Shenzhen Roundwhale Technology R-C3 User manual

INSTRUCTION MANUAL
FOR
Combo Electrotherapy Device
Shenzhen Roundwhale Technology Co., Ltd.
This manual is valid for the R-C3 Stimulator
Model: R-C3
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Be sure to read this instruction manual before operate and
keeping it where safe.
This user manual is published by Shenzhen Roundwhale
Technology Co., LTD.
Shenzhen Roundwhale Technology Co., Ltd. does not guar-
antee its contents and reserves the right to improve and
amend it at any time without prior notice. Amendments
will however be published in a new edition of this manual.
All Rights Reserved.
R-C3 Rev.V1.1 © 2019, printed in May. 6, 2019.
Declaration of conformity:
Shenzhen RoundwhaleTechnology Co., Ltd. declares that
the device complies with following normative documents:
IEC60601-1, IEC60601-1-2, IEC60601-1-11, IEC60601-2-10,
IEC62304,
ISO10993-5, ISO10993-10, ISO10993-1,ISO 14971
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1. FOREWORD 4
2. SAFETY INFORMATION 6
3. GETTING TO KNOW YOUR DEVICE 11
4. SPECIFICATION 14
5. OPERATING INSTRUCTION 15
6. INSTRUCTIONS FOR USE 21
7. CLEANING AND MAINTENANCE 29
8. TROUBLESHOOTING 31
9. STORAGE 33
10. DISPOSAL 33
11. ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES 34
12. NORMALIZED SYMBOLS 38
13. WARRANTY 39
TABLE OF CONTENS
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1. FOREWORD
1.1 Introduction
The device R-C3 is a dual channel output TENS, EMS and
MASSAGE stimulator. Before using, please read all the in-
structions in this user manual carefully and keep it safe for
future use.
The COMBO stimulator belongs to the group of electrical
stimulation systems. It has three basic functions‒ TENS
(Transcutaneous Electrical Nerve Stimulation) , EMS (Elec-
tronic Muscle Stimulation) and MASSAGE.
Function of the COMBO stimulator: The device has 22 pro-
grams (9 TENS programs, 8 EMS programs and 5 MASSAGE
programs) and applies electric currents in the low-frequen-
cy range for therapy. Each program controls the generated
electric impulses, their intensity, frequency and pulse
width.
Based on simulating the body’natural pulses,the mech-
anism of electrical stimulation equipment is to create
electric impulses that are transcutaneous transmitted to
the dual channel can be adjusted independently and can
be applied individually to one body part. This dual channel
device can be used with four pieces of electrodes, which
allows you to stimulate one muscle groups simultaneously
with a wide selection of standard programs. The electrical
transmission of stimulation in nerves as well as muscle tis-
sues in the body parts.
1.2 Medical background
1.2.1 ABOUT PAIN
s
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Pain is an important signal in the human body warning sys-
tem. It reminds us that something is wrong, without which,
abnormal conditionsmay go undetected, causing damage
or injury to vital parts of our bodies. Even though pain is a
necessary warning signal of trauma or malfunction in the
body, nature may have gone too far in its design.
Aside from its function in diagnosis, long-lasting persistent
pain serves useless purpose.
Pain does not occur until encoded message travels to the
brain where it is decoded, analyzed, and reacted to, from
the injured area along the small nerves leading to the
spinal cord. There the message is transmitted to di󽗈erent
nerves that travel up the spinal cord to the brain. Then the
pain message is interpreted, referred to and pain is felt.
1.2.2 WHAT IS TENS ?
TENS (Transcutaneous Electrical Nerve Stimulation) is ef-
fective in relief of pain. It is daily used and clinically proven
by physiotherapists, caregivers and top athletes around the
world. High-frequency TENS currents activates the pain-in-
hibiting mechanisms of the nervous system. Electrical im-
pulses from electrodes, placed on the skin over or near the
pain area, stimulate the nerves to block the pain signals to
the brain, causing the pain go unperceived. Low-frequen-
cy TENS currents facilitate the release of endorphins, the
body’s natural painkillers.
1.2.3 WHAT IS EMS ?
Electrical Muscle Stimulation is an internationally accepted
and proven way of treating muscular injuries. It works by
sending electronic pulses to the muscle needing treatment
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That causes the muscle to exercise passively. It is a product
deriving from the square waveform, originally invented by
John Faraday in 1831. Through the square wave pattern it
is able to work directly on muscle motor neurons. The EMS
System has low frequency and this in conjunction with the
square wave pattern allows direct work on muscle group-
ings.
