easyCryo America Cryo ICE COMPRESSION FIRST S1 User manual

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ICE COMPRESSION
Instruction Manual
AMERICA CRYO LLC
26841 HOT SPRINGS PL
CALABASAS CA 91301
USA
561 602 0112
[email protected]
S1 / FIRST
S1 / MALETTE
S1 / MOOVE
S2 / TWIN
America Cryo

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TABLE OF CONTENT
DESCRIPTION OF THE SYSTEM.…………………………………………………………………………………………………………
TECHNICAL FEATURES...................……………………………………………………………………………………………………
PRECAUTIONS –WARNINGS................................. ………………………………….……………………………………….
INDICATIONS …………………………………………………………………………………………………………………………………..
CONTRAINDICATIONS …………………………………………………………………………………………………………………….
INSTRUCTIONS FOR USE –GETTING STARTED......…………………………………………………………………………..
INTERFACE OF THE PROGRAMMABLE CONTROL MODULE....………………………………………………………….
PROGRAMMING TREATMENTS............ ………………………………………………………………..…………………………
MAINTENANCE OF THE DEVICE...……………………………………………………………………………………………………
TROUBLESHOOTING........ ……………………………………………………………………………………………………………….
QUICK SET-UP.............. ………………………………………………………………………………………………………………….
QUICK SET-UP............. …………………………………………………………………………………………………………………
WARRANTY GENERAL TERMS AND CONDITIONS..………………………………………………………………………….

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DESCRIPTION OF THE SYSTEM
The ICE COMPRESSION system is made up of the following elements:
1. The programmable control module,
2. The water/air pipe connections to the splints,
3. An AC adapter,
4. A user manual.
The ICE COMPRESSION device is available in 3 different versions:
-1 output version: ICE COMPRESSION S1 / FIRST
-1 output version: ICE COMPRESSION S1 /
MALETTE
-1 output version: ICE COMPRESSION S1 / Moove
-2 output version: ICE COMPRESSION S2 / DUO
Depending on the device you order, the system can also come with one or two splints. Only
splints sold by MKS PARIS are compatible with this system.
The references of the splints available are listed in the table below.
Each splint comes with a circuit for water and a circuit for air. These two circuits are independent and
are totally sealed off from each other.
LIST OF SPLINTS AVAILABLE:
NAME SIZE
REFERENCE
ICE COMPRESSION ARM SPLINT
Large
ICLegM-W
ICE COMPRESSION LEFT SHOULDER SPLINT Medium ICShoulderLL-W
ICE COMPRESSION RIGHT SHOULDER SPLINT Medium ICShoulderRL-W
ICE COMPRESSION LEFT HIP SPLINT
Large
ICHipL-W
ICE COMPRESSION RIGHT HIP SPLINT
Large
ICHipR-W
ICE COMPRESSION THIGH SPLINT
Large
ICLegM-W
ICE COMPRESSION KNEE SPLINT Medium ICKnee-W
ICE COMPRESSION ANKLE SPLINT
Large
ICAnkleL-W
ICE COMPRESSION LEG SPLINT
Large
ICLegL-W
MULTIPLE USE MASK Medium
MBVM
SINGLE USE MASK Medium
MBVU
The splints can be used with sterile jersey or with a hygienic sheath before being
placed in position on the patient.

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LIST OF ICE COMPRESSION SPLINT COVERS:
NAME SIZE
REFERENCE
ICE COMPRESSION ARM SPLINT COVER
Large
ICLegM-S
ICE COMPRESSION LEFT SHOULDER SPLINT
COVER Medium ICShoulderLL-S
ICE COMPRESSION RIGHT SHOULDER SPLINT
COVER
Medium ICShoulderRL-S
ICE COMPRESSION LEFT HIP SPLINT COVER
Large
ICHipL-S
ICE COMPRESSION RIGHT HIP SPLINT COVER
Large
ICHipR-S
ICE COMPRESSION THIGH SPLINT COVER
Large
ICLegM-S
ICE COMPRESSION KNEE SPLINT COVER Medium ICKnee-S
ICE COMPRESSION ANKLE SPLINT COVER
Large
ICAnkleL-S
ICE COMPRESSION LEG SPLINT COVER
Large
ICLegL-S
LIST OF SPARE PARTS AND REPLACEMENT ACCESSORIES AVAILABLE:
NAME
REFERENCE
BATTERY
AYE 01 2000
WATER TRAY
BIDON AVEC OU SS CONNECT
AC ADAPTER
N1173-40
DESCALING PACKAGE
DETARTRAGE
COMPRESSION FILTER
FILTRE
FEMALE COMPRESSION CONNECTOR
CONNEC F
MALE COMPRESSION CONNECTOR
CONNEC M
PHYSIO EXTENSION CABLE IC3W3M
DENTAL EXTENSION CABLE IC2W2M
FORKED EXTENSION CABLE ICY3W

