Instruction Manual 1

Automatic Upper Arm Blood Pressure Monitor

M7 Intelli IT (HEM-7361T-EBK)
X7 Smart (HEM-7361T-ESL)
EN
FR
DE
IT
Read Instruction manual and before use. ES
FR Lire le mode d’emploi et avant l’utilisation. NL
DE Lesen Sie vor der Verwendung Gebrauchsanweisung und .
IT Leggere il manuale di istruzioni e prima dell’uso. RU
ES Lea el manual de instrucciones y antes del uso. TR
NL Lees gebruiksaanwijzing en voor gebruik.
RU Прочтите руководства по эксплуатации и перед использованием. AR
TR Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun. Symbols
.‫قبل االستخدام‬ ‫و‬ ‫ اقرأ دليل اإلرشادات‬AR Symboles / Symbole / Simboli / Símbolos /
Symbolen / Символы / Semboller / ‫الرمز‬
 EN • DO NOT apply the arm cuff on your arm while on an intravenous drip or
blood transfusion.
• DO NOT use this monitor in areas containing high frequency (HF) surgical
1. Introduction equipment, magnetic resonance imaging (MRI) equipment, computerized
Thank you for purchasing the OMRON Automatic Upper Arm Blood Pressure
tomography (CT) scanners. This may result in incorrect operation of the
Monitor. This blood pressure monitor uses the oscillometric method of blood
monitor and/or cause an inaccurate reading.
pressure measurement. This means this monitor detects your blood movement
• DO NOT use this monitor in oxygen rich environments or near flammable gas.
through your brachial artery and converts the movements into a digital reading.
• Consult with your physician before using this monitor if you have common
1.1 Safety Instructions arrhythmias such as atrial or ventricular premature beats or atrial fibrillation;
This instruction manual provides you with important information about the arterial sclerosis; poor perfusion; diabetes; pregnancy; pre-eclampsia or renal
OMRON Automatic Upper Arm Blood Pressure Monitor. To ensure the safe disease. NOTE that any of these conditions in addition to patient motion,
and proper use of this monitor, READ and UNDERSTAND all of the safety and trembling, or shivering may affect the measurement reading.
operating instructions. If you do not understand these instructions or have • NEVER diagnose or treat yourself based on your readings. ALWAYS consult
any questions, contact your OMRON retail outlet or distributor before with your physician.
attempting to use this monitor. For specific information about your own • To help avoid strangulation, keep the air tube and AC adapter cable away
blood pressure, consult with your physician. from infants, toddlers and children.
• This product contains small parts that may cause a choking hazard if
1.2 Intended Use swallowed by infants, toddlers and children.
The device is a digital monitor intended for use in measuring blood pressure
and pulse rate in adult patient population. The device detects the appearance Data Transmission
of irregular heartbeats during measurement and gives a warning signal with • This product emits radio frequencies (RF) in the 2.4 GHz band. DO NOT use
readings. It is mainly designed for general household use. this product in locations where RF is restricted, such as on an aircraft or in
The device can detect an irregular pulse suggestive of Atrial Fibrillation (Afib). hospitals. Turn off the Bluetooth® feature in this monitor, remove batteries
Please note that the device is not intended to diagnose Afib. A diagnosis of Afib and/or unplug the AC adapter when in RF restricted areas.
can only be confirmed by Electrocardiogram (ECG). If the Afib symbol appears,
consult your physician. AC Adapter (optional accessory) Handling and Usage
1.3 Receiving and Inspection • DO NOT use the AC adapter if this monitor or the AC adapter cable is
Remove this monitor and other components from the packaging and inspect damaged. If this monitor or the cable is damaged, turn off the power and
for damage. If this monitor or any other components is damaged, DO NOT USE unplug the AC adapter immediately.
and consult with your OMRON retail outlet or distributor. • Plug the AC adapter into the appropriate voltage outlet. DO NOT use in a
multi-outlet plug.
2. Important Safety Information • NEVER plug in or unplug the AC adapter from the electric outlet with wet hands.
Read the Important Safety Information in this instruction manual before using • DO NOT disassemble or attempt to repair the AC adapter.
this monitor. Follow this instruction manual thoroughly for your safety.
Keep for future reference. For specific information about your own blood Battery Handling and Usage
pressure, CONSULT WITH YOUR PHYSICIAN. • Keep batteries out of the reach of infants, toddlers and children.

Indicates a potentially hazardous situation Indicates a potentially hazardous situation which, if

not avoided,may result in minor or moderate injury
2.1 Warning which, if not avoided, could result in death or 2.2 Caution to the user or patient, or cause damage to the
serious injury.
equipment or other property.
• DO NOT use this monitor on infants, toddlers, children or persons who • Stop using this monitor and consult with your physician if you experience
cannot express themselves. skin irritation or discomfort.
• DO NOT adjust medication based on readings from this blood pressure • Consult with your physician before using this monitor on an arm where
monitor. Take medication as prescribed by your physician. ONLY a physician intravascular access or therapy, or an arteriovenous (A-V) shunt, is present
is qualified to diagnose and treat high blood pressure and Afib. because of temporary interference to blood flow and could result in injury.
• DO NOT use this monitor on an injured arm or an arm under medical treatment. • Consult with your physician before using this monitor if you have had a mastectomy.
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• Consult with your physician before using this monitor if you have severe • To unplug the air plug, pull on the plastic air plug at the base of the tube, not
blood flow problems or blood disorders as cuff inflation can cause bruising. the tube itself.
• DO NOT take measurements more often than necessary because bruising, • ONLY use the AC adapter, arm cuff, batteries and accessories specified for
due to blood flow interference, may occur. this monitor. Use of unsupported AC adapters, arm cuffs and batteries may
• ONLY inflate the arm cuff when it is applied on your upper arm. damage and/or may be hazardous to this monitor.
• Remove the arm cuff if it does not start deflating during a measurement. • ONLY use the approved arm cuff for this monitor. Use of other arm cuffs may
• DO NOT use this monitor for any purpose other than measuring blood pressure result in incorrect readings.
and/or detecting the possibility of Afib. • Inflating to a higher pressure than necessary may result in bruising of the arm
• During measurement, make sure that no mobile device or any other where the cuff is applied. NOTE: refer to “If your systolic pressure is more than
electrical device that emit electromagnetic fields is within 30 cm of this 210 mmHg” in section 13 of instruction manual for additional information.
monitor. This may result in incorrect operation of the monitor and/or cause • Read and follow the “Correct Disposal of This Product” in section 7 when
an inaccurate reading. disposing of the device and any used accessories or optional parts.
• DO NOT disassemble or attempt to repair this monitor or other components.
This may cause an inaccurate reading.
Data Transmission
• DO NOT use in a location where there is moisture or a risk of water splashing • DO NOT replace batteries or unplug the AC adapter while your readings are
this monitor. This may damage this monitor. being transferred to your smart device. This may result in incorrect operation
• DO NOT use this monitor in a moving vehicle such as in a car or on an aircraft. of this monitor and failure to transfer your blood pressure data.
• DO NOT drop or subject this monitor to strong shocks or vibrations. AC Adapter (optional accessory) Handling and Usage
• DO NOT use this monitor in places with high or low humidity or high or low • Fully insert the AC adapter into the outlet.
temperatures. Refer to section 6. • When unplugging the AC adapter from the outlet, be sure to safely pull from
• During measurement, observe the arm to ensure that the monitor is not
causing prolonged impairment to blood circulation.
the AC adapter. DO NOT pull from the AC adapter cable.
• When handling the AC adapter cable: EN
• DO NOT use this monitor in high-use environments such as medical clinics or Do not damage it. / Do not break it. / Do not tamper with it. / DO NOT pinch
physician offices. it. / Do not forcibly bend or pull it. / Do not twist it. / DO NOT use it if it is
• DO NOT use this monitor with other medical electrical (ME) equipment gathered in a bundle. / DO NOT place it under heavy objects.
simultaneously. This may result in incorrect operation of the monitor and/or • Wipe any dust off of the AC adapter.
cause an inaccurate reading. • Unplug the AC adapter when not in use.
• Avoid bathing, drinking alcohol or caffeine, smoking, exercising and eating • Unplug the AC adapter before cleaning this monitor.
for at least 30 minutes before taking a measurement.
• Rest for at least 5 minutes before taking a measurement. Battery Handling and Usage
• Remove tight-fitting, thick clothing and any accessories from your arm while • DO NOT insert batteries with their polarities incorrectly aligned.
taking a measurement. • ONLY use 4 “AA” alkaline or manganese batteries with this monitor. DO NOT
• Remain still and DO NOT talk while taking a measurement. use other types of batteries. DO NOT use new and used batteries together.
• ONLY use the arm cuff on persons whose arm circumference is within the DO NOT use different brands of batteries together.
specified range of the cuff. • Remove batteries if this monitor will not be used for a long period of time.
• Ensure that this monitor has acclimated to room temperature before taking • If battery fluid should get in your eyes, immediately rinse with plenty of clean
a measurement. Taking a measurement after an extreme temperature water. Consult with your physician immediately.
change could lead to an inaccurate reading. OMRON recommends waiting
for approximately 2 hours for the monitor to warm up or cool down when
the monitor is used in an environment within the temperature specified
as operating conditions after it is stored either at the maximum or at the
minimum storage temperature. For additional information on operating and
storage / transport temperature, refer to section 6.
• DO NOT use this monitor after the durable period has ended. Refer to section 6.
• DO NOT crease the arm cuff or the air tube excessively.
• DO NOT fold or kink the air tube while taking a measurement. This may cause
an injury by interrupting blood flow.
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 • If battery fluid should get on your skin, wash your skin immediately with
plenty of clean, lukewarm water. If irritation, injury or pain persists, consult
with your physician.
• DO NOT use batteries after their expiration date.
• Periodically check batteries to ensure they are in good working condition.
2.3 General Precautions
• When you take a measurement on the right arm, the air tube should be at
the side of your elbow. Be careful not to rest your arm on the air tube.

• Blood pressure may differ between the right and left arm, and may result in a
different measurement value. Always use the same arm for measurements. If
the values between both arms differ substantially, check with your physician
on which arm to use for your measurements.
Battery Handling and Usage
• Disposal of used batteries should be carried out in accordance with local
regulations.

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•

3. Error Messages and Troubleshooting

If any of the below problems occur during measurement, check to make sure that no other electrical device is within 30 cm. If the problem persists, please refer to
the table below.
Display/Problem Possible Cause Solution

The [START/STOP] button was pressed Press the [START/STOP] button again to turn the monitor off.
while the arm cuff is not applied. After inserting the air plug securely and applying the arm cuff
correctly, press the [START/STOP] button.
Air plug is not completely plugged Insert the air plug securely.
appears or the arm into the monitor.
cuff does not inflate.
The arm cuff is not applied correctly. Apply the arm cuff correctly, then take another measurement.
Refer to section 7 of instruction manual .
Air is leaking from the arm cuff. Replace the arm cuff to the new one. Refer to section 14 of
instruction manual .
You move or talk during a measurement Remain still and do not talk during a measurement. If “E2”
appears or a and the arm cuff does not inflate
sufficiently.
appears repeatedly, inflate the arm cuff manually until the
systolic pressure is 30 to 40 mmHg above your previous
EN
measurement cannot
be completed after readings. Refer to section 13 of instruction manual .
Due to the systolic pressure is above
the arm cuff inflates. 210 mmHg, a measurement cannot be
taken.
The arm cuff is inflated exceeding the Do not touch the arm cuff and/or bend the air tube while
appears maximum allowable pressure. taking a measurement. If inflating the arm cuff manually, refer
to section 13 of instruction manual .
You move or talk during a measurement. Remain still and do not talk during a measurement.
appears Vibrations disrupt a measurement.

The pulse rate is not detected correctly. Apply the arm cuff correctly, then take another measurement.
appears Refer to section 7 of instruction manual . Remain still and
sit correctly during a measurement.
/ / If the “ ” symbol continues to appear, we recommend you
appears to consult with your physician.

does not flash during

a measurement

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 Display/Problem Possible Cause Solution
Blood pressure measurements were Apply the arm cuff correctly, then take another measurement.
not taken correctly in an Afib mode Refer to section 7 of instruction manual . Remain still and
appears
measurement. sit correctly during a measurement. Refer to section 8 of
instruction manual .
The monitor has malfunctioned. Press the [START/STOP] button again. If “Er” still appears,
appears contact your OMRON retail outlet or distributor.

The montior cannot connect to a smart Follow the instructions shown in the “OMRON connect” app. If
appears device or transmit data correctly. the “Err” symbol still appears after checking the app, contact
your OMRON retail outlet or distributor.

The monitor is waiting for pairing with Refer to section 5 of instruction manual for pairing your
flashes the smart device. monitor with your smart device, or press [START/STOP] button
to cancel pairing and turn your monitor off.
The monitor is ready to transfer your Open the “OMRON connect” app to transfer your readings.
flashes
readings to the smart device.
More than 80 readings are not Pair or transfer your readings to the “OMRON connect” app
flashes transferred. so you can keep them in memory in the app, and this error
symbol disappears.
The date and time is not set.

appears 100 readings are not transferred.

