Omron Healthcare HEM-7361T-EBK Manual de usuario

Marca: Omron Healthcare

Modelo: HEM-7361T-EBK

Categoría: Unidades de presión arterial

Tipo: Manual de usuario

Instruction Manual

Symbols

Automatic Upper Arm Blood Pressure Monitor

M7 Intelli IT (HEM-7361T-EBK)

X7 Smart (HEM-7361T-ESL)

Read Instruction manual and before use.

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

Lesen Sie vor der Verwendung Gebrauchsanweisung und .

Leggere il manuale di istruzioni e prima dell’uso.

Lea el manual de instrucciones y antes del uso.

Lees gebruiksaanwijzing en voor gebruik.

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Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

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Symboles/ Symbole/ Simboli/ Símbolos/

Symbolen/ / Semboller/



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

The device is a digital monitor intended for use in measuring blood pressure

and pulse rate in adult patient population. The device detects the appearance

of irregular heartbeats during measurement and gives a warning signal with

readings. It is mainly designed for general household use.

The device can detect an irregular pulse suggestive of Atrial Fibrillation

(Afib).

Please note that the device is not intended to diagnose Afib. A diagnosis of Afib

can only be confirmed by Electrocardiogram (ECG). If the Afib symbol appears,

consult your physician.

1.3 Receiving and Inspection

Remove this monitor and other components from the packaging and inspect

for damage. If this monitor or any other components 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 and Afib.

• 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.

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.

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 cause 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.

EN2

• 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

and/or detecting the possibility of Afib.

• 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, thick clothing and any accessories 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.

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.

EN3

• If battery fluid should get on your skin, wash your skin immediately with

plenty of clean, lukewarm water. If irritation, injury or pain persists, consult

with your physician.

• DO NOT use batteries after their expiration date.

• Periodically check batteries to ensure they are in good working condition.

2.3 General Precautions

• When you take a measurement on the right arm, the air tube should be at

the side of your elbow. Be careful not to rest your arm on the air tube.

• Blood pressure may differ between the right and left arm, and may result in a

different measurement value. Always use the same arm for measurements. If

the values between both arms differ substantially, check with your physician

on which arm to use for your measurements.

Battery Handling and Usage

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

regulations.

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

Blood pressure measurements were

not taken correctly in an Afib mode

measurement.

Apply the arm cuff correctly, then take another measurement.

Refer to section 7 of instruction manual

. Remain still and

sit correctly during a measurement. Refer to section 8 of

instruction manual

appears

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

contact your OMRON retail outlet or distributor.

appears

The montior 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 80 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

100 readings are not 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 sections 2 of instruction manual

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.

EN6

Display/Problem Possible Cause Solution

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.

Troubleshooting for Afib indicator function:

What is different between the

Afib indicator function and

ECG?

The Afib indicator function and ECG use completely different technologies. An ECG measures the electrical

activity of the heart and can be used to diagnose Afib. The Afib indicator function detects irregular

heartbeat and can suggest the possibility of Afib with a sensitivity of 95.5% and specificity of 93.8%.

Refer

to section 11 for details.

If the “ ” symbol does not

appear, it means there is no

possibility of Afib?

Even if the “ ” symbol does not appear, there is still a possibility of Afib.

Should I consult with my

physician if the “

” symbol

appears?

We recommend you to consult with your physician because there is a possibility of Afib. However, the “

”

symbol may be displayed for other reasons, such as other heart arrhythmias.

What is different between

Afib indicator function and

irregular heart beat function?

The irregular heartbeat function detects irregularities in the pulse waves in one measurement. The Afib

indicator function suggests the possibility of Afib when blood pressure is measured 3 consecutive times.

What should I do if the “

”

symbol sometimes appears?

Afib does not always have symptoms. We recommend you to consult with and follow the directions of

your physician.

I have been diagnosed with

Afib by the physician, but the

“

” symbol does not appear.

Afib may not occur at the time of specific blood pressure measurements. We recommend you to consult

with your physician regularly.

Is the blood pressure reading

reliable when the “

”

symbol appears?

Afib or an irregular heartbeat can influence your blood pressure measurements and make it difficult to get

an accurate reading. Repeated measurements may be required to overcome variabilities.* In Afib mode,

the blood pressure measurement is taken 3 times, and the average is displayed. The monitor will indicate

an error message (E5/E6) if the influence of the irregular heartbeat is too severe to give a measurement

result. If this occurs repeatedly, we recommend that you consult with your physician.

* Prof. Roland Asmar et al. European Society of Hypertension Recommendations for Conventional, Ambulatory and Home Blood Pressure Measurement

EN7

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, contact us

for information:

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.

5. Maintenance

5.1 Maintenance

To protect your monitor from damage, follow the directions below:

Changes or modifications not approved by the manufacturer will void the user

warranty.

Caution

DO NOT disassemble or attempt to repair this monitor or other components.

This may cause an inaccurate reading.

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.

• To protect your monitor during storage, an optional LCD cover is available as

accessory. Refer to section 15 of Instruction Manual

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.

EN8

6. Specications

Product Category Electronic Sphygmomanometers

Product description Automatic Upper Arm Blood Pressure

Monitor

Model (Code) M7 Intelli IT (HEM-7361T-EBK) /

X7 Smart (HEM-7361T-ESL)

Display LCD digital display

Cuff pressure range 0 to 299mmHg

Blood pressure

measurement range

SYS: 60 to 260mmHg

DIA: 40 to 215mmHg

Pulse measurement range

40 to 180 beats / min.

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

Operation mode Continuous operation

IP classification Monitor: IP20

Optional AC adapter: IP21

Rating DC6V 4.0W

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)

The number of times may decrease when

using Afib mode because one Afib indication

consists of 3 regular measurements.