2. SAFETY INFORMATION
2.1 Intended use
TENS mode
It is used for temporary relief of pain associated with sore
and aching muscles in the neck, shoulder, back, joint, hip,
hand, abdomen, foot, upper extremities (arm) and lower
extremities (leg) due to strain from exercise or normal ho-
usehold work activities.
EMS mode
The EMS stimulation program stimulates healthy muscles
in order to improve and facilitate muscle performance.
Massage mode
The Massage stimulation program provides relaxing muscle
vibration to loosen tight muscles.
2.2 Important Safety Precautions and Warnings
It is important that you read all the warnings and
precautions included in this manual because they are
intended to keep you safe, prevent risk of injury and avoid
a situation that could result in damage to the device.
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SAFETY SYMBOLS USED IN THIS MANUAL
2.2.1 Contraindication
1) Do not use this device if you are using a cardi-
ac pacemaker, implanted de󽗉brillator, or other
implanted metallic or electronic devices. Such
use could cause electric shock, burns, electrical inter-
ference, or death.
2) The device should not be used when cancerous lesions
or other lesions are present in the treatment area.
3) Stimulation should not be applied over swollen, infect-
ed, inflamed areas or skin erup-
tions (e.g. phlebitis, thrombophle-
bitis, varicose veins, etc.).
4) Electrode placements must be
avoided in the carotid sinus area (anterior neck) or
transcerebrally (through the head).
5) This device should not be used in overly enervated ar-
eas.
6) Inguinal hernia.
7) Do not use on scarred areas following a surgery for at
least 10 months after the operation.
8) Do not use with serious arterial circulatory problems in
the lower limbs.
2.2.2 WARNING
1) If you have had medical or physical treatment for your
pain, consult with your physician before use.
2) If your pain is not subdued, becomes more than mild,
or lasts for more than 󽗉ve days, stop using the device
and consult with your physician.
3) Do not apply stimulation over your neck because this
could cause severe muscle spasms resulting in closure
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of your airway, di󽗋culty in breathing, or adverse e󽗈ects
on heart rhythm or blood pressure.
4) Do not apply stimulation across your chest because the
introduction of electrical current into the chest may
cause rhythm disturbances to your heart, which could
be lethal.
5) Do not apply stimulation over, or in proximity to, can-
cerous lesions.
6) Do not apply stimulation in the presence of electronic
monitoring equipment (e.g., cardiac monitors, ECG
alarms), which may not operate properly when electri-
cal stimulation device is in use.
7) Do not apply stimulation when in bath or shower.
8) Do not apply stimulation while sleeping.
9) Do not apply stimulation while driving, operating ma-
chinery, or during any activity when electrical stimula-
tion can put you at risk of injury.
10) Apply stimulation only to normal, intact, clean, healthy
skin.
11) The long-term effects of electrical stimulation are un-
known. Electrical stimulation device cannot replace
drugs.
12) Stimulation should not take place while the user is con-
nected to high-frequency surgical equipment, which
may cause burn injuries on the skin under the elec-
trodes, as well as problems with the stimu-
lator.
13) Do not use the stimulator in the vicinity of
shortwave or microwave therapy equip-
ment, since this may a󽗈ect the output pow-
er of the stimulator.
14) Never use it near the cardiac area. Stimula-
tion electrodes should never be placed any-
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where on the front of the thorax (marked by ribs and
breastbone), but above all not on the two large pecto-
ral muscles. There it can increase the risk of ventricular
󽗉brillation and lead to cardiac arrest.
15) Never use it on the eye, head and face area.
16) Never use it near the genitals.
17) Never use it on the areas of the skin which lack normal
sensation
18) Keep electrodes separate during treatment. It could re-
sult in improper stimulation or skin burns if electrodes
are in contact with each other.
19) Keep the stimulator out of reach of children.
20) Consult your doctor if you are in any doubt whatsoever.
21) Discontinue it and do not increase the intensity level if
you feel discomfort during use.
2.2.3 Precautions
1) TENS is not e󽗈ective for pain of central origin including
headache.
2) TENS is not a substitute for pain medications and other
pain management therapies.
3) TENS is a symptomatic treatment and, as such, sup-
presses the sensation of pain that would otherwise
serve as a protective mechanism.
4) Effectiveness is highly dependent upon patient selec-
tion by a practitioner quali󽗉ed in the management of
pain patients.
5) Since the effects of stimulation of the brain are un-
known, stimulation should not be applied across your
head, and electrodes should not be placed on opposite
sides of your head.
