Omron Healthcare HEM-7155-E Kullanım kılavuzu

Marka: Omron Healthcare

Modeli: HEM-7155-E

Kategori: Kan basıncı birimleri

Tip: Kullanım kılavuzu

Instruction Manual 1

Automatic Upper Arm Blood Pressure Monitor

ω΍έΫϟ΍ϰϠϋ΄ΑΕϳΑΛΗϠϟϝΑΎϘϟ΍ϲϟϵ΍ϡΩϟ΍ρϐοαΎϳϗίΎϬΟ

M3 Comfort (HEM-7155-E)

Εέϭϔϣϭϛ3ϡ·

X3 Comfort (HEM-7155-EO)

Εέϭϔϣϭϛ3αϛ΍

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

Symbolen/ Символы/ Semboller/

ίϣέϟ΍

Read Instruction manual and before use.

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

DE Lesen Sie vor der Verwendung die Gebrauchsanweisung und .

IT Leggere il manuale di istruzioni e prima dell’uso.

ES Lea el manual de instrucciones y antes del uso.

NL Lees de gebruiksaanwijzing en voor gebruik.

Прочтите руководство по эксплуатации и перед использованием.

TR Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

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

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

indicates this via a symbol with the measurement results. 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 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 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.

• Consult 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.

• NEVER 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.

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.

EN2

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

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.

• 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.

EN3

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

• To stop a measurement, press the [START/STOP] button while taking

a measurement.

• 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.

• When using an optional AC adapter, make sure not to place your

monitor in a location where it is difficult to plug and unplug the

ACadapter.

Battery Handling and Usage

• Disposal of used batteries should be carried out in accordance with

local regulations.

• The supplied batteries may have a shorter life span than new

batteries.

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 5 of instruction manual .

Air is leaking from the arm cuff. Replace the arm cuff to the new one. Refer to section 12 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 11 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 11 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 5 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.

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

to section 3 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 3 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 3 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 .

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.

EN6

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 5 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) M3 Comfort (HEM-7155-E)

X3 Comfort (HEM-7155-EO)

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 Operating mode Continuous operation

IP classification Monitor: IP20 / Optional AC adapter: IP21 (HHP-CM01) or IP22 (HHP-BFH01)

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

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

Class II ME equipment (optional AC adapter)

Weight Monitor: approximately 337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 EN ISO 81060-2:2014 and complies with EN ISO 81060-2:2014 and

EN ISO 81060-2:2019 + A1:2020. 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 HHP-CM01 is protected

against vertically falling water drops which may cause issues during a normal operation. The optional AC adapter HHP-BFH01 is protected

against oblique 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

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-7155-E and HEM-7155-EO 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-7155-E and HEM-7155-EO on the website.

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.

• 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.

EN10

SD1

Symbols Description

FR Description des symboles NL Beschrijving van symbolen

DE Beschreibung der Symbole RU Описание символов

IT Descrizione dei simboli TR Simgelerin Açıklaması

ES Descripción de los símbolos ίϭϣέϟ΍Ρέη AR

Applied part - TypeBF Degree of protection

against electric shock (leakage current)

FR Pièce appliquée -

TypeBF Degré de protection

contre les chocs électriques

(courant de fuite)

DE Anwendungsteil–

TypBF Schutz vor Strom-

schlägen (Ableitstrom)

IT Parti applicate - TipoBF

Livello di protezione contro

le folgorazioni (corrente di

dispersione)

ES Partes en contacto:

TipoBF Grado de protección

contra descargas eléctricas

(corriente de fuga)

NL 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΍ AR

έΎϳΗϟ΍Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍Ωο

BFωϭϧϠϟΏέγΗϣϟ΍

Class II equipment.

Protection against electric shock

FR Équipement de classe II.

Protection contre les chocs

électriques

DE Gerät der Klasse II.

Schutz vor Stromschlägen

IT Apparecchiatura di

Classe II. Protezione contro le

folgorazioni

ES Equipo de Clase II.

