EN Upper arm blood pressure
monitor
Instructions for use
BM 45
2
B
C
DA
1 2 3 4
5
9
8
6
7
SYS
mmHg
DIA
mmHg
PUL
/min
10
20
19
18
17
11
12
13
141516
3
1. INCLUDED IN DELIVERY
Check that the exterior of the cardboard delivery packaging
is intact 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 re-
moved.
If you have any doubts, do not use the device and contact
your retailer or the specified Customer Services address.
1x blood pressure monitor
1x upper arm cu (22-36 cm)
ENGLISH
Read these instructions for use carefully. Observe the warnings and safety notes. Keep these
instructions for use for future reference. Make the instructions for use accessible to other
users. If the device is passed on, provide the instructions for use to the next user as well.
1. Included in delivery ....................................................... 3
2. Signs and symbols ........................................................ 4
3. Intended use ................................................................. 6
4. Warnings and safety notes ............................................ 7
5. Device description ....................................................... 10
6. Usage .......................................................................... 10
6.1 Initial use ............................................................... 10
6.2 Before the blood pressure measurement .............. 12
6.3 Taking a blood pressure measurement ................. 13
6.4 Evaluating the results ............................................ 14
6.5 Displaying and deleting measured values ............. 15
7. Cleaning and maintenance .......................................... 16
8. Accessories and replacement parts ............................ 16
9. Troubleshooting ........................................................... 17
10. Disposal ...................................................................... 18
Contents
11. Technical specifications .............................................. 18
12. Guarantee/service ....................................................... 20
4
1x instructions for use
4x 1.5V AA LR6 batteries
1x storage bag
2. SIGNS AND SYMBOLS
The following symbols are used on the device, in these instruc-
tions for use, on the packaging and on the type plate for the
device:
WARNING
Indicates a potentially impending danger. If it is not avoided,
death or serious injury will occur.
CAUTION
Indicates a potentially impending danger. If it is not avoided,
slight or minor injuries may occur.
Product information
Note on important information
Observe the instructions
Read the instructions before starting work and/
or operating devices or machines
Disposal in accordance with the Waste Electrical
and Electronic Equipment EC Directive – WEEE
Do not dispose of batteries containing harmful
substances with household waste
Manufacturer
CE labelling
This product satisfies the requirements of the
applicable European and national directives.
Dispose of packaging in an environmentally
friendly manner
5
B
A
Marking to identify the packaging material.
A = material abbreviation, B = material number:
1–7 = plastics, 20–22 = paper and cardboard
Separate the product and packaging elements
and dispose of them in accordance with local
regulations.
IP20
Protected against solid foreign objects 12.5mm
in diameter and larger
Direct current
The device is suitable for use with direct current
only
UDI
Unique device identifier (UDI)
Identifier for unique product identification
Batch designation
Item number
S
N
Serial number
Medical device
Type
Type BF applied part
Galvanically isolated applied part (F stands for
“floating”); meets the requirements for leakage
currents for type B
Temperature range
Humidity range
6
Atmospheric pressure limitation
Date of manufacture
3. INTENDED USE
Purpose
The blood pressure monitor (hereinafter, device) is intended for
the fully automatic, non-invasive measurement of arterial blood
pressure and pulse values on the upper arm.
It is designed for self-measurement by adults in a domestic en-
vironment.
Target group
The blood pressure measurement is suitable for adult users
whose upper arm circumference is within the range printed on
the cu.
Clinical benefits
The user can record their blood pressure and pulse values
quickly and easily using the device. The recorded values are
classified according to internationally applicable guidelines and
evaluated graphically. Furthermore, the device can detect any
irregular heart beats that occur during measurement and inform
the user via a symbol in the display. The device saves the re-
corded measurements and can also output average values of
previous measurements. The recorded data can provide health-
care service providers with support during the diagnosis and
treatment of blood pressure problems, and therefore it plays a
part in the long-term monitoring of the user’s health.
Indications
In the event of hypertension or hypotension, the user can in-
dependently monitor their blood pressure and pulse values at
home. However, the user does not need to be suering from
hypertension or arrhythmia in order to use the device.
Contraindications
WARNING
• Do not use the blood pressure monitor on newborns, chil-
dren or pets.
