Beurer BM 65: ENGLISH
ENGLISH: Beurer BM 65

ENGLISH
Dear Customer,
Keep these instructions carefully for further use and also let
Thank you for choosing one of our products. Our name
other users have access to them.
stands for high-quality, thoroughly tested products for the
2. Important information
applications in the areas of heat, weight, blood pressure,
body temperature, pulse, gentle therapy, massage and air.
Signs and symbols
Please read these instructions for use carefully and keep
The following symbols are used in these instructions for
them for later use, be sure to make them accessible to other
use, on the packaging and on the type plate for the device
users and observe the information they contain.
and accessories:
Best regards,
Your Beurer Team
Caution
1. Getting to know your instrument
Note
The upper arm blood pressure monitor is used for non-
Note on important information
invasive measurement and monitoring of adults‘ arterial
blood pressure.
Follow instructions for use
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.
Type BF applied part
A warning is issued for anyone suffering from cardiac ar-
rhythmia.
The values determined are classified and graphically evalu-
Direct current
ated according to WHO guidelines.
16

Disposal in accordance with EC Directive
2002/96/EC – WEEE (Waste Electrical and
Electronic Equipment).
Manufacturer
17
Storage
•
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 after eat-
ing, drinking, smoking or exercising.
•
Repeat the measurement if you are unsure of the meas-
ured value.
•
The measurements taken by you are for your information
Permissible storage temperature and
55°C
only – they are not a substitute for a medical examination!
-20°C
humidity
RH ≤90%
Discuss the measurements with your doctor, and never
Operating
Permissible operating temperature and
base any medical decisions on them (e.g. medicines and
40°C
humidity
their administration)!
10°C
RH ≤90%
•
Do not use the blood pressure monitor on newborns,
Keep dry
pregnant women or patients with preeclampsia.
•
Cardiovascular diseases may lead to incorrect measure-
ments or have a detrimental effect on measurement ac-
SN Serial number
curacy. The same also applies to very low blood pressure,
diabetes, circulatory disorders and arrhythmias as well as
The CE labelling certifies that the product
chills or shaking.
complies with the essential requirements
•
The blood pressure monitor must not be used in connec-
0483
of Directive 93/42/EEC on medical prod-
tion with a high-frequency surgical unit.
ucts.
•
Only use the device on people who have the specified up-
per arm measurement for the device.
Advice on use
•
Please note that when inflating, the functions of the limb
•
In order to ensure comparable values, always measure
in question may be impaired.
your blood pressure at the same time of day.
•
Before every measurement, relax for about five minutes.

•
During the blood pressure measurement, blood circula-
•
The device is only intended for the purpose described in
tion must not be stopped for an unnecessarily long time.
these instructions for use. The manufacturer is not liable
If the device malfunctions, remove the cuff from the arm.
for damage resulting from improper or careless use.
•
Avoid any mechanical restriction, compression or bending
Storage and Care
of the cuff line.
•
Do not allow sustained pressure in the cuff or frequent
•
The blood pressure monitor is made up of precision elec-
measurements. The resulting restriction of the blood flow
tronic components. Accuracy of readings and the instru-
may cause injury.
ment‘s service life depend on careful handling.
•
Ensure that the cuff is not placed on an arm in which the
– You should protect the device from impact, moisture,
arteries or veins are undergoing medical treatment, e.g.
dirt, major temperature fluctuations and direct exposure
intravascular access or therapy, or an arteriovenous (AV)
to the sun‘s rays.
shunt.
– Never drop the device.
•
Do not use the cuff on people who have undergone a
– Do not use near strong electromagnetic fields, i.e. keep
mastectomy.
it away from any radio systems and mobile phones.
•
Do not place the cuff over wounds as this may cause
– Only ever use the cuffs provided with the monitor or
further injury.
original replacement cuffs. Otherwise erroneous results
•
You can either use the blood pressure monitor with bat-
will be recorded.
teries or with a mains part. Please note that data transfer
•
Do not press any buttons until the cuff is in position.
and data storage is only possible when your blood pres-
•
If the instrument is not used for any length of time, we
sure monitor is supplied with power. As soon as the bat-
recommend removing the batteries.
teries are empty or the mains part is disconnected from
the power supply, the blood pressure monitor loses the
Advice on batteries
date and time.
•
Batteries can be fatal if swallowed. You should therefore
•
To conserve the batteries, the monitor switches off auto-
store the batteries and products where they are inacces-
matically if no buttons are pressed for one minute.
sible to small children. If a battery has been swallowed,
call a doctor immediately.
18

