bewell connect MyTensio BW User manual

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BW-BW1
BW-BW1
MyTensio
North American market /
Marché Nord Américain
European market /
Marché Européen
BEWELLCONNECT CORP
185 Alewife Brook Parkway 410
CAMBRIDGE - MA 02138 - USA
support.bewell-connect.com
www.bewell-connect.com
VISIOMED GROUP SA
112, Avenue Kléber
75116 PARIS - France
[email protected]
Tel : [phone]
(0,34€/mn)
www.visiomed-lab.com
www.bewell-connect.fr
MANUFACTURED FOR

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A
B
SYMBOL DEFINITIONS
Caution
Keep dry
Refer to instruction manual. Note on the equipment“Follow instructions for use”.
The device, accessories and the packaging have to be disposed of correctly at the
end of the usage. Please follow local ordinances and regulations for disposal.
FCC FCC ID: 2AF8T-BW-BW1
SN
Serial number
Year Month Day Serial number
SN
SN :
Serial number
BLOOD PRESSURE MONITOR
Model: BW-BW1 - Rating: 3.7V - 300mAh Li-ion Polymer Battery
Measurement Range: 40-180 bpm/min 0-299 mmHg
Manufactured for BEWELLCONNECT CORP
FCC ID: 2AF8T-BW-BW1
1:1
Rev.16.07.2015
SPEC. TYPE:
MODEL AFFECTED: BW-BW1_RATING-LABEL_US_012017
TO ATTN.
PREP. BY APPROVED. BY
SPEC. NO. DATE
(dd/mm/yy) 25/01/17
MODIFY
0
1
2
3
4
CMYK 37,7 x 7,6 mm
7
6
4
5
2
3
8
1
0.4 - 0.8 in / 1 - 2 cm
1
3
2
4
1
Bluetooth
2
Color coding
3
Low battery symbol
4
Systolic
5
ON/START Button
6
Diastolic
7
Heart Rate
8
Heart Rate symbol

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BW-BW1
BW-BW1
MyTensio
EN

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COMPLIANT WITH EUROPEAN STANDARDS AND WITH PART 15 OF THE FCC RULES.
CONTENTS
1. WARNINGS.................................................................................................................... 7
2. INFORMATION.............................................................................................................. 8
3. CHARACTERISTICS....................................................................................................... 10
4. USE................................................................................................................................. 11
41. INDICATIONS OF SELFMEASUREMENT ................................................................ 11
42. CONTRAINDICATIONS FOR SELFMEASUREMENT............................................... 11
43. PRECAUTIONS BEFORE USE .................................................................................... 12
44. SUGGESTIONS BEFORE MEASURING ..................................................................... 12
45. MEASUREMENT MODALITIES ................................................................................ 13
46. DOWNLOADING THE APPLICATION....................................................................... 13
47. GETTING STARTED ................................................................................................... 13
48. MEASUREMENT DIAGNOSIS ................................................................................... 14
5. CLEANING AND MAINTENANCE................................................................................. 14
6. PREVENTING MALFUNCTIONS................................................................................... 14
7. TECHNICAL SPECIFICATIONS ..................................................................................... 15
8. TROUBLESHOOTING GUIDE ....................................................................................... 16
Learn how to install and use the BewellConnect® application by logging onto our website
bewell-connect.com/bewellconnect-app
The manufacturer reserves the right to modify the product specications without prior
notice.
Dear Customer,
Thank you for purchasing MyTensio, the automatic blood pressure armband by BewellCon-
nect. We hope that you enjoy using it and recommend reading this user guide carefully to
measure your blood pressure accurately.
The ease of use of this device lets you to measure your blood pressure at any place and at
any time. Within seconds, the systolic and diastolic pressures, and heartbeat is measured
and transferred by Bluetooth 4.0, based on the oscillometric method of measuring blood
pressure.
For specic information about your own blood pressure, CONTACT YOUR PHYSICIAN.
1. WARNINGS
- Use this unit only for its intended purpose as described in these instructions.
- This unit can be used for personal use at home.
- Use this unit within an ambient temperature range between 50°F and 104°F / 10°C and 40°C.
- Do not expose this unit to extreme temperature conditions > 140°F or < -4°F > / > 60°C or < -20°C.
- Do not use this unit at a relative humidity above 90%.
- This unit should always be stored in a clean, dry place.
- Do not expose this unit to sunlight or water.
- Do not expose this unit to electrical shocks.
- Do not use this unit outdoors.
- Do not use the product while charging the device for risk of electric shock.
- Never drop this unit.
- Follow the maintenance instructions specied in this manual.
- Do not attempt to open the unit. In the event of a problem, contact customer service.
- Do not leave this unit within the reach of children.
- The measurement results are for informational purposes only. If unsure about your results,
please contact your physician.
- This product should not encourage self-medication or changes to your treatment.
- Stop using the unit in the event of a failure or malfunction.
- Electronic medical equipment requires special precautions regarding electromagnetic
compatibility, it must be installed and use in accordance with the ElectroMagnetic Com-
patibility 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
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the equipment as recommend-
ed below, according to the maximum output power of the communications equipment.