6) The safety of electrical stimulation during pregnancy
has not been established.
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7) You may experience skin irritation or hypersensitivity
due to the electrical stimulation or electrical conduc-
tive medium (silica gel).
8) If you have suspected or diagnosed heart disease or
epilepsy, you should follow precautions recommended
by your physician.
9) Caution if you have a tendency to bleed internally, e.g.
following an injury of fracture.
10) Consult with your physician prior to using the device
after a recent surgical procedure, because stimulation
may disrupt the healing process.
11) Caution if stimulation is intended to be applied over
the menstruation or pregnant uterus.
12) For single patient use only.
13) This stimulator should not be used by patients who is
noncompliant and emotionally disturbed including
whom with dementia or low IQ.
14) The instruction of use is listed and should be obeyed;
any improper use may be dangerous.
15) Rare cases of skin irritation may occur at the site of the
electrode placement following long-term application.
16) Do not use this device in the presence of other equip-
ment which sends electrical pulses to your body.
17) Do not use sharp objects such as a pencil or ballpoint
tip to operate the buttons on the control panel.
18) Check the electrode connections before each use.
19) Electrical stimulators should be used only with the
electrodes recommended for use by the manufacturer.
2.2.4 Adverse Reactions
1) Possible skin irritation or electrode burn under the
electrodes may occur.
2) On very rare occasions, first-time users of EMS report
feeling light-headed or faint. We recommend that you
use the product while seated until you become accus-
tomed to the sensation.
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3) If the stimulation makes you uncomfortable, reduce the
stimulation Intensity to a comfortable level and contact
your physician if problems continue.
3. GETTING TO KNOW YOUR DEVICE
3.1 Accessories
No. Description QTY
1 The COMBO Stimulator 1pc
2 Electrode pad (50mm×50mm ) 4pcs
3 Electrode wires 2pcs
4 USB cable 1pc
5 User manual 1pc
3.2 LCD display
No. Function description No. Function description
1 Treatment mode
8 Key locking symbol
2 Symbol of Program
9
Indicator of no load ( Channel 1 and Channel 2)
3 Low battery indicator
4 Symbol of SET
10 Intensity for Channel 2
5 Program number
11 Symbol of Channel 2
6 Symbol of Channel 1
12 Symbol of treatment time (min)
7
Intensity for Channel 1
1
2
3
4
5
6
7
16
15
14 13
12 11
10
8 9
13 Symbol of pulse width (uS)
14 Symbol of pulse rate (Hz)
15 Treatment time
16 Timer sign
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3.3 Device illustration
No. Description
1 LCD display
2
3
4
[ON/OFF/M] button:
At power saving mode, press the [ON/OFF/M] button to turn on the
device;
At standby mode, press the [ON/OFF/M] button to select treatment
mode;
At standby mode, press and hold the [ON/OFF/M] button to turn off
the device;
At treating mode, press the [ON/OFF/M] button to stop the treatment.
[+] button:
At standby or treating mode, press the [+] button to increase the in-
tensity of CH1;
At setting mode, press the [+] button to increase the corresponding
data for the pulse rate, pulse width or treatment time.
[-] button:
At treating mode, press the [-] button to decrease the intensity of
CH1;
At the key locking mode, press the [-] button to unlock the keys;
At setting mode, press the [-] button to decrease the corresponding
data for the pulse rate, pulse width or treatment time.
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No. Description
5
6
7
[-] button:
At treating mode, press the [-] button to decrease the intensity of
CH2;
At the key locking mode, press the [-] button to unlock the keys;
At setting mode, press the [-] button to decrease the corresponding
data for the pulse rate, pulse width or treatment time.
Charger indicator:
When the device is charging, the indicator light will be yellow;
When charging is completed, the indicator light will be green.
[+] button:
At standby or treating mode, press the [+] button to increase the
intensity of CH2;
At setting mode, press the [+] button to increase the corresponding
data for the pulse rate, pulse width or treatment time.
8 [P] button:
At standby mode, press the [P] button to select the treatment progr-
am;
At standby mode, press and hold [P] button to enter the setting mo-
de.
