BPU 22
Veroval
®
compact
Batteries
■
Choking hazard
Small children could swallow batteries and suffocate on them. Keep batteries out of the reach of
children!
■
Risk of explosion
Do not throw batteries into a fire.
■
Batteries must not be charged or short-circuited.
■
If a battery has leaked, wear protective gloves and clean the battery compartment with a dry
cloth. If liquid from a battery cell comes into contact with skin or eyes, clean the affected area
with water and seek medical attention if necessary.
■
Protect batteries from excessive heat.
■
Do not disassemble, open or crush batteries.
Safety information concerning the device
■
This blood pressure device is not waterproof!
■
This blood pressure device is made of high-quality electronic precision components. The accuracy of
the measured values and the lifetime of the device depend on careful handling.
■
Protect the device from strong shocks, impacts or vibrations and do not let it drop on the floor.
■
Do not excessively bend or kink the cuff or the air tube.
■
Never open the device. The device must not be modified, dismantled or repaired by the user. Repairs
may only be carried out by authorised specialists.
■
Never inflate the cuff when it is not properly applied to the upper arm.
■
Use the device only with the approved upper arm cuff. The device may otherwise sustain external or
internal damage.
■
The cuff tube may only be removed from the unit by pulling on the corresponding connector plug.
Never pull on the tube itself!
■
Do not expose the device to extreme temperatures, humidity, dust or direct sunlight because this may
cause it to malfunction.
■
Keep the packaging, batteries and device out of the reach of children.
■
Please comply with the storage and operating conditions defined in Chapter 11 ‘Technical data‘.
Storage or use outside the specified temperature and humidity range can affect the accuracy of the
measurement or the function of the device.
■
Do not use the device near strong electromagnetic fields and keep away from radio equipment or
mobile phones. Portable and mobile high-frequency and communication devices, such as telephones
and mobile phones, can impair the functionality of this electronic medical device.
Notes on electromagnetic compatibility
■
The device is suitable for use in all environments listed in these instructions for use, including
domestic environments.
■
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 device in the manner stated,
this device as well as the other devices must be monitored to ensure they are working properly.
■
The use of accessories 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 performance of the device.
Instructions for the measurement function check
Every Veroval
®
device has been carefully tested by HARTMANN for measurement accuracy and has been
developed with a view to a long service life. We recommend carrying out a metrological check every
2 years for
devices in professional use
, for example, in pharmacies, medical practices or hospitals.
Please also observe the national regulations specified by the legislator. Metrological checks may only
be carried out by the competent authorities or authorised maintenance providers against cost
reimbursement.
Disposal information
■
To protect our environment, empty batteries must not be disposed of in household waste. Please
comply with the relevant waste disposal regulations or use public collection points.
■
This product is subject to the European Directive 2012/19/EU on Used Electrical and Electronic
Equipment and is marked accordingly. Never dispose of electronic equipment in your
household waste. Please learn about your local regulations on the proper disposal of
electrical and electronic products. Proper disposal protects the environment and human
health.
3. Blood pressure information
To determine your blood pressure you need to measure two values:
■
SYS – Systolic (upper) blood pressure, which is produced when the heart contracts and pumps blood
into the blood vessels.
■
DIA – Diastolic (lower) blood pressure, which is the value measured when the heart muscle is dila-
ted and fills again with blood.
■
Blood pressure values are displayed in mmHg.
So that you can understand your results more easily, a traffic-light system is available on the left side of
the Veroval
®
BPU 22 that directly indicates the result, making it easier to categorise the measured value.