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)

Weight Monitor: approximately 460g

(notincluding batteries)

Arm cuff: approximately 163g

Dimensions

(approximately value)

Monitor: 191mm (W) × 85mm (H) ×

120mm (L) / Arm cuff:145mm ×

532mm (air tube: 750mm)

Cuff circumference

applicable to the monitor

220 to420 mm

Memory Stores up to 100 readings per user

Contents Monitor, arm cuff (HEM-FL31), 4 “AA”

batteries, Instruction Manual

and

, setup instructions, storage case

Protection against

electric shock

Internally powered ME equipment

(When using only batteries)

Class II ME equipment (Optional AC

adapter)

Applied part Type BF (arm cuff)

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**.

EN9

• 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-7361T-EBK/ESL conforms to the EN60601-1-2:2015 Electromagnetic

Compatibility (EMC) standard.

Further documentation in accordance with this EMC standard is available at

OMRON HEALTHCARE EUROPE at the address mentioned in this instruction

manual or at: www.omron-healthcare.com.

9. Guidance and Manufacturer’s Declaration

• This blood pressure monitor is designed according to the European Standard

EN1060, Non-invasive sphygmomanometers Part 1: General Requirements

and Part 3: Supplementary requirements for electromechanical blood

pressure measuring systems.

• Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipments

type HEM-7361T-EBK/ESL is in compliance with Directive 2014/53/EU.

• 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.

10. How to Calculate Weekly Averages

Morning Weekly Average Calculation

This is the average for the measurements taken during the morning (4:00 - 9:59)

between Sunday and Saturday. The 2 or 3 readings taken within the first

10minute timeframe in the morning between 4:00 - 9:59 will be used to

calculate the morning average for each day.

Evening Weekly Average Calculation

This is the average for the measurements taken during the evening (19:00 - 1:59)

between Sunday and Saturday. The 2 or 3 readings taken within the last

10minute timeframe in the evening between 19:00 - 1:59 will be used to

calculate the evening average for each day.

Within 10 min.

Measurements

in the morning

Measurements

in the morning

Within 10 min.

EN10

11. Useful Information

What is Blood Pressure?

Blood pressure is a measure of the force of blood flowing against the walls of

the arteries. Arterial blood pressure is constantly changing during the course of

the heart’s cycle.

The highest pressure in the cycle is called the Systolic Blood Pressure; the lowest

is the Diastolic Blood Pressure. Both pressures, the Systolic and Diastolic, are

necessary to enable a physician to evaluate the status of a patient’s blood pressure.

What is Arrhythmia?

Arrhythmia is a condition where the heartbeat rhythm is abnormal due to flaws in

the bio-electrical system that drives the heartbeat. Typical symptoms are skipped

heartbeats, premature contraction, an abnormally rapid (tachycardia) or slow

(bradycardia) pulse.

What is Afib?

Atrial fibrillation (also called AFib or AF) is a quivering or irregular heartbeat

(arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-

related complications. During atrial fibrillation, the heart’s two upper chambers (the

atria) beat chaotically and irregularly — out of coordination with the two lower

chambers (the ventricles) of the heart. Episodes of atrial fibrillation can come and

go, or you may develop atrial fibrillation that doesn’t go away and may require

treatment.

Afib indicator function detects the possibility of Afib with an accuracy of 94.2%

(with sensitivity of 95.5% and specificity of 93.8%) as demonstrated in the study*

with Single-lead ECG as reference measurement.

*M. Ishizawa, T. Noma, T. Minamino et al., Multiple measurements with

automated blood pressure monitor can detect atrial fibrillation with high

sensitivity and specificity in general cardiac patients, ESC Congress 2018

SD1

Symbols Description

Description des symboles

Beschrijving van symbolen

Beschreibung der Symbole

 

Descrizione dei simboli

Simgelerin Açıklaması

Descripción de los símbolos





Applied part - Type BF Degree of protection against

electric shock (leakage current)

Partie appliquée - Type BF

Degré de protection contre

les chocs électriques

(courant de fuite)

Anwendungsteil– Typ BF

Schutz vor Stromschlägen

(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)

  

-  BF 

  

 

( )

Uygulanan parça - Tip BF

Elektrik çarpmasına karşı

koruma derecesi (kaçak

akım)

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

 II.

  

 

Sınıf II ekpman. Elektrk

çarpmasına karşı koruma

IP XX

Ingress protection degree provided by IEC 60529

Degré de protection selon

CEI60529

Grad des Eindringschutzes

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

 ,



, 

 

 IEC 60529

Su grmesne karşı koruma

dereces IEC 60529

tarafından verlmştr

CE Marking

Marquage CE

CE-Kennzeichnung

Contrassegno CE

Marcado CE

CE-merkteken

 

 

CE İşaret

Serial number

Numéro de série

Seriennummer

Numero di serie

Número de serie

Serienummer

 

Ser numarası

LOT number

Numéro de LOT

LOT-Nummer

Numero di lotto

Número de lote

Partijnummer

 

Parti numarası

Medical device

Dispositif médical

Medizinprodukt

Dispositivo medico

Producto sanitario

Medisch apparaat

 

Tıbbi cihaz

BF





















)CE













II



SD2

Indicates the manufacturer’s catalogue number

Indique le numéro de

catalogue du fabricant

Angabe der Hersteller-

Katalognummer

Indica il numero di

catalogo del produttore

Indica el número de

catálogo del fabricante

Geeft het

catalogusnummer van de

fabrikant aan

  

 

Üretcnn katalog

numarasını belrtr

Temperature limitation

Limitation de température

Temperaturbegrenzung

Limite di temperatura

Limitación de la

temperatura

Temperatuurbegrenzing





Sıcaklık sınırlaması

Humidity limitation

Limitation d’humidité

Luftfeuchtigkeits-

begrenzung

Limite di umidità

Limitación de la humedad

Vochtigheidsbegrenzing

 

Nem sınırlaması

Atmospheric pressure limitation

Limitation de pression

atmosphérique

Luftdruckbegrenzung

Limite di pressione

atmosferica

Limitación de la presión

atmosférica

Luchtdrukbegrenzing

 



