VISIOMED BewellConnect MyTens Pro BW-TS1 User manual

BewellConnect - BW-TS1 - User Manual - 122016V11BW-TS1
MyTens Pro

BewellConnect - BW-TS1 - User Manual - 122016V12
SAFETY PRECAUTIONS
Caution / Attention
Keep dry/ Garder au sec
Refer to instruction manual. Note on the equipment“Follow instructions for use”/ Voir le
manuel d’instructions. Avis sur l’équipement“Suivre les instructions d’utilisation”.
Type BF applied part / Pièce appliquée de type BF
The device, accessories, and the packaging must be disposed of correctly at the end of usage.
Please follow local ordinances and regulations for disposal. / Le dispositif, ses accessoires et
son emballage doivent être recyclés de la façon appropriée au terme de leur utilisation.
Veuillez respecter les règlements et règles locaux.
SN
Serial number / numéro de série
FCC FCC ID: 2AF8T-BW-TSX
A
B
Year Month Day Serial number
SN
SN :
Serial number
4
6
1
3
2
5

3
SAFETY PRECAUTIONS
Caution / Attention
Keep dry/ Garder au sec
Refer to instruction manual. Note on the equipment“Follow instructions for use”/ Voir le
manuel d’instructions. Avis sur l’équipement“Suivre les instructions d’utilisation”.
Type BF applied part / Pièce appliquée de type BF
The device, accessories, and the packaging must be disposed of correctly at the end of usage.
Please follow local ordinances and regulations for disposal. / Le dispositif, ses accessoires et
son emballage doivent être recyclés de la façon appropriée au terme de leur utilisation.
Veuillez respecter les règlements et règles locaux.
SN
Serial number / numéro de série
FCC FCC ID: 2AF8T-BW-TSX

BewellConnect - BW-TS1 - User Manual - 122016V14

BewellConnect - BW-TS1 - User Manual - 122016V1 5
BW-TS1
MyTens
EN

BewellConnect - BW-TS1 - User Manual - 122016V16
This MyTens device complies with all the applicable standards and regulations related to expo-
sure to electromagnetic elds.
The device complies with all the standards relating to Class ll electrical medical devices and to
devices which use electrical stimulation for use at home.
Electromagnetic compatibility (EMC) : The MyTens device complies with safety standards EMC
EN 60601-1-2. It is designed to be used at home or in hospitals.
CONTENTS
Find out how to install and use the BewellConnect® app by visiting our website at
www.bewell-connect.com/bewellconnect-app
The manufacturer reserves the right to change the product’s technical specications
without prior notice.
Dear customer,
Thank you for buying the BewellConnect® electro-stimulator. We hope you get the best use out
of it, and we recommend that you read these instructions carefully so that you can use it as
eectively as possible. To gain the best treatment from your MyTens device, please follow the
treatment instructions in this user manual when using the device.
For specic information about vein, muscle, or other problems, PLEASE CONTACT YOUR DOCTOR.
1. WARNINGS
- Please read this manual carefully and always follow the treatment instructions.
- Only use this device for its intended purpose as described in these instructions.
- This device may be used for personal use at home.
- Use this device in an ambient temperature range of 41 to 104°F / 5 to 40°C.
- Do not expose this device to extreme temperature conditions > 122°F or < 14°F /> 50°C or < -10°C.
- Do not use this device at a relative humidity of over 85%.
- This device must always be placed in a clean and dry place.
- Do not expose this device to sunlight or water.
- Do not expose this device to electric shocks.
- Never drop the device.
- Follow the maintenance instructions specied in this manual.
- Do not attempt to open the device. In case of problems, contact customer service.
- This is a medical device. Keep out of the reach of children.
- Discontinue use of the device in case of anomalies or malfunction.
- Electronic medical equipment requires special precautions regarding electromechanical com-
patibility. It must be installed and used in accordance with EMC (ElectroMagnetic Compat-
ibility) information.
- The equipment is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the equipment can help prevent elec-
tromagnetic interference by maintaining a minimum distance between portable and mobile
RF communications equipment (transmitters) and the equipment, according to the maximum
output power of the communications equipment.
- This device is not designed to be used by persons (including children) whose physical, sensory
or mental capabilities are reduced, or persons without experience or knowledge, unless they
have been able to benet, by the intermediary of a person responsible for their safety, from
supervision or prior instructions concerning use of the device. It is possible that they will not
be able to use it in accordance with the instructions of this user manual and be disturbed by
the treatment.
- This product is not designed for use on children.
- Do not modify the device or the electrodes. This could cause a malfunction.
- This device is designed for use by a single person and one person only.
1. WARNINGS ......................................................................7
2. TRANSCUTANEOUS NEUROSTIMULATION INFORMATION .........................9
3. CHARACTERISTICS..............................................................10
4. USE ............................................................................11
4.1 DESCRIPTION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
4.2. PRECAUTIONS BEFORE USE....................................................11
4.3 PRESENTATION OF THE PROGRAMS ............................................12
4.3.1. FORMS OF WAVES...........................................................12
4.3.2. TENS PROGRAMS............................................................13
4.3.3. ELECTRICAL MUSCLE STIMULATION EMS PROGRAMS .......................15
4.4. DIRECTIONS BEFORE USE......................................................18
4.5. DOWNLOADING THE APPLICATION ............................................19
4.6. STARTING AND USING MYTENS................................................19
5. STORAGE AND MAINTENANCE ..................................................23
5.1. STORAGE OF THE ELECTRODES ................................................23
5.2. CLEANING ....................................................................23
6. TROUBLESHOOTING GUIDE .....................................................24
7. AVOIDING MALFUNCTIONS .....................................................24
8. TECHNICAL CHARACTERISTICS ..................................................25
9. POSITIONING THE ELECTRODES .................................................26
9.1. POSITION OF THE ELECTRODESTENS PROGRAMS..............................26
9.2. POSITION OF THE ELECTRODESEMS PROGRAMS...............................28