Protección contra descargas

eléctricas

NL Apparatuur van

KlasseII. Bescherming

tegen elektrische schokken

RU Изделие класса II

Защита от поражения

электрическим током

TR Sınıf II ünite. Elektrik

çarpmasına karşı koruma

ΩοΔϳΎϣΣϟ΍IIΔ΋ϔϟ΍ϥϣίΎϬΟ AR

Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍

IP XX Ingress protection degree provided by

IEC60529

FR Degré de protection

selon CEI60529

DE Grad des Eindring-

schutzes gemäß IEC60529

IT Livello di protezione IP

in base a IEC60529

ES Grado de protección

según la norma internacional

IEC60529

NL Beschermingsklasse

volgens IEC60529

RU Степень защиты,

обеспечиваемая

оболочками, согласно

IEC60529

TR Su girmesine karşı

koruma derecesi IEC60529

tarafından verilmiştir

ΔϣΩϘϣϟ΍ϝϭΧΩϟ΍ΔϳΎϣΣΔΟέΩ AR

,(&έΎϳόϣΔργ΍ϭΑ

CE Marking

FR Marquage CE

DE CE-Kennzeichnung

IT Contrassegno CE

ES Marcado CE

NL CE-merkteken

RU Знак соответствия

директиве ЕС

TR CE İşareti

ΔϧΟϠϟ΍ϊϣϖϓ΍ϭΗϟ΍Δϣϼϋ AR

CEΔϳΑϭέϭϷ΍

SD2

UKCA marking

FR Marquage UKCA

DE UKCA-Kennzeichnung

IT Marchio UKCA

ES Marcado UKCA

NL UKCA-markering

RU Маркировка UKCA

TR UKCA işareti

ιΎΧϟ΍ϖϓ΍ϭΗϟ΍ϡϳϳϘΗΔϣϼϋ AR

ΓΩΣΗϣϟ΍ΔϛϠϣϣϟΎΑ

Serial number

FR Numéro de série

DE Seriennummer

IT Numero di serie

ES Número de serie

NL Serienummer

RU Серийный номер

TR Seri numarası

ϝγϠγΗϣϟ΍ϡϗέϟ΍ AR

LOT number

FR Numéro de LOT

DE LOT-Nummer

IT Numero di lotto

ES Número de lote

NL Partijnummer

RU Код (номер) партии

TR Parti numarası

ΔϠϳϐηΗϟ΍ϡϗέ AR

UDI Unique device identifier

FR Identifiant unique des

dispositifs

DE Produktidentifizie-

rungsnummer

IT Identificatore univoco

del dispositivo

ES Identificador único del

producto

NL Unieke apparaat-ID

RU Уникальный

идентификатор устройства

TR Benzersiz cihaz

tanımlayıcısı

Ωϳέϔϟ΍ίΎϬΟϟ΍ϑ ˷

έόϣ AR

Medical device

FR Dispositif médical

DE Medizinprodukt

IT Dispositivo medico

ES Producto sanitario

NL Medisch apparaat

RU Медицинский прибор

TR Tıbbi cihaz

ϲΑρίΎϬΟ AR

Temperature limitation

Limitation de température

DE Temperaturbegrenzung

IT Limite di temperatura

ES Limitación de la

temperatura

Temperatuurbegrenzing

RU Температурный

диапазон

TR Sıcaklık sınırlaması

ΔΑγΎϧϣϟ΍Γέ΍έΣϟ΍ΔΟέΩΩϭΩΣ AR

Humidity limitation

FR Limitation d’humidité

DE Luftfeuchtigkeits-

begrenzung

IT Limite di umidità

Limitación de la humedad

Vochtigheidsbegrenzing

RU Диапазон влажности

TR Nem sınırlaması

ΔΑγΎϧϣϟ΍ΔΑϭρέϟ΍ΩϭΩΣ AR

Atmospheric pressure limitation

FR Limitation de pression

atmosphérique

DE Luftdruckbegrenzung

IT Limite di pressione

atmosferica

ES Limitación de la presión

atmosférica

NL Luchtdrukbegrenzing

RU Ограничение

атмосферного давления

TR Atmosferik basınç

sınırlaması

ΏγΎϧϣϟ΍ϱϭΟϟ΍ρϐοϟ΍ΩϭΩΣ AR

Indication of connector polarity

FR Indication de la polarité

des connecteurs

DE Anzeige der

Steckerpolarität

IT Indicazione della

polarità dei connettori

ES Indicación de la

polaridad del conector

NL Indicatie van polariteit

van aansluiting

RU Полярность разъема

адаптера

TR Bağlantı polarite

göstergesi

ϝλϭϣϟ΍ΔϳΑρϘϟέϳηΗΔϣϼϋ AR

SD3

For indoor use only

FR Pour un usage à

l’intérieur uniquement

DE Nur für die Nutzung in

Innenbereichen

IT Solo per uso in interni

Para uso solo en interiores

NL Alleen voor gebruik

