Wonjin Muslan POWER RECOVERY User manual

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User’s Manual
Compressible Limb and Circulation Therapy System
Model: POWER RECOVERY
Document No.: UM-PWRB0 (Feb.20,2019_Rev.1)

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1. General Information
1.1 Specification
Technical Requirement of product
Product Name Compressible Limb and Circulation Therapy System
Model Name POWER RECOVERY
Dimensions 141(W) X 245(W) X 114(H) (mm)
Power Supply 100V~240V~, 50/60Hz, 1.0A
Power Consumption 50W
Time (Selectable) 15 minutes ~ 2 hours
Maximum Pressure 150mmHg±20%
Battery Charging Time About 4 hours
Battery Use Time About 2 hours
Weight(Main Body) 2 kg
1.2 Classification
Classification
Type of protection against electric shock Class II and Internally powered
equipment
Degree of protection against electric shock Type BF applied part
Degree of protection against ingress of water
Degree of safety of application in the presence of a
flammable anaesthetic mixture with air or with oxygen or
nitrous oxide
Equipment not suitable
Mode of operation Continuous operation
1.3 Intended patient population
a) Age: 18 years old or greater
b) Weight: 40 kg or greater
c) Health: limitation to the people mentioned in contraindication of user manual
d) Nationality: multiple
e) PATIENT state:
– PATIENT is USER: alert, mentally competent (The patient is an intended operator.)
– PATIENT is not USER: not relevant, unless PATIENT is agitated
1.4 Part of the body or type of tissue applied to or interacted with
a) Part of the body: Leg, Arm, and Hip
b) Type of tissue: Skin
1.5 Intended User
a) Education:
– at least 18 years old – at least 10 years intensive reading experience (school)
– no maximum

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b) Knowledge:
– minimum:
– read and understand how to operate the device
– can distinguish: leg, arm, and hip
– understands hygiene
– no maximum
c) Language understanding:
– understand user manual which is described in English
d) Experience:
– minimum:
– laypersons
– other: no special experience needed
– no maximum
e) Permissible impairments:
– mild reading vision impairment or vision corrected to log MAR 0.2 (6/10 or 20/32)
– impaired by 40% resulting in 60% of normal hearing at 500Hz to 2kHz
1.6 User environment
a) Environment
– General: Home environment, Indoor
– Physical: Refer to environmental conditions of 6. Maintenance.
b) Frequency of use
– It is recommended to use up to 30 min / 1 time and 3 times / 1 day.
c) Mobility
– Transportable equipment
1.7 Frequently used functions
User Interface Frequently Used functions
Connecting/Disconnecting
the cuff and air hose
Connecting the cuff and air hose to main unit for operation
Disconnecting the cuff and air hose from main unit after use
Putting on/Taking off
the cuff
Putting on the cuff for operation
Taking off the cuff after use
Switching on/off the
power
Switching on the power for operation
Switching off the power after use
Setting operational mode
Setting cuff mode (Leg, Arm, and Hip), operation mode
(Sequential, Wave, Recovery, Addition, and Massage),
pressure intensity (Level 1 (60mHg) ~ Level 10 (150mmHg)),
operation time (15 min ~ 2 hours), and rest time (0, 5, 10, 30
sec).
Reading operational status Reading operational status displayed on LCD during
operation.
Operating the device Pressing the play button to operate the device when the
device is standby status.