BewellConnect - BW-TS1 - User Manual - 122016V1 7
This MyTens device complies with all the applicable standards and regulations related to expo-
sure to electromagnetic elds.
The device complies with all the standards relating to Class ll electrical medical devices and to
devices which use electrical stimulation for use at home.
Electromagnetic compatibility (EMC) : The MyTens device complies with safety standards EMC
EN 60601-1-2. It is designed to be used at home or in hospitals.
CONTENTS
Find out how to install and use the BewellConnect® app by visiting our website at
www.bewell-connect.com/bewellconnect-app
The manufacturer reserves the right to change the product’s technical specications
without prior notice.
Dear customer,
Thank you for buying the BewellConnect® electro-stimulator. We hope you get the best use out
of it, and we recommend that you read these instructions carefully so that you can use it as
eectively as possible. To gain the best treatment from your MyTens device, please follow the
treatment instructions in this user manual when using the device.
For specic information about vein, muscle, or other problems, PLEASE CONTACT YOUR DOCTOR.
1. WARNINGS
- Please read this manual carefully and always follow the treatment instructions.
- Only use this device for its intended purpose as described in these instructions.
- This device may be used for personal use at home.
- Use this device in an ambient temperature range of 41 to 104°F / 5 to 40°C.
- Do not expose this device to extreme temperature conditions > 122°F or < 14°F /> 50°C or < -10°C.
- Do not use this device at a relative humidity of over 85%.
- This device must always be placed in a clean and dry place.
- Do not expose this device to sunlight or water.
- Do not expose this device to electric shocks.
- Never drop the device.
- Follow the maintenance instructions specied in this manual.
- Do not attempt to open the device. In case of problems, contact customer service.
- This is a medical device. Keep out of the reach of children.
- Discontinue use of the device in case of anomalies or malfunction.
- Electronic medical equipment requires special precautions regarding electromechanical com-
patibility. It must be installed and used in accordance with EMC (ElectroMagnetic Compat-
ibility) information.
- The equipment is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the equipment can help prevent elec-
tromagnetic interference by maintaining a minimum distance between portable and mobile
RF communications equipment (transmitters) and the equipment, according to the maximum
output power of the communications equipment.
- This device is not designed to be used by persons (including children) whose physical, sensory
or mental capabilities are reduced, or persons without experience or knowledge, unless they
have been able to benet, by the intermediary of a person responsible for their safety, from
supervision or prior instructions concerning use of the device. It is possible that they will not
be able to use it in accordance with the instructions of this user manual and be disturbed by
the treatment.
- This product is not designed for use on children.
- Do not modify the device or the electrodes. This could cause a malfunction.
- This device is designed for use by a single person and one person only.
1. WARNINGS ......................................................................7
2. TRANSCUTANEOUS NEUROSTIMULATION INFORMATION .........................9
3. CHARACTERISTICS..............................................................10
4. USE ............................................................................11
4.1 DESCRIPTION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
4.2. PRECAUTIONS BEFORE USE....................................................11
4.3 PRESENTATION OF THE PROGRAMS ............................................12
4.3.1. FORMS OF WAVES...........................................................12
4.3.2. TENS PROGRAMS............................................................13
4.3.3. ELECTRICAL MUSCLE STIMULATION EMS PROGRAMS .......................15
4.4. DIRECTIONS BEFORE USE......................................................18
4.5. DOWNLOADING THE APPLICATION ............................................19
4.6. STARTING AND USING MYTENS................................................19
5. STORAGE AND MAINTENANCE ..................................................23
5.1. STORAGE OF THE ELECTRODES ................................................23
5.2. CLEANING ....................................................................23
6. TROUBLESHOOTING GUIDE .....................................................24
7. AVOIDING MALFUNCTIONS .....................................................24
8. TECHNICAL CHARACTERISTICS ..................................................25
9. POSITIONING THE ELECTRODES .................................................26
9.1. POSITION OF THE ELECTRODESTENS PROGRAMS..............................26
9.2. POSITION OF THE ELECTRODESEMS PROGRAMS...............................28

BewellConnect - BW-TS1 - User Manual - 122016V18
Do not treat the the following parts or areas :
Do not apply stimulation on your chest, the introduction of electric cur-
rent on this area can cause heart rhythm disturbances, with a risk of death.
Its eects on the brain are unknown. Stimulation to the head or on each
side of the skull must be avoided.
Stimulation on the sides of the neck or on the carotid artery can cause seri-
ous adverse eects on your blood pressure or your heart rhythm.
Stimulation on the front of the neck can cause severe muscle spasms that
can block your airways and cause breathing diculties.
Do not place the electrodes on the inside of body cavities, such as in the
mouth. This device is only designed for external application.
Do not place the electrodes on the genitals. They could stimulate inappro-
priate muscles or organs.
- Do not position the electrodes on broken or injured skin, or that which is dirty or unhealthy.
Skin with irritation, sores or other lesions can lead to the injection of too much current on the
area, which can cause burns.
- Do not place the electrodes near cancerous lesions because this may have a negative impact
on these injuries.
- Do not place the electrodes on skin areas on which sensations are not normal. You may burn
yourself due to a lack of perception of the high intensity of the current.
- Do not put the electrodes on areas that are swollen, red, infected or inamed or on skin rashes
(eg. phlebitis, thrombophlebitis and varicose veins). Stimulation should not be performed on
areas of thrombosis or thrombophlebitis because it can promote the circulation and lead to a
greater risk of embolism.
- Do not put the electrodes on redness or open wounds. Open wounds may lead to applying too
much current on the area, causing burns. They can also further the penetration of substances
from the electrode into the skin.
-
Do not make sudden movements during a session. This could cause a dysfunction of the device.
Do not use the device in the following conditions :
- Do not use the device if you are connected to high frequency surgical equipment. This could
lead to burns on the skin under the electrodes and damage the device.
- Do not use the electro-stimulator if you are monitored by a doctor and you have not consulted
him before using it.
- In the case of internal bleeding due to impacts or injury, do not use the device.
- Do not use electrical muscle stimulation if muscle contraction can disrupt the healing process.
If the tendon or the muscle is torn, a muscle contraction can aggravate the tear. This can also
occur after recent surgery or after an acute trauma or fracture. A muscle contraction can also
aggravate the symptoms of tendonitis.
- Do not use the device while driving, operating machinery or any other activity during which
the electrical stimulation may lead to a risk of injury.
- Do not use the device if you are subject to falling asleep during the session, as this may cause
you to feel pain too late. If using at the time of going to bed, set the timer so that the device
does not turn itself o automatically.
- Never use MyTens in contact with water (in the bathroom, in the shower or in the pool, etc. )
because this increases the risk of an electric shock and skin burns.
2. TRANSCUTANEOUS NEUROSTIMULATION INFORMATION
My Tens is a device designed for adults to alleviate acute post surgical pain or low to moder-
ate chronic pain. It works on the principle of transcutaneous electrical neurostimulation (TENS),
which enables you to relieve pain and soothe muscle tension. This device also helps to promote
venous return and to strengthen the muscle mass. The device has been specially designed to be
used at home.Transcutaneous electrical neurostimulation (TENS) is a non-analgesic drug therapy
without secondary eects, used by doctors and physical therapists for more than 30 years. The
electrodes are placed on dierent areas of the body and transmit a low electrical current to the
nerves. This stimulation brings the body to produce and disseminate endogenous analgesic-
painkilling substances (endorphins, enkephaline) whose function is to anesthetize the pain.
In case of pain or muscle tension, mini-electrical impulses in the nervous tissue may block the
transmission of pain signals to the nervous system and trigger the release of endorphins. You
can choose your program among 11 preset TENS protocols on the MyTens application.
For the strengthening of your muscle mass, you can select a program among 8 protocols of elec-
trical muscle stimulation (EMS). MyTens sends, via the electrodes placed on the area to stimu-
late, electrical pulses causing a muscle contraction which strengthens the muscle.
It is controlled from the MyTens application. A diagram of the human body with treatment
zones helps you to position the electrodes correctly (see paragraph 10).
The MyTens application is available on the BewellConnect® website or as a free app in the Apple
store or Google Play store.
Contraindications
- On a damaged skin area , desensitized to the electrodes or the intermediate paste.
- On an anterior area of the neck (near the carotid) or sides.
- During an electrocardiogram or an electroencephalogram.
- In case of heart disease
- If you have epilepsy
- If you wear a pacemaker, a debrillator or any other active implantable or metallic medical
device (for example a drug administration system). In these conditions, use could cause an
electric shock, interference, burns or even death.
- If you are pregnant, during the rst trimester. The eects of TENS on the development of the
fetus are not yet known. During pregnancy, do not use the device on the uterus or abdomen
to avoid triggering of contractions. Always consult your doctor or midwife if you are pregnant
and intend to use the device.
- If you suer from venous thrombosis or high blood pressure, or thrombophlebitis. Using the
electrical muscle stimulation (EMS) device could, in this case, cause a blood clot.
- In case of cognitive impairment