Batteries are low. Replacing all 4 batteries with new ones is recommended.
flashes
Refer to section 4 of instruction manual .
appears or the Batteries are depleted. Immediately replace all 4 batteries with new ones. Refer to
monitor is turned off section 4 of instruction manual .
unexpectedly during
a measurement

Nothing appears on the display

of the monitor. Battery polarities are not properly Check the battery installation for proper placement. Refer to
aligned. section 4 of instruction manual .
Readings appear too high or Blood pressure varies constantly. Many factors including stress, time of day, and/or how you apply the arm
too low. cuff, may affect your blood pressure. Review sections 2 of instruction manual .
Any other communication Follow the instructions shown in the smart device, or visit the “Help” section in the “OMRON connect” app
issue occurs. for further help. If the problem still persists, contact your OMRON retail outlet or distributor.
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 Display/Problem Possible Cause Solution
Press the [START/STOP] button to turn the monitor off, then press it again to take a measurement. If the
Any other problem occurs. problem continues, remove all batteries and wait for 30 seconds. Then re-install batteries. If the problem
still persists, contact your OMRON retail outlet or distributor.
Troubleshooting for Afib indicator function:
The Afib indicator function and ECG use completely different technologies. An ECG measures the electrical
What is different between the
activity of the heart and can be used to diagnose Afib. The Afib indicator function detects irregular
Afib indicator function and
heartbeat and can suggest the possibility of Afib with a sensitivity of 95.5% and specificity of 93.8%. Refer
ECG?
to section 11 for details.

If the “ ” symbol does not Even if the “ ” symbol does not appear, there is still a possibility of Afib.
appear, it means there is no
possibility of Afib?
Should I consult with my We recommend you to consult with your physician because there is a possibility of Afib. However, the “ ”
physician if the “ ” symbol symbol may be displayed for other reasons, such as other heart arrhythmias.
appears? EN
What is different between The irregular heartbeat function detects irregularities in the pulse waves in one measurement. The Afib
Afib indicator function and indicator function suggests the possibility of Afib when blood pressure is measured 3 consecutive times.
irregular heart beat function?

What should I do if the “ ” Afib does not always have symptoms. We recommend you to consult with and follow the directions of
your physician.
symbol sometimes appears?
I have been diagnosed with Afib may not occur at the time of specific blood pressure measurements. We recommend you to consult
Afib by the physician, but the with your physician regularly.
“ ” symbol does not appear.

Afib or an irregular heartbeat can influence your blood pressure measurements and make it difficult to get
Is the blood pressure reading an accurate reading. Repeated measurements may be required to overcome variabilities.* In Afib mode,
reliable when the “ ” the blood pressure measurement is taken 3 times, and the average is displayed. The monitor will indicate
symbol appears? an error message (E5/E6) if the influence of the irregular heartbeat is too severe to give a measurement
result. If this occurs repeatedly, we recommend that you consult with your physician.
* Prof. Roland Asmar et al. European Society of Hypertension Recommendations for Conventional, Ambulatory and Home Blood Pressure Measurement

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 4. Limited Warranty 5.2 Storage
• Keep your monitor in the storage case when not in use.
Thank you for buying an OMRON product. This product is constructed of high
1. Remove the arm cuff from the monitor.
quality materials and great care has been taken in its manufacturing. It is
designed to give you every satisfaction, provided that it is properly operated Caution
and maintained as described in the instruction manual.
To unplug the air plug, pull on the plastic air plug at the base of the tube, not
This product is warranted by OMRON for a period of 3 years after the date of
the tube itself.
purchase. The proper construction, workmanship and materials of this product
is warranted by OMRON. During this period of warranty OMRON will, without 2. Gently fold the air tube into the arm cuff. Note: Do not bend or crease the
air tube excessively.
charge for labour or parts, repair or replace the defect product or any defective
3. Place your monitor and other components in the storage case.
parts. • Store your monitor and other components in a clean, safe location.
The warranty does not cover any of the following: • Do not store your monitor and other components:
A. Transport costs and risks of transport. • If your monitor and other components are wet.
B. Costs for repairs and / or defects resulting from repairs done by unauthorised • In locations exposed to extreme temperatures, humidity, direct sunlight,
persons. dust or corrosive vapors such as bleach.
C. Periodic check-ups and maintenance. • In locations exposed to vibrations or shocks.
• To protect your monitor during storage, an optional LCD cover is available as
D. Failure or wear of optional parts or other attachments other than the main
accessory. Refer to section 15 of Instruction Manual .
device itself, unless explicitly warranted above.
E. Costs arising due to non-acceptance of a claim (those will be charged for). 5.3 Cleaning
F. Damages of any kind including personal caused accidentally or from misuse. • Do not use any abrasive or volatile cleaners.
G. Calibration service is not included within the warranty. • Use a soft dry cloth or a soft cloth moistened with mild (neutral) detergent to
clean your monitor and arm cuff, and then wipe them with a dry cloth.
H. Optional parts have a one (1) year warranty from date of purchase. Optional
• Do not wash or immerse your monitor and arm cuff or other components in
parts include, but are not limited to the following items: cuff and cuff tube. water.
Should warranty service be required please apply to the dealer whom the • Do not use gasoline, thinners or similar solvents to clean your monitor and
product was purchased from or an authorised OMRON distributor. For the arm cuff or other components.
address refer to the product packaging / literature or to your specialised
5.4 Calibration and Service
retailer. If you have difficulties in finding OMRON customer services, contact us
• The accuracy of this blood pressure monitor has been carefully tested and is
for information: designed for a long service life.
www.omron-healthcare.com • It is generally recommended to have the unit inspected every two years to
Repair or replacement under the warranty does not give rise to any extension ensure correct functioning and accuracy. Please consult your authorised
or renewal of the warranty period. OMRON dealer or the OMRON Customer Service at the address given on the
The warranty will be granted only if the complete product is returned together packaging or attached literature.
with the original invoice / cash ticket issued to the consumer by the retailer.

5. Maintenance
5.1 Maintenance
To protect your monitor from damage, follow the directions below:
Changes or modifications not approved by the manufacturer will void the user
warranty.

Caution
DO NOT disassemble or attempt to repair this monitor or other components.
This may cause an inaccurate reading.
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6. Specifications Battery life Approximately 1000 measurements
Product Category Electronic Sphygmomanometers (using new alkaline batteries)
The number of times may decrease when
Product description Automatic Upper Arm Blood Pressure using Afib mode because one Afib indication
Monitor consists of 3 regular measurements.

Model (Code) M7 Intelli IT (HEM-7361T-EBK) / Durable period (Service Monitor: 5 years / Cuff: 5 years /
X7 Smart (HEM-7361T-ESL) life) Optional AC adapter: 5 years

Display LCD digital display Operating conditions +10 to +40°C / 15 to 90% RH

(non-condensing) / 800 to 1060 hPa
Cuff pressure range 0 to 299 mmHg
Storage / Transport -20 to +60°C / 10 to 90% RH
Blood pressure SYS: 60 to 260 mmHg conditions (non-condensing)
measurement range DIA: 40 to 215 mmHg
Weight Monitor: approximately 460 g
Pulse measurement range 40 to 180 beats / min. (not including batteries)
Arm cuff: approximately 163 g
Accuracy Pressure: ±3 mmHg
Pulse: ±5% of display reading Dimensions Monitor: 191 mm (W) × 85 mm (H) ×
Inflation Automatic by electric pump
(approximately value) 120 mm (L) / Arm cuff:145 mm × EN
532 mm (air tube: 750 mm)
Deflation Automatic pressure release valve
Cuff circumference 220 to 420 mm
Measurement method Oscillometric method applicable to the monitor
Transmission method Bluetooth® Low Energy Memory Stores up to 100 readings per user
Wireless communication Frequency range: 2.4 GHz (2400 - Contents Monitor, arm cuff (HEM-FL31), 4 “AA”
2483.5 MHz) / Modulation: GFSK batteries, Instruction Manual and
Effective radiated power: < 20 dBm , setup instructions, storage case
Operation mode Continuous operation Protection against Internally powered ME equipment
electric shock (When using only batteries)
IP classification Monitor: IP20 Class II ME equipment (Optional AC
Optional AC adapter: IP21 adapter)
Rating DC6 V 4.0 W Applied part Type BF (arm cuff )
Power source 4 “AA” batteries 1.5 V or optional
AC adapter (INPUT AC 100 - 240 V Note
50/60 Hz 0.12 - 0.065 A) • These specifications are subject to change without notice.
• This monitor is clinically investigated according to the requirements of
ISO 81060-2:2013. In the clinical validation study, K5 was used on 85 subjects
for determination of diastolic blood pressure.
• This device has been validated for use on pregnant and pre-eclampsia patients
according to the Modified European Society of Hypertension Protocol*.
• This device has been validated for use on diabetic (Type II) population**. EN8
 • IP classification is degrees of protection provided by enclosures in • The full text of the EU declaration of conformity is available at the following
accordance with IEC 60529. This monitor and optional AC adapter are internet address: www.omron-healthcare.com
protected against solid foreign objects of 12.5 mm diameter and greater • This OMRON product is produced under the strict quality system of OMRON
such as a finger. The optional AC adapter is protected against vertically HEALTHCARE Co., Ltd., Japan. The Core component for OMRON blood
falling water drops which may cause issues during a normal operation. pressure monitors, which is the Pressure Sensor, is produced in Japan.
• Please report to the manufacturer and the competent authority of the
* Topouchian J et al. Vascular Health and Risk Management 2018:14 189–197
Member State in which you are established about any serious incident that
** Chahine M.N. et al. Medical Devices: Evidence and Research 2018:11 11–20
has occurred in relation to this device.
About a wireless communication interference
This product operates in an unlicensed ISM band at 2.4 GHz. In the event 10. How to Calculate Weekly Averages
this product is used near other wireless devices such as microwave and Morning Weekly Average Calculation
wireless LAN, which operate on the same frequency band as this product, This is the average for the measurements taken during the morning (4:00 - 9:59)
there is a possibility that interference may occur. If interference occurs, stop between Sunday and Saturday. The 2 or 3 readings taken within the first
the operation of the other devices or relocate this product away from other 10 minute timeframe in the morning between 4:00 - 9:59 will be used to
wireless devices before attempting to use it. calculate the morning average for each day.
7. Correct Disposal of This Product (Waste Evening Weekly Average Calculation
Electrical & Electronic Equipment) This is the average for the measurements taken during the evening (19:00 - 1:59)
This marking shown on the product or its literature, indicates that between Sunday and Saturday. The 2 or 3 readings taken within the last
it should not be disposed of, with other household wastes at the 10 minute timeframe in the evening between 19:00 - 1:59 will be used to
end of its working life. calculate the evening average for each day.
To prevent possible harm to the environment or human health
from uncontrolled waste disposal, please separate this product
Within 10 min. Within 10 min.
from other types of wastes and recycle it responsibly to promote
the sustainable reuse of material resources.
Household users should contact either the retailer where they purchased this
product, or their local government office, for details of where and how they can
return this item for environmentally safe recycling.
Business users should contact their supplier and check the terms and
conditions of the purchase contract. This product should not be mixed with
other commercial waste for disposal. Measurements Measurements
8. Important Information regarding in the morning in the morning
Electromagnetic Compatibility (EMC)
HEM-7361T-EBK/ESL conforms to the EN60601-1-2:2015 Electromagnetic
Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at
OMRON HEALTHCARE EUROPE at the address mentioned in this instruction
manual or at: www.omron-healthcare.com.

9. Guidance and Manufacturer’s Declaration

• This blood pressure monitor is designed according to the European Standard
EN1060, Non-invasive sphygmomanometers Part 1: General Requirements
and Part 3: Supplementary requirements for electromechanical blood
pressure measuring systems.
• Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipments
type HEM-7361T-EBK/ESL is in compliance with Directive 2014/53/EU.
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11. Useful Information
What is Blood Pressure?
Blood pressure is a measure of the force of blood flowing against the walls of
the arteries. Arterial blood pressure is constantly changing during the course of
the heart’s cycle.
The highest pressure in the cycle is called the Systolic Blood Pressure; the lowest
is the Diastolic Blood Pressure. Both pressures, the Systolic and Diastolic, are
necessary to enable a physician to evaluate the status of a patient’s blood pressure.

What is Arrhythmia?
Arrhythmia is a condition where the heartbeat rhythm is abnormal due to flaws in
the bio-electrical system that drives the heartbeat. Typical symptoms are skipped
heartbeats, premature contraction, an abnormally rapid (tachycardia) or slow
(bradycardia) pulse.