•
Batteries should not be charged or reactivated with any
3. Unit description
other means, nor should they be taken apart, thrown in
the fire or short-circuited.
•
Remove the batteries from the instrument if they are worn
out or if you are not going to use the instrument for any
1
4
9
length of time. This prevents any damage as a result of
3
8
leakage. Always replace all the batteries at the same time.
•
Never use different types of battery, battery brands or
2
batteries with different capacities. You should preferably
use alkaline batteries.
5
MEM
6
Repair and disposal
•
Batteries do not belong in domestic refuse. Used batteries
should be disposed of at the collection points provided.
•
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.
1. Cuff tube
We can no longer guarantee perfect functioning if you do.
2. Cuff
•
Repairs may only be performed by Beurer Customer
3. Cuff connector
7
Service or authorized dealers. However, always check the
4. Display
batteries and replace them if necessary prior to making
5. MEM memory button
any complaint.
6. START/STOP button
•
The appliance should be disposed of according to
7. Connection for cuff connector
Regulation 2002/96/EC-WEEE (Waste Electrical
8. USB interface
and Electronic Equipment). In case of queries,
9. Connection for mains part
please contact the municipal authorities responsible for
waste disposal in your area.
19

Icons in the display:
To do this you require a USB cable (included in delivery) and
the Beurer “Health Manager” PC software.
5
The software can be downloaded free of charge from
4
www.beurer.com/service/download.
S YS
mm Hg
6
3
P UL
/m in
7
System requirements for the Beurer “Health Manager”
DIA
2
mm Hg
computer software
8
1. Supported operating systems:
•
Windows XP SP3
•
Windows Vista SP1 or later
1
•
Windows 7
•
Windows 8
1. Time and date
•
Windows 7 SP1
2. Diastolic pressure
2. Supported architectures:
3. Memory display, average value (
),
•
x86 (32 bit)
morning (
), evening ( ),
number of memory space
•
x64 (64 bit)
4. Systolic pressure
3. Hardware requirements:
5. WHO classification
•
Recommended: at least Pentium 1 GHz or faster with at
6. Arrhythmia recognition
least 1 GB RAM.
7. Measured pulse
•
Free memory on the primary partition of at least:
8. Change battery icon
– x86 – 600 MB
PC interface
– x64 – 1.5 GB
•
Graphic resolution from: 1024 x 768 pixels.
The Beurer blood pressure monitor also allows you to trans-
•
USB port 1.0 or later.
fer your measured values to the PC.
20