The World Health Organisation (WHO) and the European Society of Cardiology (ESC) & European Society of
Hypertension (ESH) have developed the following summary for classifying blood pressure values:
Results
indicator
Evaluation
Systolic pressure
Diastolic
pressure
Red
Grade 3 hypertension
above 179 mmHg
and/or
above 109 mmHg
Orange
Grade 2 hypertension
160 – 179 mmHg
and/or
100 – 109 mmHg
Yellow
Grade 1 hypertension
140 – 159 mmHg
and/or
90 – 99 mmHg
Green
High normal
130 – 139 mmHg
and/or
85 – 89 mmHg
Green
Normal
120 – 129 mmHg
and/or
80 – 84 mmHg
Green
Optimal
up to 119 mmHg
and
up to 79 mmHg
Classification of Office Blood Pressure and definition of Hypertension Grade
(Source: 2018 ESC/ESH Guidelines)
4. Preparing the measurement
Inserting/changing the batteries
■
Open the battery cover on the underside of the device. Insert the batteries (see Chapter 11
‘Technical data’). Ensure correct polarity (‘+’ and ‘–’) when inserting batteries. Close the battery lid.
or
flashes on the display. Set date and time as described below.
■
If the ‘Change battery’ symbol
is permanently illuminated, blood pressure can no longer be
measured and you must replace all the batteries.
Setting the date and time
Be sure to set the date and time correctly. This is the only way to save your measured values
correctly with date and time for subsequent retrieval.
■
To switch to setting mode, reinsert the batteries or hold the START/ STOP button down for 5
seconds. Proceed as follows:
Hours
The hour format flashes on the display.
• Select the desired hour format using the Save buttons / and confirm using
the START / STOP button .
Date
The display shows the year (a), the month (b) and the day (c).
• Depending on the display, use the Save buttons / to select the year,
the month or the day and confirm using the START / STOP button .
If the 12-hour format is selected, the month is displayed before the day.
Time
The hour (d) and the minutes (e) flash consecutively on the display.
• Depending on the display, use the Save buttons / to select the current
hour or minutes and confirm using the START / STOP button .
The device switches off automatically once all data has been set.
5. Measuring your blood pressure
Application of the cuff
■
Before applying the cuff, insert the cuff socket into the connector socket on the left side of the
device.
■
Do not mechanically constrict, compress or bend the sleeve tube.
■
The blood pressure must be measured on a bare upper arm. If the cuff is completely open, thread
the end of the cuff through the metal ring to form a loop (see Fig. 1). Position the cuff on the upper
arm so that the lower edge is 2-3 cm above the crook of the arm and above the artery (see Fig. 2).
The tube points to the centre of the palm.
Fig. 1
Fig. 2
■
Now bend your arm slightly, grasp the free end of the cuff, wrap it firmly round your arm and close
the hook-and-loop fastener.
The cuff should fit securely but not tightly. You should be able to insert
two fingers between the arm and the cuff. Make sure the tube is not bent
or damaged.
Important: It is essential that the cuff is correctly applied to obtain correct measurements.
The cuff included with the device is a universal cuff for upper arm circumferences of 22 cm
to 42 cm. The white arrow must point to an area within the sizing scale. If it is outside the
range, it is not possible to guarantee a correct measurement result.
This innovative Veroval
®
device with Comfort Air Technology ensures comfortable
measurement. The individual inflation pressure is determined independently for each
measurement and depends on the corresponding systolic blood pressure value. This allows for
more comfortable upper arm measurements.
Carrying out the measurement
■
Rest for approx. 5 minutes before measurement.
■
You should take your blood pressure in a quiet place, in a relaxed and comfortable seated position.
■
Measurement can be taken on the right or left arm. We recommend you perform the measurement
on the left upper arm. Over the long term, the arm giving higher readings should be used for blood
pressure monitoring. However, if there is a very clear difference between readings on either arm, you
need to check with your doctor which arm you should use for the measurement.
■
Always measure on the same arm and place your forearm in a relaxed position on a support.
■
We recommend that you measure your blood pressure while sitting with your back supported by the
back of the chair. Place both feet flat on the floor next to each other. Do not cross your legs. Relax
your forearm and hand with your palm facing upwards on a support and make sure the cuff is at
the height of your heart.
