Weightworld CIRCULATOR User manual

USER MANUAL OF
NERVE & MUSCLE STIMULATOR
WEIGHTWORLD™
Document No.: CWL-URM-04A | Revision No.: 00. | Revision Date: 20.06.2022
Manufactured By
Camex Wellness Limited
16 Plot Number, Sector 2, Akshar Industrial Park,
Opp Zydus Cadila Pharma, Sarkhej-Bavla National Highway,
Moriaya, Ahmedabad-382213, Gujarat, India.
Manufactured For
COMFORT CLICK LIMITED
Number 7, Doctor Croke Place,
CLONMEL, TIPPERARY.
E91 E7D0, Ireland.
For Technical Support
Contact No.: + 44 203 322 7970
Website: www.weightworld.uk
2265

Contents
1. Introduction 4
1.1.
1.2.
1.3.
1.4.
1.5.
1.6.
1.7.
1.8.
1.9.
1.10.
Intended Use
Intended User
Patient Population
Medical Condition
Known Characteristics of Repeat Application of the device
Performance Characteristics
Clinical Benefits
Principle of Operation
Contraindications
Adverse Reactions
4
4
4
5
5
5
5
6
7
7
2. Warnings
3. Cautions
4. Precaution
5. Package Content
6. Charging the Circulator (Nerve and muscle stimulator)
7. Charging related warnings
8. Technical Specification
9. Care Cleaning and maintenance
10. Purchasing consumables
11. Expected service life
12. Disposal of product WEEE
13. Troubleshooting
14. EMC and Electrical standard requirement
8
9
10
11
11
11
12
13
13
14
14
15
18
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15. Notice to Users and/or Patients
16. Applicable symbol
17. Warranty
18. Batteries
19. Serviceability
20. Spillage of liquid
21. Technical Specification
22. Technical data
23. Recommendation
24. Device electrode patches body intensity
25. Recommendation
26. Accuracy of Controls and Instruments
18
19
21
21
22
22
22
22
23
24
27
28
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7 DC USB Cable
6 Power & Battery Sockets
8 Electrode Patches
5 Power Button
1 Foot Pads
3 Foot Intensity Level Button
-/+ 1-99 (Foot Pads)
2 Prog/Time Button Default time - 30
minutes Program- P1 (EMS) and P2
(TENS)
4 Body Intensity Level Button
-/+ 1-99 (Electrode Patches)
1. Introduction
1.1. Intended Use
To increase local blood circulation
To relieve neuropathy pain, osteoarthritic pain,
acute and chronic body pain, varicose vein
To provide paralytic nervous activation
For strengthening body muscle and relieve
body muscle pain
For muscle toning
1.
2.
3.
4.
5.
1.3. Patient Population
Device can be used by patients with age 15 and above. Contraindicated for:
Pregnant ladies
Patient with pacemaker, implanted defibrillator or other implanted electronic
devices as this may cause electric shock, electric interference, burns or death.
Patient with Deep Vein Thrombosis
Epileptic Patient
Patient with cardiac condition
1.2. Intended User
Device can be used by patients aged 15 and above.

