BM 27
EN Upper arm blood pressure monitor
Instructions for use
2
Included in delivery
•
Blood pressure monitor
•
Upper arm cuff
•
4 x 1.5 V LR6 AA batteries
•
Storage bag
•
Instructions for use
Dear customer,
Thank you for choosing one of our products. Our name
stands for high-quality, thoroughly tested products for ap-
plications 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.
With kind regards,
Your Beurer team
1. Getting to know your device
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 ac-
cessories and that all packaging material has been removed.
If you have any doubts, do not use the device and contact
your retailer or the specified Customer Services address.
The upper arm blood pressure monitor is used to carry out
non-invasive measurement and monitoring of the arterial
blood pressure values in adults.
ENGLISH
1. Getting to know your device ......................................... 2
2. Important notes ............................................................. 3
3. Device description ......................................................... 7
4. Preparing the measurement .......................................... 8
5. Measuring blood pressure ............................................. 9
6. Evaluating results ........................................................ 11
7. Saving, displaying and deleting measured values ...... 12
8. Error messages/troubleshooting ................................. 12
9. Cleaning and storing the device and cuff .................... 12
10. Technical specifications .............................................. 13
11. Replacement parts and wearing parts ........................ 14
12. Warranty / service ......................................................... 14
Contents
3
This allows you to quickly and easily measure your blood
pressure, save the measured values and display the devel-
opment and average values of the measured values taken.
You are also warned of possible existing cardiac arrhythmia.
The recorded values are classified and evaluated graphically.
2. Important notes
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 the 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 tem-
perature and humidity
Operating
Permissible operating temperature and
humidity
IP21
Protected against solid foreign objects
12.5 mm in diameter and larger, and
against vertically falling drops of water
S
N
Serial number
The CE labelling certifies that the product
complies with the essential requirements
of Directive 93/42/EEC on medical pro-
ducts.
4
Certification symbol for products that are
exported to the Russian Federation and
members of the CIS
Notes on use
•
In order to ensure comparable values, always measure
your blood pressure at the same time of day.
•
Before every measurement, relax for about five minutes.
•
If you want to perform several measurements on the same
person, wait five minutes between each measurement.
•
Do not take a measurement within 30 minutes of eating,
drinking, smoking or exercising.
•
Repeat the measurement if you are unsure of the meas-
ured value.
•
The measured values taken by you are for your informa-
tion only – they are no substitute for a medical examina-
tion. Discuss the measured values with your doctor and
never base any medical decisions on them (e.g. medi-
cines 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 pre-eclampsia. 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 ac-
curacy. 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, un-
less 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 up-
per arm measurement for the device.
•
Please note that when inflating, the functions of the limb
in question may be impaired.
•
During the blood pressure measurement, the blood circu-
lation must not be stopped for an unnecessarily long time.
If the device malfunctions remove the cuff from the arm.
5
•
Avoid any mechanical restriction, compression or bending
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.
•
Make sure that the cuff is not placed on an arm in which
the arteries or veins are undergoing medical treatment,
e.g. intravascular access or intravascular 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
further injury.
•
Place the cuff on your upper arm only. Do not place the
cuff on other parts of the body.
•
The blood pressure monitor can only be operated with
batteries.
•
To conserve the batteries, the blood pressure monitor
switches off automatically if you do not press any buttons
for 30seconds.
•
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.
Instructions for storage and maintenance
•
The blood pressure monitor is made from precision and
electronic components. The accuracy of the measured
values and service life of the device depend on its careful
handling:
– Protect the device from impacts, humidity, dirt, marked
temperature fluctuations and direct sunlight.
– Do not drop the device.
– Do not use the device in the vicinity of strong electro-
magnetic fields and keep it away from radio systems or
mobile telephones.
– Only use the cuff included with the delivery or original
replacement parts. Otherwise incorrect measured val-
ues will be recorded.
•
We recommend that the batteries be removed if the de-
vice will not be used for a prolonged period of time.
Notes on handling batteries
•
If your skin or eyes come into contact with battery fluid,
rinse the affected areas with water and seek medical as-
sistance.
•
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.
6
•
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.
Instructions for repairs and disposal
•
Batteries do not belong in household waste. Please dis-
pose of empty batteries at the collection points intended
for this purpose.
•
Do not open the device. Failure to comply will result in
voiding of the warranty.
•
Do not repair or adjust the device yourself. Proper opera-
tion can no longer be guaranteed in this case.
•
Repairs must only be carried out by Customer Services
or authorised suppliers. Before making a claim, please
check the batteries first and replace them if necessary.
•
Please 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.
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 de-
vice 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 other than those specified or
provided 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.
