ARCHEON EOlifeX User manual

INSTRUCTIONS FOR USE
INSTRUCTION D’UTILISATION

Instructions for use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Instruction d’utilisation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
LIFE COMES FIRST
[EN]
[FR]

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EN EN
The EOlife X equipment is manufactured by ARCHEON,
2 Chemin des Aiguillettes, 25000 Besançon, France.
I. Symbols used on product labelling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
II. Acronyms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
III. Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
IV. Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
V. Product description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
VI. Equipment and accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
VII. How to use the device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1. Initial product set-up. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
2. Using EOlife X . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
VIII. Detailed product description and operating instructions . . . . . . . . . . . . . . . . . . . . . . 10
1. Using the device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
a) Assembly/disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
b) EOlife X blind ventilation training mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
c) EOlife X monitored ventilation training mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
d) Alarm conditions and alarm signals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
e) Standby mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
2. EOlife X device set-up screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
a) Set-up screen display. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
b) Choice of interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
c) Data transfer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
d) Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
3. Cleaning and maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
a) Charging the battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
b) Cleaning EOlife X and its accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
c) Storing EOlife X. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21
d) Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
IX. Technical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
1. Technical data relating to the device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
2. Technical data relating to the power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
X. Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
XI. Warranty and limits of liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
XII. Certifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
TABLE OF CONTENTS I. Symbols used on product labelling
Symbol Definition
Manufacturer’s lot number
Manufacturer
Part number
Serial number
Use by date
IP44
Ingress protection against:
oIntrusion of solid objects larger than 1mm
oWater splashing from any direction
Do not dispose of with general waste
CE marking
Temperature limitation
Humidity limitation
Warning
Quantity
II. Acronyms
AHA
BLS
WEEE
ERC
LED
CPR
American Heart Association
Basic life support
Waste Electrical and Electronic Equipment
European Resuscitation Council
Light-Emitting Diode
Cardiopulmonary resuscitation

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EN EN
III. Intended use
EOlife X is a manual ventilation training device for CPR. It is intended for use on an adult manikin or adult patient simulator
and is not intended for use on humans.
EOlife X is not approved for the following uses:
oIn a hyperbaric chamber
oNear magnetic resonance imaging machines
IV. Safety
oBefore using the product, read these instructions carefully. Failure to follow the instructions can lead to improper use
and expose the user or persons nearby to risks.
oThe use of defective devices may put the user at risk.
oThe EOlife X device, its battery, charger and the FlowSense X sensor must be stored and used as described in the
instructions for use (see “X. Technical data”).
oThe device can be safely used outdoors, as it is rainproof, splashproof and cannot be penetrated by solid objects larger
than 1mm (IP44 rating). However, it should be handled with care and kept away from powerful water jets and dust.
oAlways check the battery level before using EOlife X. We advise recharging the battery after each use. Change the battery
if the charge is below 20%. We also advise having a spare operational battery in case this is needed.
oUsing a battery with a low charge at temperatures below 0°C greatly reduces the run time and can cause EOlife X to stop
functioning after a short time. If the device is used at low temperatures, the battery should be fully charged.
oDo not remove the battery when EOlife X is switched on.
• Use the device as intended (see “III. Intended use”).
• Comply with the restrictions on use (see “III. Intended use”).
• Carefully read the safety instructions in these instructions for use.
• Comply with all the sections in these instructions.
Precautions
• Only use the EOlife X device and its accessories if they do not show any visible damage.
EOlife X is not intended for use on humans. EOlife X should only be used on a manikin or patient simulator.
Avoid using EOlife X next to or in combination with other devices as this could cause it to malfunction. If devices must
be used next to each other or together, monitor both devices to check that they are functioning properly.
To ensure that EOlife X functions effectively you must follow the instructions provided by ARCHEON.
Never use the EOlife X device or its accessories in a hyperbaric chamber as this could cause an explosion.
Portable high frequency communication devices (e.g. wireless devices, antennas and their cables) in close proximity
to EOlife X can interfere with the device and reduce its performance. Keep EOlife X at least 30 cm from portable high
frequency communication devices.