Safe for use in patients with age 15 and above,
Increases local blood circulation,
Strengthens body muscles,
Provides pain relief.
1.4. Medical Condition
It is used in multiple conditions for pain in legs, shoulder, upper back, waist, upper
extremities and lower extremities in ailments osteoarthritis, fibromyalgia, tendinitis,
diabetic neuropathy etc.
1.5. Known Characteristics of Repeat Application of the device
The device can be used not more than 30 minutes, twice daily. The foot pads come in
direct contact with the skin.
The electrode patches also come in direct contact with the skin and the patches can be
used up to 30 applications.
1.6. Performance Characteristics
The Circulator (Nerve & Muscle Stimulator) is indicated for increasing local blood
circulation; relieve neuropathy pain, osteoarthritic pain, acute and chronic body pain,
varicose vein; provide paralytic nervous activation; strengthening body muscle and
relieve body muscle pain; muscle toning.
1.7. Clinical Benefits
The Circulator (Nerve & Muscle Stimulator):
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1.8. Principle of Operation
The Circulator (Nerve & Muscle Stimulator) works on the two principles i.e. TENS
(Transcutaneous Electrical Nerve Stimulation) and EMS (Electrical Muscle Stimulation)
TENS is a method of electrical stimulation which
primarily aims to provide a degree of
symptomatic pain relief by exciting sensory
nerves and thereby stimulating either the pain
gate mechanism and/or the opioid system. The
type of stimulation delivered by the TENS unit aims
to excite (stimulate) the sensory nerves, and by
doing so, activate specific natural pain relief
mechanisms. The unit sends light electrical pulses
into the body through the skin via Foot pads and
electrode patches which are placed over peripheral nerves. Then Circulator (Nerve
& Muscle Stimulator). Works by sending high-frequency electrical signals that are
both continuous and mild to block out the pain signals being delivered to the brain.
The Circulator (Nerve & Muscle Stimulator) device was designed with specific pulse
frequency and pulse length that are suitable for its intended use. Low frequency
bursts of mild electrotherapy also help activate the natural pain control response,
releasing beta endorphins to ease pain felt by the patient.
EMS is a protocol that elicits a muscle contraction
using electrical impulses that directly stimulate
motor neurons. This stimulation creates muscle
contractions that can be quick and frequent, fast
with long pauses, or contractions that are held for
several (uncomfortable) seconds or minutes at a
time. Normally, it is your body that fires your
muscles by sending electrical impulses from brain
through central nervous system (CNS). But an
EMS device allows to engage in deep, intense, and
complete muscular contractions without actually activating (or stressing) CNS.
Circulator (Nerve & Muscle Stimulator) helps in expanding and contracting the
muscles through which there is an increase in blood circulation and also strength-
ening of muscles.

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1.9. Contraindications
Circulator (Nerve & Muscle Stimulator) should not be used by following person:
1.10. Adverse Reactions
Do not use the product if you experience skin irritation or burns on the skin surface,
if you have experienced any adverse reactions, immediately contact your doctor.
Pregnant ladies.
Patient with pacemaker, implanted defibrillator or other implanted electronic
devices as this may cause electric shock, electric interference, burns or death.
Patient with Deep Vein Thrombosis.
Patient with cardiac condition.
Epileptic patient.
2. Warnings
Consult with your physician before using Circulator (Nerve & Muscle Stimulator) in case of
following:
If you are in care of physician
If you have any medical or physical treatment ongoing
Do not apply stimulation over the chest because introduction of electrical current to chest
may cause disturbance to heart which could be lethal.
Do not apply stimulation over neck, there is a chance that using the electrode patches
on neck may cause the closure of airway difficulty in breathing Stimulation over the neck
could adversely impact hearing or blood pressure.
Do not apply stimulation or place the electrode patches around or on head. The
effect of stimulation of the brain are unknown.
Use the electrode patches only on normal, dry, healthy and clean skin.
Do not apply foot Electrode patches or electrode patches directly:
On open wounds or rashes, swollen, red, infected, or inflamed areas or skin
eruptions (such as phlebitis, thrombophlebitis and varicose veins).
On or close to, cancerous lesions/tumours.
On areas treated with radiotherapy (within the past 6 months).
On reproductive organs.
On bones and joint (knee, elbow and shoulder joint).
The electrode patches are for single person use only. Do not share electrode patches with others.
Do not use while sleeping, or in or close to water (eg. bath, shower) or in environment
of elevated humidity (eg. Sauna, hydrotherapy etc.)
You must use the device as indicated in this manual.
Avoid placing the Electrode patches over metal implants.
Do not use the device in oxygen rich environment
Avoid areas of injury or restricted movement (eg. Fracture or sprains)

