Omron Healthcare M4 Intelli IT - HEM-7155T-EBK El kitabı

Marka: Omron Healthcare

Modeli: M4 Intelli IT - HEM-7155T-EBK

Kategori: Kan basıncı birimleri

Tip: El kitabı

Bu kılavuz aynı zamanda aşağıdakiler için de uygundur:

Automatic Upper Arm Blood Pressure Monitor

M4 Intelli IT (HEM-7155T-EBK)

X4 Smart (HEM-7155T-ESL)

Instruction Manual

Symboles/ Symbole/ Simboli/ Símbolos/

Symbolen/ Символы/ Semboller/

ίϣέϟ΍

Read Instruction manual and before use.

Lire le mode d’emploi et avant l’utilisation.

Lesen Sie vor der Verwendung die Gebrauchsanweisung und .

Leggere il manuale di istruzioni e prima dell’uso.

Lea el manual de instrucciones y antes del uso.

Lees de gebruiksaanwijzing en voor gebruik.

Прочтите руководство по эксплуатации и перед использованием.

Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

ϡ΍ΩΧΗγϻ΍ϝΑϗ

ϭ Ε΍ΩΎηέϹ΍ϝϳϟΩ΃έϗ΍

EN1

1. Introduction

Thank you for purchasing the OMRON Automatic Upper Arm Blood

Pressure Monitor. This blood pressure monitor uses the oscillometric

method of blood pressure measurement. This means this monitor

detects your blood movement through your brachial artery and

converts the movements into a digital reading.

1.1 Safety Instructions

This instruction manual provides you with important information

about the OMRON Automatic Upper Arm Blood Pressure Monitor.

To ensure the safe and proper use of this monitor, READ and

UNDERSTAND all of the safety and operating instructions. If you do

not understand these instructions or have any questions, contact

your OMRON retail outlet or distributor before attempting to

use this monitor. For specific information about your own blood

pressure, consult with your physician.

1.2 Intended Use

This device is a digital monitor intended for use in measuring blood

pressure and pulse rate in adult patient population. The device detects

the appearance of irregular heartbeats during measurement and

gives a warning signal with readings. It is mainly designed for general

household use.

1.3 Receiving and Inspection

Remove this monitor from the packaging and inspect for damage. If

this monitor is damaged, DO NOT USE and consult with your OMRON

retail outlet or distributor.

2. Important Safety Information

Read the Important Safety Information in this instruction manual

before using this monitor. Follow this instruction manual thoroughly

for your safety.

Keep for future reference. For specific information about your own

blood pressure, CONSULT WITH YOUR PHYSICIAN.

2.1 Warning

Indicates a potentially hazardous

situation which, if not avoided, could

result in death or serious injury.

• DO NOT use this monitor on infants, toddlers, children or persons

who cannot express themselves.

• DO NOT adjust medication based on readings from this blood

pressure monitor. Take medication as prescribed by your physician.

ONLY a physician is qualified to diagnose and treat high blood

pressure.

• DO NOT use this monitor on an injured arm or an arm under medical

treatment.

•

DO NO

T 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 equipment, magnetic resonance imaging (MRI) equipment,

computerized tomography (CT) scanners. This may result in incorrect

operation of the monitor and/or cause an inaccurate reading.

• DO NOT use this monitor in oxygen rich environments or near

flammable gas.

•

onsult with your physician before using this monitor if you have

common arrhythmias such as atrial or ventricular premature beats

or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes;

pregnancy; pre-eclampsia or renal disease. NOTE that any of these

conditions in addition to patient motion, trembling, or shivering

may affect the measurement reading.

•

VER diagnose or treat yourself based on your readings. ALWAYS

consult with your physician.

• To help avoid strangulation, keep the air tube and AC adapter cable

away from infants, toddlers and children.

• This product contains small parts that may cause a choking hazard if

swallowed by infants, toddlers and children.

Data Transmission

• This product emits radio frequencies (RF) in the 2.4GHz band.

DO NOT use this product in locations where RF is restricted, such as

on an aircraft or in hospitals. Turn off the Bluetooth® feature in this

monitor, remove batteries and/or unplug the AC adapter when in

RFrestricted areas.

EN2

AC Adapter (optional accessory) Handling and Usage

• DO NOT use the AC adapter if this monitor or the AC adapter cable is

damaged. If this monitor or the cable is damaged, turn off the power

and unplug the AC adapter immediately.

• Plug the AC adapter into the appropriate voltage outlet. DO NOT

use in a multi-outlet plug.

• NEVER plug in or unplug the AC adapter from the electric outlet

with wet hands.

• DO NOT disassemble or attempt to repair the AC adapter.

Battery Handling and Usage

• Keep batteries out of the reach of infants, toddlers and children.

2.2 Caution

Indicates a potentially hazardous

situation which, if not avoided,may

result in minor or moderate injury to

the user or patient or damage to the

equipment or other property.

• Stop using this monitor and consult with your physician if you

experience skin irritation or discomfort.

• Consult with your physician before using this monitor on an arm

where intravascular access or therapy, or an arteriovenous (A-V)

shunt, is present because of temporary interference to blood flow

and could result in injury.

• Consult with your physician before using this monitor if you have

had a mastectomy.

• Consult with your physician before using this monitor if you have

severe blood flow problems or blood disorders as cuff inflation can

cause bruising.

• DO NOT take measurements more often than necessary because

bruising, due to blood flow interference, may occur.

• ONLY inflate the arm cuff when it is applied on your upper arm.

• Remove the arm cuff if it does not start deflating during a

measurement.

• DO NOT use this monitor for any purpose other than measuring

blood pressure.

• During measurement, make sure that no mobile device or any other

electrical device that emit electromagnetic fields is within 30 cm of

this monitor. This may result in incorrect operation of the monitor

and/or cause an inaccurate reading.

• DO NOT disassemble or attempt to repair this monitor or other

components. This may cause an inaccurate reading.

• DO NOT use in a location where there is moisture or a risk of water

splashing this monitor. This may damage this monitor.

• DO NOT use this monitor in a moving vehicle such as in a car or on

an aircraft.

• DO NOT drop or subject this monitor to strong shocks or vibrations.

• DO NOT use this monitor in places with high or low humidity or high

or low temperatures. Refer to section 6.

• During measurement, observe the arm to ensure that the monitor is

not causing prolonged impairment to blood circulation.

• DO NOT use this monitor in high-use environments such as medical

clinics or physician offices.

• DO NOT use this monitor with other medical electrical (ME)

equipment simultaneously. This may result in incorrect operation of

the monitor and/or cause an inaccurate reading.

• Avoid bathing, drinking alcohol or caffeine, smoking, exercising and

eating for at least 30 minutes before taking a measurement.

• Rest for at least 5 minutes before taking a measurement.

• Remove tight-fitting or thick clothing from your arm while taking a

measurement.

• Remain still and DO NOT talk while taking a measurement.

• ONLY use the arm cuff on persons whose arm circumference is

within the specified range of the cuff.

• Ensure that this monitor has acclimated to room temperature before

taking a measurement. Taking a measurement after an extreme

temperature 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.

• To unplug the air plug, pull on the plastic air plug at the base of the

tube, not the tube itself.

EN3

• ONLY use the AC adapter, arm cuff, batteries and accessories

specified for this monitor. Use of unsupported AC adapters, arm

cuffs and batteries may damage and/or may be hazardous to this

monitor.

• ONLY use the approved arm cuff for this monitor. Use of other arm

cuffs may result in incorrect readings.

• Inflating to a higher pressure than necessary may result in bruising

of the arm where the cuff is applied. NOTE: refer to “If your systolic

pressure is more than 210mmHg” in section 13 of instruction

manual

for additional information.

• Read and follow the “Correct Disposal of This Product” in section 7

when disposing of the device and any used accessories or optional

parts.

Data Transmission

• DO NOT replace batteries or unplug the AC adapter while your

readings are being transferred to your smart device. This may result

in incorrect operation of this monitor and failure to transfer your

blood pressure data.

AC Adapter (optional accessory) Handling and Usage

• Fully insert the AC adapter into the outlet.

• When unplugging the AC adapter from the outlet, be sure to safely

pull from the AC adapter. DO NOT pull from the AC adapter cable.

• When handling the AC adapter cable:

Do not damage it. / Do not break it. / Do not tamper with it.

DO NOT pinch it. / Do not forcibly bend or pull it. / Do not twist it.

DO NOT use it if it is gathered in a bundle.

DO NOT place it under heavy objects.

• Wipe any dust off of the AC adapter.

• Unplug the AC adapter when not in use.

• Unplug the AC adapter before cleaning this monitor.

Battery Handling and Usage

• DO NOT insert batteries with their polarities incorrectly aligned.

• ONLY use 4 “AA” alkaline or manganese batteries with this monitor.

DO NOT use other types of batteries. DO NOT use new and used

batteries together. DO NOT use different brands of batteries

together.

• Remove batteries if this monitor will not be used for a long period of

time.

• If battery fluid should get in your eyes, immediately rinse with

plenty of clean water. Consult with your physician immediately.

• 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.

Remember to have a record of your blood pressure and pulse

readings for your physician. A single measurement does not provide

an accurate indication of your true blood pressure.

Please use the Blood Pressure Diary to keep records of several

readings over a certain period of time. To download PDF files of the

diary, visit www.omron-healthcare.com.

EN4

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

appears or the arm

cuff does not inflate.

The [START/STOP] button was pressed

while the arm cuff is not applied.

Press the [START/STOP] button again to turn the monitor off.

After inserting the air plug securely and applying the arm cuff

correctly, press the [START/STOP] button.

Air plug is not completely plugged into

the monitor.

Insert the air plug securely.

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

appears or a

measurement

cannot be

completed after the

arm cuff inflates.

You move or talk during a measurement

and the arm cuff does not inflate

sufficiently.