The EOlife X electronic unit, the FlowSense X sensor, the battery and the charger must be discarded at the end of their
lifetime as instructed in “IX. 3 d) Disposal”.
Handling the battery improperly could seriously injure the user and persons nearby. The battery must not be disposed
of in a fire, opened, deformed or short-circuited. The battery must be protected from humidity, high temperatures and
high pressure (see “X. Technical data”).
The use of accessories, transducers and cables other than those specified or supplied could increase the
electromagnetic emissions or decrease the electromagnetic immunity of the device and cause it to malfunction.
Warnings
FlowSense X sensor
Removable battery
Touch screen
Red
LED
Bumpers
Physical
ON/OFF button
V. Product description
oThe device is a portable machine that includes the EOlife X electronic unit, its removable and rechargeable battery, its
charger and the FlowSense X sensor.
oEOlife X is used with the FlowSense X sensor which is positioned between a non-invasive ventilation interface (mask),
invasive ventilation interface (endotracheal tube), or any type of supraglottic airway device, and a standard self-inflating
bag to manually ventilate a manikin.
oEOlife X allows the user to choose the resuscitation mode (continuous ventilation or CPR with a 30:2 compression/
ventilation ratio), the patient’s height and the training mode (blind ventilation or monitored ventilation).
oEOlife X records the ventilation data, which can be exported to another device for research and analysis. EOlife X includes
a Bluetooth low energy wireless module to communicate with such devices.
• Monitored ventilation training:
Based on the inspiratory and expiratory flow rates measured during ventilation, EOlife X calculates and records the
main ventilation parameters (insufflation volumes, tidal volumes, ventilation frequency and leakage) and gives real-
time feedback on the ventilation performed. EOlife X also shows the target ventilation values (in accordance with the
guidelines issued by the AHA and ERC international scientific committees in 2015) to guarantee adequate ventilation.
• Blind ventilation training:
Based on the inspiratory and expiratory flow rates measured during ventilation, EOlife X calculates and records the
main ventilation parameters (insufflation volumes, tidal volumes, ventilation frequency and leakage) but does not give
the user real-time feedback on the ventilation performed and does not show target ventilation values.
Note
The ventilation interface and the
self-inflating bag are accessories not
supplied by ARCHEON.
Self-inflating bag
Mask

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EN EN
VI. Equipment and accessories
Equipment Part number
EOlife X A0000089
Charger and 4 adapters A0000029
FlowSense X (x1) A0000093
FlowSense X (x10) A0000095
The equipment and accessories can be ordered from approved distributors.
VII. How to use the device
This section gives a short step-by-step description of how to use the EOlife X device. There is a more detailed description in the
next section, “IX. Detailed product description and operating instructions”.
1. Initial product set-up
Note
The initial set-up process must be implemented only once, when you receive the EOlife X device.
Charge the battery fully
• See “IX 3 a) Charging the battery”
Start up EOlife X by pressing
the physical ON/OFF button
Press the physical ON/OFF button
to show the summary screen
Display the
set-up screen
1 4
5
2
3
Select the date, time and language
and choose the desired interface
• See “IX 2 a) Set-up screen display”
and “IX 2 b) Choice of interface” Summary screen
Date
Interface
mode
Time
Language
Set-up
screen
Small
140 / 160 cm
Medium
160 / 180 cm
Tall
180 / 200 cm
55%
Patient’s height
55%
Ventilation
Mode
30 : 2
Continuous
Assembly with the bag
EOlife X assembly
with the FlowSense X sensor
Assemble EOlife X, attaching the FlowSense X sensor and other devices to carry out ventilation on the manikin (ventilation
interface and bag)
2. Using EOlife X
• See “IX 1 a) Assembly”
Choose the type of training
oBlind ventilation
oMonitored ventilation
Ventilation screen
• See “IX 1 b) EOlife X ventilation method”
• and “IX 1 c) Alarm conditions and alarm signals”
Start up EOlife X by pressing
the physical ON/OFF button
Press on the height of the adult
patient
in cardiopulmonary arrest
oSmall: the patient’s height
is between 140 and 160cm
oMedium: the patient’s
height
is between 160 and 180cm
oTall: the patient’s height
is between 180 and 200cm
Choose the type of resuscitation
performed
o30:2 mode:
alternating between 30
chest compressions and 2
ventilations
oContinuous mode:
continuous ventilation at a
frequency of 10 breaths per
minute
55%
Training mode
Blind
ventilation
Monitored
ventilation
Medium Continuous Rotate 55%
Vi Vt Freq.