Do not make any kind of unauthorized modification in the Circulator Device as by doing
so, risks like breakdown of the device/improper performance of the device might occur.
This Device is considered to be the home health care unit. So while doing any surgery or
treatment please do not use this product.
Indicates a potential hazard situation or unsafe practice that, if not avoided,
could result in serious personal injury.
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3. Cautions
After recent surgical procedures as stimulation may impede healing process.
There is a tendency to hemorrhage following acute trauma or fracture.
After a long period of immobility or inactivity — use a low intensity and shorter time to
avoid over-stimulation or muscle fatigue.
It is possible Circulator (Nerve & Muscle Stimulator) may reduce the sensation
of pain that would normally act as a warning of an underlying problem.
Circulator (Nerve & Muscle Stimulator) is not intended to be used by person
with reduced physical, sensory or mental capabilities.
Use caution when/ if:
4. Precaution
Use the device when sitting down. Do not stand on the device.
Do not expose device to extreme heat (Extreme Heat - ≥ 65˚C)
Keep this device out of the reach of children.
Check Electrode Foot Pads, electrode patches, electrode patches cables periodically damage.
Do not spill liquid or water on the device.
Do not use this device with Electrode Patches Cable / Electrode Patches other than those
provided by Camex Wellness Limited. The performance of the device has not been evaluated
and may be compromised.
In the unlikely event your Circulator (Nerve & Muscle Stimulator) malfunctions, disconnect
it from the power source and contact distributor.
Avoid opening the device or repairing it yourself. Doing so will void the warranty.
Contact the distributor if the device does not function properly
After use, unplug the device from the socket.
Do not immerse the device in water or clean it with chemicals.
Clean the foot pads with a wet cloth and dry cleaning brush.
Place the electrode patches on the protective membrane after use.
Acoustic energies like infrasound and ultrasound do not affect the performance of the device.
There is no DC component preset. Because of we are using an H bridge and both will have
the same DC value so differential voltage will be zero.
After recent surgical procedures as stimulation may impede healing process.
There is a tendency to hemorrhage following acute trauma or fracture.
After a long period of immobility or inactivity — use a low intensity and shorter time to
avoid over-stimulation or muscle fatigue.
It is possible Circulator (Nerve & Muscle Stimulator) may reduce the sensation
of pain that would normally act as a warning of an underlying problem.
Circulator (Nerve & Muscle Stimulator) is not intended to be used by person
with reduced physical, sensory or mental capabilities.

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5. Package Content
Circulator (Nerve & Muscle Stimulator) Device
Electrode Patches
Electrode Patches Cable
DC USB Cable
User Manual
Circulator (Nerve & Muscle Stimulator) Bag
The device packaging consists of the following inclusive content:
6. Charging the Circulator (Nerve and muscle stimulator)
Place charger output pin in Circulator (Nerve & Muscle Stimulator) charging slot.
Plug the charger into any working 110V 50/60Hz or 220/240v 50/60Hz mains electrical outlet.
Both the Glowing Green and Red Light indicates that the charging is on.
When the device is fully charged, it indicates the 'Solid Green' light.
Your device will be fully charged in 4 1/2 hours.
When the battery is low, it is indicated by short beep sound and when the battery is
completely discharged it is indicated by a long beep sound.
7. Charging related warnings
Charging with any other types of DC USB Cable may damage the device.
Usage of any other attachment that is not with your charger may result in electric
shock or injury to people.
Shortening the terminal of the charging socket or plug may cause permanent
damage to the device,
To ensure the optimum battery performance, always store the device in a fully charged state.
Model
Dimensions
Weight
No. of Programs
Input Voltage
Input Power
Chargeable
Circulator
458 mm x 343 mm x 72 mm
2 kg with Box Pack
2 (PI-EMS, P2-TENS)
5VDC
10 Watt
Yes
Working Time 30 min
Mode of Machine 1
Operational Frequency 0-99Hz
Delay Frequency 300ms
Batteries Lithium ion batteries
Accessories Electrode Patches Cable,
DC USB Cable and Electrode Patches
Operating conditions: 41°F - 104°F (5°C - 40°C), 30% — 75% RH,
700 hPa - 1060 hPa atmospheric pressure
Transportation and storage environment: 14°F - 122°F (-10°C - 50°C), 10% - 90% RH,
700 hPa - 1060 hPa atmospheric pressure
Name of product Circulator
(Nerve and Muscle Stimulator)
Electrode patches
Foot pads
BF
BF
Applied parts Applicable type verification
Applied parts
8. Technical Specification
Electrode patches
Foot pads
BF
BF
Applied parts Applicable type verification

