Amoul i6 User manual

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i6-English Instructions
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1
www.amoulmed.com

I
Table of Contents
Table of Contents...........................................................................................................................I
1 Safety Instructions....................................................................................................................... 1
1.1 Safety Signs....................................................................................................................1
1.2 Safety Overview.............................................................................................................1
1.2.1 Hazards...............................................................................................................1
1.2.2 Warnings............................................................................................................ 2
1.2.3 Considerations....................................................................................................3
1.3 Contraindications.......................................................................................................... 3
2 Product Introduction....................................................................................................................5
2.1 Scope of application......................................................................................................5
2.2 User Qualification..........................................................................................................5
2.3 Symbols Used on the Equipment..................................................................................5
2.4 ProductStructure and Function.....................................................................................7
2.4.1 Product Structure...............................................................................................7
2.4.2 Product Functions.............................................................................................. 7
2.4.3 Views.................................................................................................................. 7
3 System Operation.......................................................................................................................13
3.1 Installation and Use.....................................................................................................13
3.1.1 Unpacking and Inspection............................................................................... 13
3.1.2 Environmental Requirement............................................................................14
3.1.3 Connecting the Power Supply..........................................................................14
3.1.4 Switching On.................................................................................................... 14
3.1.5 Start Using the Device......................................................................................15
3.1.6 Power Off......................................................................................................... 15
3.2 Screen Description...................................................................................................... 16
3.2.1 Main Screen..................................................................................................... 16
3.2.2 Main Menu.......................................................................................................17
3.3 System Settings........................................................................................................... 18
3.3.1 Alarm Settings.................................................................................................. 18
3.3.2 Brightness Adjustment.....................................................................................19
3.3.3 Volume Level Settings...................................................................................... 19
3.3.4 Language Settings............................................................................................ 20
3.3.5 Time and Date Settings.................................................................................... 21
3.4 Waveform Settings...................................................................................................... 21
3.5 Monitoring Parameter Settings...................................................................................22
4 AED.............................................................................................................................................23
4.1 Overview..................................................................................................................... 23
4.2 AED Screen.................................................................................................................. 23
4.3 AED Steps.................................................................................................................... 24
4.3.1 AED Settings..................................................................................................... 24
4.3.2 Defibrillation Operation................................................................................... 25

II
4.3.3 Shock Recommended...................................................................................... 26
4.3.4 Shock Not Recommended............................................................................... 26
4.4 CPR Operation............................................................................................................. 27
5 Manual Defibrillation.................................................................................................................28
5.1 Overview..................................................................................................................... 28
5.2 Manual Defibrillation Screen...................................................................................... 28
5.3 Manual Defibrillation Settings.................................................................................... 29
5.4 Manual Defibrillation Steps........................................................................................ 30
5.1.1 External Defibrillation...................................................................................... 30
5.1.2 Internal Defibrillation.......................................................................................32
5.5 Manual Synchronous Defibrillation............................................................................ 33
5.5.1 Manual Synchronous Defibrillation Steps....................................................... 33
5.5.2 Deliver an Additional Synchronous Shock....................................................... 34
5.5.3 Stop Synchronous Defibrillation...................................................................... 34
6 ECG Monitoring..........................................................................................................................34
6.1 Overview..................................................................................................................... 34
6.2 Monitoring Screen.......................................................................................................35
6.3 ECG Monitoring Settings............................................................................................. 36
6.4 ECG Monitoring Steps................................................................................................. 37
6.4.1 Lead Monitoring Operation............................................................................. 37
6.4.2 Lead Electrode Placement............................................................................... 37
6.4.3 Monitoring Operation with Paddles/Pads.......................................................38
6.4.4 Placement of Paddles/Pads............................................................................. 39
6.4.5 Check Pacing Status......................................................................................... 39
7 Non-invasive Pacing................................................................................................................... 41
7.1 Overview..................................................................................................................... 41
7.2 Pacing Screen.............................................................................................................. 42
7.3 Pacing Settings............................................................................................................ 42
7.4 Pacing Steps.................................................................................................................43
8 CO2Monitoring.......................................................................................................................... 45
8.1 Overview..................................................................................................................... 45
8.2 CO2Monitoring Display...............................................................................................45
8.3 Mainstream CO2Module............................................................................................ 46
8.4 CO2Monitoring Settings..............................................................................................46
8.5 Atmosphere Pressure Compensation......................................................................... 47
8.6 Measuring Influencing Factors....................................................................................47
9 SpO2Monitoring........................................................................................................................ 48
9.1 Overview..................................................................................................................... 48
9.2 SpO2Monitoring Display............................................................................................. 48
9.3 Monitoring Settings.....................................................................................................49
9.4 Monitoring Steps.........................................................................................................50
9.5 Measuring Influencing Factors....................................................................................50
10 NIBP Monitoring...................................................................................................................... 51
10.1 Overview................................................................................................................... 51