420 mL 390 mL 11/min
Good Ventilation
Main screen
(advanced interface)
Bar graph
(real-time Vi)
Alarm signal
display area
Information area (advanced
interface)
• Vi = insufflated volume
• Vt = tidal volume
• Freq. = ventilation frequency
1
4 5 6
7
8
Assembly with the
ventilation interface
2 3

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EN EN
Switch off EOlife X by pressing the ON/OFF button, then on
the OFF icon or by pressing the ON/OFF button for 3 seconds.
Disconnect the ventilation bag and interface
(mask or endotracheal tube) and unclip
the FlowSense X sensor by pulling the tab
outwards, as shown by the arrow.
Disconnecting EOlife XSwitching off using
the summary screen
9 10
click
Notch
Ridge
Tab
VIII. Detailed product description and operating instructions
EOlife X is controlled via the touch screen and the physical ON/OFF button.
Avoid using any object that could scratch the screen.
Caution
a) Assembly/disassembly
Assembly
Remove the FlowSense X sensor from its packaging by using the notch to tear the antistatic bag to avoid damaging
the sensor.
Connect the FlowSense X sensor to the EOlife X unit, taking care not to expose the printed circuit board to dust or
splash it with water.
First insert the part of the FlowSense X with a notch into the connector ridge, and then press firmly on the sensor so
that it comes into contact with the connector pins. You will hear a click when the connector tab holds the FlowSense
X sensor in place.
Check that the FlowSense X sensor is held properly in place before starting up the EOlife X unit.
1. Using the device
Connect the ventilation interface (mask or
endotracheal tube) to the compatible end of the
FlowSense X sensor. The sensor ends are shaped
differently to ensure that the interface cannot be
connected to the wrong end.
Connect the bag to the other end of the FlowSense
X sensor. The device must be assembled as shown
here:
Disassembly
To remove the accessories from the product, take the FlowSense X sensor out of the ventilation interface (mask or
endotracheal tube) by gently pulling vertically on the FlowSense X sensor. Then remove the ventilation bag at the other
end in the same way.
When ventilating with a mask, ensure it is correctly held on the manikin's face during insufflation and for the entire
duration of expiration so that EOlife X can measure the volume expired.
Warning
b) EOlife X blind ventilation training mode
c) EOlife X monitored ventilation training mode
In blind ventilation mode, EOlife X calculates the volumes insufflated and expired, the ventilation frequency and
leakage, estimates the tidal volumes, and records the data. After recording the ventilation session, EOlife X provides a
statistical report on the quality of the ventilation performed.
In monitored ventilation mode, EOlife X gives the user real-time feedback on the quality of the ventilation performed
based on a cyclic analysis of inspiratory and expiratory flow rates. It must therefore be positioned proximally to be able
to measure both the inspiratory and expiratory flow rates, calculate the volumes insufflated and expired, the ventilation
frequency and leakage, estimate the tidal volumes, and generate user information signals and alarm signals if the
ventilation parameters are unacceptable.
EOlife X also uses algorithms to filter out small airflows generated by chest compressions so as not to display
anomalous volume and ventilation frequency values and to avoid measurement artefacts. During ventilation, be sure to
generate enough flow to be detected by the device.
REC
STOP
Recording session
Medium Continuous Rotate 55%
Blind ventilation
training screen
Recording indicator
Click on stop to
stop recording

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EN EN
Medium Continuous Rotate 55%
Vi Vt Freq.