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Photo 1: front view of the device
Photo 2: rear view and inside view of the device

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TECHNICAL FEATURES
DIMENSIONS
327 H x 478 l x 405 L S1 / First ET S2 / Twin,
290 H x 240 l x 390 L S1 / Moove
320 H x 282 l x 390 L S1 / Malette
WEIGHT WHEN EMPTY 5 kg for S1 / First and 6 Kg for S2 / DUO
2.5 kg for S1 / Moove and 5 kg for S1 / Malette
WEIGHT WHEN FILLED WITH WATER 7 kg for S1/ Move and 10kg for S2/ DUO
7kg for S1 / Moove and 7kg for S1/Malette
MAXIMUM PRESSURE IN THE SPLINT
75 mmHg
PRECISION OF AIR PRESSURE
±10 mmHg
PRECISION OF WATER TEMPERATURE
±1°C*
POWER SUPPLY
In: 110-220Vac, 50-60Hz, 0.32-0.19A
Out: 12Vdc, 1A
STORAGE TEMPERATURE Between 5 and 40 ° with humidity of 10 to 90 %
TEMPERATURE WHEN IN USE
1 °C à 40 °C
RELATIVE HUMIDITY WHEN IN USE Between 20 and 80 % humidity and 5 to 40 °C
MAX. ALTITUDE WHEN IN USE
< 2000m
LIFE EXPECTANCY OF THE CONTROL MODULE 5 years
LIFE EXPECTANCY OF PARTS AND ACCESSORIES 2 years for parts and 1 year for accessories
*The temperature of the circulating ice water can be set between 5°C and 25°C, provided that there
is a sufficient supply of ice.
USAGE PRECAUTIONS –WARNINGS
Users MUST read this manual before using the device.
Type B parts which are applied
Continous power supply
Refer to the instruction manual
DO NOT DISPOSE OF IN HOUSEHOLD WASTE: This pictogram on the
product itself and which appears in this manual, indicates that batteries
and electronics must be kept separate from household waste. In order to
ensure the correct treatment, recovery and recycling of batteries and
used devices, please take them to one of the collection points for this
purpose, as per the applicable legislation in your country.
Do not walk on the surface

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Do not sit
Do not spray with water
Warning
Serial number
Warning: refer to the instruction manual
Manufacturer
Reference
Date of manufacture
Ensure that the splint is correctly positioned and that the surface is in contact with the patient's
limb. If a crease forms, it may slow down the flow of water and damage the water pump.
If in doubt, we recommend that you first check the splint and then the extension.
WARNINGS:
▪Incorrect positioning or prolonged use of the ICE COMPRESSION system may result in tissue
damage.
▪Stop using the system immediately if the patient feels a sensation of burning or itching,
increased pain or swelling.
▪Frequently monitor the skin at the cryotherapy site and stop using the system immediately if
changes such as blistering, increased redness, abnormal discoloration, or edema swelling
occur.
▪Take extra care during the initial postoperative period, especially in the case where sedation
or medication which could alter the normal sensation of pain is being taken. Check the skin of
the area treated regularly and, if necessary, adjust the temperature range or wait longer
between treatments.
▪A layer of clothing between the splint and the skin is recommended for all patients.
▪The splints which are compatible with the ICE COMPRESSION device are not sterile, do not
place in direct contact with an open wounds, a lesion, erythema, infection or stitches. The
splint may be placed over clothing or a bandage.
▪Splints which are compatible with the ICE COMPRESSION device are available for many parts
of the body and come in several sizes, but are not suitable for all possible physiological uses.
The ankle splint, for example, is not designed for use on the toes.
IMPORTANT: READ ALL INSTRUCTIONS, CONTRAINDICATIONS, CAUTIONS AND WARNINGS
BEFORE USING THIS PRODUCT.

