DECELL

User Manual

DAEYANG MEDICAL CO., LTD.

Publishing details

DECELL User Manual

Document No.: DY2202-Manual-EG
Revision No.: 0
Part Code: ML5117-0
Revision date: 2022.04.07

Manufacturer

Daeyang Medical Co., Ltd

147, Donghwagongdan-ro, Munmak-eup,
Wonju-si, Gangwon-do, Republic of Korea, 26365
T +82) 33-747-4466
F +82) 33-747-1133
http:// www.daeyangmed.com

Copyright
This document is protected by copyright. All rights reserved. Notably, no portion of this publication may be
reproduced or made available to third parties, in any form, online or offline, without the written consent of
Daeyang Medical Co., Ltd. Further, no portion of this publication may be translated into a language or code that
can be utilized for machines data processing systems, or the internet. This document may exclusively be used
to properly use the products described herein in accordance with the contractual terms for such product.
Copyright ©2022 Daeyang Medical Co., Ltd.
DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 2 / 24
Contents

General Information .................................................................................................................................... 4

Warranty ...................................................................................................................................................... 4
Precautionary Instructions ......................................................................................................................... 4
CAUTION .............................................................................................................................................. 5
WARNING ............................................................................................................................................. 6
DANGER ............................................................................................................................................... 8
Introduction ................................................................................................................................................. 9
Intended use .......................................................................................................................................... 9
What is the DECELL? ............................................................................................................................. 9
Features of DECELL .................................................................................................................................. 10
Unit ...................................................................................................................................................... 10
Accessories .......................................................................................................................................... 12
User Interface ............................................................................................................................................ 13
Technical Specification. ............................................................................................................................ 15
General ................................................................................................................................................ 15
Output Parameter ................................................................................................................................. 15
Environmental Conditions for Transport and Storage ............................................................................ 15
Environmental Conditions for Operation ................................................................................................ 15
Intended operator ................................................................................................................................. 15
How to Use................................................................................................................................................. 16
Operation Method ................................................................................................................................. 16
Indications ................................................................................................................................................. 19
Troubleshooting ........................................................................................................................................ 20
Self-Checking Point ................................................................................................................................... 21
Maintain ..................................................................................................................................................... 22
Cleaning method .................................................................................................................................. 22
Technical Maintenance ......................................................................................................................... 22
End of life ............................................................................................................................................. 22
Safety and Performance standards ....................................................................................................... 22
Label Symbol ............................................................................................................................................. 23
GUARANTEE ............................................................................................................................................. 24

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 3 / 24

General Information

This section provides Safety information critical to use of the Shock Wave Systems.
Read, understand, and follow all of the Safety Precautions found in this section and throughout this manual
prior to System use.
Observe all applicable precautionary measures for treatment.
Keep informed on appropriate indications and contraindication for the use of Shock Wave Systems.

Warranty

This product is warranted against defects in materials and workmanship for a period of one year from the date
of shipment.
The Company will at its option, repair or replace components which prove to be defective during the warranty
period, provided that the repairs or replacements are carried out by the Company or its approved agents.
The Company will consider itself responsible for the effects on safety, reliability and performance of the
product: -only if assembly operations, re-adjustments, modifications or repairs are carried out by persons
authorized by it, only if the product is used in accordance with the instructions for use, only if the electrical
installation of the relevant room complies with the appropriate national requirements.
Should the product be returned to the Company for repair it must be sent carriage paid.
Consumable items, for example, electrodes are not excluded from the above warranty.

Precautionary Instructions

The precautionary instructions found in this section and throughout this manual are indicated by specific
symbols. Understand these symbols and their definitions before operating this equipment. The definition of
these symbols is as follows.

Text with a “CAUTION” indicator will explain possible

Safety infractions that could have the potential to cause minor to moderate injury or damage to
CAUTION equipment.

Text with a “WARNING” indicator will explain possible

WARNING Safety infractions that will potentially cause serious injury and equipment damage.

Text with a “DANGER” indicator will explain possible

Safety infractions that are imminently hazardous situations that would result in death or serious
DANGER injury.

