Omron M4 Intelli IT - HEM-7155T-EBK El manual del propietario

Categoría
Unidades de presión arterial
Tipo
El manual del propietario

Este manual también es adecuado para

Automatic Upper Arm Blood Pressure Monitor
M4 Intelli IT (HEM-7155T-EBK)
X4 Smart (HEM-7155T-ESL)
Instruction Manual
Symboles/ Symbole/ Simboli/ Símbolos/
Symbolen/ Символы/ Semboller/
ίϣέϟ΍
Read Instruction manual and before use.
FR
Lire le mode d’emploi et avant l’utilisation.
DE
Lesen Sie vor der Verwendung die Gebrauchsanweisung und .
IT
Leggere il manuale di istruzioni e prima dell’uso.
ES
Lea el manual de instrucciones y antes del uso.
NL
Lees de gebruiksaanwijzing en voor gebruik.
RU
Прочтите руководство по эксплуатации и перед использованием.
TR
Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.
ϡ΍ΩΧΗγϻ΍ϝΑϗ
ϭ Ε΍ΩΎηέϹ΍ϝϳϟΩ΃έϗ΍
AR
EN1
EN
1. Introduction
Thank you for purchasing the OMRON Automatic Upper Arm Blood
Pressure Monitor. This blood pressure monitor uses the oscillometric
method of blood pressure measurement. This means this monitor
detects your blood movement through your brachial artery and
converts the movements into a digital reading.
1.1 Safety Instructions
This instruction manual provides you with important information
about the OMRON Automatic Upper Arm Blood Pressure Monitor.
To ensure the safe and proper use of this monitor, READ and
UNDERSTAND all of the safety and operating instructions. If you do
not understand these instructions or have any questions, contact
your OMRON retail outlet or distributor before attempting to
use this monitor. For specific information about your own blood
pressure, consult with your physician.
1.2 Intended Use
This device is a digital monitor intended for use in measuring blood
pressure and pulse rate in adult patient population. The device detects
the appearance of irregular heartbeats during measurement and
gives a warning signal with readings. It is mainly designed for general
household use.
1.3 Receiving and Inspection
Remove this monitor from the packaging and inspect for damage. If
this monitor is damaged, DO NOT USE and consult with your OMRON
retail outlet or distributor.
2. Important Safety Information
Read the Important Safety Information in this instruction manual
before using this monitor. Follow this instruction manual thoroughly
for your safety.
Keep for future reference. For specific information about your own
blood pressure, CONSULT WITH YOUR PHYSICIAN.
2.1 Warning
Indicates a potentially hazardous
situation which, if not avoided, could
result in death or serious injury.
DO NOT use this monitor on infants, toddlers, children or persons
who cannot express themselves.
DO NOT adjust medication based on readings from this blood
pressure monitor. Take medication as prescribed by your physician.
ONLY a physician is qualified to diagnose and treat high blood
pressure.
DO NOT use this monitor on an injured arm or an arm under medical
treatment.
DO NO
T apply the arm cuff on your arm while on an intravenous
drip or blood transfusion.
DO NOT use this monitor in areas containing high frequency (HF)
surgical equipment, magnetic resonance imaging (MRI) equipment,
computerized tomography (CT) scanners. This may result in incorrect
operation of the monitor and/or cause an inaccurate reading.
DO NOT use this monitor in oxygen rich environments or near
flammable gas.
C
onsult with your physician before using this monitor if you have
common arrhythmias such as atrial or ventricular premature beats
or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes;
pregnancy; pre-eclampsia or renal disease. NOTE that any of these
conditions in addition to patient motion, trembling, or shivering
may affect the measurement reading.
NE
VER diagnose or treat yourself based on your readings. ALWAYS
consult with your physician.
To help avoid strangulation, keep the air tube and AC adapter cable
away from infants, toddlers and children.
This product contains small parts that may cause a choking hazard if
swallowed by infants, toddlers and children.
Data Transmission
This product emits radio frequencies (RF) in the 2.4GHz band.
DO NOT use this product in locations where RF is restricted, such as
on an aircraft or in hospitals. Turn off the Bluetooth® feature in this
monitor, remove batteries and/or unplug the AC adapter when in
RFrestricted areas.
EN2
EN
AC Adapter (optional accessory) Handling and Usage
DO NOT use the AC adapter if this monitor or the AC adapter cable is
damaged. If this monitor or the cable is damaged, turn off the power
and unplug the AC adapter immediately.
Plug the AC adapter into the appropriate voltage outlet. DO NOT
use in a multi-outlet plug.
NEVER plug in or unplug the AC adapter from the electric outlet
with wet hands.
DO NOT disassemble or attempt to repair the AC adapter.
Battery Handling and Usage
Keep batteries out of the reach of infants, toddlers and children.
2.2 Caution
Indicates a potentially hazardous
situation which, if not avoided,may
result in minor or moderate injury to
the user or patient or damage to the
equipment or other property.
Stop using this monitor and consult with your physician if you
experience skin irritation or discomfort.
Consult with your physician before using this monitor on an arm
where intravascular access or therapy, or an arteriovenous (A-V)
shunt, is present because of temporary interference to blood flow
and could result in injury.
Consult with your physician before using this monitor if you have
had a mastectomy.
Consult with your physician before using this monitor if you have
severe blood flow problems or blood disorders as cuff inflation can
cause bruising.
DO NOT take measurements more often than necessary because
bruising, due to blood flow interference, may occur.
ONLY inflate the arm cuff when it is applied on your upper arm.
Remove the arm cuff if it does not start deflating during a
measurement.
DO NOT use this monitor for any purpose other than measuring
blood pressure.
During measurement, make sure that no mobile device or any other
electrical device that emit electromagnetic fields is within 30 cm of
this monitor. This may result in incorrect operation of the monitor
and/or cause an inaccurate reading.
DO NOT disassemble or attempt to repair this monitor or other
components. This may cause an inaccurate reading.
DO NOT use in a location where there is moisture or a risk of water
splashing this monitor. This may damage this monitor.
DO NOT use this monitor in a moving vehicle such as in a car or on
an aircraft.
DO NOT drop or subject this monitor to strong shocks or vibrations.
DO NOT use this monitor in places with high or low humidity or high
or low temperatures. Refer to section 6.
During measurement, observe the arm to ensure that the monitor is
not causing prolonged impairment to blood circulation.
DO NOT use this monitor in high-use environments such as medical
clinics or physician offices.
DO NOT use this monitor with other medical electrical (ME)
equipment simultaneously. This may result in incorrect operation of
the monitor and/or cause an inaccurate reading.
Avoid bathing, drinking alcohol or caffeine, smoking, exercising and
eating for at least 30 minutes before taking a measurement.
Rest for at least 5 minutes before taking a measurement.
Remove tight-fitting or thick clothing from your arm while taking a
measurement.
Remain still and DO NOT talk while taking a measurement.
ONLY use the arm cuff on persons whose arm circumference is
within the specified range of the cuff.