7
• Persons with reduced physical, sensory or mental capabili-
ties should be supervised by a person responsible for their
safety and receive instructions from that person on how to
use the device.
• If you have any of the following conditions, it is essential
you consult your doctor before using the device: Cardiac
arrhythmia, circulatory problems, diabetes, pregnancy,
pre-eclampsia, hypotension, chills, shaking
• Do not use the device if you are using electrical implants
(e.g. pacemakers).
• Do not use the cu on people who have undergone a mas-
tectomy.
• Do not place the cu over wounds as this may cause fur-
ther injury.
• Make sure that the cu is not placed on an arm whose
arteries or veins are undergoing medical treatment, e.g.
intravascular access or intravascular therapy, or an arte-
riovenous (AV) shunt.
4. WARNINGS AND SAFETY NOTES
General warnings
WARNING
• The measurements you take are for your information only –
they are not a substitute for a medical examination! Discuss
your measured values with your doctor and never make
your own medical decisions based on them (e.g. regarding
medicine doses).
• 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 incorrect use.
• Using the blood pressure monitor outside your home envi-
ronment or while on the move (e.g. while travelling in a car,
ambulance or helicopter, or while undertaking physical ac-
tivity such as playing sport) can influence the measurement
accuracy and cause incorrect measurements.
• Cardiovascular diseases may lead to incorrect measure-
ments or have a detrimental eect on measurement accu-
racy.
• Do not use the device at the same time as other medical
electrical devices (ME equipment). This could cause the
measuring device to malfunction and/or an inaccurate
measurement.
8
• Do not use the device outside of the specified storage and
operating conditions. This could lead to incorrect measure-
ments.
• Only use the cus included in delivery or described in these
instructions for use with the device. Using a dierent cu
may lead to inaccurate measurements.
• Note that when inflating the cu, the functions of the limb
aected may be impaired.
• Do not perform measurements more frequently than nec-
essary. Due to the restriction of blood flow, some bruising
may occur.
• Blood circulation must not be stopped for an unnecessarily
long time during the blood pressure measurement. If the
device malfunctions, remove the cu from the arm.
• Place the cu on the upper arm only. Do not place the cu
on other parts of the body.
• The air line poses a risk of strangulation for small children.
• Small parts may present a choking hazard for small children
if swallowed. They should therefore always be supervised.
• Do not drop, step on or shake the device.
• Do not disassemble the device as this may cause damage,
faults and malfunctions.
• Do not use the device if you have metal implants.
General precautions
CAUTION
• The blood pressure monitor is made from precision and
electronic components. The accuracy of the measure-
ments and service life of the device depend on its careful
handling.
• Protect the device and its mains adapter from impacts,
humidity, dirt, marked temperature fluctuations and direct
sunlight.
• Ensure the device is at room temperature before taking a
measurement. If the measuring device has been stored
close to the maximum or minimum storage and transport
temperatures and is placed in an environment with a tem-
perature of 20°C, it is recommended that you wait approx.
2 hours before using the measuring device.
• Do not use the device in the vicinity of strong electromag-
netic fields and keep it away from radio systems or mobile
telephones.
• We recommend removing the batteries if the device is not
going to be used for a prolonged period of time.
• Avoid any mechanical restriction, compression or bending
of the cu line.
• Do not use the device on people with allergies or sensitive
skin.
9
Notes on handling batteries
WARNING
• If your skin or eyes come into contact with battery fluid,
rinse the aected areas with water and seek medical as-
sistance.
• Choking hazard! Small children may swallow and choke
on batteries. Therefore, store batteries out of the reach of
small children.
• Seek medical attention immediately if swallowed.
• Risk of explosion! Do not throw batteries into a fire.
• If a battery has leaked, put on protective gloves and clean
the battery compartment with a dry cloth.
• Do not disassemble, open or crush the batteries.
• Observe the plus (+) and minus (-) polarity signs.
CAUTION
• Protect batteries from excessive heat.
• Do not charge or short-circuit the batteries.
• If the device is not going to be used for a long period of
time, remove the batteries from the battery compartment.
• Use identical or equivalent battery types only.
• Always replace all batteries at the same time.
• Do not use rechargeable batteries.