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- This unit is not intended for use by persons (including children) with reduced physical, sen-
sory or mental capabilities, or persons lacking experience or knowledge, unless they have
been given, through a person responsible for their safety, supervision or prior instructions
regarding the use of this unit.
2. INFORMATION
Blood Pressure
Heart contraction
(pressure increase) Heart at rest
(pressure decrease)
Systolic (Top number)
Diastolic (Bottom number)
Blood pressure is the pressure inside the arteries. This pressure is exerted by the blood on
the artery walls, and is expressed in millimeters of mercury (mmHg).
When the heart contracts (systolic or maximum pressure): the pressure suddenly increases
in the arteries, this is the rst number that your physician gives you when measuring your
blood pressure. It is normally under 14 (140 mmHg).
When the heart relaxes between beats, the pressure decreases (diastolic or minimum pres-
sure): This pressure corresponds to the second number your physician gives you when
measuring your blood pressure. It is generally between 5 and 9 (50 and 90 mmHg).
Both numbers provide important information about your health. The harder it is for the
blood to ow through the arteries, the higher these two numbers will be. If the blood pres-
sure is persistently above normal, this is called hypertension.
Blood pressure varies considerably throughout the day, and these variations are even more
signicant in hypertensive subjects. It is lower in the morning and increases in the afternoon
and the evening. When sleeping, it decreases. Blood pressure is lower in summer than in win-
ter, and it rises noticeably with age. Blood pressure also increases during exercise, sex, preg-
nancy, stress, etc.
EXAMPLE OF THE BLOOD PRESSURE VARIATION IN A 35 YEAR OLD MALE
cmHg
12h
0
4
6
8
10
12
14
14h 16h 18h 20h 22h 24h 02h 04h 06h 08h 10h
TV
SYS.
DIA.
Factors that may cause blood pressure include: heavy breathing, exercise, stress, anxiety,
changes in temperature and/or environment, meals, arguments, bathing, smoking, or drink-
ing alcohol.
Note : One or two blood pressure readings may not provide a true indication of your blood pressure, it is
important to measure it daily and regularly in order to obtain accurate data. Sharing your results with
your physician, may help him/her diagnose you and prevent potential health problems.
In 2013, the American Heart Association (AHA) dened a blood pressure classication shown
in the table below. This classication is just a general guide, as blood pressure varies from
one person to another, based on age, weight, and health.
IT IS RECOMMENDED THAT YOU CONSULT WITH YOUR PHYSICIAN IN ORDER TO DETERMINE
YOUR NORMAL BLOOD PRESSURE.
This blood pressure chart reects categories dened by the American Heart Association.
TABLE FOR CLASSIFYING BLOOD PRESSURE VALUES MMHG
Blood Pressure Cat-
egory Systolic (upper) Diastolic (lower)
Normal less than 120 and less than 80
Prehypertension 120 - 139 or 80 - 89
High Blood Pressure
(Hypertension) Stage I 140 - 159 or 90 - 99

