Beurer BM 58 User manual

EN Blood pressure monitor
Instructions for use
BM 58

2
Included in delivery:
Blood pressure monitor
Upper arm cuff
USB cable
4 x LR6 AA batteries
Storage bag
Instructions for use
Dear Customer,
thank you for choosing a product from our range. Our name
stands for high-quality, thoroughly tested products for appli-
cations in the areas of heat, weight, blood pressure, body
temperature, pulse, gentle therapy, massage, beauty and
air. Please read these instructions for use carefully and keep
them for later use, be sure to make them accessible to other
users and observe the information they contain.
Best regards,
Your Beurer Team
1. Getting to know your instrument
Check that the device packaging has not been tampered
with and make sure that all contents are present. Before
use, ensure that there is no visible damage to the device
or accessories and that all packaging material has been
removed. If you have any doubts, do not use the device and
ENGLISH
1. Getting to know your instrument...............................2
2. Important information................................................3
3. Unit description ........................................................7
4. Prepare measurement ...............................................8
5. Measuring blood pressure.......................................10
6. Evaluating results ....................................................12
7. Saving, retrieving and deleting results ....................13
8. Transferring measurements...................................14
9. Error messages/trouble-shooting .........................14
10. Cleaning and storing the device and cu..............15
11. Specifications........................................................15
12. Mains part..............................................................16
13. Replacement parts and wearing parts ..................17
14. Warranty/service...................................................17
Content

3
contact your retailer or the specified Customer Services
address.
The upper arm blood pressure monitor is used for non-inva-
sive measurement and monitoring of adults’ arterial blood
pressure. You can use it to measure your blood pressure
quickly and easily, storing the results and displaying the
progression of readings together with the average.
A warning is issued for anyone suffering from cardiac
arrhythmia.
The recorded values are classified and evaluated graphi-
cally.
Store these instructions for use for future reference and
make them accessible to other users.
2. Important information
Signs and symbols
The following symbols are used in these instructions for
use, on the packaging and on the type plate for the device
and accessories:
Attention
Note
Note on important information
Observe the instructions for use
Application part, type BF
Direct current
Disposal in accordance with the Waste
Electrical and Electronic Equipment EC
Directive – WEEE
21
PAP
Dispose of packaging in an environmen-
tally friendly manner
Manufacturer
Storage / Transport
Permissible storage and transport tempe-
rature and humidity
Operating
Permissible operating temperature and
humidity.
Protect from moisture

4
S N
Serial number
The CE labelling certifies that the prod-
uct complies with the essential require-
ments of Directive 93/42/EEC on medical
products.
Advice on use
• In order to ensure comparable values, always measure
your blood pressure at the same time of day.
• Do not take a measurement within 30 minutes after eat-
ing, drinking, smoking or exercising.
• Before the initial blood pressure measurement, make sure
always to rest for about 5 minutes.
• Furthermore, if you want to take several measurements in
succession, make sure always to wait for at least 1 minute
between the individual measurements.
• Repeat the measurement if you are unsure of the meas-
ured value.
• The measurements taken by you are for your information
only – they are not a substitute for a medical examination!
Discuss the measurements with your doctor, and never
base any medical decisions on them (e.g. medicines and
their administration)!
• Using the blood pressure monitor outside your home
environment or whilst on the move (e.g. whilst travelling
in a car, ambulance or helicopter, or whilst undertaking
physical activity such as playing sport) can influence the
measurement accuracy and cause incorrect measure-
ments.
• Do not use the blood pressure monitor on newborns or
patients with preeclampsia. We recommend consulting
a doctor before using the blood pressure monitor during
pregnancy.
• Cardiovascular diseases may lead to incorrect measure-
ments or have a detrimental effect on measurement accu-
racy. The same also applies to very low blood pressure,
diabetes, circulatory disorders and arrhythmias as well as
chills or shaking.
• This device is not intended for use by people (including
children) with restricted physical, sensory or mental skills
or a lack of experience and/or a lack of knowledge, unless
they are supervised by a person who is responsible for
their safety or are instructed by such a person in how to
use the device. Supervise children around the device to
ensure they do not play with it.
• The blood pressure monitor must not be used in connec-
tion with a high-frequency surgical unit.
• Only use the device on people who have the specified
upper arm measurement for the device.
• Please note that when inflating, the functions of the limb
in question may be impaired.