Atmosferk basınç

sınırlaması

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

 



Bağlantı polarite

göstergesi

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

 

 



Sadece ç mekanda

kullanım çn

OMRON’s trademarked technology for blood

pressure measurement

Technologie brevetée

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



 

 

OMRON

OMRON'un kan basıncı

ölçümü çn tcar markalı

teknolojsdr

















OMRON











SD3

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

,  



Chaz le uyumlu

kollukların tanıtım şaret

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

  

  



Kolluk üzerndek şaretn

konumu artern üzerne

gelmeldr

Manufacturer’s quality control mark

Marque de contrôle de la

qualité du fabricant

Qualitätskontrollzeichen

des Herstellers

Contrassegno controllo

qualità del produttore

Marca del control de

calidad del fabricante

Symbool voor

kwaliteitscontrole van

fabrikant

 

  

Üretcnn kalte kontrol

şaret

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

 

 

Doğal kauçuk lateksten

üretlmemştr

Arm circumference

Circonférence du bras

Armumfang

Circonferenza del braccio

Perímetro de brazo

Armomtrek

 

Kol çevres

Necessity for the user to consult this instruction manual

L’utilisateur doit consulter

le 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

De gebruiker dient deze

gebruiksaanwijzing te

raadplegen

 

 

  

 

Kullanıcı, bu kullanım

kılavuzuna başvurmalıdır























SD4

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.

Voor de eigen veiligheid

dient de gebruiker zich

zorgvuldig aan deze

gebruiksaanwijzing te

houden.

  

 

  

  

.

Güvenlk açısından

kullanıcının bu kullanım

kılavuzuna dkkatle

uyması gerekr.

Direct current

Courant continu

Gleichstrom

Corrente diretta

Corriente directa

Gelijkstroom

 

Doğru akım

Alternating current

Courant alternatif

Wechselstrom

Corrente alternata

Corriente alterna

Wisselstroom

 

Alternatf akım

Date of manufacture

Date de fabrication

Herstellungsdatum

Data di fabbricazione

Fecha de fabricación

Productiedatum

 

Üretm tarh

Prohibited action

Action interdite

Verbotene Aktion

Operazione proibita

Acción prohibida

Verboden handeling

 

Yasaklanmış eylem















SD5

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.

Pour indiquer des niveaux généralement élevés, potentiellement

dangereux, de rayonnement non ionisant, ou pour indiquer

l’équipement ou les systèmes, par exemple dans le domaine de

l’électricité médicale qui comprennent des émetteurs RF ou qui

utilisent intentionnellement 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 electro médico, 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.

     

     

  (,    

),    

 ,  

      .

Genellkle yüksek ve zararlı olablecek yonlaşmayan radyasyon

sevyelern belrtr veya RF vercler çeren veya tanı ya da tedav

amacıyla blnçl olarak RF elektromanyetk enerj uygulayan (örneğn

medkal elektrk alanında bulunan) ekpman ve sstemler belrtr.











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 is a service mark of Apple Inc., registered in the U.S and other

countries. 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 est

une marque de service d’Apple Inc., déposées aux États-Unis et dans d’autres

pays. Le logo GooglePlay est une marque commerciale 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 ist eine

Dienstleistungsmarke der AppleInc., die in den USA und anderen Ländern

eingetragen ist. Das Google Play-Logo ist eine Marke der 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 è un marchio commerciale di

Apple Inc., registrato negli Stati Uniti e in altri Paesi. Il logo Google Play è un

marchio commerciale 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 es una marca de servicio registrada de Apple Inc. en EE. UU. y en

otros países. El logotipo de Google Play es una marca comercial 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 is een servicemerk van Apple Inc. en gedeponeerd in de V.S. en in

andere landen. Het Google Play-logo is een handelsmerk van Google LLC.

    Bluetooth®  

 ,    Bluetooth

SIG, Inc.,       OMRON

HEALTHCARE Co., Ltd.  .  

      

. App Store    Apple Inc.,

     .  Google Play

   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, Apple Inc. firmasının ABD ve diğer ülkelerde

tescilli hizmet markasıdır. Google Play logosu, GoogleLLC firmasının ticari

markasıdır.

Bluetooth





















.

Play

Issue Date:

2019-09-04

Date de publication:

Ausgabedatum:

Data di pubblicazione:

Fecha de publicación:

Uitgiftedatum

 :

Teslim Tarihi:



IM1-HEM-7361T-E-02-09/2019

2895864-6B

Automatic Upper Arm

Blood Pressure Monitor

M7 Intelli IT (HEM-7361T-EBK)

X7 Smart (HEM-7361T-ESL)

Instruction Manual

Read Instruction manual and before use.

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

Lesen Sie vor der Verwendung Gebrauchsanweisung und .

Leggere il manuale di istruzioni e prima dell’uso.

Lea el manual de instrucciones y antes del uso.

Lees gebruiksaanwijzing en voor gebruik.

      .

Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.

  

Package Contents...........................................1

Contenu de l’emballage

Inhoud van de verpakking

Packungsinhalt

 

Contenuto della confezione

Paketin İçindekiler

Contenido del envase



Preparing for a Measurement........................4

Préparation pour une prise

de mesure

Een meting voorbereiden

Vorbereiten einer Messung

  

Preparazione per la

misurazione

Ölçüm Hazırlığı

Preparación para una

medición



Downloading the "OMRON connect" App.....5

Téléchargement de

l’application «OMRON

connect»

De app “OMRON connect“

downloaden

Herunterladen der App

„OMRON connect“

 

«OMRON connect»

Download dell'app “OMRON

connect”

"OMRON Connect"

Uygulamasını İndirme

Descarga de la aplicación

“OMRON connect”



Inserting Batteries..........................................6

Mise en place des piles

De batterijen plaatsen

Einlegen von Batterien

 