Throughout this manual “NOTE” may be found. These Notes are helpful information to aid in
the area or function being described.
NOTE

4 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

 CAUTION
• The device in operation must be regularly inspected for safety by qualified personnel authorized by the
manufacturer.
• Since the device cannot be repaired except by professional personnel authorized by the manufacturer,
do not disassemble or assemble the device at your own discretion.
• For electrical safety, the device must be connected to a safety grounded power source.
• The operator and manager of the device must be familiar with the user manual, and the user manual
should be kept close to the device.
• For the prevention of safety accidents and proper maintenance, provide safety signs and instructions
provided with the device in a place that is easily visible around the device.
• It is managed so that there is no water, alcohol, flammable glue, etc. around the device.
• Do not use electronic devices such as mobile phones, walkie-talkies, mobile radio transmitters, radio
toys, etc. while the device is in operation.
• Do not use the device with wet hands.
• The application site according to the disease is decided by the user or operator and is entirely
responsible.
• Observe the recommended operating time and method.
• Install on a flat surface.
• After use, clean all parts with a soft cloth / disinfecting gauze and alcohol.
• Do not use agents containing chlorine or those with a high alcohol content (more than 20 %)
• When in use, you must constantly communicate with the patient. The patient should never be left
indifferent.
• Do not place the device in direct sunlight or near a heat source.
• When the device is brought from a cold environment to a warm environment, wait for the temperature to
equalize before connecting it to the power supply before use. (Minimum 2 hours)
• The main power supply to which the device will be connected must be installed and calibrated in
accordance with current standards for electrical installations in medical institutions.
• Check if the input power is correct.
• Before starting, make sure that all the setting parameters match the requirements.
• The instrument displays a message about the fault or defect of the instrument and components. If you
are not sure of the meaning, stop using the device and contact an authorized service center.
• Do not bend the electrical cord or accessories using force or place a sharp or heavy object on them.
(There may be a risk of electrical shock or fire.)
• Do not plug several power cords of electrical appliances into one receptacle at the same time. (There
may be a risk of fire.)
• Do not touch the exterior of the instrument while it is operating.
• The pressure pulse is attenuated during passage through tissue, and that additional energy is absorbed
by bone.
• Even if anti-collision devices are installed, the operator shall always watch for any movements that may
cause danger to the patient or operator
• Do not apply more than 300-500 shots to the same point.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 5 / 24

 WARNING
• Use the device according to the instruction manual.
• The instruction manual explains how to operate the machine properly. Please read the instruction manual
carefully and keep it well.
• The device must be used under the supervision of a person with professional medical certification or a
person who has completed the related education.
• We are not responsible for any problems arising from the use of the product by persons without
professional medical certification or those who have not completed related training.
• This device should not be tampered with or modified or used for any other purpose than intended use.
• In case of natural disasters such as thunder, lightning, earthquake, etc., immediately stop using the
product, turn off the power, and unplug the power cord.
• Patients should not be contacted with a conductive component that is grounded or has a well-grounded
capacitance and may provide an unwanted path for induced current. In particular, do not use a bed or
chair with a metal frame.
• The connection cables related to the applicator should be arranged so that they do not come into contact
with the patient or conductive or energy absorbing objects.
• Keep people with pacemakers away from the machine during operation.
• If the device is used despite its defect, the user is fully responsible for any damage caused by the device.
• The device must be disposed of in a common method of disposal for general electronic and electrical the
device.
• Arrange the device so that the power cord can be easily disconnected in case of an emergency.
• If the patient moves after correct positioning, re-perform localization if necessary. Failure to maintain
correct positioning could result in misdirection of the shockwave and injury to adjacent nerves or blood
vessels.
• If electromagnetic interference between the extracorporeal shock wave system and nearby electronic
equipment is suspected (as evidenced by erratic behaviour with either device), it is recommended that
their distance be increased until proper operation resumes. If it is necessary to operate an electronic
device in close proximity to the ESWT system during treatment, the device and the ESWT system should
be tested for proper simultaneous operation prior to clinical use.
• Never remove any of the cabinet covers to the system’s electronics. The high voltage power supply
circuits utilized by extracorporeal shock wave systems use voltages that are capable of causing serious
injury or death from electric shock.
• If you have any problems with this product, immediately stop using this product and contact our customer
service center or stores where you bought this product.
• Patients currently undergoing systemic anticoagulation therapy (example—coumadin, heparin) should
consult their physicians regarding temporary discontinuation of such medications before ESWT to
prevent potential ecchymosis/bruising.
• Patients on daily aspirin therapy should temporarily discontinue aspirin intake 1week before ESWT
therapy.
• If the device malfunctions during treatment or the treatment is discontinued, the therapeutic effects may
not be as noticeable.