5
• During the blood pressure measurement, blood circula-
tion must not be stopped for an unnecessarily long time.
If the device malfunctions, remove the cuff from the arm.
• Avoid any mechanical restriction, compression or bend-
ing of the cuff line.
• Do not allow sustained pressure in the cuff or frequent
measurements. The resulting restriction of the blood flow
may cause injury.
• Ensure that the cuff is not placed on an arm in which the
arteries or veins are undergoing medical treatment, e.g.
intravascular access or therapy, or an arteriovenous (AV)
shunt.
• Do not use the cuff on people who have undergone a
mastectomy.
• Do not place the cuff over wounds as this may cause fur-
ther injury.
• You can either use the blood pressure monitor with bat-
teries or with a mains part. Please note that data transfer
and data storage is only possible when your blood pres-
sure monitor is supplied with power. As soon as the bat-
teries are empty or the mains part is disconnected from
the power supply, the blood pressure monitor loses the
date and time.
• To conserve the batteries, the monitor switches off auto-
matically if no buttons are pressed for one minute.
• The device is only intended for the purpose described in
these instructions for use. The manufacturer is not liable
for damage resulting from improper or careless use.
Storage and Care
• The blood pressure monitor is made up of precision elec-
tronic components. Accuracy of readings and the instru-
ment’s service life depend on careful handling.
– You should protect the device from impact, moisture,
dirt, major temperature fluctuations and direct exposure
to the sun’s rays.
– Never drop the device.
– Do not use near strong electromagnetic fields, i.e. keep
it away from any radio systems and mobile phones.
– Only ever use the cuffs provided with the monitor or
original replacement cuffs. Otherwise erroneous results
will be recorded.
• Do not press any buttons until the cuff is in position.
• If the instrument is not used for any length of time, we
recommend removing the batteries.

6
Notes on handling batteries
• If your skin or eyes come into contact with battery fluid,
rinse the affected areas with water and seek medical
assistance.
• Choking hazard! Small children may swallow and
choke on batteries. Store the batteries out of the reach of
small children.
• Observe the plus (+) and minus (-) polarity signs.
• If a battery has leaked, put on protective gloves and clean
the battery compartment with a dry cloth.
• Protect batteries from excessive heat.
• Risk of explosion! Never throw batteries into a fire.
• Do not charge or short-circuit batteries.
• If the device is not to be used for a relatively long period,
take the batteries out of the battery compartment.
• Use identical or equivalent battery types only.
• Always replace all batteries at the same time.
• Do not use rechargeable batteries.
• Do not disassemble, split or crush the batteries.
Repair and disposal
• Batteries do not belong in domestic refuse. Used batter-
ies should be disposed of at the collection points pro-
vided.
• Never open the instrument. If these instructions are not
heeded, the warranty will be null and void.
• Never attempt to repair the instrument or adjust it yourself.
We can no longer guarantee perfect functioning if you do.
• Repairs may only be performed by Beurer Customer Ser-
vice or authorized dealers. However, always check the
batteries and replace them if necessary prior to making
any complaint.
• For environmental reasons, do not dispose of the
device in the household waste at the end of its
useful life. Dispose of the unit at a suitable local
collection or recycling point. Dispose of the device in
accordance with EC Directive – WEEE (Waste Electrical
and Electronic Equipment). If you have any questions,
please contact the local authorities responsible for waste
disposal.