What is Afib?
Atrial fibrillation (also called AFib or AF) is a quivering or irregular heartbeat
(arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-
related complications. During atrial fibrillation, the heart’s two upper chambers (the
atria) beat chaotically and irregularly — out of coordination with the two lower
chambers (the ventricles) of the heart. Episodes of atrial fibrillation can come and EN
go, or you may develop atrial fibrillation that doesn’t go away and may require
treatment.
Afib indicator function detects the possibility of Afib with an accuracy of 94.2%
(with sensitivity of 95.5% and specificity of 93.8%) as demonstrated in the study*
with Single-lead ECG as reference measurement.
*M. Ishizawa, T. Noma, T. Minamino et al., Multiple measurements with
automated blood pressure monitor can detect atrial fibrillation with high
sensitivity and specificity in general cardiac patients, ESC Congress 2018

EN10
 Symbols Description IP XX Ingress protection degree provided by IEC 60529
FR Description des symboles NL Beschrijving van symbolen FR Degré de protection selon NL Beschermingsklasse
DE Beschreibung der Symbole RU Описание символов CEI 60529 volgens IEC 60529
IT Descrizione dei simboli TR Simgelerin Açıklaması DE Grad des Eindringschutzes RU Степень защиты,
ES Descripción de los símbolos ‫ وصف الرموز‬AR gemäß IEC 60529 обеспечиваемая

Applied part - Type BF Degree of protection against IT Livello di protezione IP in оболочкой, в

base a IEC 60529 соответствии со
electric shock (leakage current)
ES Grado de protección según стандартом IEC 60529
FR Partie appliquée - Type BF NL Toegepast
Degré de protection contre onderdeel - Type BF-
la norma internacional TR Su girmesine karşı koruma
IEC 60529 derecesi IEC 60529
les chocs électriques beschermingsgraad tegen
tarafından verilmiştir
(courant de fuite) elektrische schokken
‫ درجة الحماية من التسرب وف ًقا‬AR
DE Anwendungsteil – Typ BF (lekstroom)
IEC 60529 ‫لمعيار‬
Schutz vor Stromschlägen RU Рабочая часть аппарата
(Ableitstrom) - Тип BF Степень CE Marking
IT Parti applicate - Tipo BF защиты от поражения FR Marquage CE NL CE-merkteken
Livello di protezione contro электрическим током DE CE-Kennzeichnung RU Знак соответствия
le folgorazioni (corrente di (токи утечки) IT Contrassegno CE директиве ЕС
dispersione) TR Uygulanan parça - Tip BF ES Marcado CE TR CE İşareti
ES Partes en contacto: Tipo Elektrik çarpmasına karşı ‫ عالمة التوافق مع اللجنة األوروبية‬AR
BF Grado de protección koruma derecesi (kaçak )CE(
contra descargas eléctricas akım) Serial number
(corriente de fuga) ‫ درجة‬- BF ‫ جزء مطبق من النوع‬AR FR Numéro de série NL Serienummer
‫الحماية ضد الصدمات الكهربائية‬ DE Seriennummer RU Серийный номер
)‫(التيار المتسرب‬ IT Numero di serie TR Seri numarası
Class II equipment. Protection against electric shock ES Número de serie ‫ الرقم المتسلسل‬AR
FR Équipement de classe II. NL Apparatuur van Klasse II. LOT number
Protection contre les chocs Bescherming tegen FR Numéro de LOT NL Partijnummer
électriques elektrische schokken DE LOT-Nummer RU Номер ПАРТИИ
DE Gerät der Klasse II. Schutz RU Оборудование класса II. IT Numero di lotto TR Parti numarası
vor Stromschlägen Защита от поражения ES Número de lote ‫ رقم التشغيلة‬AR
IT Apparecchiatura di электрическим током Medical device
Classe II. Protezione contro TR Sınıf II ekipman. Elektrik
FR Dispositif médical NL Medisch apparaat
le folgorazioni çarpmasına karşı koruma
DE Medizinprodukt RU Медицинский прибор
ES Equipo de Clase II. ‫ الحماية ضد‬.II ‫ جهاز من الفئة‬AR IT Dispositivo medico TR Tıbbi cihaz
Protección contra ‫الصدمات الكهربائية‬ ‫ جهاز طبي‬AR
ES Producto sanitario
descargas eléctricas
SD1
Indicates the manufacturer’s catalogue number Indication of connector polarity
FR Indique le numéro de NL Geeft het FR Indication de la polarité NL Indicatie van polariteit van
catalogue du fabricant catalogusnummer van de des connecteurs aansluiting
DE Angabe der Hersteller- fabrikant aan DE Anzeige der RU Индикация полярности
Katalognummer RU Указывает номер в Steckerpolarität разъема
IT Indica il numero di каталоге производителя IT Indicazione della polarità TR Bağlantı polarite
catalogo del produttore TR Üreticinin katalog dei connettori göstergesi
ES Indica el número de numarasını belirtir ES Indicación de la polaridad ‫ عالمة تشير إلى قطبية الموصل‬AR
catálogo del fabricante ‫ لإلشارة إلى رقم القائمة الخاص‬AR del conector
‫بالشركة المصنعة‬ For indoor use only
Temperature limitation FR Pour un usage à l’intérieur NL Alleen voor gebruik
FR Limitation de température NL Temperatuurbegrenzing uniquement binnenshuis
DE Temperaturbegrenzung RU Температурный DE Nur für die Nutzung in RU Для использования
IT Limite di temperatura диапазон Innenbereichen только внутри
ES Limitación de la TR Sıcaklık sınırlaması IT Solo per uso in interni помещений
temperatura ‫ حدود درجة الحرارة المناسبة‬AR ES Para uso solo en interiores TR Sadece iç mekanda
Humidity limitation kullanım için
‫ صالح لالستخدام في األماكن‬AR
FR Limitation d’humidité NL Vochtigheidsbegrenzing
‫المغلقة فقط‬
DE Luftfeuchtigkeits- RU Диапазон влажности
begrenzung TR Nem sınırlaması OMRON’s trademarked technology for blood
IT Limite di umidità ‫ حدود الرطوبة المناسبة‬AR
pressure measurement
ES Limitación de la humedad FR Technologie brevetée NL Technologie voor
OMRON pour la mesure de bloeddrukmeting onder
Atmospheric pressure limitation
la pression artérielle handelsmerk van OMRON
FR Limitation de pression NL Luchtdrukbegrenzing
atmosphérique RU Диапазон атмосферного DE Markenrechtlich RU Зарегистрированная
geschützte Technologie технология измерения
DE Luftdruckbegrenzung давления
von OMRON zur артериального давления
IT Limite di pressione TR Atmosferik basınç
atmosferica sınırlaması Blutdruckmessung OMRON

ES Limitación de la presión ‫ حدود الضغط الجوي المناسب‬AR

IT Tecnologia brevettata TR OMRON'un kan basıncı
OMRON per la misurazione ölçümü için ticari markalı
atmosférica
della pressione arteriosa teknolojisidir
ES La tecnología de OMRON OMRON ‫ تقنية العالمة التجارية‬AR
para medir la presión ‫لقياس ضغط الدم‬
arterial

SD2
 Identifier of cuffs compatible for the device Not made with natural rubber latex
FR Identificateur des brassards NL Identificatie van FR Ne contient pas de latex de NL Bevat geen
compatibles avec l’appareil manchetten die caoutchouc naturel natuurrubberlatex
DE Kennzeichnung der mit compatibel zijn met het DE Enthält kein Naturlatex RU Не содержит
dem Gerät kompatiblen apparaat IT Non contiene lattice di натуральный латекс
Manschetten RU Манжеты, совместимые с gomma naturale TR Doğal kauçuk lateksten
IT Identifica i bracciali устройством ES No contiene látex de üretilmemiştir
compatibili con il TR Cihaz ile uyumlu caucho natural ‫ تم التصنيع دون استخدام التيكس‬AR
dispositivo kollukların tanıtım işareti ‫المطاط الطبيعي‬
ES Identificador para ‫ عالمات تحديد الشرائط الضاغطة‬AR Arm circumference
manguitos compatibles ‫المتوافقة مع الجهاز‬ FR Circonférence du bras NL Armomtrek
con el dispositivo DE Armumfang RU Окружность плеча
Marker on the cuff to be positioned above the IT Circonferenza del braccio TR Kol çevresi
artery ES Perímetro de brazo ‫ محيط الذراع‬AR
FR Repère sur le brassard, à NL Markering op de manchet Necessity for the user to consult this instruction manual
positionner au-dessus de die boven de slagader
FR L’utilisateur doit consulter NL De gebruiker dient deze
l’artère moet worden geplaatst le mode d’emploi gebruiksaanwijzing te
DE Markierung auf der RU Указатель на манжете DE Der Benutzer muss diese raadplegen
Manschette, die oberhalb для расположения над Gebrauchsanweisung RU Необходимость для
der Arterie liegen muss артерией lesen пользователя обратиться
IT Contrassegno sul bracciale TR Kolluk üzerindeki işaretin IT L’utente deve consultare к данному руководству
da posizionare al di sopra konumu arterin üzerine il presente manuale di по эксплуатации
dell’arteria gelmelidir istruzioni TR Kullanıcı, bu kullanım
ES La marca del manguito ‫ عالمة بالشريط الضاغط لإلشارة‬AR ES Es necesario que el usuario kılavuzuna başvurmalıdır
debe colocarse sobre la ‫إلى وجوب وضعه فوق الشريان‬ consulte este manual de ‫ ضرورة رجوع المستخدم إلى‬AR
arteria instrucciones ‫دليل اإلرشادات هذا‬
Manufacturer’s quality control mark
, FR Marque de contrôle de la NL Symbool voor
qualité du fabricant kwaliteitscontrole van
DE Qualitätskontrollzeichen fabrikant
des Herstellers RU Отметка производителя
IT Contrassegno controllo о контроле качества
qualità del produttore TR Üreticinin kalite kontrol
ES Marca del control de işareti
calidad del fabricante ‫ عالمة التحكم في الجودة الخاصة‬AR
‫بالشركة المصنعة‬

SD3
Need for the user to follow this instruction manual Prohibited action
thoroughly for your safety. FR Action interdite NL Verboden handeling
FR L’utilisateur doit suivre NL Voor de eigen veiligheid DE Verbotene Aktion RU Запрещенные действия
attentivement ce mode dient de gebruiker zich IT Operazione proibita TR Yasaklanmış eylem
d’emploi pour votre zorgvuldig aan deze ES Acción prohibida ‫ إجراء محظور‬AR
sécurité. gebruiksaanwijzing te
DE Damit die Sicherheit houden.
gewährleistet ist, muss RU В целях обеспечения
der Benutzer diese безопасности строго
Gebrauchsanweisung следуйте указаниям в
sorgfältig befolgen. данном руководстве по
IT Per la propria sicurezza, эксплуатации.
l’utente deve seguire TR Güvenlik açısından
attentamente il presente kullanıcının bu kullanım
manuale di istruzioni. kılavuzuna dikkatle
ES Es necesario que el usuario uyması gerekir.
siga rigurosamente este ‫ حاجة المستخدم إلى اتباع دليل‬AR
manual de instrucciones ‫اإلرشادات بالكامل للحفاظ على‬
para su seguridad. .‫السالمة‬
Direct current
FR Courant continu NL Gelijkstroom
DE Gleichstrom RU Постоянный ток
IT Corrente diretta TR Doğru akım
ES Corriente directa ‫ التيار المباشر‬AR
Alternating current
FR Courant alternatif NL Wisselstroom
DE Wechselstrom RU Переменный ток
IT Corrente alternata TR Alternatif akım
ES Corriente alterna ‫ التيار المتناوب‬AR
Date of manufacture
FR Date de fabrication NL Productiedatum
DE Herstellungsdatum RU Дата изготовления
IT Data di fabbricazione TR Üretim tarihi
ES Fecha de fabricación ‫ تاريخ التصنيع‬AR

SD4
 To indicate generally elevated, potentially hazardous, levels of non-ionizing radiation, or to indicate equipment or systems.
e.g. in the medical electrical area that include RF transmitters or that intentionally apply RF electromagnetic energy for
diagnosis or treatment.
FR Pour indiquer des niveaux généralement élevés, potentiellement NL Geeft in het algemeen verhoogde, potentieel gevaarlijke niveaus aan
dangereux, de rayonnement non ionisant, ou pour indiquer van niet-ioniserende straling of duidt op apparatuur of systemen,
l’équipement ou les systèmes, par exemple dans le domaine de bijvoorbeeld in de medische elektrische omgeving, die RF-zenders
l’électricité médicale qui comprennent des émetteurs RF ou qui bevatten of die opzettelijk elektromagnetische RF-energie toepassen
utilisent intentionnellement l’énergie électromagnétique RF pour le voor diagnose of behandeling.
diagnostic ou le traitement. RU Для указания повышенных и потенциально опасных
DE Als Hinweis auf allgemein erhöhte, potenziell gefährliche Stufen уровней неионизирующей радиации или же оборудования
nicht-ionisierender Strahlung oder als Hinweis auf Geräte oder или систем (например, в зоне размещения медицинского
Systeme zum Beispiel im medizinisch-elektrischen Bereich, etwa HF- электрооборудования), включающих в себя радиопередатчики
Übertragungsgeräte, bzw. auf solche, die elektromagnetische HF- или устройства, использующие радиочастотную
Strahlung zur Diagnose oder Behandlung verwenden. электромагнитную энергию в целях диагностики или терапии.
IT Indica livelli generalmente elevati, potenzialmente pericolosi, di TR Genellikle yüksek ve zararlı olabilecek iyonlaşmayan radyasyon
radiazioni non ionizzanti oppure indica apparecchiature o sistemi seviyelerini belirtir veya RF vericileri içeren veya tanı ya da tedavi
(ad esempio per le aree elettromedicali in cui sono presenti amacıyla bilinçli olarak RF elektromanyetik enerji uygulayan (örneğin
trasmettitori RF o in cui viene intenzionalmente applicata energia medikal elektrik alanında bulunan) ekipman ve sistemleri belirtir.
elettromagnetica a radiofrequenza per la diagnosi o il trattamento). ‫ لإلشارة إلى مستويات األشعة غير المؤينة المرتفعة بوجه عام ومن المحتمل أن تكون‬AR
ES Para indicar niveles de radiación no ionizante generalmente ‫ مثل الموجودة في األماكن المحتوية على‬،‫ أو لإلشارة إلى األجهزة أو األنظمة‬،‫خطرة‬
elevados y potencialmente peligrosos, o bien para indicar equipos ‫أجهزة كهربائية طبية تشتمل على أجهزة إرسال تنبعث منها ترددات السلكية أو حيث يتم‬
o sistemas, como los usados en el ámbito electro médico, que ‫استخدام الطاقة الكهرومغناطيسية ذات الترددات الالسلكية عن عمد ألغراض التشخيص‬
.‫أو العالج‬
incorporen transmisores de radiofrecuencia o que apliquen energía
electromagnética de radiofrecuencia intencionadamente para
diagnósticos o tratamientos.