III
10.2 NIBP Measurement Steps......................................................................................... 52
10.2.1 Measurement Preparation............................................................................ 52
10.2.2 Measurement Method...................................................................................52
10.2.3 Correct Measurement Results....................................................................... 53
10.3 Limitations of the Measurement.............................................................................. 53
10.4 Measurement Mode................................................................................................. 53
10.5 Set initial Pressure.....................................................................................................54
11 TEMP monitoring..................................................................................................................... 55
11.1 Overview................................................................................................................... 55
11.2 TEMP monitoring display.......................................................................................... 55
11.3 TEMP measurement steps........................................................................................ 55
11.4 Temperature Unit Setting..........................................................................................56
12 RESP Monitoring...................................................................................................................... 57
12.1 Overview................................................................................................................... 57
12.2 RESP Monitoring Display...........................................................................................57
12.3 RESP Monitoring Settings..........................................................................................57
12.4 Place Respiratory Electrodes.....................................................................................58
13 Recording Settings................................................................................................................... 60
13.1 Recorder.................................................................................................................... 60
13.2 Recording Type..........................................................................................................60
13.3 Recorder Use............................................................................................................. 60
13.4 Recording Settings.....................................................................................................61
13.5 Recording Paper Loading.......................................................................................... 62
13.6 Clear Paper Jam.........................................................................................................62
13.7 Clean Recorder.......................................................................................................... 63
14 Marking Events........................................................................................................................ 64
15 Trend Review............................................................................................................................65
16 Battery Management...............................................................................................................66
16.1 Overview................................................................................................................... 66
16.2 Installing the Battery.................................................................................................66
16.3 Check Battery Performance...................................................................................... 66
16.4 Charging the Battery................................................................................................. 67
16.5 Battery storage..........................................................................................................67
16.6 Battery Recycling.......................................................................................................67
17 Cleaning and Disinfection........................................................................................................ 69
18 Inspection and Maintenance...................................................................................................70
18.1 Routine Inspection.................................................................................................... 70
18.2 Inspection period...................................................................................................... 70
18.3 Service....................................................................................................................... 70
19 Alarms...................................................................................................................................... 72
19.1 Alarm Information and Prompts...............................................................................72
19.2 Alarm Settings........................................................................................................... 73
19.2.1 Alarm System Settings................................................................................... 73
19.2.2 Alarm Level Settings.......................................................................................73