binnenshuis

RU Для использования

только внутри помещений

TR Sadece iç mekanda

kullanım için

ϖρΎϧϣϟ΍ϲϓϡ΍ΩΧΗγϼϟ΢ϟΎλ AR

ρϘϓΔϘϠϐϣϟ΍

OMRON’s trademarked technology for

blood pressure measurement

FR Technologie protégée

par la marque de commerce

OMRON pour la mesure de

la pression artérielle

DE Markenrechtlich

geschützte Technologie

von OMRON zur

Blutdruckmessung

IT Tecnologia brevettata

OMRON per la misurazione

della pressione arteriosa

La tecnología de OMRON

para medir la presión arterial

NL Technologie voor

bloeddrukmeting onder

handelsmerk van OMRON

RU Зарегистрированная

технология измерения

артериального давления

OMRON

TR OMRON'un kan basıncı

ölçümü için ticari markalı

teknolojisidir

ΔϳέΎΟΗϟ΍Δϣϼόϟ΍ΔϳϧϘΗ AR

ϡΩϟ΍ρϐοαΎϳϘϟOMRON

Identifier of cuffs compatible for the device

FR Identificateur des

brassards compatibles avec

l’appareil

DE Kennzeichnung der

mit dem Gerät kompatiblen

Manschetten

IT Identifica i bracciali

compatibili con il dispositivo

ES Identificador para

manguitos compatibles con

el dispositivo

NL Identificatie van

manchetten die compatibel

zijn met het apparaat

Манжеты совместимые

с устройством

TR Cihaz ile uyumlu

kollukların tanıtım işareti

ρ΋΍έηϟ΍ΩϳΩΣΗΕΎϣϼϋ AR

ίΎϬΟϟ΍ϊϣΔϘϓ΍ϭΗϣϟ΍ΔρϏΎοϟ΍

Marker on the cuff to be positioned above

the artery

FR Repère sur le brassard,

à positionner au-dessus de

l’artère

DE Markierung auf der

Manschette, die oberhalb

der Arterie liegen muss

IT Contrassegno sul

bracciale da posizionare al di

sopra dell’arteria

ES La marca del manguito

debe colocarse sobre la

arteria

Markering op de manchet

die boven de slagader moet

worden geplaatst

RU Указатель располо-

жения плечевой артерии

TR Kolluk üzerindeki

işaretin konumu arterin

üzerine gelmelidir

ρϏΎοϟ΍ρϳέηϟΎΑΔϣϼϋ AR

ϕϭϓϪόοϭΏϭΟϭϰϟ·ΓέΎηϺϟ

ϥΎϳέηϟ΍

SD4

Manufacturer’s quality control mark

FR Marque de contrôle de

la qualité du fabricant

DE Qualitätskontroll-

zeichen des Herstellers

IT Contrassegno controllo

qualità del produttore

ES Marca del control de

calidad del fabricante

Symbool voor kwaliteits-

controle van fabrikant

RU Отметка произво-

дителя о контроле качества

TR Üreticinin kalite kontrol

işareti

ΓΩϭΟϟ΍ϲϓϡϛΣΗϟ΍Δϣϼϋ AR

Δόϧλϣϟ΍ΔϛέηϟΎΑΔλΎΧϟ΍

Not made with natural rubber latex

FR Ne contient pas de latex

de caoutchouc naturel

DE Enthält kein Naturlatex

IT Non contiene lattice di

gomma naturale

ES No contiene látex de

caucho natural

NL Bevat geen

natuurrubberlatex

RU Не содержит

натуральный латекс

TR Doğal kauçuk lateksten

üretilmemiştir

ϡ΍ΩΧΗγ΍ϥϭΩϊϳϧλΗϟ΍ϡΗ AR

ϲόϳΑρϟ΍ρΎρϣϟ΍αϛϳΗϻ

Arm circumference

FR Circonférence du bras

DE Armumfang

Circonferenza del braccio

ES Perímetro de brazo

NL Armomtrek

RU Окружность плеча

TR Kol çevresi

ω΍έΫϟ΍ρϳΣϣ AR

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 Es necesario que el

usuario consulte este manual

de instrucciones

NL Noodzaak voor de

gebruiker om deze gebruiks-

aanwijzing te raadplegen

RU Необходимость для

пользователя обратиться

к данному руководству по

эксплуатации

TR Kullanıcı, bu kullanım

kılavuzuna başvurmalıdır

ϡΩΧΗγϣϟ΍ωϭΟέΓέϭέο AR

ϝϳϟΩϲϓΓΩέ΍ϭϟ΍ΕΎϣϭϠόϣϟ΍ϰϟ·

΍ΫϫΕ΍ΩΎηέϹ΍

SD5

Need for the user to follow this instruction

manual thoroughly for your safety.