7
Notes on electromagnetic compatibility
• The device is suitable for use in all environments listed
in these instructions for use, including domestic environ-
ments.
• The use of the device may be limited in the presence of
electromagnetic disturbances. This could result in issues
such as error messages or the failure of the display/
device.
• Avoid using this device directly next to other devices or
stacked on top of other devices, as this could lead to
faulty operation. If, however, it is necessary to use the
device in the manner stated, this device as well as the
other devices must be monitored to ensure they are work-
ing properly.
• The use of accessories other than those specified or pro-
vided by the manufacturer of this device can lead to an
increase in electromagnetic emissions or a decrease in
the device’s electromagnetic immunity; this can result in
faulty operation.
• Failure to comply with the above can impair the perfor-
mance of the device.
3. Unit description
1. Cuff tube
2. Cuff
3. Cuff connector
4. Touch screen activation
switch
5. USB interface
6. Cuff holder
7. Cuff connector port
(left side)
8. Memory button MEM
9. START/STOP button
10. Mains part port
11. Display
MEM
4
7
10
9
11
8
1
3
2
ON
OFF
4
5
6

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Touch screen activation switch
The device features a touch screen display. To prevent the
screen from being activated accidentally, keep the touch
screen activation switch set to OFF when the device is not
in use. To operate the device, move the touch screen activa-
tion switch to ON. When the touch screen display is touched
(START/STOP button or MEM button), a beep is output.
Tip: You can switch off the device at any time by setting the
touch screen activation switch to the OFF position.
Cuff holder
Thanks to the cuff holder on the underside of the device,
you have the option of conveniently storing the cuff. To do
so, push out the cuff holder with both thumbs until it locks
into place (see also Chapter: Inserting battery).
Icons in the display:
1. Time and date
2. Systolic pressure
3. Diastolic pressure
4. Measured pulse
5. Release air (arrow)
6. Memory display, average value ( ),
morning ( ), evening ( )
7. Risk indicator
8. “Change battery” icon
9. Arrhythmia recognition
PC interface
The blood pressure monitor also allows you to transfer your
measured values to the computer.
For this, you will need a standard USB cable (included in
delivery) and the "beurer HealthManager" computer soft-
ware.
The software can be downloaded free of charge from the
download area under Service at www.beurer.com.
System requirements for the "beurer HealthManager"
PC software
• Windows 7 SP1 or higher
• USB 2.0 (Type A) or higher
4. Prepare measurement
Inserting battery
• Push the cuff holder
upwards at the rear of the
device until it locks into
place.
• Open the battery com-
partment lid.
• Insert four AA 1.5V alka-
line batteries. making absolutely sure that you insert them
with the correct polarity as marked. Never use recharge-
able batteries.
• Replace the battery cover carefully.
2
3
4
6
7
8
9 1
5

9
If the battery change is continuously illuminated,
measurement is no longer possible and you must replace all
the batteries. Once batteries have been removed from the
device, the time must be reset.
Used batteries do not belong in the household waste. You
are legally obliged to dispose of the batteries. Dispose of
them via your specialist electrical supplier or local collecting
point for recyclable waste.
Battery disposal
• The empty, completely flat batteries must be disposed of
through specially designated collection boxes, recycling
points or electronics retailers. You are legally required to
dispose of the batteries.
• The codes below are printed on batteries containing
harmful substances:
Pb = Battery contains lead,
Cd = Battery contains cadmium,
Hg = Battery contains mercury
Setting date and time
You should set the date and time without fail. Otherwise,
you will not be able to save your measured values correctly
with a date and time and to access them again later.
Tip: If you press and hold the MEM button, you can set the
values more quickly.
To set the date and time, proceed as follows:
• Move the touch screen activation switch to the ON posi-
tion.
• Press the START/STOP and MEM buttons simultane-
ously, 24h begins to flash. Select 12h or 24h mode using
the MEM button. Press START/STOP to confirm your
selection. The year display will start to flash. Set the year
with the MEM button and confirm with START/STOP .
• Then set the month, day, hour and minutes and confirm
each setting with START/STOP .
• Pressing the START/STOP button again will switch the
display off.
Note: In 24h mode, the date is displayed as day/month. In
12h mode, as month/day.
Operation with the mains part
You can also operate this device with a mains part.
When doing so, there must not be any batteries in the bat-
tery compartment. The mains part can be obtained from
specialist retailers or from the service address using order
number 071.95.
• To prevent possible damage to the device, the blood
pressure monitor must only be used with the mains part
described here.
• Insert the mains part into the connection provided for
this purpose on the right-hand side of the blood pressure