Remain still and do not talk during a measurement. If “E2”

appears repeatedly, inflate the arm cuff manually until the

systolic pressure is 30 to 40 mmHg above your previous

readings. Refer to section 13 of instruction manual

Due to the systolic pressure is above

210mmHg, a measurement cannot be

taken.

appears

The arm cuff is inflated exceeding the

maximum allowable pressure.

Do not touch the arm cuff and/or bend the air tube while taking

a measurement. If inflating the arm cuff manually, refer to

section 13 of instruction manual

appears

You move or talk during a measurement.

Vibrations disrupt a measurement.

Remain still and do not talk during a measurement.

appears

The pulse rate is not detected correctly. Apply the arm cuff correctly, then take another measurement.

Refer to section 7 of instruction manual . Remain still and sit

correctly during a measurement.

If the “

” symbol continues to appear, we recommend you to

consult with your physician.

/ /

appears

does not flash during

a measurement.

EN5

Display/Problem Possible Cause Solution

appears

The monitor has malfunctioned. Press the [START/STOP] button again. If “Er” still appears, contact

your OMRON retail outlet or distributor.

appears

The monior cannot connect to a smart

device or transmit data correctly.

Follow the instructions shown in the “OMRON connect” app.

If the “Err” symbol still appears after checking the app, contact

your OMRON retail outlet or distributor.

flashes

The monitor is waiting for pairing with

the smart device.

Refer to section 5 of instruction manual

for pairing your

monitor with your smart device, or press [START/STOP] button

to cancel pairing and turn your monitor off.

flashes

The monitor is ready to transfer your

readings to the smart device.

Open the “OMRON connect” app to transfer your readings.

flashes

More than 48 readings are not

transferred.

Pair or transfer your readings to the “OMRON connect” app so

you can keep them in memory in the app, and this error symbol

disappears.

The date and time is not set.

appears

There are 60 readings in memory to be

transferred

flashes

Batteries are low. Replacing all 4 batteries with new ones is recommended. Refer

to section 4 of instruction manual

appears or the

monitor is turned

off unexpectedly

during a

measurement

Batteries are depleted. Immediately replace all 4 batteries with new ones. Refer to

section 4 of instruction manual

Nothing appears on the

display of the monitor.

Battery polarities are not properly

aligned.

Check the battery installation for proper placement. Refer to

section 4 of instruction manual

Readings appear too high or

too low.

Blood pressure varies constantly. Many factors including stress, time of day, and/or how you apply the arm

cuff, may affect your blood pressure. Review section 2 of instruction manual

EN6

Display/Problem Possible Cause Solution

Any other communication

issue occurs.

Follow the instructions shown in the smart device, or visit the “Help” section in the “OMRON

connect" app for further help. If the problem still persists, contact your OMRON retail outlet or

distributor.

Any other problem occurs.

Press the [START/STOP] button to turn the monitor off, then press it again to take a measurement.

If the 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.

4. Limited Warranty

Thank you for buying an OMRON product. This product is constructed of high 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 and maintained as described in the instruction manual.

This product is warranted by OMRON for a period of 3 years after the date of purchase. The proper construction, workmanship and materials of

this product is warranted by OMRON. During this period of warranty OMRON will, without charge for labour or parts, repair or replace the defect

product or any defective parts.

The warranty does not cover any of the following:

A. Transport costs and risks of transport.

B. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.

C. Periodic check-ups and maintenance.

D. Failure or wear of optional parts or other attachments other than the main device itself, unless explicitly warranted above.

E. Costs arising due to non-acceptance of a claim (those will be charged for).

F. Damages of any kind including personal caused accidentally or from misuse.

G. Calibration service is not included within the warranty.

H. Optional parts have a one (1) year warranty from date of purchase. Optional parts include, but are not limited to the following items: cuff and

cuff tube.

Should warranty service be required please apply to the dealer whom the product was purchased from or an authorised OMRON distributor. For

the address refer to the product packaging / literature or to your specialised retailer. If you have difficulties in finding OMRON customer services,

www.omron-healthcare.com

Repair or replacement under the warranty does not give rise to any extension or renewal of the warranty period.

The warranty will be granted only if the complete product is returned together with the original invoice / cash ticket issued to the consumer by the

retailer.

EN7

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.

DO NOT disassemble or attempt to repair this monitor or other components. This may cause an inaccurate reading.

5.2 Storage

• Keep your monitor in the storage case when not in use.

1. Remove the arm cuff from the monitor.

Caution

To unplug the air plug, pull on the plastic air plug at the base of the tube, not the tube itself.

2. Gently fold the air tube into the arm cuff. Note: Do not bend or crease the air tube excessively.

3. Place your monitor and other components in the storage case.

• Store your monitor and other components in a clean, safe location.

• Do not store your monitor and other components:

• If your monitor and other components are wet.

• In locations exposed to extreme temperatures, humidity, direct sunlight, dust or corrosive vapors such as bleach.

• In locations exposed to vibrations or shocks.

5.3 Cleaning

• Do not use any abrasive or volatile cleaners.

• 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.

• Do not wash or immerse your monitor and arm cuff or other components in water.

• Do not use gasoline, thinners or similar solvents to clean your monitor and arm cuff or other components.

5.4 Calibration and Service

• The accuracy of this blood pressure monitor has been carefully tested and is designed for a long service life.

• It is generally recommended to have the unit inspected every two years to ensure correct functioning and accuracy. Please consult your

authorised OMRON dealer or the OMRON Customer Service at the address given on the packaging or attached literature.

Caution

EN8

6. Specifications

Product description Automatic Upper Arm Blood Pressure Monitor

Product category Electronic Sphygmomanometers

Model (code) M4 Intelli IT (HEM-7155T-EBK)

X4 Smart (HEM-7155T-ESL)

Display LCD digital display

Cuff pressure range 0 to 299mmHg

Pulse measurement range

40 to 180 beats / min.

Blood pressure measurement range

SYS: 60 to 260mmHg / DIA: 40 to 215mmHg

Accuracy Pressure: ±3mmHg / Pulse: ±5% of display reading

Inflation Automatic by electric pump Deflation

Automatic pressure release valve

Measurement method Oscillometric method Transmission method Bluetooth

Low Energy

Wireless communication Frequency range: 2.4GHz (2400 - 2483.5MHz) / Modulation: GFSK

Effective radiated power: <20dBm

Operating mode Continuous operation

IP classification Monitor: IP20 / Optional AC adapter: IP21

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 50 - 60Hz 0.12 - 0.065A)

Battery life Approximately 1000 measurements (using new alkaline batteries)

Durable period (Service life) Monitor: 5 years / Cuff: 5 years / Optional AC adapter: 5 years

Operating conditions +10 to +40°C / 15 to 90% RH (non-condensing) / 800 to 1060hPa

Storage / Transport conditions -20 to +60°C / 10 to 90% RH (non-condensing)

Contents Monitor, arm cuff (HEM-FL31), 4 “AA” batteries, storage case, Instruction Manual

and

, setup instructions

Protection against electric shock Internally powered ME equipment (when using only batteries)

Class II ME equipment (optional AC adapter)

Weight Monitor: approximately 340g (not including batteries) / Arm cuff: approximately 163g

Dimensions (approximately value) Monitor: 105mm (W) × 85mm (H) × 152mm (L)

Arm cuff: 145mm × 532mm (air tube: 750mm)

Memory Stores up to 60 readings per user

EN9

Note

• 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**.

• IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This monitor and optional AC adapter are

protected against solid foreign objects of 12.5 mm diameter and greater such as a finger. The optional AC adapter is protected against vertically

falling water drops which may cause issues during a normal operation.

* Topouchian J et al. Vascular Health and Risk Management 2018:14 189–197

** Chahine M.N. et al. Medical Devices: Evidence and Research 2018:11 11–20

About a wireless communication interference

This product operates in an unlicensed ISM band at 2.4 GHz. In the event this product is used near other wireless devices such as microwave and

wireless LAN, which operate on the same frequency band as this product, there is a possibility that interference may occur. If interference occurs,

stop the operation of the other devices or relocate this product away from other wireless devices before attempting to use it.

7. Correct Disposal of This Product (Waste Electrical & Electronic Equipment)

This marking shown on the product or its literature, indicates that it should not be disposed of, with other household wastes at the

end of its working life.

To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate this product 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.

8. Important Information Regarding Electromagnetic Compatibility (EMC)

HEM-7155T-EBK and HEM-7155T-ESL conform to EN60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.

Further documentation in accordance with this EMC standard is available at

www.omron-healthcare.com

Refer to the EMC information for HEM-7155T-EBK and HEM-7155T-ESL on the website.

EN10

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-7155T-EBK and HEM-7155T-ESL are complied with Directive

2014/53/EU. The full text of the EU declaration of conformity is available at the following internet address: www.omron-healthcare.com

• This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan. The Core component for OMRON

blood pressure monitors, which is the Pressure Sensor, is produced in Japan.

• Please report to the manufacturer and the competent authority of the Member State in which you are established about any serious incident

that has occurred in relation to this device.

SD1

Symbols Description

Description des symboles

Beschrijving van symbolen

Beschreibung der Symbole

Описание символов

Descrizione dei simboli

Simgelerin Açıklaması

Descripción de los símbolos

ίϭϣέϟ΍Ρέη

Applied part - TypeBF Degree of protection

against electric shock (leakage current)

Pièce appliquée -

TypeBF Degré de protection

contre les chocs électriques

(courant de fuite)

Anwendungsteil–

TypBF Schutz vor Strom-

schlägen (Ableitstrom)

Parti applicate - TipoBF

Livello di protezione contro

le folgorazioni (corrente di

dispersione)

Partes en contacto:

TipoBF Grado de protección

contra descargas eléctricas

(corriente de fuga)

Toegepast onderdeel -

TypeBF-beschermingsgraad

tegen elektrische schokken

(lekstroom)

Рабочая часть аппарата

- Степень защиты от

поражения электрическим

током (токи утечки) ТипBF

Uygulanan parça - TipBF

Elektrik çarpmasına karşı

koruma derecesi (kaçak akım)

ΔϳΎϣΣϟ΍ΔΟέΩϖΑρϣϟ΍˯ίΟϟ΍

έΎϳΗϟ΍Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍Ωο

BFωϭϧϠϟΏέγΗϣϟ΍

Class II equipment.