Notes on electromagnetic compatibility
CAUTION
• The device is suitable for use in all environments listed
in these instructions for use, including domestic environ-
ments.
• The device may not be fully usable in the presence of elec-
tromagnetic 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 working properly.
• The use of accessories or replacement parts other than
those specified or provided by the manufacturer of this de-
vice can lead to an increase in electromagnetic emissions
or a decrease in the device’s electromagnetic immunity;
this can result in faulty operation.
• Keep portable RF communication devices (including pe-
ripheral equipment, such as antenna cables or external an-
tennas) at least 30 cm away from all device parts, including
all cables included in delivery.
• Failure to comply with the above can impair the perfor-
mance of the device.
10
5. DEVICE DESCRIPTION
The associated drawings are shown on page 2.
1
Cu
2
Cu line
3
Cu connector
4
Connection for mains part*
(rear of device)
5
Display
6
Memory buttons M1/M2
7
Start/stop button
8
Risk indicator
9
Connection for cu connector (left-hand side)
* not included in delivery
Information on the display
10
Date / time
11
Systolic pressure
12
Diastolic pressure
13
Calculated pulse value
14
Pulse symbol
15
Release air
16
Number of memory space/memory display average value
( ), morning ( ), evening ( )
17
Battery replacement
symbol
18
User memory
19
Risk indicator
20
Cardiac arrhythmia symbol
6. USAGE
6.1 Initial use
Inserting the batteries
• Remove the battery compartment cover on the back of the
device
A
.
• Insert four 1.5 V AA (alkaline type LR6) batteries. Insert the
batteries, making sure the polarity is correct according to
the label
A
.
• Close the battery compartment cover.
If the
symbol is displayed and does not disappear, meas-
urement is no longer possible. Replace all the batteries. Once
the batteries have been removed from the device, the date
and time must be set again. Any saved measured values are
retained.
Operation with the mains part
You can alternatively also operate this device with a mains part
(not included in delivery). However, before connecting the de-
vice with the mains part, please ensure that you have removed
the batteries from the device. During mains operation, there
must not be any batteries in the battery compartment, as this
could damage the device.
11
• To avoid any potential damage, the device may only be
operated with a mains part that meets the specifications
described in the chapter “Technical specifications”.
• Furthermore, the mains part must only be connected to the
mains voltage that is specified on the type plate.
• First, remove the protective cap of the mains part connec-
tor – located on the rear of the device – and insert the mains
part into the connection intended for this purpose.
• 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 measured values are retained.
Adjusting the settings
Make sure that the device’s settings have been set correctly so
you can make full use of all its functions. Otherwise you will not
be able to save your measured values with the date and time
and access them later.
There are two dierent ways to access the settings menu:
• Before initial use and after each time you replace the bat-
tery:
When inserting batteries into the device, you will be taken
to the relevant menu automatically.
• If the batteries have already been inserted:
With the device switched o, press and hold the START/
STOP button
for approx. 5 seconds.
Set these settings in the order shown below:
Hour format
➔
Date
➔
Time
Press
to confirm your selection each time.
Time format
Time format flashes:
• Press M1/M2 to select the time format
Date
The year flashes:
• Press M1/M2 to select the year
The month flashes:
• Press M1/M2 to select the month
The day flashes:
• Press M1/M2 to select the day
If the time format is set to the 12-hour format, the order
in which the day and month are displayed is reversed.
12
Time
The hour flashes:
• Press M1/M2 to select the hour
The minutes flash:
• Press M1/M2 to select the minutes
6.2 Before the blood pressure measurement
General rules when measuring your own blood
pressure
• In order to generate an informative profile of changes in
your blood pressure that can be used for comparisons, you
should measure your blood pressure regularly and always
at the same time of day.
Measure your blood pressure twice a day: once in the
morning after getting up and once in the evening.
• Always perform the measurement when you are suciently
physically rested. Avoid taking measurements at stressful
times.
• Do not take a measurement within 30 minutes of eating,
drinking, smoking or exercising.
• Before the initial blood pressure measurement, make sure
always to rest for about 5minutes.
• If you want to take several measurements in succession,
always make sure that you leave at least 1 minute between
each measurement.
• Repeat the measurement if you have doubts about the
measured value.