SD5
The Bluetooth® word mark and logos are registered trademarks owned by the Bluetooth SIG, Inc. and any use of such marks by OMRON HEALTHCARE Co., Ltd. is
under license. Other trademarks and trade names are those of their respective owners. App Store is a service mark of Apple Inc., registered in the U.S and other
countries. Google Play logo are trademarks of Google LLC.
FR La marque verbale et les logos Bluetooth® sont des marques déposées NL Het woordmerk en de logo’s van Bluetooth® zijn gedeponeerde
détenues par Bluetooth SIG, Inc. et l’utilisation de ces marques par OMRON handelsmerken van Bluetooth SIG, Inc. en enig gebruik hiervan door
HEALTHCARE Co., Ltd. se fait sous licence. Les autres marques commerciales OMRON HEALTHCARE Co., Ltd. geschiedt onder licentie. Overige
et noms de marque sont ceux de leurs détenteurs respectifs. App Store est handelsmerken en handelsnamen zijn van hun respectievelijke eigenaren.
une marque de service d’Apple Inc., déposées aux États-Unis et dans d’autres App Store is een servicemerk van Apple Inc. en gedeponeerd in de V.S. en in
pays. Le logo Google Play est une marque commerciale de Google LLC. andere landen. Het Google Play-logo is een handelsmerk van Google LLC.
DE Die Bluetooth®-Wortmarke und -Logos sind eingetragene Marken RU Словесный знак и логотип Bluetooth® являются зарегистрированными
der Bluetooth SIG, Inc. und die Verwendung solcher Marken durch товарными знаками, являющимися собственностью компании Bluetooth
OMRON HEALTHCARE Co., Ltd. erfolgt in Lizenz. Andere Marken und SIG, Inc., и любое использование этих знаков компанией OMRON
Markennamen gehören ihren jeweiligen Eigentümern. App Store ist eine HEALTHCARE Co., Ltd. обеспечивается лицензией. Другие товарные
Dienstleistungsmarke der Apple Inc., die in den USA und anderen Ländern знаки и торговые марки являются собственностью соответствующих
eingetragen ist. Das Google Play-Logo ist eine Marke der Google LLC. владельцев. App Store является знаком обслуживания Apple Inc.,
IT Il marchio e i logotipi Bluetooth® sono marchi commerciali registrati di зарегистрированным в США и других странах. Логотип Google Play
Bluetooth SIG, Inc. e l’utilizzo di tali marchi da parte di OMRON HEALTHCARE является товарным знаком Google LLC.
Co., Ltd. è stato concesso in licenza. Gli altri marchi e nomi commerciali sono TR Bluetooth® marka adı ve logoları, Bluetooth SIG Inc. kuruluşunun tescilli
di proprietà dei rispettivi titolari. App Store è un marchio commerciale di ticari markalarıdır ve OMRON HEALTHCARE Co., Ltd. bu markaları lisans
Apple Inc., registrato negli Stati Uniti e in altri Paesi. Il logo Google Play è un kapsamında kullanmaktadır. Diğer ticari markalar ve ticari isimler, ilgili
marchio commerciale di Google LLC. sahiplerine aittir. App Store, Apple Inc. firmasının ABD ve diğer ülkelerde
ES El nombre y los logotipos de Bluetooth® son marcas registradas de tescilli hizmet markasıdır. Google Play logosu, Google LLC firmasının ticari
Bluetooth SIG, Inc. y cualquier uso de dichas marcas hecho por OMRON markasıdır.
HEALTHCARE Co., Ltd. se ha llevado a cabo con su licencia correspondiente. ‫ وشعاراتها هي عالمات تجارية مسجلة مملوكة‬Bluetooth® ‫ إن عالمة كلمة‬AR
Otras marcas registradas también pertenecen a sus respectivos propietarios. ‫ ويكون أي استخدام لهذه العالمات بواسطة شركة‬Bluetooth SIG, Inc. ‫لشركة‬
App Store es una marca de servicio registrada de Apple Inc. en EE. UU. y en ‫ تكون العالمات التجارية‬.‫ بموجب ترخيص‬OMRON HEALTHCARE Co., Ltd.
otros países. El logotipo de Google Play es una marca comercial de Google ‫ عالمة خدمة لشركة‬App Store ‫ يُعد‬.‫األخرى واألسماء التجارية لهذا المنتج خاصة بمالكيه‬
LLC. Google ‫ يُعد شعار‬.‫ وهي مسجلة في الواليات المتحدة األمريكية وبلدان أخرى‬Apple Inc.
.Google LLC ‫ عالمة تجارية لشركة‬Play

SD6
Issue Date:
Date de publication :
Ausgabedatum:
Data di pubblicazione:
Fecha de publicación: 2019-09-04
Uitgiftedatum
Дата выпуска:
Teslim Tarihi:
:‫تاريخ اإلصدار‬

IM1-HEM-7361T-E-02-09/2019
2895864-6B
Instruction Manual 2
Automatic Upper Arm
Blood Pressure Monitor
M7 Intelli IT (HEM-7361T-EBK)
X7 Smart (HEM-7361T-ESL)

Read Instruction manual and before use.

FR Lire le mode d’emploi et vant l’utilisation.
DE Lesen Sie vor der Verwendung Gebrauchsanweisung und .
IT Leggere il manuale di istruzioni e prima dell’uso.
ES Lea el manual de instrucciones y antes del uso.
NL Lees gebruiksaanwijzing en voor gebruik.
RU Прочтите руководства по эксплуатации и перед использованием.
TR Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.
.‫و قبل االستخدام‬ ‫ اقرأ دليل اإلرشادات‬AR
1 Package Contents...........................................1
FR Contenu de l’emballage NL Inhoud van de verpakking
5 Pairing Your Smart Device..............................7
FR Jumelage de votre appareil NL Uw smartapparaat koppelen
DE Packungsinhalt RU Комплект поставки intelligent
DE Koppeln mit Smartphone RU Синхронизация со смарт-
IT Contenuto della confezione TR Paketin İçindekiler oder Tablet устройством
ES Contenido del envase ‫ محتويات العلبة‬AR IT Associazione del dispositivo TR Akıllı Cihazınızın
smart Eşleştirilmesi
2 Preparing for a Measurement........................4
FR Préparation pour une prise NL Een meting voorbereiden
ES Sincronización con un ‫ إقران هاتفك الذكي‬AR
dispositivo inteligente
de mesure
DE Vorbereiten einer Messung RU Подготовка к измерению
6 Setting Date and Time Manually....................8
FR Réglage manuel de la date NL Datum en tijd handmatig
IT Preparazione per la TR Ölçüm Hazırlığı
misurazione et de l’heure instellen
ES Preparación para una DE Manuelles Einstellen von RU Установка даты и времени
‫ التجهيز لعملية القياس‬AR
medición Datum und Uhrzeit вручную
IT Impostazione manuale di TR Tarih ve Saatin Manuel
3 Downloading the "OMRON connect" App.....5
FR Téléchargement de NL De app “OMRON connect“
data e ora Olarak Ayarlanması
ES Ajuste manual de la fecha y ‫ ضبط الوقت والتاريخ يدويًا‬AR
l’application « OMRON downloaden la hora
connect »
DE Herunterladen der App
„OMRON connect“
RU Загрузка приложения
«OMRON connect»
7 Applying the Cuff on the Left Arm.................9
FR Pose du brassard sur le bras NL De manchet op de linkerarm
IT Download dell'app “OMRON TR "OMRON Connect" gauche aanbrengen
connect” Uygulamasını İndirme DE Anbringen der Manschette RU Расположение манжеты на
ES Descarga de la aplicación am linken Arm левой руке
"OMRON ‫ تنزيل تطبيق "اتصال‬AR
“OMRON connect” IT Applicazione del bracciale TR Kolluğun Sol Kola Takılması
sul braccio sinistro
4 Inserting Batteries..........................................6
FR Mise en place des piles NL De batterijen plaatsen
ES Colocación del manguito en
el brazo izquierdo
‫ لف الشريط الضاغط على الذراع األيسر‬AR

DE Einlegen von Batterien RU Установка элементов

питания 8 Sitting Correctly..............................................11
FR Position assise correcte NL Correct zitten
IT Inserimento delle batterie TR Pilleri Takma
ES Introducción de las pilas DE Korrekte Körperhaltung RU Сядьте правильно
‫ إدخال البطاريات‬AR
IT Come sedersi nel modo TR Düzgün Oturma
corretto
ES Cómo sentarse ‫ الجلوس بشكل صحيح‬AR
correctamente

1
9 Selecting User ID (1 or 2)................................13
FR Sélection de l’ID Utilisateur NL Gebruikers-ID selecteren
13 Other Settings...............................................26
FR Autres réglages NL Andere instellingen
(1 ou 2) (1 of 2) DE Weitere Einstellungen RU Другие настройки
DE Auswahl der Benutzer-ID RU Выберите идентификатор
(1 oder 2) пользователя (1 или 2) IT Altre impostazioni TR Diğer Ayarlar
IT Selezione dell’ID utente TR Kullanıcı Kimliğini Seçme ES Otros ajustes ‫ اإلعدادات األخرى‬AR
(1 o 2) (1 veya 2)
ES Selección de ID de usuario )2 ‫ أو‬1( ‫ تحديد هوية المستخدم‬AR 14 Optional Medical Accessories........................29
FR Accessoires médicaux en NL Optionele medische
(1 o 2)
option accessoires
10 Taking a Measurement...................................14
FR Réalisation d’une mesure NL Een meting verrichten
DE Medizinisches optionales
Zubehör
RU Дополнительно
принадлежности
DE Eine Messung vornehmen RU Выполнение измерений IT Accessori medicali opzionali TR Opsiyonel Tıbbi Aksesuarlar
IT Misurazione TR Bir Ölçüm Yapma ES Accesorios médicos ‫ الملحقات الطبية االختيارية‬AR
opcionales
ES Obtención de una lectura ‫ إجراء قياس‬AR

11 Checking Readings in Comparison Mode......18 15 Other Optional Parts.......................................30

FR Autres pièces en option NL Overige optionele
FR Vérification des mesures en NL Metingen bekijken in onderdelen
mode de comparaison vergelijkingsmodus
DE Weitere optionale Teile RU Другие дополнительно
DE Überprüfen von Messwerten RU Проверка результатов приобретаемые запасные
im Vergleichsmodus измерений в режиме
части
сравнения
IT Altri componenti opzionali TR Diğer Aksesuarlar
IT Controllo dei risultati in TR Karşılaştırma Modunda
modalità Confronto Ölçüm Değerlerini Kontrol ES Otras piezas opcionales ‫ أجزاء اختيارية أخرى‬AR
Etme
ES Comprobación de ‫ التحقق من القراءات في وضع المقارنة‬AR
las lecturas en modo
comparativo

12 Using Memory Functions...............................23

FR Utilisation des fonctions de NL Geheugenfuncties
mémoire gebruiken
DE Verwendung der RU Использование функции
Speicherfunktion памяти
IT Uso delle funzioni di TR Hafıza Fonksiyonunun
memoria Kullanılması
ES Uso de las funciones de ‫ استخدام وظائف الذاكرة‬AR
memoria
2
1 Package Contents
FR Contenu de l’emballage NL Inhoud van de verpakking
DE Packungsinhalt RU Комплект поставки
IT Contenuto della confezione TR Paketin İçindekiler
ES Contenido del envase ‫محتويات العلبة‬ AR

Instru
ction
Manua
l 1

Instru
ction
Manua
l 2

3
2 Preparing for a Measurement
FR Préparation pour une prise de mesure NL Een meting voorbereiden
DE Vorbereiten einer Messung RU Подготовка к измерению
IT Preparazione per la misurazione TR Ölçüm Hazırlığı
ES Preparación para una medición ‫التجهيز لعملية القياس‬ AR

30 minutes before
FR 30 minutes avant

DE 30 Minuten vorher

IT 30 minuti prima

ES 30 minutos antes

NL 30 minuten ervoor

RU За 30 минут до

TR 30 dakika önce

‫ لقة في تصمم واعيد التصمم والمحتوى مثل يدية ألو‬.‫ لق إلى مع‬AR

5 minutes before: Relax and rest.

FR 5 minutes avant : détente et repos.

DE 5 Minuten vorher: ruhig hinsetzen.

IT 5 minuti prima: rilassarsi e stare a riposo.

ES 5 minutos antes: relájese y descanse.

NL 5 minuten ervoor: ontspan en rust.

RU За 5 минут до: расслабьтесь и отдохните.

TR 5 dakika önce: Gevşeyin ve dinlenin.

‫واسترخ‬
ِ ‫ استرح‬:‫ دقائق‬5 ‫ قبل القياس بمدة تبلغ‬AR
4
3 Downloading the "OMRON connect" App
FR Téléchargement de l’application « OMRON connect » NL De app “OMRON connect“ downloaden
DE Herunterladen der App „OMRON connect“ RU Загрузка приложения «OMRON connect»
IT Download dell'app “OMRON connect” TR "OMRON Connect" Uygulamasını İndirme
ES Descarga de la aplicación “OMRON connect” "OMRON ‫تنزيل تطبيق "اتصال‬ AR

omron connect

5
4 Inserting Batteries
FR Mise en place des piles NL De batterijen plaatsen
DE Einlegen von Batterien RU Установка элементов питания
IT Inserimento delle batterie TR Pilleri Takma
ES Introducción de las pilas ‫إدخال البطاريات‬ AR

1 2 3

AA, 1.5V × 4

6
5 Pairing Your Smart Device
FR Jumelage de votre appareil intelligent NL Uw smartapparaat koppelen
DE Koppeln mit Smartphone oder Tablet RU Синхронизация со смарт-устройством
IT Associazione del dispositivo smart TR Akıllı Cihazınızın Eşleştirilmesi
ES Sincronización con un dispositivo inteligente ‫ إقران هاتفك الذكي‬AR

1 2 3 Follow the instructions.