■
Always take measurements at the same time of day. Only regular measurements taken at the same
time each day over a longer period of time give a meaningful assessment of blood pressure values.
■
Do not measure when you have a strong urge to urinate. A full bladder can increase blood pressure
by about 10 mmHg.
■
Do not take your blood pressure after taking a bath or playing sport.
■
Do not eat, drink or exercise for at least 30 minutes before the measurement.
■
Please wait for at least one minute between two measurements.
■
Start a measurement only after applying the cuff. Press the START/ STOP button . The appearance
of all display segments followed by the time and date indicates that the device is carrying out its
self-test and is ready for use.
■
Check the display segments for completion (see Chapter 1).
■
After about 0,5 seconds the cuff will automatically inflate. If this inflation pressure is insufficient or
if the measurement is interrupted, the device continues to pump in increments of 40 mmHg until a
high enough pressure is reached. During inflation, the results indicator on the left also increases at
the same time.
(a)
(b)
(c)
(d)
(e)
Operating mode
Continuous mode
Nominal voltage
DC 6V
Power supply
4× 1.5 V alkaline manganese (AA/LR06) batteries
Expected service life
20,000 measurements
Battery capacity
Approx. 1,000 measurements
Protection against electric
shock
Medical-electrical equipment with internal power supply (only when
batteries are used); applied part: type BF
Protection against harmful
ingress of water or solid
materials
IP21 (not protected against moisture)
Inflation pressure
Comfort Air Technology:
Individual inflation pressure depends on systolic blood pressure
Automatic switch-off
function
1 minute after measurement/otherwise 30 sec.
Cuff
Veroval
®
cuff for BPU 22, cuff for arm circumference of 22 to 42 cm
Model number: 30601
Memory capacity
2 × 100 measurements with average of all measurements and morning/
evening average of the last 7 days
Operating conditions
Ambient temperature: +10 °C to +40 °C
Relative humidity: <90 %, non-condensing
Air pressure: 800 hPa – 1050 hPa
Storage/transport
conditions
Ambient temperature: –20 °C to +55 °C
Relative humidity: <90 %, non-condensing
Serial number
inside the battery compartment
Reference to standards
IEC 60601-1; IEC 60601-1-2 (In accordance with CISPR11,
IEC 61000-4-2, IEC 61000-4-3, IEC 61000-4-8)
Weight
Approx. 220 g (without batteries)
Dimensions
Approx. 134(L) x 48(W) x 91(H) mm
Legal requirements and guidelines
■
The Veroval BPU 22 conforms to the European regulations, which are based on the European
Medical Device Directive 93/42/EEC, and bears the CE mark.
■
The device complies, for example, with the European standard EN 1060: Non-invasive
sphygmomanometers – Part 3: Additional requirements for electro-mechanical blood pressure
measuring systems and the standard IEC 80601-2-30.
■
Clinical testing of measuring accuracy was performed in accordance with the European Standard
EN 1060-4.
■
Beyond statutory requirements, the device has been clinically validated by the ESH-IP2 Protocol of
the European Society of Hypertension (ESH) and the protocol of the German society of hypertension
(DHL).
Subject to errors and changes
Upper arm blood pressure monitor
EN
Dear customer
We are pleased that you have chosen to buy a blood pressure monitor from HARTMANN.
The Veroval
®
BPU 22 is a quality product for fully automatic blood pressure measurement on the upper arm
of adults and is suitable for clinical and domestic use. Requiring no preliminary settings, this blood pressure
monitor easily and automatically inflates for simple, quick and reliable measurement of the systolic and
diastolic blood pressure and the pulse rate. The monitor also indicates if it detects an irregular heartbeat.
We wish you all the best for your health.
Please read these instructions for use carefully before using the device the first time because
correctly measuring your blood pressure depends on appropriate handling of the device.