Ensure that this monitor has acclimated to room temperature before
taking a measurement. Taking a measurement after an extreme
temperature change could lead to an inaccurate reading. OMRON
recommends waiting for approximately 2 hours for the monitor to
warm up or cool down when the monitor is used in an environment
within the temperature specified as operating conditions after
it is stored either at the maximum or at the minimum storage
temperature. For additional information on operating and storage/
transport temperature, refer to section 6.
DO NOT use this monitor after the durable period has ended. Refer
to section 6.
DO NOT crease the arm cuff or the air tube excessively.
DO NOT fold or kink the air tube while taking a measurement. This
may cause an injury by interrupting blood flow.
To unplug the air plug, pull on the plastic air plug at the base of the
tube, not the tube itself.
EN3
ONLY use the AC adapter, arm cuff, batteries and accessories
specified for this monitor. Use of unsupported AC adapters, arm
cuffs and batteries may damage and/or may be hazardous to this
monitor.
ONLY use the approved arm cuff for this monitor. Use of other arm
cuffs may result in incorrect readings.
Inflating to a higher pressure than necessary may result in bruising
of the arm where the cuff is applied. NOTE: refer to “If your systolic
pressure is more than 210mmHg in section 13 of instruction
manual
for additional information.
Read and follow the “Correct Disposal of This Product” in section 7
when disposing of the device and any used accessories or optional
parts.
Data Transmission
DO NOT replace batteries or unplug the AC adapter while your
readings are being transferred to your smart device. This may result
in incorrect operation of this monitor and failure to transfer your
blood pressure data.
AC Adapter (optional accessory) Handling and Usage
Fully insert the AC adapter into the outlet.
When unplugging the AC adapter from the outlet, be sure to safely
pull from the AC adapter. DO NOT pull from the AC adapter cable.
When handling the AC adapter cable:
Do not damage it. / Do not break it. / Do not tamper with it.
DO NOT pinch it. / Do not forcibly bend or pull it. / Do not twist it.
DO NOT use it if it is gathered in a bundle.
DO NOT place it under heavy objects.
Wipe any dust off of the AC adapter.
Unplug the AC adapter when not in use.
Unplug the AC adapter before cleaning this monitor.
Battery Handling and Usage
DO NOT insert batteries with their polarities incorrectly aligned.
ONLY use 4 “AA alkaline or manganese batteries with this monitor.
DO NOT use other types of batteries. DO NOT use new and used
batteries together. DO NOT use different brands of batteries
together.
Remove batteries if this monitor will not be used for a long period of
time.
If battery fluid should get in your eyes, immediately rinse with
plenty of clean water. Consult with your physician immediately.
If battery fluid should get on your skin, wash your skin immediately
with plenty of clean, lukewarm water. If irritation, injury or pain
persists, consult with your physician.
DO NOT use batteries after their expiration date.
Periodically check batteries to ensure they are in good working
condition.
2.3 General Precautions
When you take a measurement on the right arm, the air tube should
be at the side of your elbow. Be careful not to rest your arm on the
air tube.
Blood pressure may differ between the right and left arm, and
may result in a different measurement value. Always use the same
arm for measurements. If the values between both arms differ
substantially, check with your physician on which arm to use for
your measurements.
Remember to have a record of your blood pressure and pulse
readings for your physician. A single measurement does not provide
an accurate indication of your true blood pressure.
Please use the Blood Pressure Diary to keep records of several
readings over a certain period of time. To download PDF files of the
diary, visit www.omron-healthcare.com.
EN4
EN
3. Error Messages and Troubleshooting
If any of the below problems occur during measurement, check to make sure that no other electrical device is within 30 cm. If the problem persists,
please refer to the table below.
Display/Problem Possible Cause Solution
appears or the arm
cuff does not inflate.
The [START/STOP] button was pressed
while the arm cuff is not applied.
Press the [START/STOP] button again to turn the monitor off.
After inserting the air plug securely and applying the arm cuff
correctly, press the [START/STOP] button.
Air plug is not completely plugged into
the monitor.
Insert the air plug securely.
The arm cuff is not applied correctly. Apply the arm cuff correctly, then take another measurement.
Refer to section 7 of instruction manual
.
Air is leaking from the arm cuff. Replace the arm cuff to the new one. Refer to section 14 of
instruction manual
.
appears or a
measurement
cannot be
completed after the
arm cuff inflates.
You move or talk during a measurement
and the arm cuff does not inflate
sufficiently.
Remain still and do not talk during a measurement. If “E2”
appears repeatedly, inflate the arm cuff manually until the
systolic pressure is 30 to 40 mmHg above your previous
readings. Refer to section 13 of instruction manual
.
Due to the systolic pressure is above
210mmHg, a measurement cannot be
taken.
appears
The arm cuff is inflated exceeding the
maximum allowable pressure.
Do not touch the arm cuff and/or bend the air tube while taking
a measurement. If inflating the arm cuff manually, refer to
section 13 of instruction manual
.
appears
You move or talk during a measurement.
Vibrations disrupt a measurement.
Remain still and do not talk during a measurement.
appears
The pulse rate is not detected correctly. Apply the arm cuff correctly, then take another measurement.
Refer to section 7 of instruction manual . Remain still and sit
correctly during a measurement.
If the
symbol continues to appear, we recommend you to
consult with your physician.
/ /
appears
does not flash during
a measurement.
EN5
Display/Problem Possible Cause Solution
appears
The monitor has malfunctioned. Press the [START/STOP] button again. If “Er still appears, contact
your OMRON retail outlet or distributor.
appears
The monior cannot connect to a smart
device or transmit data correctly.
Follow the instructions shown in the “OMRON connect” app.
If the “Err symbol still appears after checking the app, contact
your OMRON retail outlet or distributor.
flashes
The monitor is waiting for pairing with
the smart device.
Refer to section 5 of instruction manual
for pairing your
monitor with your smart device, or press [START/STOP] button
to cancel pairing and turn your monitor off.
flashes
The monitor is ready to transfer your
readings to the smart device.
Open the “OMRON connect” app to transfer your readings.
flashes
More than 48 readings are not
transferred.
Pair or transfer your readings to the “OMRON connect app so
you can keep them in memory in the app, and this error symbol
disappears.
The date and time is not set.
appears
There are 60 readings in memory to be
transferred
flashes
Batteries are low. Replacing all 4 batteries with new ones is recommended. Refer
to section 4 of instruction manual
.
appears or the
monitor is turned
off unexpectedly
during a
measurement
Batteries are depleted. Immediately replace all 4 batteries with new ones. Refer to
section 4 of instruction manual
.
Nothing appears on the
display of the monitor.
Battery polarities are not properly
aligned.
Check the battery installation for proper placement. Refer to
section 4 of instruction manual
.
Readings appear too high or
too low.
Blood pressure varies constantly. Many factors including stress, time of day, and/or how you apply the arm
cuff, may affect your blood pressure. Review section 2 of instruction manual
.
EN6
EN
Display/Problem Possible Cause Solution
Any other communication
issue occurs.