Inserimento delle batterie

Pilleri Takma

Introducción de las pilas



Pairing Your Smart Device..............................7

Jumelage de votre appareil

intelligent

Uw smartapparaat koppelen

Koppeln mit Smartphone

oder Tablet

  -



Associazione del dispositivo

smart

Akıllı Cihazınızın

Eşleştirilmesi

Sincronización con un

dispositivo inteligente



Setting Date and Time Manually....................8

Réglage manuel de la date

et de l’heure

Datum en tijd handmatig

instellen

Manuelles Einstellen von

Datum und Uhrzeit

   



Impostazione manuale di

data e ora

Tarih ve Saatin Manuel

Olarak Ayarlanması

Ajuste manual de la fecha y

la hora







Applying the Cuff on the Left Arm.................9

Pose du brassard sur le bras

gauche

De manchet op de linkerarm

aanbrengen

Anbringen der Manschette

am linken Arm

  

 

Applicazione del bracciale

sul braccio sinistro

Kolluğun Sol Kola Takılması

Colocación del manguito en

el brazo izquierdo



Sitting Correctly..............................................11

Position assise correcte

Correct zitten

Korrekte Körperhaltung

 

Come sedersi nel modo

corretto

Düzgün Oturma

Cómo sentarse

correctamente



Selecting User ID (1 or 2)................................13

Sélection de l’ID Utilisateur

(1 ou 2)

Gebruikers-ID selecteren

(1of 2)

Auswahl der Benutzer-ID

(1oder 2)

 

 (1  2)

Selezione dell’ID utente

(1o 2)

Kullanıcı Kimliğini Seçme

(1veya 2)

Selección de ID de usuario

(1o 2)

)

Taking a Measurement...................................14

Réalisation d’une mesure

Een meting verrichten

Eine Messung vornehmen

 

Misurazione

Bir Ölçüm Yapma

Obtención de una lectura



Checking Readings in Comparison Mode......18

Vérification des mesures en

mode de comparaison

Metingen bekijken in

vergelijkingsmodus

Überprüfen von Messwerten

im Vergleichsmodus

 

  



Controllo dei risultati in

modalità Confronto

Karşılaştırma Modunda

Ölçüm Değerlerini Kontrol

Etme

Comprobación de

las lecturas en modo

comparativo



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

Utilisation des fonctions de

mémoire

Geheugenfuncties

gebruiken

Verwendung der

Speicherfunktion

 



Uso delle funzioni di

memoria

Hafıza Fonksiyonunun

Kullanılması

Uso de las funciones de

memoria



Other Settings...............................................26

Autres réglages

Andere instellingen

Weitere Einstellungen

 

Altre impostazioni

Diğer Ayarlar

Otros ajustes



Optional Medical Accessories........................29

Accessoires médicaux en

option

Optionele medische

accessoires

Medizinisches optionales

Zubehör





Accessori medicali opzionali

Opsiyonel Tıbbi Aksesuarlar

Accesorios médicos

opcionales



Other Optional Parts.......................................30

Autres pièces en option

Overige optionele

onderdelen

Weitere optionale Teile

 

 



Altri componenti opzionali

Diğer Aksesuarlar

Otras piezas opcionales



Package Contents

Contenu de l’emballage

Inhoud van de verpakking

Packungsinhalt

Комплект поставки

Contenuto della confezione

Paketin İçindekiler

Contenido del envase



Instruction Manual

Preparing for a Measurement

Préparation pour une prise de mesure

Een meting voorbereiden

Vorbereiten einer Messung

Подготовка к измерению

Preparazione per la misurazione

Ölçüm Hazırlığı

Preparación para una medición





30 minutes before

30minutes avant

30 Minuten vorher

30 minuti prima

30minutos antes

30 minuten ervoor

 30  

30 dakika önce





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.

 5  :   .

5 dakika önce: Gevşeyin ve dinlenin.





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 dell'app “OMRON connect”

"OMRON Connect" Uygulamasını İndirme

Descarga de la aplicación “OMRON connect”



omron connect

Inserting Batteries

Mise en place des piles

De batterijen plaatsen

Einlegen von Batterien

Установка элементов питания

Inserimento delle batterie

Pilleri Takma

Introducción de las pilas



AA, 1.5V × 4

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 un dispositivo inteligente



2 3

Bluetooth

Follow the instructions.

Suivez les instructions.

Befolgen Sie die Anweisungen.

Attenersi alle istruzioni.

Siga las instrucciones.

Volg de instructies.

 .

Talimatları izleyin.



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.

        .

Ölçüm cihazınız uygulamayla eşleştirildiğinde tarih ve saat otomatik olarak ayarlanır.











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







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.



    -,   

 .    

,   >  >  >  > .

Ölçüm cihazınız akıllı cihazınızla eşleştirilmişse tarih ve saat otomatik

olarak ayarlanır. Bunları manuel olarak ayarlamanız gerektiğinde,

yıl>ay > gün > saat > dakika değerini ayarlayın.



Year

Month

Day

Hour

Minute

Back / Forward

Arrière / Avant

Terug / vooruit

Zurück / Vorwärts

 / 

Indietro / Avanti

İleri / Geri

Atrás / Adelante









daymonthyear





minutehour

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



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 del

gomito interno, 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.

       1 - 2

  .

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

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.

,     

     

,      .

Hava borusunun kolunuzun iç tarafında olduğundan emin

olun ve kolluğu kaymayacak şekilde sabit şekilde sarın.

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:

Instruction Manual

     .

Sağ koldan ölçüm yapıyorsanız aşağıdakilere bakın:









Sitting Correctly

Position assise correcte

Correct zitten

Korrekte Körperhaltung

Сядьте правильно

Come sedersi nel modo corretto

Düzgün Oturma

Cómo sentarse correctamente





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.

 ,       -.

Sırtınız ve kolunuz desteklenecek şekilde oturun.

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.

     .

Kolluğu kalbinizle aynı düzeye getirin.

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.

  ,   ,     .

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











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)

(

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.

       2- .