Attaching the cu
You can measure your blood pressure on either arm. Some de-
viations between the values in the right and left arm are perfect-
ly normal. Always perform the measurement on the arm with the
higher blood pressure values. Consult your doctor about this
before starting self-measurement.
• Always measure your blood pressure on the same arm.
• Place the cu onto the bare upper arm. The circulation of
the arm must not be hindered by tight clothing or similar.
• The cu must be placed on the upper arm so that the bot-
tom edge is positioned 2-3cm above the elbow and over
the artery. The line should point to the centre of the palm
here
B
.
• Guide the end of the cu that is sticking out through the
metal ring, fold it back over the arm and close the cu using
the hook-and-loop fastener. The cu should be fastened
tightly, but not too tightly, so that two fingers can still fit
under the closed cu
C
.
13
• The cu is suitable for you if the index mark (
) is within
the OK range after fitting the cu.
• Now insert the cu line into the connection for the cu con-
nector.
Adopting the correct posture
• Sit in a comfortable upright position when taking the blood
pressure measurement. Lean back so that your back is
supported.
• Place your arm on a surface
D
.
• Place your feet flat on the ground next to one another.
• The cu must be level with your heart.
• Stay as still as possible during the measurement and do
not talk.
Selecting the user
This device has 2 users with 60 memory spaces each in order
that you can save measurements from 2 dierent people sepa-
rately from each other.
If multiple people are using the device, make sure that the cor-
rect user has been selected before each measurement:
• Use the M1 or M2 memory button to select the desired
user. Confirm your selection by pressing
.
• If you do not select a user memory, the measurement is
stored in the most recently used user memory. The relevant
symbol M1 or M2 appears on the display.
• Using the Start/stop button
, switch o the blood pres-
sure monitor. The measurement is then stored in the select-
ed user memory.
If you forget to turn o the device, it will switch o automat-
ically after approx. 3 minutes. In this case too, the value is
stored in the selected or most recently used user memory.
6.3 Taking a blood pressure measurement
Requirement: cu attached, user selected.
Measurement
1. Press
. All display elements are briefly displayed. The cu
inflates itself automatically. The measurement process starts.
is displayed as soon as a pulse is detected.
To cancel the measurement, press .
2.
The systolic pressure, diastolic pressure and pulse measure-
ments are displayed.
is displayed if the measurement could not be performed
properly. In this case, please refer to the “Troubleshooting”
section.
If necessary, re-attach the cu after 1 minute.
14
The device switches o automatically after approx. 3min-
utes. The value is saved to the selected or most recently
used user.
6.4 Evaluating the results
General information about blood pressure
• Blood pressure is always stated in the form of two values:
• The highest pressure is the systolic blood pressure. This
occurs when the heart muscle contracts and blood is
pumped into the blood vessels.
• The lowest pressure is the diastolic blood pressure. This
occurs when the heart muscle has completely relaxed
again and the heart is filling with blood.
• Fluctuations in blood pressure are normal. Even during
repeat measurements, there may be considerable dier-
ences between the measured values. One-o or irregular
measurements therefore do not provide reliable information
about the actual blood pressure. Reliable assessment is
only possible when you perform the measurement regularly
under comparable conditions.
Cardiac arrhythmia
The device can identify heart rhythm abnormalities during the
blood pressure measurement. If
is displayed after the
measurement, this indicates that an irregularity has been de-
tected in your pulse.
Repeat the measurement if
is displayed.
When assessing your blood pressure, only use the results that
have been recorded without any irregularities in your pulse.
Consult your doctor if is displayed frequently. Only they
can determine, through an examination, whether there is an
abnormality.
Risk indicator
Measured blood
pressure value range
Classification
Risk
indicator
colour
Systolic
(in mmHg)
Diastolic
(in mmHg)
≥ 180 ≥ 110
Stage 3 high blood
pressure (severe)
Red
160 – 179 100 – 109
Stage 2 high blood
pressure (moderate)
Orange
140 – 159 90 – 99
Stage 1 high blood
pressure (mild)
Yellow
130 – 139 85 – 89 High normal Green
120 – 129 80 – 84 Normal Green
< 120 < 80 Optimal Green
Source:
15
The risk indicator
8
/
19
indicates which category the record-
ed blood pressure values fall into. If the measured values are
in two dierent categories (e.g. systolic pressure in the “high
normal” range and diastolic pressure in the “normal” range), the
risk indicator always indicates the higher range – “high normal”
in the example described.