FR L’utilisateur doit suivre

attentivement ce mode

d’emploi pour votre sécurité.

DE Damit die Sicherheit

gewährleistet ist, muss

der Benutzer diese

Gebrauchsanweisung

sorgfältig befolgen.

IT Per la propria sicurezza,

l’utente deve seguire

attentamente il presente

manuale di istruzioni.

ES Es necesario que el

usuario siga rigurosamente

este manual de instrucciones

para su seguridad.

NL Noodzaak voor de

gebruiker om zich voor de

eigen veiligheid zorgvuldig

aan deze gebruiksaanwijzing

te houden.

RU В целях обеспечения

безопасности строго

следуйте указаниям в

данном руководстве по

эксплуатации.

TR Güvenlik açısından

kullanıcının bu kullanım

kılavuzuna dikkatle uyması

gerekir.

ωΎΑΗ΍ϰϟ·ϡΩΧΗγϣϟ΍ΔΟΎΣ AR

ϝϳϟΩϲϓΓΩέ΍ϭϟ΍Ε΍ΩΎηέϹ΍

υΎϔΣϠϟ΍ΫϫϝϣΎϛϟΎΑΕ΍ΩΎηέϹ΍

Δϣϼγϟ΍ϰϠϋ

Direct current

FR Courant continu

DE Gleichstrom

IT Corrente diretta

ES Corriente directa

NL Gelijkstroom

RU Постоянный ток

TR Doğru akım

έηΎΑϣϟ΍έΎϳΗϟ΍ AR

Alternating current

FR Courant alternatif

DE Wechselstrom

IT Corrente alternata

ES Corriente alterna

NL Wisselstroom

RU Переменный ток

TR Alternatif akım

ΏϭΎϧΗϣϟ΍έΎϳΗϟ΍ AR

Date of manufacture

FR Date de fabrication

DE Herstellungsdatum

IT Data di fabbricazione

ES Fecha de fabricación

NL Productiedatum

RU Дата изготовления

TR Üretim tarihi

ϊϳϧλΗϟ΍ΦϳέΎΗ AR

Prohibited action

FR Action interdite

DE Verbotene Aktion

IT Operazione proibita

ES Acción prohibida

NL Verboden handeling

Запрещенные действия

TR Yasaklanmış eylem

έϭυΣϣ˯΍έΟ· AR

SD6

Issue Date:

2022-05-25

Date de publication:

Ausgabedatum:

Data di pubblicazione:

Fecha de publicación:

Uitgiftedatum:

Дата выпуска:

Teslim Tarihi:

έ΍ΩλϹ΍ΦϳέΎΗ

IM1-HEM-7155-E-05-01/2022

2870433-4D

IM2-HEM-7155-E-05-01/2022

2870434-2D

Instruction Manual 2

Instruction Manual

2.3

Automatic Upper Arm Blood Pressure Monitor

ω΍έΫϟ΍ϰϠϋ΄ΑΕϳΑΛΗϠϟϝΑΎϘϟ΍ϲϟϵ΍ϡΩϟ΍ρϐοαΎϳϗίΎϬΟ

M3 Comfort (HEM-7155-E)

Εέϭϔϣϭϛ3ϡ·

X3 Comfort (HEM-7155-EO)

Εέϭϔϣϭϛ3αϛ΍

Read Instruction manual and before use.

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

DE Lesen Sie vor der Verwendung die Gebrauchsanweisung und .

IT Leggere il manuale di istruzioni e prima dell’uso.

ES Lea el manual de instrucciones y antes del uso.

NL Lees de gebruiksaanwijzing en voor gebruik.

RU 

Прочтите руководство по эксплуатации и перед использованием.

TR Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

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

1Package 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 ΓϭΑόϟ΍ΕΎϳϭΗΣϣ 

Instruction Manual

Instruction Manual2

2Preparing for a Measurement

FR Préparation d’une 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 αΎϳϘϟ΍ΔϳϠϣόϟίϳϬΟΗϟ΍ 

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

ΔϘϳϗΩ˼˹ώϠΑΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ 

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.

˶ΥέΗγ΍ϭΡέΗγ΍ϖ΋ΎϗΩ˾ώϠΑΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ

5Applying 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 ϥϣϳϷ΍ω΍έΫϟ΍ϰϠϋρϏΎοϟ΍ρϳέηϟ΍ϑϟ 

1-2 cm





Click

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

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

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

IT 

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.

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

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

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

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

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

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

securely so it can no longer slip round.