Follow the instructions shown in the smart device, or visit the “Help” section in the “OMRON
connect" app for further help. If the problem still persists, contact your OMRON retail outlet or
distributor.
Any other problem occurs.
Press the [START/STOP] button to turn the monitor off, then press it again to take a measurement.
If the problem continues, remove all batteries and wait for 30 seconds. Then re-install batteries.
If the problem still persists, contact your OMRON retail outlet or distributor.
4. Limited Warranty
Thank you for buying an OMRON product. This product is constructed of high quality materials and great care has been taken in its manufacturing.
It is designed to give you every satisfaction, provided that it is properly operated and maintained as described in the instruction manual.
This product is warranted by OMRON for a period of 3 years after the date of purchase. The proper construction, workmanship and materials of
this product is warranted by OMRON. During this period of warranty OMRON will, without charge for labour or parts, repair or replace the defect
product or any defective parts.
The warranty does not cover any of the following:
A. Transport costs and risks of transport.
B. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.
C. Periodic check-ups and maintenance.
D. Failure or wear of optional parts or other attachments other than the main device itself, unless explicitly warranted above.
E. Costs arising due to non-acceptance of a claim (those will be charged for).
F. Damages of any kind including personal caused accidentally or from misuse.
G. Calibration service is not included within the warranty.
H. Optional parts have a one (1) year warranty from date of purchase. Optional parts include, but are not limited to the following items: cuff and
cuff tube.
Should warranty service be required please apply to the dealer whom the product was purchased from or an authorised OMRON distributor. For
the address refer to the product packaging / literature or to your specialised retailer. If you have difficulties in finding OMRON customer services,
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.
EN7
5. Maintenance
5.1 Maintenance
To protect your monitor from damage, follow the directions below:
Changes or modifications not approved by the manufacturer will void the user warranty.
DO NOT disassemble or attempt to repair this monitor or other components. This may cause an inaccurate reading.
5.2 Storage
Keep your monitor in the storage case when not in use.
1. Remove the arm cuff from the monitor.
Caution
To unplug the air plug, pull on the plastic air plug at the base of the tube, not the tube itself.
2. Gently fold the air tube into the arm cuff. Note: Do not bend or crease the air tube excessively.
3. Place your monitor and other components in the storage case.
Store your monitor and other components in a clean, safe location.
Do not store your monitor and other components:
If your monitor and other components are wet.
In locations exposed to extreme temperatures, humidity, direct sunlight, dust or corrosive vapors such as bleach.
In locations exposed to vibrations or shocks.
5.3 Cleaning
Do not use any abrasive or volatile cleaners.
Use a soft dry cloth or a soft cloth moistened with mild (neutral) detergent to clean your monitor and arm cuff, and then wipe them with a dry
cloth.
Do not wash or immerse your monitor and arm cuff or other components in water.
Do not use gasoline, thinners or similar solvents to clean your monitor and arm cuff or other components.
5.4 Calibration and Service
The accuracy of this blood pressure monitor has been carefully tested and is designed for a long service life.
It is generally recommended to have the unit inspected every two years to ensure correct functioning and accuracy. Please consult your
authorised OMRON dealer or the OMRON Customer Service at the address given on the packaging or attached literature.
Caution
EN8
EN
6. Specifications
Product description Automatic Upper Arm Blood Pressure Monitor
Product category Electronic Sphygmomanometers
Model (code) M4 Intelli IT (HEM-7155T-EBK)
X4 Smart (HEM-7155T-ESL)
Display LCD digital display
Cuff pressure range 0 to 299mmHg
Pulse measurement range
40 to 180 beats / min.
Blood pressure measurement range
SYS: 60 to 260mmHg / DIA: 40 to 215mmHg
Accuracy Pressure: ±3mmHg / Pulse: ±5% of display reading
Inflation Automatic by electric pump Deflation
Automatic pressure release valve
Measurement method Oscillometric method Transmission method Bluetooth
®
Low Energy
Wireless communication Frequency range: 2.4GHz (2400 - 2483.5MHz) / Modulation: GFSK
Effective radiated power: <20dBm
Operating mode Continuous operation
IP classification Monitor: IP20 / Optional AC adapter: IP21
Rating DC6 V 4.0W Applied part Type BF (arm cuff)
Power source
4 AA” batteries 1.5V or optional AC adapter (INPUT AC 100 - 240V 50 - 60Hz 0.12 - 0.065A)
Battery life Approximately 1000 measurements (using new alkaline batteries)
Durable period (Service life) Monitor: 5 years / Cuff: 5 years / Optional AC adapter: 5 years
Operating conditions +10 to +40°C / 15 to 90% RH (non-condensing) / 800 to 1060hPa
Storage / Transport conditions -20 to +60°C / 10 to 90% RH (non-condensing)
Contents Monitor, arm cuff (HEM-FL31), 4 “AA batteries, storage case, Instruction Manual
and
, setup instructions
Protection against electric shock Internally powered ME equipment (when using only batteries)
Class II ME equipment (optional AC adapter)
Weight Monitor: approximately 340g (not including batteries) / Arm cuff: approximately 163g
Dimensions (approximately value) Monitor: 105mm (W) × 85mm (H) × 152mm (L)
Arm cuff: 145mm × 532mm (air tube: 750mm)
Memory Stores up to 60 readings per user
EN9
Note
These specifications are subject to change without notice.
This monitor is clinically investigated according to the requirements of ISO 81060-2:2013. In the clinical validation study, K5 was used on
85subjects for determination of diastolic blood pressure.
This device has been validated for use on pregnant and pre-eclampsia patients according to the Modified European Society of Hypertension
Protocol*.
This device has been validated for use on diabetic (Type II) population**.
IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This monitor and optional AC adapter are
protected against solid foreign objects of 12.5 mm diameter and greater such as a finger. The optional AC adapter is protected against vertically
falling water drops which may cause issues during a normal operation.
* Topouchian J et al. Vascular Health and Risk Management 2018:14 189–197
** Chahine M.N. et al. Medical Devices: Evidence and Research 2018:11 11–20
About a wireless communication interference
This product operates in an unlicensed ISM band at 2.4 GHz. In the event this product is used near other wireless devices such as microwave and
wireless LAN, which operate on the same frequency band as this product, there is a possibility that interference may occur. If interference occurs,
stop the operation of the other devices or relocate this product away from other wireless devices before attempting to use it.
7. Correct Disposal of This Product (Waste Electrical & Electronic Equipment)
This marking shown on the product or its literature, indicates that it should not be disposed of, with other household wastes at the
end of its working life.
To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate this product from
other types of wastes and recycle it responsibly to promote the sustainable reuse of material resources.
Household users should contact either the retailer where they purchased this product, or their local government office, for details of
where and how they can return this item for environmentally safe recycling.
Business users should contact their supplier and check the terms and conditions of the purchase contract. This product should not be mixed with
other commercial waste for disposal.
8. Important Information Regarding Electromagnetic Compatibility (EMC)
HEM-7155T-EBK and HEM-7155T-ESL conform to EN60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at
www.omron-healthcare.com
Refer to the EMC information for HEM-7155T-EBK and HEM-7155T-ESL on the website.