10
monitor. The mains part must only be connected to the
mains voltage that is specified on the type plate.
• Then insert the mains plug of the mains part into the
mains socket.
• After using the blood pressure monitor, unplug the mains
part from the mains socket first and then disconnect it
from the blood pressure monitor. As soon as you unplug
the mains part, the blood pressure monitor loses the
date and time setting but the saved measurements are
retained.
5. Measuring blood pressure
Ensure the device is at room temperature before measuring.
The measurement can be performed on the left or right arm.
Attaching the cuff
Place the cuff onto the bare upper
arm. The circulation of the arm
must not be hindered by tight
clothing or similar.
The cuff must be placed on the
upper arm so that the bottom
edge is positioned 2 – 3 cm above
the elbow and over the artery. The
line should point to the centre of
the palm.
Now tighten the free end of the
cuff, but make sure that it is not
too tight around the arm and close
the hook-and-loop fastener. The
cuff should be fastened so that
two fingers can fit under the cuff.
Now insert the cuff line into the
connection for the cuff connector.
This cuff is suitable for you if the
index mark ( ) is within the OK
range after fitting the cuff on the
upper arm.
If the measurement is performed on the right upper arm,
the line should be located on the inside of your elbow.
Ensure that your arm is not pressing on the line.
Blood pressure may vary between the right and left arm,
which may mean that the measured blood pressure val-
ues are different. Always perform the measurement on the
same arm.

11
If the values between the two arms are significantly differ-
ent, please consult your doctor to determine which arm
should be used for the measurement.
Important: The instrument should only be operated with the
original cuff. The cuff is suitable for an arm circumference
of 22 to 30 cm. A larger cuff for upper arm circumferences
from 30 to 42 cm is available from retailers or the service
address under order no. 163.246.
Correct posture
• Before the initial blood pressure measurement, make sure
always to rest for about 5 minutes. Otherwise there may
be divergences.
• Furthermore, if you want to take several measurements in
succession, make sure always to wait for at least 1 minute
between the individual measurements.
• You can perform the measurement either sitting or lying
down. Always make sure that the cuff is on a level with
your heart.
• To carry out a blood pressure measurement, make sure
you are sitting comfortably with your arms and back lean-
ing on something. Do not cross your legs. Place your feet
flat on the ground.
• In order not to distort the result, it is important to keep still
during the measurement and not talk.
Measuring blood pressure
• Move the touch screen activation switch to the ON posi-
tion.
• Put on the cuff as described previously and assume the
position in which you want to carry out the measurement.
• Switch on the blood pressure monitor with the START/
STOP button . After the full-screen display, the most
recently used user memory appears ( or ). To change
the user memory, press the MEM button and confirm
your selection with the START/STOP button . If no but-
ton is pressed, the most recently used user memory is
automatically used after 5 seconds.
• Before the measurement, the last saved test result is
briefly displayed. If there is no measurement in the mem-
ory, the instrument always displays the value .
• The cuff automatically inflates. Cuff air pressure is
released slowly. If a tendency towards high blood pres-
sure is already detectable, the cuff is pumped up again
and cuff pressure increased further. As soon as a heart
rate is detected, the heart rate symbol is displayed.