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9. Care Cleaning and maintenance
The electrode patches supplied with Circulator (nerve and muscle stimulator) are
self-adhesive and can be clean up to 30 times, when not in use the electrode patches
should be concealed in a bag to keep them clean. It is important to ensure that electrode
patches electrodes patches remain dust free and tidy. The electrode patches should be
replaced once they lose its adhesiveness poor connection can harm and cause irritation
and discomfort. Storage life of an unopen pack of electrode is 2 years.
Store these electrode patches in cool areas with temperature under 30°C in a dry and
ventilated place. Avoid exposure to sunlight.
If these electrode patches get dry and lose their sickness, then put a few drops of
water on them and rub them evenly and gently to rehydrate them.
The electrode patches are latex free.
Electrode patches
Clean the foot pads with a wet clothe and dry cleaning brush. The foot pads are latex free.
Circulator (Nerve and muscle stimulator)
Do not clean the device while charging.
10. Purchasing consumables
Electrode Patches, electrode patches cable and USB cable can be purchased by
calling Customer care on +447411139760.
11. Expected service life
The machine will often last for more than 5 years, but is warranted for 1 years.
Damage to the batteries is not covered by the warranted.
Lead life depends greatly on use. Always handle the lead with care.
Electrode patches should last 30 applications depending on skin condition and humidity.
Fully charged battery should last about 4 hours continuous use.
12. Disposal of product WEEE
One of the provisions of the European Directive 2002/96/CE is that anything electrical or
electronic should not be treated as domestic waste and simply thrown away. To remind
you of this directive all affected products are now being marked with a crossed out
wheelie bin symbol, To comply with the Directive the device should be disposed of following
the local regulation for the disposal of electrical and electronic devices.

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Problem Possible Cause Solution
Leg pain after use
of device
You may have set the
intensity too high Adjust and set the intensity at a lower
level (where you can feel the mild elec
trical stimulation & it is comfortable)
The device turns on,
but does not generate
electric impulse
The device is not being
used correctly Check whether your hands can feel the
stimulation. To test this, place both your
bare hands on both the footpads and
increase the intensity. If you feel the
stimulation then the device is working
fine but if you do not feel it even at the
highest intensity then please contact
your authorised dealer.
Not placing both bare
feet on the foot pads
at the same time
Ensure that both your feet are bare and
they are placed properly and
simultaneously on the foot pads. Then
increase the intensity until you feel the
stimulation.
The intensity level may
be too low Keep increasing the intensity and take it
to the maximum level until you feel the
stimulation.
Do not compare yourself with other
people who feel the stimulation at lower
level of intensity because everyone is
different.
Electrodes patches
cable broken Replace the cable
Electrodes patches
cable not connected
properly
Connect the cable properly
You are using this
device too frequently Keep sufficient gap between two
consecutive treatments to allow the
muscles to recover. Reduce the duration
until your muscles have acclimatized to
the stimulation
13. Troubleshooting
Problem Possible Cause Solution
The device turns on,
but does not generate
electric impulse
Your feet may be dry Moisturize the soles of your feet to
improve conductivity and stimulation
and try the procedure again. You may
also have to increase the intensity level.
The device does not
turn on/ No indication
of light
Batteries not recharged Recharge the batteries
The device turns on
and then goes off
again
Batteries not recharged Recharge the batteries
Blinking red light
when trying to turn
on the device.
Low batteries. Recharge battery.
The device does not
turn on even after
new batteries have
been inserted
contact the authorized dealer
The device does
not vibrate
The device is not
designed to vibrate
You may be dehydrated Drink plenty of water before and after
using the device. The device uses your
body to create the electrical circuit.
Water is an excellent conductor of
electricity and if your body is less
hydrated (below 60%) then the
stimulation may be less, therefore
it is important to always remain well
hydrated.

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Problem Possible Cause Solution
The electrode patches
do not stick properly
to the skin.
The electrode patches
will undergo wear and
tear with regular use.
To improve their longevity, please
ensure that the skin on which they are
applied is dry, clean and free of lotions.
Put a few drops of water on the sticky
side of the pad and rub it on the
surface. This should improve its
stickiness.
Also ensure that the electrode patches
are stuck on the protective plastic after
use.
If the electrode patches still do not stick
then contact the authorized dealer to
get them replaced.
Weak sensation, even
on high setting.
Electrode patches
have been over-used,
or are dry.
Replace electrode patches
Sensation is too strong Setting is too high Press the button to decrease the setting
Sensation is too weak Sensation is too low Press the button to increase the setting
No sensation Incorrect connection Make sure that wires are connected
and are not damaged
Verify that the device is turned on
Make sure both electrode patches
are attached to the body
1.
2.
3.
14. EMC and Electrical standard requirement
Precautions with respect to electromagnetic compatibility are taken.
The Circulator must be installed and prepared to use as described in this manual.
Do not use accessories other than specified or sold by the manufacturer. Use of
replacement parts may lead to increased emission or decrease the immunity of the unit.
15. Notice to Users and/or Patients:
Any serious incident that has occurred in relation to the device, should be REPORTED to
the Manufacturer & the Competent Authority.