These instructions for use are designed to teach you each step for self-measurement of
blood pressure using the Veroval
®
BPU 22. You will be given important and useful hints to
ensure that you obtain reliable results for your personal blood pressure profile. Use this device in
accordance with the information provided in the instructions for use. Please store these instructions
carefully and ensure other users can access them. Check that the outside of the package is undamaged
and that the contents are complete.
Package contents:
• Blood pressure monitor
• Universal upper arm cuff
• 4× 1.5 V AA batteries
• Storage bag
• Instructions for use with warranty certificate
1. Device and display description
Blood pressure monitor
1 Extra large LCD display
2 START/STOP button
3 Memory button for User 1
4 Memory button for User 2
5 Cuff connector socket
6 Battery compartment
Cuff
7 Cuff with application instructions
8 Size indicator to correctly fit cuff
9 Cuff plug
10 Cuff tube
Display
11 Systolic blood pressure
12 Diastolic blood pressure
13 Pulse rate
14 Flashes when the device is measuring
and the pulse rate is detected
15 Irregular heartbeat
16 Display to check the fit of the cuff
17 Battery symbol
18 Traffic light system for your values
19 Average value (A), morning (AM), evening (PM) /
memory allocation number
20 User memory
21 Date and time display
2. Important information
Signs and symbols
The following symbols are used in the operating instructions, on the packaging and on the type plate of
the device and accessories:
Labelling in accordance with Medical Devices Directive 93/42/EEC
Manufacturer
Authorised representative in the European Community
Batch code
Catalogue number
SN
Serial number
Follow instructions for use
Caution (Please note)
Temperature limit
Humidity limitation
Protection against electric shock
(type BF)
Direct current
Protected against solid objects with a diameter of ≥12.5 mm and against
vertically falling drops of water
Symbol for the marking of electrical and electronic equipment
Dispose of packaging in an environmentally responsible way
Cardboard recycling code
Important instructions for use
■
Only use the device to take blood pressure measurements on the upper arm. Do not place the cuff on
other areas of the body.
■
Use only the supplied cuff or an original replacement cuff. The measured values may otherwise be
incorrect.
■
Only use the device on persons whose upper arm circumference is within the range indicated for the
device.
■
If measured values are questionable, repeat the measurement.
■
Do not leave the device unattended near small children or persons who cannot operate it
themselves. There is a risk of strangulation if the cuff tube becomes wrapped around the neck.
Swallowing small parts that have detached from the device can also result in suffocation.
■
Do not under any circumstances carry out blood pressure measurements on newborns, babies or
toddlers.
■
Please do not place the cuff over a wound as this may cause further injuries.
■
Do not place the cuff on persons who have had a mastectomy.
■
Please note that the pressure build-up in the cuff can lead to temporary disruption of medical
devices being used at the same time on the same arm.
■
Do not use the blood pressure monitor together with a high frequency surgical device.
■
If an intravenous treatment is being carried out or a venous catheter is inserted in the arm, blood
pressure measurements can lead to injuries. Never use the cuff on the arm to which these
conditions apply.
■
The function of the arm on which the cuff is placed may become impaired during inflation.
■
If you are carrying out the measurement on another person, please ensure that using the blood
pressure monitor does not have a lasting negative effect on the blood circulation.
■
Taking measurements too often within a short time period as well as maintaining continuous
cuff pressure can disrupt the blood circulation and cause injuries. Please take a break between
measurements and do not bend or fold the air tube. If the monitor malfunctions, remove the cuff
from the arm.
■
Do not use the blood pressure monitor on patients with pre-eclampsia during pregnancy.
Important instructions for self-measurements
■
Even minor changes in internal and external factors (e.g. deep breathing, stimulants, talking,
excitement, environmental factors) can lead to fluctuations in blood pressure. This explains why
deviating values are often measured at the doctor or pharmacist.