Protection against electric shock

Équipement de classe II.

Protection contre les chocs

électriques

Gerät der Klasse II.

Schutz vor Stromschlägen

Apparecchiatura di

Classe II. Protezione contro le

folgorazioni

Equipo de Clase II.

Protección contra descargas

eléctricas

Apparatuur van

KlasseII. Bescherming tegen

elektrische schokken

Изделие класса II

Защита от поражения

электрическим током

Sınıf II ünite. Elektrik

çarpmasına karşı koruma

ΩοΔϳΎϣΣϟ΍IIΔ΋ϔϟ΍ϥϣίΎϬΟ

Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍

IP XX

Ingress protection degree provided by

IEC60529

Degré de protection

selon CEI60529

Grad des Eindring-

schutzes gemäß IEC60529

Livello di protezione IP

in base a IEC60529

Grado de protección

según la norma internacional

IEC60529

Beschermingsklasse

volgens IEC60529

Степень защиты,

обеспечиваемая

оболочками, согласно

IEC60529

Su girmesine karşı

koruma derecesi IEC60529

tarafından verilmiştir

ΔϣΩϘϣϟ΍ϝϭΧΩϟ΍ΔϳΎϣΣΔΟέΩ

,(&έΎϳόϣΔργ΍ϭΑ

CE Marking

Marquage CE

CE-Kennzeichnung

Contrassegno CE

Marcado CE

CE-merkteken

Знак соответствия

директиве ЕС

CE İşareti

ΔϧΟϠϟ΍ϊϣϖϓ΍ϭΗϟ΍Δϣϼϋ

&(ΔϳΑϭέϭϷ΍

SD2

Serial number

Numéro de série

Seriennummer

Numero di serie

Número de serie

Serienummer

Серийный номер

Seri numarası

ϝγϠγΗϣϟ΍ϡϗέϟ΍

LOT number

Numéro de LOT

LOT-Nummer

Numero di lotto

Número de lote

Partijnummer

Код (номер) партии

Parti numarası

ΔϠϳϐηΗϟ΍ϡϗέ

Medical device

Dispositif médical

Medizinprodukt

Dispositivo medico

Producto sanitario

Medisch apparaat

Медицинский прибор

Tıbbi cihaz

ϲΑρίΎϬΟ

Temperature limitation

Limitation de température

Temperaturbegrenzung

Limite di temperatura

Limitación de la

temperatura

Temperatuurbegrenzing

Температурный

диапазон

Sıcaklık sınırlaması

ΔΑγΎϧϣϟ΍Γέ΍έΣϟ΍ΔΟέΩΩϭΩΣ

Humidity limitation

Limitation d’humidité

Luftfeuchtigkeits-

begrenzung

Limite di umidità

Limitación de la humedad

Vochtigheidsbegrenzing

Диапазон влажности

Nem sınırlaması

ΔΑγΎϧϣϟ΍ΔΑϭρέϟ΍ΩϭΩΣ

Atmospheric pressure limitation

Limitation de pression

atmosphérique

Luftdruckbegrenzung

Limite di pressione

atmosferica

Limitación de la presión

atmosférica

Luchtdrukbegrenzing

Ограничение

атмосферного давления

Atmosferik basınç

sınırlaması

ΏγΎϧϣϟ΍ϱϭΟϟ΍ρϐοϟ΍ΩϭΩΣ

Indication of connector polarity

Indication de la polarité

des connecteurs

Anzeige der

Steckerpolarität

Indicazione della

polarità dei connettori

Indicación de la

polaridad del conector

Indicatie van polariteit

van aansluiting

Полярность разъема

адаптера

Bağlantı polarite

göstergesi

ϝλϭϣϟ΍ΔϳΑρϘϟέϳηΗΔϣϼϋ

For indoor use only

Pour un usage à

l’intérieur uniquement

Nur für die Nutzung in

Innenbereichen

Solo per uso in interni

Para uso solo en interiores

Alleen voor gebruik

binnenshuis

Для использования

только внутри помещений

Sadece iç mekanda

kullanım için

ϖρΎϧϣϟ΍ϲϓϡ΍ΩΧΗγϼϟ΢ϟΎλ

ρϘϓΔϘϠϐϣϟ΍

SD3

OMRON’s trademarked technology for

blood pressure measurement

Technologie protégée

par la marque de commerce

OMRON pour la mesure de

la pression artérielle

Markenrechtlich

geschützte Technologie

von OMRON zur

Blutdruckmessung

Tecnologia brevettata

OMRON per la misurazione

della pressione arteriosa

La tecnología de OMRON

para medir la presión arterial

Technologie voor

bloeddrukmeting onder

handelsmerk van OMRON

Зарегистрированная

технология измерения

артериального давления

OMRON

OMRON’un kan basıncı

ölçümü için ticari markalı

teknolojisidir

ΔϳέΎΟΗϟ΍Δϣϼόϟ΍ΔϳϧϘΗ

ϡΩϟ΍ρϐοαΎϳϘϟOMRON

Identifier of cuffs compatible for the device

Identificateur des

brassards compatibles avec

l’appareil

Kennzeichnung der

mit dem Gerät kompatiblen

Manschetten

Identifica i bracciali

compatibili con il dispositivo

Identificador para

manguitos compatibles con

el dispositivo

Identificatie van

manchetten die compatibel

zijn met het apparaat

Манжеты совместимые

с устройством

Cihaz ile uyumlu

kollukların tanıtım işareti

ρ΋΍έηϟ΍ΩϳΩΣΗΕΎϣϼϋ

ίΎϬΟϟ΍ϊϣΔϘϓ΍ϭΗϣϟ΍ΔρϏΎοϟ΍

Marker on the cuff to be positioned above

the artery

Repère sur le brassard,

à positionner au-dessus de

l’artère

Markierung auf der

Manschette, die oberhalb

der Arterie liegen muss

Contrassegno sul

bracciale da posizionare al di

sopra dell’arteria

La marca del manguito

debe colocarse sobre la

arteria

Markering op de manchet

die boven de slagader moet

worden geplaatst

Указатель располо-

жения плечевой артерии

Kolluk üzerindeki

işaretin konumu arterin

üzerine gelmelidir

ρϏΎοϟ΍ρϳέηϟΎΑΔϣϼϋ

ϕϭϓϪόοϭΏϭΟϭϰϟ·ΓέΎηϺϟ

ϥΎϳέηϟ΍

Manufacturer’s quality control mark

Marque de contrôle de

la qualité du fabricant

Qualitätskontroll-

zeichen des Herstellers

Contrassegno controllo

qualità del produttore

Marca del control de

calidad del fabricante

Symbool voor kwaliteits-

controle van fabrikant

Отметка произво-

дителя о контроле качества

Üreticinin kalite kontrol

işareti

ΓΩϭΟϟ΍ϲϓϡϛΣΗϟ΍Δϣϼϋ

Δόϧλϣϟ΍ΔϛέηϟΎΑΔλΎΧϟ΍

Not made with natural rubber latex

Ne contient pas de latex

de caoutchouc naturel

Enthält kein Naturlatex

Non contiene lattice di

gomma naturale

No contiene látex de

caucho natural

Bevat geen

natuurrubberlatex

Не содержит

натуральный латекс

Doğal kauçuk lateksten

üretilmemiştir

ϡ΍ΩΧΗγ΍ϥϭΩϊϳϧλΗϟ΍ϡΗ

ϲόϳΑρϟ΍ρΎρϣϟ΍αϛϳΗϻ

SD4

Arm circumference

Circonférence du bras

Armumfang

Circonferenza del braccio

Perímetro de brazo

Armomtrek

Окружность плеча

Kol çevresi

ω΍έΫϟ΍ρϳΣϣ

Necessity for the user to consult this

instruction manual

L’utilisateur doit consulter

le présent mode d’emploi

Der Benutzer muss diese

Gebrauchsanweisung lesen

L’utente deve consultare il

presente manuale di istruzioni

Es necesario que el

usuario consulte este manual

de instrucciones

Noodzaak voor de

gebruiker om deze gebruiks-

aanwijzing te raadplegen

Необходимость для

пользователя обратиться

к данному руководству по

эксплуатации

Kullanıcı, bu kullanım

kılavuzuna başvurmalıdır

ϡΩΧΗγϣϟ΍ωϭΟέΓέϭέο

ϝϳϟΩϲϓΓΩέ΍ϭϟ΍ΕΎϣϭϠόϣϟ΍ϰϟ·

΍ΫϫΕ΍ΩΎηέϹ΍

Need for the user to follow this instruction

manual thoroughly for your safety.

L’utilisateur doit suivre

attentivement ce mode

d’emploi pour votre sécurité.

Damit die Sicherheit

gewährleistet ist, muss

der Benutzer diese

Gebrauchsanweisung

sorgfältig befolgen.

Per la propria sicurezza,

l’utente deve seguire

attentamente il presente

manuale di istruzioni.

Es necesario que el

usuario siga rigurosamente

este manual de instrucciones

para su seguridad.

Noodzaak voor de

gebruiker om zich voor de

eigen veiligheid zorgvuldig

aan deze gebruiksaanwijzing

te houden.

В целях обеспечения

безопасности строго

следуйте указаниям в

данном руководстве по

эксплуатации.

Güvenlik açısından

kullanıcının bu kullanım

kılavuzuna dikkatle uyması

gerekir.