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High Blood Pressure
(Hypertension) Stage II 160 or higher or 100 or higher
Hypertensive crisis
(emercency care
needed)
higher than 180 or higher than 110
Self-measurement of blood pressure
- MAM (Mean Arterial Measurement): MAM technology makes it possible to automatically
perform three repeated measurements in moments. Repetition is essential when measur-
ing blood pressure oneself, because isolated readings are often wrong for many reasons,
including the high variability of blood pressure, and high susceptibility to factors such as
recent exercise or stress… Taking 3 consecutive readings and averaging them can improve
the reliability of blood pressure measurement at home by a non-professional. This mode of
use is especially recommended by the American Heart Association (AHA).
Reference: Blood Pressure Measurement Instructions. Available on http://www.heart.org/idc/groups/heart-public/@wcm/@hcm/docu-
ments/downloadable/ucm_445846.pdf (Last Visited Sept 21st 2016)
- Rule of 3s: 3 readings recommended while sitting, resting, 3 days in a row: in the morning
before taking medications, 3 consecutive readings (MAM); in the evening after taking med-
ications, 3 readings in a row (MAM). A single reading is not necessarily signicant, especially
in terms of monitoring your blood pressure.
-Self-measurement of blood pressure: The monitoring targets, for a known hypertensive
subject, using self-measurement at home, are dierent from those of the AHA, which es-
tablishes the classication of the blood pressure) and lower. These targets are based on age
and may vary depending on your condition.
General case: SBP* < 135 mmHg and DBP* < 85 mmHg
Age > 80 years: SBP* < 150 mmHg
Chronic renal failure: SBP* < 130 mmHg and DBP* < 80 mmHg
* SBP: Systolic Blood Pressure - DBP: Diastolic Blood Pressure
The gures above are for general, informational purposes only and they must be re-validated in each case
with a physician. It is important to check your targets, especially in cases of serious illness or preg-
nancy.
3. CHARACTERISTICS
- Oscillometric method, measures on ination
- Series of 3 consecutive measurements, automatically
- Screen with a clear display of readings: systolic pressure, diastolic pressure, heart rate
- Display screen of the unit: Displays the rst two readings and the average of the three
- Application: Automatic calculation and display of the average of the three readings
- Easy adjustment of rigid cu
- Compact size, easy to carry
- Easy to use
- Automatic shuto
- Data transfer to a smartphone/tablet that supports Bluetooth 4.0.
4. USE
41. INDICATIONS OF SELFMEASUREMENT
Self-measurement of blood pressure is recommended for:
- Patients starting antihypertensive treatment to determine its eectiveness
- Patients requiring closer monitoring in between and prior to appointments (patients with
coronary heart disease, diabetes and / or renal disease)
- Pregnant women looking to prevent preeclampsia
- Patients at cardiovascular risk
- People displaying high blood pressure during an appointment, to eliminate a white coat
eect or conrm real hypertension
- Elderly patients whose blood pressure variability is increased, and whose frequency of
white coat eect gradually increases with age
- People suspected to mask hypertension (not detected at the doctor)
- In case of resistant hypertension
42. CONTRAINDICATIONS FOR SELFMEASUREMENT
Self-measurement of blood pressure is contraindicated on:
- People under 18 years
- Patients suering from:
Atrial brillation or other serious heart conditions;
Anxiety or obsessional disorders;
Elderly cognitive impairment (unless used by a third party);
Physical disability, Handicap
- An arm wearing a dialysis stula, peripheral venous catheter: to avoid impair functioning of
the stula or the catheter, the formation of blood clots in the vein,
- An arm having undergone axillary lymphadenectomy. The increase of the pressure in near-
by blood vessels can lead to the swelling of the arms and hands (lymphedema)
- A hemiplegic arm