12
• Heart rate, systolic and diastolic blood pressure are dis-
played.
• You can cancel the measurement at any time by press-
ing the START/STOP button or by pushing the touch
screen activation button to OFF.
• _ appears if it has not been possible to perform the
measurement properly. Observe the section in these
instructions on error messages/troubleshooting and
repeat the measurement.
• The test result is saved automatically.
• To switch off the device, press the START/STOP button
or push the touch screen activation switch to OFF. If
you forget to switch off the device, it switches off auto-
matically after approx. 1 minute.
Wait for at least 1 minute before taking another
measurement.
6. Evaluating results
Cardiac arrhythmia:
This instrument can identify possible cardiac arrhythmia dis-
orders during measurement and if necessary indicates the
measurement with the flashing icon .
This may be an indicator for arrhythmia. Arrhythmia is a
condition where the heart rhythm is abnormal as a result
of defects in the bioelectrical system controlling the heart
beat. The symptoms (omitted or premature heart beats,
slow or excessively fast heart rate) may be caused, among
other things, by heart disease, age, physical predisposition,
excessive use of stimulants, stress or lack of sleep. Arrhyth-
mia can only be ascertained through examination by your
doctor.
Repeat the measurement if the flashing icon is dis-
played after the measurement. Please note that you should
rest for 5 minutes between measurements and not talk or
move during the measurement. If the icon appears
often, please contact your doctor. Any self-diagnosis and
treatment based on the test results may be dangerous. It is
vital to follow your doctor’s instructions.
Risk indicator:
The measurements can be classified and evaluated in
accordance with the following table.
However, these standard values serve only as a general
guideline, as the individual blood pressure varies in different
people and different age groups etc.
It is important to consult your doctor regularly for advice.
Your doctor will tell you your individual values for normal
blood pressure as well as the value above which your blood
pressure is classified as dangerous.
The bar chart on the display and the scale on the unit show
which category the recorded blood pressure values fall into.
If the values of systole and diastole fall into two different
categories (e.g. systole in the High normal category and

13
diastole in the Normal category), the graphical classifica-
tion on the device always shows the higher category; for the
example given this would be High normal.
Blood pressure
value category Systole (in mmHg) Diastole (in mmHg) Action
Setting 3:
severe
hypertension ≥180 ≥110 seek medical
attention
Setting 2:
moderate
hypertension 160–179 100–109 seek medical
attention
Setting 1:
mild hyperten-
sion 140–159 90–99 regular monito-
ring by doctor
High normal 130 –139 85 –89 regular monito-
ring by doctor
Normal 120–129 80–84 self-monitoring
Optimal <120 <80 self-monitoring
Source: WHO, 1999 (World Health Organization)
7. Saving, retrieving and deleting results
• The results of each successful measurement are stored
together with date and time. With more than 60 items of
measured data, the earliest items of data measured are
lost.
• Move the touch screen activation switch to the ON posi-
tion.
• Make a selection with the MEM button, and then confirm
the desired user memory with the START/STOP button .
If you press the MEM button again, the average value of
all the stored measured values in the user memory will be
displayed. If you press the MEM button again, the aver-
age value of the last 7 days for the morning measurement
will be displayed (Morning: 5 a.m. – 9 a.m., display ). If
you press the MEM button again, the average value of the
last 7 days for the evening measurement will be displayed
(Evening: 6 p.m. – 8 p.m., display ). If you continue to
press the MEM button, the most recent individual meas-
ured values with date and time are displayed in turn.
• You can delete the memory by pressing and holding the
MEM button for 3 seconds. All the values in the current
user memory are deleted after three beeps are output.
• To switch off the device, press the MEM button again or
the START/STOP button or push the touch screen acti-
vation switch to OFF.
• If you forget to switch off the device, it will switch off
automatically after 2 minutes.