7
3. Device description
8910
7
6
5
4
1 2 3
1. Cuff
2. Cuff line
3. Cuff connector
4. Display
5. Connection for cuff connector
6. Risk indicator
7. Function buttons -/+
8. START/STOPbutton
9. Memory button M
10. Setting button SET
Information on the display:
5
678
2
3
4
9
10
11
1
1. Time and date
2. Systolic pressure
3. Diastolic pressure
4. Calculated pulse value
5. Cardiac arrhythmia symbol
6. Memory display: average value ( ), morning( ),
evening (
), memory space number
7. Release air
8. User memory
9. Battery replacement symbol
10. Risk indicator
11. Cuff position control
8
4. Preparing the measurement
Inserting the batteries
•
Open the battery compartment lid.
•
Insert four 1.5V AA (alkaline type
LR6) batteries. Make sure that the
batteries are inserted the correct
way round.
Do not use rechargeable batteries.
•
Close the battery compartment lid
again carefully.
•
All display elements are briefly dis-
played, 24 h flashes in the display. Now set the date and
time as described below.
If the low battery indicator
is permanently displayed,
you can no longer perform any measurements and must re-
place the batteries. Once the batteries have been removed
from the device, the time must be set again.
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 the hour format, date and time
It is essential to set the date and time. Otherwise, you will
not be able to save your measured values correctly with a
date and time and access them again later.
To set the date and time, proceed as follows:
•
Insert the batteries, or
press and hold the setting button
SET
for at least 5 seconds if the batteries have already
been inserted.
•
Select 12h or 24h mode using the function buttons -/+.
Press
SET
to confirm. The year display will start to flash.
Set the year with the function buttons -/+ and confirm with
SET.
•
Set the month, day, hour and minute and confirm each
with the
setting button
SET.
•
The blood pressure monitor switches itself off automatically.
9
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 values
are different. Always perform the measurement on the same
arm.
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 unit may only be operated with the original
cuff. The cuff is suitable for an arm circumference of 22 to
42 cm.
10
Adopting the correct posture
•
Before every measurement, relax for about five minutes.
Otherwise deviations can occur.
•
You can take the measurement while sitting or lying. Al-
ways make sure that the cuff is at heart level.
•
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.
•
To avoid falsifying the measurement, it is important to
remain still during the measurement and not to speak.
Performing the blood pressure measurement
•
As described above, attach the cuff and adopt the pos-
ture in which you want to perform the measurement.
•
Start the blood pressure monitor with the START/STOP
button .
•
The cuff automatically inflates. The cuff’s air pressure is
slowly released. If you already recognise a tendency for
high blood pressure, you should reinflate the cuff and
increase the cuff’s pressure again. As soon as a pulse is
found, the pulse symbol
will be displayed.
•
The cuff position control symbol is displayed
throughout the entire measurement. If the cuff is ap-
plied too tightly or too loosely, then and “ ” are
displayed. In such cases, the measurement is cancelled
after approx. 5 seconds and the device switches itself off.
Apply the cuff correctly and take a new measurement.
•
The systolic pressure, diastolic pressure and pulse rate
measurements are displayed.
•
You can cancel the measurement at any time by pressing
the START/STOP button .
•
_ appears if the measurement has not been performed
properly. Observe the chapter on error messages/trou-
bleshooting in these instructions for use and repeat the
measurement.
•
Now select the desired user memory by pressing the
memory button M. If you do not select a user memory,
the measurement is stored in the most recently used user
memory. The relevant , , or symbol appears on
the display.
•
To switch off, press the
START/STOP
button
. If you
forget to turn off the device, it will switch itself off auto-
matically after approx. 3 minutes.
Wait at least 5 minutes before taking another measurement.
11
6. Evaluating results
Cardiac arrhythmia:
This device can identify potential disruptions of the heart
rhythm when measuring and if necessary, indicates this
after the measurement with the symbol . This can be an
indicator for arrhythmia. Arrhythmia is an illness in which the
heart rhythm is abnormal because of flaws in the bioelectri-
cal system that regulates the heartbeat. The symptoms
(skipped or premature heart beats, pulse being slow or too
fast) can be caused by factors such as heart disease, age,
physical make-up, excess stimulants, stress or lack of sleep.
Arrhythmia can only be determined through an examination
by your doctor. If the symbol is shown on the display
after the measurement has been taken, repeat the measure-
ment. Please ensure that you rest for 5 minutes beforehand
and do not speak or move during the measurement. If the
symbol appears frequently, please consult your doctor.
Self-diagnosis and treatment based on the measurements
can be dangerous. Always follow your GP’s instructions.
Risk indicator:
The measurements can be classified and evaluated in ac-
cordance 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
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: mode-
rate hypertension
160 – 179 100 – 109
seek medical
attention
Setting 1: mild
hypertension
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)
12
7. Saving, displaying and deleting measured
values
The results of every successful measurement are stored
together with the date and time. If there are more than 30
measurements, the oldest measurements are lost.