ωΎΑΗ΍ϰϟ·ϡΩΧΗγϣϟ΍ΔΟΎΣ

ϝϳϟΩϲϓΓΩέ΍ϭϟ΍Ε΍ΩΎηέϹ΍

υΎϔΣϠϟ΍ΫϫϝϣΎϛϟΎΑΕ΍ΩΎηέϹ΍

Δϣϼγϟ΍ϰϠϋ

Direct current

Courant continu

Gleichstrom

Corrente diretta

Corriente directa

Gelijkstroom

Постоянный ток

Doğru akım

έηΎΑϣϟ΍έΎϳΗϟ΍

Alternating current

Courant alternatif

Wechselstrom

Corrente alternata

Corriente alterna

Wisselstroom

Переменный ток

Alternatif akım

ΏϭΎϧΗϣϟ΍έΎϳΗϟ΍

SD5

Date of manufacture

Date de fabrication

Herstellungsdatum

Data di fabbricazione

Fecha de fabricación

Productiedatum

Дата изготовления

Üretim tarihi

ϊϳϧλΗϟ΍ΦϳέΎΗ

Prohibited action

Action interdite

Verbotene Aktion

Operazione proibita

Acción prohibida

Verboden handeling

Запрещенные действия

Yasaklanmış eylem

έϭυΣϣ˯΍έΟ·

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.

Indique des niveaux de rayonnement non ionisant,

potentiellement dangereux, généralement élevés, ou un équipement

ou des systèmes, par exemple dans le domaine médical électrique,

incluant des émetteurs RF ou utilisant intentionnellement de l’énergie

électromagnétique RF pour le diagnostic ou le traitement.

Als Hinweis auf allgemein erhöhte, potenziell gefährliche Stufen

nicht ionisierender Strahlung oder als Hinweis auf Geräte oder

Systeme zum Beispiel im medizinisch-elektrischen Bereich, etwa HF-

Übertragungsgeräte, bzw. auf solche, die elektromagnetische HF-

Strahlung zur Diagnose oder Behandlung verwenden.

Indica livelli generalmente elevati, potenzialmente pericolosi,

di radiazioni non ionizzanti oppure indica apparecchiature o

sistemi, ad esempio per le aree elettromedicali in cui sono presenti

trasmettitori RF o in cui viene intenzionalmente applicata energia

elettromagnetica a radiofrequenza per la diagnosi o il trattamento.

Para indicar niveles de radiación no ionizante generalmente

elevados y potencialmente peligrosos, o bien para indicar equipos

o sistemas, como los usados en el ámbito electromédico, que

incorporen transmisores de radiofrecuencia o que apliquen energía

electromagnética de radiofrecuencia intencionadamente para

diagnósticos o tratamientos.

Geeft in het algemeen verhoogde, potentieel gevaarlijke niveaus

aan van niet-ioniserende straling of duidt op apparatuur of systemen,

bijvoorbeeld in de medische elektrische omgeving, die RF-zenders

bevatten of die opzettelijk elektromagnetische RF-energie toepassen

voor diagnose of behandeling.

Для указания повышенных и потенциально опасных

уровней неионизирующей радиации или же оборудования

или систем (например, в зоне размещения медицинского

электрооборудования), включающих в себя радиопередатчики

или устройства, использующие радиочастотную

электромагнитную энергию в целях диагностики или терапии.

Genellikle yüksek ve zararlı olabilecek iyonlaşmayan radyasyon

seviyelerini belirtir veya RF vericileri içeren veya tanı ya da tedavi

amacıyla bilinçli olarak RF elektromanyetik enerji uygulayan (örneğin

medikal elektrik alanında bulunan) ekipman ve sistemleri belirtir.

έϳϏΔόηϷ΍ϥϣΩΎΗόϣϟ΍ΩΣϟ΍ϥϋΔόϔΗέϣϟ΍ΕΎϳϭΗγϣϟ΍ϰϟ·ϡΎϋϪΟϭΑΓέΎηϺϟ

ϝΛϣˬΔϣυϧϷ΍ϭ΃ΓίϬΟϷ΍ϰϟ·ΓέΎηϺϟϭ΃ˬΓέρΧϥϭϛΗϥ΃ϝϣΗΣϣϟ΍ϥϣϲΗϟ΍Δϧϳ΅ϣϟ΍

ΓίϬΟ΃ϰϠϋϝϣΗηΗΔϳ΋ΎΑέϬϛΔϳΑρΓίϬΟ΃ϰϠϋΔϳϭΗΣϣϟ΍ϥϛΎϣϷ΍ϲϓΩΟϭΗϲΗϟ΍ϙϠΗ

Ε΍ΫΔϳγϳρΎϧϐϣϭέϬϛϟ΍ΔϗΎρϟ΍ϡ΍ΩΧΗγ΍ϡΗϳΙϳΣϭ΃ΔϳϛϠγϻΕ΍ΩΩέΗΎϬϧϣΙόΑϧΗϝΎγέ·

Νϼόϟ΍ϭ΃ιϳΧηΗϟ΍ν΍έϏϷΩϣϋϥϋΔϳϛϠγϼϟ΍Ε΍ΩΩέΗϟ΍

SD6

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 and AppStore logo are

service marks of AppleInc., registered in the U.S and other countries. GooglePlay and GooglePlay logo are trademarks of GoogleLLC.

La marque verbale et les logos Bluetooth® sont des marques

déposées détenues par Bluetooth SIG, Inc. et l’utilisation de ces marques

par OMRONHEALTHCARECo.,Ltd. se fait sous licence. Les autres marques

commerciales et noms de marque sont ceux de leurs détenteurs respectifs.

AppStore et le logo AppStore sont des marques de service d’Apple Inc.,

déposées aux États-Unis et dans d’autres pays. GooglePlay et le logo

GooglePlay sont des marques commerciales de GoogleLLC.

Die Bluetooth®-Wortmarke und -Logos sind eingetragene Marken

der BluetoothSIG, Inc. und die Verwendung solcher Marken durch

OMRONHEALTHCARECo.,Ltd. erfolgt in Lizenz. Andere Marken und

Markennamen gehören ihren jeweiligen Eigentümern. AppStore und das

AppStore-Logo sind Dienstleistungsmarken der AppleInc., die in den USA

und anderen Ländern eingetragen sind. GooglePlay und das GooglePlay-

Logo sind Marken von GoogleLLC.

Il marchio e i logotipi Bluetooth® sono marchi commerciali

registrati di Bluetooth SIG, Inc. e l’utilizzo di tali marchi da parte di

OMRONHEALTHCARECo.,Ltd. è stato concesso in licenza. Gli altri marchi e

nomi commerciali sono di proprietà dei rispettivi titolari. AppStore e il logo

AppStore sono marchi commerciali di AppleInc., registrati negli Stati Uniti

e in altri Paesi. GooglePlay e il logo GooglePlay sono marchi commerciali di

GoogleLLC.

El nombre y los logotipos de Bluetooth® son marcas registradas

de Bluetooth SIG, Inc. y cualquier uso de dichas marcas hecho por

OMRONHEALTHCARECo.,Ltd. se ha llevado a cabo con su licencia

correspondiente. Otras marcas registradas también pertenecen a sus

respectivos propietarios. App Store y el logotipo de App Store son marcas de

servicios registradas de Apple Inc. en EE.UU. y en otros países. GooglePlay y

el logotipo de GooglePlay son marcas comerciales de GoogleLLC.

Het woordmerk en de logo’s van Bluetooth® zijn gedeponeerde

handelsmerken van Bluetooth SIG, Inc. en enig gebruik hiervan door

OMRONHEALTHCARECo.,Ltd. geschiedt onder licentie. Overige

handelsmerken en handelsnamen zijn van hun respectievelijke eigenaren.

App Store en het logo van App Store zijn handelsmerken van Apple Inc. die

gedeponeerd zijn in de V.S. en in andere landen. GooglePlay en het logo van

GooglePlay zijn handelsmerken van GoogleLLC.

Словесный знак Bluetooth® и логотип являются

зарегистрированными товарными знаками, являющимися

собственностью компании Bluetooth SIG, Inc., и любое использование

этих знаков компанией OMRONHEALTHCARECo.,Ltd. обеспечивается

лицензией. Другие товарные знаки и торговые марки являются

собственностью соответствующих владельцев. App Store и логотип App

Store являются знаками обслуживания Apple Inc., зарегистрированными

в США и других странах. GooglePlay и логотип GooglePlay являются

товарными знаками GoogleLLC.

Bluetooth® marka adı ve logoları, Bluetooth SIG Inc. kuruluşunun

tescilli ticari markalarıdır ve OMRONHEALTHCARECo.,Ltd. bu markaları

lisans kapsamında kullanmaktadır. Diğer ticari markalar ve ticari isimler, ilgili

sahiplerine aittir. App Store ve App Store logosu, Apple Inc. firmasının ABD

ve diğer ülkelerde tescilli hizmet markalarıdır. GooglePlay ve GooglePlay

logosu, GoogleLLC firmasının ticari markalarıdır.

ΔϛϭϠϣϣΔϠΟγϣΔϳέΎΟΗΕΎϣϼϋϲϫΎϬΗ΍έΎόηϭBluetooth

ΔϣϠϛΔϣϼϋϥ·

ΔϛέηΔργ΍ϭΑΕΎϣϼόϟ΍ϩΫϬϟϡ΍ΩΧΗγ΍ϱ΃ϥϭϛϳϭ%OXHWRRWK6,*,QFΔϛέηϟ

ΔϳέΎΟΗϟ΍ΕΎϣϼόϟ΍ϥϭϛΗιϳΧέΗΏΟϭϣΑ20521+($/7+&$5(&R/WG.