■
Measurement results depend fundamentally on the measurement location and the position of the
patient (sitting, standing, reclining). They are also influenced by physical activity and physiological
preconditions of the patient, for example. For comparable values, carry out the measurement in the
same location and the same position.
■
Diseases of the cardiovascular system can lead to erroneous readings or lower the accuracy of the
measurement. The accuracy may also be affected if you have very low blood pressure, diabetes,
circulatory disorders and arrhythmias as well as chills or tremors.
Consult your doctor before measuring your own blood pressure if …
■
you are pregnant. Blood pressure may vary during pregnancy. Regular blood pressure monitoring
is particularly important if you have high blood pressure because elevated values may affect foetal
development. Check with your doctor in any case to find out if and when you should measure your
own blood pressure, especially if you suffer from pre-eclampsia.
■
you have diabetes, liver function disorders or narrowing of blood vessels (e.g. arteriosclerosis,
peripheral arterial occlusive disease) because deviating measurements may occur in such cases.
■
you have certain blood disorders (e.g. haemophilia) or severe circulatory disorders or are taking
blood-thinning drugs.
■
you wear a cardiac pacemaker because it may lead to deviating measured values. The blood pressure
monitor itself has no impact on a cardiac pacemaker. Please note that the pulse rate displayed is not
suitable for checking the frequency of cardiac pacemakers.
■
you tend to bruise easily and/or are sensitive to pressure pain.
■
you suffer from severe irregular heartbeat or cardiac arrhythmias. Because of the oscillometric
measurement method that is used, in some cases incorrect measured values are obtained or the
blood pressure cannot be measured.
■
If this symbol
appears often, it may indicate heart rhythm disorders (arrhythmias). If this is the
case, please consult your doctor. Severe heart rhythm disorders may sometimes produce false
measurements or lower the measurement accuracy. Please discuss with your doctor whether taking
your own blood pressure readings is suitable for you.
■
Your self-measured values are for your information only – they are not a substitute for a medical
examination! Discuss your measured values with your doctor and under no circumstances make your
own medical decisions based on these measurements (e.g. medications and their dosages)!
■
Measuring your own blood pressure is not a substitute for medical treatment! Do not interpret your
measured values by yourself and do not use them for self-prescribed treatment. Take measurements
based on the instructions of your doctor and trust his or her diagnosis. Take medications as
prescribed by your doctor and never change the dose on your own. Discuss the appropriate time to
measure your blood pressure with your doctor.
Handling batteries
■
Observe the polarity labels plus (+) and minus (-).
■
Only use high-quality batteries (see specification in Chapter 11 ‘Technical data’). If you use
low-quality batteries, we cannot guarantee the specified number of measurements.
■
Never mix old and new batteries or batteries from different manufacturers.
■
Remove empty batteries immediately.
■
Replace batteries if the battery symbol
remains illuminated.
■
Always replace all the batteries at the same time.
■
If the device remains unused for a longer period of time, you should remove the batteries to prevent
possible leakage.
5
6
10
9
8
7
1
2
5
3
4
11
17
18
19
21
20
12
13
14
15
16
Date of revision of the text: 2021-06-15
Made under the control of PAUL HARTMANN AG
Globalcare Medical Technology Co., Ltd.
7th Building, 39 Middle Industrial Main Road
European Industrial Zone, Xiaolan Town
528415 Zhongshan City, Guangdong Province
P.R.C.
Donawa Lifescience Consulting Srl
Piazza Albania, 10
00153 Rome
Italy
■
If the cuff has been applied securely enough on the arm, the cuff symbol appears
on the
display. If the cuff symbol does not appear in the display, the cuff has not been fitted securely
enough and the error message ‘
E3
’ appears on the display after a few seconds.
Important: Please do not speak or move during the measurement.
■
As the air pressure in the cuff decreases, the heart symbol
and the dropping pressure in the cuff
are shown on the display.