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



Taking a Measurement

Réalisation d’une mesure

Een meting verrichten

Eine Messung vornehmen

Выполнение измерений

Misurazione

Bir Ölçüm Yapma

Obtención de una lectura



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.

 ,   [START/STOP] ,    

.  ,   .

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

aktarmak için uygulamayı açın.

Instruction Manual

P.18







Taking a measurement in Afib mode

Réalisation d’une mesure en mode fibrillation auriculaire

Vornehmen einer Messung im Afib-Modus

Misurazione in modalità Afib

Obtención de una lectura en modo fibrilación auricular

Een meting in Afib-modus afnemen

    

Afib modunda ölçüm yapma

In the Afib mode, your monitor automatically takes 3

consecutive readings at 30-second intervals and displays

the average. If there is a possibility of Afib, “Afib indicator

symbol” (

) will appear.

This is not a diagnosis, it is only a potential finding for Afib.

You should contact your physician to discuss the findings.

If you are experiencing any symptoms, contact a medical

professional.

En mode fibrillation auriculaire, votre moniteur effectue

automatiquement 3mesures consécutives à 30secondes d’intervalle

et affiche la moyenne. S’il y a une possibilité de fibrillation auriculaire,

le «symbole indicateur de fibrillation auriculaire» (

) s’affiche.

Il ne s’agit pas d’un diagnostic mais seulement de l’indication

d’une fibrillation auriculaire possible. Vous devriez consulter votre

médecin pour discuter des résultats. Si vous ressentez un symptôme

quelconque, consultez un professionnel de la santé.

Im Afib-Modus nimmt das Messgerät automatisch 3Messungen

hintereinander im Abstand von je 30Sekunden vor und zeigt den

Mittelwert an. Wenn die Möglichkeit von Vorhofflimmern besteht,

erscheint das „Afib-Hinweissymbol“ (

).

Dabei handelt es sich nicht um eine Diagnose, sondern lediglich um

einen Befund, dass Vorhofflimmern vorliegen könnte. Wenden Sie sich

an Ihren Arzt, um den Befund weiter abzuklären. Konsultieren Sie bei

Auftreten von Symptomen eine medizinische Fachkraft.

Nella modalità Afib, il misuratore esegue automaticamente 3

misurazioni consecutive a intervalli di 30 secondi e visualizza la media.

In caso di potenziale presenza di fibrillazione atriale (Afib) viene

visualizzato il “simbolo dell’indicatore Afib” (

).

Questa non è una diagnosi ma è soltanto un rilevamento della

potenziale presenza di fibrillazione atriale (Afib). È opportuno

rivolgersi al proprio medico curante per discutere questo risultato. Se

si dovessero riscontrare eventuali sintomi, rivolgersi a un medico.

En el modo fibrilación auricular, el monitor realiza 3 mediciones

consecutivas automáticamente a intervalos de 30 segundos y muestra

el valor promedio. Si existe una posible fibrilación auricular, aparecerá

el “símbolo indicador de fibrilación auricular” (

).

Esto no es un diagnóstico, simplemente la detección de una posible

fibrilación auricular. Deberá ponerse en contacto con su médico para

hablar de los resultados. En caso de padecer síntomas, póngase en

contacto con un profesional sanitario.

In de Afib-modus neemt uw meter automatisch 3 achtereenvolgende

metingen met intervallen van 30 seconden en toont vervolgens het

gemiddelde. Als er een mogelijkheid is op Afib verschijnt het “Afib-

indicatorsymbool” (

Dit is geen diagnose, het is slechts een vaststelling dat er mogelijk

sprake is van Afib. Neem contact op met uw arts om de bevindingen

te bespreken. Neem contact op met een medische professional als u

symptomen ondervindt.

     3  

 30- ,     .

     «  » (

).

  ,     . 

     

 .     -  

,   .

Cihazınız Afib modunda iken, otomatik olarak 30 saniyelik aralıklarda

ardışık 3 ölçüm yapar ve ortalamayı gösterir. Afib olasılığı varsa "Afib

gösterge sembolü" (

) görünür.

Bu bir tanı değildir, yalnızca olası Afib bulgusudur. Doktorunuzla

iletişime geçerek bulguları konuşmanız gerekir. Semptom yaşıyorsanız

bir tıp uzmanıyla iletişime geçin.









































2 sec+

Instruction Manual

P.18

Taking a measurement in guest mode

Réalisation d’une mesure en mode Invité

Vornehmen einer Messung im Gast-Modus

Misurazione in modalità Ospite

Obtención de una lectura en modo de invitado

Een meting in gastmodus afnemen

    

Konuk modunda ölçüm yapma

The guest mode can be used to take a single measurement

for another user. No readings are stored in the memory,

and the Afib mode is not available when the guest mode is

selected.

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 et le mode fibrillation auriculaire n’est pas disponible

lorsque le mode Invité est sélectionné.

Soll eine einzelne Messung bei einem anderen Benutzer durchgeführt

werden, kann dafür der Gast-Modus aktiviert werden. Im Gast-Modus

werden keine Messwerte gespeichert und der Afib-Modus steht nicht

zur Verfügung.

La modalità Ospite può essere utilizzata per eseguire una singola

misurazione su un diverso utente. I risultati ottenuti non vengono

memorizzati e la modalità Afib non è disponibile quando si seleziona

la modalità Ospite.

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 en la memoria y el modo de fibrilación auricular no

está disponible.

De gastmodus kan worden gebruikt om één enkele meting uit

te voeren voor een andere gebruiker. Er worden geen metingen

opgeslagen in het geheugen en de Afib-modus is niet beschikbaar

wanneer de gastmodus is geselecteerd.

     

    .   

,      ,  

 .

Konuk modu, başka bir kişi için tek bir ölçüm yapmak üzere

kullanılabilir. Konuk modu seçildiğinde, ölçüm değerleri hafızada

saklanmaz ve Afib modu kullanılamaz.











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

Tout en maintenant le bouton enfoncé, appuyer sur le bouton [START/STOP].