EN10
EN
9. Guidance and Manufacturer’s Declaration
This blood pressure monitor is designed according to the European Standard EN1060, Non-invasive sphygmomanometers Part 1: General
Requirements and Part 3: Supplementary requirements for electromechanical blood pressure measuring systems.
Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipments type HEM-7155T-EBK and HEM-7155T-ESL are complied with Directive
2014/53/EU. The full text of the EU declaration of conformity is available at the following internet address: www.omron-healthcare.com
This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan. The Core component for OMRON
blood pressure monitors, which is the Pressure Sensor, is produced in Japan.
Please report to the manufacturer and the competent authority of the Member State in which you are established about any serious incident
that has occurred in relation to this device.
SD1
Symbols Description
FR
Description des symboles
NL
Beschrijving van symbolen
DE
Beschreibung der Symbole
RU
Описание символов
IT
Descrizione dei simboli
TR
Simgelerin Açıklaması
ES
Descripción de los símbolos
ίϭϣέϟ΍Ρέη
AR
Applied part - TypeBF Degree of protection
against electric shock (leakage current)
FR
Pièce appliquée -
TypeBF Degré de protection
contre les chocs électriques
(courant de fuite)
DE
Anwendungsteil–
TypBF Schutz vor Strom-
schlägen (Ableitstrom)
IT
Parti applicate - TipoBF
Livello di protezione contro
le folgorazioni (corrente di
dispersione)
ES
Partes en contacto:
TipoBF Grado de protección
contra descargas eléctricas
(corriente de fuga)
NL
Toegepast onderdeel -
TypeBF-beschermingsgraad
tegen elektrische schokken
(lekstroom)
RU
Рабочая часть аппарата
- Степень защиты от
поражения электрическим
током (токи утечки) ТипBF
TR
Uygulanan parça - TipBF
Elektrik çarpmasına karşı
koruma derecesi (kaçak akım)
ΔϳΎϣΣϟ΍ΔΟέΩϖΑρϣϟ΍˯ίΟϟ΍
AR
έΎϳΗϟ΍Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍Ωο
BFωϭϧϠϟΏέγΗϣϟ΍
Class II equipment.
Protection against electric shock
FR
Équipement de classe II.
Protection contre les chocs
électriques
DE
Gerät der Klasse II.
Schutz vor Stromschlägen
IT
Apparecchiatura di
Classe II. Protezione contro le
folgorazioni
ES
Equipo de Clase II.
Protección contra descargas
eléctricas
NL
Apparatuur van
KlasseII. Bescherming tegen
elektrische schokken
RU
Изделие класса II
Защита от поражения
электрическим током
TR
Sınıf II ünite. Elektrik
çarpmasına karşı koruma
ΩοΔϳΎϣΣϟ΍IIΔ΋ϔϟ΍ϥϣίΎϬΟ
AR
Δϳ΋ΎΑέϬϛϟ΍ΕΎϣΩλϟ΍
IP XX
Ingress protection degree provided by
IEC60529
FR
Degré de protection
selon CEI60529
DE
Grad des Eindring-
schutzes gemäß IEC60529
IT
Livello di protezione IP
in base a IEC60529
ES
Grado de protección
según la norma internacional
IEC60529
NL
Beschermingsklasse
volgens IEC60529
RU
Степень защиты,
обеспечиваемая
оболочками, согласно
IEC60529
TR
Su girmesine karşı
koruma derecesi IEC60529
tarafından verilmiştir
ΔϣΩϘϣϟ΍ϝϭΧΩϟ΍ΔϳΎϣΣΔΟέΩ
AR
,(&έΎϳόϣΔργ΍ϭΑ
CE Marking
FR
Marquage CE
DE
CE-Kennzeichnung
IT
Contrassegno CE
ES
Marcado CE
NL
CE-merkteken
RU
Знак соответствия
директиве ЕС
TR
CE İşareti
ΔϧΟϠϟ΍ϊϣϖϓ΍ϭΗϟ΍Δϣϼϋ
AR
&(ΔϳΑϭέϭϷ΍
SD2
Serial number
FR
Numéro de série
DE
Seriennummer
IT
Numero di serie
ES
Número de serie
NL
Serienummer
RU
Серийный номер
TR
Seri numarası
ϝγϠγΗϣϟ΍ϡϗέϟ΍
AR
LOT number
FR
Numéro de LOT
DE
LOT-Nummer
IT
Numero di lotto
ES
Número de lote
NL
Partijnummer
RU
Код (номер) партии
TR
Parti numarası
ΔϠϳϐηΗϟ΍ϡϗέ
AR
Medical device
FR
Dispositif médical
DE
Medizinprodukt
IT
Dispositivo medico
ES
Producto sanitario
NL
Medisch apparaat
RU
Медицинский прибор
TR
Tıbbi cihaz
ϲΑρίΎϬΟ
AR
Temperature limitation
FR
Limitation de température
DE
Temperaturbegrenzung
IT
Limite di temperatura
ES
Limitación de la
temperatura
NL
Temperatuurbegrenzing
RU
Температурный
диапазон
TR
Sıcaklık sınırlaması
ΔΑγΎϧϣϟ΍Γέ΍έΣϟ΍ΔΟέΩΩϭΩΣ
AR
Humidity limitation
FR
Limitation d’humidité
DE
Luftfeuchtigkeits-
begrenzung
IT
Limite di umidità
ES
Limitación de la humedad
NL
Vochtigheidsbegrenzing
RU
Диапазон влажности
TR
Nem sınırlaması
ΔΑγΎϧϣϟ΍ΔΑϭρέϟ΍ΩϭΩΣ
AR
Atmospheric pressure limitation
FR
Limitation de pression
atmosphérique
DE
Luftdruckbegrenzung
IT
Limite di pressione
atmosferica
ES
Limitación de la presión
atmosférica
NL
Luchtdrukbegrenzing
RU
Ограничение
атмосферного давления
TR
Atmosferik basınç
sınırlaması
ΏγΎϧϣϟ΍ϱϭΟϟ΍ρϐοϟ΍ΩϭΩΣ
AR
Indication of connector polarity
FR
Indication de la polarité
des connecteurs
DE
Anzeige der
Steckerpolarität
IT
Indicazione della
polarità dei connettori
ES
Indicación de la
polaridad del conector
NL
Indicatie van polariteit
van aansluiting
RU
Полярность разъема
адаптера
TR
Bağlantı polarite
göstergesi
ϝλϭϣϟ΍ΔϳΑρϘϟέϳηΗΔϣϼϋ
AR
For indoor use only
FR
Pour un usage à
l’intérieur uniquement
DE
Nur für die Nutzung in
Innenbereichen
IT
Solo per uso in interni
ES
Para uso solo en interiores
NL
Alleen voor gebruik
binnenshuis
RU
Для использования
только внутри помещений
TR
Sadece iç mekanda
kullanım için
ϖρΎϧϣϟ΍ϲϓϡ΍ΩΧΗγϼϟ΢ϟΎλ
AR