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43. PRECAUTIONS BEFORE USE
- Do not confuse personal blood pressure measurement and self-diagnosis. Blood pressure
readings should be interpreted only by a medical professional, who has knowledge of your
medical condition. The readings do not replace a treatment or a regular examination per-
formed by your physician.
- In the event of medical treatment, consult a physician to nd out the best time to take your
blood pressure.
- Do not use this unit on children and elderly people without medical advice.
- This product should not encourage self-medication or changes to your treatment.
- If the cu pressure is too high or in the event of discomfort, immediately press the ON/
START button to deate the cu.
- Do not use the unit in a moving vehicle. This can result in inaccurate readings.
- The blood pressure readings detected by this monitor are equivalent to those obtained by
a trained observer using the cu/stethoscope auscultation method, within the limits pre-
scribed by the American National Standards Institute for electronic or automated sphyg-
momanometers.
Reference: Association for the Advancement of Medical Instrumentation. American National Standard. Manual, electronic or automa-
ted sphygmomanometers ANSI/AAMI SP10-2002.
44. SUGGESTIONS BEFORE MEASURING
- Choice of the arm for the blood pressure measurement:
The rst time, it’s recommended to take the measurement in both arms. If one arm
consistently has higher blood pressure than the other (> 10 mmHg), that arm should be
used to measure your blood pressure except in the event of contraindications in this arm
(You should discuss dierences higher than 10 mm Hg with your doctor). If there is no
dierence, the readings are often more easily taken in the non-dominant arm ( left for
right-handed, right for left-handed).
Reference: American Heart Association. How to Monitor and Record Your Blood Pressure. http://www.heart.org/HEARTORG/Condi-
tions/HighBloodPressure/SymptomsDiagnosisMonitoringofHighBloodPressure/How-to-Monitor-and-Record-Your-Blood-Pressure_
UCM_303323_Article.jsp (Last visited Sept 2st, 2016)
- When rst using the unit, be sure to charge the battery using the USB port provided for this
purpose. Connect the USB cable from the unit to a computer to charge the product. Once
unit is charged, unplug the USB cable.
- Avoid eating, smoking, or exercising 30 minutes before measurement. Stay calm in the 15
minutes before taking your blood pressure.
- Stress raises your blood pressure. Avoid taking blood pressure readings during stressful times.
- The blood pressure reading should be taken in a quiet place, you must be relaxed and
seated, resting your arm on a table so that the cu is at the same level as your heart
- Sit still and do not talk as the blood pressure reading is taken.
45. MEASUREMENT MODALITIES
See Diagram B on page 2
Do not take measurements over clothing. Remove all jewelry on the arm to be measured before use
(watch, ring, bracelet, etc.).
- Make sure you have a smartphone or tablet with the BewellConnect® application installed
at hand.
- With the palm of the hand facing upward, thread the cu so that the display screen of the
monitor is pointed toward you in the reading direction.
- The cu must be one or two centimeters from the palm.
- Wrap the cu comfortably around the wrist, both edges of the cu should be tightened at
the wrist and forearm.
- When the cu is positioned correctly, hold it in place by pressing the tab rmly against
the velcro.
- Press the ON/START button to turn the monitor on. The blue LED will light up.
- Place your arms on the table, palm up, so that the monitor is at heart level.
- Sit on a chair with your feet at (do not cross your legs), place your arm on the table, palm
upward. The cu should be at the same level as your heart. The heart is located slightly
below the armpit. In the event of diculties in positioning your wrist at heart level, use a
support under your arm.
- Sit quietly for two minutes before the blood pressure measurement.
Note: For a better interpretation of the results, always take measurements using the same arm.
46. DOWNLOADING THE APPLICATION
The following information is subject to change.
bw
My
Download the BewellConnect® application on your smartphone or tablet:
- Through the app store or Google Play
- Or by scanning the QR code on the side of the box.
Then click on the MyTensio icon.
47. GETTING STARTED
- Position the monitor as explained in Chapter 4-6.
- Launch the BewellConnect® application and click on MyTensio.
- Hit START on the screen (application) to start the measurement.
- The cu will inate automatically. The 3 blood pressure readings in a row are taken auto-
matically. The cu inates and deates 3 times, following the procedure in the MyTensio
application. Do not remove the cu before the end of the 3 readings. The readings are sent
automatically to the application via Bluetooth 4.0.