IV
19.2.3 Limit Settings..................................................................................................74
19.2.4 Alarm Parameter Settings..............................................................................76
19.2.5 Clear Technical Alarms................................................................................... 76
19.2.6 Technical Alarm List........................................................................................76
20 Accessories...............................................................................................................................79
21 Technical Parameters............................................................................................................... 80
21.1 Medical Device Management Class.......................................................................... 80
21.2 Main Unit Specifications........................................................................................... 80
21.3 Defibrillation Specifications...................................................................................... 81
21.4 AED Algorithm Performance.....................................................................................84
21.5 Noninvasive Pacing Specifications............................................................................ 85
21.6 Monitoring Specifications......................................................................................... 85
21.6.1 Basic Monitoring Specifications.....................................................................85
21.6.2 SpO2Monitoring Specifications..................................................................... 88
21.6.3 Respiratory (RESP) Monitoring Specifications...............................................89
21.6.4 Temperature (TEMP) Monitoring Specifications........................................... 89
21.6.5 Non-Invasive Blood Pressure (NIBP)..............................................................91
21.6.6 Carbon Dioxide (CO2) Monitoring Specifications...........................................92
21.7 Recording Specifications........................................................................................... 93
21.8 Environmental Specifications:...................................................................................94
22 EMC.......................................................................................................................................... 95
22.1 Warnings................................................................................................................... 95
22.2 Considerations...........................................................................................................95
22.3 Electromagnetic Compatibility Information of the Equipment................................95
23 Product Assurance................................................................................................................. 102
24 Classification Description of Toxic and Harmful Substances.................................................103
25 Storage and Transportation................................................................................................... 104
26 Defibrillator Monitor Shift Check List....................................................................................105
27 List of Terms........................................................................................................................... 106

V
Product Information
Thank you for purchasing the i6 defibrillator monitor.
Please read and understand the contents of this instruction manual carefully before use, to
operate the device correctly. Keep this manual in a safe place so that it can be easily referred to
during the use of this product.
Product name: Defibrillator Monitor
Specifications and model No.: i6
Medical device registration No.:
Production license No.: YSYJXSCX No. 20020533
Registrant: Ambul (Shenzhen) Tech Co., Ltd.
Registrant's address: Room A1302, Shenzhen National Engineering Laboratory
Building, No.20, High-tech South 7th Road, High-tech Zone, Yuehai Street, Nanshan
District, Shenzhen
Manufacturer's name: Ambul (Shenzhen) Tech Co., Ltd.
Manufacturing Address: 3rd Floor, Building 5#C, Innovation Valley, SKYWORTH
Industrial Zone, No. 1 Tangtou Road, Shiyan Street, Baoan District, Shenzhen
Date of manufacture: located on the main unit
Serviceable life: 8 years
Revision date of this manual: January 2022
Caution: this instrument is not intended for household use.

VI
Intellectual property
@2022 Ambul (Shenzhen). Tech Co., Ltd., all rights reserved.
The intellectual property rights of this product and its instruction manual belong to
Ambulanc (Shenzhen) Tech Co., Ltd., including but not limited to patents, trademarks,
copyrights, etc.
Ambulanc (Shenzhen) Tech Co., Ltd. reserves the right of final interpretation of this
instruction manual.
Ambulanc (Shenzhen) Tech Co., Ltd. reserves the right to treat this instruction manual as
confidential. No individual or organization shall disclose all or part of the information in this
Manual by any means, and shall not allow other person or organizations to obtain all or part
of the information in this Manual by any means without the written permission of Ambulanc
(Shenzhen) Tech Co., Ltd.
No individual or organization may publish, modify, reproduce, distribute, rent, recompose or
translate this manual in whole or in part, but not limited to, into other languages without
the written permission of Ambulanc (Shenzhen) Tech Co., Ltd.
is the registered trademark or trademark of Ambul (Shenzhen) Tech Co.,
Ltd., and these trademarks and related security logos are the intangible property of Ambul
(Shenzhen) Tech Co., Ltd. The use of trademarks or logos of Ambulanc (Shenzhen) Tech Co.,
Ltd. in this Manual is editorial purposes only and for no other purpose, and their rights
belong to their respective right holders.