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Only use compression therapy with the ICE COMPRESSION system under the supervision
of a licensed healthcare professional in the following patients:
▪Patients with an open lesion in the affected area (the lesion should be covered with a dressing
before using the ICE COMPRESSION system).
▪Patients with an unstable (untreated) acute fracture in the affected area.
▪Patients under the age of 18, or patients with barriers to communication, be they
temporary, drug-related or permanent.
▪Patients suffering from heart failure or congestive heart failure (with associated edema of the
limbs or lungs).
▪Patients presenting with an unstable localized skin condition (e.g. dermatitis, venous ligation,
gangrene or a recent skin graft) in the affected area.
▪Patients with erysipelas or other active infection in the affected area.
Only use cryotherapy with the ICE COMPRESSION system under the supervision of a
licensed healthcare professional in the following patients:
▪Patients with Raynaud's disease or hypersensitivity to cold (cold urticaria).
▪Hypersensitive patients or patients with extremely low blood pressure.
▪Diabetic patients.
▪Patients with compromised local circulation or neurological impairment (including
paralysis or localized impairment due to multiple surgeries) in the affected area.
▪Patients suffering from an instable localized skin condition (e.g.: dermatitis, venous ligation,
gangrene or a recent skin graft) in the affected area.
▪Patients with rheumatoid arthritis in the affected area.
▪Patients under the age of 18 or patients with cognitive or communication issues, be
they temporary, drug-related or permanent.
CAUTION:
▪To avoid the risk of electric shock, do not attempt to remove the control pannel or to open
the part which contains the pumps and the electronic cards. Any attempt or actual opening
of these parts will render the MKS PARIS warranty void. For repairs, contact the MKS PARIS
customer service department on 04 99 64 21 05 or your distributor.
▪To avoid the risk of electric shock, always switch the system off and unplug the power cable
from the electrical outlet when not in use and before adding or emptying ice and water.
▪Do not use any AC adapter other than the one supplied by MKS PARIS. Use of other
adapters may cause electric shock and render the MKS PARIS warranty void.
▪To avoid damaging the product, do not operate the system without water, unless the water
function is canceled.
▪To prevent electric shocks, breakdowns or damage to the product, never use the system with
damaged power cables or pipes, or in the event of other mechanical damage, or if the unit is
not working properly.
▪Only use ice and water in the ice compartment.
▪Limit the filling of the water tank to 2 liters.

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▪To avoid damage to the product, do not pick the control module up by the compartment
closing system. Only transport the control module using the handle provided.
▪To avoid potentially damaging the product, do not use splints from other manufacturers.
▪To avoid damaging the product, do not use the control module without a hose connected to
the circuit.
▪To avoid damaging the product, do not walk on the hoses or the splints, and do not set
objects on top of them. They may lose their shape, be crushed or even pierced.
▪To avoid injury, ensure that the power cables and hoses are not left lying around so as not to
trip over them.
▪Monitor the position of the hose and the cord when they are in use. Tidy away when they are
not in use to avoid any risk of strangulation.
▪Keep the device, hoses and cords out of the reach of children and animals.
▪Use caution when handling small parts to reduce the risk of ingestion or inhalation.
▪The ICE COMPRESSION system is a technical medical device. To avoid damage to the product,
handle it with care, as if it were a laptop computer. Do not let it fall, do not knock it, do not sit
on it and do not climb on it. This type of misuse will render all MKS PARIS warranties invalid.
▪Do not place the AC adapter inside the ice compartment for storage or transportation.
▪This symbol on the controller or its packaging means that the product must not be
disposed of with household waste. To find out about where to dispose of electric and
electronic waste, contact the waste recycling department.
▪No special disposal measures are required for splints.
Safety in the presence of flammable anesthetics or oxygen:
Not suitable for use in an oxygen-enriched environment or in the presence of flammable
anesthetics.
Electromagnetic interference:
This device has been tested as complying to the limits of the IEC 60601-1: 2012 and IEC
60601-1-2:2014 norms for medical devices. These limits are set to ensure reasonable
protection against harmful interference in a typical medical installation.
This device generates and radiates radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to other devices in the vicinity.
There is no guarantee however that interference will not occur in a particular installation.
If this device creates harmful interference with other devices, which can be determined by turning
the unit off and on, we recommend that the user attempt to rectify the cause by taking one one or
more of the following measures:
▪Reorient or move the receiving device.
▪Increase the distance between the devices. Connect the equipment to a different outlet or
circuit from the other devices.
▪Contact the manufacturer for assitance.
This device is intended for use in health facilities, rehabilitation centers, sports therapy centers,
sports training establishments, hospitals, nursing homes, medical centers and physiotherapy
practices.