ϲΗϣϼϋϩέΎόηϭ$SS6WRUHΩό

ϳϪϳϛϟΎϣΑΔλΎΧΞΗϧϣϟ΍΍ΫϬϟΔϳέΎΟΗϟ΍˯ΎϣγϷ΍ϭϯέΧϷ΍

Ωό

ϳϭϯέΧ΃ϥ΍ΩϠΑϭΔϳϛϳέϣϷ΍ΓΩΣΗϣϟ΍ΕΎϳϻϭϟ΍ϲϓΔϠΟγϣϟ΍$SSOH,QFΔϛέηϟΔϣΩΧ

.*RRJOH//&ΔϛέηϟϥϳΗϳέΎΟΗϥϳΗϣϼϋϩέΎόηϭ*RRJOH3OD\

2019-07-29

IM1-HEM-7155T-E-01-03/2019

2870440-7A

Issue Date:

Date de publication:

Ausgabedatum:

Data di pubblicazione:

Fecha de publicación:

Uitgiftedatum

Дата выпуска:

Teslim Tarihi:

έ΍ΩλϹ΍ΦϳέΎΗ

Automatic Upper Arm

Blood Pressure Monitor

M4 Intelli IT (HEM-7155T-EBK)

X4 Smart (HEM-7155T-ESL)

IM2-HEM-7155T-E-01-03/2019

2870441-5A

Instruction Manual

2.3

Read Instruction manual and before use.

Lire le mode d’emploi et avant l’utilisation.

Lesen Sie vor der Verwendung die Gebrauchsanweisung und .

Leggere il manuale di istruzioni e prima dell’uso.

Lea el manual de instrucciones y antes del uso.

Lees de gebruiksaanwijzing en voor gebruik.

Прочтите руководство по эксплуатации и перед использованием.

Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

ϡ΍ΩΧΗγϻ΍ϝΑϗ ϭ Ε΍ΩΎηέϹ΍ϝϳϟΩ΃έϗ΍

Package Contents

Contenu de l’emballage

Inhoud van de verpakking

Packungsinhalt

Комплект поставки

Contenuto della confezione

Paketin İçindekiler

Contenido del envase

ΓϭΑόϟ΍ΕΎϳϭΗΣϣ

Instruction Manual

Preparing for a Measurement

Préparation d’une mesure

Een meting voorbereiden

Vorbereiten einer Messung

Подготовка к измерению

Preparazione per la misurazione

Ölçüm Hazırlığı

Preparación para una medición

αΎϳϘϟ΍ΔϳϠϣόϟίϳϬΟΗϟ΍

30 minutes before

30minutes avant

30 Minuten vorher

30 minuti prima

30minutos antes

30 minuten ervoor

За 30 минут до

30 dakika önce

ΔϘϳϕΩ˼˹ώϟΏΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ 

5 minutes before: Relax and rest.

5minutes avant: détente et repos.

5 Minuten vorher: ruhig hinsetzen.

5 minuti prima: rilassarsi e stare a riposo.

5minutos antes: relájese y descanse.

5 minuten ervoor: ontspan en rust.

За 5 минут до: расслабьтесь и отдохните.

5 dakika önce: Gevşeyin ve dinlenin.



ΥέΗγ΍ϭΡέΗγ΍ϖ΋ΎϗΩ˾ώϟΏΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ 

Downloading the “OMRON connect” App

Téléchargement de l’application

«OMRONconnect»

De app “OMRON connect” downloaden

Herunterladen der App „OMRON connect“

Загрузка приложения «OMRON connect»

Download della app “OMRON connect”

“OMRON connect” Uygulamasını indirme

Descarga de la aplicación “OMRONconnect”

"20521FRQQHFWϖϳΑρΗϝϳίϧΗ

Pairing Your Smart Device

Jumelage de votre appareil intelligent

Uw smartapparaat koppelen

Koppeln mit Smartphone oder Tablet

Синхронизация со смарт-устройством

Associazione del dispositivo smart

Akıllı Cihazınızın Eşleştirilmesi

Sincronización con su dispositivo inteligente

ϲϛΫϟ΍ϙϔΗΎϫϥ΍έϗ·





Bluetooth

Follow the instructions.

Suivez les instructions.

Befolgen Sie die Anweisungen.

Attenersi alle istruzioni.

Siga las instrucciones.

Volg de instructies.

Выполняйте инструкции.

Talimatları izleyin.

Ε΍ΩΎηέϹ΍ϊΑΗ΍ 

The date and time will automatically be set when your monitor is paired with the app.

La date et l’heure seront automatiquement réglées lorsque votre tensiomètre sera jumelé avec l’application.

Wenn Ihr Messgerät mit der App verknüpft ist, werden Datum und Uhrzeit automatisch eingestellt.

La data e l’ora verranno impostate automaticamente una volta che il misuratore verrà associato alla app.

La fecha y la hora se ajustarán automáticamente cuando el monitor se sincronice con la aplicación.

De datum en tijd worden automatisch ingesteld wanneer uw bloeddrukmeter is gekoppeld aan de app.

Дата и время установятся автоматически после синхронизации с приложением.

Ölçüm cihazınız uygulamayla eşleştirildiğinde tarih ve saat otomatik olarak ayarlanır.

ϖϳΑρΗϟΎΑϙΑιΎΧϟ΍αΎϳϘϟ΍ίΎϬΟϥ΍έϗ·ΩϧϋΎ

ϳ΋ΎϘϠΗΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑοϡΗϳγ 

Applying the Cuff on the Left Arm

Pose du brassard sur le bras gauche

De manchet op de linkerarm aanbrengen

Anbringen der Manschette am linken Arm

Расположение манжеты на левой руке

Applicazione del bracciale sul braccio sinistro

Kolluğun Sol Kola Takılması

Colocación del manguito en el brazo izquierdo

ϥϣϳϷ΍ω΍έΫϟ΍ϰϠϋρϏΎοϟ΍ρϳέηϟ΍ϑϟ

1-2 cm





Click

Tube side of the cuff should be 1 - 2 cm above the inside elbow.

Le côté tuyau du brassard doit être positionné 1 à 2cm au-dessus de l’intérieur du coude.

Das Manschettenstück mit dem Schlauch muss 1 bis 2cm oberhalb des Ellbogens liegen.

Il lato del bracciale con il tubo deve trovarsi al di sopra dell’interno del gomito, a una distanza di circa 1 o 2 cm.

El lado del tubo del manguito deberá quedar 1 o 2cm por encima de la parte interna del codo.

De kant met de slang van de manchet moet 1 - 2 cm boven de binnenkant van de elleboog liggen.

Край манжеты с трубкой должен находиться на 1–2 см выше локтевого сгиба.

Kolluğun boru tarafı, dirsek içinin 1 ila 2 cm üstünde olmalıdır.

ϖϓέϣϟ΍ϥϋϡα˻ϰϟ·˺ϥϣρϏΎοϟ΍ρϳέηϟ΍ϥϣϡϭρέΧϟ΍ΏϧΎΟϊϔΗέϳϥ΃ΏΟϳ 

Make sure that air tube is on the inside of your arm and wrap the cuff

securely so it can no longer slip round.

Assurez-vous que le tuyau à air se trouve du côté intérieur de votre bras et enroulez fermement le brassard

de manière qu’il ne puisse plus tourner.

Stellen Sie sicher, dass der Luftschlauch an der Arminnenseite sitzt, und befestigen Sie die Manschette sicher, so dass sie nicht verrutscht.

Assicurarsi che il tubo dell’aria si trovi all’interno del braccio e avvolgere il bracciale saldamente in modo che non possa ruotare.

Asegúrese de que el tubo de aire se encuentra en la cara interna del brazo y enrolle el manguito con

firmeza para que no pueda deslizarse.

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.

Убедитесь, что воздуховодная трубка находится на внутренней поверхности плеча и надежно

оберните манжету, чтобы она не прокручивалась вокруг руки.

Hava borusunun kolunuzun iç tarafında olduğundan emin olun ve kolluğu kaymayacak şekilde sabit şekilde sarın.

ω΍έΫϟ΍ϝϭΣϖϟίϧϳϻΙϳΣΑϡΎϛΣΈΑρϏΎοϟ΍ρϳέηϟ΍ϑϟϭϙϋ΍έΫϥϣϲϠΧ΍Ωϟ΍ΏϧΎΟϟ΍ϰϠϋ˯΍ϭϬϟ΍ϡϭρέΧϥ΃ϥϣΩϛ΄Η 

If taking measurements on the right arm, refer to:

Pour la prise de mesures au bras droit, voir:

Bei Messungen am rechten Arm siehe:

Se la misurazione viene eseguita al braccio destro, fare riferimento a:

Si va a realizar mediciones en el brazo derecho, consulte:

Als u metingen aan de rechterarm uitvoert, raadpleeg dan:

При измерении на правой руке см:

Sağ koldan ölçüm yapıyorsanız aşağıdakilere bakın:

ϰϟ·ϊΟέ΍ˬϥϣϳϷ΍ω΍έΫϟ΍ϰϠϋαΎϳϘϟ΍˯΍έΟ·ϝΎΣϲϓ 

Installing Batteries

Mise en place des piles

Batterijen plaatsen

Einsetzen der Batterien

Установка элементов питания

Installazione delle batterie

Pillerin Takılması

Instalación de las pilas

ΕΎϳέΎρΑϟ΍ΏϳϛέΗ

AA, 1.5V × 4







Sitting Correctly

Position assise correcte

Correct zitten

Korrekte Körperhaltung

Сядьте правильно

Come sedere nel modo corretto

Düzgün Oturma

Cómo sentarse correctamente

΢ϳΣλϝϛηΑαϭϠΟϟ΍









Sit with your back and arm supported.

S’asseoir de façon à ce que le dos et le bras soient bien soutenus.

Mit dem Rücken anlehnen und den Arm auf eine Unterlage legen.

Sedere con la schiena e il braccio ben sostenuti.

Siéntese de modo que la espalda y el brazo estén bien apoyados.