420 mL 390 mL 11/min
Good Ventilation
Medium 30 : 2 Rotate 55%
Good Ventilation
Perform 2
ventilations
Advanced interface Basic interface
510
7
8
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1. Displays the patient height selected and quick access key to change the patient’s height.
2. Displays the chosen resuscitation mode and quick access key to change the resuscitation mode.
3. Rotation icon and key to rotate the screen 180° to adjust the direction of the screen to the user’s position during
ventilation.
The user can perform ventilation and change the patient’s height or the resuscitation mode in this position.
The screen returns to its normal position if the user:
• Presses again on the rotation icon
• Presses the physical ON/OFF button to show the summary screen
• Presses the physical ON/OFF button for 3 seconds to switch the device off
4. Displays the battery level (between 0% and 100%).
oSee “IX. 3 a) Charging the battery”.
5. On the advanced interface: displays the actual volume insufflated (Vi) for each ventilation cycle (value in mL).
6. On the advanced interface: displays the tidal volume (Vt) (value in mL):
oFor the 30:2 mode → mean tidal volume based on the two consecutive ventilation cycles
oFor the continuous mode → actual value of tidal volume at each ventilation cycle
2 3
6
Note
The tidal volume is the estimated volume of air/oxygen actually reaching the patient’s lungs based on both
the measurement of the volume of air expired and the leakage calculated during the insufflation/expiration
phases.
The ERC and AHA recommend that an adult patient in cardiopulmonary arrest should be ventilated with a
tidal volume of 6 to 7mL/kg-1 of theoretical ideal weight, i.e. a volume of around 420 to 490mL for an average
adult weighing 70kg.
7. On the advanced interface: displays the trend value of the ventilation frequency (Freq.) (breaths/minute) taking
into account the frequency of the last ventilation cycles performed:
oFor the 30:2 mode → value available from the fourth ventilation cycle
oFor the continuous mode → value available from the second ventilation cycle
Note
The ERC and AHA recommend that an adult patient in cardiopulmonary arrest should be ventilated at a
frequency of 10 breaths per minute during continuous cardiac massage.
8. Real-time indication of how to ventilate:
oA bar graph shows whether the volume insufflated/expired is sufficient:
Note
• The bar graph is displayed on each breath and is incremented in proportion to the volume insufflated.
• During expiration, the bar graph is decremented in proportion to the measured volume of air/oxygen
expired.
• Take care to generate enough flow for the system to detect the insufflation and ensure that it is not
mistaken for an artefact or an involuntary movement of air caused by chest compressions or handling the
bag.
Orange:
volume insufflated
insufficient. Green:
volume insufflated
sufficient.
Red:
volume insufflated
excessive.
• When the user ventilates, the bar graph shows in real time the quantity of air/oxygen that must be insufflated
based on ERC and AHA guidelines.
oRate display in continuous mode:
oDisplay in 30:2 mode:
• In continuous resuscitation mode, EOlife X generates a visual countdown to show the user when to ventilate
to deliver 10 breaths per minute. When the green lung is displayed, the user must ventilate.
In 30:2 mode, the rate function is disabled as the person ventilating must wait for 30 chest compressions
before delivering 2 ventilations.
In this mode the ventilation frequency depends on the person (or machine) performing the chest
compressions.
The green lung is shown permanently to indicate that the device is waiting to detect a ventilation to display
the bar graph.
Note
Check that the manikin’s airways are completely sealed so that all of the air insufflated via the mouth is
fully expired. If this is not the case, EOlife X will not be able to analyse the ventilation cycles or calculate the
ventilation parameters correctly.
The main screen guides the user by displaying the ventilation parameters (advanced interface) or ventilation
instructions (basic interface) and visual indicators showing the ideal air/oxygen volume to administer and when to
administer it. The main screen also uses alarm signals to warn the user if the manikin is not ventilated correctly.