VII
Statement
Ambulanc (Shenzhen) Tech Co., Ltd. reserves the right to modify the contents of the Manual
without prior notice.
Ambulanc (Shenzhen) Tech Co., Ltd. reserves the right to change the technology without
prior notice.
Ambulanc (Shenzhen) Tech Co., Ltd. reserves the right to modify product specifications
without prior notice.
Ambulanc (Shenzhen) Tech Co., Ltd. makes no warranty of any kind with respect to this
material, including (but not limited to) the implied liability for guarantee with respect to
merchantability and fitness for a particular purpose.
Ambulanc (Shenzhen) Tech Co., Ltd. is responsible for the safety, reliability, and performance
of the device only under the following circumstances, namely:
•The assembly operations, extensions, re-adjustments, making improvement and repairs
are carried out by personnel approved by Ambulanc (Shenzhen) Tech Co., Ltd.
•The relevant electrical equipment complies with the national standards.
•The device is used according to the operating instructions.
•Ambulanc (Shenzhen) Tech Co., Ltd. is not responsible for the safety, reliability, and
operation of the product in case of the following situations:
•Components are disassembled, tensioned and re-commissioned.
•The device repaired or modified by personnel who are not authorized by Ambulanc
(Shenzhen) Tech Co., Ltd.
•The product is not used correctly according to the Instruction Manual.

VIII
Maintenance service
Scope of free service:
•The free service is available for all devices that meet the warranty service regulations of
Ambulanc (Shenzhen) Tech Co., Ltd.
Scope of fee-based services:
•Ambulanc (Shenzhen) Tech Co., Ltd. will implement fee-based services for any device
that exceeds the scope of warranty service regulations of Ambulanc (Shenzhen) Tech
Co., Ltd.;
•During the warranty period, the following conditions are not covered by the warranty:
1. Man-made damage.
2. Improper use.
3. Grid voltage exceeds the specified range of the device.
4. Unavoidable natural disasters.
5. Replace parts or consumables that are not licensed by Ambulanc (Shenzhen) Tech Co.,
Ltd. or have the device repaired by personnel not authorized by Ambulanc (Shenzhen)
Tech Co., Ltd.
Warnings:
Failure to implement a satisfactory repair/maintenance program for each hospital or
institution responsible for the use of this device may result in abnormal device failure and
may endanger human health.
Assurance
The manufacturing process and raw materials:
Ambulanc (Shenzhen) Tech Co., Ltd. guarantees that under normal operation and
maintenance conditions, the equipment will be free of the production process and raw
material failures during the warranty period.
Aftersales service is provided by:
After-sales Service Department of Ambulanc (Shenzhen) Tech Co., Ltd.
Address: 3rd Floor, Building 5# C, Innovation Valley, SKYWORTH Industrial Zone, No. 1
Tangtou Road, Shiyan Street, Baoan District, Shenzhen
Zipcode: 518108

IX
Toll-free service hotline: [phone]
Tel: [phone] Fax: [phone]
Website: http://www.ambulgroup.com
E-mail: mana[email protected]
Product returns
Returning procedure
For necessary product returns to Ambulanc (Shenzhen) Tech Co., Ltd., please follow the
steps below:
•Approval for product returns: please contact the After-sales Service Department of
Ambulanc (Shenzhen) Tech Co., Ltd. and provide the Ambulanc product serial number
marked on the outside of the packing case. The return will be rejected if the serial number is
not legible. Please specify the product model and provide a brief description of the reason
for the return.
•Cost of shipping: The user shall be responsible for the shipping costs (including customs
fees) to transport the device to Ambulanc (Shenzhen) Tech Co., Ltd. for repairs.
Important information
1. After product purchase, the customer will be solely responsible for the maintenance
and management of the product.
2. During the warranty period, the following are not covered by the warranty:
•Damage or loss caused by improper or rough handling.
•Damage or loss caused by force majeure such as fire, earthquake, flood, or lightning.
•Failure to meet conditions of use specified for the system, such as damage or loss
caused by the insufficient power supply, incorrect installation, or unsatisfactory
environmental conditions.
•Damage or loss caused by not using the system in the area where it was originally
purchased.
•Damage or loss of systems not purchased from Ambulanc (Shenzhen) Tech Co., Ltd. or
its authorized dealers or agents.
3. Only qualified medical personnel with professional qualifications are allowed to
operate this device.
4. Unauthorized modification of the software or hardware or any other parts of this
product is prohibited.
5. Ambul (Shenzhen) Tech Co., Ltd. is not responsible for any issues, damages or losses
caused by the re-installation, alteration, or repair of the system by personnel not designated