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INDICATIONS
The ICE COMPRESSION system combines two types of treatment: compression therapy and
cryotherapy.
It has been designed to treat post-surgical and accute injuries to reduce edema, swelling and pain,
when cold and compression are indicated. It is designed for use by healthcare professionals in a
hospital or outpatient clinic setting, and in sports training environments.
CONTRAINDICATIONS
The ICE COMPRESSION S2 / TWIN device has two functions:
▪A compression function, which allows compression therapy to be performed,
▪A cold function, which allows for cryotherapy.
These two actions may be combined or not.
Compression Therapy (vasopneumatic compression) is contraindicated for:
▪Patients with severe phlebitis in the part of the body to be treated.
▪Patients with a history of or is predisposed to a diagnosis of severe venous thrombosis or
pulmonary embolism in the part of the body to be treated. The same is true for patients who
have been prescribed extended medical rest.
▪Patients affected by significant arteriosclerosis or any other ischemic cardiovascular disorder
in the part of the body to be treated.
▪Patients where the part of the body to be treated has a sensitive lymphatic or venous blood
flow (as can be the case with cancer).
▪Patients suffering from heart failure.
▪Patients presenting with any significant risk factors or clinical signs of embolism (for example,
pulmonary embolism, cerebral infarction, atrial fibrillation, endocarditis, myocardial
infatction or embolic atherosclerotic plaque).
▪Patients with decompensated hypertonia in the affected area.
Cryotherapyis contraindicated for patients:
▪Suffering from a serious vascular insufficiency in the area of the affected limb
▪Suffering from cryoglobulinemia orhemoglobinuria.

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Button to press
INSTRUCTIONS FOR USE - GETTING STARTED
In order to get the ICE COMPRESSION system up and running, you need to ensure that you have
the following elements:
▪The programmable control module containing one or two containers filled with water
(depending on the number of circuits used) and ice up to the fill line. Each container needs to
be filled with a minimum of 1.5 liters of water, so that the water can fill the splint and
circulate in the system. Then it is possible to add ice up to the level indicated on the water
containers.
▪The water/air tubes to connect to the splints.
▪The AC adapter.
▪One splint per circuit.
Each splint consists of a pouch containing the water circuit and the air circuit, and a material
protective cover, which keeps the splint in position on the patient.
The control module must be placed on a flat, horizontal surface, for example a table, to prevent
water leakage inside the unit. Also, you need to take care not to position the hoses and the mains
cable in an area where people walk, to prevent trips and damage to the system.
If the system is used n an environment with a high ambiant temperature, it may impact the system's
ability to deliver cold and how long the ice lasts in the water tray.
WARNING:
▪To avoid the risk of electric shock, it is recommended that you unplug the mains adapter
from the electrical outlet before refilling with water and ice.
STARTUP PROCEDURE:
1. Place the control module on a flat, horizontal surface.
2. Open the control module to access the water containers inside. To do this, all you need to do
is to press the button.
3. Disconnect the water tank by unclipping or removing the 2 hoses for incoming and outgoing
water and the temperature sensor. Remove the water tray. 2 versions of water container are
available ( 1 with connectors with clips and 1 with openings on the tray)
NOTE: If you want to use the 2 circuits of the device, you need to procede in the same
manner to fill the second tray.