ρϘϓΔϘϠϐϣϟ΍
SD3
OMRON’s trademarked technology for
blood pressure measurement
FR
Technologie protégée
par la marque de commerce
OMRON pour la mesure de
la pression artérielle
DE
Markenrechtlich
geschützte Technologie
von OMRON zur
Blutdruckmessung
IT
Tecnologia brevettata
OMRON per la misurazione
della pressione arteriosa
ES
La tecnología de OMRON
para medir la presión arterial
NL
Technologie voor
bloeddrukmeting onder
handelsmerk van OMRON
RU
Зарегистрированная
технология измерения
артериального давления
OMRON
TR
OMRON’un kan basıncı
ölçümü için ticari markalı
teknolojisidir
ΔϳέΎΟΗϟ΍Δϣϼόϟ΍ΔϳϧϘΗ
AR
ϡΩϟ΍ρϐοαΎϳϘϟOMRON
Identifier of cuffs compatible for the device
FR
Identificateur des
brassards compatibles avec
l’appareil
DE
Kennzeichnung der
mit dem Gerät kompatiblen
Manschetten
IT
Identifica i bracciali
compatibili con il dispositivo
ES
Identificador para
manguitos compatibles con
el dispositivo
NL
Identificatie van
manchetten die compatibel
zijn met het apparaat
RU
Манжеты совместимые
с устройством
TR
Cihaz ile uyumlu
kollukların tanıtım işareti
ρ΋΍έηϟ΍ΩϳΩΣΗΕΎϣϼϋ
AR
ίΎϬΟϟ΍ϊϣΔϘϓ΍ϭΗϣϟ΍ΔρϏΎοϟ΍
Marker on the cuff to be positioned above
the artery
FR
Repère sur le brassard,
à positionner au-dessus de
l’artère
DE
Markierung auf der
Manschette, die oberhalb
der Arterie liegen muss
IT
Contrassegno sul
bracciale da posizionare al di
sopra dell’arteria
ES
La marca del manguito
debe colocarse sobre la
arteria
NL
Markering op de manchet
die boven de slagader moet
worden geplaatst
RU
Указатель располо-
жения плечевой артерии
TR
Kolluk üzerindeki
işaretin konumu arterin
üzerine gelmelidir
ρϏΎοϟ΍ρϳέηϟΎΑΔϣϼϋ
AR
ϕϭϓϪόοϭΏϭΟϭϰϟ·ΓέΎηϺϟ
ϥΎϳέηϟ΍
,
Manufacturer’s quality control mark
FR
Marque de contrôle de
la qualité du fabricant
DE
Qualitätskontroll-
zeichen des Herstellers
IT
Contrassegno controllo
qualità del produttore
ES
Marca del control de
calidad del fabricante
NL
Symbool voor kwaliteits-
controle van fabrikant
RU
Отметка произво-
дителя о контроле качества
TR
Üreticinin kalite kontrol
işareti
ΓΩϭΟϟ΍ϲϓϡϛΣΗϟ΍Δϣϼϋ
AR
Δόϧλϣϟ΍ΔϛέηϟΎΑΔλΎΧϟ΍
Not made with natural rubber latex
FR
Ne contient pas de latex
de caoutchouc naturel
DE
Enthält kein Naturlatex
IT
Non contiene lattice di
gomma naturale
ES
No contiene látex de
caucho natural
NL
Bevat geen
natuurrubberlatex
RU
Не содержит
натуральный латекс
TR
Doğal kauçuk lateksten
üretilmemiştir
ϡ΍ΩΧΗγ΍ϥϭΩϊϳϧλΗϟ΍ϡΗ
AR
ϲόϳΑρϟ΍ρΎρϣϟ΍αϛϳΗϻ
SD4
Arm circumference
FR
Circonférence du bras
DE
Armumfang
IT
Circonferenza del braccio
ES
Perímetro de brazo
NL
Armomtrek
RU
Окружность плеча
TR
Kol çevresi
ω΍έΫϟ΍ρϳΣϣ
AR
Necessity for the user to consult this
instruction manual
FR
L’utilisateur doit consulter
le présent mode d’emploi
DE
Der Benutzer muss diese
Gebrauchsanweisung lesen
IT
L’utente deve consultare il
presente manuale di istruzioni
ES
Es necesario que el
usuario consulte este manual
de instrucciones
NL
Noodzaak voor de
gebruiker om deze gebruiks-
aanwijzing te raadplegen
RU
Необходимость для
пользователя обратиться
к данному руководству по
эксплуатации
TR
Kullanıcı, bu kullanım
kılavuzuna başvurmalıdır
ϡΩΧΗγϣϟ΍ωϭΟέΓέϭέο
AR
ϝϳϟΩϲϓΓΩέ΍ϭϟ΍ΕΎϣϭϠόϣϟ΍ϰϟ·
΍ΫϫΕ΍ΩΎηέϹ΍
Need for the user to follow this instruction
manual thoroughly for your safety.
FR
L’utilisateur doit suivre
attentivement ce mode
d’emploi pour votre sécurité.
DE
Damit die Sicherheit
gewährleistet ist, muss
der Benutzer diese
Gebrauchsanweisung
sorgfältig befolgen.
IT
Per la propria sicurezza,
l’utente deve seguire
attentamente il presente
manuale di istruzioni.
ES
Es necesario que el
usuario siga rigurosamente
este manual de instrucciones
para su seguridad.
NL
Noodzaak voor de
gebruiker om zich voor de
eigen veiligheid zorgvuldig
aan deze gebruiksaanwijzing
te houden.
RU
В целях обеспечения
безопасности строго
следуйте указаниям в
данном руководстве по
эксплуатации.
TR
Güvenlik açısından
kullanıcının bu kullanım
kılavuzuna dikkatle uyması
gerekir.
ωΎΑΗ΍ϰϟ·ϡΩΧΗγϣϟ΍ΔΟΎΣ
AR
ϝϳϟΩϲϓΓΩέ΍ϭϟ΍Ε΍ΩΎηέϹ΍
υΎϔΣϠϟ΍ΫϫϝϣΎϛϟΎΑΕ΍ΩΎηέϹ΍
Δϣϼγϟ΍ϰϠϋ
Direct current
FR
Courant continu
DE
Gleichstrom
IT
Corrente diretta
ES
Corriente directa
NL
Gelijkstroom
RU
Постоянный ток
TR
Doğru akım
έηΎΑϣϟ΍έΎϳΗϟ΍
AR
Alternating current
FR
Courant alternatif
DE
Wechselstrom
IT
Corrente alternata
ES
Corriente alterna
NL
Wisselstroom
RU
Переменный ток
TR
Alternatif akım
ΏϭΎϧΗϣϟ΍έΎϳΗϟ΍
AR
SD5
Date of manufacture
FR
Date de fabrication
DE
Herstellungsdatum
IT
Data di fabbricazione
ES
Fecha de fabricación
NL
Productiedatum
RU
Дата изготовления
TR
Üretim tarihi
ϊϳϧλΗϟ΍ΦϳέΎΗ
AR
Prohibited action
FR
Action interdite
DE
Verbotene Aktion
IT
Operazione proibita
ES
Acción prohibida
NL
Verboden handeling
RU
Запрещенные действия
TR
Yasaklanmış eylem
έϭυΣϣ˯΍έΟ·
AR
To indicate generally elevated, potentially hazardous, levels of non-ionizing radiation, or to indicate
equipment or systems. e.g. in the medical electrical area that include RF transmitters or that intentionally
apply RF electromagnetic energy for diagnosis or treatment.