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- The rst 2 readings are displayed on the screen of the unit.
- The 3rd reading that appears on the screen is the average of the 3 readings
- Once the readings are taken, the average of your three readings is also displayed on the
application screen.
- Press the ON/START button again to turn the monitor o. If you forget, the unit turns itself
o automatically after about 1 minute.
Choice of the arm for the blood pressure measurement:
The rst time, it’s recommended to take the measurement in both arms. If one arm con-
sistently has higher blood pressure than the other (> 10 mmHg), that arm should be used
to measure your blood pressure except in the event of contraindications in this arm (You
should discuss dierences higher than 10 mm Hg with your doctor).
If there is no asymmetry, the readings are often more easily taken in the non-dominant arm
( left for right-handed, right for left-handed).
Reference: American Heart Association. How to Monitor and Record Your Blood Pressure. http://www.heart.org/HEARTORG/Condi-
tions/HighBloodPressure/SymptomsDiagnosisMonitoringofHighBloodPressure/How-to-Monitor-and-Record-Your-Blood-Pressure_
UCM_303323_Article.jsp (Last visited Sept 2st, 2016)
Notes:
- The reading will be too low if the cuff is kept above heart level, and too high if it is kept below
heart level.
- If you wish to stop measurement during a pressure reading, simply press the ON/START button
to automatically stop the unit.
- Consult your physician if in doubt about using the blood pressure monitor.
48. MEASUREMENT DIAGNOSIS
The application automatically evaluates the MAM (Mean Arterial Measurement) and uses
AHA color coding in interpreting the results.
5. CLEANING AND MAINTENANCE
-
Use a soft, dry cloth to clean the unit. If necessary, use a cloth lightly moistened with tap water.
- Do not use alcohol, benzene, thinner, or other chemicals to clean the unit or cu.
- Before any use, it is advisable to wash your hands. Do not wash or wet the cu.
- Avoid placing the unit in direct contact with sunlight, high humidity, or dust.
6. PREVENTING MALFUNCTIONS
-
Do not drop the unit, avoid jolts and shocks.
- Do not insert anything into the unit.
- Do not disassemble the unit.
- Do not put the device in water.
- Do not crush the pressure pocket of the cu.
- Follow the temperature and humidity ranges outlined in the specications.
7. TECHNICAL SPECIFICATIONS
Product name BewellConnect® MyTensio
Model BW-BW1
Classication Class II
Measurement
method Oscillometric system, measures on ination
Dimensions 2.8 x 2.8 x 0.5 in / 70 x 72 x 13 mm - Cu 5.3 x 8.5 in / 13.5 x 21.5 cm
diameter
Weight 2.8 oz / 80 g
Measuring range Pressure: 0~299 mmHg
Heart rate: 40~180 beats/minute
Accuracy Pressure: ± 3mmHg
Heart rate: ± 5%
Ination Ination by electric pump
Deation Pressure released by valve
Normal conditions
of use Temperature: 50°F - 104°F / 10°C - 40°C Humidity: 15-90%RH
Storage conditions Temperature: -4°F - 140°F / -20°C - 60°C
Humidity: 10-95%RH
Barometric Pressure: 80-105Kpa
Bluetooth Technology 4.0
Bluetooth Led Unit working: LED on
Low Battery: appears on the screen
Charging: LED light
Battery Rechargeable Li-ion battery (300mAh)
Battery life Between 100 and 150 measures
USB USB 2.0 port
Voltage 3.7 V
Accessories provided 5.3 x 8.5 in / 13.5 x 21.5 cm cu, instruction manual, storage case, USB
cable 31.5 in / 800 mm

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16
8. TROUBLESHOOTING GUIDE
If any of the following problems occur when using your MyTensio,refer to this
troubleshooting guide. If the problem persists, please contact our customer support.
PROBLEM POSSIBLE CAUSE SOLUTION
Abnormal
results
The cu is not
properly positioned
or is not tight enough Apply the cu correctly and try again
The position was not
correct during the
measurement Reread "Measurement Modalities" and try again
You spoke, moved,
or you were angry,
excited, or nervous
during the
measurement
Try again when you are calmer without talking or
moving during the test
Arrhythmia The unit is not suitable for people with a serious
cardiac arrhythmia
The blue
colored Blue-
tooth LED light
blinks or does
not light up
Low battery Recharge the unit with the USB cable
No data transfer
to your smart-
phone/tablet
Bluetooth Disabled Enable Bluetooth on your smartphone/tablet. Make sure that the Bluetooth function (Bluetooth Low
Energy 4.0 only) of your smartphone is turned on
Incompatible smart-
phone or tablet
Check that your smartphone or tablet has Bluetooth
4.0. Make sure the version of the operating system of
your smartphone/tablet is up to date (Android 4.3 or
later Or iOS 7.1 or later).

WARRANTY
This device complies with part 15 of the FCC rules.
Changes or modications not expressly approved by the party responsible for compliance
could void the user’s authority to operate the equipment.
This equipment has been tested and found to comply with the limits for a Class B digital
device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reason-
able protection against harmful interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to radio communications.
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to radio or television reception, which can
be determined by turning the equipment o and on, the user is encouraged to try to correct
the interference by one or more of the following measures:
- Reorient or relocate the receiving antenna.
- Increase the separation between the equipment and receiver.
- Connect the equipment into an outlet on a circuit dierent from that to which the receiver
is connected.
- Consult customer service or an experienced radio/TV technician for help.
Operation is subject to the following two conditions: (1) this device may not cause harmful
interference, and (2) this device must accept any interference received, including interfer-
ence that may cause undesired operation.