4. Prepare measurement
Setting date and time
Inserting battery
You should set the date and time without fail. Otherwise,
you will not be able to save your measured values correctly
•
Replace the battery cover
with a date and time and to access them again later.
carefully.
Tip: If you press and hold the MEM button, you can set the
•
Insert four AAA 1.5 V alkaline
values more quickly.
(LR 03) batteries. making
To set the date and time, proceed as follows:
absolutely sure that you
•
Press the START/STOP and MEM buttons simultane-
insert them with the correct
ously, 24h begins to flash. Select 12h or 24h mode using
polarity as marked. Never use
the MEM button. Press START/STOP to confirm your
rechargeable batteries.
selection. The year display will start to flash. Set the year
•
Replace the battery cover
with the MEM button and confirm with START/STOP .
carefully.
•
Then set the month, day, hour and minutes and confirm
If the battery change
is continuously illuminated,
each setting with START/STOP .
measurement is no longer possible and you must replace all
•
Pressing the START/STOP button again will switch the
the batteries. Once batteries have been removed from the
display off; the date and time are permanently displayed.
device, the time must be reset.
Note: In 24h mode, the date is displayed as day/month. In
Used batteries do not belong in the household waste. You
12h mode, as month/day.
are legally obliged to dispose of the batteries. Dispose of
them via your specialist electrical supplier or local collec ting
Operation with the mains part
point for recyclable waste.
You can also operate this device with a mains part.
When doing so, there must not be any batteries in the bat-
Note: Batteries containing pollutant substances
tery compartment. The mains part can be obtained from
are marked as follows:
specialist retailers or from the service address using order
Pb = Battery contains lead,
number 071.19.
Cd = Battery contains cadmium,
Hg = Battery contains mercury.
21

•
To prevent possible damage to the device, the blood
The cuff should be placed on the
pressure monitor must only be used with the mains part
upper arm so that the lower edge
described here.
is 2 to 3 cm above the bend of the
•
Insert the mains part into the connection provided for
elbow and above the artery. The
this purpose on the right-hand side of the blood pressure
tube should be in line with the
monitor. The mains part must only be connected to the
centre of the palm.
mains voltage that is specified on the type plate.
Now place the free end of the cuff
•
Then insert the mains plug of the mains part into the
snugly, but not too tightly, around
mains socket.
the arm, and fix it with the Velcro
•
After using the blood pressure monitor, unplug the mains
fastener. The cuff should be fitted
part from the mains socket first and then disconnect it
tight enough to allow just two fin-
from the blood pressure monitor. As soon as you unplug
gers to fit beneath the cuff.
the mains part, the blood pressure monitor loses the
Insert the cuff tubing into the socket
date and time setting but the saved measurements are
for the cuff attachment.
retained.
Important: The device may only be
operated with the original cuffs. The
5. Measuring blood pressure
device comes with 2 cuffs: a stand-
Please ensure the device is at room temperature before
ard cuff for arm circumferences of 22 to 30 cm and a larger
measuring.
cuff for upper arm circumferences of 30 to 42 cm.
Positioning cuff
Fit the cuff round your bare left
upper arm. Blood circulation in the
arm should not be restricted by
tight clothing or other objects.
22

Correct posture
If no button 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 memo-
ry, the instrument always displays the value
.
•
The cuff automatically inflates. Cuff air pressure is re-
leased slowly. If a tendency towards high blood pressure
•
Rest for approx. 5 minutes before each measurement.
is already detectable, the cuff is pumped up again and
Otherwise there may be divergences.
cuff pressure increased further. As soon as a heart rate is
•
You can perform the measurement either sitting or lying
detected, the heart beat symbol is displayed.
down. Always make sure that the cuff is on a level with
•
Heart rate, systolic and diastolic blood pressure are dis-
your heart.
played.
•
To carry out a blood pressure measurement, make sure
•
Measuring can be cancelled at any time by pressing the
you are sitting comfortably with your arms and back lean-
START/STOP button
.
ing on something. Do not cross your legs. Place your feet
•
appears if it has not been possible to perform the
flat on the ground.
measurement properly. Observe the section in these in-
•
In order not to distort the result, it is important to keep still
structions on error messages/troubleshooting and repeat
during the measurement and not talk.
the measurement.
•
The test result is saved automatically.
Measuring blood pressure
•
To switch off, press the START/STOP button . If you
•
Put on the cuff as described previously and assume the
forget to turn off the device, it will switch off automatically
position in which you want to carry out the measurement.
after approx. 1 minute.
•
Switch on the blood pressure monitor with the START/
Wait at least 5 minutes before taking another measurement!
STOP button . After the full-screen display, the most
recently used user memory appears ( U0, U1....U9 ). To
change the user memory, press the MEM button and
confirm your selection with the START/STOP button .
23