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Stopping the device Pressing the pause button to stop the device when the device
is working status.
Cleaning Cleaning the main unit and accessories
Moving Moving the main unit and accessories for operation
Storing Storing the main unit and accessories when not in use.
1.8 Intended Use
This device is intended for use by medical professionals and patents at home, in treating
many conditions, such as:
① Primary lymphedema
② Edema following trauma and sport injuries
③ Post-immobilization edema
④ Venous insufficiencies
⑤ Lymphedema
The device is a pneumatic pressure treatment system that inflates sleeves (cuffs) to help
blood circulation and prevent blood clots or clogs.
2. Precautions
- This is for user safety and prevention against the property damage.
Please read it carefully prior to using the product.
Indications
Manufacturer Serial Number Caution
Date of Manufacture Follow the
instructions for use Operating Instruction
Temperature Limit Humidity Limitation Atmospheric pressure
limitation
Sitting prohibited General prohibition
sign Keep dry
Stepping prohibited This means not to
take the device apart Type BF applied part
Authorized
representative in the
European communit
y
This means to
unplug the power
cord
2 Level Insulation
(Class II)
Complied with MDD
93/42/EEC
General mandatory
action sign General warning sign
Please do not throw any electrical equipment (including hose marked with this symbol in
your bin)
Protected from touch by fingers or objects greater than 12.5 mm
Protected from vertically falling water drops

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Contraindication
Do not use the device as follows;
• A person with medical electronic implant device (artificial heart)
• A person who is in pulmonary edema, heart disease, vein cancer, high blood
pressure, and high fever.
• A person who have skin disease such as skin burn, dermatitis, bedsore, purulent
disease, malignant tumor and etc.
• A person who took skin surgery (skin graft) on the part of use.
• A person who has blood vessel disease such as serious artery hardening or
other angina, cardiac infarction and etc.
• Cases the suspected blood clot presence
• A person who has extreme malformation or a person who inserted pin on using
part (artificial joint, beads, metal, silicon and so on)
• Right after the operation as varicose veins
• Recovering patients since after the surgery, pregnant woman, children
• In the case of increasing of pain after using this machine
Please avoid same time with medical equipment
for artificial life preservation, installation st
y
le
Do not use this product if you are experiencing
inflammation, an infection, pain of unknown
origin, or bleeding (internal or external) at near
the site of application.
medical equipment like
electrocardiograph etc.
Please avoid to user’s the
device to whom in too high
blood pressure or obstacle in
blood circulation.
Do not place the heavy things on the power
cord. Also do not press it with a table or a chair.
(It may cause an electric shock, and electric
leaka
g
e, or fire.
)
Do not soak the device in the water because it is
an electrical product.
When plugging or unplugging the power cord
from the wall outlet, please remove moisture
from hands. (It may cause the electric shock,
electric leakage or fire.)
Check up the suitable voltage to be used and
use the device. (The user may be burned, get
shocked or be injured.)
Please use after wearing underwear or
sportswear not to touch directly in skin with the
cuffs or pad.
Do not use the device if you feel pain or make
you feel uncomfortable. Stop the use
immediately.
Be careful when you zip up the cuff. Clothes,
hair or skin may get stuck in the zipper.

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Try not to drop the device on the floor because if
might be much vibration or shock on it. (The
device may be damaged.)
Do not use by purpose except massage.
Keep infants and children away from this device
sue to the risk of electric shock or other injuries.
Do not use it in an environment with too much
electromagnetic wave.
It may cause damage to the device and/or
cause malfunctioning.
Do not store the garments near a stove,
cigarette or other heat generating device as this
is a file hazard. Do not store the garments near
needles, scissors or other sharp objects as they
may damage the garments.
Be careful that water or other substance cannot
be inserted inside of the device.
If this device should malfunction or fail to
operate, do not attempt to open, repair, or
disassemble the main unit or this device. (It may
lead to a risk or file, electric shock, or injury to
the user.
)
While using this product, remain stationary and
do not attempt to walk or move around.
Use the device within 30 minutes when using it
once. (At first, start from 15 minutes, and
increase the time slowly considering your
physical strength. “If you use it continuously for a
long time, it may have a
reverse effect on you.”)
If you have not used the device for a long time,
or if you wise to use it in cold areas.
The device may not operate normally. In this
case, use the device after operating it three
Keep the product out of the direct rays of the sun
or heatin
g
equipment includin
g
g
as stove.
It may cause the
product modification or
discoloration.
or four times
at the strength
of Low-
Medium -High
in regular
sequence.

