Beurer BM 58: ENGLISH
ENGLISH: Beurer BM 58

ENGLISH
Dear Customer,
2. Important information
Thank you for choosing one of our products. Our name
Signs and symbols
stands for high-quality, thoroughly tested products for the
applications in the areas of heat, weight, blood pressure,
The following symbols are used in these instructions for
body temperature, pulse, gentle therapy, massage and air.
use, on the packaging and on the type plate for the device
Please read these instructions for use carefully and keep
and accessories:
them for later use, be sure to make them accessible to other
Caution
users and observe the information they contain.
Best regards,
Your Beurer Team
Note
Note on important information
1. Getting to know your instrument
The upper arm blood pressure monitor is used for non-inva-
Follow instructions for use
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
Type BF applied part
progression of readings together with the average.
A warning is issued for anyone suffering from cardiac
arrhythmia.
Direct current
The values determined are classified and graphically evalu-
Disposal in accordance with EC Directive
ated according to WHO guidelines.
2002/96/EC – WEEE (Waste Electrical and
Keep these instructions carefully for further use and also let
Electronic Equipment).
other users have access to them.
17

•
Do not take a measurement within 30 minutes after eat-
Manufacturer
ing, drinking, smoking or exercising.
•
Repeat the measurement if you are unsure of the meas-
Storage
Permissible transport and storage tempe-
ured value.
55°C
rature. Permissible transport and storage
•
The measurements taken by you are for your information
-20°C
RH ≤95%
humidity.
only – they are not a substitute for a medical examination!
Operating
Discuss the measurements with your doctor, and never
Permissible operating temperature and
40°C
base any medical decisions on them (e.g. medicines and
humidity.
5°C
RH ≤90%
their administration)!
•
Do not use the blood pressure monitor on newborns or
Keep dry
patients with preeclampsia. We recommend consulting
a doctor before using the blood pressure monitor during
SN Serial number
pregnancy.
•
Cardiovascular diseases may lead to incorrect measure-
The CE labelling certifies that the prod-
ments or have a detrimental effect on measurement accu-
uct complies with the essential require-
racy. The same also applies to very low blood pressure,
0483
ments of Directive 93/42/EEC on medical
diabetes, circulatory disorders and arrhythmias as well as
products.
chills or shaking.
•
The blood pressure monitor must not be used in connec-
Advice on use
tion with a high-frequency surgical unit.
•
Only use the device on people who have the specified
•
In order to ensure comparable values, always measure
upper arm measurement for the device.
your blood pressure at the same time of day.
•
Please note that when inflating, the functions of the limb
•
Before every measurement, relax for about five minutes.
in question may be impaired.
•
If you want to perform several measurements on the same
person, wait five minutes between each measurement.
18

•
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 fur-
– Only ever use the cuffs provided with the monitor or
ther 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.
19

•
Batteries should not be charged or reactivated with any
please contact the municipal authorities responsible for
other means, nor should they be taken apart, thrown in
waste disposal in your area.
the fire or short-circuited.
3. Unit description
•
Remove the batteries from the instrument if they are worn
1
4
out or if you are not going to use the instrument for any
3
length of time. This prevents any damage as a result of
leakage. Always replace all the batteries at the same time.
2
11
10
•
Never use different types of battery, battery brands or
batteries with different capacities. You should preferably
7
use alkaline batteries.
Repair and disposal
•
Batteries do not belong in domestic refuse. Used batter-
ies should be disposed of at the collection points pro-
8
MEM
9
vided.
•
Never open the instrument. If these instructions are not
heeded, the warranty will be null and void.
1. Cuff tube
•
Never attempt to repair the instrument or adjust it yourself.
2. Cuff
We can no longer guarantee perfect functioning if you do.
3. Cuff connector
4
O
F
F
•
Repairs may only be performed by Beurer Customer Ser-
4. Touch screen activation
O
N
vice or authorized dealers. However, always check the
switch
5
batteries and replace them if necessary prior to making
5. USB interface
any complaint.
6. Cuff holder
6
•
The appliance should be disposed of according to
7. Cuff connector port (left side)
Regulation 2002/96/EC-WEEE (Waste Electrical
8. Memory button MEM
and Electronic Equipment). In case of queries,
9. START/STOP button
20