■
After the measurement is complete, the systolic and diastolic blood pressure as
well as the pulse rate (see Fig. 3) appear simultaneously.
■
In addition to the measured values, the time, date, the associated user memory or as well as
the associated memory numbers (e.g.
M
) appear. The measured value is automatically stored in the
displayed user memory. As long as the result of the measurement is displayed, you can assign values to
the corresponding user memory by pressing the or button. If you do not assign them, the
measured value is automatically stored in the displayed user memory. You can use the results
indicator on the left of the display to classify your measurement result (see table in Chapter 3
‘Blood pressure information’).
■
To switch off the device, press the START/STOP button , otherwise the device will automatically
switch off after 1 minute.
If you wish to stop the measurement for any reason, simply press the START/STOP button . The
cuff inflation or measurement is interrupted and the pressure is automatically released.
■
If this symbol
is shown in the display, the unit has detected an irregular heartbeat during the
measurement. However, the measurement may also have been disrupted by body movement or
speaking. It is best to repeat the measurement. If you see this symbol regularly when measuring your
blood pressure, we recommend that your doctor checks your heart rhythm.
6. Memory function
User memory
■
The Veroval
®
BPU 22 stores up to 100 measurements in each user memory. Once all memory slots
are occupied, the oldest value is deleted. Memory recall is activated by pressing the or button
when the device is switched off. For values saved in the first user memory, press the button, for
the second user memory press the button.
Average values
■
After selecting the particular user memory, the corresponding symbol or
and an
A
. appear on the display. The average value of all the data stored for the
particular user memory is displayed (see Fig. 4).
■
By pressing the button again (or button if you are in user memory 2), the
average values for all morning measurements ‘
AM
’ (5 am to 9 am) taken on the
last 7 days appear.
1
M
■
By pressing the button again (or button if you are in user memory 2) the
average values for all evening measurements ‘
PM
’ (6.00 pm to 8.00 pm) taken on
the last 7 days appear.
1
M
Individual measured values
■
By pressing the button again (or button, if you are in user memory 2), all
memory values can be retrieved one after the other, starting with the most recent
measured value.
1
M
■
If an irregular heartbeat was detected during measurement, that information
is also
stored and displayed when the measured value is retrieved from the device‘s memory
along with the systolic and diastolic blood pressure readings, pulse rate, time, date and
year.
■
You can cancel the memory recall at any time by pressing the START/STOP button .
Otherwise, the device will switch off automatically after a few seconds.
■
Even if the power supply is interrupted, e.g. when changing the batteries, the stored
values will still be available.
Deleting saved readings
All data saved for each user can be separately deleted for user memory and user memory . To do
so, press the button of the corresponding user memory ( or ). The average value will then appear
on the display.
Press and hold the user memory button for 5 seconds. ‘
CL 00
’ appears on the display. All data in the
selected user memory are now deleted. If you release the button ahead of time, no data will be deleted.
7. Explanation of error messages
Error that has
occurred
Possible causes
Remedy
Monitor cannot be
switched on
Batteries are missing, inserted
incorrectly or flat.
Check batteries and insert four
identical new batteries if necessary.
Cuff will not inflate
Cuff connector plug is incorrectly
positioned in the connector socket
of the monitor.
Check the connection between the
cuff connector plug and socket.
Wrong cuff type connected.
Verify that only an approved Veroval
®
cuff and connector are being used.
E I
Pulse could not be detected
correctly.
Check whether the cuff has been
applied correctly. Do not talk or move
during the measuring procedure.
E2
The pulse could not be detected.
Check whether the cuff has been
positioned correctly. Do not talk or
move during the measuring
procedure.
E3
The cuff was applied too firmly or
too loosely.
Apply the cuff so that two fingers fit
between the cuff and the upper arm.
Air tube is not correctly connected to
the monitor. Check that the connec-
tor plug is correctly positioned. If this
error occurs frequently, you should
use a new cuff.