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4. Unscrew the filler cap and fill the tank with a minimum of 1 liter of water and with ice. It is
also possible to fill the tray with just water up to 1200ml and to place it in the fridge for
several hours before the start of the treatment. The water containers must be filled with a
maximum of 2500 ml of water in order to avoid water overflowing inside the device.
5. Screw the filler cap back on. Replace the water tank in the container, ensuring that you
reconnect the 2 water inlet and outlet hoses and the temperature probe.
6. Close the cover of the control unit.
7. Connect the air/ water hoses to the control module, using the quick connectors. To do this,
insert the female connector into the hose in the male connector attached to the control
module. Push the female connector to the stop. Connect the other end of the air/ water
hoses to a splint.
8. Connect the AC adapter to the back of the machine. Then plug the mains adapter into a wall
electrical outlet.
9. Press the on/off button on the control module. The following startup screen should appear.
Water inlet and outlet hoses
Temperature probe
Filler cap

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10. After a few seconds, the Home screen will appear.
"Treatment"key: 10 PRE-SET and 10 FREE CHOICE TREATMENTS
By pressing this key, you can select between several pre-set treatment programs. For the
parameters of the pres-set treatments and to find out how to set them, refer to the chapter
on "Programming treatments".
"Manual" key:
By pressing this key, you will be able to create a treatment program, which you will be able
to save for future use. If you want to save a program you have created, you need to adjust all
the air and water settings, leave manual mode, then press "validate" when you go to "exit".
Do you want to save the program in "treatments"? You will be able to find it later in the list
of saved programs. This will automatically be added to the pre-set treatments.
"Settings" key:
By pressing this key, you will have acces to information about your device, such as:
▪Brightness as a %
▪Volume (as a %)
▪Language: French, English
▪Updates
▪Purge
▪Screen calibration
▪Software Version: Treatment
mode
Treatment
Manual
Settings

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11. We recommend that you select the treatment using the protocol sheet or page 15 of the
manual.
The green part of the screen is related to the air circuit, the blue part to the water circuit, the
treatment time is at the top and the splint model is displayed in the middle of the screen.
12. When the treatment program has been selected or modified, press on the "select" button to
select the program. Then you need to press the key to start the
treatment program. The splint will be filled up.
13. We recommend that you don't place the splint on the patient, in order to allow the water to
fill up correctly in the pouch of the splint, or at least that you do not tighten the splint on the
patient so as not to obstruct the flow of water.
14. Position the splint on the patient. Ensure that the splint is suitable for the area to be treated
(there are different splints for different parts of the body) and that the size is right for the
patient. You need to be able to attach the splint to the patient without tightening it too
much. Otherwise when the splint is inflated, it may uncomfortable for the patient.
15. Check that the patient can feel the cold or wait until the circuit has been filled, the device
will ask you to validate the start of the treatment.
16. You will hear a beep lasting a few seconds at the end of the treatment and the device will
offer to purge the splint. If the next treatment will use the same splint, there is no need to
purge. If you are going to change the splint, start the purge. If you are not going to be using
the splint again, start the purge program, so that the water does not stagnate in the pouch.
INTERFACE OF THE PROGRAMMABLE CONTROL MODULE
The ICE COMPRESSION S1 / FIRST device has a single output and so allows you to connect a single
splint. The ICE COMPRESSION S2 / TWIN device has two channels, which allow you to collect two
different splints and to deliver two different treatments. The programming systems are specific to
each channel. It is therefore possible to program each output independently.
On/off button for
channel 1
On/ off button for
channel 2
Control keypad for
both channels

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The meanings of the programmable Control Module Keys:
On/off: this button is used to start or stop the control module of the
relevant channel.
Stop: this button is used to stop a treatment program
Start/pause: this button us used to launch a treatment program or to pause it.
Enter: this button is used to validate an entry and move on to the next entry.
"Up" or "plus": directional arrow used to navgate up the menu or to increase the
value of a parameter.
"Down" or "minus": directional arrow used to navigate down the menu or to
decrease the value of a parameter.
Left: directional arrow to navigate to the left of a menu
Right: directional arrow to navigate to the right of a menu
TContextual keys to select an option
Meaning of battery charge indications:
Battery charge = 100%
Battery charge = 80%
Battery charge = 60%
Battery charge= 40%
Battery charge = 20%
Battery discharged, the device will power off
Battery charging, unit is connected to the mains