FR Suivez les instructions.
Bluetooth
ON DE Befolgen Sie die Anweisungen.
IT Attenersi alle istruzioni.
ES Siga las instrucciones.
NL Volg de instructies.
RU Выполняйте инструкции.
TR Talimatları izleyin.
.‫ اتبع اإلرشادات‬AR

The date and time will automatically be set when your monitor is paired with the app.
FR La date et l’heure seront automatiquement réglées lorsque votre tensiomètre sera jumelé avec l’application.
DE Wenn Ihr Messgerät mit der App verknüpft ist, werden Datum und Uhrzeit automatisch eingestellt.
IT La data e l’ora verranno impostate automaticamente una volta che il misuratore verrà associato alla app.
ES La fecha y la hora se ajustarán automáticamente cuando el monitor se sincronice con la aplicación.
NL De datum en tijd worden automatisch ingesteld wanneer uw bloeddrukmeter is gekoppeld aan de app.
RU Дата и время установятся автоматически после синхронизации с приложением.
TR Ölçüm cihazınız uygulamayla eşleştirildiğinde tarih ve saat otomatik olarak ayarlanır.
.‫ سيتم ضبط الوقت والتاريخ تلقائيًا عند إقران جهاز القياس الخاص بك بالتطبيق‬AR

7
6 Setting Date and Time Manually
FR Réglage manuel de la date et de l’heure NL Datum en tijd handmatig instellen
DE Manuelles Einstellen von Datum und Uhrzeit RU Установка даты и времени вручную
IT Impostazione manuale di data e ora TR Tarih ve Saatin Manuel Olarak Ayarlanması
ES Ajuste manual de la fecha y la hora ‫ضبط الوقت والتاريخ يدو ًيا‬ AR

If your monitor is paired with your smart device, date ES Si el monitor está sincronizado con su dispositivo inteligente, la
and time is set automatically. When you need to set them fecha y la hora se ajustarán automáticamente. Cuando tenga que
configurarlas manualmente, ajuste año > mes > día > hora > minuto.
manually, set year > month > day > hour > minute.
NL Als uw bloeddrukmeter gekoppeld is met uw smartapparaat, worden
FR Si votre tensiomètre est jumelé avec votre appareil intelligent, la date de datum en tijd automatisch ingesteld. Wanneer u ze handmatig
et l’heure sont réglées automatiquement. Si vous devez les régler moet instellen, stelt u jaar > maand > dag > uur > minuut in.
manuellement, réglez dans l’ordre année > mois > jour > heure > RU Если прибор синхронизирован со смарт-устройством, дата и время
minute. устанавливаются автоматически. Если необходимо установить их
DE Wenn Ihr Messgerät mit Ihrem Smartphone oder Tablet gekoppelt ist, вручную, выберите год > месяц > день > час > минута.
werden Datum und Uhrzeit automatisch eingestellt. Bei manueller TR Ölçüm cihazınız akıllı cihazınızla eşleştirilmişse tarih ve saat otomatik
Einstellung müssen Sie Jahr > Monat > Tag > Stunde > Minute olarak ayarlanır. Bunları manuel olarak ayarlamanız gerektiğinde,
einstellen. yıl > ay > gün > saat > dakika değerini ayarlayın.
IT Se il misuratore viene accoppiato con un dispositivo smart, la data
e l’ora verranno impostate automaticamente. Se occorre impostarle ‫عند‬ ‫ يتم ضبط الوقت والتاريخ تلقائي‬،‫ في حال إقران جهاز القياس الخاص بك بالجهاز الذكي‬AR
.‫ًا‬
manualmente, impostare anno > mese > giorno > ore > minuti. > )‫ (اليوم‬day > )‫ (الشهر‬month > )‫ (السنة‬year ‫ اضبط‬،‫الحاجة إلى ضبطهما يدويًا‬
.)‫ (الدقيقة‬minute > )‫ (الساعة‬hour
Year Month Day Hour Minute

Back / Forward
FR Arrière / Avant NL Terug / vooruit
DE Zurück / Vorwärts RU Назад / Вперед
IT Indietro / Avanti TR İleri / Geri
ES Atrás / Adelante ‫ التقدم‬/ ‫ الرجوع‬AR
8
7 Applying the Cuff on the Left Arm
FR Pose du brassard sur le bras gauche NL De manchet op de linkerarm aanbrengen
DE Anbringen der Manschette am linken Arm RU Расположение манжеты на левой руке
IT Applicazione del bracciale sul braccio sinistro TR Kolluğun Sol Kola Takılması
ES Colocación del manguito en el brazo izquierdo ‫لف الشريط الضاغط على الذراع األيسر‬ AR

1 2

Click

3 4
A 1-2 cm
B

9
A Tube side of the cuff should be 1 - 2 cm above the B Make sure that air tube is on the inside of your
inside elbow. arm and wrap the cuff securely so it can no
FR Le côté tuyau du brassard doit être positionné 1 à 2 cm longer slip round.
au-dessus de l’intérieur du coude.
DE Das Manschettenstück mit dem Schlauch muss 1 bis 2 cm FR Assurez-vous que le tuyau à air se trouve du côté intérieur de
oberhalb des Ellbogens liegen. votre bras et enroulez fermement le brassard de manière qu’il
ne puisse plus tourner.
IT Il lato del bracciale con il tubo deve trovarsi al di sopra del
gomito interno, a una distanza di circa 1 o 2 cm. DE Stellen Sie sicher, dass der Luftschlauch an der Arminnenseite
sitzt, und befestigen Sie die Manschette sicher, so dass sie
ES El lado del tubo del manguito deberá quedar 1 o 2 cm por nicht verrutscht.
encima de la parte interna del codo.
IT Assicurarsi che il tubo dell’aria si trovi all’interno del braccio
NL De kant met de slang van de manchet moet 1 - 2 cm boven de e avvolgere il bracciale saldamente in modo che non possa
binnenkant van de elleboog liggen. ruotare.
RU Край манжеты с трубкой должен находиться на 1 - 2 см ES Asegúrese de que el tubo de aire se encuentra en la cara
выше локтевого сгиба. interna del brazo y enrolle el manguito con firmeza para que
TR Kolluğun boru tarafı, dirsek içinin 1-2 cm üstünde olmalıdır. no pueda deslizarse.
.‫ سم عن المرفق‬2 ‫ إلى‬1 ‫ يجب أن يرتفع جانب الخرطوم من الشريط الضاغط من‬AR NL Zorg ervoor dat de luchtslang zich aan de binnenkant van uw
arm bevindt en wikkel de manchet stevig rond uw arm zodat
deze niet meer kan wegglijden.
RU Убедитесь, что воздуховодная трубка находится на
внутренней поверхности плеча и надежно оберните
If taking measurements on the right arm, refer to: манжету, чтобы она не прокручивалась вокруг руки.
FR Pour la prise de mesures au bras droit, TR Hava borusunun kolunuzun iç tarafında olduğundan emin
voir : Instru
ction
Manu
olun ve kolluğu kaymayacak şekilde sabit şekilde sarın.
al 1

DE Bei Messungen am rechten Arm siehe:

‫ تأكد من أن خرطوم الهواء على الجانب الداخلي من ذراعك ولف الشريط الضاغط‬AR
IT Se la misurazione viene eseguita al .‫بإحكام بحيث ال ينزلق حول الذراع‬
braccio destro, fare riferimento a:
ES Si va a realizar mediciones en el brazo
derecho, consulte:
NL Als u metingen aan de rechterarm
uitvoert, raadpleeg dan:
RU При измерении на правой руке см.
TR Sağ koldan ölçüm yapıyorsanız aşağıdakilere bakın:
:‫ ارجع إلى‬،‫ في حال إجراء القياس على الذراع األيمن‬AR

10
8 Sitting Correctly
FR Position assise correcte NL Correct zitten
DE Korrekte Körperhaltung RU Сядьте правильно
IT Come sedersi nel modo corretto TR Düzgün Oturma
ES Cómo sentarse correctamente ‫الجلوس بشكل صحيح‬ AR

1
2

11
1 Sit with your back and arm supported.
FR S’asseoir de façon à ce que le dos et le bras soient bien soutenus.
DE Mit dem Rücken anlehnen und den Arm auf eine Unterlage legen.
IT Sedere con la schiena e il braccio ben sostenuti.
ES Siéntese de modo que la espalda y el brazo estén bien apoyados.
NL Zit met uw rug en arm ondersteund.
RU Сядьте так, чтобы спина и рука опирались на что-либо.
TR Sırtınız ve kolunuz desteklenecek şekilde oturun.
.‫ اجلس بحيث يكون الظهر والذراع في وضع استناد‬AR

2 Place the arm cuff at the same level as your heart.

FR Le brassard doit se trouver au même niveau que votre cœur.
DE Die Manschette auf Herzhöhe platzieren.
IT Posizionare il bracciale allo stesso livello del cuore.
ES Coloque el manguito al mismo nivel que el corazón.
NL Plaats de armmanchet op hetzelfde niveau als uw hart.
RU Манжета должна находиться на уровне сердца.
TR Kolluğu kalbinizle aynı düzeye getirin.
.‫ ضع الشريط الضاغط للذراع في مستوى القلب نفسه‬AR

3 Keep feet flat, legs uncrossed, remain still and do not talk.
FR Garder les pieds à plat, les jambes non croisées, ne pas bouger et ne pas parler.
DE Füße flach auf den Boden stellen, die Beine nicht kreuzen, still halten und nicht sprechen.
IT Tenere i piedi ben poggiati, non incrociare le gambe, rimanere fermi e non parlare.
ES Mantenga los pies planos, las piernas sin cruzar, quédese quieto y no hable.
NL Houd de voeten plat, benen niet gekruist, zit stil en praat niet.
RU Поставьте ноги ровно, не перекрещивая их, не двигайтесь и не разговаривайте.
TR Ayaklarınızı düz, bacaklarınızı açık tutun, hareketsiz kalın ve konuşmayın.
ّ
.‫مسطح وساقيك في وضع متباعد وحافظ على ثباتك وال تتحدث‬ ‫ اجعل قدميك في وضع‬AR
12
9 Selecting User ID (1 or 2)
FR Sélection de l’ID Utilisateur (1 ou 2) NL Gebruikers-ID selecteren (1 of 2)
DE Auswahl der Benutzer-ID (1 oder 2) RU Выберите идентификатор пользователя (1 или 2)
IT Selezione dell’ID utente (1 o 2) TR Kullanıcı Kimliğini Seçme (1 veya 2)
ES Selección de ID de usuario (1 o 2) (2 ‫ أو‬1( ‫ تحديد هوية المستخدم‬AR

Switching user ID enables you to save readings for 2 people.

FR Changer d’ID Utilisateur permet d’enregistrer les résultats pour 2 personnes.
DE Mit verschiedenen Benutzer-IDs lassen sich Messwerte für 2 Personen speichern.
IT Cambiare ID utente permette di registrare i risultati relativi a 2 persone.
ES Cambiar de ID de usuario le permite guardar las lecturas de 2 personas.
NL Door het wisselen van gebruikers-ID kunt u metingen voor 2 personen opslaan.
RU Переключение идентификатора пользователя позволяет сохранять результаты для 2-х людей.
TR Kullanıcı kimlikleri arasında geçiş yapma, 2 kişi için ölçüm değerlerini kaydetmenizi sağlar.
.‫ تتيح لك إمكانية تبديل معرف المستخدم حفظ القراءات لشخصين‬AR

13
10 Taking a Measurement
FR Réalisation d’une mesure NL Een meting verrichten
DE Eine Messung vornehmen RU Выполнение измерений
IT Misurazione TR Bir Ölçüm Yapma
ES Obtención de una lectura ‫إجراء قياس‬ AR

P.18
When the [START/STOP] button is pressed, the measurement is taken and saved
automatically. Open the app to transfer the reading.
FR Après une pression sur le bouton [START/STOP], la mesure démarre et le résultat est enregistré
automatiquement. Ouvrir l’application pour transférer le résultat.
DE Beim Drücken der Taste [START/STOP] erfolgt die Messung. Die Messwerte werden automatisch
gespeichert. Öffnen Sie die App, um die Messwerte zu übertragen.
IT Quando si preme il pulsante [START/STOP], la misurazione viene eseguita e salvata
automaticamente. Aprire la app per trasferire i risultati.
ES Al pulsar el botón [START/STOP], se obtiene la medición, que se guarda automáticamente. Abra la
aplicación para transferir la lectura.
NL Wanneer op de knop [START/STOP] wordt gedrukt, wordt de meting automatisch uitgevoerd en Instru
ction
Manu
al 1

opgeslagen. Open de app om de meting te versturen.