BewellConnect - BW-TS1 - User Manual - 122016V1 9
Do not treat the the following parts or areas :
Do not apply stimulation on your chest, the introduction of electric cur-
rent on this area can cause heart rhythm disturbances, with a risk of death.
Its eects on the brain are unknown. Stimulation to the head or on each
side of the skull must be avoided.
Stimulation on the sides of the neck or on the carotid artery can cause seri-
ous adverse eects on your blood pressure or your heart rhythm.
Stimulation on the front of the neck can cause severe muscle spasms that
can block your airways and cause breathing diculties.
Do not place the electrodes on the inside of body cavities, such as in the
mouth. This device is only designed for external application.
Do not place the electrodes on the genitals. They could stimulate inappro-
priate muscles or organs.
- Do not position the electrodes on broken or injured skin, or that which is dirty or unhealthy.
Skin with irritation, sores or other lesions can lead to the injection of too much current on the
area, which can cause burns.
- Do not place the electrodes near cancerous lesions because this may have a negative impact
on these injuries.
- Do not place the electrodes on skin areas on which sensations are not normal. You may burn
yourself due to a lack of perception of the high intensity of the current.
- Do not put the electrodes on areas that are swollen, red, infected or inamed or on skin rashes
(eg. phlebitis, thrombophlebitis and varicose veins). Stimulation should not be performed on
areas of thrombosis or thrombophlebitis because it can promote the circulation and lead to a
greater risk of embolism.
- Do not put the electrodes on redness or open wounds. Open wounds may lead to applying too
much current on the area, causing burns. They can also further the penetration of substances
from the electrode into the skin.
-
Do not make sudden movements during a session. This could cause a dysfunction of the device.
Do not use the device in the following conditions :
- Do not use the device if you are connected to high frequency surgical equipment. This could
lead to burns on the skin under the electrodes and damage the device.
- Do not use the electro-stimulator if you are monitored by a doctor and you have not consulted
him before using it.
- In the case of internal bleeding due to impacts or injury, do not use the device.
- Do not use electrical muscle stimulation if muscle contraction can disrupt the healing process.
If the tendon or the muscle is torn, a muscle contraction can aggravate the tear. This can also
occur after recent surgery or after an acute trauma or fracture. A muscle contraction can also
aggravate the symptoms of tendonitis.
- Do not use the device while driving, operating machinery or any other activity during which
the electrical stimulation may lead to a risk of injury.
- Do not use the device if you are subject to falling asleep during the session, as this may cause
you to feel pain too late. If using at the time of going to bed, set the timer so that the device
does not turn itself o automatically.
- Never use MyTens in contact with water (in the bathroom, in the shower or in the pool, etc. )
because this increases the risk of an electric shock and skin burns.
2. TRANSCUTANEOUS NEUROSTIMULATION INFORMATION
My Tens is a device designed for adults to alleviate acute post surgical pain or low to moder-
ate chronic pain. It works on the principle of transcutaneous electrical neurostimulation (TENS),
which enables you to relieve pain and soothe muscle tension. This device also helps to promote
venous return and to strengthen the muscle mass. The device has been specially designed to be
used at home.Transcutaneous electrical neurostimulation (TENS) is a non-analgesic drug therapy
without secondary eects, used by doctors and physical therapists for more than 30 years. The
electrodes are placed on dierent areas of the body and transmit a low electrical current to the
nerves. This stimulation brings the body to produce and disseminate endogenous analgesic-
painkilling substances (endorphins, enkephaline) whose function is to anesthetize the pain.
In case of pain or muscle tension, mini-electrical impulses in the nervous tissue may block the
transmission of pain signals to the nervous system and trigger the release of endorphins. You
can choose your program among 11 preset TENS protocols on the MyTens application.
For the strengthening of your muscle mass, you can select a program among 8 protocols of elec-
trical muscle stimulation (EMS). MyTens sends, via the electrodes placed on the area to stimu-
late, electrical pulses causing a muscle contraction which strengthens the muscle.
It is controlled from the MyTens application. A diagram of the human body with treatment
zones helps you to position the electrodes correctly (see paragraph 10).
The MyTens application is available on the BewellConnect® website or as a free app in the Apple
store or Google Play store.
Contraindications
- On a damaged skin area , desensitized to the electrodes or the intermediate paste.
- On an anterior area of the neck (near the carotid) or sides.
- During an electrocardiogram or an electroencephalogram.
- In case of heart disease
- If you have epilepsy
- If you wear a pacemaker, a debrillator or any other active implantable or metallic medical
device (for example a drug administration system). In these conditions, use could cause an
electric shock, interference, burns or even death.
- If you are pregnant, during the rst trimester. The eects of TENS on the development of the
fetus are not yet known. During pregnancy, do not use the device on the uterus or abdomen
to avoid triggering of contractions. Always consult your doctor or midwife if you are pregnant
and intend to use the device.
- If you suer from venous thrombosis or high blood pressure, or thrombophlebitis. Using the
electrical muscle stimulation (EMS) device could, in this case, cause a blood clot.
- In case of cognitive impairment