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PROGRAMMING TREATMENTS
PRE-SET PROGRAMS
The ICE COMPRESSION system comes with 10 pre-set treatment programs. These programs are described below.
Program n° 1 : Edema, inflammation
▪Total treatment time: 1800 seconds (30 minutes)
▪Splint/ default: Knee
▪Type of pressure: static
▪Pressure value: 50mmHg
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds
▪Temperature: 8°C (Goal)
▪Number of cycles: 1
Program n° 2:Shoulder Treatment
▪Total treatment time: 1200 seconds (20 minutes)
▪Splint/ default: Shoulder
▪Type of pressure: static
▪Pressure value: 25mmHg
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds
▪Temperature: 10°C(Goal)
▪Number of cycles: 1
Program n° 3: Recovery
▪Total treatment time: 1200 seconds (20 minutes)
▪Splint/ default: thigh
▪STATIC phase
oDuration of the phase: 5 minutes
oPressure value: 50mmHg
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
▪DYNAMIQUE phase
oDuration of the phase: 15 minutes
oMaximum pressure value: 75 mmHg
oMinimum pressure value: 25 mmHg
oApplication time of the maximum pressure:20 seconds
oApplication time of the minimum pressure:10 seconds
oWater circulation time : 30 seconds
oWater renewal time: 30 seconds
▪Temperature: 8°C (Goal)
▪Number of cycles: 1

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Program n° 4: Ankle or wrist
▪Total treatment time: 1200 seconds (20 minutes)
▪Splint/ default: Ankle
▪Type of pressure: dynamic
▪Maximum pressure value: 35mmHg
▪Minimum pressure value: 10mmHg
▪Application time of the minimum pressure: 30 seconds
▪Application time of the maximum pressure: 30 seconds
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds
▪Temperature: 12°C
▪Number of cycles: 20
Program n° 5 : Deep treatment
▪Total treatment time: 1500 seconds (20 minutes)
▪Splint/ default: Thigh
▪DYNAMIC phase
oDuration of the phase: 5 minutes
oMaximum pressure value: 60mmHg
oMinimum pressure value: 25mmHg
oApplication time of the maximum pressure: 15 seconds
oApplication time of the minimum pressure: 15 seconds
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
oTemperature: 8°C(Goal)
▪STATIC phase
oDuration of the phase: 15 minutes
oPressure value: 60mmHg
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
Program n° 6: Face
▪Total treatment time: 3600 seconds (1 hour)
▪Splint/ default: face
▪Type of pressure: static
▪Pressure value: 10mmHg
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds
▪Temperature: 10°to 14 ° (Goal)
▪Number of cycles: 1
Program n° 7: Spasms
▪Total treatment time: 1200 seconds (20 minutes)
▪Splint/ default: thigh
▪Type of pressure: dynamic
▪Minimum pressure value: 20mmHg
▪Application time of the minimum pressure: 10 seconds
▪Maximum pressure value: 50mmHg
▪Application time of the maximum pressure: 30 seconds
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds

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▪Temperature: 8°C (Goal)
▪Number of cycles: 30
Program n° 8: Sprains
▪Total treatment time: 1500 seconds (30 minutes)
▪Splint/ default: ankle
▪STATIC phase
oDuration of the phase: 15 minutes
oPressure value: 50mmHg
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
▪DYNAMIC phase
oDuration of the phase: 15 minutes
oMaximum pressure value: 35mmHg
oMinimum pressure value: 15mmHg
oApplication time of the maximum pressure: 20 seconds
oApplication time of the minimum pressure: 20 seconds
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
▪Temperature: 10°C
▪Number of cycles: 40
Program n° 9: Hematomas
▪Total treatment time: 1500 seconds (25 minutes)
▪Splint/ default: thigh
▪Type of pressure: dynamic
▪Minimum pressure value: 20mmHg
▪Application time of the minimum pressure: 15 seconds
▪Maximum pressure value: 65mmHg
▪Application time of the minimum pressure: 15 seconds
▪Water circulation time: 30 seconds
▪Water renewal time: 30 seconds
▪Temperature: 8°C
▪Number of cycles: 50
Program n° 10: Post-op treatment
▪Total treatment time: 10 800 seconds (3 hours)
▪STATIC phase
oPressure value: 50mmHg
oWater circulation time: 30 seconds
oWater renewal time: 30 seconds
oTemperature: 6°C
oDuration of the phase: 3600 secondes (1 hour)
oNumber of cycles: 1
▪DYNAMIC phase
oMinimum pressure value: 15mmHg
oApplication time of the minimum pressure: 15 seconds
oMaximum pressure value: 50mmHg
oApplication time of the maximum pressure: 30 seconds
oWater circulation time: 30 seconds