FR
Indique des niveaux de rayonnement non ionisant,
potentiellement dangereux, généralement élevés, ou un équipement
ou des systèmes, par exemple dans le domaine médical électrique,
incluant des émetteurs RF ou utilisant intentionnellement de l’énergie
électromagnétique RF pour le diagnostic ou le traitement.
DE
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.
IT
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.
ES
Para indicar niveles de radiación no ionizante generalmente
elevados y potencialmente peligrosos, o bien para indicar equipos
o sistemas, como los usados en el ámbito electromédico, que
incorporen transmisores de radiofrecuencia o que apliquen energía
electromagnética de radiofrecuencia intencionadamente para
diagnósticos o tratamientos.
NL
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.
RU
Для указания повышенных и потенциально опасных
уровней неионизирующей радиации или же оборудования
или систем (например, в зоне размещения медицинского
электрооборудования), включающих в себя радиопередатчики
или устройства, использующие радиочастотную
электромагнитную энергию в целях диагностики или терапии.
TR
Genellikle yüksek ve zararlı olabilecek iyonlaşmayan radyasyon
seviyelerini belirtir veya RF vericileri içeren veya tanı ya da tedavi
amacıyla bilinçli olarak RF elektromanyetik enerji uygulayan (örneğin
medikal elektrik alanında bulunan) ekipman ve sistemleri belirtir.
έϳϏΔόηϷ΍ϥϣΩΎΗόϣϟ΍ΩΣϟ΍ϥϋΔόϔΗέϣϟ΍ΕΎϳϭΗγϣϟ΍ϰϟ·ϡΎϋϪΟϭΑΓέΎηϺϟ
AR
ϝΛϣˬΔϣυϧϷ΍ϭ΃ΓίϬΟϷ΍ϰϟ·ΓέΎηϺϟϭ΃ˬΓέρΧϥϭϛΗϥ΃ϝϣΗΣϣϟ΍ϥϣϲΗϟ΍Δϧϳ΅ϣϟ΍
ΓίϬΟ΃ϰϠϋϝϣΗηΗΔϳ΋ΎΑέϬϛΔϳΑρΓίϬΟ΃ϰϠϋΔϳϭΗΣϣϟ΍ϥϛΎϣϷ΍ϲϓΩΟϭΗϲΗϟ΍ϙϠΗ
Ε΍ΫΔϳγϳρΎϧϐϣϭέϬϛϟ΍ΔϗΎρϟ΍ϡ΍ΩΧΗγ΍ϡΗϳΙϳΣϭ΃ΔϳϛϠγϻΕ΍ΩΩέΗΎϬϧϣΙόΑϧΗϝΎγέ·
Νϼόϟ΍ϭ΃ιϳΧηΗϟ΍ν΍έϏϷΩϣϋϥϋΔϳϛϠγϼϟ΍Ε΍ΩΩέΗϟ΍
SD6
The Bluetooth® word mark and logos are registered trademarks owned by the Bluetooth SIG, Inc. and any use of such marks by OMRON
HEALTHCARECo.,Ltd. is under license. Other trademarks and trade names are those of their respective owners. AppStore and AppStore logo are
service marks of AppleInc., registered in the U.S and other countries. GooglePlay and GooglePlay logo are trademarks of GoogleLLC.
FR
La marque verbale et les logos Bluetooth® sont des marques
déposées détenues par Bluetooth SIG, Inc. et l’utilisation de ces marques
par OMRONHEALTHCARECo.,Ltd. se fait sous licence. Les autres marques
commerciales et noms de marque sont ceux de leurs détenteurs respectifs.
AppStore et le logo AppStore sont des marques de service d’Apple Inc.,
déposées aux États-Unis et dans d’autres pays. GooglePlay et le logo
GooglePlay sont des marques commerciales de GoogleLLC.
DE
Die Bluetooth®-Wortmarke und -Logos sind eingetragene Marken
der BluetoothSIG, Inc. und die Verwendung solcher Marken durch
OMRONHEALTHCARECo.,Ltd. erfolgt in Lizenz. Andere Marken und
Markennamen gehören ihren jeweiligen Eigentümern. AppStore und das
AppStore-Logo sind Dienstleistungsmarken der AppleInc., die in den USA
und anderen Ländern eingetragen sind. GooglePlay und das GooglePlay-
Logo sind Marken von GoogleLLC.
IT
Il marchio e i logotipi Bluetooth® sono marchi commerciali
registrati di Bluetooth SIG, Inc. e l’utilizzo di tali marchi da parte di
OMRONHEALTHCARECo.,Ltd. è stato concesso in licenza. Gli altri marchi e
nomi commerciali sono di proprietà dei rispettivi titolari. AppStore e il logo
AppStore sono marchi commerciali di AppleInc., registrati negli Stati Uniti
e in altri Paesi. GooglePlay e il logo GooglePlay sono marchi commerciali di
GoogleLLC.
ES
El nombre y los logotipos de Bluetooth® son marcas registradas
de Bluetooth SIG, Inc. y cualquier uso de dichas marcas hecho por
OMRONHEALTHCARECo.,Ltd. se ha llevado a cabo con su licencia
correspondiente. Otras marcas registradas también pertenecen a sus
respectivos propietarios. App Store y el logotipo de App Store son marcas de
servicios registradas de Apple Inc. en EE.UU. y en otros países. GooglePlay y
el logotipo de GooglePlay son marcas comerciales de GoogleLLC.
NL
Het woordmerk en de logos van Bluetooth® zijn gedeponeerde
handelsmerken van Bluetooth SIG, Inc. en enig gebruik hiervan door
OMRONHEALTHCARECo.,Ltd. geschiedt onder licentie. Overige
handelsmerken en handelsnamen zijn van hun respectievelijke eigenaren.
App Store en het logo van App Store zijn handelsmerken van Apple Inc. die
gedeponeerd zijn in de V.S. en in andere landen. GooglePlay en het logo van
GooglePlay zijn handelsmerken van GoogleLLC.
RU
Словесный знак Bluetooth® и логотип являются
зарегистрированными товарными знаками, являющимися
собственностью компании Bluetooth SIG, Inc., и любое использование
этих знаков компанией OMRONHEALTHCARECo.,Ltd. обеспечивается
лицензией. Другие товарные знаки и торговые марки являются
собственностью соответствующих владельцев. App Store и логотип App
Store являются знаками обслуживания Apple Inc., зарегистрированными
в США и других странах. GooglePlay и логотип GooglePlay являются
товарными знаками GoogleLLC.