BewellConnect - BW-TS1 - User Manual - 122016V110
- If the source of your pain has not been diagnosed, unless otherwise given permission from
your doctor.
Side eects
Side eects are few and often represented by skin irritation (redness) associated to electrodes.
They usually disappear within two hours following a session of electro -stimulation. If they per-
sist for more than 24 hours, consult your doctor.
Users can also present myoclonus (involuntary muscle contractions) if the stimulation intensity
is too high, or sensory disturbances.
In case of side eects during the use such as nausea or fainting, burns at the locations of the
electrodes, painful sensations or headache, stop using the device and consult your doctor.
3. CHARACTERISTICS
- Pain relief and healing of muscle tension (TENS : 11 preset programs)
- Strengthening of the muscular mass (EMS : 8 standard programs)
- Stimulation of the venous return (TENS)
- Easy to use
- Designed to be used for temporary relief of pain.
- Designed to be used for the stimulation of healthy muscles.
4. USE
4.1 DESCRIPTION
See digram A page 2
1
On / o button
2
Status indicator
3
Removable
connector
4
Micro-USB socket
of the device
5
Electrodes
6
Micro-USB cable
4.2. PRECAUTIONS BEFORE USE
- Use the transcutaneous electrical neurostimulation programs in bursts (TENS Burst) at rest.
They can cause a muscle contraction in the treatment area.
- Before using the device, consult your doctor in the case: you take insulin for diabetes; muscle
contractions stimulate glucose uptake / recent surgery; the use of this device may aect the
healing process.
- It is necessary to complete the treatment in the MyTens application or press the on/o but-
ton of the device before removing the electrodes. If you do not complete the treatment and
remove the electrodes or the device, and if you touch the connectors, it is possible to feel pain
in the ngers. This sensation, however, is not dangerous.
- Before any use of electrodes, check their expiration date on the packaging. If the date has
expired, do not use them.
- Use new electrodes when the electrodes are damaged, dirty, less adhesive or if you begin to
feel discomfort during stimulation (uncomfortable pinching, tingling).
- This product must only be used with the adapter, the cable and accessories recommended by
the manufacturer.
- Before use, check that the device and the electrodes are not damaged. In case of any damage,
do not use the electrodes.
- Usable indoors and outdoors, the device is not designed to withstand all weather conditions.
- The device is not waterproof. Do not get wet and never use it in a damp environment.
- Do not use plaster or tape to attach the electrodes to the skin.
- For storing the electrodes, please follow the instructions in section 5.1 “Storage of electrodes”.
- In case of abnormal operation of the device in accordance with this user manual, discontinue
use and contact customer service. Consult section 6 “Troubleshooting Guide” for information
concerning potential malfunctions of the device.
4.3 PRESENTATION OF THE PROGRAMS
4.3.1. FORMS OF WAVES
CONT : Form of continuous wave
*CONT = CONTINUOUS
HANS : Form of alternating wave

BewellConnect - BW-TS1 - User Manual - 122016V1 11
- If the source of your pain has not been diagnosed, unless otherwise given permission from
your doctor.
Side eects
Side eects are few and often represented by skin irritation (redness) associated to electrodes.
They usually disappear within two hours following a session of electro -stimulation. If they per-
sist for more than 24 hours, consult your doctor.
Users can also present myoclonus (involuntary muscle contractions) if the stimulation intensity
is too high, or sensory disturbances.
In case of side eects during the use such as nausea or fainting, burns at the locations of the
electrodes, painful sensations or headache, stop using the device and consult your doctor.
3. CHARACTERISTICS
- Pain relief and healing of muscle tension (TENS : 11 preset programs)
- Strengthening of the muscular mass (EMS : 8 standard programs)
- Stimulation of the venous return (TENS)
- Easy to use
- Designed to be used for temporary relief of pain.
- Designed to be used for the stimulation of healthy muscles.
4. USE
4.1 DESCRIPTION
See digram A page 2
1
On / o button
2
Status indicator
3
Removable
connector
4
Micro-USB socket
of the device
5
Electrodes
6
Micro-USB cable
4.2. PRECAUTIONS BEFORE USE
- Use the transcutaneous electrical neurostimulation programs in bursts (TENS Burst) at rest.
They can cause a muscle contraction in the treatment area.
- Before using the device, consult your doctor in the case: you take insulin for diabetes; muscle
contractions stimulate glucose uptake / recent surgery; the use of this device may aect the
healing process.
- It is necessary to complete the treatment in the MyTens application or press the on/o but-
ton of the device before removing the electrodes. If you do not complete the treatment and
remove the electrodes or the device, and if you touch the connectors, it is possible to feel pain
in the ngers. This sensation, however, is not dangerous.
- Before any use of electrodes, check their expiration date on the packaging. If the date has
expired, do not use them.
- Use new electrodes when the electrodes are damaged, dirty, less adhesive or if you begin to
feel discomfort during stimulation (uncomfortable pinching, tingling).
- This product must only be used with the adapter, the cable and accessories recommended by
the manufacturer.
- Before use, check that the device and the electrodes are not damaged. In case of any damage,
do not use the electrodes.
- Usable indoors and outdoors, the device is not designed to withstand all weather conditions.
- The device is not waterproof. Do not get wet and never use it in a damp environment.
- Do not use plaster or tape to attach the electrodes to the skin.
- For storing the electrodes, please follow the instructions in section 5.1 “Storage of electrodes”.
- In case of abnormal operation of the device in accordance with this user manual, discontinue
use and contact customer service. Consult section 6 “Troubleshooting Guide” for information
concerning potential malfunctions of the device.
4.3 PRESENTATION OF THE PROGRAMS
4.3.1. FORMS OF WAVES
CONT : Form of continuous wave
*CONT = CONTINUOUS
HANS : Form of alternating wave

