical force.
The ventilator or its part should be positioned so that is easy to view.
The ventilator is intended to be used in the patient environment.
Additional MULTIPLE SOCKET- OUTLET or extension cord shall not be
connected to the system.
When pushing the ventilator over the obstacles such as threshold, force the
ventilator downwards to avoid getting tilted.

1-6
1.1.4 Notes
NOTE
Put the equipment in a location where you can easily see the screen and access the
operating controls.
Keep this manual close to the equipment so that it can be obtained conveniently
when needed.
The software was developed in compliance with IEC 60601-1-4. The possibility of
hazards arising from software errors is minimized.
This manual describes all features and options. Your equipment may not have all
of them.