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When cleaning the product, wipe off with a dry
cloth without any chemical substance or
detergent.
It may cause the product external damage such
as discoloration and peeling off.
This product contains a lithium ion battery.
Dispose of this product in accordance with
local regulations.
Please use the exclusive power outlet and do not
plug several cords at once.
It may cause the fire, electric shock or other
injuries.
Be careful about air hose not to be twisted or
bent.
Do not keep the device at too low temperature in
winter time. It may be hardened and damaged.
Do not wash the cuffs in washing machine or
submerge them in water. The cuffs may be
gently wiped with a moistened towel or cloth. If
necessary, a mild detergent may be used.
If you wish to keep the device for a long time,
place it in its box.
Use of accessories other than those specified
or provided by the manufacturer of this
equipment could result in improper operation.

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3. Device Description
Main Body and AC-DC Adapter
Main Body AC-DC Adapter
Basic Accessories
Leg Cuff Main Hose Hose Adapter
Optional Accessories
Arm Cuff Hip Cuff Carrier
* Remark
- Applied part: Leg cuff, Arm cuff, Hip cuff.

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4. Preparation before use
1) Select proper cuff to use. (Leg cuff, Arm cuff, Hip cuff)
2) In case you use two cuffs.
① Connect one terminal of main hose to air outlet of main body. Press main hose into
main body until you hear an audible ‘click’.
② Connect another terminal of main hose in the direction which there is one outlet in
hose adapter. Press main hose into hose adapter until you hear an audible ‘click’.

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③ Connect two terminals of cuff hoses in the direction which there are two outlets in
hose adapter. Press cuff hoses into hose adapter until you hear an audible ‘click’.
④ In this case, there are the following combinations.
a. Two leg cuffs
b. Two arm cuffs
c. One hip cuff with two cuff hoses
d. One leg cuff + One arm cuff
3) In case you use only one cuff, such as one leg cuff or one arm cuff, directly connect cuff
hose to air outlet of main body. In this case, main hose and hose adapter are not required.
4) If cuff connection is completed, wear the cuff.
Use of cuff of hose other than those specified or provided by the manufacturer of
this equipment could result in improper operation.
5. How to use
1) Connect AC-DC adapter into an electrical outlet and then into the main body.
This device is equipped with a rechargeable lithium ion battery. The battery
automatically charges when the AC-DC adapter is connected to an electrical
outlet and main body.
Use of AC-DC adapter other than those specified or provided by the manufacturer
of this equipment could result in improper operation.
The time required for the ME EQUIPMENT to warm from the minimum storage
temperature between uses until the ME EQUIPMENT is ready for its INTENDED
USE when the ambient temperature is 20 °C: one hou
r
The time required for the ME EQUIPMENT to cool from the maximum storage
temperature between uses until the ME EQUIPMENT is ready for its INTENDED
USE when the ambient temperature is 20°C: one hour
2) Press power switch to turn on the power.
3) How to operate the program

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Play/Pause
Button
That Play icon is displayed means that the device
is not operating now.
That PAUSE icon is displayed means that the
device is operating now.
Cuff
Selection
Button
There are three cuff modes. (Leg, Arm, and Hip)
If you select one among Leg, Arm, and Hip, Leg
picture, Shoulder/Arm picture, or hip picture will
be displayed.
Operation
Mode
Selection
Button
SEQUENTIAL is the mode that the air pressure
sequentially moves from foot (1st chamber) to
thigh (6th chamber).
WAVE is the mode that the air pressure
sequentially moves from foot (1st chamber) to
thigh (6th chamber), and If the next chamber
inflates, the previous chamber deflates in 3
seconds. (Overlapped for 3 seconds)
RECOVERY is the mode that the air pressure
sequentially moves from foot (1st chamber) to
thigh (6th chamber). If the operation of 4th
chamber is completed, 1st chamber deflates and
5th chamber inflates. If the operation of 5th
chamber is completed, 2nd chamber deflates and
6th chamber inflates. If the operation of 6th
chamber is completed, 3rd chamber deflates.
Each of 4th/5th/6th chambers sequentially deflates
in 10 seconds.