6 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

• Do not disassemble, repair and remodel the product at discretion of a user. Please contact the sales
store or customer service center for help to repair it. (There may be a risk of electrical shock or fire)
• Please insert a plug in a wall socket with grounded.
• Do not use a damaged electrical cord or aged receptacle.
(There may be a risk of electrical shock or fire)
• Do not give a shock to the product or accessories.
• No modification of this equipment is allowed without authorization of the manufacturer.
• Equipment must be connected to an appropriate power source.
• To avoid risk of electric shock, this equipment must only be connected to a supply main with protective
earth.
• The pressure pulses may cause unwanted cardiac activity.
• Operate the air release lever on the back of device once a month to drain air and water.
• Do not lay down the product. (It can cause oil leakage)
• The use time and stop time should be adjust and used. (Stop for 10 minutes after operating for 20
minutes)
(If not adjusted, a lot of oil may leak or the tank and motor connection hose may burst)
• Oil should be replenished every two to three months.
• Never operate with the tip(head) of the applicator removed.
• Do not operate the applicator in the air.
(When operating without contact with the patient, the life of the device may be shortened)
• At first use, the intensity (POWER) should be set low and gradually increase the intensity (POWER)
depending on the patient’s condition. (1 ~ 7 bar)
• At first use, the number of operations (SHOCKS) should be set less and the number of operations
(SHOCKS) should be gradually increased depending on the patient’s condition.
(1000, 2000, 3000, 4000)
• When operating the applicator, it should not operation on objects (metal, stone, etc.) other than the
patient.
• Do not turn off the main power switch while the compressor inside the main body is operating.
• The intake cap should be closed during transport and the intake cap should be opened and used during
operation.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 7 / 24

 DANGER
• A user shall avoid using the product in the following cases of for the specific regions or person;
- Growing child.
- Pregnant women.
- Patients younger than 18 years of age.
- Patients with a coagulation abnormality, thrombopathy, infection, tumours, cervical compression
syndrome, cervical or upper extremity arthritis, local arthrosis, neurologic abnormality, or radial nerve
entrapment.
- Patients who have had previous surgery for lateral epicondylitis.
- Patients who suffer from severe systemic diseases that may lead to sensory changes or neuropathic
pain. For example, this may include diseases such as gout, diabetes mellitus, rheumatoid arthritis.
- Patients with cardiac pacemaker
- Patients who received physical or occupational therapy less than four (4) weeks prior to ESWT.
- Patients who received a local steroid injection less than six (6) weeks prior to ESWT.
- Patients with tennis elbow affecting both arms or who have had previous surgery for this condition.
• Do not put the electrode to your eye directly to prevent from your eye damage.
• Do not pull the power cord using force or touch the power plug with a wet hand.
(There may be a risk of electrical shock or fire)
• Stop using the product and unplug the power cord immediately when there is thunder and lightning or an
earthquake. (There may be a risk of electrical shock or fire)

8 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

Introduction

Extracorporeal Shock Wave Therapy (ESWT) is a popular treatment method used to combat common
concerns including heel pain, plantar fasciitis, Achilles tendonitis, tennis elbow, shoulder tendonitis, lateral
epicondylitis, and more. It is considered a breakthrough treatment that can make common problems like heel
pain virtually obsolete. Many people with chronic pain problems are turning to ESWT to find relief from their
pain.

Intended use
It is a device which is used for relieving pain on injury and stimulating the body by generating shock wave that
uses energy level with 1~7 bar and frequency (1, 3, 5, 10Hz).

What is the DECELL?

What is ESWT?
ESWT is an FDA approved form of treatment. It is a non-surgical approach to pain relief that is used regularly
to cure common problems like plantar fasciitis and Achilles tendonitis. The therapy works by targeting shock
waves directly to the area that is experiencing pain. This non-invasive procedure typically lasts less than 30
minutes.

Success Rate
Statistically, over 90 percent of patients that receive this therapy experience a reduction in their pain. In patients
that suffered from plantar fasciitis and heel pain related problems, the pain reduction was remarkable. Nearly
all patients had successful results with only one treatment of ESWT. For this reason, many people are turning
to ESWT to treat their injuries.