6. Evaluating results
move during the measurement. If the icon appears
Cardiac arrhythmia:
often, please contact your doctor. Any self-diagnosis and
This instrument can identify possible cardiac arrhythmia dis-
treatment based on the test results may be dangerous. It is
orders during measurement and if necessary indicates the
vital to follow your doctor‘s instructions.
measurement with the flashing icon .
WHO classification:
This may be an indicator for arrhythmia. Arrhythmia is a
In accordance with the guidelines/definitions of the World
condition where the heart rhythm is abnormal as a result of
Heath Organization and the latest findings, the measure-
defects in the bioelectrical system controlling the heart beat.
ments can be classified and assessed according to the
The symptoms (omitted or premature heart beats, slow or
following table.
excessively fast heart rate) may be caused, among other
However, these standard values serve only as a general
things, by heart disease, age, physical predisposition, ex-
guideline, as the individual blood pressure varies in different
cessive use of stimulants, stress or lack of sleep. Arrhythmia
people and different age groups etc.
can only be ascertained through examination by your doctor.
It is important to consult your doctor regularly for advice.
Repeat the measurement if the flashing icon is dis-
Your doctor will tell you your individual values for normal
played after the measurement. Please note that you should
blood pressure as well as the value above which your blood
rest for 5 minutes between measurements and not talk or
pressure is classified as dangerous.
Range of blood pressure values Systolic
Diastolic
Measure
(in mmHg)
(in mmHg)
Grade 3: Severe hypertension > = 180 > = 110 Seek medical advice
Grade 2: Moderate hypertension 160 – 179 100 – 109 Seek medical advice
Grade 1: Mild hypertension 140 – 159 90 – 99 Have it checked regularly by doctor
High-normal 130 – 139 85 – 89 Have it checked regularly by doctor
Normal 120 – 129 80 – 84 Check it yourself
Optimal < 120 < 80 Check it yourself
Source: WHO, 1999
24

The WHO classification in the display shows the range of
•
To switch off, press the MEM button again or the START/
the measured blood pressure.
STOP button .
If the values for systolic and diastolic pressure are in two
•
If you forget to switch off the device, it will switch off
different WHO ranges (e.g. systolic in the grade hyperten-
automatically after 2 minutes.
sion range and diastolic pressure in the normal range), the
8. Error messages/trouble-shooting
WHO classification on the unit always indicates the higher
range (grade hypertension in the example described).
In case of faults, the _ message appears in the display.
Error messages may appear if:
7. Saving, retrieving and deleting results
• systolic or diastolic pressure could not be measured (
•
The results of each successful measurement are stored
or appears on the display)
together with date and time. With more than 30 items of
• systolic or diastolic pressure was outside the measure-
measured data, the earliest items of data measured are lost.
ment range („ “ or „ “ appears on the display)
•
Press MEM button to activate the memory function and
• the cuff is fastened too tightly or loosely ( or ap-
choose the desired user memory by using the
START/STOP
pears on the display)
button
. If you press the MEM button again, the average
• the pump pressure is higher than 300 mmHg ( ap-
value of all the stored measured values in the user memory
pears on the display)
will be displayed. If you press the MEM button again, the av-
• pumping up takes longer than 160 seconds ( appears
erage value of the last 7 days for the morning measurement
on the display)
will be displayed (Morning: 5 a.m. – 9 a.m., display ). If
• there is a system or device error ( , , or
you press the MEM button again, the average value of the
appears on the display)
last 7 days for the evening measurement will be displayed
• the batteries are almost empty .
(Evening: 6 p.m. – 8 p.m., display ). If you continue to
In such cases, repeat the measurement. Ensure you do not
press the MEM button, the most recent individual measured
move or speak.
values with date and time are displayed in turn.
If necessary, re-insert or replace the batteries.
•
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.
25