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ADDITION is the mode that the mode that the air
pressure sequentially moves from foot (1st
chamber) to thigh (6th chamber), and each
chamber doesn’t deflate until the operation of 6th
chamber is completed. If the operation of 6th
chamber is completed, all of chambers deflate at
the same time.
MASSAGE is the combination of SEQUENTIAL,
RECOVERY, and ADDITION modes.
Pressure
Intensity
Selection
Button
You can select pressure intensity from LEVEL 1
(60mmHg) to LEVEL 10 (150 mmHg).
Operation
Time
You can select operation time from 15 minutes to
2 hours. On the operation, the remaining time is
displayed.
Rest Time
You can adjust rest time at Interval of 0/5/10/30
sec.
Rest time is fixed at 30 sec at ADDITION and
MASSAGE modes.
Memory User
1~7
SAVE
You can save operation
mode up to seven
modes.
CHOICE
You can operate the
selected USER mode by
clicking PLAY.
PRIOROTY
If the power is turned off
and on, the selected
USER mode is
displayed, and operated
by clicking PLAY.
Reset
Data in memory are deleted and all of functions
are returned to factory release mode.
Factory release mode: LEG / RECOVERY /
LEVEL 3 (80 mmHg) / 30 min
Brightness You can adjust screen brightness with MIN ~
MAX.
You can adjust pressure intensity of each chamber by clicking
the chamber picture. If you press and hold the chamber for 3
seconds, the chamber can be selected or be skipped.
Full charging status of battery / Charging status

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When closing the Use
If the use is completed,
① Press the power switch to turn off the power,
② Disconnect AC-DC adapter from an electrical outlet and main
body.
Disconnect main hose from the main body.
-Press red button on main hose and pull off main hose.
Disconnect main hose and cuff hoses from hose adapter.
If you wish to keep the device for a long time, place it in its box
6. Maintenance
No modification of this equipment is allowed.
Do not modify this equipment without authorization of the manufacturer.
If this equipment is modified, appropriate inspection and testing must be
conducted to ensure continued safe use of the equipment.
We will make available on request circuit diagrams, component part lists,
descriptions, or other information that will assist SERVICE PERSONNEL to repair
those parts of ME EQUIPMENT that are designated by us as repairable by
SERVICE PERSONNEL.
All the cuffs are not to be repaired as consumption goods. Be always careful.
Do not place the cuff near the sharp things such as furnaces, needles, scissors,
etc.
Keep the device in the dry place where there is no water or humidity
Do not wash the cuffs in washing machine nor submerge them in water.
Do not keep the device at too low temperature in winter time.
[It may be hardened and damaged.]
If you wish to keep the device for a long time, place it in its carrier.
Cleaning
When cleaning the product, wipe off with a dry cloth without any chemical

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substance or detergent.
It may cause the product external damage such as discoloration and peeling off.
The cuffs may be gently wiped with a moistened towel or cloth. If necessary, a mild
detergent may be used.
Environmental conditions
○,1 Operation
- a temperature range of +5°C to +40°C;
- a relative humidity range of 15% to 90%, non-condensing, but not requiring
a water vapour partial pressure greater than 50hPa; and
- an atmospheric pressure range of 700hPa to 1060hPa.
- home use as well as professional, indoor use only
○,2 Transport/Storage
- -25 °C to + 5 °C , and
- +5 °C to + 35°C at a relative humidity up to 90%, non-condensing;
- >35°C to 70°C at a water vapour pressure up to 50hPa
7. Temporary action taken during usage
Contents Check-up
When it doesn’t work
• Check up if the power switch is turned on.
• Check up if there is any problem in AC-DC adapter.
• Check up if it is low battery. If yes, connect AC-DC adapter
into main device to charge the battery.
When there is a strange
sound like air leakage
• Check up if there is any damage in the connecting hose and
hose adapter.
• Check up if you have connected the connector with the
device.
• Check up if the connecting hose is pressed or bent.
When the air does not
go into the cuffs or when
there is no pressure
• Check up if you have connected the connector with the
device.
• Check up if any heavy stuff is placed on the connecting
hose or the connecting hose is bent.
• Check up if the connecting hose is connected to main body
and hose adapte
r
until you hear an audible ‘click’.
When the air continues
to go into the cuffs and
when the air leakage
sound is made
• Check up where there is air leakage in the cuff. If there is no
air leakage, turn off the power, and then, turn on the power
again and check up if it does work properly. (the cuffs are
consumption goods.)
When the pressure is
too strong or discomfort
to the patient
• Press the PAUSE button to deflate the cuff, set the pressure
to the reduced one, and perform the operation again.