E4
There was an error during the
measurement.
Please rest for at least 1 minute and
take the measurement again.
E5
Inflation pressure is higher than
300 mmHg.
Please rest for at least 1 minute and
take the measurement again.
E6
There is a system error.
Contact customer service if this error
message appears.
The batteries are almost empty.
Replace batteries.
Implausible measured
values
Implausible measured values often
occur due to inappropriate
handling of the device or mistakes
during the measuring procedure.
Please observe Chapter 5 ‘Measuring
your blood pressure’ as well as the
safety information. Then repeat the
measurement.
Switch the device off if an error symbol appears. Check for all possible causes and note the instructions
for self-measurement from Chapter 2 ‘Important information’. Relax for a minute and then take the
measurement again.
8. Device care
■
Only ever use a soft, damp cloth to clean the device. Please do not use thinner, alcohol, detergents
or solvents.
■
The cuff can be cleaned carefully using a slightly damp cloth and mild soap solution. Do not
completely immerse the cuff in water.
■
It is recommended to clean and disinfect the cuff regularly or after each use, especially when used
by several users, to prevent infection. The cuff should be disinfected, particularly on the inside, by
wiping with a disinfectant. Use a disinfectant that is compatible with the cuff materials, e.g. 75 %
ethanol or isopropyl alcohol. To protect from external influences, keep the device, the cuff and these
instructions in the storage bag.
■
If you store a device and cuff, do not place any heavy objects on the device and the cuff. Remove the
batteries.
9. Warranty conditions
■
We offer a 3-year warranty for this premium quality blood pressure monitor from the day of purchase
and in accordance with the conditions listed below.
■
Claims must be made during the warranty period. The date of purchase must be documented by an
appropriately completed and stamped warranty certificate or proof of purchase.
■
Within the warranty period, HARTMANN will replace or repair free of charge any faulty device
components caused by material faults or manufacturing errors. This does not extend the warranty
period.
■
The device is intended for the purpose described in this instruction manual only.
■
The warranty does not cover damage resulting from improper use or unauthorised interference.
Accessory parts that are subject to wear and tear (batteries, cuffs, etc.) are excluded from the
warranty. Claims for compensation are limited to the value of the merchandise; compensation for
consequential damage or injury is expressly excluded.
■
In warranty cases, please send the device with cuff together with the fully completed and stamped
warranty certificate or purchase receipt directly or via your dealer to the Customer Services
department for your country.
10. Contact details for customer queries
HK PAUL HARTMANN Asia-Pacific Ltd.
Suite 3102-3103, 31/F Manhattan Place
23 Wang Tai Road, Kowloon Bay,
Kowloon, Hong Kong
www.veroval.info
Tel: +852 2953-7100
Fax: +852 2796-7610
[email protected]
ZA
HARTMANN South Africa
Epsom Avenue, Northriding,
2169 Johannesburg
www.veroval.info
Tel. +27 860 4278 6266
[email protected]
11. Technical data
Model
Veroval
®
BPU 22
Type
GCE606
Measuring method
oscillometric
Display range
0 – 300 mmHg
Measuring range
Systolic (SYS): 50–280 mmHg
Diastolic (DIA): 30–200 mmHg
Pulse: 40–199 pulse beats per minute
Displaying of correct values outside the measuring range cannot be
guaranteed.
Display unit
1 mmHg
Technical
measuring accuracy
Cuff pressure: ±3 mmHg
Pulse: ±5 % of the displayed pulse rate
Clinical measuring
accuracy
Complies with the requirements of DIN EN 1060-4;
Korotkoff validation method: Phase I (SYS), Phase V (DIA)
1
M
Fig. 3
Fig. 4
1
M
Warranty certificate
BPU 22
Upper arm blood pressure monitor
Purchase date
Serial number (see battery compartment)
Reason for complaint
Dealer’s stamp
Veroval
®
compact