Halten Sie die Taste gedrückt und drücken Sie gleichzeitig die Taste [START/STOP].

Mentre si tiene premuto il pulsante

premere il pulsante [START/STOP].

Mientras mantiene pulsado el botón , pulse el botón [START/STOP].

Houd de knop

ingedrukt en druk tegelijkertijd op de knop [START/STOP].

    ,   [START/STOP].

düğmesn basılı tutarken, [START/STOP] düğmesne basın.

 



Checking Readings in Comparison Mode

Vérification des mesures en mode de comparaison

Metingen bekijken in vergelijkingsmodus

Überprüfen von Messwerten im Vergleichsmodus

Проверка результатов измерений в режиме

сравнения

Controllo dei risultati in modalità Confronto

Karşılaştırma Modunda Ölçüm Değerlerini Kontrol

Etme

Comprobación de las lecturas en modo comparativo



Prior reading

Mesure antérieure

Vorheriger Messwert

Valore precedente

Lectura anterior

Eerdere meting

 

Önceki ölçüm değeri



Appears when the reading was taken in Afib mode.

S’affiche lorsque la mesure a été effectuée en mode Fibrillation

auriculaire.

Erscheint, wenn der Messwert im AFib-Modus ermittelt wurde.

Appare quando la misurazione è stata effettuata in modalità Afib.

Aparece cuando la lectura fue realizada en el modo de fibrilación

auricular.

Verschijnt wanneer de meting in de Afib-modus werd verricht.

,      .

Ölçüm Afb moduna alınınca görünür.



Appears if an atrial fibrillation (Afib)* was detected

during the Afib mode measurement. If it continues

to appear, we recommend you to consult with and

follow the directions of your physician.

S’affiche si une fibrillation auriculaire* a été détectée durant une

mesure en mode fibrillation auriculaire. S’il continue d’apparaître,

nous vous recommandons de consulter votre médecin et de

suivre ses recommandations.

Wird angezeigt, wenn bei einer Messung im Afib-Modus

Vorhofflimmern (Afib)* erkannt wurde. Wird das Symbol weiterhin

angezeigt, sollten Sie sich an einen Arzt wenden und dessen

Anweisungen befolgen.

Viene visualizzato se durante una misurazione in modalità Afib

è stata rilevata la presenza di fibrillazione atriale (Afib)*. Se il

simbolo continua ad apparire, è consigliabile rivolgersi al proprio

medico curante e seguirne le indicazioni.

Aparece si se detecta fibrilación auricular (Afib)* durante la

medición en modo fibrilación auricular. Si esto sigue apareciendo, le

recomendamos que consulte a su médico y siga sus recomendaciones.

Verschijnt als er een atriumfibrillatie (Afib)* is gedetecteerd tijdens

de Afib-modusmeting. Als dit blijft verschijnen raden we u aan

contact op te nemen met uw arts en zijn of haar aanwijzingen op

te volgen.

,       

  ()*.    

,      

  .

Afib modunda ölçüm esnasında bir atrial fibrilasyon (Afib)*

saptandığında görünür. Görünmeye devam ediyorsa doktorunuza

danışmanızı ve kendisinin yönergelerini izlemenizi öneririz.

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mmHg**

o superior.

Verschijnt als “SYS” 135 mmHg of hoger is en/of “DIA” 85 mmHg**

of hoger is.

,  «SYS» 135 ...   / «DIA»

85...**  .

"SYS" 135 mmHg ya da üstünde olduğunda ve/veya "DIA"

85mmHg** ya da üstünde olduğunda görünür.

Cuff 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.

   .

Kolluk yeterince sıkıdır.

Apply cuff 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.

     .

Kolluğu tekrar, DAHA SIKI bir şekilde takın.

DIA







SYS























Appears when your body moves during a

measurement. Remove the arm cuff, wait

2-3minutes and try again.

(It does not appear when the possibility of Afib is

detected during a Afib mode measurement)

S’affiche si vous bougez pendant une mesure. Retirer le brassard,

attendre 2 à 3 minutes et essayer à nouveau.

(Ne s’affiche pas si la possibilité d’une fibrillation auriculaire est

détectée pendant une mesure en mode fibrillation auriculaire.)

Wird angezeigt, wenn Sie sich während der Messung bewegen.

Nehmen Sie die Manschette ab, warten Sie 2–3Minuten und

versuchen Sie es erneut.

(Wird nicht angezeigt, wenn bei einer Messung im Afib-Modus

mögliches Vorhofflimmern erkannt wird)

Viene visualizzato se l’utilizzatore si muove durante la misurazione.

Rimuovere il bracciale, attendere 2-3minuti e riprovare.

(Il simbolo non appare quando viene rilevata una potenziale presenza

di fibrillazione atriale durante una misurazione in modalità Afib)

Aparece cuando se mueve el cuerpo durante una medición. Retire

el manguito, espere unos 2 o 3minutos e inténtelo de nuevo.

(No aparece cuando se detecta una posible fibrilación auricular

durante una medición en modo fibrilación auricular)

Verschijnt wanneer uw lichaam tijdens een meting beweegt.

Verwijder de armmanchet, wacht 2-3 minuten en probeer het

opnieuw.

(Het verschijnt niet wanneer de mogelijkheid op Afib is gedetecteerd

tijdens de Afib-modusmeting)

      .

 ,  2-3    .

( ,       

 )

Bir ölçüm esnasında vücudunuz hareket ettiğinde görünür.

Kolluğu çıkarın, 2-3 dakika bekleyip tekrar deneyin.

(Afib modundaki bir ölçümde Afib olasılığı tespit edildiğinde

görünmez)

Appears when an irregular rhythm* is detected

during a measurement. If it continues to appear, it

is recommended to consult your physician.

(It does not appear during a Afib mode measurement)

S’affiche lorsqu’un rythme irrégulier* est détecté pendant une

mesure. S’il continue d’apparaître, il est recommandé de consulter

votre médecin.