FR 

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.

DE 

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

IT 

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

ES 

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.

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

манжету, чтобы она не прокручивалась вокруг руки.

TR 

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 

3Installing Batteries

FR Mise en place des piles NL Batterijen plaatsen

DE Einsetzen der Batterien RUУстановка элементов питания

IT Installazione delle batterie TR Pillerin Takılması

ES Instalación de las pilas ΕΎϳέΎρΑϟ΍ΏϳϛέΗ

AA, 1.5V × 4





6Sitting Correctly

FR Position assise correcte NL Correct zitten

DE Korrekte Körperhaltung RUСядьте правильно

IT Come sedere nel modo corretto TR Düzgün Oturma

ES Cómo sentarse correctamente ΢ϳΣλϝϛηΑαϭϠΟϟ΍ 







Sit comfortably with your back and arm supported.

FR 

6DVVHRLUFRQIRUWDEOHPHQWGHPDQLqUHjFHTXHOHGRVHWOHEUDVVRLHQWELHQVRXWHQXV

DE 

%HTXHPKLQVHW]HQPLWGHP5FNHQDQOHKQHQXQGGHQ$UPDXIHLQH8QWHUODJHOHJHQ

IT 

6HGHUHFRPRGDPHQWHFRQODVFKLHQDHLOEUDFFLREHQVRVWHQXWL

ES 

6LpQWHVHFyPRGDPHQWHGHPRGRTXHODHVSDOGD\HOEUD]RHVWpQELHQDSR\DGRV

NL 

1HHPHHQFRPIRUWDEHOH]LWSRVLWLHLQPHWXZUXJHQDUPRQGHUVWHXQG

RU

ɋɹɞɶɬɟɭɞɨɛɧɨɱɬɨɛɵɫɩɢɧɚɢɪɭɤɚɨɩɢɪɚɥɢɫɶɧɚɱɬɨɥɢɛɨ

TR 

6ÕUWÕQÕ]YHNROXQX]GHVWHNOHQHUHNUDKDWELUúHNLOGHRWXUXQ

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

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.

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

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.

ΙΩΣΗΗϻϭϙΗΎΑΛϰϠϋυϓΎΣϭΩϋΎΑΗϣϊοϭϲϓϙϳϗΎγϭ΢˷ργϣϊοϭϲϓϙϳϣΩϗϝόΟ΍ 

AR 8

7Selecting 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)

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

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.

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

4Setting Date and Time

FR Réglage de la date et de l’heure NL Datum en tijd instellen

DE Einstellen von Datum und Uhrzeit RUУстановка даты и времени

IT Impostazione di data e ora TR Tarih ve Saatin Ayarlanması

ES Ajuste de la fecha y la hora ΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑο AR

Set year > month > day > hour > minute.

FR Réglez l’année > le mois > le jour > les heures > les minutes.

DE Stellen Sie Jahr > Monat > Tag > Stunde > Minute ein.

IT Impostare anno > mese > giorno > ora > minuti.

ES Ajuste de año > mes > día > hora > minuto.

NL Instellen van jaar > maand > dag > uur > minuut.

RUУстановите год > месяц > день > час > минута.

TR Yıl > ay > gün > saat > dakika ayarlayın.

ΔϘϳϗΩϟ΍ΔϋΎγϟ΍ϡϭϳϟ΍έϬηϟ΍ϡΎόϟ΍ρΑο AR

Year

Month

Day

Hour

Minute

Back / Forward

FR Arrière / Avant

DE Zurück / Vorwärts

IT Indietro / Avanti

ES Atrás / Adelante

NL Terug / vooruit

RUНазад / Вперед

TR İleri / Geri

ϡΩϘΗϟ΍ωϭΟέϟ΍

If taking measurements on the right arm, refer to:

FR 

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

DE 

Bei Messungen am rechten Arm siehe:

IT 

Se la misurazione viene eseguita al 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:

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

Instruction Manual

9Checking Readings

FR Vérication des résultats NL Metingen bekijken

DE Prüfen der Messwerte RU 

IT Controllo dei risultati TR Ölçüm Değerlerini Kontrol Etme

ES 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*.

DE

Wird angezeigt, wenn „SYS“ 135mmHg oder

mehr beträgt und/oder wenn „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*.

ES 

Aparece si “SYS” es 135mmHg o superior y/o

“DIA” es 85mmHg* o superior.

NL 

Verschijnt als “SYS” 135 mmHg of hoger is

en/of “DIA” 85 mmHg* of hoger is.