RU После того, как кнопка [START/STOP] нажата, измерение выполняется и сохраняется
автоматически. Откройте приложение, чтобы передать результаты.
TR [START/STOP] düğmesine basıldığında ölçüm yapılır ve otomatik olarak kaydedilir. Ölçüm değerini Instruction Manual
aktarmak için uygulamayı açın. 3.
.‫ افتح التطبيق لنقل القراءة‬.‫ يتم إجراء القياس وحفظه تلقائيًا‬،]START/STOP[ ‫ عند الضغط على زر‬AR
14
Taking a measurement in Afib mode ES Obtención de una lectura en modo fibrilación auricular

FR Réalisation d’une mesure en mode fibrillation auriculaire NL Een meting in Afib-modus afnemen
DE Vornehmen einer Messung im Afib-Modus RU Выполнение измерений в режиме ФП

IT Misurazione in modalità Afib TR Afib modunda ölçüm yapma

‫ إجراء القياس باستخدام وضع الرجفان األذيني‬AR
In the Afib mode, your monitor automatically takes 3 ES En el modo fibrilación auricular, el monitor realiza 3 mediciones
consecutive readings at 30-second intervals and displays consecutivas automáticamente a intervalos de 30 segundos y muestra
el valor promedio. Si existe una posible fibrilación auricular, aparecerá
the average. If there is a possibility of Afib, “Afib indicator el “símbolo indicador de fibrilación auricular” ( ).
symbol” ( ) will appear. Esto no es un diagnóstico, simplemente la detección de una posible
This is not a diagnosis, it is only a potential finding for Afib. fibrilación auricular. Deberá ponerse en contacto con su médico para
hablar de los resultados. En caso de padecer síntomas, póngase en
You should contact your physician to discuss the findings. contacto con un profesional sanitario.
If you are experiencing any symptoms, contact a medical
NL In de Afib-modus neemt uw meter automatisch 3 achtereenvolgende
professional. metingen met intervallen van 30 seconden en toont vervolgens het
FR En mode fibrillation auriculaire, votre moniteur effectue gemiddelde. Als er een mogelijkheid is op Afib verschijnt het “Afib-
automatiquement 3 mesures consécutives à 30 secondes d’intervalle indicatorsymbool” ( ).
et affiche la moyenne. S’il y a une possibilité de fibrillation auriculaire, Dit is geen diagnose, het is slechts een vaststelling dat er mogelijk
le « symbole indicateur de fibrillation auriculaire » ( ) s’affiche. sprake is van Afib. Neem contact op met uw arts om de bevindingen
Il ne s’agit pas d’un diagnostic mais seulement de l’indication te bespreken. Neem contact op met een medische professional als u
d’une fibrillation auriculaire possible. Vous devriez consulter votre symptomen ondervindt.
médecin pour discuter des résultats. Si vous ressentez un symptôme RU В режиме ФП автоматически выполняется 3 последовательных измерения
quelconque, consultez un professionnel de la santé. с 30-секундным интервалом, после чего отображается среднее значение.
В случае вероятности ФП отображается «Значок индикатора ФП» ( ).
DE Im Afib-Modus nimmt das Messgerät automatisch 3 Messungen
Это не диагноз, а только вероятность обнаружения ФП. Для
hintereinander im Abstand von je 30 Sekunden vor und zeigt den
обсуждения полученных результатов необходимо обратиться к
Mittelwert an. Wenn die Möglichkeit von Vorhofflimmern besteht,
лечащему врачу. Если у Вас существуют какие-либо жалобы на
erscheint das „Afib-Hinweissymbol“ ( ).
самочувствие, обратитесь к врачу.
Dabei handelt es sich nicht um eine Diagnose, sondern lediglich um
einen Befund, dass Vorhofflimmern vorliegen könnte. Wenden Sie sich TR Cihazınız Afib modunda iken, otomatik olarak 30 saniyelik aralıklarda
an Ihren Arzt, um den Befund weiter abzuklären. Konsultieren Sie bei ardışık 3 ölçüm yapar ve ortalamayı gösterir. Afib olasılığı varsa "Afib
Auftreten von Symptomen eine medizinische Fachkraft. gösterge sembolü" ( ) görünür.
Bu bir tanı değildir, yalnızca olası Afib bulgusudur. Doktorunuzla
IT Nella modalità Afib, il misuratore esegue automaticamente 3
iletişime geçerek bulguları konuşmanız gerekir. Semptom yaşıyorsanız
misurazioni consecutive a intervalli di 30 secondi e visualizza la media.
bir tıp uzmanıyla iletişime geçin.
In caso di potenziale presenza di fibrillazione atriale (Afib) viene
visualizzato il “simbolo dell’indicatore Afib” ( ). ‫ قراءات متتابعة تلقائيًا على فترات‬3 ‫ يقوم جهاز القياس بالتقاط‬،‫ في وضع الرجفان األذيني‬AR
Questa non è una diagnosi ma è soltanto un rilevamento della ً
‫ فسوف‬،‫محتمل‬ ‫ إذا كان الرجفان األذيني أمرً ا‬.‫ ثانية ومن ثم يعرض المعدل‬30 ‫منتظمة مدتها‬
potenziale presenza di fibrillazione atriale (Afib). È opportuno .) ( "‫يظهر "رمز مؤشر الرجفان األذيني‬
rivolgersi al proprio medico curante per discutere questo risultato. Se ‫ يجب‬،‫ ومن ث ّم‬.‫ فما هو إال اكتشاف محتمل لحدوث رجفان أذيني‬،‫ال يُعد هذا اإلجراء تشخيصًا‬
si dovessero riscontrare eventuali sintomi, rivolgersi a un medico. ‫ فيجب عليك االتصال‬،‫ إذا تعرضت ألي أعراض‬.‫عليك االتصال بالطبيب لمناقشة النتائج‬
.‫بطبيب مختص‬
15
1

2 sec+

Instru
ction
Manua
l 1

Instruction Manual
3.

P.18
16
Taking a measurement in guest mode ES Obtención de una lectura en modo de invitado
FR Réalisation d’une mesure en mode Invité NL Een meting in gastmodus afnemen
DE Vornehmen einer Messung im Gast-Modus RU Выполнение измерений в гостевом режиме
IT Misurazione in modalità Ospite TR Konuk modunda ölçüm yapma
.‫ إجراء القياس باستخدام وضع الضيف‬AR
The guest mode can be used to take a single measurement ES Para realizar una única medición para otro usuario, se puede utilizar
for another user. No readings are stored in the memory, el modo de invitado. Cuando se selecciona el modo de invitado, no se
and the Afib mode is not available when the guest mode is guardan lecturas en la memoria y el modo de fibrilación auricular no
está disponible.
selected.
NL De gastmodus kan worden gebruikt om één enkele meting uit
FR Le mode Invité permet de mesurer la pression artérielle d’une autre te voeren voor een andere gebruiker. Er worden geen metingen
personne une seule fois. Les résultats ne sont pas enregistrés dans opgeslagen in het geheugen en de Afib-modus is niet beschikbaar
la mémoire et le mode fibrillation auriculaire n’est pas disponible wanneer de gastmodus is geselecteerd.
lorsque le mode Invité est sélectionné. RU Гостевой режим используется для единичного измерения
DE Soll eine einzelne Messung bei einem anderen Benutzer durchgeführt артериального давления у другого лица. Если выбран гостевой
werden, kann dafür der Gast-Modus aktiviert werden. Im Gast-Modus режим, то измерения не сохраняются в памяти, и недоступен
werden keine Messwerte gespeichert und der Afib-Modus steht nicht режим ФП.
zur Verfügung. TR Konuk modu, başka bir kişi için tek bir ölçüm yapmak üzere
IT La modalità Ospite può essere utilizzata per eseguire una singola kullanılabilir. Konuk modu seçildiğinde, ölçüm değerleri hafızada
misurazione su un diverso utente. I risultati ottenuti non vengono saklanmaz ve Afib modu kullanılamaz.
memorizzati e la modalità Afib non è disponibile quando si seleziona ‫ ال يتم تخزين أي‬.‫ ويمكن استخدام وضع الضيف إلجراء عملية قياس واحدة لمستخدم آخر‬AR
la modalità Ospite. .‫قراءة داخل الذاكرة كما أن وضع الرجفان األذيني ال يكون متاحً ا عند تحديد وضع الضيف‬

1 While holding the button down, press the [START/STOP] button.

FR Tout en maintenant le bouton enfoncé, appuyer sur le bouton [START/STOP].
DE Halten Sie die Taste gedrückt und drücken Sie gleichzeitig die Taste [START/STOP].
IT Mentre si tiene premuto il pulsante , premere il pulsante [START/STOP].
ES Mientras mantiene pulsado el botón , pulse el botón [START/STOP].
NL Houd de knop ingedrukt en druk tegelijkertijd op de knop [START/STOP].
RU Удерживая кнопку в нажатом положении, нажмите кнопку [START/STOP].
TR düğmesini basılı tutarken, [START/STOP] düğmesine basın.
.)‫إيقاف‬/‫] (بدء‬START/STOP[ ‫ اضغط على الزر‬، ‫ أثناء االستمرار في الضغط على الزر‬AR
2

17
11 Checking Readings in Comparison Mode
FR Vérification des mesures en mode de comparaison NL Metingen bekijken in vergelijkingsmodus
DE Überprüfen von Messwerten im Vergleichsmodus RU Проверка результатов измерений в режиме
сравнения
TR Karşılaştırma Modunda Ölçüm Değerlerini Kontrol
IT Controllo dei risultati in modalità Confronto Etme
ES Comprobación de las lecturas en modo comparativo ‫ التحقق من القراءات في وضع المقارنة‬AR

Prior reading
FR Mesure antérieure 1
DE Vorheriger Messwert 1
IT Valore precedente 2 2
ES Lectura anterior 3
NL Eerdere meting 3
RU Прошлое значение 5 4
TR Önceki ölçüm değeri 4 5
‫ ةقبسم ةءارق‬AR 6
6

1 Appears when the reading was taken in Afib mode. ES Aparece cuando la lectura fue realizada en el modo de fibrilación
auricular.
FR S’affiche lorsque la mesure a été effectuée en mode Fibrillation
auriculaire. NL Verschijnt wanneer de meting in de Afib-modus werd verricht.
DE Erscheint, wenn der Messwert im AFib-Modus ermittelt wurde. RU Отображается, если значение получено в режиме ФП.
IT Appare quando la misurazione è stata effettuata in modalità Afib. TR Ölçüm Afib moduna alınınca görünür.
.‫ يظهر عندما يتم الحصول على القراءة في وضع الرجفان األذيني‬AR

18
 2 Appears if an atrial fibrillation (Afib)* was detected ES Aparece si se detecta fibrilación auricular (Afib)* durante la
medición en modo fibrilación auricular. Si esto sigue apareciendo, le
during the Afib mode measurement. If it continues recomendamos que consulte a su médico y siga sus recomendaciones.
to appear, we recommend you to consult with and NL Verschijnt als er een atriumfibrillatie (Afib)* is gedetecteerd tijdens
follow the directions of your physician. de Afib-modusmeting. Als dit blijft verschijnen raden we u aan
FR S’affiche si une fibrillation auriculaire* a été détectée durant une contact op te nemen met uw arts en zijn of haar aanwijzingen op
mesure en mode fibrillation auriculaire. S’il continue d’apparaître, te volgen.
nous vous recommandons de consulter votre médecin et de RU Отображается, если в режиме измерения ФП была определена
suivre ses recommandations. фибрилляция предсердий (ФП)*. Если эти нарушения ритма
DE Wird angezeigt, wenn bei einer Messung im Afib-Modus продолжаются, рекомендуем обратиться к лечащему врачу и
Vorhofflimmern (Afib)* erkannt wurde. Wird das Symbol weiterhin следовать его указаниям.
angezeigt, sollten Sie sich an einen Arzt wenden und dessen TR Afib modunda ölçüm esnasında bir atrial fibrilasyon (Afib)*
Anweisungen befolgen. saptandığında görünür. Görünmeye devam ediyorsa doktorunuza
IT Viene visualizzato se durante una misurazione in modalità Afib danışmanızı ve kendisinin yönergelerini izlemenizi öneririz.
è stata rilevata la presenza di fibrillazione atriale (Afib)*. Se il ‫)* خلل إجراء القياس باستخدام‬Afib( ‫ تظهر في حالة اكتشاف الرجفان األذيني‬AR
simbolo continua ad apparire, è consigliabile rivolgersi al proprio ‫ فإننا نوصيك باستشارة الطبيب‬،‫ وإذا استمرت في الظهور‬.‫وضع الرجفان األذيني‬
medico curante e seguirne le indicazioni. .‫الخاص بك واتباع تعليماته‬

3 Appears if "SYS" is 135 mmHg or above and/or ES Aparece si “SYS” es 135 mmHg o superior y/o “DIA” es 85 mmHg**
o superior.
"DIA" is 85 mmHg** or above.
NL Verschijnt als “SYS” 135 mmHg of hoger is en/of “DIA” 85 mmHg**
FR S’affiche si « SYS » est égale ou supérieure à 135 mmHg et/ou of hoger is.
« DIA » égale ou supérieure à 85 mmHg**.
RU Отображается, если «SYS» 135 мм.рт.ст. и выше и/или «DIA»
DE Wird angezeigt, wenn „SYS“ 135 mmHg oder mehr beträgt und/ 85 мм.рт.ст.** и выше.
oder wenn „DIA“ 85 mmHg** oder mehr beträgt.
TR "SYS" 135 mmHg ya da üstünde olduğunda ve/veya "DIA"
IT Viene visualizzato se la pressione sistolica “SYS” è pari o superiore 85 mmHg** ya da üstünde olduğunda görünür.
a 135 mmHg e/o la pressione diastolica “DIA” è pari o superiore a
85 mmHg**. 85 "DIA" ‫ أو‬/‫ ملليمترً ا زئبقيًا أو أكثر و‬135 ‫" يبلغ‬SYS" ‫ تظهر إذا كان‬AR
.‫ملليمترً ا زئبقيًا** أو أكثر‬

4 Cuff is tight enough. 4 Apply cuff again MORE TIGHTLY.

FR Le brassard est suffisamment serré. FR Poser le brassard en le serrant davantage.
DE Manschette sitzt ausreichend straff. DE Manschette STRAFFER ziehen.
IT Il bracciale è stretto a sufficienza. IT Applicare di nuovo il bracciale STRINGENDOLO DI PIÙ.
ES El manguito está lo suficientemente prieto. ES Vuelva a poner el manguito MÁS PRIETO.
NL Manchet zit strak genoeg. NL Breng de manchet STRAKKER aan.
RU Манжета затянута достаточно туго. RU Наложите манжету еще раз БОЛЕЕ ТУГО.
TR Kolluk yeterince sıkıdır. TR Kolluğu tekrar, DAHA SIKI bir şekilde takın.
.‫ الشريط الضاغط محكم بما يكفي‬AR .‫ لف الشريط الضاغط مرة أخرى بشكل أكثر إحكامًا‬AR