10. Mains part port
7. WHO classification
11. Display
8. “Change battery” icon
9. Arrhythmia recognition
Touch screen activation switch
The device features a touch screen display. To prevent the
PC interface
screen from being activated accidentally, keep the touch
The Beurer blood pressure monitor also allows you to trans-
screen activation switch set to OFF when the device is not
fer your measured values to the PC.
in use. To operate the device, move the touch screen activa-
To do this you require a USB cable (included in delivery) and
tion switch to ON. When the touch screen display is touched
the Beurer “Health Manager” PC software.
(START/STOP button or MEM button), a beep is output.
The software can be downloaded free of charge from the
Tip: You can switch off the device at any time by setting the
download area under Service at www.beurer.com.
touch screen activation switch to the OFF position.
System requirements for the Beurer “Health Manager”
Cuff holder
computer software
Thanks to the cuff holder on the underside of the device,
1. Supported operating systems:
you have the option of conveniently storing the cuff. To do
•
Windows XP SP3
so, push out the cuff holder with both thumbs until it locks
•
Windows Vista SP1 or later
into place (see also Chapter: Inserting battery).
•
Windows 7
•
Windows 7 SP1
Icons in the display:
9 1
•
Windows 8
1. Time and date
8
2. Systolic pressure
2. Supported architectures:
2
3. Diastolic pressure
•
x86 (32 bit)
4. Measured pulse
7
•
x64 (64 bit)
5. Release air (arrow)
3
3. Hardware requirements:
6.
Memory display, average value ( ),
•
Recommended: at least Pentium 1 GHz or faster with at
6
4
morning ( ), evening ( )
least 1 GB RAM
5
21

•
Free memory on the primary partition of at least:
them via your specialist electrical supplier or local collec ting
– x86 – 600 MB
point for recyclable waste.
– x64 – 1.5 GB
Note: Batteries containing pollutant substances
•
Graphic resolution from: 1024 x 768 pixels
are marked as follows: Pb = Battery contains
•
USB port 1.0 or later
lead, Cd = Battery contains cadmium,
Hg = Battery contains mercury.
4. Prepare measurement
Setting date and time
Inserting battery
You should set the date and time without fail. Otherwise,
•
Push the cuff holder
you will not be able to save your measured values correctly
upwards at the rear of the
with a date and time and to access them again later.
device until it locks into
Tip: If you press and hold the MEM button, you can set the
place.
values more quickly.
•
Open the battery com-
partment lid.
To set the date and time, proceed as follows:
•
Insert four AA 1.5 V alka-
•
Move the touch screen activation switch to the ON posi-
line batteries. making absolutely sure that you insert them
tion.
with the correct polarity as marked. Never use recharge-
•
Press the START/STOP and MEM buttons simultane-
able batteries.
ously, 24h begins to flash. Select 12h or 24h mode using
•
Replace the battery cover carefully.
the MEM button. Press START/STOP to confirm your
selection. The year display will start to flash. Set the year
If the battery change
is continuously illuminated,
with the MEM button and confirm with START/STOP .
measurement is no longer possible and you must replace all
•
Then set the month, day, hour and minutes and confirm
the batteries. Once batteries have been removed from the
each setting with START/STOP .
device, the time must be reset.
•
Pressing the START/STOP button again will switch the
Used batteries do not belong in the household waste. You
display off.
are legally obliged to dispose of the batteries. Dispose of
22