X
by Ambul (Shenzhen) Tech Co., Ltd.
6. This system is designed to provide physicians with the aids they need for clinical care.
7. The physician is responsible for the treatment process. Ambulanc (Shenzhen) Tech Co.,
Ltd. shall not bear any responsibilities for the treatment process.
8. Be sure to back up important data such as clinical records and notebooks to the
external storage medium.
9. Ambulan (Shenzhen) Tech Co., Ltd. is not responsible for the loss of data stored in the
system due to operator error or unusual circumstances.
10. This Manual contains warning about foreseeable potential hazards. Be always on high
alert for dangers that are not stated. Ambul (Shenzhen) Tech Co., Ltd. shall not be liable for
any damage or loss caused by negligence or disregard of the Considerations specified in
these Operating Instructions.
11. Once the administrator of this system changes, this Manual must be handed over.

1
1 Safety Instructions
Please read these Safety Instructions carefully. These Safety Instructions are inseparable
parts of the device and must be always available. For safety reasons, please pay attention to the
following matters:
1.1 Safety Signs
Safety instructions are marked this Manual as follows:
Hazards:
Warn patients and users of the risk of death or serious personal injuries.
Warnings:
Warn patients and users of the risk of injuries.
Caution:
Provide warning for conditions that can cause damage to the device and possibly improper
treatment results.
Prompts: provides helpful advice.
The i6 Defibrillator Monitor is hereinafter referred to as "i6".
1.2 Safety Overview
Function check must be performed before using this device (see "Inspection and
Maintenance (19)").
•Please follow the instructions stipulated in "18 Cleaning and Disinfection" to prevent
infection or bacterial contamination.
1.2.1 Hazards
•This device releases a large amount of electrical discharge during defibrillation, which
may cause serious personal injury or even death. All operating instructions in this manual
must be followed when using this device. Do not operate the device before you are familiar
with all operating instructions.
•Do not open the housing of the device to avoid the possibility of electric shock. Repairs
or upgrades to the device can only be performed by the service personnel trained and
authorized by the Company.
•Avoid using this device near combustible agents or in oxygen-rich environments to
prevent explosions or fires. In addition, the Defibrillator Monitor and its surrounding area
should be kept clean and dry

2
•During defibrillation, keep a sufficient distance from the patient and metal objects
connected to the patient to avoid electric shocks.
1.2.2 Warnings
•The equipment, connection lines and accessories must be checked for proper operation
before use. Do not use this device in case of failure is discovered.
•The user should confirm that the synchronous input device is suitable for the
Defibrillator Monitor and that the input signal is valid.
•This device can only be used for a single patient at one time.
•This device is not suitable for use in a magnetic resonance imaging (MRI) environment.
•This device uses only disposable batteries provided by our company.
•Do not disassemble the Defibrillator Monitor to prevent electric shocks.
•The pad should be adhered strongly to the patient's skin without leaving any gap, and
the patient's chest hair should be removed if necessary.
•If you want to use the device with any equipment not mentioned in this Manual, please
consult the manufacturer.
•During operation, keep the device away from sources of electromagnetic interference
(e.g. electric motors, generators, X-ray devices, radio transmitters, cell phones, nuclear
magnetic resonance and other such devices) as they may interfere with the signals being
collected and analyzed. See Chapter 23 "EMC" for details.
•Do not operate the device in standing water, do not immerse any part of the device in
water, or drop any liquid on it. If the equipment gets wet, please dry it thoroughly.
•Do not store or use the device in a damp environment. If the device gets wet, wipe its
surface with a dry towel, and place the device in a dry, environment with a temperature of
20℃for a period of time, until the equipment is completely dry before use.
•Always prepare a fully charged and properly maintained spare battery. Replace the
battery when the device displays a low battery warning, otherwise, the device may shut
down.
•Disconnect all other devices without defibrillation protection from the patient during
defibrillation.
•The alarm volume and alarm limit should be set according to the patient's actual
condition. Do not rely solely on an audible alarm system for patient monitoring. Low alarm
volume setting may result in patients being in danger.
•When the device is attached to the patient, no functional examination should be
performed to avoid accidental electric shock to the patient.
•When using this device for treatment, attention should always be paid to the actual
condition of the patient. If there is a delay in delivering a shock, there may be a situation
where a heart rate that has been analyzed as shockable changes to a non-shockable heart
rate, resulting in electric shocks being delivered incorrectly.