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16. Applicable symbol
Symbol Description
Serial Number
Catalogue number
Manufacturer
Authorized
representative in the
European community.
CE Mark with notified
body number
Date of manufacture
Refer to instruction
manual
The product is
latex free
Direct Current
2265
Symbol Description
Ingress Protection
The IP code
(International Protection
code) indicates the
degree of protection
provided by an
enclosure.
• IPX0: Protection
against ingress of
solid foreign objects
is not specified, and
no protection against
ingress of water with
harmful effects
• IPX8: Protection
against continuous
immersion in water
up to 1 meter or as
specified by user
“ON” (power)
General Warning Sign
Country of
manufacture
(To identify the
country of
manufacture of
products)
Do not use if packing
is found damaged
or opened
IN
IPXX
Symbol Description
Keep away from
direct sunlight
Keep away from
moisture
Caution, consult
accompanying
documents.
BF Type applied Part.
Non-sterile Product
The product is
recyclable
Symbol Description
Follow Operating
Instructions
Medical device
(Indicates the item
is a medical device)
Unique Device
Identifier
General
Prohibition Sign
The system cannot be
disposed of as
unsorted municipal
waste. Please contact
your local distributor
for unit disposal.
Dispose of product at
the end of its useful life
according to local
regulations.
Class II Equipment

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17. Warranty 19. Serviceability
Our products are well tested and they come with reasonable confidence from us that they
are free of defects at the time of distribution. The product you bought is warranted for one
year from the date of purchase. During this one year, the company is liable to replace the
device or provide a refund to you for any major failure of the device. You also have the right
to get the product repaired or parts replaced if they fail to operate at acceptable level of
quality without being qualified as major failure.
The warranty is not transferrable and so it is extended only to the original user. You are
entitled to the warranty only against original parts. The warranty stands void if any part of the
device has been opened and repaired or replaced by the customer or unauthorized third
party technician. Additionally, the warranty will also be voided if the device is misused or
abused in any form.
If the device was bought online, the customer has to make the arrangements and bear the
expenses for returning the product. In case of an approved replacement, the customer has
to also bear the expenses for delivering the replacement. If the device was bought from an
authorised dealer, the customer may return the device to the dealer.
Please ensure that you have read and tried the troubleshooting steps mentioned in the
'Troubleshooting' chapter of this manual before approaching us for exercising the warranty.
If the device is not turned on or the battery of the device gets damaged then contact nearby
authorized distributor or call to our customer care on +447411139760.
This limited warranty shall only apply to defects that are reported to the Distributor from
whom the Customer purchased the product within the applicable warranty period. If there is
not a Distributor, you must contact Camex Wellness Limited directly.
20. Device foot pads and foot intensity
The device should be charged for at least 6 hours before first use.
NOTE: It is recommended to not use Circulator (Nerve & Muscle Stimulator) for more than 2
sessions of 30 minutes (or the equivalent) per day.
21. Spillage of liquid
The equipment is not protected against liquid ingress. Spillage of liquids which may bring live
parts of the equipment into contact with conductive enclosures or direct contact with
operator, other personnel or the patient, must be prevented. It’s recommended to not use the
device around any kind of water of particulate matter. Same information is also provided in
the caution section. IP rating of the Circulator (Nerve & Muscle Stimulator) device is IP20.
22. Technical data
Standard and regulation
18. Batteries
Battery Handling and Usage to prevent the risk of overheating, fire or explosion: •Do not
puncture, crush, disassemble or modify the device.
Do not throw the device into fire.
Do not recharge, use, or leave the device in any high temperature environment such as in a
location near a fire or in direct sunlight. The device contains a built-in rechargeable
Lithium-Ion battery which must be disposed of properly. Dispose of the device according
to applicable local government regulations. Do not disassemble the device by yourself.
The device contains a built-in rechargeable Lithium-Ion battery which must be disposed
of properly. Dispose of the device according to applicable local government regulations.
Do not disassemble the device by yourself.
The system is developed and manufactured with observance of a number of directives,
regulations and standards. Information regarding the compliance status with relevant
national and international standards, regulations and laws can be obtained on request
from your Camex Wellness Limited’s representative.
The system conforms to IEC 60601-1 3rd edition, ordinary equipment (enclosed without
protection against ingress of water).