BewellConnect - BW-TS1 - User Manual - 122016V112
BURST : Wave form deviation
EMS : wave form
4.3.2. TENS PROGRAMS
Traditional transcutaneous neurostimulation program :
A common transcutaneous neurostimulation program is performed with a high frequency stimula-
tion. This stimulation is intended to block the transmission of the pain signal to the nervous system.
Generally, people use traditional transcutaneous neurostimulation for a session of about 30 min-
utes. It is possible to use these programs for a variable period and frequency according to what you
want. It is normal to feel the eects of this program more intensely during the stimulation and to
experience a decline after the end of the session. To improve eectiveness, adjust the intensity of
the program, avoiding any painful or unpleasant sensation.
Burst transcutaneous neurostimulation program :
A burst program (Burst TENS) allows low frequency stimulation in the form of a series of im-
pulses. It enables the release of endorphins. It is possible to use the transcutaneous neurostimu-
lation in bursts for 30 minutes. The frequency can be up to several times per day: for example,
3 times. For a sensation of strong stimulation, it is advisable to adjust the intensity of the burst
program. An unpleasant sensation may then appear. You can also adjust the intensity of the
program at a level leading to perceptible muscle contractions in the stimulation area. These con-
tractions are not dangerous. However, if you experience discomfort, it is advisable to decrease
the intensity of the program, change or move the electrodes. The burst transcutaneous electri-
cal neurostimulation (Burst TENS) can trigger a muscle contraction in the area of stimulation, so
you should to perform this program at rest.
Summary Table of the TENS Programs
TENS Impulses
Treatment
site
Indication
Treatment
time
Treatment
phases
Frequency
(time)
Width
in µS Wave form
Description
Shoulder
Shoulder
pain and
frozen
shoulder
30mn
Phase 1
2Hz (10s) 250
CONT
Continuous
output
Phase 2 4Hz (8s) 250
Phase 3
6Hz (6s) 250
Lumbar
areas
Pain in
the lower
back
30mn
Phase 1
2Hz (10s) 250
CONT
Continuous
output
Phase 2 4Hz (8s) 250
Phase 3 6Hz (6s) 250
Phase 4 2Hz (10s) 250
Phase 5 4Hz (8s) 250
Phase 6 6Hz (6s) 250
Elbow Pain in the
elbow 30mn Phase 1
2Hz (3s) 150 HANS
Alternating
output
Phase 2 100Hz (3s) 200
Forearm
Pain in the
forearm
30mn
Phase 1
2Hz (3s) 200 HANS
Alternating
output
Phase 2 100Hz (3s) 150 HANS
Phase 3 3Hz 250 EMS
Up : 1.5s
Down : 3s
10s cycle
with 2/5
strength
Wrist
Pain in
the wrist
and carpal
tunnel
syndrome
30mn Phase 1 2Hz 250 CONT
Continuous
output
Hip
Pain in
the hip
30mn
Phase 1
6Hz (30s) 250
CONT
Continuous
output
Phase 2 6Hz (30s) 250
Phase 3 8Hz (20s) 250
Phase 4 8Hz (20s) 250
Phase 5 10Hz (20s) 250
Phase 6 10Hz (20s) 250
Thigh Sciatic pain 30mn Phase 1 100Hz 200 EMS
Up : 0.5s
Cont : 7s
Down : 0.5s
Rest : 7s

BewellConnect - BW-TS1 - User Manual - 122016V1 13
BURST : Wave form deviation
EMS : wave form
4.3.2. TENS PROGRAMS
Traditional transcutaneous neurostimulation program :
A common transcutaneous neurostimulation program is performed with a high frequency stimula-
tion. This stimulation is intended to block the transmission of the pain signal to the nervous system.
Generally, people use traditional transcutaneous neurostimulation for a session of about 30 min-
utes. It is possible to use these programs for a variable period and frequency according to what you
want. It is normal to feel the eects of this program more intensely during the stimulation and to
experience a decline after the end of the session. To improve eectiveness, adjust the intensity of
the program, avoiding any painful or unpleasant sensation.
Burst transcutaneous neurostimulation program :
A burst program (Burst TENS) allows low frequency stimulation in the form of a series of im-
pulses. It enables the release of endorphins. It is possible to use the transcutaneous neurostimu-
lation in bursts for 30 minutes. The frequency can be up to several times per day: for example,
3 times. For a sensation of strong stimulation, it is advisable to adjust the intensity of the burst
program. An unpleasant sensation may then appear. You can also adjust the intensity of the
program at a level leading to perceptible muscle contractions in the stimulation area. These con-
tractions are not dangerous. However, if you experience discomfort, it is advisable to decrease
the intensity of the program, change or move the electrodes. The burst transcutaneous electri-
cal neurostimulation (Burst TENS) can trigger a muscle contraction in the area of stimulation, so
you should to perform this program at rest.
Summary Table of the TENS Programs
TENS Impulses
Treatment
site
Indication
Treatment
time
Treatment
phases
Frequency
(time)
Width
in µS Wave form
Description
Shoulder
Shoulder
pain and
frozen
shoulder
30mn
Phase 1
2Hz (10s) 250
CONT
Continuous
output
Phase 2 4Hz (8s) 250
Phase 3
6Hz (6s) 250
Lumbar
areas
Pain in
the lower
back
30mn
Phase 1
2Hz (10s) 250
CONT
Continuous
output
Phase 2 4Hz (8s) 250
Phase 3 6Hz (6s) 250
Phase 4 2Hz (10s) 250
Phase 5 4Hz (8s) 250
Phase 6 6Hz (6s) 250
Elbow Pain in the
elbow 30mn Phase 1
2Hz (3s) 150 HANS
Alternating
output
Phase 2 100Hz (3s) 200
Forearm
Pain in the
forearm
30mn
Phase 1
2Hz (3s) 200 HANS
Alternating
output
Phase 2 100Hz (3s) 150 HANS
Phase 3 3Hz 250 EMS
Up : 1.5s
Down : 3s
10s cycle
with 2/5
strength
Wrist
Pain in
the wrist
and carpal
tunnel
syndrome
30mn Phase 1 2Hz 250 CONT
Continuous
output
Hip
Pain in
the hip
30mn
Phase 1
6Hz (30s) 250
CONT
Continuous
output
Phase 2 6Hz (30s) 250
Phase 3 8Hz (20s) 250
Phase 4 8Hz (20s) 250
Phase 5 10Hz (20s) 250
Phase 6 10Hz (20s) 250
Thigh Sciatic pain 30mn Phase 1 100Hz 200 EMS
Up : 0.5s
Cont : 7s
Down : 0.5s
Rest : 7s