RU

Ɉɬɨɛɪɚɠɚɟɬɫɹɟɫɥɢ©6<6ªɦɦɪɬɫɬ

ɢɜɵɲɟɢɢɥɢ©',$ªɦɦɪɬɫɬɢɜɵɲɟ

TR 

“SYS” 135 mmHg ya da üstünde olduğunda

ve/veya “DIA” 85 mmHg* ya da üstünde

olduğunda görünür.

έΛϛ΃ϭ΃Ύ˱ϳϘΑ΋ί΍˱

έΗϣϳϠϠϣ˺˼˾ώϠΑϳ6<6ϥΎϛϝΎΣϲϓέϬυΗ 

έΛϛ΃ϭ΃Ύ˱ϳϘΑ΋ί΍˱

έΗϣϳϠϠϣ́˾',$ϭ΃ϭ

2Appears when an irregular rhythm** is detected during a measurement.

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

FR 

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

àplusieurs reprises, OMRON recommande de consulter votre médecin.

DE

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

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

IT 

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.

ES 

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

veces, OMRON recomienda que consulte a su médico.

NL 

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

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

RU

,      **.   

 ,  OMRON     .

TR 

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

OMRON doktorunuza danışmanızı önerir.

ϙΑϳΑρΓέΎηΗγΎΑ20521ϲλϭΗˬέέϛΗϣϝϛηΑΎϫέϭϬυΩϧϋαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓΏϠϘϟ΍ΕΎΑέοϡΎυΗϧ΍ϡΩϋϑΎηΗϛ΍ΩϧϋέϬυΗ

3Appears 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 3minutes et essayer à nouveau.

DE

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

warten Sie 2–3Minuten und versuchen Sie es erneut.

IT 

Viene visualizzato se l’utilizzatore si muove durante la misurazione. Rimuovere il bracciale,

attendere 2-3 minuti e riprovare.

ES 

Aparece cuando se mueve el cuerpo durante una medición. Retire el manguito, espere unos

2o3minutos e inténtelo de nuevo.

NL

Verschijnt wanneer uw lichaam tijdens een meting beweegt. Verwijder de armmanchet,

wacht2-3minuten en probeer het opnieuw.

RU

      .  , 

2-3    .

TR 

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 

4Cu is tight enough.

FR Le brassard est suffisamment serré.

DE Manschette sitzt ausreichend straff.

IT Il bracciale è stretto a sufficienza.

ES El manguito está lo suficientemente prieto.

NL Manchet zit strak genoeg.

RUɆɚɧɠɟɬɚɡɚɬɹɧɭɬɚɞɨɫɬɚɬɨɱɧɨɬɭɝɨ

TR Kolluk yeterince sıkıdır.

ϲϔϛϳΎϣΑϡϛΣϣρϏΎοϟ΍ρϳέηϟ΍ 

4Apply cu again MORE TIGHTLY.

FR 

Poser le brassard en le serrant davantage.

DE 

Manschette STRAFFER ziehen.

IT 

Applicare di nuovo il bracciale

STRINGENDOLO DI PIÙ.



Vuelva a poner el manguito MÁS PRIETO.

NL 

Breng de manchet STRAKKER aan.



ɇɚɥɨɠɢɬɟɦɚɧɠɟɬɭɟɳɟɪɚɡȻɈɅȿȿɌɍȽɈ



Kolluğu tekrar, DAHA SIKI bir şekilde takın.

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

*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*       2018 ESH/ESC.

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

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

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

more than the average rhythm detected during a measurement.

FR 

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

rythme moyen détecté durant une mesure.

DE 

** 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.

IT 

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

rispetto al ritmo medio rilevato durante una misurazione.

ES 

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

medio detectado durante una medición.

NL 

** 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.

RU

**    —  ,   25%   

  .

TR 

** 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 NL



Geheugenfuncties gebruiken



Verwendung der Speicherfunktionen RU



  



Uso delle funzioni di memoria TR



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.

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.



      .

TR 

Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.

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

10.1 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   

TR Hafızada Saklanan Ölçüm Değerleri

Γέϛ΍Ϋϟ΍ϲϓΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ 

Up to 60 readings

arestored.

FR 

Jusqu’à 60mesures

sont stockées.

DE

Es werden bis zu

60Messwerte

gespeichert.

IT 

Vengono conservati

fino a 60 risultati.

ES 

Se almacenan hasta

60lecturas.



Er kunnen tot 60 meetwaarden

worden opgeslagen.

RU

 

60.

TR 

60 adede kadar ölçüm

değeri saklanır.

ΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ΩΩϋϝλϳ 

Γ˯΍έϗ˿˹ϰϟ·

10.2

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 wurden

IT 

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

RU

    2-  3- ,

   10 

TR 

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+

10.3 Deleting All Readings



Suppression de toutes les mesures

DE 

Löschen aller Messwerte



Cancellazione di tutti i risultati



Eliminación de todas las lecturas

NL Alle metingen verwijderen

RU

  

TR 

Tüm Ölçüm Değerlerini Silme

Ε΍˯΍έϘϟ΍ϊϳϣΟϑΫΣ 

4sec+ 4sec+

   

Other Settings



Autres réglages NL



Andere instellingen



Weitere Einstellungen RU



 



Altre impostazioni TR



Diğer Ayarlar



Otros ajustes ϯέΧϷ΍Ε΍Ω΍ΩϋϹ΍ 

11.1 Restoring to the Default Settings

FR Réinitialisation aux réglages par défaut

DE Wiederherstellen der Standardeinstellungen

IT Ripristino delle impostazioni predefinite

ES Restablecimiento a los ajustes de fábrica

NL De standaardinstellingen herstellen

RU   

TR Varsayılan Ayarları Geri Yükleme

Δϳο΍έΗϓϻ΍Ε΍Ω΍ΩϋϹ΍ΓΩΎόΗγ΍



4sec+

 

4sec+



Optional Medical Accessories



Accessoires médicaux optionnels NL



Optionele medische accessoires



Optionales medizinisches Zubehör RU



 



Accessori medicali opzionali TR



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 cu.

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 conec-

tor 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

   . 

    .

TR 

Hava tıpasını atmayın. Hava tıpası steğe bağlı

kolluğa uygulanablr.

˯΍ϭϬϟ΍ΓΩ΍ΩγϝΎϣόΗγ΍ϥϛϣϳ˯΍ϭϬϟ΍ΓΩ΍ΩγϥϣιϠΧΗΗϻ

ϱέΎϳΗΧϻ΍ρϏΎοϟ΍ρϳέηϟ΍ϊϣ

Error messages or other problems? Refer to:

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

DE Weitere Fehlermeldungen oder Probleme siehe:

IT Messaggi di errore o altri problemi? Fare riferimento a:

ES ¿Hay mensajes de error u otros problemas? Consulte:

NL Foutmeldingen of andere problemen? Raadpleeg:

RU

     ? :

TR Hata mesajları veya başka sorunlar mı var? Bkz:

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

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

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.

DE 

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.

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

Если систолическое давление выше 210 мм.рт.ст.:  ,  

    ,    

[START/STOP]   ,        ,

     30–40..

TR 

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.

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

ϥϣϰϠϋ΃Ύ˱ϳϘΑ΋ί΍ ˱

έΗϣϳϠϠϣ˽˹ϰϟ·˼˹ϥϣΦϔϧϟΎΑίΎϬΟϟ΍ϡϭϘϳϰΗΣϑΎϘϳ·˯ΩΑ>67$576723@έίϟ΍ϰϠϋέ΍έϣΗγϻ΍

ϙϳΩϟΔόϗϭΗϣϟ΍ϲοΎΑϘϧϻ΍ϡΩϟ΍ρϐοΔϣϳϗ

8Taking a Measurement

FR Réalisation d’une mesure NL Een meting doen

DE Vornehmen einer Messung RU 

IT Misurazione TR Ölçüm Yapma

ES Obtención de una lectura αΎϳϘϟ΍˯΍έΟ· 

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

automatically.



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

DE

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

IT 

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

ES 

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

NL

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

RU

 ,   [START/STOP] ,     .

TR 

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

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

Taking a measurement in guest mode

FR Réalisation d’une mesure en mode Invité

DE Vornehmen einer Messung im Gast-Modus

IT Misurazione in modalità Ospite

Obtención de una lectura en modo de invitado

NL Een meting in gastmodus afnemen

RU     

TR Konuk modunda ölçüm yapma

ϑϳοϟ΍ϊοϭϡ΍ΩΧΗγΎΑαΎϳϘϟ΍˯΍έΟ· 

The guest mode can be used to take a single measurement for another user.

Noreadings are stored in the memory.

Le mode Invité permet de mesurer la pression

artérielle d’une autre personne une seule fois.

Les résultats ne sont pas enregistrés dans

lamémoire.

Soll eine einzelne Messung bei einem anderen

Benutzer durchgeführt werden, kann dafür der

Gast-Modus aktiviert werden. Im Gast-Modus

werden keine Messwerte gespeichert.