Zit met uw rug en arm ondersteund.

Сядьте так, чтобы спина и рука опирались на что-либо.

Sırtınız ve kolunuz desteklenecek şekilde oturun.

ΩΎϧΗγ΍ϊοϭϲϓω΍έΫϟ΍ϭέϬυϟ΍ϥϭϛϳΙϳΣΑαϠΟ΍ 



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

Le brassard doit se trouver au même niveau que votre cœur.

Die Manschette auf Herzhöhe platzieren.

Posizionare il bracciale allo stesso livello del cuore.

Coloque el manguito al mismo nivel que el corazón.

Plaats de armmanchet op hetzelfde niveau als uw hart.

Манжета должна находиться на уровне сердца.

Kolluğu kalbinizle aynı düzeye getirin.

ϪγϔϧΏϠϘϟ΍ϯϭΗγϣϲϓω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍ϊο 



Keep feet flat, legs uncrossed, remain still and do not talk.

Garder les pieds à plat, les jambes non croisées, ne pas bouger et ne pas parler.

Füße flach auf den Boden stellen, die Beine nicht kreuzen, still halten und nicht sprechen.

Tenere i piedi ben poggiati, non incrociare le gambe, rimanere fermi e non parlare.

Mantenga los pies planos, las piernas sin cruzar, quédese quieto y no hable.

Houd de voeten plat, benen niet gekruist, zit stil en praat niet.

Поставьте ноги ровно, не перекрещивая их, не двигайтесь и не разговаривайте.

Ayaklarınızı düz, bacaklarınızı açık tutun, hareketsiz kalın ve konuşmayın.

ΙΩΣΗΗϻϭϙΗΎΑΛϰϠϋυϓΎΣϭΩϋΎΑΗϣϊοϭϲϓϙϳϗΎγϭ΢

ργϣϊοϭϲϓϙϳϣΩϗϝόΟ΍ 

Setting Date and Time Manually

Réglage manuel de la date et de l’heure

Datum en tijd handmatig instellen

Manuelles Einstellen von Datum und Uhrzeit

Установка даты и времени вручную

Impostazione manuale di data e ora

Tarih ve Saatin Manuel Olarak Ayarlanması

Ajuste manual de la fecha y la hora

ϳϭΩϳΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑο

If your monitor is paired with your smart device, date and time is set automatically.

When you need to set them manually, set year > month > day > hour > minute.

Si votre tensiomètre est jumelé avec votre appareil intelligent, la date et l’heure sont réglées automatiquement.

Si vous devez les régler manuellement, réglez dans l’ordre année > mois > jour > heure > minute.

Wenn Ihr Messgerät mit Ihrem Smartphone oder Tablet gekoppelt ist, werden Datum und Uhrzeit automatisch

eingestellt. Bei manueller Einstellung müssen Sie Jahr > Monat > Tag > Stunde > Minute einstellen.

Se il misuratore viene accoppiato con un dispositivo smart, la data e l’ora verranno impostate

automaticamente. Se occorre impostarle manualmente, impostare anno > mese > giorno > ore > minuti.

Si el monitor está sincronizado con su dispositivo inteligente, la fecha y la hora se ajustarán

automáticamente. Cuando tenga que configurarlas manualmente, ajuste año > mes > día > hora > minuto.

Als uw bloeddrukmeter gekoppeld is met uw smartapparaat, worden de datum en tijd automatisch

ingesteld. Wanneer u ze handmatig moet instellen, stelt u jaar > maand > dag > uur > minuut in.

Если прибор синхронизирован со смарт-устройством, дата и время устанавливаются автоматически.

Если необходимо установить их вручную, выберите год > месяц > день > час > минута.

Ölçüm cihazınız akıllı cihazınızla eşleştirilmişse tarih ve saat otomatik olarak ayarlanır. Bunları manuel

olarak ayarlamanız gerektiğinde, yıl > ay > gün > saat > dakika değerini ayarlayın.

ρΑο΍ˬΎ

ϳϭΩϳΎϣϬρΑοϰϟ·ΔΟΎΣϟ΍ΩϧϋΎ

ϳ΋ΎϘϠΗΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑοϡΗϳˬϲϛΫϟ΍ίΎϬΟϟΎΑϙΑιΎΧϟ΍αΎϳϘϟ΍ίΎϬΟϥ΍έϗ·ϝΎΣϲϓ 

ΔϘϳϗΩϟ΍PLQXWHΔϋΎγϟ΍KRXUϡϭϳϟ΍dayέϬηϟ΍PRQWKΔϧγϟ΍\HDU

Year

Month

Day

Hour

Minute

Back / Forward

Arrière / Avant

Zurück / Vorwärts

Indietro / Avanti

Atrás / Adelante

Terug / vooruit

Назад / Вперед

İleri / Geri

ϡΩϘΗϟ΍ωϭΟέϟ΍ 

Instruction Manual

Checking Readings

Vérication des résultats

Metingen bekijken

Prüfen der Messwerte

Проверка результатов

Controllo dei risultati

Ölçüm Değerlerini Kontrol Etme

Comprobación de lecturas

Ε΍˯΍έϘϟ΍ϥϣϖϘΣΗϟ΍

Appears if “SYS” is 135 mmHg or above

and/or “DIA” is 85 mmHg* or above.

S’affiche si «SYS» est égale ou supérieure à

135mmHg et/ou «DIA» égale ou supérieure

à 85mmHg*.

Wird angezeigt, wenn „SYS“ 135mmHg oder

mehr beträgt und/oder wenn „DIA“ 85mmHg*

oder mehr beträgt.

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*.

Aparece si “SYS” es 135mmHg o superior

y/o “DIA” es 85mmHg* o superior.

Verschijnt als “SYS” 135 mmHg of hoger is

en/of “DIA” 85 mmHg* of hoger is.

Отображается, если «SYS» 135 мм.рт.ст. и

выше и/или «DIA» 85 мм.рт.ст.* и выше.

“SYS” 135 mmHg ya da üstünde olduğunda

ve/veya “DIA” 85 mmHg* ya da üstünde

olduğunda görünür.

έΛϛ΃ϭ΃Ύ

ϳϘΑ΋ί΍

έΗϣϳϠϠϣ˺˼˾ώϠΑϳSYSϥΎϛϝΎΣϲϓέϬυΗ 

έΛϛ΃ϭ΃Ύ

ϳϘΑ΋ί΍

έΗϣϳϠϠϣ́˾DIAϭ΃ϭ

Appears when an irregular rhythm** is detected during a measurement.

If it appears repeatedly, OMRON recommends to consult your physician.

S’affiche lorsqu’un rythme irrégulier** est détecté pendant une mesure. S’il s’affiche à

plusieurs reprises, OMRON recommande de consulter votre médecin.

Wird angezeigt, wenn während einer Messung ein unregelmäßiger Herzschlag** festgestellt

wird. Wird das Symbol wiederholt angezeigt, empfiehlt OMRON, sich an Ihren Arzt zu wenden.

Viene visualizzato se nel corso di una misurazione viene rilevato un ritmo cardiaco irregolare**.

Se il simbolo appare ripetutamente, OMRON consiglia di consultare il medico curante.

Aparece cuando se detecta un ritmo irregular** durante una medición. Si aparece varias veces,

OMRON recomienda que consulte a su médico.

Verschijnt wanneer tijdens een meting een onregelmatig ritme** wordt gedetecteerd. Als dit

herhaaldelijk verschijnt, raadt OMRON aan om uw arts te raadplegen.

Отображается, если при измерении определяется нерегулярный ритм**. Если этот символ

отображается неоднократно, компания OMRON рекомендует обратиться к лечащему врачу.

Bir ölçüm esnasında düzensiz ritim** saptandığında görünür. Tekrarlı şekilde görünürse

OMRON doktorunuza danışmanızı önerir.

ϙΑϳΑρΓέΎηΗγΎΑOMRONϲλϭΗˬέέϛΗϣϝϛηΑΎϫέϭϬυΩϧϋαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓΏϠϘϟ΍ΕΎΑέοϡΎυΗϧ΍ϡΩϋϑΎηΗϛ΍ΩϧϋέϬυΗ 

Appears when your body moves during a measurement. Remove the

arm cu, wait 2-3 minutes and try again.

S’affiche si vous bougez pendant une mesure. Retirer le brassard, attendre 2 à 3minutes et essayer à nouveau.

Wird angezeigt, wenn Sie sich während der Messung bewegen. Nehmen Sie die Manschette ab, warten Sie

2–3Minuten und versuchen Sie es erneut.

Viene visualizzato se l’utilizzatore si muove durante la misurazione. Rimuovere il bracciale, attendere 2-3 minuti e riprovare.

Aparece cuando se mueve el cuerpo durante una medición. Retire el manguito, espere unos 2 o 3minutos e

inténtelo de nuevo.

Verschijnt wanneer uw lichaam tijdens een meting beweegt. Verwijder de armmanchet, wacht 2-3 minuten

en probeer het opnieuw.

Отображается при движении тела во время измерения. Снимите манжету, подождите 2-3 минуты и

попробуйте еще раз.

Bir ölçüm esnasında vücudunuz hareket ettiğinde görünür. Kolluğu çıkarın, 2-3 dakika bekleyip tekrar deneyin.

ϯέΧ΃ΓέϣΔϟϭΎΣϣϟ΍ϭϖ΋ΎϗΩ˼ϰϟ·˻ϥϣέΎυΗϧϻ΍ϭω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍Δϟ΍ίΈΑϡϗαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϙϣγΟϙέΣΗΩϧϋέϬυΗ 

Cu is tight enough.

Le brassard est suffisamment serré.

Manschette sitzt ausreichend straff.

Il bracciale è stretto a sufficienza.

El manguito está lo suficientemente prieto.

Manchet zit strak genoeg.

Манжета затянута достаточно туго.