TR
Bluetooth® marka adı ve logoları, Bluetooth SIG Inc. kuruluşunun
tescilli ticari markalarıdır ve OMRONHEALTHCARECo.,Ltd. bu markaları
lisans kapsamında kullanmaktadır. Diğer ticari markalar ve ticari isimler, ilgili
sahiplerine aittir. App Store ve App Store logosu, Apple Inc. firmasının ABD
ve diğer ülkelerde tescilli hizmet markalarıdır. GooglePlay ve GooglePlay
logosu, GoogleLLC firmasının ticari markalarıdır.
ΔϛϭϠϣϣΔϠΟγϣΔϳέΎΟΗΕΎϣϼϋϲϫΎϬΗ΍έΎόηϭBluetooth
®
ΔϣϠϛΔϣϼϋϥ·
AR
ΔϛέηΔργ΍ϭΑΕΎϣϼόϟ΍ϩΫϬϟϡ΍ΩΧΗγ΍ϱ΃ϥϭϛϳϭ%OXHWRRWK6,*,QFΔϛέηϟ
ΔϳέΎΟΗϟ΍ΕΎϣϼόϟ΍ϥϭϛΗιϳΧέΗΏΟϭϣΑ20521+($/7+&$5(&R/WG.
ϲΗϣϼϋϩέΎόηϭ$SS6WRUHΩό
˵
ϳϪϳϛϟΎϣΑΔλΎΧΞΗϧϣϟ΍΍ΫϬϟΔϳέΎΟΗϟ΍˯ΎϣγϷ΍ϭϯέΧϷ΍
Ωό
˵
ϳϭϯέΧ΃ϥ΍ΩϠΑϭΔϳϛϳέϣϷ΍ΓΩΣΗϣϟ΍ΕΎϳϻϭϟ΍ϲϓΔϠΟγϣϟ΍$SSOH,QFΔϛέηϟΔϣΩΧ
.*RRJOH//&ΔϛέηϟϥϳΗϳέΎΟΗϥϳΗϣϼϋϩέΎόηϭ*RRJOH3OD\
2019-07-29
IM1-HEM-7155T-E-01-03/2019
2870440-7A
Issue Date:
Date de publication:
Ausgabedatum:
Data di pubblicazione:
Fecha de publicación:
Uitgiftedatum
Дата выпуска:
Teslim Tarihi:
έ΍ΩλϹ΍ΦϳέΎΗ
Automatic Upper Arm
Blood Pressure Monitor
M4 Intelli IT (HEM-7155T-EBK)
X4 Smart (HEM-7155T-ESL)
9
IM2-HEM-7155T-E-01-03/2019
2870441-5A
1
Instruction Manual
Instruction Manual
2.3
Read Instruction manual and before use.
FR
Lire le mode d’emploi et avant l’utilisation.
DE
Lesen Sie vor der Verwendung die Gebrauchsanweisung und .
IT
Leggere il manuale di istruzioni e prima dell’uso.
ES
Lea el manual de instrucciones y antes del uso.
NL
Lees de gebruiksaanwijzing en voor gebruik.
RU
Прочтите руководство по эксплуатации и перед использованием.
TR
Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.
ϡ΍ΩΧΗγϻ΍ϝΑϗ ϭ Ε΍ΩΎηέϹ΍ϝϳϟΩ΃έϗ΍
AR
1
Package Contents
FR
Contenu de l’emballage
NL
Inhoud van de verpakking
DE
Packungsinhalt
RU
Комплект поставки
IT
Contenuto della confezione
TR
Paketin İçindekiler
ES
Contenido del envase
ΓϭΑόϟ΍ΕΎϳϭΗΣϣ
AR
1
Instruction Manual
Instruction Manual
2
2
Preparing for a Measurement
FR
Préparation d’une mesure
NL
Een meting voorbereiden
DE
Vorbereiten einer Messung
RU
Подготовка к измерению
IT
Preparazione per la misurazione
TR
Ölçüm Hazırlığı
ES
Preparación para una medición
αΎϳϘϟ΍ΔϳϠϣόϟίϳϬΟΗϟ΍
AR
30 minutes before
FR
30minutes avant
DE
30 Minuten vorher
IT
30 minuti prima
ES
30minutos antes
NL
30 minuten ervoor
RU
За 30 минут до
TR
30 dakika önce
ΔϘϳϕΩ˼˹ώϟΏΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ
AR
5 minutes before: Relax and rest.
FR
5minutes avant: détente et repos.
DE
5 Minuten vorher: ruhig hinsetzen.
IT
5 minuti prima: rilassarsi e stare a riposo.
ES
5minutos antes: relájese y descanse.
NL
5 minuten ervoor: ontspan en rust.
RU
За 5 минут до: расслабьтесь и отдохните.
TR
5 dakika önce: Gevşeyin ve dinlenin.
˶
ΥέΗγ΍ϭΡέΗγ΍ϖ΋ΎϗΩ˾ώϟΏΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ
AR
3
Downloading the OMRON connect” App
FR
Téléchargement de l’application
«OMRONconnect»
NL
De app “OMRON connect downloaden
DE
Herunterladen der App „OMRON connect“
RU
Загрузка приложения «OMRON connect»
IT
Download della app “OMRON connect”
TR
“OMRON connect” Uygulamasını indirme
ES
Descarga de la aplicación “OMRONconnect
"20521FRQQHFWϖϳΑρΗϝϳίϧΗ
AR
5
Pairing Your Smart Device
FR
Jumelage de votre appareil intelligent
NL
Uw smartapparaat koppelen
DE
Koppeln mit Smartphone oder Tablet
RU
Синхронизация со смарт-устройством
IT
Associazione del dispositivo smart
TR
Akıllı Cihazınızın Eşleştirilmesi
ES
Sincronización con su dispositivo inteligente
ϲϛΫϟ΍ϙϔΗΎϫϥ΍έϗ·
AR

Bluetooth
ON
Follow the instructions.
FR
Suivez les instructions.
DE
Befolgen Sie die Anweisungen.
IT
Attenersi alle istruzioni.
ES
Siga las instrucciones.
NL
Volg de instructies.
RU
Выполняйте инструкции.
TR
Talimatları izleyin.
Ε΍ΩΎηέϹ΍ϊΑΗ΍
AR
The date and time will automatically be set when your monitor is paired with the app.
FR
La date et l’heure seront automatiquement réglées lorsque votre tensiomètre sera jumelé avec l’application.
DE
Wenn Ihr Messgerät mit der App verknüpft ist, werden Datum und Uhrzeit automatisch eingestellt.
IT
La data e l’ora verranno impostate automaticamente una volta che il misuratore verrà associato alla app.
ES
La fecha y la hora se ajustarán automáticamente cuando el monitor se sincronice con la aplicación.
NL
De datum en tijd worden automatisch ingesteld wanneer uw bloeddrukmeter is gekoppeld aan de app.
RU
Дата и время установятся автоматически после синхронизации с приложением.