Low Risk
One of the main benefits of ESWT is the low risk attached to the procedure. The therapy is treated extra-
corporeally. Patients receive the therapy outside of their body instead of receiving an invasive surgery. This
promotes a faster recovery time, and it also minimizes the side effects from the treatment itself.

Recovering From ESWT

Recovery from ESWT is a gradual process, however the pain will not get worse. In the process of ESWT,
damaged tissue cells begin to rebuild. Therefore, healing of the injured area will occur over a few days, weeks
or months as these new cells develop. In some rare cases individuals will experience soreness or bruising after
the treatment.

Why ESWT?
ESWT is a great option for patients that have chronic pain. Individuals that have tried other options with no
results and are still experiencing pain will benefit from ESWT. It is important to try this therapy before the pain
gets worse. If the injury gets worse or spreads to other areas of the body, ESWT may not be an option.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 9 / 24

Features of DECELL

Unit

Front View Rear View

Side View (Right) Side View (Left)

10 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

 No. Parts Description

1 LCD LCD display for control.

2 Sub On/Off Switch Sub power switch.

3 Applicator Holder (Left) Applicator holder (Left).

4 Applicator Holder (Right) Applicator holder (Right).

5 Pressure gauge Gauge for air pressure.

6 Power Inlet Power Inlet Socket.

7 Power On/Off Switch Power On/Off.
8 Air release lever Lever for air pressure release.
9 Applicator (left) Applicator for output (left).
10 Applicator (Right) Applicator for output (Right).
11 Air outlet Hole for air pressure release.
12 Air intake Hole for air pressure intake.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 11 / 24

Accessories

Picture Parts Description Quantity Remarks

Applicator Applicator for Output. 2 -

Power cord Power cord for power supply. 1 -

Expendables (Tip)

Picture Parts Description Quantity Remarks

Ø 6 Tip Applicator head part

1 -
connector.
(acupuncture)

Ø 10 Tip Applicator head part

1 -
connector.
(trigger)

Ø 15 Tip Applicator head part

2 -
connector.
(eswt)

Ø 20 Tip Applicator head part

1 -
connector.
(rswt)

12 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

User Interface

No. Name Function

1 Select applicator (LEFT) Select the left applicator.

2 Select applicator (RIGHT) Select the right applicator.

Mode selection.
SINGLE (1 Hz), SLOW (3 Hz),
3 MODE MIDDLE (5 Hz), FAST (10 Hz)
* Single: output only when the output generation button is
pressed.
4 POWER Air pressure strength setting. (1~7 bar)
Select maximum number of outputs available.
5 SHOCKS
(1000, 2000, 3000, 4000)
6 LEFT CONFIG Display selected applicator settings.

7 RIGHT CONFIG Display selected applicator settings.

8 START Output start.

9 Treatment part Select the treatment part.

10 ENVIRONMENT Go to the environment setting value screen.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 13 / 24

No. Name Function
1 Select applicator (LEFT) Select the left applicator.

2 Select applicator (RIGHT) Select the right applicator.

Display selected mode.

3 MODE
* Control with the UP & DOWN button

Display selected power.

4 POWER
* Control with the UP & DOWN button

Display selected shocks.

5 SHOCKS
* Control with the UP & DOWN button
6 LEFT CONFIG Display selected applicator settings.

7 RIGHT CONFIG Display selected applicator settings.

8 STOP Output stop.

9 Treatment part Display selected treatment part.

10 TOTAL COUNT Display total number of shocks.

14 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

Technical Specification.

General
Power Input………………………………………………………………………………………220-240 Vac, 50/60 Hz
Maximum Power Consumption…………………………………………………….……………………………300VA
Classification ………………………………………………………………………….…………….…Class 1, Type BF
Mains Fuses…………………………………………………………………………...……………2 x T8A (5 x 20 mm)
Size (width x depth x height) ……………………………………………………….……………452 x 415 x 983 mm
Weight…………………………………………………………………………………………………………………20 kg

Output Parameter
Energy Level ………………………………………………………………………………………………… 1~7 bar
SHOCKS ….……………………………………………………………………………….… 1000 / 2000 / 3000 / 4000
MODE …………………………………………………………………………………………… SINGLE: 1 Hz
SLOW: 3 Hz
MIDDLE: 5 Hz
FAST: 10 Hz

The DECELL is designed to operate from any 50/60Hz single phase supply between 220 and 240 Vac.
All information on model, serial number, and month/year of manufacture is located on the rear panel.