•
Press the memory button M. Select the desired user
memory (
... ) by pressing the memory button M again.
•
If you press the function button +, the average value of
all the stored measured values in the user memory will be
displayed. If you press the function button + again, the
average value of the morning measurements for the last
7days will be displayed (morning: 5 a.m. – 9 a.m., display
). If you press the function button + again, the average
value of the evening measurements for the last 7 days will
be displayed (evening: 6 p.m. – 8 p.m., display ). If you
continue to press the function button +, the most recent
individual measured values are displayed in turn with the
date and time.
•
To switch off, press the START/STOP button
.
•
If you forget to switch off the device, it will switch itself off
automatically after 30 seconds.
•
If you want to delete the whole memory for a specific
user, press the memory button M. Press and hold down
the memory button M and the setting button SET simulta-
neously for 5 seconds.
8. Error messages/troubleshooting
In the event of errors, the error message _ appears on the
screen. Error messages may appear if:
•
It was not possible to correctly record the pulse:
1
;
•
No measurement could be taken:
2
;
•
The cuff is fastened too tightly or loosely:
3;
•
Errors occur during the measurement:
4
;
•
The pump pressure is higher than 300 mmHg:
5
;
•
There is a system error. If this error message appears,
please contact Customer Services:
6
.
•
The batteries are almost empty: .
In such cases, repeat the measurement. Ensure that the cuff
line is correctly attached and that you do not move or speak
during the measurement.
If necessary, reinsert or replace the batteries.
9. 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 ob-
jects on the device and cuff. Remove the batteries. The
cuff line should not be bent sharply.
13
10. Technical specifications
Model No. BM 27
Measurement
method
Oscillometric, non-invasive blood pres-
sure measurement on the upper arm
Measurement
range
Cuff pressure 0-300 mmHg,
Systolic 50-280 mmHg,
Diastolic 30-200 mmHg,
Pulse 40-199 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 4 x 30 memory spaces
Dimensions L 112 mm x W 110 mm x H 53 mm
Weight Approximately 341 g (without batteries,
with cuff)
Cuff size
22 to 42 cm
Permissible opera-
ting conditions
+10°C to +40°C, 10 to 85% relative
humidity (non-condensing)
Permissible sto-
rage conditions
-20°C to +55°C, 10-90% relative humi-
dity, 800-1050 hPa ambient pressure
Power supply 4 x 1.5 V
AA batteries
Battery life For approx. 300measurements, depen-
ding on levels of blood pressure and
pump pressure
Classification Internal supply, IP21, no AP or APG,
continuous operation, application part
type BF
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 device complies with European Standard EN60601-
1-2 (In accordance with CISPR 11, IEC 61000-4-2, IEC
61000-4-3 and IEC 61000-4-8) 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 the EU Medical Devices
Directive 93/42/EEC, the German Medical Devices Act
(Medizinproduktgesetz) and the standards EN1060-1
(Non-invasive sphygmomanometers – Part1: General
requirements), EN1060-3 (Non-invasive sphygmoma-
nometers – Part 3: Supplementary requirements for
14
electro-mechanical blood pressure measuring systems)
and IEC80601-2-30 (Medical electrical equipment – Part
2 – 30: Particular requirements for the basic safety and
essential performance of automated non-invasive sphyg-
momanometers).
•
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.
11. 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
Universal cuff (22 – 42 cm) 163.911
12. Warranty / service
In case of a claim under the warranty please contact your
local dealer or the local representation which is mentioned
in the list “service international”.
In case of returning the unit please add a copy of your re-
ceipt and a short report of the defect.
The following warranty terms shall apply:
1
. The warranty period for BEURER products is either
5years or- if longer- the country specific warranty period
from date of Purchase.
In case of a warranty claim, the date of purchase has to
be proven by means of the sales receipt or invoice.
2
. Repairs (complete unit or parts of the unit) do not extend
the warranty period.
3
. The warranty shall not be valid for damages because of
a. improper treatment, e.g. nonobservance of the user
instructions.
b. repairs or tampering by the customer or unauthorised
third parties.
c. transport from the manufacturer to the consumer or
during transport to the service centre.
d. The warranty shall not be valid for accessories
which are subject to normal wear and tear (cuff,
batteries etc.).
4
. Liability for direct or indirect consequential losses
caused by the unit are excluded even if the damage
to the unit is accepted as a warranty claim.
Subject to errors and changes
15
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Beurer GmbH • Söflinger Straße 218 • 89077 Ulm, Germany
www.beurer.com • www.beurer-healthguide.com
658.18_BM27_2019-03-21_05_IM1_BEU_EN