BewellConnect - BW-TS1 - User Manual - 122016V114
Knee Knee pain 30mn Phase 1 100Hz 150 BURST
On : 0.25s
O : 0.25s
Lower leg Pain in the
lower leg 30mn Phase 1
100Hz 150 BURST
On : 0.25s
O : 0.25s
Ankle
Pain in the
ankle and
Achilles
tendon
problem
30mn Phase 1 100Hz 200 CONT
Continuous
output
Foot
Pain in
the foot
30mn
Phase 1
40Hz (5s) 250
CONT
Continuous
output
Phase 2 6Hz (10s) 250
Phase 3 50Hz (5s) 250
4.3.3. ELECTRICAL MUSCLE STIMULATION EMS PROGRAMS
These programs, commonly called “neuromuscular electrical stimulation” (NMES) or “electro-
myostimulation”, emit impulses to cause a muscle contraction. They are especially used for
strengthening the muscle mass. Only perform the electrical muscle stimulation program on in-
tact and healthy muscles. Because they involve muscle contraction, they need to be performed
at rest (lying or sitting).
When using for the rst time, the electrical stimulation can lead to an atypical and strange sensa-
tion. It is advisable to begin the program on low intensity and change to a higher one to become
used to it. The stimulation must remain comfortable and muscle contractions must not be harsh
or painful. If your program is part of intensive physical exercise or after eort, you are advised to
choose a low intensity to limit muscular fatigue.
Summary Table of the EMS Programs
EMS Impulses
Treatment
site
Indication
Treatment
time
Treatment
phases
Frequency
(time)
Width
in µS
Wave
form
Description
Shoulder
Tightness
of the
trapezius
muscle
28mn
Phase 1
5Hz (5mn) 280
EMS
Preparation
phase
Phase 2 55Hz (10s) 280
Intensity :
50%
Up : 1,5s
Down :
0,75s
Phase 3
6Hz (8s) 280 Intensity:
25%
Phase 4 3Hz (10mn) 280
Phase of
relaxation
Intensity :
40%
Abdo-
minal
Tightness
of ab-
dominal
muscles
22mn
Phase 1
30Hz (2mn) 200
EMS
Up : 10s
Cont : 5s
Down : 10s
Rest : 5s
Phase 2 45Hz (9mn) 200
Up : 5s
Cont : 5s
Down : 5s
Rest : 5s
Phase 3 60Hz (9mn) 200
Up : 6s
Cont : 8s
Down : 6s
Rest : 5s
Phase 4 30Hz (2mn) 200
Up : 10s
Cont : 5s
Down : 10s
Rest : 5s
Lumbar
areas
Tightness
of the
lower
back
28mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 55Hz (10s) 300
Intensity :
50%
Up : 1,5s
Down :
0,75s
Phase 3 6Hz (8s) 300
Intensity:
25%
Phase 4 3Hz (10mn) 300
Phase of
relaxation
Intensity :
40%

BewellConnect - BW-TS1 - User Manual - 122016V1 15
Knee Knee pain 30mn Phase 1 100Hz 150 BURST
On : 0.25s
O : 0.25s
Lower leg Pain in the
lower leg 30mn Phase 1
100Hz 150 BURST
On : 0.25s
O : 0.25s
Ankle
Pain in the
ankle and
Achilles
tendon
problem
30mn Phase 1 100Hz 200 CONT
Continuous
output
Foot
Pain in
the foot
30mn
Phase 1
40Hz (5s) 250
CONT
Continuous
output
Phase 2 6Hz (10s) 250
Phase 3 50Hz (5s) 250
4.3.3. ELECTRICAL MUSCLE STIMULATION EMS PROGRAMS
These programs, commonly called “neuromuscular electrical stimulation” (NMES) or “electro-
myostimulation”, emit impulses to cause a muscle contraction. They are especially used for
strengthening the muscle mass. Only perform the electrical muscle stimulation program on in-
tact and healthy muscles. Because they involve muscle contraction, they need to be performed
at rest (lying or sitting).
When using for the rst time, the electrical stimulation can lead to an atypical and strange sensa-
tion. It is advisable to begin the program on low intensity and change to a higher one to become
used to it. The stimulation must remain comfortable and muscle contractions must not be harsh
or painful. If your program is part of intensive physical exercise or after eort, you are advised to
choose a low intensity to limit muscular fatigue.
Summary Table of the EMS Programs
EMS Impulses
Treatment
site
Indication
Treatment
time
Treatment
phases
Frequency
(time)
Width
in µS
Wave
form
Description
Shoulder
Tightness
of the
trapezius
muscle
28mn
Phase 1
5Hz (5mn) 280
EMS
Preparation
phase
Phase 2 55Hz (10s) 280
Intensity :
50%
Up : 1,5s
Down :
0,75s
Phase 3
6Hz (8s) 280 Intensity:
25%
Phase 4 3Hz (10mn) 280
Phase of
relaxation
Intensity :
40%
Abdo-
minal
Tightness
of ab-
dominal
muscles
22mn
Phase 1
30Hz (2mn) 200
EMS
Up : 10s
Cont : 5s
Down : 10s
Rest : 5s
Phase 2 45Hz (9mn) 200
Up : 5s
Cont : 5s
Down : 5s
Rest : 5s
Phase 3 60Hz (9mn) 200
Up : 6s
Cont : 8s
Down : 6s
Rest : 5s
Phase 4 30Hz (2mn) 200
Up : 10s
Cont : 5s
Down : 10s
Rest : 5s
Lumbar
areas
Tightness
of the
lower
back
28mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 55Hz (10s) 300
Intensity :
50%
Up : 1,5s
Down :
0,75s
Phase 3 6Hz (8s) 300
Intensity:
25%
Phase 4 3Hz (10mn) 300
Phase of
relaxation
Intensity :
40%

