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.