Kolluk yeterince sıkıdır.

ϲϔϛϳΎϣΑϡϛΣϣρϏΎοϟ΍ρϳέηϟ΍ 

Apply cu again MORE TIGHTLY.

Poser le brassard en le serrant davantage.

Manschette STRAFFER ziehen.

Applicare di nuovo il bracciale

STRINGENDOLO DI PIÙ.

Vuelva a poner el manguito MÁS PRIETO.

Breng de manchet STRAKKER aan.

Наложите манжету еще раз БОЛЕЕ ТУГО.

Kolluğu tekrar, DAHA SIKI bir şekilde takın.

Ύ

ϣΎϛΣ·έΛϛ΃ϝϛηΑϯέΧ΃ΓέϣρϏΎοϟ΍ρϳέηϟ΍ϑϟ 

Error messages or other problems? Refer to:

Messages d’erreur ou autres problèmes? Voir:

Weitere Fehlermeldungen oder Probleme siehe:

Messaggi di errore o altri problemi? Fare riferimento a:

¿Hay mensajes de error u otros problemas? Consulte:

Foutmeldingen of andere problemen? Raadpleeg:

Сообщения об ошибках или другие неисправности? См:

Hata mesajları veya başka sorunlar mı var? Bkz:

ϰϟ·ϊΟέ΍ˮϯέΧϷ΍Εϼϛηϣϟ΍ϭ΃΄ρΧϟ΍ϝ΋Ύγέ 

*The high blood pressure definition is based on the 2018 ESH/ESC Guidelines.

*La définition de l’hypertension est basée sur les recommandations ESH/ESC 2018.

*Die Definition für Bluthochdruck basiert auf den 2018 ESH/ESC Richtlinien.

*La definizione di alta pressione arteriosa si basa sulle linee guida 2018 di ESH/ESC.

*La definición de presión arterial alta se basa en las guías 2018 ESH/ESC.

*De definitie van hoge bloeddruk is gebaseerd op de ESH/ESC-richtlijnen uit 2018.

*Определение высокого артериального давления основано на Рекомендациях 2018 ESH/ESC.

*Yüksek kan basıncı tanımı, 2018 ESH/ESC Kılavuzlarını temel alır.

.2018ϡΎόϟESCΏϠϘϟ΍ΏρϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍ESHϡΩϟ΍ρϐορέϔϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍Ε΍ΩΎηέ·ϰϟ·ΩϧΗγϳϊϔΗέϣϟ΍ϡΩϟ΍ρϐοϑϳέόΗ 

** An irregular heart beat rhythm is defined as a rhythm that is 25% less or 25%

more than the average rhythm detected during a measurement.

** Un rythme cardiaque irrégulier est défini comme un rythme inférieur ou supérieur de 25% au

rythme moyen détecté durant une mesure.

** Ein unregelmäßiger Herzschlag ist definiert als ein Herzrhythmus, der weniger als 25% oder mehr

als 25% des mittleren Herzrhythmus beträgt, der während der Blutdruckmessung erkannt wird.

** Si definisce ritmo cardiaco irregolare un ritmo cardiaco inferiore del 25% o superiore del 25%

rispetto al ritmo medio rilevato durante una misurazione.

** Latido arrítmico se define como un ritmo que es un 25% menor o un 25% mayor que el ritmo

medio detectado durante una medición.

** Een onregelmatig hartslagritme wordt gedefinieerd als een ritme dat 25% lager of 25% hoger is dan

het gemiddelde ritme dat tijdens een meting wordt gedetecteerd.

** Нерегулярный ритм сердцебиения — это ритм, который на 25% медленнее или быстрее

измеренного среднего ритма.

** Düzensiz kalp atışı ritmi, bir ölçüm sırasında saptanan ortalamadan %25 daha düşük veya %25 daha

yüksek ritim olarak tanımlanır.

̃˻˾ϝΩόϣΑϪϧϣέΛϛ΃ϭ΃̃˻˾ϝΩόϣΑαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϪϓΎηΗϛ΍ϡΗϳϱΫϟ΍ϲόϳΑρϟ΍ϡ

υϧϟ΍ϥϣϝϗ΃ϡ

υϧϪϧ΄ΑΏϠϘϟ΍ΕΎΑέοΏ΍έρο΍ϑέό

ϳ 

Using Memory Functions

Utilisation des fonctions de mémoire

Geheugenfuncties gebruiken

Verwendung der Speicherfunktionen

Использование функции памяти

Uso delle funzioni di memoria

Hafıza Fonksiyonunun Kullanılması

Uso de las funciones de memoria

Γέϛ΍Ϋϟ΍ϑ΋Ύυϭϡ΍ΩΧΗγ΍

Before using memory functions, select your user ID.

Avant d’utiliser les fonctions de mémoire, sélectionner votre ID Utilisateur.

Wählen Sie vor dem Verwenden der Speicherfunktionen Ihre Benutzer-ID aus.

Prima di utilizzare le funzioni di memoria selezionare il proprio ID utente.

Antes de usar las funciones de memoria, seleccione su ID de usuario.

Selecteer uw gebruikers-ID voordat u geheugenfuncties gebruikt.

Перед использованием функции памяти выберите идентификатор пользователя.

Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.

ϙΑιΎΧϟ΍ϡΩΧΗγϣϟ΍ϑέόϣΩΩΣˬΓέϛ΍Ϋϟ΍ϑ΋Ύυϭϡ΍ΩΧΗγ΍ϝΑϗ 

12.1 Readings Stored in Memory

Mesures stockées en mémoire

Gespeicherte Messungen

Risultati conservati in memoria

Lecturas guardadas en la memoria

Meetwaarden opgeslagen in het geheugen

Сохранение результатов в памяти

Hafızada Saklanan Ölçüm Değerleri

Γέϛ΍Ϋϟ΍ϲϓΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ 

Up to 60 readings

arestored.

Jusqu’à 60mesures

sont stockées.

Es werden bis zu

60Messwerte

gespeichert.

Vengono conservati

fino a 60 risultati.

Se almacenan hasta

60lecturas.

Er kunnen tot 60 meetwaar-

den worden opgeslagen.

Сохраняется до

60 результатов.

60 adede kadar ölçüm

değeri saklanır.

ΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ΩΩϋϝλϳ 

Γ˯΍έϗ˿˹ϰϟ·

12.2 Average of the Latest 2 or 3 Readings Taken

within a 10 Minute Span

Moyenne des 2 ou 3 dernières mesures prises en l’espace de 10minutes

Mittelwert der letzten 2 oder 3Messwerte, die in einem 10-Minuten-

Zeitrahmen erfasst wurden

Media degli ultimi 2 o 3 risultati ottenuti nell’arco di 10 minuti

Promedio de las 2 o 3últimas lecturas realizadas en un intervalo de 10minutos

Gemiddelde van de laatste 2 of 3 metingen uitgevoerd binnen een

tijdspanne van 10 minuten

Среднее значение из последних 2-х или 3-х результатов

полученных в течение 10 минут

10 Dakika Aralıkta Alınan Son 2 veya 3 Ölçüm Değerinin Ortalaması

ϖ΋ΎϗΩ˺˹ώϠΑΗΔϳϧϣίΓΩϣϲϓΎϬϳϠϋϝϭλΣϟ΍ϡΗΕ΍˯΍έϗ˼ϭ΃ϥϳΗ˯΍έϗέΧ΁ργϭΗϣ 

3 sec+

12.3 Deleting All Readings

Suppression de toutes les mesures

Löschen aller Messwerte

Cancellazione di tutti i risultati

Eliminación de todas las lecturas

Alle metingen verwijderen

Удаление всех результатов

Tüm Ölçüm Değerlerini Silme

Ε΍˯΍έϘϟ΍ϊϳϣΟϑΫΣ 

4sec+ 4sec+





Other Settings

Autres réglages

Andere instellingen

Weitere Einstellungen

Другие настройки

Altre impostazioni

Diğer Ayarlar

Otros ajustes

ϯέΧϷ΍Ε΍Ω΍ΩϋϹ΍ 

13.1 Disabling/Enabling Bluetooth

Désactivation/activation de Bluetooth

Deaktivieren/Aktivieren der Bluetooth-Funktion

Disattivazione/attivazione della funzione Bluetooth

Activar o desactivar el Bluetooth

Bluetooth uitschakelen/inschakelen

Выключение/включение Bluetooth

Bluetooth’u Devre Dışı Bırakma/Etkinleştirme

%OXHWRRWKΔϳλΎΧϝϳρόΗϥϳϛϣΗ 

10 sec+

3 sec+

Bluetooth is enabled

by default.

Bluetooth est activé

par défaut.

Die Bluetooth-Funktion ist

standardmäßig aktiviert.

La funzione Bluetooth è

attiva per impostazione

predefinita.

El Bluetooth está

activado por defecto.

Bluetooth is standaard

ingeschakeld.

Bluetooth включен по

умолчанию.

Bluetooth varsayılan

olarak etkindir.

%OXHWRRWKΔϳλΎΧϥϳϛϣΗϡΗϳ 

ϲο΍έΗϓ΍ϝϛηΑ

13.2 Restoring to the Default Settings

Réinitialisation aux réglages par défaut

Wiederherstellen der Standardeinsttellungen

Ripristino delle impostazioni predefinite

Restablecimiento a los ajustes de fábrica

De standaardinstellingen herstellen

Восстановление настроек по умолчанию

Varsayılan Ayarları Geri Yükleme

Δϳο΍έΗϓϻ΍Ε΍Ω΍ΩϋϹ΍ΓΩΎόΗγ΍ 

4sec+

 

4sec+



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.

Si votre pression systolique est supérieure à 210mmHg: Lorsque le brassard se gonfle, 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.

Wenn Ihr systolischer Druck höher ist als 210mmHg: 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.

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.

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.

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.