19
5 Appears when your body moves during a ES Aparece cuando se mueve el cuerpo durante una medición. Retire
el manguito, espere unos 2 o 3 minutos e inténtelo de nuevo.
measurement. Remove the arm cuff, wait (No aparece cuando se detecta una posible fibrilación auricular
2-3 minutes and try again. durante una medición en modo fibrilación auricular)
(It does not appear when the possibility of Afib is NL Verschijnt wanneer uw lichaam tijdens een meting beweegt.
detected during a Afib mode measurement) Verwijder de armmanchet, wacht 2-3 minuten en probeer het
opnieuw.
FR S’affiche si vous bougez pendant une mesure. Retirer le brassard,
(Het verschijnt niet wanneer de mogelijkheid op Afib is gedetecteerd
attendre 2 à 3 minutes et essayer à nouveau.
tijdens de Afib-modusmeting)
(Ne s’affiche pas si la possibilité d’une fibrillation auriculaire est
détectée pendant une mesure en mode fibrillation auriculaire.) RU Отображается при движении тела во время измерения.
Снимите манжету, подождите 2-3 минуты и попробуйте еще раз.
DE Wird angezeigt, wenn Sie sich während der Messung bewegen.
(Не отображается, если при измерении в режиме ФП выявлена
Nehmen Sie die Manschette ab, warten Sie 2–3 Minuten und
вероятность ФП)
versuchen Sie es erneut.
(Wird nicht angezeigt, wenn bei einer Messung im Afib-Modus TR Bir ölçüm esnasında vücudunuz hareket ettiğinde görünür.
mögliches Vorhofflimmern erkannt wird) Kolluğu çıkarın, 2-3 dakika bekleyip tekrar deneyin.
(Afib modundaki bir ölçümde Afib olasılığı tespit edildiğinde
IT Viene visualizzato se l’utilizzatore si muove durante la misurazione.
görünmez)
Rimuovere il bracciale, attendere 2-3 minuti e riprovare.
(Il simbolo non appare quando viene rilevata una potenziale presenza ‫ قم بإزالة الشريط الضاغط للذراع‬.‫ تظهر عند تحرك جسمك في أثناء عملية القياس‬AR
di fibrillazione atriale durante una misurazione in modalità Afib) .‫ دقائق وحاول مرة أخرى‬3 ‫ إلى‬2 ‫وانتظر من‬
)‫(ال تظهر عند اكتشاف احتمالية الرجفان األذيني أثناء القياس باستخدام وضع الرجفان األذيني‬

6 Appears when an irregular rhythm* is detected ES Aparece cuando se detecta un ritmo irregular* durante una medición. Si
esto sigue apareciendo, le recomendamos que consulte a su médico.
during a measurement. If it continues to appear, it (No aparece durante una medición en modo fibrilación auricular)
is recommended to consult your physician.
NL Verschijnt wanneer tijdens een meting een onregelmatig ritme*
(It does not appear during a Afib mode measurement) wordt gedetecteerd. Neem contact op met uw arts als dit blijft
verschijnen.
FR S’affiche lorsqu’un rythme irrégulier* est détecté pendant une
(Het verschijnt niet tijdens een Afib-modusmeting)
mesure. S’il continue d’apparaître, il est recommandé de consulter
votre médecin. RU Отображается, если при измерении определяется нерегулярный
(Ne s’affiche pas pendant une mesure en mode fibrillation auriculaire) ритм*. Если этот значок продолжает отображаться, рекомендуем
обратиться к лечащему врачу.
DE Wird angezeigt, wenn während einer Messung ein
(Не отображается при измерении в режиме ФП)
unregelmäßiger Herzschlag* erkannt wird. Wird das Symbol
weiterhin angezeigt, sollten Sie sich an Ihren Arzt wenden. TR Bir ölçüm esnasında düzensiz ritim* saptandığında görünür.
(Wird bei einer Messung im Afib-Modus nicht angezeigt) Görünmeye devam ederse doktorunuza danışmanız önerilir.
(Afib modundaki ölçüm esnasında görünmez)
IT Viene visualizzato se nel corso di una misurazione viene rilevato
un ritmo cardiaco irregolare*. Se il simbolo continua ad apparire ،‫ إذا استمرت في الظهور‬.‫ تظهر عند اكتشاف عدم انتظام ضربات القلب* أثناء القياس‬AR
è consigliabile rivolgersi al proprio medico curante. .‫يُوصى باستشارة الطبيب المختص‬
(Il simbolo non viene visualizzato durante le misurazioni in modalità Afib) )‫(ال تظهر أثناء إجراء عملية القياس باستخدام وضع الرجفان األذيني‬
20
* Afib and an irregular heartbeat rhythm are defined as a rhythm that is 25 % less or 25 % more than the
average rhythm detected while your monitor is measuring blood pressure. The difference between the Afib
indicator function and irregular heartbeat function is:
Afib indicator function: detects Afib possibility in 3-times measurement.
Irregular heartbeat function: detects irregular heartbeat including Afib in 1 measurement.
FR * La fibrillation auriculaire et les pulsations cardiaques irrégulières sont des pulsations dont la fréquence est supérieure ou inférieure de 25 % par
rapport à la moyenne détectée lorsque l’appareil mesure la pression artérielle. La différence entre la fonction indicateur de fibrillation auriculaire
et la fonction pulsations cardiaques irrégulières est la suivante :
Fonction indicateur de fibrillation auriculaire : détecte la possibilité d’une fibrillation auriculaire par une mesure répétée 3 fois.
Fonction pulsations cardiaques irrégulières : détecte des pulsations cardiaques irrégulières, y compris une fibrillation auriculaire, en 1 mesure.
DE * Vorhofflimmern (Afib) und unregelmäßiger Herzschlag sind definiert als ein Herzrhythmus, der 25 % unter oder 25 % über dem mittleren
Herzrhythmus liegt, der während der Blutdruckmessung erkannt wird. Der Unterschied zwischen Afib-Hinweisfunktion und Erkennung
unregelmäßiger Herzschläge ist:
Afib-Hinweisfunktion: Erkennt bei 3-maliger Messung möglicherweise vorliegendes Vorhofflimmern.
Erkennung unregelmäßiger Herzschläge: Erkennt unregelmäßigen Herzschlag einschließlich Vorhofflimmern bei 1-maliger Messung.
IT * Per Afib e battito cardiaco irregolare si intende la presenza di variazioni inferiori del 25% o superiori del 25% nel ritmo rispetto al ritmo medio
rilevato dall’apparecchio durante la misurazione della pressione arteriosa. La differenza tra la funzione dell’indicatore Afib e la funzione battito
cardiaco irregolare è la seguente:
la funzione dell’indicatore Afib rileva la potenziale presenza di fibrillazione atriale mediante 3 misurazioni ripetute.
La funzione battito cardiaco irregolare rileva il battito irregolare inclusa la fibrillazione atriale in 1 misurazione.
ES * La fibrilación auricular y un ritmo de latido cardíaco irregular se definen como aquel ritmo que es el 25% inferior o el 25% superior al ritmo
cardíaco medio detectado mientras el monitor mide la presión arterial. La diferencia entre la función de indicador de fibrilación auricular y la
función de latido cardíaco arrítmico es:
Función de indicador de fibrilación auricular: detecta una posible fibrilación auricular en 3 mediciones.
Función de latido cardíaco irregular: detecta un latido irregular incluyendo fibrilación auricular en 1 medición.
NL * Afib en onregelmatige hartslag zijn gedefinieerd als een hartritme dat meer dan 25% lager of 25% hoger is dan het gemiddelde hartritme
tijdens het meten van de bloeddruk door de meter. Het verschil tussen de Afib-indicatorfunctie en onregelmatige hartslagfunctie is: Afib-
indicatorfunctie: detecteert de mogelijkheid op Afib in een driemalige meting.
Onregelmatige hartslagfunctie: detecteert onregelmatige hartslag inclusief Afib in één meting.
RU * ФП и нерегулярный ритм сердцебиения — это ритм, который на 25 % медленнее или на 25 % быстрее среднего ритма, определенного
прибором при измерении артериального давления. Различия между функцией индикатора ФП и функцией нерегулярного сердцебиения:
Функция индикатора ФП: определяет вероятность ФП при трехкратном измерении.
Функция нерегулярного сердцебиения: определяет нерегулярные сердечные сокращения, включая ФП, при однократном измерении.
TR * Afib ve düzensiz kalp atışı ritmi, ölçüm cihazınız tansiyon ölçümü yaparken saptanan ortalama ritme göre %25’ten az ya da %25'ten fazla sapma
gösteren ritim olarak tanımlanır. Afib göstergesi fonksiyonu ve düzensiz kalp atışı fonksiyonu arasındaki fark şu şekildedir:
Afib göstergesi fonksiyonu: 3 kez yapılan ölçümde Afib olasılığını tespit eder.
Düzensiz kalp atışı fonksiyonu: 1 ölçümde, Afib de dahil olmak üzere düzensiz kalp atışını tespit eder.
‫ االختلف بين‬.‫ عن اإليقاع المتوسط الذي يتم اكتشافه أثناء قياس الجهاز لضغط الدم‬%25 ‫ أو يزيد بنسبة‬%25 ‫ * يعبر كل من الرجفان األذيني واضطراب ضربات القلب عن إيقاع يقل بنسبة‬AR
:‫وظيفة مؤشر الرجفان األذيني ووظيفة اضطراب ضربات القلب هو أن‬
.‫ مرات‬3 ‫ تكتشف احتمالية حدوث رجفان أذيني عند إجراء عمليات القياس‬:‫وظيفة مؤشر الرجفان األذيني‬
.‫ تشير إلى ضربات القلب غير المنتظمة بما في ذلك الرجفان األذيني وذلك عند إجراء عملية قياس واحدة‬:‫وظيفة اضطراب ضربات القلب‬
21
** The high blood pressure definition is based on the 2018 ESH/ESC Guidelines.
FR ** La définition de l’hypertension est basée sur les recommandations ESH/ESC 2018.
DE ** Die Definition für Bluthochdruck basiert auf den 2018 ESH/ESC-Richtlinien.
IT ** La definizione di alta pressione arteriosa si basa sulle linee guida 2018 di ESH/ESC.
ES ** La definición de presión arterial alta se basa en las guías 2018 ESH/ESC.
NL ** De definitie van hoge bloeddruk is gebaseerd op de ESH/ESC-richtlijnen uit 2018.
RU ** Определение высокого артериального давления основано на Рекомендациях 2018 ESH/ESC.
TR ** Yüksek tansiyon tanımı, 2018 ESH/ESC Kılavuzlarını temel alır.
‫ الجمعية األوروبية لطب القلب‬/)ESH( ‫ ** تعريف ضغط الدم المرتفع يستند إلى إرشادات الجمعية األوروبية لفرط ضغط الدم‬AR
.2018 ‫) لعام‬ESC(

Error messages or other problems? Refer to:

FR Messages d’erreur ou autres problèmes ? Voir : NL Foutmeldingen of andere problemen? Instru
ction

Raadpleeg:
Manu
al 1

DE Weitere Fehlermeldungen oder Probleme siehe:

RU Сообщения об ошибках или другие
IT Messaggi di errore o altri problemi? Fare
неисправности? См.
riferimento a:
TR Hata mesajları veya başka sorunlar mı var? Bkz:
ES ¿Hay mensajes de error u otros problemas?
Consulte: :‫ رسائل الخطأ أو المشكلت األخرى؟ ارجع إلى‬AR

22
12 Using Memory Functions
FR Utilisation des fonctions de mémoire NL Geheugenfuncties gebruiken
DE Verwendung der Speicherfunktion RU Использование функции памяти
IT Uso delle funzioni di memoria TR Hafıza Fonksiyonunun Kullanılması
ES Uso de las funciones de memoria ‫استخدام وظائف الذاكرة‬ AR

Before using memory functions, select your user ID.