WARRANTY CARD
Purchase date
Date : ......... / .......... / ..........
Serial number
SN: ...................................................
Retailer’s seal Stamp :
EN: The Bewellconnect® device limited warranty provides that the Bewellconnect® devices will be
free from material defects impacting performance in accordance with the documentation for a
period of one (1) year when used under normal conditions consistent with the documentation,
subject to the terms and limitations set forth below.
The Bewellconnect® device limited warranty is granted only to the original purchaser of the
Bewellconnect® device, and is non-transferable. For the sake of clarity, in the case of a refurbish-
ment of the Bewellconnect® device for the use of a dierent end-user during the original one-year
term of the Bewellconnect® device limited warranty, the Bewellconnect® device limited warranty
shall continue to be in eect for the remainder of such original one-year term. A purchase invoice
or other proof of purchase will be required for after-sales service, in accordance with the Bewell-
connect® device limited warranty. The purchase invoice is mandatory to be able to benet from
the Bewellconnect® device limited warranty.
The Bewellconnect® device limited warranty will be invalidated where serial numbers on products
are changed, replaced, illegible, absent or if a repair has been made without any outcome by any
unauthorized service, including the user.
The Bewellconnect® device limited warranty covers only defective equipment or parts, and
only defects that arise during normal use of the product for its intended purpose in accordance
with the documentation. It does not cover damage caused during the dispatch or carriage of
the device, caused by repairs made by a distributor, by alterations made, by the connection of
equipment not approved by Bewellconnect®, or caused by use that is contrary to the documen-
tation. Furthermore, the Bewellconnect® device limited warranty does not cover damage related
to items being dropped, improper handling, improper installation, re damage, ood, lightning,
or any other natural disaster.
The Bewellconnect® device limited warranty does not cover product packaging, accessories, or
any defective appearance due to the display of the product for sale, in showrooms, retail out-
lets, for demonstration purposes, etc. Normal use, cleaning and replacement of parts with normal
wear and tear are not covered by the terms of this guarantee.
Repair or replacement of the defective Bewellconnect® device is the customer’s sole remedy for
the Bewellconnect® device limited warranty, or, if the defective Bewellconnect® device cannot
be repaired or replaced, refund of the amounts paid by the customer for the defective Bewell-
connect® device will be the customer’s sole remedy.
BEWELLCONNECT® PROVIDES ONLY THIS BEWELLCONNECT® DEVICE LIMITED WARRANTY, AND
MAKES NO OTHER WARRANTIES OF ANY KIND. WITHOUT LIMITING THE FOREGOING, BEWELL
CONNECT® EXPRESSLY DISCLAIMS ALL OTHER WARRANTIES, WHETHER ORAL OR WRITTEN,
EXPRESSLY IMPLIED, STATUTORY OR OTHERWISE, INCLUDING, WITHOUT LIMITATION, THE IM-
PLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, AND ALL
WARRANTIES ARISING FROM COURSE OF PERFORMANCE, COURSE OF DEALING OR USAGE IN
TRADE. BEWELLCONNECT® SHALL NOT BE RESPONSIBLE FOR ANY WARRANTIES OR GUARANTEES
GRANTED BY ANY DISTRIBUTOR OR OTHER THIRD PARTY.
TO THE MAXIMUM EXTENT PERMITTED BY APPLICABLE LAW, IN NO EVENT SHALL BEWELL
CONNECT® OR ANY OF ITS AFFILIATES BE LIABLE WITH RESPECT TO ANY BEWELLCONNECT®
DEVICE FOR (a) ANY SPECIAL, INDIRECT, INCIDENTAL, CONSEQUENTIAL, RELIANCE OR PUNITIVE
DAMAGES, INCLUDING, WITHOUT LIMITATION, LOSS OF PROFITS, OR (b) ANY DIRECT DAMAGES IN
EXCESS OF THE PRICE THAT CUSTOMER PAID FOR THE BEWELLCONNECT® DEVICE
EN: The device, accessories, and the packaging must be disposed of correctly at the end of
usage. Please follow local ordinances and regulations for disposal
© 02/2017 BW-BW1
EN: BewellConnect® is a brand registered by Visiomed Group SA. The constructor keeps the right to
modify the photographs and characteristics without previous notice. Registered design. The logos and
trademarks are the property of their respective owners.