3
•When treating patients with implantable pacemakers, pads or paddles should be placed
as far away from implantable pacemaker as possible.
•Please place the power cord and cables of various accessories carefully to avoid
entanglement or suffocation of the patient, or the cables from being tangled and electrically
disturbed
•Do not contact the patient and the device interface, the recorder thermal head or other
electrically charged devices at the same time to avoid injury to the patient.
•The operator must not touch the patient and the conductive part of the device at the
same time.
•To avoid causing danger or environmental pollution, the main unit, accessories, and
packaging materials must be handled with relevant local regulations or the waste disposal
policy of the hospital. The main unit, accessories and packaging materials must be kept out
of the reach of children.
•Do not make any modifications to the device.
•Maintenance measures, such as inspection and repairs, may only be carried out by the
manufacturer, Ambulanc (Shenzhen) Tech Co., Ltd. or by its authorized professionals.
1.2.3 Considerations
•Please proper care of the device to prevent it from falling, colliding, or being damaged
by strong shocks or other mechanical external forces.
•Do not different types and brands of electrodes. Mixing electrodes may cause greater
baseline wander or lead to longer baseline recovery time after defibrillation.
•To avoid contamination or infection to the personnel, environment or other equipment,
the device and its accessories that have reached the end of their useful life must be
disposed of according to the relevant local regulations or hospital rules.
•Please keep this Manual near the device so that it can be easily and promptly accessed
during the device operation.
•When operating the device, the operator should stand in front of it.
•To always keep the device in a usable state, please install batteries and connect the
electrode plugs in advance.
•A user test should be carried out first after a device drop or an improper operation. Do
not use the device again and contact the designated maintenance personnel for repair if any
malfunction is detected.
•Please install the device in a location where it can be easy to be observed, operated,
and maintained.
1.3 Contraindications
•AED Treatment:

4
Patients who are responsive, breathing and have a pulse.
•Manual defibrillation and asynchronous defibrillation:
A conscious patient with a pulse.
Patients with no pulse and no shockable rhythm (cardiac arrest or pulseless electrical
activity).
•Synchronous defibrillation:
Patients with pulseless and unresponsive ventricular fibrillation, pulseless ventricular
tachycardia or polymorphic tachycardia, pulseless activity, and cardiac arrest.
•Non-invasive external pacing:
Patients with prolonged cardiac arrest.
Contraindicated for the treatment of ventricular fibrillation and use with caution in cases of
severe hypothermia.
•NIBP monitoring:
Not for use in patients with sickle cell disease and skin lesions that have occurred or are
expected to occur.
NIBP measurements cannot be performed in patients with extreme heart rate (<40bpm
or >300bpm) or in patients who are being connected to a cardiopulmonary machine.
•ETCO2:
Not yet found
•ECG monitoring:
Not yet found
•SpO2:
Not yet found