Note: In 24h mode, the date is displayed as day/month. In
5. Measuring blood pressure
12h mode, as month/day.
Please ensure the device is at room temperature before
Operation with the mains part
measuring.
You can also operate this device with a mains part.
Positioning cuff
When doing so, there must not be any batteries in the bat-
Fit the cuff round your bare left
tery compartment. The mains part can be obtained from
upper arm. Blood circulation in the
specialist retailers or from the service address using order
arm should not be restricted by
number 071.60.
tight clothing or other objects.
•
To prevent possible damage to the device, the blood
pressure monitor must only be used with the mains part
described here.
The cuff should be placed on the
•
Insert the mains part into the connection provided for
upper arm so that the lower edge
this purpose on the right-hand side of the blood pressure
is 2 to 3 cm above the bend of the
monitor. The mains part must only be connected to the
elbow and above the artery. The
mains voltage that is specified on the type plate.
tube should be in line with the
•
Then insert the mains plug of the mains part into the
centre of the palm.
mains socket.
Now place the free end of the cuff
•
After using the blood pressure monitor, unplug the mains
snugly, but not too tightly, around
part from the mains socket first and then disconnect it
the arm, and fix it with the Velcro
from the blood pressure monitor. As soon as you unplug
fastener. The cuff should be fitted
the mains part, the blood pressure monitor loses the date
tight enough to allow just two
and time setting but the saved measurements are retai-
fingers to fit beneath the cuff.
ned.
23

Insert the cuff tubing into the socket
ing on something. Do not cross your legs. Place your feet
for the cuff attachment.
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
Important: The instrument should only be operated with the
•
Move the touch screen activation switch to the ON position.
original cuff. The cuff is suitable for an arm circumference
•
Put on the cuff as described previously and assume the
of 22 to 30 cm. A larger cuff for upper arm circumferences
position in which you want to carry out the measurement.
from 30 to 42 cm is available from retailers or the service
•
Switch on the blood pressure monitor with the START/
address under order no. 163.246.
STOP button
. After the full-screen display, the most
recently used user memory appears (
or ). To change
Correct posture
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 .
•
Rest for approx. 5 minutes before each measurement.
•
The cuff automatically inflates. Cuff air pressure is
Otherwise there may be divergences.
released slowly. If a tendency towards high blood pres-
•
You can perform the measurement either sitting or lying
sure is already detectable, the cuff is pumped up again
down. Always make sure that the cuff is on a level with
and cuff pressure increased further. As soon as a heart
your heart.
rate is detected, the heart rate symbol is displayed.
•
To carry out a blood pressure measurement, make sure
•
Heart rate, systolic and diastolic blood pressure are dis-
you are sitting comfortably with your arms and back lean-
played.
24

•
You can cancel the measurement at any time by press-
sive use of stimulants, stress or lack of sleep. Arrhythmia can
ing the START/STOP button or by pushing the touch
only be ascertained through examination by your doctor.
screen activation button to OFF.
Repeat the measurement if the flashing icon is dis-
•
_ appears if it has not been possible to perform the
played after the measurement. Please note that you should
measurement properly. Observe the section in these
rest for 5 minutes between measurements and not talk or
instructions on error messages/troubleshooting and
move during the measurement. If the icon
appears
repeat the measurement.
often, please contact your doctor. Any self-diagnosis and
•
The test result is saved automatically.
treatment based on the test results may be dangerous. It is
•
To switch off the device, press the START/STOP button
vital to follow your doctor’s instructions.
or push the touch screen activation switch to OFF. If
WHO classification:
you forget to switch off the device, it switches off auto-
In accordance with the guidelines/definitions of the World
matically after approx. 1 minute.
Heath Organization and the latest findings, the measure-
Wait at least 5 minutes before taking another measurement!
ments can be classified and assessed according to the fol-
lowing table.
6. Evaluating results
However, these standard values serve only as a general
Cardiac arrhythmia:
guideline, as the individual blood pressure varies in different
This instrument can identify possible cardiac arrhythmia dis-
people and different age groups etc.
orders during measurement and if necessary indicates the
It is important to consult your doctor regularly for advice.
measurement with the flashing icon
.
Your doctor will tell you your individual values for normal
This may be an indicator for arrhythmia. Arrhythmia is a
blood pressure as well as the value above which your blood
condition where the heart rhythm is abnormal as a result of
pressure is classified as dangerous.
defects in the bioelectrical system controlling the heart beat.
The WHO classification in the display shows the range of
The symptoms (omitted or premature heart beats, slow or
the measured blood pressure.
excessively fast heart rate) may be caused, among other
If the values for systolic and diastolic pressure are in two
things, by heart disease, age, physical predisposition, exces-
different WHO ranges (e.g. systolic in the grade hyperten-
sion range and diastolic pressure in the normal range), the
25