9 USB socket
10 Output sockets
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4. SPECIFICATION
4.1Technical information
Device name Combo Electrotherapy Device
Model/type R-C3
Power Sources 3.7 V Li-ion batteries
Power Supply Input: 100-240V AC, 50/60Hz,0.2A;
Output:
5V DC, 300mA
Output Channel Dual channel
Waveform Bi-phase square-wave pulse
Output current Max. 120mA (at 500-ohm load)
Output intensity 0 to 40 levels, adjustable
Treatment mode: TENS, EMS and MASSAGE mode
Output characteristics 5℃ to 40℃ with a relative humidity
of
15%-93%, atmospheric pressure from
700
hPa to 1060 hPa
Operating condition -10℃ to 55℃ with a relative humidity
of
10%-95%, atmospheric pressure from
700
hPa to 1060 hPa
Dimension 142*50*21.4mm (L x W x T)
Weight About 85g
1 minute
BF type applied part, internal power equip-
ment, IP22
Size of electrodes pad 50 x 50mm, square
Output precision ±20% error is allowed forall the output
parameters
TENS mode
Number of programs 9 programs
P.W. (Pulse Width) 100-300μs
P.R. (Pulse Rate) 2-100Hz (Hz=vib ration per second)
Treatment time 5-90 minutes
EMS mode
Classification
Automatic shutoff
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Number of programs 8 programs
P.W. (Pulse Width) 100 - 300μs
P.R. (Pulse Rate) 2 - 100Hz (Hz=vibration per second)
Treatment time 5-90 minutes
MASSAGE mode
Number of programs 5 programs
P.W. (Pulse width) 100 - 250μs
P.R. (Pulse Rate) 8 -100Hz (Hz=vib ration per second)
Treatment time 30 minutes
5. OPERATING INSTRUCTION
5.1 Connect electrode pads to electrode wires
Insert the electrode wires connector into electrode connec-
tor. Make sure they are properly connected to ensure the
good performance. Please refer to the picture.
Caution
Always use the electrode pads which comply with the re-
quirements of the IEC/EN60601-1, ISO10993-1/-5/-10 and IEC/
EN60601-1-2, as well as CE and FDA 510(K) regulation.
5.2 Connect electrode wires to device
Before proceeding to this step, be sure the device is com-
pletely switched OFF.
Hold the insulated portion of the electrode wire connector,
and insert the plug into the receptacle on the top of the
main device.
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Ensure the electrode wires are inserted correctly. The de-
vice has two output receptacles controlled by Channel A
and Channel B at the top of the unit. You may choose to
use one channel with one pair of
electrode wires or both channels
with two pairs of electrode wires. Us-
ing both channels gives the user the
advantage of stimulating two differ-
ent areas at the same time.
Caution
Do not insert the plug of the electrode wires into any AC
power supply socket.
5.3 Electrode
5.3.1 Electrode options
The electrodes should be routinely replaced when they
start to lose their adhesiveness. If you are unsure of your
electrode adhesive properties, please order new replace-
ment electrodes. Replacing electrodes should be re-or-
dered under the advice of your physician or the device
manufacturer to ensure proper quality. Follow application
procedures outlined on electrode packing when using the
new replacement electrodes to maintain optimal stimula-
tion and to prevent skin irritation.
5.3.2 Place electrodes on skin
Place the electrode on the body part
in need of treatment, according to the
instruction of this user manual. Please
make the skin clean before use and en-
sure the skin and electrode connect well.
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Caution
1. Always remove the electrodes from the skin with a mod-
erate pull in order to avoid injury in the event of highly
sensitive skin.
2. Before applying the self-adhesive electrodes, it is recom-
mended to wash and degrease the skin, and then dry it.
3. Do not turn on the device when the self-adhesive elec-
trodes are not positioned on the body.
or the appropriate channel first in order to avoid un-
wanted irritation.
5. It is recommended that, at minimum, 1.97”x 1.97”
self-adhesive square electrodes are used at the treat-
ment area.
6. Never remove the self-adhesive electrodes from the skin
while the device is still on.
5.3.3 Electrode placement
R-C3 is a kind of OTC stimulator, suitable for home use. You
only have to use according to the user manual, place the
electrode on the position where you feel pain. Conducting
exercise, treatment and adjustment based on your own
feeling.
Different programs with corresponding applicable symp-
toms as below:
Position of electrode placement under TENS programs
Neck
4.To remove or move the electrodes, switch off the device
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Shoulder
Arm
Hand
Back 1
1
2
2
Abdomen
Hip
Leg
1２
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Foot
Joint (knee)
Joint
(elbow)
Joint
(ankle)
Joint
(wrist)
Position of electrode placement under EMS programs
Neck 1
2
1
2
Shoulder
1
1
2
2
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Arm
Hand
Back
Abdomen
1
2
1 2
Hip
Leg
Foot
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