BewellConnect - BW-TS1 - User Manual - 122016V116
Forearm
Front-
arm :
exing
of the
wrist and
ngers
Front-
arm :
Bending
of the
wrist and
ngers
28mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 55Hz (10s) 200
Intensity :
50%
Up : 1.5s
Down :
0.75s
Phase 3 6Hz (8s) 200
Intensity:
25%
Phase 4 3Hz (10mn) 200
Phase of
relaxation
Intensity :
40%
Hip
Tightness
of the hip
muscle
32mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 75Hz (6,3s) 300
Intensity :
50%
Up : 1.5s
Down :
0.75s
Phase 3 4Hz (8s) 300
Intensity:
25%
Phase 4 3Hz (10mn) 300
Phase of
relaxation
Intensity :
40%
Thigh
Tightness
of the
hamstring
muscle
28mn
Phase 1
5Hz (5mn) 370
EMS
Preparation
phase
Phase 2 55Hz (10s) 370
Intensity:
50% Up:
1.5s Down:
0.75s
Phase 3 6Hz (8s) 370
Intensity:
25%
Phase 4 3Hz (10mn) 370
Phase of
relaxation
Intensity:
40%
Lower leg
Tightness
of the calf
muscles
28mn
Phase 1
5Hz (5mn) 370
EMS
Preparation
phase
Phase 2 55Hz (10s) 370
Intensity:
50% Up:
1.5s Down:
0.75s
Phase 3 6Hz (8s) 370
Intensity:
25%
Phase 4 3Hz (10mn) 370
Phase of
relaxation
Intensity:
40%
Foot
Training
the foot
30mn Phase 1 50Hz 200 EMS
Up : 2s
Con : 8s
Down : 2s
Rest : 4s
4.4. DIRECTIONS BEFORE USE
Charging the device
Charge the device before the rst use. In normal conditions (ambient temperature), it takes 5
hours to charge the device. A full charge allows a battery life of about 8 hours continuously
when functioning in normal conditions. Please charge the device fully before beginning a ses-
sion. If the charge is not complete at the beginning of a program, the battery may become
depleted before the end of the session. You cannot use the device when it is charging.
Plugging in the device gure B on page 2
1. Disconnect the cable used to connect the two connector units from the unit with the battery
light and micro-USB socket.
2. Insert the micro-USB cable into the micro-USB socket for the respective connector unit .
3. Insert the USB plug into a computer to charge the device.
4. When the battery light goes into continuous orange (which means that the battery is
being charged) to a continuous green (the battery is full), remove the micro-USB plug from
the micro-USB socket of the connector unit with the battery indicator (see diagram 4). Use the
USB plug only for the use described above (to charge and connect to the cable connecting
the two connectors units).
5. Reconnect the cable connecting the two connectors units : Insert the unit with the cable into
the micro-USB socket for the unit with the battery light .

BewellConnect - BW-TS1 - User Manual - 122016V1 17
Forearm
Front-
arm :
exing
of the
wrist and
ngers
Front-
arm :
Bending
of the
wrist and
ngers
28mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 55Hz (10s) 200
Intensity :
50%
Up : 1.5s
Down :
0.75s
Phase 3 6Hz (8s) 200
Intensity:
25%
Phase 4 3Hz (10mn) 200
Phase of
relaxation
Intensity :
40%
Hip
Tightness
of the hip
muscle
32mn
Phase 1
5Hz (5mn) 300
EMS
Preparation
phase
Phase 2 75Hz (6,3s) 300
Intensity :
50%
Up : 1.5s
Down :
0.75s
Phase 3 4Hz (8s) 300
Intensity:
25%
Phase 4 3Hz (10mn) 300
Phase of
relaxation
Intensity :
40%
Thigh
Tightness
of the
hamstring
muscle
28mn
Phase 1
5Hz (5mn) 370
EMS
Preparation
phase
Phase 2 55Hz (10s) 370
Intensity:
50% Up:
1.5s Down:
0.75s
Phase 3 6Hz (8s) 370
Intensity:
25%
Phase 4 3Hz (10mn) 370
Phase of
relaxation
Intensity:
40%
Lower leg
Tightness
of the calf
muscles
28mn
Phase 1
5Hz (5mn) 370
EMS
Preparation
phase
Phase 2 55Hz (10s) 370
Intensity:
50% Up:
1.5s Down:
0.75s
Phase 3 6Hz (8s) 370
Intensity:
25%
Phase 4 3Hz (10mn) 370
Phase of
relaxation
Intensity:
40%
Foot
Training
the foot
30mn Phase 1 50Hz 200 EMS
Up : 2s
Con : 8s
Down : 2s
Rest : 4s
4.4. DIRECTIONS BEFORE USE
Charging the device
Charge the device before the rst use. In normal conditions (ambient temperature), it takes 5
hours to charge the device. A full charge allows a battery life of about 8 hours continuously
when functioning in normal conditions. Please charge the device fully before beginning a ses-
sion. If the charge is not complete at the beginning of a program, the battery may become
depleted before the end of the session. You cannot use the device when it is charging.
Plugging in the device gure B on page 2
1. Disconnect the cable used to connect the two connector units from the unit with the battery
light and micro-USB socket.
2. Insert the micro-USB cable into the micro-USB socket for the respective connector unit .
3. Insert the USB plug into a computer to charge the device.
4. When the battery light goes into continuous orange (which means that the battery is
being charged) to a continuous green (the battery is full), remove the micro-USB plug from
the micro-USB socket of the connector unit with the battery indicator (see diagram 4). Use the
USB plug only for the use described above (to charge and connect to the cable connecting
the two connectors units).
5. Reconnect the cable connecting the two connectors units : Insert the unit with the cable into
the micro-USB socket for the unit with the battery light .