14
8. Transferring measurements
Connect the blood pressure monitor to your PC using the
USB cable.
No data transfer may be launched whilst performing a
measurement.
PC is shown on the display. Begin the data transfer
in the "beurer HealthManager" PC software.
During the data transfer, an animation is shown
on the display. A successful data transfer is
displayed as in figure 1. If the data transfer is
unsuccessful, an error message appears as in
figure 2. In this case, interrupt the PC connec-
tion and start the data transfer again.
After 30 seconds of not being in use or if com-
munication with the PC is interrupted, the blood
pressure monitor switches itself off automati-
cally.
9. Error messages/trouble-shooting
In case of faults, the _ message appears in the display.
Error messages may appear if:
• systolic or diastolic pressure could not be measured
(or appears on the display)
• systolic or diastolic pressure was outside the measure-
ment range ( or Lo appears on the display)
• the cuff is fastened too tightly or loosely
(or appears on the display)
• the pump pressure is higher than 300 mmHg
(appears on the display)
• pumping up takes longer than 160 seconds
(appears on the display)
• there is a system or device error
(, , or appears on the display)
• the batteries are almost empty .
In the above cases, you must repeat the measurement.
Make sure that the cuff tube is properly inserted and that
you do not move or talk.
Re-insert the batteries if necessary, or else replace them.
Technical alarm – description
Should the recorded blood pressure (systolic or diastolic) lie
outside the limits specified in the section “Technical speci-
fications”, the technical alarm will appear on the display
indicating either “ ” or “Lo”. In such cases, you should seek
medical assistance and check the accuracy of your proce-
dure.
The limit values for the technical alarm are factory set and
cannot be adjusted or deactivated. These alarm limit values
Abb. 1
Abb. 2

15
are accorded second priority under the standard
IEC 60601-1-8.
The technical alarm is a non-locking alarm and must not be
reset. The signal shown on the display will disappear auto-
matically after about 8 seconds.
10. Cleaning and storing the device and cuff
• Clean the device and cuff carefully using a slightly damp
cloth only.
• Do not use any cleaning agents or solvents.
• Under no circumstances hold the device and cuff under
water, as this can cause liquid to enter and damage the
device and cuff.
• If you store the device and cuff, do not place heavy
objects on the device and cuff. Remove the batteries. The
cuff line should not be bent sharply.
11. Specifications
Model no. BM 58
Measurement
method Oscillometric, non-invasive blood pres- sure measurement on the upper arm
Measurement
range Cuff pressure 0–300 mmHg, systolic 60–260 mmHg,
diastolic 40–199 mmHg,
Pulse 40–180 beats/minute
Display accuracy Systolic ±3 mmHg, diastolic ±3 mmHg,
pulse ±5% of the value shown
Measurement
inaccuracy Max. permissible standard deviation according to clinical testing:
systolic 8 mmHg/diastolic 8 mmHg
Memory 2x 60 memory spaces
Dimensions L 100 mm x W 150 mm x H 58 mm
Weight Approx. 508 g
(without batteries, with cuff)
Cuff size 22 to 30 cm
Permissible oper-
ating conditions +5°C to +40°C, ≤90% relative air humidity (non-condensing)
Permissible
storage conditions -20°C to +55°C, ≤95% relative air humidity, 800–1050 hPa ambient pres-
sure
Power supply 4x 1,5V AA batteries
Battery life For approx. 500 measurements,
depending on the blood pressure level
and/or pump pressure
Classification Internal supply, IPX0, no AP or APG,
continuous operation, type BF applied
part