Если систолическое давление выше 210 мм.рт.ст.: После того, как началось автоматическое нагнетание

воздуха в манжету, нажмите и удерживайте кнопку [START/STOP] до тех пор, пока электронный блок не

поднимет давление до значения, превышающего ожидаемое систолическое давление на 30–40ммрт.ст.

Sistolik basıncınız 210 mmHg’den fazlaysa: Kolluk şişmeye başladıktan sonra, [START/STOP] düğmesine basın

ve ölçüm cihazı beklediğiniz sistolik basınç değerinden 30 ila 40 mmHg daha fazla şişene kadar basılı tutun.

έίϟ΍ϰϠϋέ΍έϣΗγϻ΍ϊϣρϐο΍ˬω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍ΥΎϔΗϧ΍˯ΩΑΩόΑΔϳϘΑ΋ίΕ΍έΗϣϳϠϠϣ˻˺˹ϥϣέΛϛ΃ϲοΎΑϘϧϻ΍ϙϣΩρϐοϥΎϛ΍Ϋ·

ϙϳΩϟΔόϗϭΗϣϟ΍ϲοΎΑϘϧϻ΍ϡΩϟ΍ρϐοΔϣϳϗϥϣϰϠϋ΃Ύ

ϳϘΑ΋ί΍

έΗϣϳϟϝϣ˽˹ϰϟ·˼˹ϥϣΦϔϧϟΎΑίΎϬΟϟ΍ϡϭϘϳϰΗΣϑΎϘϳ·˯ΩΑ>67$576723]

Optional Medical Accessories

Accessoires médicaux optionnels

Optionele medische accessoires

Optionales medizinisches Zubehör

Дополнительно принадлежности

Accessori medicali opzionali

Opsiyonel Tıbbi Aksesuarlar

Accesorios médicos opcionales

ΔϳέΎϳΗΧϻ΍ΔϳΑρϟ΍ΕΎϘΣϠϣϟ΍

Arm Cuff

(HEM-FL31)

22 - 42 cm

AC Adapter

(HHP-CM01) (HHP-BFH01)

Do not throw the air plug away. The air

plug can be applicable to the optional cuff.

Ne pas jeter la prise de gonflage. La prise de gonflage

peut être utilisée pour le brassard en option.

Entsorgen Sie den Luftschlauchstecker nicht. Der Luft-

schlauch stecker wird für die optionale Manschette verwendet.

Non gettare via l’attacco del tubo dell’aria. L’attacco del

tubo dell’aria può essere applicato al bracciale opzionale.

No tire el conector para tubo de aire. El conector para tubo

de aire puede ser utilizado con el manguito opcional.

Gooi de plug van de luchtslang niet weg. De

plug van de luchtslang kan worden gebruikt op

de optionele manchet.

Не выбрасывайте воздушный штекер. Он

может подойти к дополнительной манжете.

Hava tıpasını atmayın. Hava tıpası isteğe bağlı

kolluğa uygulanabilir.

ϱέΎϳΗΧϻ΍ρϏΎοϟ΍ρϳέηϟ΍ϊϣ˯΍ϭϬϟ΍ΓΩ΍ΩγϝΎϣόΗγ΍ϥϛϣϳ˯΍ϭϬϟ΍ΓΩ΍Ωγϥϻ 

Taking a Measurement

Réalisation d’une mesure

Een meting doen

Vornehmen einer Messung

Выполнение измерений

Misurazione

Ölçüm Yapma

Obtención de una lectura

αΎϳϘϟ΍˯΍έΟ·

When the [START/STOP] button is pressed, the measurement is taken and saved

automatically. Open the app to transfer the reading.

Après une pression sur le bouton [START/STOP], la mesure démarre et le résultat est enregistré

automatiquement. Ouvrir l’application pour transférer le résultat.

Beim Drücken der Taste [START/STOP] erfolgt die Messung. Die Messwerte werden automatisch

gespeichert. Öffnen Sie die App, um die Messwerte zu übertragen.

Quando si preme il pulsante [START/STOP], la misurazione viene eseguita e salvata automaticamente.

Aprire la app per trasferire i risultati.

Al pulsar el botón [START/STOP], se obtiene la medición, que se guarda automáticamente. Abra la

aplicación para transferir la lectura.

Wanneer op de knop [START/STOP] wordt gedrukt, wordt de meting automatisch uitgevoerd en

opgeslagen. Open de app om de meting te versturen.

После того, как кнопка [START/STOP] нажата, измерение выполняется и сохраняется

автоматически. Откройте приложение, чтобы передать результаты.

[START/STOP] düğmesine basıldığında ölçüm yapılır ve otomatik olarak kaydedilir. Ölçüm değerini

aktarmak için uygulamayı açın.

Γ˯΍έϘϟ΍ϝϘϧϟϖϳΑρΗϟ΍΢Ηϓ΍Ύ

ϳ΋ΎϘϠΗϪυϔΣϭαΎϳϘϟ΍˯΍έΟ·ϡΗϳˬ>67$576723@έίϰϠϋρϐοϟ΍Ωϧϋ 

Selecting User ID (1 or 2)

Sélection de l’ID Utilisateur (1 ou 2)

Gebruikers-ID selecteren (1 of 2)

Auswahl der Benutzer-ID (1 oder 2)

Выберите идентификатор

пользователя (1 или 2)

Selezione dell’ID UTENTE (1 o 2)

Kullanıcı Kimliğini Seçme (1 veya 2)

Selección de ID de usuario (1 o 2)

(˻ϭ΃˺ϙΑΔλΎΧϟ΍ϡΩΧΗγϣϟ΍ΔϳϭϫΩϳΩΣΗ

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

Changer d’ID Utilisateur permet d’enregistrer les résultats pour 2personnes.

Mit verschiedenen Benutzer-IDs lassen sich Messwerte für 2Personen speichern.

Cambiare ID utente permette di registrare i risultati relativi a 2 persone.

Cambiar de ID de usuario le permite guardar las lecturas de 2personas.

Door het wisselen van gebruikers-ID kunt u metingen voor 2 personen opslaan.

Переключение идентификатора пользователя позволяет сохранять результаты для 2-х людей.

Kullanıcı kimlikleri arasında geçiş yapma, 2 kişi için ölçüm değerlerini kaydetmenizi sağlar.

ϥϳλΧηϟΕ΍˯΍έϘϟ΍υϔΣϡΩΧΗγϣϟ΍ϑέόϣϝϳΩΑΗΔϳϧΎϛϣ·ϙϟ΢ϳΗΗ 

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

Manufacturer

Fabricant

Hersteller

Produttore

Fabricante

Fabrikant

Производитель

Üretici

Δόϧλ

ϣϟ΍Δϛέηϟ΍

OMRON HEALTHCARE Co., Ltd.

53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN

EU-representative

Mandataire dans l’UE

EU-Repräsentant

Rappresentante per l’UE

Representante en la UE

Vertegenwoordiging in de EU

Представитель в ЕС

AB temsilcisi

ϲΑϭέϭϷ΍ΩΎ Σ ΗϻΎΑϝ ϳ Λ ϣ Η ϟ΍ΔϬΟ

OMRON HEALTHCARE EUROPE B.V.

Scorpius 33, 2132 LR Hoofddorp,

THE NETHERLANDS

www.omron-healthcare.com

Importer in EU

Importateur dans l’UE

Importeur in der EU

Importatore per l’UE

Importador en la UE

Importeur in de EU

Импортер в ЕС

AB’de İthalatçı

ϲΑϭέϭϷ΍ΩΎΣΗϻ΍ϲϓΩέϭΗγϣϟ΍

Production facility

Site de production

Produktionsstätte

Stabilimento di produzione

Planta de producción

Productiefaciliteit

Производственное

подразделение

Üretim Tesisi

ϊϳϧλΗϟ΍Γ΄ηϧϣ

OMRON HEALTHCARE MANUFACTURING

VIETNAM CO., LTD.

No.28 VSIP II, Street 2, Vietnam-Singapore Industrial Park II,

Binh Duong Industry-Services-Urban Complex, Hoa Phu Ward,

Thu Dau Mot City, Binh Duong Province, Vietnam

Subsidiaries

Succursales

Niederlassungen

Consociate

Empresas filiales

Dochteronder-

nemingen

Филиалы

Yan Kuruluşlar

ΔόΑΎΗϟ΍ΕΎϛέηϟ΍

OMRON HEALTHCARE UK LTD.

Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK

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

Issue Date / Date de publication / Ausgabedatum/

Datadipubblicazione / Fecha de publicación /

Uitgiftedatum / Дата выпуска / Teslim Tarihi /

έ΍ΩλϹ΍ΦϳέΎΗ

: 2019-07-29

Made in Vietnam / Fabriqué en Vietnam / Hergestellt in Vietnam/

Prodottoin Vietnam / Fabricado en Vietnam / Geproduceerd in Vietnam/

Сделано во Вьетнаме / Vietnam’da Üretilmiştir /

ϡΎϧΗϳϓϲϓϊϧλ

Omron Healthcare M4 Intelli IT - HEM-7155T-EBK El kitabı

Marka: Omron Healthcare

Modeli: M4 Intelli IT - HEM-7155T-EBK

Kategori: Kan basıncı birimleri

Tip: El kitabı

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PDF''yi indir

rapor

diğer dillerde

español: Omron Healthcare M4 Intelli IT - HEM-7155T-EBK El manual del propietario
français: Omron Healthcare M4 Intelli IT - HEM-7155T-EBK Le manuel du propriétaire
italiano: Omron Healthcare M4 Intelli IT - HEM-7155T-EBK Manuale del proprietario
English: Omron Healthcare M4 Intelli IT - HEM-7155T-EBK Owner's manual
Nederlands: Omron Healthcare M4 Intelli IT - HEM-7155T-EBK de handleiding

Omron Healthcare M4 Intelli IT - HEM-7155T-EBK El kitabı

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