BewellConnect - BW-TS1 - User Manual - 122016V118
4.5. DOWNLOADING THE APPLICATION
Download the BewellConnect® application to your phone or tablet:
- through the Apple store or Google Play Store.
- or by ashing the QR Code on the side of the box.
Then, download the subapplication MyTens by clicking on the icon MyTens.
4.6. STARTING AND USING MYTENS
Preparation of the treatment areas and installation of MyTens
1. Before placing the electrodes, ensure that the skin is healthy and shows no: injuries, open
wounds, redness, pre-cancerous lesions.
• Transcutaneous electrical neurostimulation (TENS) programs : Do not position the electrodes
on irritated skin or skin with open wounds, rashes or cancerous lesions
• Electrical muscle stimulation (EMS) programs : Position the electrodes only on intact and
healthy muscles. (in case of doubt, contact your doctor or physiotherapist).
2. Clean skin thoroughly prior to each application of the electrodes. Electrodes do not stick well
if any lotion, oil, make-up, dirt, etc. is left on skin. Always moisten skin with a damp cloth prior
to applying the electrodes. This will improve the electrode adhesion and life.
3. Remove the electrodes from the bag, ensure they are not damaged or worn. If the expiration
date has past / is exceeded, do not use these electrodes.
4. Attach the electrodes to the device using the pressure buttons provided for this purpose.
5. Put the rst electrode on the treatment area chosen. See the section “Arranging the elec-
trodes”and the electrode positioning diagrams at the end of this manual (see paragraph 9).
6. Put the second electrode on the area of the body to treat (see paragraph 9). Avoid any contact
between both of the electrodes, do not place them on top of eachother.
7. To apply the second pair of electrodes, proceed in the same manner (steps 1 to 6).The second
pair must be placed symmetrically (e.g. for treatment of the left thigh with one pair of elec-
trodes, the second pair must be applied symmetrically on the right thigh).The intensity of the
electrical impulses will be identical in both pairs, unless otherwise selected.
Remarks
- It is possible that you may need additional assistance for placing the electrodes on certain
areas.
- Make sure that the device is switched o when moving the electrodes to avoid risk of injury
to yourself or others.
Placing the electrodes
Warning
As indicated in“Do not treat the the following parts or areas” :
Do not place the electrodes on the head, carotid artery, at the front or on the sides (right or
left) of the neck or on chest. Do not position the electrodes on swollen skin or skin with open
wounds, rashes or cancerous lesions or on irritated skin.
The eectiveness of your sessions will depend in part on how you place your electrodes on
the skin. Before placing the electrodes, ensure you have good sensation in the area. If in doubt
about the ideal placement you can move the electrodes to nd the best sensation. If you nd
an area to be eective, note the placement for future use. If you suer discomfort (unpleas-
ant contractions during burst electrical neurostimulation programs), it is advisable to move
the electrodes. If during electrical muscle stimulation programs (intended especially to create
a contraction of the muscle) no contraction occurs, this may mean an intensity is too low or the
electrodes have been placed incorrectly.
Starting a session through the use of the MyTens application
1. Ensure that the Bluetooth (4.0) connection is activated on your smartphone or tablet. Open
the MyTens application .
2. Press the on/o button so that the device is put on standby mode (Continuous green light :
Standby mode, ready for the session). The App detects the MyTens which is switched on. In
case of inactivity for more than 5 min, the device switches o. Press the on/o button again
to begin a session.
3. Choose between a TENS session (transcutaneous electrical neurostimulation) or EMS session
(neuromuscular electrical stimulation).
4. If you’ve used MyTens previously, you can start with the last session or choose another one
in the history.
History Button

BewellConnect - BW-TS1 - User Manual - 122016V1 19
4.5. DOWNLOADING THE APPLICATION
Download the BewellConnect® application to your phone or tablet:
- through the Apple store or Google Play Store.
- or by ashing the QR Code on the side of the box.
Then, download the subapplication MyTens by clicking on the icon MyTens.
4.6. STARTING AND USING MYTENS
Preparation of the treatment areas and installation of MyTens
1. Before placing the electrodes, ensure that the skin is healthy and shows no: injuries, open
wounds, redness, pre-cancerous lesions.
• Transcutaneous electrical neurostimulation (TENS) programs : Do not position the electrodes
on irritated skin or skin with open wounds, rashes or cancerous lesions
• Electrical muscle stimulation (EMS) programs : Position the electrodes only on intact and
healthy muscles. (in case of doubt, contact your doctor or physiotherapist).
2. Clean skin thoroughly prior to each application of the electrodes. Electrodes do not stick well
if any lotion, oil, make-up, dirt, etc. is left on skin. Always moisten skin with a damp cloth prior
to applying the electrodes. This will improve the electrode adhesion and life.
3. Remove the electrodes from the bag, ensure they are not damaged or worn. If the expiration
date has past / is exceeded, do not use these electrodes.
4. Attach the electrodes to the device using the pressure buttons provided for this purpose.
5. Put the rst electrode on the treatment area chosen. See the section “Arranging the elec-
trodes”and the electrode positioning diagrams at the end of this manual (see paragraph 9).
6. Put the second electrode on the area of the body to treat (see paragraph 9). Avoid any contact
between both of the electrodes, do not place them on top of eachother.
7. To apply the second pair of electrodes, proceed in the same manner (steps 1 to 6).The second
pair must be placed symmetrically (e.g. for treatment of the left thigh with one pair of elec-
trodes, the second pair must be applied symmetrically on the right thigh).The intensity of the
electrical impulses will be identical in both pairs, unless otherwise selected.
Remarks
- It is possible that you may need additional assistance for placing the electrodes on certain
areas.
- Make sure that the device is switched o when moving the electrodes to avoid risk of injury
to yourself or others.
Placing the electrodes
Warning
As indicated in“Do not treat the the following parts or areas” :
Do not place the electrodes on the head, carotid artery, at the front or on the sides (right or
left) of the neck or on chest. Do not position the electrodes on swollen skin or skin with open
wounds, rashes or cancerous lesions or on irritated skin.
The eectiveness of your sessions will depend in part on how you place your electrodes on
the skin. Before placing the electrodes, ensure you have good sensation in the area. If in doubt
about the ideal placement you can move the electrodes to nd the best sensation. If you nd
an area to be eective, note the placement for future use. If you suer discomfort (unpleas-
ant contractions during burst electrical neurostimulation programs), it is advisable to move
the electrodes. If during electrical muscle stimulation programs (intended especially to create
a contraction of the muscle) no contraction occurs, this may mean an intensity is too low or the
electrodes have been placed incorrectly.
Starting a session through the use of the MyTens application
1. Ensure that the Bluetooth (4.0) connection is activated on your smartphone or tablet. Open
the MyTens application .
2. Press the on/o button so that the device is put on standby mode (Continuous green light :
Standby mode, ready for the session). The App detects the MyTens which is switched on. In
case of inactivity for more than 5 min, the device switches o. Press the on/o button again
to begin a session.
3. Choose between a TENS session (transcutaneous electrical neurostimulation) or EMS session
(neuromuscular electrical stimulation).
4. If you’ve used MyTens previously, you can start with the last session or choose another one
in the history.
History Button

BewellConnect - BW-TS1 - User Manual - 122016V120
Select treatment area
Before you resume a previous session or begin a new MyTens session, you must select a treat-
ment area and a program.
Estimate the intensity of pain (in TENS mode)
On a scale of 1 to 10, evaluate the intensity of the pain. For no pain press 0, for extremely intense
pain press 10.
Select and start a session.
1. Starting a session : Click on the Play Button.