16
The serial number is located on the device or in the battery
compartment.
Technical information is subject to change without notifica-
tion to allow for updates.
• This unit is in line with European Standard EN 60601-1-2
(In accordance with CISPR 11, IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-4, IEC 61000-4-5,
IEC 61000-4-6, IEC 61000-4-8, IEC 61000-4-11) and is
subject to particular precautions with regard to electro-
magnetic compatibility (EMC). Please note that portable
and mobile HF communication systems may interfere with
this unit.
• This device is in line with the EU Medical Devices Direc-
tive 93/42/EEC, the „Medizinproduktegesetz“ (German
Medical Devices Act) and the standards EN1060-1 (non-
invasive sphygmomanometers, Part 1: General require-
ments), EN1060-3 (non-invasive sphygmomanometers,
Part 3: Supplementary requirements for electro-mechani-
cal blood pressure measuring systems) and
IEC80601-2-30 (Medical electrical equipment –
Part 2–30: Particular requirements for the safety and
essential performance of automated non-invasive blood
pressure monitors).
• The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life. If using the device for commercial medical pur-
poses, it must be regularly tested for accuracy by appro-
priate means. Precise instructions for checking accuracy
may be requested from the service address.
12. Mains part
Model no. LXCP12-006060BEH
Input 100–240V, 50– 60 Hz, 0.5A max
Output 6V DC, 600mA, only in connection with beurer
blood pressure monitor.
Supplier Shenzhen Iongxc power supply co., ltd
Protection This device is double insulated and protected
against short circuit and overload by a primary
thermal fuse.
Make sure to take the batteries out of the com-
partment before using the mains adapter.
Polarity of the the DC voltage
connection
Double insulated/equipment class 2
Enclo-
sures and
Protective
Covers
Equipment enclosed to protect against con-
tact with live parts, and with parts which can
become live (finger, pin, hook test).
The operator shall not contact the patient and
the output plug of AC mains adapter simulta-
neously.

17
13. Replacement parts and wearing parts
Replacement parts and wearing parts are available from
the corresponding listed service address under the stated
material number.
Designation Item number and/or order
number
Standard cuff (22-30 cm) 162.829
XL cuff (30-42 cm) 163.246
Mains part (EU) 071.95
USB cable 162.043
14. Warranty/service
Beurer GmbH,Söflinger Straße 218, 89077 Ulm, Germany
(hereinafter referred to as “Beurer”) provides a warranty for
this product, subject to the requirements below and to the
extent described as follows.
The warranty conditions below shall not aect the
seller’s statutory warranty obligations which ensue from
the sales agreement with the buyer.
The warranty shall apply without prejudice to any man-
datory statutory provisions on liability.
Beurer guarantees the perfect functionality and complete-
ness of this product.
The worldwide warranty period is 5 years, commencing
from the purchase of the new, unused product from the
seller.
The warranty only applies to products purchased by the
buyer as a consumer and used exclusively for personal
purposes in the context of domestic use.
German law shall apply.
During the warranty period, should this product prove to be
incomplete or defective in functionality in accordance with
the following provisions, Beurer shall carry out a repair or
a replacement delivery free of charge, in accordance with
these warranty conditions.
If the buyer wishes to make a warranty claim, they
should approach their local retailer in the first instance:
see the attached “International Service” list of service
addresses.
The buyer will then receive further information about the
processing of the warranty claim, e.g. where they can send
the product and what documentation is required.

18
A warranty claim shall only be considered if the buyer can
provide Beurer, or an authorised Beurer partner, with
– a copy of the invoice/purchase receipt, and
– the original product.
The following are explicitly excluded from this warranty:
– deterioration due to normal use or consumption of the
product;
– accessories supplied with this product which are worn
out or used up through proper use (e.g. batteries,
rechargeable batteries, cus, seals, electrodes, light
sources, attachments and nebuliser accessories);
– products that are used, cleaned, stored or maintained
improperly and/or contrary to the provisions of the
instructions for use, as well as products that have been
opened, repaired or modified by the buyer or by a ser-
vice centre not authorised by Beurer;
– damage that arises during transport between manu-
facturer and customer, or between service centre and
customer;
– products purchased as seconds or as used goods;
– consequential damage arising from a fault in this pro-
duct (however, in this case, claims may exist arising from
product liability or other compulsory statutory liability
provisions).
Repairs or an exchange in full do not extend the warranty
period under any circumstances.

19

20
656.16_BM58_2019-11-12_04_IM2_BEU_EN
Beurer GmbH Söflinger Straße 218 89077 Ulm, Germany www.beurer.com
www.beurer-gesundheitsratgeber.com www.beurer-healthguide.com • www.beurer-blutdruck.de
Subject to errors and changes