WHO classification on the unit always indicates the higher
measured data, the earliest items of data measured are
range (grade hypertension in the example described).
lost.
•
Move the touch screen activation switch to the ON posi-
Range of
Systolic
Diastolic
Measure
tion.
blood pressure
(in mmHg)
(in mmHg)
•
Make a selection with the MEM button, and then confirm
values
the desired user memory with the START/STOP button .
Grade 3: Severe
≥ 180 ≥ 110 Seek medical
If you press the MEM button again, the average value of
hypertension
advice
all the stored measured values in the user memory will be
Grade 2: Mode-
160 – 179 100 – 109 Seek medical
displayed. If you press the MEM button again, the aver-
rate hyperten-
advice
age value of the last 7 days for the morning measurement
sion
will be displayed (Morning: 5 a.m. – 9 a.m., display ). If
Grade 1: Mild
140 – 159 90 – 99 Have it che-
you press the MEM button again, the average value of the
hypertension
cked regularly
last 7 days for the evening measurement will be displayed
by doctor
(Evening: 6 p.m. – 8 p.m., display ). If you continue to
press the MEM button, the most recent individual meas-
High-normal 130 – 139 85 – 89 Have it che-
ured values with date and time are displayed in turn.
cked regularly
•
You can delete the memory by pressing and holding the
by doctor
MEM button for 3 seconds. All the values in the current
Normal 120 – 129 80 – 84 Check it
user memory are deleted after three beeps are output.
yourself
•
To switch off the device, press the MEM button again or
Optimal < 120 < 80 Check it
the START/STOP button or push the touch screen acti-
yourself
vation switch to OFF.
Source: WHO, 1999
•
If you forget to switch off the device, it will switch off
automatically after 2 minutes.
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
26

8. Transferring measurements
• systolic or diastolic pressure was outside the measure-
ment range (
or Lo appears on the display)
Connect the blood pressure monitor to your PC using the
• the cuff is fastened too tightly or loosely (
or
USB cable.
appears on the display)
No data transfer may be launched whilst performing a
• the pump pressure is higher than 300 mmHg (
measurement.
appears on the display)
PC is shown on the display. Begin the data transfer
• pumping up takes longer than 160 seconds ( appears
in the “HealthManager” PC software. During the
on the display)
data transfer, an animation is shown on the
• there is a system or device error ( , , or
display. A successful data transfer is displayed
appears on the display)
as in figure 1. If the data transfer is unsuccessful,
• the batteries are almost empty .
an error message appears as in figure 2. In this
A
bb. 1
In such cases, repeat the measurement. Ensure you do not
case, interrupt the PC connection and start the
move or speak.
data transfer again.
If necessary, re-insert or replace the batteries.
After 30 seconds of not being in use or if com-
munication with the PC is interrupted, the blood
Technical alarm – description
pressure monitor switches itself off automati-
Should the recorded blood pressure (systolic or diastolic) lie
cally
.
outside the limits specified in the section “Technical speci-
fications”, the technical alarm will appear on the display
A
bb. 2
indicating either “
” or “Lo”. In such cases, you should seek
9. Error messages/trouble-shooting
medical assistance and check the accuracy of your proce-
In case of faults, the _ message appears in the display.
dure.
Error messages may appear if:
The limit values for the technical alarm are factory set and
• systolic or diastolic pressure could not be measured (
cannot be adjusted or deactivated. These alarm limit val-
or appears on the display)
ues are accorded second priority under the standard IEC
60601-1-8.
27