(Ne s’affiche pas pendant une mesure en mode fibrillation auriculaire)

Wird angezeigt, wenn während einer Messung ein

unregelmäßiger Herzschlag* erkannt wird. Wird das Symbol

weiterhin angezeigt, sollten Sie sich an Ihren Arzt wenden.

(Wird bei einer Messung im Afib-Modus nicht angezeigt)

Viene visualizzato se nel corso di una misurazione viene rilevato

un ritmo cardiaco irregolare*. Se il simbolo continua ad apparire

è consigliabile rivolgersi al proprio medico curante.

(Il simbolo non viene visualizzato durante le misurazioni in modalità Afib)

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

esto sigue apareciendo, le recomendamos que consulte a su médico.

(No aparece durante una medición en modo fibrilación auricular)

Verschijnt wanneer tijdens een meting een onregelmatig ritme*

wordt gedetecteerd. Neem contact op met uw arts als dit blijft

verschijnen.

(Het verschijnt niet tijdens een Afib-modusmeting)

,     

*.     , 

   .

(      )

Bir ölçüm esnasında düzensiz ritim* saptandığında görünür.

Görünmeye devam ederse doktorunuza danışmanız önerilir.

(Afib modundaki ölçüm esnasında görünmez)

















* Afib and an irregular heartbeat rhythm are defined as a rhythm that is 25% less or 25% more than the

average rhythm detected while your monitor is measuring blood pressure. The difference between the Afib

indicator function and irregular heartbeat function is:

Afib indicator function: detects Afib possibility in 3-times measurement.

Irregular heartbeat function: detects irregular heartbeat including Afib in 1 measurement.

* La fibrillation auriculaire et les pulsations cardiaques irrégulières sont des pulsations dont la fréquence est supérieure ou inférieure de 25% par

rapport à la moyenne détectée lorsque l’appareil mesure la pression artérielle. La différence entre la fonction indicateur de fibrillation auriculaire

et la fonction pulsations cardiaques irrégulières est la suivante:

Fonction indicateur de fibrillation auriculaire: détecte la possibilité d’une fibrillation auriculaire par une mesure répétée 3fois.

Fonction pulsations cardiaques irrégulières: détecte des pulsations cardiaques irrégulières, y compris une fibrillation auriculaire, en 1mesure.

* Vorhofflimmern (Afib) und unregelmäßiger Herzschlag sind definiert als ein Herzrhythmus, der 25% unter oder 25% über dem mittleren

Herzrhythmus liegt, der während der Blutdruckmessung erkannt wird. Der Unterschied zwischen Afib-Hinweisfunktion und Erkennung

unregelmäßiger Herzschläge ist:

Afib-Hinweisfunktion: Erkennt bei 3-maliger Messung möglicherweise vorliegendes Vorhofflimmern.

Erkennung unregelmäßiger Herzschläge: Erkennt unregelmäßigen Herzschlag einschließlich Vorhofflimmern bei 1-maliger Messung.

* Per Afib e battito cardiaco irregolare si intende la presenza di variazioni inferiori del 25% o superiori del 25% nel ritmo rispetto al ritmo medio

rilevato dall’apparecchio durante la misurazione della pressione arteriosa. La differenza tra la funzione dell’indicatore Afib e la funzione battito

cardiaco irregolare è la seguente:

la funzione dell’indicatore Afib rileva la potenziale presenza di fibrillazione atriale mediante 3 misurazioni ripetute.

La funzione battito cardiaco irregolare rileva il battito irregolare inclusa la fibrillazione atriale in 1 misurazione.

* La fibrilación auricular y un ritmo de latido cardíaco irregular se definen como aquel ritmo que es el 25% inferior o el 25% superior al ritmo

cardíaco medio detectado mientras el monitor mide la presión arterial. La diferencia entre la función de indicador de fibrilación auricular y la

función de latido cardíaco arrítmico es:

Función de indicador de fibrilación auricular: detecta una posible fibrilación auricular en 3 mediciones.

Función de latido cardíaco irregular: detecta un latido irregular incluyendo fibrilación auricular en 1 medición.

* Afib en onregelmatige hartslag zijn gedefinieerd als een hartritme dat meer dan 25% lager of 25% hoger is dan het gemiddelde hartritme

tijdens het meten van de bloeddruk door de meter. Het verschil tussen de Afib-indicatorfunctie en onregelmatige hartslagfunctie is: Afib-

indicatorfunctie: detecteert de mogelijkheid op Afib in een driemalige meting.

Onregelmatige hartslagfunctie: detecteert onregelmatige hartslag inclusief Afib in één meting.

*      —  ,   25%    25%   , 

    .         :

  :      .

  :    ,  ,   .

* Afib ve düzensiz kalp atışı ritmi, ölçüm cihazınız tansiyon ölçümü yaparken saptanan ortalama ritme göre %25’ten az ya da %25'ten fazla sapma

gösteren ritim olarak tanımlanır. Afib göstergesi fonksiyonu ve düzensiz kalp atışı fonksiyonu arasındaki fark şu şekildedir:

Afib göstergesi fonksiyonu: 3 kez yapılan ölçümde Afib olasılığını tespit eder.

Düzensiz kalp atışı fonksiyonu: 1 ölçümde, Afib de dahil olmak üzere düzensiz kalp atışını tespit eder.









Error messages or other problems? Refer to:

Instruction Manual

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:

    

? .

Hata mesajları veya başka sorunlar mı var? Bkz:

** 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.

**        2018 ESH/ESC.

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



ESH

.ESC(

Using Memory Functions

Utilisation des fonctions de mémoire

Geheugenfuncties gebruiken

Verwendung der Speicherfunktion

Использование функции памяти

Uso delle funzioni di memoria

Hafıza Fonksiyonunun Kullanılması

Uso de las funciones de memoria



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.

      .

Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.

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

   

Hafızada Saklanan Ölçüm Değerleri

Stores up to 100 readings.

Mémorise jusqu’à

100résultats.