Note that these default values are for general guidance
only, as individual blood pressures may vary.
Please note that self-measurement at home usually results in
values lower than those recorded at a doctor’s surgery. Consult
your doctor at regular intervals. Only they are able to give you
personal target values for controlled blood pressure, particular-
ly if you are receiving medical therapy.
6.5 Displaying and deleting measured
values
User
The results of every successful measurement are saved with
the date and time. If there are more than 60 measurements, the
oldest measurements are deleted.
1.
To access memory recall mode, the blood pressure mon-
itor must first be started. To do this press the Start/stop
button .
2.
After the full-screen display, select the relevant user mem-
ory that you want to see the measurement data for within
3 seconds using the M1 or M2 memory button (M1 for
or M2 for ).
3. Your last measurement will appear on the display.
4. Press the relevant memory button (M1 or M2).
If you have selected user memory1, the M1 memory
button must be pressed.
If you have selected user memory2, the M2 memory
button must be pressed.
Average value
flashes:
The average value of all this user’s saved meas-
ured values is displayed.
1. Press the relevant memory button (M1 or M2).
flashes:
The average value of the morning measurements
for the last 7 days is displayed (morning: 5:00–
9:00).
2. Press the relevant memory button (M1 or M2).
16
flashes:
The average value of the evening measurements
for the last 7 days is displayed (evening: 18:00–
20:00).
Individual measured values
1.
When the relevant memory button (M1 or M2) is
pressed again, the last individual measurement
is displayed (in this example, measurement 03).
2. When the relevant memory button (M1 or M2)
is pressed again, you can view your individual
measurements.
3. Press
to switch the device o again.
Press
to exit the menu.
Deleting measured values
1.
To delete all of a user’s measured values, select the corre-
sponding user.
Start individual measurement access.
2.
Press and hold the M1 & M2 memory buttons for 5 seconds.
appears on the display. All this user’s values are
deleted.
The device switches o automatically.
7. CLEANING AND MAINTENANCE
• Clean the device and cu carefully using only a slightly
damp cloth.
• Do not use any cleaning solutions or solvents.
• Under no circumstances hold the device or cu under wa-
ter, as this can cause liquid to enter and damage the device
and cu.
• If you store the device and cu, do not place heavy objects
on the device and cu. The cu line should not be bent
sharply.
• Remove the batteries if the device is not going to be used
for a long period of time.
8. ACCESSORIES AND
REPLACEMENT PARTS
Accessories and replacement parts are available on the home-
page www.beurer.de, under “Service”. Please state the corre-
sponding order number.
Designation Item number and/or
order number
Standard cu (22-36 cm) 163.388
17
Designation Item number and/or
order number
XL cu (35-44 cm) 163.387
Mains part (EU) 071.95
9. TROUBLESHOOTING
Error
message
Possible cause Solution
Unable to record
a pulse.
Please wait one minute
and repeat the measure-
ment.
Ensure that you do not
speak or move during the
measurement.
You moved or
spoke during the
measurement.
The cu was
not attached
correctly.
Please observe the
information in chapter
“Attaching the cu”.
Error
message
Possible cause Solution
An error occurred
during the meas-
urement.
Please wait one minute
and repeat the measure-
ment.
Ensure that you do not
speak or move during the
measurement.
The inflation
pressure is higher
than 300mmHg.
Please take another meas-
urement to check whether
the cu can be correctly
inflated.
Make sure that neither
your arm nor other heavy
objects are pressing on
the line, and that the line is
not bent.
The batteries are
almost empty.
Insert new batteries into
the device.
18
10. DISPOSAL
Repairing and disposing of the device
• Do not repair or modify the device yourself. Proper opera-
tion can no longer be guaranteed in this case.
• Do not open the device except for the battery compart-
ment. Failure to comply will invalidate the warranty.
• Repairs must only be carried out by Customer Services or
authorised retailers. Before making a complaint, first check
the batteries and replace them if necessary.
• The device must not be disposed of with household waste.
Dispose of the device at a suitable local collection
or recycling point in your country. Dispose of the
device in accordance with EC Directive – WEEE
(Waste Electrical and Electronic Equipment).
