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.

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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 EN1060-1

load by a primary thermal fuse.

(non-invasive sphygmomanometers, Part 1: General

Make sure to take the batteries out

requirements), EN1060-3 (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 IEC80601-2-30 (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