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EN EN
9. Alarm signal display area:
o“Good ventilation”: all the ventilation parameters calculated are within the appropriate range of values as
defined in the international guidelines.
o“Insufficient volume”: the volume of air insufflated to the patient is significantly lower than the values given in
the international guidelines.
o“Excessive volume”: the volume of air insufflated to the patient is significantly higher than the values given in
the international guidelines.
o“Low frequency”: the ventilation frequency is significantly lower than the values given in the international
guidelines.
o“High frequency” (for continuous mode): the ventilation frequency is significantly higher than the values given
in the international guidelines.
o“Important leakage”: the difference calculated between the volume of air/oxygen insufflated and the volume
expired is too great. This may be because the mask is not positioned correctly, due to improper intubation
(oesophageal intubation) or because the ventilation circuit is not properly sealed.
10. On the basic interface: displays an operating instruction based on the resuscitation mode chosen instead of the
Vi, Vt and Freq. values.
Note
See details of alarms in “IX. 1 c) Alarm conditions and alarm signals”.
d) Alarm conditions and alarm signals
Alarm messages related to ventilation parameters
Alarm messages may appear during ventilation when the ventilation parameters exceed the threshold values and are
persistently outside the ranges given below.
The screen shows the alarms in the alarm signal display area (lower part of the screen) as a message and in the same
way for both the basic and advanced interface.
The alarm messages concern:
• The tidal volume (Vt):
Alarm conditions
Cause
Solution
Patient height Tidal volume value
Insufficient volume
Small < 175mL
Insufflate a volume of air within the
appropriate range as defined in the
international guidelines
Medium < 235mL
Tall < 295mL
Excessive volume
Small > 500 mL
Medium > 600 mL
Tall > 750 mL
• The ventilation frequency (Freq.):
Alarm conditions Ventilation frequency value Solution
Low frequency
(continuous mode)
No insufflation for more than 5 seconds after
the green lung is displayed
Ventilate at an appropriate frequency,
as recommended in the international
guidelines
Low frequency (30:2
mode)
If the pause time (time between the end
of expiration in one cycle and the start of
insufflation in the next cycle) is greater than 24
seconds
High frequency > 15 bpm
Note
• In continuous resuscitation mode the alarm condition is calculated based on the trend value of the volumes.
If the trend value and the current value of the tidal volume are as described in the table above, the tidal
volume alarm is triggered.
• In 30:2 CPR mode the alarm condition is calculated based on the mean value of the tidal volumes during two
consecutive ventilation cycles.
Note
• In continuous resuscitation mode the frequency is calculated based on the trend value of the ventilation
frequency. If the trend value and the current value of the frequency are as described in the table above, the
ventilation frequency alarm is triggered.
• In 30:2 CPR mode the alarm condition is calculated based on the actual value of the pause time.
• Leakage:
Alarm conditions Leakage value Solution
Important leakage > 40%
Depending on the cause of the leakage, several solutions are
possible (non-exhaustive list):
oReposition the tracheal tube if the manikin is improperly
intubated (selective intubation, tube not deep enough inside
the trachea) or inflate the bag more if the ventilation circuit is
not properly sealed
oReposition the mask properly on the manikin's face to ensure
that the ventilation circuit is properly sealed
oCompletely free the manikin's airways

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EN EN
• Alarm prioritisation:
Note
• In continuous resuscitation mode leakage is calculated based on the trend value of the leakages. If
the trend value and the current leakage value are as described in the table above, the leakage alarm is
triggered.
• In 30:2 CPR mode the alarm condition is calculated based on the mean value of the leakages during two
consecutive ventilation cycles.
All alarm messages appear in the same display area, therefore a system is necessary to prioritise the alarms. Alarm
prioritisation also enables the user to focus first on correcting the most critical problem, and avoids the additional
stress of multiple simultaneous alarms.
The alarms were prioritised with clinical experts, using a structured risk management process.