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oWater renewal time: 30 seconds
oTemperature: 8°C
oDuration of the phase: 7200 seconds (2 hours)
oNumber of cycles: 160
CREATING A TREATMENT PROGRAM
The system offers the possibility of creating a specific treatment program. For
this, you can:
▪Either use the "Manual" mode: When you have adjusted the settings and are coming out of manual
mode, the system asks you if you would like to save your program in the treatments. So, you can save it in
the list of the 10 free treatments in order to use it again in the future.
▪Or use the "Treatment" mode, select the appropriate program and set the parameters you want. The
press "SET" and modify the parameters and press SAVE. The treatment will be added to the list.
The settings you can program are as follows:
PARAMETERSMIN VALUE MAX VALUE
STATIC MODE
Pressure in the splint
0 mmHg
75mmHg
Temperature
5°C
25°C
Number of cycles
0
200
DYNAMIC MODE
Maximum pressure in the splint
0 mmHg
75mmHg
Application time of the maximum pressure 0 seconds 55 seconds
Minimum pressure in the splint
0 mmHg
75mmHg
Application time of the minimum pressure 0 seconds 55 seconds
Temperature
5°C
25°C
Number of cycles
0
200
Number of phases
1
2
Duration of a phase
0 minutes
6000 seconds

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MAINTENANCE OF THE DEVICE
▪Don't forget to purge at the end of a treatment so that the water does not stagnate in the splints.
▪If a splint has not been purged and is not used, a deposit can build up and it will sit on the splint
connection when used, which will put pressure on the pump and break the splint…
▪Change the water in the tank every day. We recommend that you use demineralized water if your tap
water is too soft.
▪Clean the water circuit with white vinegar once a month: 1/3 white vinegar to 2/3 water. Fill up to the
line on the water tray.Circulate the water in the system as during a treatment session
▪If the machine is not used for several days, we recommend you empty the water containers.
▪Check the water filter regularly: it should be transparent, otherwise it is necessary to change it.
Depending on the use of the machine, the quality of the water and the maintenance, you will need to
change the filter (ref. FILTER) every 3 to 6 months.
▪Change the male connectors (ref. CONNEC M) and female connectors (ref. CONNEC F) every 6
months in case of intensive use ( + 4 hours a day) or at least once a year.
▪Remember to fully drain the water in the splints before storing them. For this, we recommend that you
roll them towards the connections so that the water can escape and to press on the two white nozzles at
the same time.
▪Remember to empty the water in the water containers if you need to move the device.
CLEANING THE CONTROL MODULE
▪The outer surface of the control module can be cleaned with a soft cloth and one of the following
products:
oMild detergent
oIsopropyl 70 % alcohol
▪DO NOT USE:
oPhenolic disinfectants
oSolvent-based cleaning products. These may damage the plastics and render the warranty void.
oAbrasive materials. These may damage the plastics and render the warranty void.
▪WARNING: the control module is not watertight if liquid is directly sprayed onto it, do not soak, do not
liquids run down the surface.
CLEANING THE HOSES
▪The outer surface of the hoses can be wiped with a soft cloth and one of the following products:
oMild detergent
oIsopropyl 70% alcohol
▪DO NOT USE:
oPhenolic disinfectants
oSolvent-based cleaning products. These may damage the plastics and render the warranty void.
oAbrasive materials. These may damage the plastics and render the warranty void.
oPetrolium-based lubricants. These may damage the o-rings and render the warranty void. If
lubrication is required, we recommend that you use a silicone spray.
CLEANING THE SPLINTS
▪Carefully remove the pouch from inside the protective cover. Wash the protective cover with cold or
lukewarm water, using a mild detergent or an antibacterial solution. Do not use fabric softener. Hang to
dry.
▪The outer surface of the pouch can be cleaned with a damp cloth. Machine wash on a delicate setting. Do
not expose to the sun.