Please contact the local authorities responsible for waste
disposal if you have any questions regarding disposal.
Disposal of the batteries
• Used, completely discharged batteries must not be dis-
posed of with household waste. Dispose of the batteries
in specially designated collection boxes, at recycling points
or at electronics retailers. You are legally required to dis-
pose of the batteries correctly.
• The codes below are printed on batteries containing harm-
ful substances:
- Pb = battery contains lead
- Cd = battery contains cadmium
- Hg = battery contains mercury
11. TECHNICAL SPECIFICATIONS
Device
Type BM 45
Measurement
method
Oscillometric, non-invasive blood pres-
sure measurement on the upper arm
Measurement range Cu pressure 0 – 300 mmHg,
systolic 60– 250 mmHg,
diastolic 30 – 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 2 x 60 memory spaces
19
Dimensions L 160 mm x W 107 mm x H 50 mm
Weight Approx. 408 g
(without batteries, with cu)
Cu size Standard cu (22-36 cm)
XL cu (35-44 cm)
Permissible operating
conditions
+5 °C to + 40 °C, 15 – 90 % relative air
humidity (non-condensing)
Permissible storage
and transport con-
ditions
- 25 °C to + 70 °C, ≤90 % relative air
humidity, 700hPa – 1060hPa ambient
pressure
Power supply
4x 1,5 V
AA batteries (LR6)
Battery life For approx. 250 measurements,
depending on the blood pressure level
and/or pump pressure
Classification Internal supply, IP20, no AP or APG,
continuous operation, application part
type BF (cu), CLASS II (when using a
mains part)
The serial number is located on the device or in the battery
compartment.
Technical specifications are subject to change without notifica-
tion to allow for updates.
• This device conforms with the European stand-
ard EN 60601-1-2 (in accordance with CISPR-11,
IEC 61000-3-2, IEC 61000-3-3, IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-4, IEC 61000-4-5,
IEC 61000-4-6, IEC 61000-4-7, IEC 61000-4-8,
IEC 61000-4-11) and is subject to particular precautions
with regard to electromagnetic compatibility. Please note
that portable and mobile HF communication systems may
interfere with this unit.
• The device complies with Regulation (EU) 2017/745 of the
European Parliament and of the Council for medical devic-
es as well as the respective national regulations and the
standard IEC 80601-2-30 (Medical electrical equipment
Part 2-30 – Particular requirements for basic safety and
essential performance of automated non-invasive sphyg-
momanometers).
• The accuracy of this blood pressure monitor has been care-
fully checked and developed with regard to a long useful
life. If the device is used for commercial medical purpos-
es, it must be regularly tested for accuracy by appropriate
means. Precise instructions for checking accuracy may be
requested from the service address.
20
Mains part
Model no. LXCP12-006060BEH
Input 100 – 240 V, 50 – 60 Hz, 0.5 A max
Output 6 V DC, 600 mA, in conjunction with Beurer
blood pressure monitors only
Manufacturer Shenzhen Longxc Power Supply Co., Ltd.
Protection This device is double protected and has a
primary-side cutout switch which discon-
nects the device from the mains in case of
malfunction.
Ensure that you have removed the batteries
from the battery compartment before you
use the mains part.
Polarity of the DC voltage connection
Insulated/protection class 2
Housing and
protective
covers
The housing of the mains part protects users
from touching live parts or parts that could
be live (for example with their fingers, or with
a needle or checking hook).
The user must not touch the patient and the
output connector of the AC/DC mains part at
the same time.
12. GUARANTEE/SERVICE
Further information on the guarantee and guarantee condi-
tions can be found in the guarantee leaflet supplied.
Notification of incidents
For users/patients in the European Union and identical
regulation systems (EU Medical Device Regulation (MDR)
2017/745), the following applies: If during or through use of
the product a major incident occurs, notify the manufacturer
and/or their representative of this as well as the respective
national authority of the member state in which the user/
patient is located.
658.06_BM45_2023-05-03_07_IM2_BEU_MDR_EN Subject to errors and changes
Beurer GmbH
•
Söflinger Str. 218
•
89077 Ulm, Germany
www.beurer.com
•
www.beurer-healthguide.com