FR Avant d’utiliser les fonctions de mémoire, sélectionner votre ID Utilisateur.
DE Wählen Sie vor dem Verwenden der Speicherfunktionen Ihre Benutzer-ID aus.
IT Prima di utilizzare le funzioni di memoria selezionare il proprio ID utente.
ES Antes de usar las funciones de memoria, seleccione su ID de usuario.
NL Selecteer uw gebruikers-ID voordat u geheugenfuncties gebruikt.
RU Перед использованием функции памяти выберите идентификатор пользователя.
TR Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.
.‫ حدد معرف المستخدم الخاص بك‬،‫ قبل استخدام وظائف الذاكرة‬AR

12.1 Readings Stored in Memory

FR Mesures stockées en mémoire
DE Gespeicherte Messungen
IT Risultati conservati in memoria
ES Lecturas guardadas en la memoria
NL Meetwaarden opgeslagen in het geheugen
RU Сохранение результатов в памяти
TR Hafızada Saklanan Ölçüm Değerleri
‫ القراءات المخزنة في الذاكرة‬AR
Stores up to 100 readings. ES Almacena hasta 100 lecturas.
FR Mémorise jusqu’à NL Slaat tot maximaal
100 résultats. 100 metingen op.
DE Es werden bis zu RU Сохраняется до
100 Messwerte gespeichert. 100 результатов.
IT Conserva fino a 100 risultati. TR 100 adede kadar ölçüm değeri
saklar.
23 .‫ قراءة‬100 ‫ تقوم بتخزين ما يصل إلى‬AR
Morning/Evening Weekly Averages
FR Moyennes hebdomadaires matin/soir
DE Wöchentliche Morgen-/Abendmittelwerte
IT Media settimanale mattutina e serale
ES Valor promedio semanal de mañana y noche
wk ago
NL Weekgemiddelden van ochtend- en avondwaarden
RU Утренние/вечерние средние значения за неделю
TR Sabah/Akşam Haftalık Ortalamaları
‫المسائية لضغط الدم‬/‫ المعدالت األسبوعية الصباحية‬AR
wks ago

wks ago

Appears if "SYS" is 135 mmHg or above and/or

"DIA" is 85 mmHg or above in the morning
wks ago
weekly average.
FR S’affiche si « SYS » est égale ou supérieure à 135 mmHg et/ou « DIA » égale ou supérieure à 85 mmHg dans la moyenne hebdomadaire du matin.
DE Wird angezeigt, wenn im wöchentlichen Morgenmittelwert „SYS“ 135 mmHg oder mehr und/oder „DIA“ 85 mmHg oder mehr beträgt.
IT Viene visualizzato se la pressione sistolica “SYS” è pari o superiore a 135 mmHg e/o la pressione diastolica “DIA” è pari o superiore a 85 mmHg
nella media mattutina settimanale.
ES Aparece si “SYS” es 135 mmHg o superior y/o “DIA” es 85 mmHg o superior en el promedio semanal de mañana.
NL Verschijnt als “SYS” 135 mmHg of hoger is en/of “DIA” 85 mmHg of hoger is in het ochtendweekgemiddelde.
RU Отображается, если средние утренние значения за неделю «SYS» 135 мм.рт.ст. и выше и/или «DIA» 85 мм.рт.ст. и выше.
TR Sabah haftalık ortalamasında "SYS" 135 mmHg ya da üstünde olduğunda ve/veya "DIA" 85 mmHg** ya da üstünde olduğunda görünür.
.‫ ملليمترً ا زئبقيًا أو أكثر في المعدل األسبوعي الصباحي‬85 "DIA" ‫ أو‬/‫ ملليمترً ا زئبقيًا أو أكثر و‬135 ‫" يبلغ‬SYS" ‫ تظهر إذا كان‬AR
To know how to calculate weekly averages, refer to section 10 of the Instruction Manual .
FR Pour savoir comment calculer les moyennes hebdomadaires, se reporter à la section 10 du Mode d’emploi .
DE Wie die wöchentlichen Mittelwerte berechnet werden, ist in Abschnitt 10 der Gebrauchsanweisung beschrieben.
IT Per sapere come calcolare le medie settimanali, consultare la sezione 10 del manuale di istruzioni .
ES Para saber cómo calcular mediciones semanales, consulte la sección 10 del manual de instrucciones .
NL Zie paragraaf 10 van de gebruiksaanwijzing voor aanwijzingen hoe u het wekelijkse gemiddelde kunt berekenen.
RU О том, как рассчитываются средние значения за неделю, см. раздел 10 этого руководства по эксплуатации .
TR Haftalık ortalamaların nasıl hesaplanacağını öğrenmek için, Kullanım Kılavuzu 'de bölüm 10'a bakın.
. ‫ من دليل اإلرشادات‬10 ‫ ارجع إلى القسم‬،‫ لمعرفة كيفية حساب المعدالت األسبوعية‬AR
24
12.3 Average of the Latest 2 or 3 Readings Taken within a
10 Minute Span
FR Moyenne des 2 ou 3 dernières mesures prises en l’espace de 10 minutes
DE Mittelwert der letzten 2 oder 3 Messwerte, die in einem 10-Minuten-Zeitrahmen erfasst 3 sec+
wurden
IT Media degli ultimi 2 o 3 risultati ottenuti nell’arco di 10 minuti
ES Promedio de las 2 o 3 últimas lecturas realizadas en un intervalo de 10 minutos
NL Gemiddelde van de laatste 2 of 3 metingen uitgevoerd binnen een tijdspanne van
10 minuten
RU Среднее значение последних 2-х или 3-х результатов, полученных в течение
10 минут
TR 10 Dakika Aralıkta Alınan Son 2 veya 3 Ölçüm Değerinin Ortalaması
‫ دقائق‬10 ‫ قراءات مسجلة خلل مدة زمنية تبلغ‬3 ‫ معدل آخر قراءتين أو‬AR

12.4 Deleting All Readings for 1 User NL Alle meetresultaten voor 1 gebruiker wissen
FR Suppression de toutes les mesures pour 1 utilisateur RU Удаление всех измерений одного пользователя
DE Löschen aller Messwerte für Benutzer 1 TR 1 Kullanıcı için Tüm Ölçüm Değerlerini Silme
IT Eliminazione di tutti i risultati relativi a 1 utente ‫ مسح جميع القراءات الخاصة بمستخدم واحد‬AR
ES Eliminación de todas las lecturas de un usuario

1 2 4sec+ 3 4 4sec+ 5

25
13 Other Settings
FR Autres réglages NL Andere instellingen
DE Weitere Einstellungen RU Другие настройки
IT Altre impostazioni TR Diğer Ayarlar
ES Otros ajustes ‫اإلعدادات األخرى‬ AR

13.1 Disabling/Enabling Bluetooth

FR Désactivation/activation de Bluetooth
10 sec+
DE Deaktivieren/Aktivieren der Bluetooth-Funktion
IT Disattivazione/attivazione della funzione Bluetooth
ES Activar o desactivar el Bluetooth
NL Bluetooth uitschakelen/inschakelen
RU Выключение/включение Bluetooth
TR Bluetooth'u Devre Dışı Bırakma/Etkinleştirme
Bluetooth ‫ تعطيل خاصية‬/‫ تمكين‬AR 3 sec+

Bluetooth is enabled by default. ES El Bluetooth está activado por defecto.

FR Bluetooth est activé par défaut. NL Bluetooth is standaard ingeschakeld.
DE Die Bluetooth-Funktion ist standardmäßig aktiviert. RU Bluetooth включен по умолчанию.
IT La funzione Bluetooth è attiva per impostazione TR Bluetooth varsayılan olarak etkindir.
predefinita.
.‫ بشكل افتراضي‬Bluetooth ‫ يتم تمكين خاصية‬AR

26
13.2 Restoring to the Default Settings NL De standaardinstellingen herstellen
FR Réinitialisation aux réglages par défaut RU Восстановление настроек по умолчанию
DE Wiederherstellen der Standardeinstellungen TR Varsayılan Ayarları Geri Yükleme
IT Ripristino delle impostazioni predefinite ‫ استعادة اإلعدادات االفتراضية‬AR
ES Restablecimiento a los ajustes de fábrica

1 4sec+ 2 3 4sec+ 4

27
If your systolic pressure is more than 210 mmHg:
After the arm cuff starts to inflate, press and hold the [START/STOP] button until the monitor inflates 30 to 40 mmHg higher
than your expected systolic pressure.
FR Si votre pression systolique est supérieure à 210 mmHg :
Lorsque le brassard commence à se gonfler, appuyer sur le bouton [START/STOP] et le maintenir enfoncé jusqu’à ce que le tensiomètre atteigne une pression
de gonflage supérieure de 30 à 40 mmHg à votre pression systolique attendue.
DE Nachdem die Manschette begonnen hat, sich aufzupumpen, drücken Sie die [START/STOP]-Taste, und halten Sie sie gedrückt, bis ein Druck von
30 bis 40 mmHg über Ihrem erwarteten systolischen Druck erreicht ist.
IT Se la pressione sistolica è superiore a 210 mmHg:
Quando il bracciale inizia a gonfiarsi, premere e mantenere premuto il pulsante [START/STOP] finché il misuratore non raggiunge una pressione da
30 a 40 mmHg superiore rispetto al valore di pressione sistolica atteso.
ES En caso de que su presión arterial sistólica esté por encima de 210 mmHg:
Una vez que el manguito comience a inflarse, mantenga pulsado el botón [START/STOP] hasta que el monitor indique que el inflado está entre 30 y 40 mmHg
por encima de la presión arterial sistólica estimada.
NL Als uw systolische druk hoger is dan 210 mmHg:
Zodra de armmanchet wordt opgepompt, houdt u de knop [START/STOP] ingedrukt totdat de meter 30 tot 40 mmHg hoger aangeeft dan uw verwachte
systolische druk.
RU После того, как началось автоматическое наполнение манжеты воздухом, нажмите и удерживайте кнопку [START/STOP] до тех пор,
пока прибор не поднимет давление до значения, превышающего ожидаемое систолическое давление на 30-40 мм.рт.ст.
TR Sistolik basıncınız 210 mmHg'den fazlaysa:
Manşet şişmeye başladıktan sonra, [START/STOP] düğmesine basın ve ölçüm cihazı beklediğiniz sistolik basınç değerinden 30 ila 40 mmHg daha fazla şişene
kadar basılı utun.
:‫ ملليمترات زئبقية‬210 ‫ إذا كان ضغط الدم االنقباضي أكثر من‬AR
.‫ ملليمترً ا زئبقيًا أعلى من قيمة ضغط الدم االنقباضي المتوقعة‬40 ‫ إلى‬30 ‫] حتى يقوم الجهاز بالنفخ من‬START/STOP[ ‫ اضغط مع االستمرار على الزر‬،‫بعد بدء انتفاخ الشريط الضاغط للذراع‬

28
14 Optional Medical Accessories
FR Accessoires médicaux en option NL Optionele medische accessoires
DE Medizinisches optionales Zubehör RU Дополнительно принадлежности
IT Accessori medicali opzionali TR Opsiyonel Tıbbi Aksesuarlar
ES Accesorios médicos opcionales ‫الملحقات الطبية االختيارية‬ AR

Arm Cuff AC Adapter

(HEM-FL31) (HHP-CM01) (HHP-BFH01)
22 - 42 cm

Do not throw the air plug away. The air plug can be applicable to the optional cuff.
FR Ne pas jeter la prise de gonflage. La prise de gonflage peut être utilisée pour le brassard en option.
DE Entsorgen Sie den Luftschlauchstecker nicht. Der Luftschlauchstecker wird für die optionale Manschette verwendet.
IT Non gettare via l’attacco del tubo dell’aria. L’attacco del tubo dell’aria può essere applicato al bracciale opzionale.
ES No tire el conector para tubo de aire. El conector para tubo de aire puede ser utilizado con el manguito opcional.
NL Gooi de plug van de luchtslang niet weg. De plug van de luchtslang kan worden gebruikt op de optionele manchet.
RU Не выбрасывайте воздушный штекер. Он может подойти к дополнительной манжете.
TR Hava tıpasını atmayın. Hava tıpası isteğe bağlı kolluğa uygulanabilir.
.‫ يمكن استعمال سدادة الهواء مع الشريط الضاغط االختياري‬.‫ ال تتخلص من سدادة الهواء‬AR

29
15 Other Optional Parts
FR Autres pièces en option NL Overige optionele onderdelen
DE Weitere optionale Teile RU Другие дополнительно приобретаемые запасные части
IT Altri componenti opzionali TR Diğer Aksesuarlar
ES Otras piezas opcionales ‫أجزاء اختيارية أخرى‬ AR

Protective LCD Cover

(HEM-CACO-734)

https://www.omron-healthcare.com/

30
 Manufacturer Produttore Производитель OMRON HEALTHCARE Co., Ltd.
Fabricant Fabricante Üretici
53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN
Hersteller Fabrikant ‫الشركةالمُصنعة‬
EU-Repräsentant Представитель в ЕС OMRON HEALTHCARE EUROPE B.V.
Rappresentante per l’UE AB temsilcisi
Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS
Representante en la UE ‫جهة التمثيل باالتحاد األوروبي‬
EU-representative Vertegenwoordiging in de EU www.omron-healthcare.com
Mandataire dans l’UE
Importer in EU Importatore per l’UE Импортер в ЕС
Importateur dans l’UE Importador en la UE AB’de İthalatçı
Importeur in der EU Importeur in de EU ‫المستورد في االتحاد األوروبي‬
Production facility Stabilimento di produzione Производственное OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.
Site de production Planta de producción подразделение
Produktionsstätte Productiefaciliteit Üretim Tesisi No.28 VSIP II, Street 2, Vietnam-Singapore Industrial Park II,
‫ منشأةالتصنيع‬Binh Duong Industry-Services-Urban Complex, Hoa Phu Ward,
Thu Dau Mot City, Binh Duong Province, Vietnam
Subsidiaries Consociate Филиалы OMRON HEALTHCARE UK LTD.
Succursales Empresas filiales Yan Kuruluşlar
Niederlassungen Dochteronder- Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
‫الشركات التابعة‬
nemingen www.omron-healthcare.com
OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH
Konrad-Zuse-Ring 28, 68163 Mannheim, GERMANY
www.omron-healthcare.com
OMRON SANTÉ FRANCE SAS
3, Parvis de la Gare, 94130 Nogent-sur-Marne, FRANCE
Uniquement pour le marché français:
OMRON Service Après Vente
Nº Vert 0 800 91 43 14
www.omron-healthcare.com
Made in Vietnam / Fabriqué en Vietnam / Hergestellt in Vietnam / Prodotto in Vietnam / Fabricado en Vietnam / Geproduceerd in Vietnam / Сделано во Вьетнаме /
Vietnam'da Üretilmiştir / ‫صنع في فيتنام‬
Issue Date / Date de publication / Ausgabedatum / Data di pubblicazione / Fecha de publicación / Uitgiftedatum / Дата выпуска / Teslim Tarihi / ‫تاريخ اإلصدار‬: 2019-09-05

IM2-HEM-7361T-E-02-09/2019
2895865-4B