La modalità Ospite può essere utilizzata

per eseguire una singola misurazione su un

diverso utente. I risultati ottenuti non vengono

memorizzati.

Para realizar una única medición para otro

usuario, se puede utilizar el modo de invitado.

Cuando se selecciona el modo de invitado,

nose guardan lecturas.

NL De gastmodus kan worden gebruikt om

één enkele meting uit te voeren voor een

andere gebruiker. Er worden geen metingen

opgeslagen in het geheugen.

RU    

  

   .  

 ,   

  .

TR Konuk modu, başka br kş çn tek br ölçüm

yapmak üzere kullanılablr. Konuk modu

seçldğnde, ölçüm değerler hafızada saklanmaz.

ΓΩΣ΍ϭαΎϳϗΔϳϠϣϋ˯΍έΟϹϑϳοϟ΍ϊοϭϡ΍ΩΧΗγ΍ϥϛϣϳϭ

ϥ΃ΎϣϛΓέϛ΍Ϋϟ΍ϝΧ΍ΩΓ˯΍έϗϱ΃ϥϳίΧΗϡΗϳϻέΧ΁ϡΩΧΗγϣϟ





3 sec+

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

Manufacturer

Fabricant

Hersteller

Produttore

Fabricante

Fabrikant



Üretici

Δόϧλ˵ϣϟ΍Δϛέηϟ΍

OMRON HEALTHCARE Co., Ltd.

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

ΓΩϭΩΣϣϟ΍έϳϛΙϠϳϫϥϭέϣ΍Δϛέη

ϭηϭΩ΍έΗϭΑϭγΗϭϧϭϛ

ϭΗϭϳΎϛˬϭϛϭϣ

ϥΎΑΎϳϟ΍

EU-representative

Mandataire dans l’UE

EU-Repräsentant

Rappresentante per l’UE

Representante en la UE

Vertegenwoordiging in de EU

  

AB temsilcisi

ϲΑϭέϭϷ΍ΩΎ ΣΗϻΎΑϝ ϳΛ ϣΗϟ΍Δ ϬΟ

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

  

AB’de İthalatçı

ϲΑϭέϭϷ΍ΩΎΣΗϻ΍ϲϓΩέϭΗγϣϟ΍

Production facility

Site de

production

Produktionsstätte

Stabilimento di produzione

Planta de producción

Productiefaciliteit





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



Yan Kuruluşlar

ΔόΑΎΗϟ΍ΕΎϛέηϟ΍

Importer in the United Kingdom and UK responsible person

Importateur au Royaume-Uni et la personne responsable au Royaume-Uni

Importeur im Vereinigten Königreich und Verantwortliche Person für UK

Importatore per il Regno Unito e Responsabile in UK

Importador en el Reino Unido y persona responsable en el RU

Importeur voor het Verenigd Koninkrijk en verantwoordelijke in het VK

Импортер в Великобританию и ответственное лицо в Великобритании

Birleşik Krallık’taki İthalatçı ve Birleşik Krallık sorumlusu

ΓΩΣΗϣϟ΍ΔϛϠϣϣϟ΍ϲϓϝϭ΅γϣϟ΍ιΧηϟ΍ϭΓΩΣΗϣϟ΍ΔϛϠϣϣϟ΍ϲϓΓΩέϭΗγϣϟ΍ΔϬΟϟ΍

OMRON HEALTHCARE UK LTD.

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

www.omron-healthcare.com/distributors

OMRON MEDIZINTECHNIK

HANDELSGESELLSCHAFT mbH

www.omron-healthcare.com/distributors

OMRON SANTÉ FRANCE SAS

www.omron-healthcare.com/distributors

Issue Date / Date de publication / Ausgabedatum/

Datadipubblicazione / Fecha de publicación /

Uitgiftedatum /   / Teslim Tarihi / έ΍ΩλϹ΍ΦϳέΎΗ

: 2022-05-25

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

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

   / Vietnam'da Üretilmiştir /

ϡΎϧΗϳϓϲϓϊϧλ

Omron Healthcare HEM-7155-E Kullanım kılavuzu

Marka: Omron Healthcare

Modeli: HEM-7155-E

Kategori: Kan basıncı birimleri

Tip: Kullanım kılavuzu

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diğer dillerde

español: Omron Healthcare HEM-7155-E Manual de usuario
français: Omron Healthcare HEM-7155-E Manuel utilisateur
italiano: Omron Healthcare HEM-7155-E Manuale utente
English: Omron Healthcare HEM-7155-E User manual