Multiple alarm conditions
Priority alarm
Ventilation frequency Tidal volume Leakage
Low frequency Insufficient volume Low frequency
Low frequency Insufficient volume Important leakage Low frequency
Low frequency Low frequency
Low frequency Important leakage Low frequency
Low frequency Excessive volume Low frequency
Low frequency Excessive volume Important leakage Low frequency
Insufficient volume Insufficient volume
Insufficient volume Important leakage Important leakage
Important leakage Important leakage
Excessive volume Excessive volume
Excessive volume Important leakage Excessive volume
High frequency Insufficient volume High frequency
High frequency Insufficient volume Important leakage High frequency
High frequency High frequency
High frequency Important leakage High frequency
High frequency Excessive volume High frequency
High frequency Excessive volume Important leakage High frequency
Alarm message linked to the FlowSense X sensor
During ventilation, if the FlowSense X sensor is defective or not properly connected or if a foreign object on the
connector interferes with the signal transmission, an alarm screen is displayed:
EOlife X device failure
If there is a device failure, EOlife X will be unusable: the screen switches off (or no longer comes on) and the red LED in
the top right corner of the screen comes on.
See “XI. Troubleshooting”.
You must reconnect a functional FlowSense X sensor as described above to clear the
“FlowSense X failure” alarm.
FlowSense X failure
Alarm screen
“FlowSense X failure”
Note
The “FlowSense X failure” alarm screen can only be displayed from the main screen.
e) Standby mode
If there is no user activity (no ventilation or no action on EOlife X) for 3 minutes, the device goes into “standby” mode
and the screen turns off.
To turn the screen on again, simply press the physical ON/OFF button and the summary screen will reappear.
If EOlife X remains in standby mode for more than 10 minutes, the device will turn itself off completely.
a) Set-up screen display
1. Start up EOlife X by pressing the physical ON/OFF button.
2. Press normally on the physical ON/OFF button to show the summary screen.
2. EOlife X device set-up screen
Summary screen

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EN EN
Summary screen
3. Next, select the [wrench ] to display the EOlife X set-up screen.
Set-up screen
To set
the time
Data transfer
To set
the date
Choice of
interface
Language
selection
Access to main
information
b) Choice of interface
c) Data transfer
EOlife X offers two interfaces:
o Basic interface: the EOlife X device guides the user by displaying instructions based on how it interprets the
volumes insufflated, tidal volumes and ventilation frequency, without displaying the values of the ventilation
parameters in real time.
o Advanced interface: the EOlife X device guides the user by displaying instructions based on how it interprets
the volumes insufflated, tidal volumes and ventilation frequency, but at the same time displays the values of the
ventilation parameters if users wish to interpret them themselves.
EOlife X records the ventilation parameters in each ventilation cycle and can record for approximately 5 hours. This data
can then be transferred via Bluetooth to a compatible device to extract and analyse the data. To avoid losing the data
recorded, it is advisable to transfer the data recorded by EOlife X after each use.
Note
Transferring data requires the use of a device compatible with EOlife X, not included with the equipment and
accessories sold with EOlife X.
Please contact an approved distributor or the manufacturer for more information.
Download the data recorded by EOlife X from the set-up screen:
1. Select [the icon]. The EOlife X Bluetooth
connection is automatically turned on and an
hourglass is displayed until the device detects the
compatible device.
2. After a few seconds, a pairing code is displayed on
both devices. Check that they are the same:
oPress on [the icon] if the codes are different and
repeat this step.
oIf they are the same:
3. Press on [the icon]. The devices
are paired and the connection screen is displayed.
Connection screen
55%
Update
Data transfer
Remote device
Paired
Transfer confirmation
screen
55%
Transfer to Remote
device?
Remote device
Paired
4. Press on [the “Data transfer” icon]. The transfer
confirmation screen is displayed.
5. To confirm the transfer, press on [the icon]. A
gauge appears to show the progress of the data
transfer.
Transfer complete screen
55%
Transfer done
Remote device
Paired
The transfer complete screen appears automatically.
Note
• To cancel the transfer and return to the connection screen, press on [the icon] on the transfer
confirmation screen.
• [The icon] lets you return to the set-up screen.
• If the Bluetooth connection between EOlife X and the compatible device is lost after pairing, the
reconnection screen is displayed, which lets the user re-establish the Bluetooth connection between the
two devices.
Reconnection screen
55%
Connection failure.
Try again?