10. Specifications
Technical alarm – description
Should the recorded blood pressure (systolic or diastolic)
Model no. BM 65
lie outside the limits specified in the section “Technical
Measurement
Oscillometric, non-invasive blood pres-
specifications”, the technical alarm will appear on the dis-
method
sure measurement on the upper arm
play indicating either “
” or “ ”. In such cases, you should
Measurement
Cuff pressure 0 – 300 mmHg,
seek medical assistance and check the accuracy of your
range
systolic 60 – 260 mmHg,
procedure.
diastolic 40 –199 mmHg,
The limit values for the technical alarm are factory set and
Pulse 40 –180 beats/minute
cannot be adjusted or deactivated. These alarm limit values
Display accuracy Systolic ± 3 mmHg,
are accorded second priority under the standard IEC 60601-
diastolic ± 3 mmHg,
1-8.
pulse ± 5 % of the value shown
The technical alarm is a non-locking alarm and must not be
reset. The signal shown on the display will disappear auto-
Measurement inac-
Max. permissible standard deviation
matically after about 8 seconds.
curacy
according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
9. Cleaning and storing the instrument
Memory 10 x 30 memory spaces
•
Clean your blood pressure computer carefully only with a
Dimensions L 240 mm x W 120 mm x H 50 mm
slightly moistened cloth.
•
Do not use detergents or solvents.
Weight Approx. 419 g (without batteries)
•
On no account must you immerse the computer in water,
Cuff size 22 – 30 cm / 30 – 42 cm
otherwise liquid can enter it and cause demage.
Permissible operat-
+10 °C to +40 °C, ≤ 90 % relative air
•
When storing the device, make sure that no heavy objects
ing conditions
humidity (non-condensing)
are placed on top of it. Remove the batteries. The cuff
Permissible storage
-20 °C to +55 °C, ≤ 90 % relative air
tube should not have any sharp kinks.
conditions
humidity, 800 –1050 hPa ambient
pressure
26

nometers, Part 3: Supplementary requirements for
Power supply
4 x 1,5 V
AAA batteries
electro-mechanical blood pressure measuring systems)
Battery life For approx. 220 measurements, de-
and IEC80601-2-30 (Medical electrical equipment –
pending on the blood pressure level
Part 2 – 30: Particular requirements for the safety and
and/or pump pressure
essential performance of automated non-invasive blood
Accessories Instruction for use, 4 x 1.5 V AAA bat-
pressure monitors).
teries, storage pouch
•
The accuracy of this blood pressure monitor has been
Classification Internal supply, IPX0, no AP or APG,
carefully checked and developed with regard to a long
continuous operation, type BF applied
useful life. If using the device for commercial medical pur-
part
poses, it must be regularly tested for accuracy by appro-
priate means. Precise instructions for checking accuracy
Technical information is subject to change without notifica-
may be requested from the service address.
tion to allow for updates.
•
This unit is in line with European Standard EN 60601-1-2
and is subject to particular precautions with regard to
electromagnetic compatibility (EMC). Please note that
portable and mobile HF communication systems may in-
terfere with this unit. More details can be requested from
the stated Customer Service address or found at the end
of the instructions for use.
•
This device is in line with the EU Medical Devices Direc-
tive 93/42/EC, the „Medizinproduktegesetz“ (German
Medical Devices Act) and the standards EN1060-1
(non-invasive sphygmomanometers, Part 1: General
requirements), EN1060-3 (non-invasive sphygmoma-
27

11. Adapter
Model No. FW 7575M/EU/6/06
Input 100 – 240 V, 50 – 60 Hz
Output 6 V DC, 600 mA, only in connection
with beurer blood pressure monitor
Supplier Friwo Gerätebau GmbH
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 compartment before using the
mains part
Double insulated / equipment class 2
Polarity of the DC voltage connection
Enclosures and
Equipment enclosed to protect
Protective Covers
against contact with live parts, and
with parts which can become live
(finger, pin, hook test).
The operator shall not contact the pa-
tient and the output plug of AC mains
part simultaneously.
28