5
2 Product Introduction
2.1 Scope of application
The defibrillator monitori6 provides semi-automatedmated external defibrillation, manual
asynchronous external defibrillation, externally synchronized cardioversion, and non-invasive
external pacing for adults and children (including infants) and it also offers ECG, NIBP, SpO2, and
ETCO2monitoring for patients.
Semi-automated external defibrillation is for patients with suspected cardiac arrest who are
unresponsive, breathless, and pulseless; manual asynchronous external defibrillation is used to
terminate symptoms of tachycardia and ventricular fibrillation; externally synchronized
cardioversion is used to terminate atrial fibrillation; external non-invasive pacing is used in
patients with symptomatic bradycardia.
2.2 User Qualification
The defibrillator monitori6 is intended for use by personnel authorized by a doctor or chief
physician who have at least the following training and appropriate skills:
•Training on the use of defibrillator monitor i6.
•Trained in CPR or other physician-authorized emergency response plans.
•The Defibrillator Monitor i6 can be used in a medical institution or public places and
supports pre-hospital or in-hospital use.
•When used as a semi-automated external defibrillator in AED mode, the i6 is intended
for use by medical personnel trained in basic life support (including the use of AEDs).
•The i6 is intended for use by healthcare professionals trained in advanced life support
protocols when operating in monitoring, manual defibrillation, or pacer mode.
2.3 Symbols Used on the Equipment
The following table describes the symbols used on this device or in this Manual.
Symbol
Description
Symbol
Description
Refer to the documents
provided
Refer to the Instructions for
Use
Date of manufacture
Serial Number
The effective date for use
Anti-defibrillation BF type
application section
I/O
Anti-defibrillation CF type
application section

6
Symbol
Description
Symbol
Description
sternum paddle icon
Apex paddle icon
Do not discard in trash
Refer to the attached
Handbook/Instructions
"Shock" button
Select Adult or Child
Level of protection against
ingress of solid particles
Level of protection against
ingress of liquid
Keep away from high heat
and open flame, and do not
dispose of battery in fire
Do not recharge the battery
Do not crush the battery
Do not deform the battery or
open the battery housing
USB
Charging
Adults
AC Power Supply
Children
Battery-powered
Neonates
Status of battery capacity
Pausing alarm
Lead selection
Silencing Alarms
I/O
Alarm suppression
Computer network
is232 interface
Menu
Printing
CPR
NIBP
Video output
Event marking
Sync

7
Symbol
Description
Symbol
Description
Environmental life of electronic products (20 years)
This product complies with the EUMDD 93/42/EEC and meets the basic
requirements of Annex I of the Directive, therefore bears the CE marking
2.4 ProductStructure and Function
2.4.1 Product Structure
The Defibrillator Monitor i6 consists of the main unit, battery, and pads (disposable pads for
both adult and pediatric patients).
2.4.2 Product Functions
There are four operating modes of the i6 defibrillator monitor: manual defibrillation, AED,
pacer and monitoring. In which, the monitoring module includes ECG monitoring, Resp
monitoring, SpO2monitoring, NIBP monitoring, Temp monitoring, and CO2monitoring.
2.4.3 Views
•Main Unit - Front View
2- 1 Front view
Num
ber
Parts
Description
1
Handle
Used for manual defibrillation to provide defibrillator discharge to
the patient.

8
Num
ber
Parts
Description
2
Alarm
Indicator
When an alarm sounds, red and yellow flashes are displayed to
indicate different alarm priorities. Red flashing = high, yellow flashing
= medium, steady yellow = low.
3
Display Screen
To bring up the main menu; display waveform changes; observe the
monitoring parameters; for executing repeat operations to close the
main menu.
4
Mode Button
For selecting adults or children.
5
Lead Button
Button for lead switching.
6-9
Soft Key
Corresponds to the hotkey on the screen. The function of the same
soft key is not the same under different operating modes.
10
Printing
Button
Start/stop printing.
11
NIBP Button
Manually enable/disable NIBP measurement.
12
Speaker
For sounding alarms and giving voice prompts.
13
Event marking
button
Used for event marking.
14
System Alarm
Silence Button
Alarm silencing on/off.
15
Microphone
Port
Used for voice recording.
16
Navigation
knob
Rotate clockwise or counterclockwise to move the cursor Press:
pressing the knob to confirm an operation.
17
Defibrillation
Button
Press the button to provide defibrillation.
18
Charge Button
Press the button to charge the defibrillator.
19
Sync Button
Turn synchronization on/off.
20
Mode Knob
For selecting a different mode.
21
Battery
Indicator
Indicates the current battery status.
22
AC Indicator
Indicates the current AC status.
23
Status
indicator
Indicates device status.
•Main unit - rear view