23. Recommendation
Although it is not mandatory, we recommend you to apply balm on your feet to improve its
conductivity.
Important Note
Selected Program will be displayed every 5 mins for 10 seconds during the therapy in the
PROG/TIME display segment.
Please note that the optimal intensity level varies from person to person.
For optimum result, please do not lift your feet while the device is on.
The device should not be on the charging mode while in use
24. Device electrode patches body intensity
Sit down on a chair or a sofa and place your both bare feet on the foot
shaped pad of device and press the power button placed at the
bottom of device.
Step 1
Select the program PI or P2 by using the +/Prog/ Time button on the
device.
Step 2
Adjust the intensity through +/- foot intensity level buttons.
Continue to increase the foot intensity at your comfort level.
Step 3
As the device is set on Auto Timer for 30 mins, post 30 mins the
device will automatically switch off. Take off your bare feet and
restore the device in the bag properly.
Step 4
Auto shutdown after 30 sec in standby condition.
Shutdown procedure
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Circulator (Nerve & Muscle Stimulator) comes with one pair of reusable (up to 30 applications)
electrode patches that can be used to deliver electrical stimulation to the upper back, lower
back, shoulders, upper extremities and lower extremities.
Electrodes that have current delivered densities are 0.8 mA/cm².
Electrode patches are for single person use only. DO NOT share the electrode
patches with others.

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Thoroughly wash the intended treatment site and then dry it properly.
Connect the electrode patches with the connecting wire. Now plug this
wire into the accessories socket on the device
Step 1
Ensure that the device is turned off when you are attaching the
electrode patches. Peel off the protective membrane from the
electrode patches and carefully place on the clean, dry, uninjured skin.
Step 2
Turn on the device through the power button of device
Step 3
Adjust the intensity through the 4+ button for body Adjust still your
comfort level.
Step 4
As the device is set on Auto Timer for 30 mins, post 30 mins the
device will automatically switch off.
Step 5
Carefully peel the electrode patches from the skin and place it
back on the protective membrane
Step 6
Please do not pull the electrode wires. They may get damaged.
Carefully remove the wire and restore the accessories.
Step 7

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25. Recommendation
Please note that the optimal intensity level varies from person to person.
For optimum result, please do not peel the electrode patches while the device is on.
Important
Store these electrode patches in cool areas with temperature under 30°C in a dry and
ventilated place. Avoid exposure to sunlight.
If these electrode patches get dry and lose their stickiness, then put a few drops of water on
them and rub them evenly and gently to rehydrate them.
Using the foot pads and electrode patches at the same time
If you want to use electrode patches and the foot pads at the same time:
Follow the steps for using the Foot Pads
Then follow the steps for using the Electrode Patches.
Important note
Selected program will be displayed every 5 mins for 10 seconds during the therapy in the
PROG/TIME display segment.
Information
The poly fuse has been used in the devices and that is resettable. We uses on board SMD
1812L150 LF150 Fuse
Note
Camex wellness Limited will make available on request circuit diagrams, component part
lists, descriptions, calibration instructions, or other information that will assist service person-
nel to repair those parts of the Circulator (Nerve & Muscle Stimulator) that are designed by
the Camex Wellness Limited as repairable by the service personnel.
26. Accuracy of Controls and Instruments
Device is to produce strong non-painful pulsating sensations, often accompanied by
muscle twitching. Suggests that currents with pulse amplitudes (mA) that generate a
strong, non-painful pulse sensation are critical for response and therefore pulse amplitude
should be titrated during treatment to maintain this intensity level last 1 to 85 in some
scenario above >85 its to be sensation are critical and may harm to user.
Intensity equation:
pulse_voltage_legs = ( 31V + INT_SETTING_LEGS) * 1.2;
pulse_voltage_pads = ( 21V + INT_SETTING_LEGS) * 1.2;

Document No.: CWL-URM-04A | Revision No.: 00. | Revision Date: 20.06.2022
Document No.: CWL-URM-04A | Revision No.: 00. | Revision Date: 20.06.2022
29 30
EMS Voltage Waveform
Foot
Body
12-85v
8-58v
Section Voltage Range
Foot
Body
20-120v
12-84v
Section Voltage Range
TENS output waveform
TENS Program Sequence

Document No.: CWL-URM-04A | Revision No.: 00. | Revision Date: 20.06.2022
Document No.: CWL-URM-04A | Revision No.: 00. | Revision Date: 20.06.2022
31 32
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