Es werden bis zu

100Messwerte gespeichert.

Conserva fino a 100 risultati.

Almacena hasta 100lecturas.

Slaat tot maximaal

100metingen op.

 

100.

100 adede kadar ölçüm değeri

saklar.







Morning/Evening Weekly Averages

Moyennes hebdomadaires matin/soir

Wöchentliche Morgen-/Abendmittelwerte

Media settimanale mattutina e serale

Valor promedio semanal de mañana y noche

Weekgemiddelden van ochtend- en avondwaarden

/    

Sabah/Akşam Haftalık Ortalamaları

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

"DIA" is 85mmHg or above in the morning

weekly average.

wk ago

wks ago

S’affiche si «SYS» est égale ou supérieure à 135mmHg et/ou «DIA» égale ou supérieure à 85mmHg dans la moyenne hebdomadaire du matin.

Wird angezeigt, wenn im wöchentlichen Morgenmittelwert „SYS“ 135mmHg oder mehr und/oder „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

nellamedia mattutina settimanale.

Aparece si “SYS” es 135mmHg o superior y/o “DIA” es 85mmHg o superior en el promedio semanal de mañana.

Verschijnt als “SYS” 135 mmHg of hoger is en/of “DIA” 85 mmHg of hoger is in het ochtendweekgemiddelde.

,       «SYS» 135...   / «DIA» 85...  .

Sabah haftalık ortalamasında "SYS" 135 mmHg ya da üstünde olduğunda ve/veya "DIA" 85 mmHg** ya da üstünde olduğunda görünür.

To know how to calculate weekly averages, refer to section10 of the Instruction Manual .

Pour savoir comment calculer les moyennes hebdomadaires, se reporter à la section10 du Mode d’emploi .

Wie die wöchentlichen Mittelwerte berechnet werden, ist in Abschnitt10 der Gebrauchsanweisung beschrieben.

Per sapere come calcolare le medie settimanali, consultare la sezione10 del manuale di istruzioni .

Para saber cómo calcular mediciones semanales, consulte la sección10 del manual de instrucciones .

Zie paragraaf 10 van de gebruiksaanwijzing voor aanwijzingen hoe u het wekelijkse gemiddelde kunt berekenen.

 ,      , . 10     .

Haftalık ortalamaların nasıl hesaplanacağını öğrenmek için, Kullanım Kılavuzu 'de bölüm 10'a bakın.











DIA







SYS



12.3 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

   2-  3- ,   

10

10 Dakika Aralıkta Alınan Son 2 veya 3 Ölçüm Değerinin Ortalaması

3 sec+

12.4 Deleting All Readings for 1 User

Suppression de toutes les mesures pour 1utilisateur

Löschen aller Messwerte für Benutzer 1

Eliminazione di tutti i risultati relativi a 1 utente

Eliminación de todas las lecturas de un usuario

Alle meetresultaten voor 1 gebruiker wissen

    

1 Kullanıcı için Tüm Ölçüm Değerlerini Silme

4sec+ 4sec+

1 2 3 4 5





Other Settings

Autres réglages

Andere instellingen

Weitere Einstellungen

Другие настройки

Altre impostazioni

Diğer Ayarlar

Otros ajustes



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

/ Bluetooth

Bluetooth'u Devre Dışı Bırakma/Etkinleştirme

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   .

Bluetooth varsayılan olarak etkindir.

Bluetooth

Bluetooth

13.2 Restoring to the Default Settings

Réinitialisation aux réglages par défaut

Wiederherstellen der Standardeinstellungen

Ripristino delle impostazioni predefinite

Restablecimiento a los ajustes de fábrica

De standaardinstellingen herstellen

   

Varsayılan Ayarları Geri Yükleme

4 sec+



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 commence à se gonfler, appuyer sur le bouton [START/STOP] et le maintenir enfoncé jusqu’à ce que le tensiomètre atteigne une pression

de gonflage supérieure de 30 à 40mmHg à votre pression systolique attendue.

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.

 ,      ,     [START/STOP]   ,

     ,      30-40...

Sistolik basıncınız 210 mmHg'den fazlaysa:

Manşet şişmeye başladıktan sonra, [START/STOP] düğmesine basın ve ölçüm cihazı beklediğiniz sistolik basınç değerinden 30 ila 40 mmHg daha fazla şişene

kadar basılı utun.













Optional Medical Accessories

Accessoires médicaux en option

Optionele medische accessoires

Medizinisches optionales Zubehör

Дополнительно принадлежности

Accessori medicali opzionali

Opsiyonel Tıbbi Aksesuarlar

Accesorios médicos opcionales



(HHP-CM01)

(HHP-BFH01)

AC Adapter

Arm Cu

(HEM-FL31)

22 - 42 cm

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 Luftschlauchstecker 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.

   .      .

Hava tıpasını atmayın. Hava tıpası isteğe bağlı kolluğa uygulanabilir.



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

Other Optional Parts

Autres pièces en option

Overige optionele onderdelen

Weitere optionale Teile

Другие дополнительно приобретаемые запасные части

Altri componenti opzionali

Diğer Aksesuarlar

Otras piezas opcionales



Protective LCD Cover

(HEM-CACO-734)

Manufacturer

Fabricant

Hersteller

Produttore

Fabricante

Fabrikant



Üretici







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

  

AB temsilcisi



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



Production facility

Site de production

Produktionsstätte

Stabilimento di produzione

Planta de producción

Productiefaciliteit





Üretim Tesisi



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



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

Made in Vietnam / Fabriqué en Vietnam / Hergestellt in Vietnam/ Prodottoin Vietnam / Fabricado en Vietnam / Geproduceerd in Vietnam/    /

Vietnam'da Üretilmiştir /



Issue Date / Date de publication / Ausgabedatum / Datadipubblicazione / Fecha de publicación / Uitgiftedatum /  / Teslim Tarihi /



: 2019-09-05

IM2-HEM-7361T-E-02-09/2019

2895865-4B