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8. Label
8.1 ID Label
The ID label is affixed on main unit and inner box.
8.2 Type BF Applied Part
The type BF applied part label is affixed near air outlet of main unit.

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9. Electromagnetic Compatibility
Guidance and manufacturer’ declaration –electromagnetic emissions
This equipment is intended for use in the electromagnetic environment specified below. The
customer or the user of this equipment should assure that is used in such an environment.
Emissions test Compliance Electromagnetic environment-guidance
RF emissions
CISPR 11
Group 1 The equipment uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely
to cause any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B The equipment is suitable for use in all establishments
including domestic establishments and those directly
connected to the public low-voltage power supply network
that supplies buildings used for domestic purposes.
Harmonic
emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies
Guidance and manufacturer’ declaration –electromagnetic immunity
This equipment is intended for use in the electromagnetic environment specified below. The
customer or the user of this equipment should assure that is used in such an environment.
Immunity test IEC60601
test level Compliance level Electromagnetic environment- guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±8 kV contact
±15 kV air
±8 kV contact
±15 kV air
Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material, the relative
humidity should be at least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
±2kV for power
supply lines
±1kV for input/
output lines
±2 kV for power
supply lines
±1 kV for
input/output lines
Mains power quality should be that of
a typical commercial or hospital
environment.
Surge
IEC61000-4-5
±1 kV line(s) to
lines
±2 kV line(s) to
earth
±1 kV line(s) to
lines
±2 kV line(s) to
earth
Mains power quality should be that of
a typical commercial or hospital
environment.
Power frequency
(50/60Hz)
Magnetic field
IEC61000-4-8
3 A/m 3 A/m Power frequency magnetic fields
should be at levels characteristic of a
typical location in a typical hospital or
home environment.
Voltage dips,
short interruptions
and voltage
variations on
power supply
<5% UT
(>95%dip in UT)
for 0.5 cycle
40% UT (60%
<5% UT (>95%dip
in UT) for 0.5 cycle
40% UT
(
60% dip
Mains power quality should be that of
a typical commercial or hospital
environment. If the user of the
equipment requires continued
operation during power mains

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lines
IEC6100-4-11
dip in UT) for 5
cycles
70% UT (30%
dip in UT) for 25
cycles
<5% UT (>95%
dip in UT) for 5
sec
in UT) for 5 cycles
70% UT (30% dip
in UT) for 25
cycles
<5% UT (>95%
dip in UT) for 5
sec
interruptions, it is recommended that
the equipment be powered from an
uninterruptible power supplied or a
battery.
Guidance and manufacturer’ declaration –electromagnetic immunity
The equipment is intended for use in the electromagnetic environment specified below. The
customer or the user of this equipment should assure that it is used in such an environment
Immunity test IEC60601
test level
Complia
nce
level
Electromagnetic environment-guidance
Conductive RF
IEC61000-4-6
3Vrms
150kHz to
80MHz
3Vrms
Portable and mobile RF communications
equipment should be used no closer to any part of the
equipment Including cables, than the recommended
separation distances calculated from the equation
applicable to the frequency of the transmitter
Recommended separation distance:
d=1.2√P
d=1.2√P 80 MHz to 800 MHz
d=2.3√P 800 MHz to 2.5 GHz
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site surveya, should
be less than the compliance level in each frequency
rangeb.
Interference may occur in the vicinity of
equipment marked with the following symbol:
Radiated RF
IEC61000-4-3
3V/m
80MHz to
2,5GHz
3V/m
Note 1 At 80MHz and 800MHz the higher frequency range applies.
Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a : Field strengths from fixed transmitted, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast cannot be
predicted theoretically with accuracy. To assess the electromagnetic environment in the
location due to fixed RF transmitters, an electromagnetic site survey should be considered. If
the measured field strength in the location in which this equipment is used exceeds the
applicable RF compliance level above, this equipment should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such
as reorienting or relocating this equipment.
b : Over the frequency range 150kHz to 80MHz, field strengths should be less than 3V/m.