The technical alarm is a non-locking alarm and must not be
Measurement
Max. permissible standard deviation
reset. The signal shown on the display will disappear auto-
inaccuracy
according to clinical testing:
matically after about 8 seconds.
systolic 8 mmHg /diastolic 8 mmHg
10. Cleaning and storing the instrument
Memory 2 x 60 memory spaces
•
Clean your device and cuff carefully only with a slightly
Dimensions L 100 mm x W 150 mm x H 58 mm
moistened cloth.
Weight Approx. 364 g (without batteries)
•
Do not use detergents or solvents.
Cuff size 22 to 30 cm
•
On no account must you immerse the computer in water,
otherwise liquid can enter it and cause demage.
Permissible oper-
+5 °C to +40 °C, ≤ 90 % relative air
•
When storing the device, make sure that no heavy objects
ating conditions
humidity (non-condensing)
are placed on top of it. Remove the batteries. The cuff
Permissible
-20 °C to +55 °C, ≤ 95 % relative air
tube should not have any sharp kinks.
storage conditions
humidity, 800 –1050 hPa ambient pres-
sure
11. Specifications
Power supply
4 x 1,5 V
AA batteries
Model no. BM 58
Battery life For approx. 500 measurements,
Measurement
Oscillometric, non-invasive blood pres-
depending on the blood pressure level
method
sure measurement on the upper arm
and/or pump pressure
Measurement
Cuff pressure 0 – 300 mmHg,
Accessories
Cuff, instructions for use, 4 x 1.5 V AAA
range
systolic 60 – 260 mmHg,
batteries, USB cable, storage pouch
diastolic 40 –199 mmHg,
Classification Internal supply, IPX0, no AP or APG,
Pulse 40 –180 beats/minute
continuous operation, type BF applied
Display accuracy Systolic ± 3 mmHg, diastolic ± 3 mmHg,
part
pulse ± 5 % of the value shown
Technical information is subject to change without notifica-
tion to allow for updates.
28

•
This unit is in line with European Standard EN 60601-1-2
12. Mains part
and is subject to particular precautions with regard to
Model No. FW 7575M/EU/6/06
electromagnetic compatibility (EMC). Please note that
Input 100 – 240 V, 50 – 60 Hz
portable and mobile HF communication systems may
interfere with this unit. More details can be requested
Output 6 V DC, 600 mA, only in connection with
from the stated Customer Service address or found at the
beurer blood pressure monitor
end of the instructions for use.
Supplier Friwo Gerätebau GmbH
•
This device is in line with the EU Medical Devices Direc-
Protection This device is double insulated and pro-
tive 93/42/EC, the „Medizinproduktegesetz“ (German
tected against short circuit and over-
Medical Devices Act) and the standards EN1060-1
load by a primary thermal fuse.
(non-invasive sphygmomanometers, Part 1: General
Make sure to take the batteries out
requirements), EN1060-3 (non-invasive sphygmoma-
of the compartment before using the
nometers, Part 3: Supplementary requirements for elec-
mains part.
tro-mechanical blood pressure measuring systems)
and IEC80601-2-30 (Medical electrical equipment –
Double insulated / equipment class 2
Part 2 – 30: Particular requirements for the safety and
Polarity of the the DC voltage con-
essential performance of automated non-invasive blood
nection
pressure monitors).
Enclosures and
Equipment enclosed to protect against
•
The accuracy of this blood pressure monitor has been
Protective Covers
contact with live parts, and with parts
carefully checked and developed with regard to a long
which can become live (finger, pin,
useful life. If using the device for commercial medical pur-
hook test).
poses, it must be regularly tested for accuracy by appro-
The operator shall not contact the
priate means. Precise instructions for checking accuracy
patient and the output plug of mains
may be requested from the service address.
part simultaneously.
29