Environmental Conditions for Transport and Storage

• Temperature: -10 to +55 C
• Relative Humidity: 10 to 80%
• Atmospheric Pressure: 500 to 1060 hPa

Environmental Conditions for Operation

• Temperature: 10 to 40 ℃

• Relative Humidity: 30 to 75%

• Atmospheric Pressure: 700 to 1060 hPa

Intended operator
1) Education
- A physician who specializes in therapy
2) Knowledge
- Read and understand English
- Understands human body such as physician
3) Experience
- The physician who have been educated or trained the electrosurgical unit system.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 15 / 24

How to Use

Operation Method

1) Preparation to use

(1) Check whether this equipment has all accessories necessary. If the connector is loose or do not make
good connection, then ask to the agent where you purchased it.
(2) Connect the power cable into the Inlet socket.
(3) Turn on the power switch on the back of the equipment and the auxiliary power switch on the front.
(4) The pain position of the human body is checked using an ultrasound imaging diagnostic device or
x-ray.
(5) Clean the patient’s skin and apply enough gel.

2) How to Use
The operation of DECELL is extremely simple.
(1) Check whether the connector of Applicator
is connected to the proper position of the
equipment.

(2) Combine the applicator tip you want to

use.

(3) Select the applicator you want to use.

16 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

 (4) Select a treatment part.

(5) Select the desired Program.

Mode Name Description

SINGLE 1 Hz
SLOW 3 Hz
MIDDLE 5 Hz
FAST 10 Hz

* Single: output only when the output

generation button is pressed.

(6) Set the air pressure level and shocks

value.

Name Description
Power 1~7 Bar
1000, 2000,
Shocks
3000, 4000

(7) Check the setting value you want to use

and press the Start button.

* Possible control the setting value even

after pressing the start button

(8) Place the applicator on the area to be

treated and press the output generation
button.

* Applicator output Generation button press

for more than 3 seconds to continuously
output.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 17 / 24

3) How to store and manage after use
(1) Press sub switch to turn off the power.
(2) Press main switch to shut off power completely.

(3) Keep the equipment away from humid places or firearms.

(4) Be careful not to touch children.
(5) Do not touch the power supply with wet hands.

4) Air pressure release method

(1) Turn the air release lever on the back of the product as shown in the figure below.
(2) Exhaust the air pressure while checking the pressure gauge.
(3) When the air release is complete, return the air release lever.

Operate the air release lever on the back of device once a month to drain air and water.

18 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

Indications

1 EPICONDYLITIS HUMERI RADIALIS

Painful inflammation of the tendon attachment on the medial elbow.
2 TENDINOSIS CALCAREA
Painful limitation of shoulder movement due to calcification.
3 EPICONDYLITIS HUMERI ULNARIS
Painful inflammation of the tendon attachment on the lateral elbow.
4 BURSITIS TROCHANTERICA
Painful periostitis of the outer femur.
5 PATELLA TIP SYNDROME
Inflammation of the point of attachment of
the patellar ligament.
6 TIBIALIS ANTERIOR SYNDROME
Inflammation of the tibial edge due to
excessive strain.
7 ACHILLODYNIA
Painful irritation of the Achilles tendon.
8 FASCIITIS PLANTARIS
Painful, mostly chronic inflammation of the
plantar fascia.

CHRONIC ENTHESOPATHIES
Painful irritation of tendon attachments due to overexertion or improper strain, or due to degenerative
processes.

ACUPUNCTURE POINTS
Pain therapy via treatment of acupuncture points.

PAINFUL TRIGGER POINTS

Acute and chronic pain in the back, shoulder, neck, etc. due to permanently shortened and thickened
muscles.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 19 / 24

Troubleshooting

Issue Description Recommended action(s)

• Change fuse.
Back of main body fuse
• Replace the extra fuse on the back of the
disconnection.
main body power connector.

Power supply Mian PCB damage from electric

• Contact agency or manufacturer.
shock.

• Check the main power switch.

The display does not light up • Check/replace the fuses and replace them
when the device is switched on. only with the type indicated on the back of
the unit.