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Recommended separation distances between portable and mobile communication
equipment and this equipment
This equipment is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of this equipment can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communication equipment (transmitters) and this equipment as recommended below, according to
the maximum output power of the communications equipment.
Rated maximum
output power of
transmitter W
Separation distance according to frequency of transmitter (m)
150kHz to 80MHz
d=1.2√P
80MHz to 800MHz
d=1.2√P
800MHz to 2.5GHz
d=2.3√P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1.0 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitter rated at a maximum output power not listed above, the recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter, where P is the maximum output power of the transmitter in watts (W) according to the
transmitter manufacturer.
Note 1. At 80MHz and 800MHz the higher frequency range applies.
Note 2. These guidelines may not apply in all situations. Electromagnetic propagation is affected
by absorption and reflection from structures, objects and people.

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WARRANTY
Name of
Products
Compressible Limb and
Circulation Therapy System
Applicable
Model POWER RECOVERY
Date of
Purchase Serial No.
Agent of
Purchase Warranty
Period
Body : 1 Year
Cuffs (Consumption Goods) :
3 Months (Work Place)
The life cycle of the device is 6 YEARS based on the motor pump which are the shortest life
cycle part of the device.
About Our Service
This is a product that we, Wonjin Mulsan Co., Ltd. manufactured though its own strict quality
management and inspection process.
Paid Services
Please be careful about the fact that the service fee will be charged even within the warranty
period if the consumer requests the service due to his/her carelessness or if no defects are
found in it.
In case of faults due to the consumer’s mistake (When the faults occur due to consumer’s
carelessness or wrong repair)
※ When the fault occurs due to the wrong use for the electrical capacity.
※ When the fault occurs because the consumer has fallen down the device during the transfer
after installation.
※ When the fault occur because the consumer has used the consumption and optional goods
that we did not designated.
※ When the fault occurs because other companies’ repairman has repaired the product
concerned.
※ When the fault occurs because the consumer has used the product in the prohibited
area(outdoors) or beyond the original use, because the consumer has disassembled,
alternated and repaired at his/her discretion.
※ When the consumer has not Abide by the matters that require attention in this instruction
manual (Please red the matters that require attention carefully.)
Other cases
※ In case of natural disasters(fire, damage from sea wind, flood damage, thunder, lightening,
earthquake, etc.)
※ Where the consumption goods are used up or their warranty period has already lapsed.
- Unprofessional operators or untrained operators need information service such as
installation, maintain of the device
- Report unexpected operation or event.
- Circuit diagrams, component part lists, etc. are needed for service personal.
Manufacturer: Wonjin Mulsan Co., Ltd.
Address : 2F, 89, Geomdan-ro, Seo-gu, Incheon, Rep. of KOREA
A/S telephone : + 82-32-816-0552

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CMC Medical Devices & Drugs S.L.
C/Horacio Lengo N 18, CP 29006, Málaga, Spain
Wonjin Mulsan Co., Ltd.
http://www.wonjininc.net
89, Geomdan-ro, Seo-gu, Incheon, Korea
A
/S : 82-32-816-0552