Applicator Damage caused by external

• Contact agency or manufacturer.
malfunction impact.

Applicator’s head is untied. • Tighten the head part.

Applicator’s Defect or deterioration of internal

• Contact agency or manufacturer.
strength problem solenoid valves.

Damaged Tip or O-ring. • Contact agency or manufacturer.

Applicator don’t connect properly

• Contact agency or manufacturer.
to the main body.

Defect or deterioration of internal

• Contact agency or manufacturer.
solenoid valves.

• Check the pressure available for the device.

Device air defective Pressure not adjustable. • Check the compressor.
• Contact agency or manufacturer.

Pressure reduction during • Check the compressed air supply.

operation. • Contact agency or manufacturer.

Pressure too high. • Contact agency or manufacturer.

Damage caused by external

• Contact agency or manufacturer.
impact.
LCD power connector
LCD defective • Contact agency or manufacturer.
disconnection.
Mian PCB damage from external
• Contact agency or manufacturer.
impact.

20 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

Self-Checking Point

1) Before using the product

(1) Does the power code Insert a plug in a wall outlet?

(2) Did you check the connection between main frame and etc.?

(3) Did you check the connection line?

(4) Did you check the power switch ON?

(5) Do you see any problem with Display?

2) After using the product

(1) Did you check the power switch OFF?

(2) Did you check the plug off in a wall outlet?

(3) Did you clean the etc.?

3) How to replace the fuse

1) Check that the machine's power is off.

2) Check if the fuse is blown.

3) Replace the fuse (250V, 8 A).

4) Remove the fuse, replace 1 or 2 new fuses, and close the cover.

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 21 / 24

Maintain

Cleaning method
• After all treatment, it is recommended to wipe with a dry cloth or cotton gauze to clean.
• When cleaning the touch LCD screen, wipe with a soft surface.
• Clean the surface of the product, wipe with a soft surface, not greasy and that water is moderate.
• Separate the applicator and the tip and clean them.

Technical Maintenance
If there are any defective parts of Accessories, you can replace the accessories by Daeyang medical
company directly. In case of any defective parts of main device, we need to receive the device to repair or
calibration. Please send the address as below.

Repair Center: DAEYANG MEDICAL CO., LTD

Address: #147 Donghwagongdan-ro Munmak-eup Wonju-si, Gangwon-do, KOREA
Contact: [email protected]

CAUTION:
• Electrical safety of the device relies on a properly earthed electrical connection via the power cord. It is
therefore necessary to have this connection checked annually.

WARNING:
• This unit operates with high voltages. No attempt should be made to disassemble the unit. Maintenance
and repair should be carried out by authorized personnel only. The manufacturer will not be held
responsible for the results of maintenance or repairs by unauthorized persons.

All other technical maintenance is restricted to authorized Daeyang Medical maintenance personnel.

End of life
The DECELL contains materials that can be recycled and/or are noxious to the environment.
Specialized companies can dismantle the unit and sort out these materials. When you dispose of
the unit, find out about local regulations concerning waste management.

Safety and Performance standards

• IEC 60601-1: General requirements for the safety of electrical medical systems.

• Safety class according to IEC 60601-1: class I type BF

22 / 24 DAEYANG MEDICAL CO., LTD DY2202-Manual-EG(Rev.0)

Label Symbol

Symbol Meaning

Serial number

Manufacturer information

Type BF applied part

Follow instructions for use

Waste Electrical and Electronic The device Directive

Warning

Top

Fragile

Keep dry

Temperature limit

Atmospheric pressure limitation

Humidity limitation

DY2202-Manual-EG(Rev.0) DAEYANG MEDICAL CO., LTD 23 / 24

 GUARANTEE

All Daeyang Medical units are guaranteed against defects in material and workmanship for a period of
one year after the date of purchase – with the exception of accessories and subject to normal wear.

Should your unit develop a fault, please return it to the distributor in the country where the unit was
purchased.

Local Distributor

DISTRIBUTOR

DAEYANG MEDICAL CO. LTD.

#147 Donghwagongdan-ro Munmak-eup Wonju-si
Gangwon-do, KOREA
MANUFACTURER
Phone No.: +82-33-747-4466
Fax No.: +82-33-747-1133
http://www.daeyangmed.com