TR
Ölçüm cihazınız uygulamayla eşleştirildiğinde tarih ve saat otomatik olarak ayarlanır.
ϖϳΑρΗϟΎΑϙΑιΎΧϟ΍αΎϳϘϟ΍ίΎϬΟϥ΍έϗ·ΩϧϋΎ
˱
ϳ΋ΎϘϠΗΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑοϡΗϳγ
AR
7
Applying the Cuff on the Left Arm
FR
Pose du brassard sur le bras gauche
NL
De manchet op de linkerarm aanbrengen
DE
Anbringen der Manschette am linken Arm
RU
Расположение манжеты на левой руке
IT
Applicazione del bracciale sul braccio sinistro
TR
Kolluğun Sol Kola Takılması
ES
Colocación del manguito en el brazo izquierdo
ϥϣϳϷ΍ω΍έΫϟ΍ϰϠϋρϏΎοϟ΍ρϳέηϟ΍ϑϟ
AR
1-2 cm


Click
A
B
A
Tube side of the cuff should be 1 - 2 cm above the inside elbow.
FR
Le côté tuyau du brassard doit être positionné 1 à 2cm au-dessus de l’intérieur du coude.
DE
Das Manschettenstück mit dem Schlauch muss 1 bis 2cm oberhalb des Ellbogens liegen.
IT
Il lato del bracciale con il tubo deve trovarsi al di sopra dell’interno del gomito, a una distanza di circa 1 o 2 cm.
ES
El lado del tubo del manguito deberá quedar 1 o 2cm por encima de la parte interna del codo.
NL
De kant met de slang van de manchet moet 1 - 2 cm boven de binnenkant van de elleboog liggen.
RU
Край манжеты с трубкой должен находиться на 1–2 см выше локтевого сгиба.
TR
Kolluğun boru tarafı, dirsek içinin 1 ila 2 cm üstünde olmalıdır.
ϖϓέϣϟ΍ϥϋϡα˻ϰϟ·˺ϥϣρϏΎοϟ΍ρϳέηϟ΍ϥϣϡϭρέΧϟ΍ΏϧΎΟϊϔΗέϳϥ΃ΏΟϳ
AR
B
Make sure that air tube is on the inside of your arm and wrap the cuff
securely so it can no longer slip round.
FR
Assurez-vous que le tuyau à air se trouve du côté intérieur de votre bras et enroulez fermement le brassard
de manière quil ne puisse plus tourner.
DE
Stellen Sie sicher, dass der Luftschlauch an der Arminnenseite sitzt, und befestigen Sie die Manschette sicher, so dass sie nicht verrutscht.
IT
Assicurarsi che il tubo dell’aria si trovi all’interno del braccio e avvolgere il bracciale saldamente in modo che non possa ruotare.
ES
Asegúrese de que el tubo de aire se encuentra en la cara interna del brazo y enrolle el manguito con
firmeza para que no pueda deslizarse.
NL
Zorg ervoor dat de luchtslang zich aan de binnenkant van uw arm bevindt en wikkel de manchet stevig
rond uw arm zodat deze niet meer kan wegglijden.
RU
Убедитесь, что воздуховодная трубка находится на внутренней поверхности плеча и надежно
оберните манжету, чтобы она не прокручивалась вокруг руки.
TR
Hava borusunun kolunuzun iç tarafında olduğundan emin olun ve kolluğu kaymayacak şekilde sabit şekilde sarın.
ω΍έΫϟ΍ϝϭΣϖϟίϧϳϻΙϳΣΑϡΎϛΣΈΑρϏΎοϟ΍ρϳέηϟ΍ϑϟϭϙϋ΍έΫϥϣϲϠΧ΍Ωϟ΍ΏϧΎΟϟ΍ϰϠϋ˯΍ϭϬϟ΍ϡϭρέΧϥ΃ϥϣΩϛ΄Η
AR
If taking measurements on the right arm, refer to:
FR
Pour la prise de mesures au bras droit, voir:
DE
Bei Messungen am rechten Arm siehe:
IT
Se la misurazione viene eseguita al braccio destro, fare riferimento a:
ES
Si va a realizar mediciones en el brazo derecho, consulte:
NL
Als u metingen aan de rechterarm uitvoert, raadpleeg dan:
RU
При измерении на правой руке см:
TR
Sağ koldan ölçüm yapıyorsanız aşağıdakilere bakın:
ϰϟ·ϊΟέ΍ˬϥϣϳϷ΍ω΍έΫϟ΍ϰϠϋαΎϳϘϟ΍˯΍έΟ·ϝΎΣϲϓ
AR
4
Installing Batteries
FR
Mise en place des piles
NL
Batterijen plaatsen
DE
Einsetzen der Batterien
RU
Установка элементов питания
IT
Installazione delle batterie
TR
Pillerin Takılması
ES
Instalación de las pilas
ΕΎϳέΎρΑϟ΍ΏϳϛέΗ
AR
AA, 1.5V × 4
8
Sitting Correctly
FR
Position assise correcte
NL
Correct zitten
DE
Korrekte Körperhaltung
RU
Сядьте правильно
IT
Come sedere nel modo corretto
TR
Düzgün Oturma
ES
Cómo sentarse correctamente
΢ϳΣλϝϛηΑαϭϠΟϟ΍
AR
Sit with your back and arm supported.
FR
S’asseoir de façon à ce que le dos et le bras soient bien soutenus.
DE
Mit dem Rücken anlehnen und den Arm auf eine Unterlage legen.
IT
Sedere con la schiena e il braccio ben sostenuti.
ES
Siéntese de modo que la espalda y el brazo estén bien apoyados.
NL
Zit met uw rug en arm ondersteund.
RU
Сядьте так, чтобы спина и рука опирались на что-либо.
TR
Sırtınız ve kolunuz desteklenecek şekilde oturun.
ΩΎϧΗγ΍ϊοϭϲϓω΍έΫϟ΍ϭέϬυϟ΍ϥϭϛϳΙϳΣΑαϠΟ΍
AR
Place the arm cuff at the same level as your heart.
FR
Le brassard doit se trouver au même niveau que votre cœur.
DE
Die Manschette auf Herzhöhe platzieren.
IT
Posizionare il bracciale allo stesso livello del cuore.
ES
Coloque el manguito al mismo nivel que el corazón.
NL
Plaats de armmanchet op hetzelfde niveau als uw hart.
RU
Манжета должна находиться на уровне сердца.
TR
Kolluğu kalbinizle aynı düzeye getirin.
ϪγϔϧΏϠϘϟ΍ϯϭΗγϣϲϓω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍ϊο
AR
Keep feet flat, legs uncrossed, remain still and do not talk.
FR
Garder les pieds à plat, les jambes non croisées, ne pas bouger et ne pas parler.
DE
Füße flach auf den Boden stellen, die Beine nicht kreuzen, still halten und nicht sprechen.
IT
Tenere i piedi ben poggiati, non incrociare le gambe, rimanere fermi e non parlare.
ES
Mantenga los pies planos, las piernas sin cruzar, quédese quieto y no hable.
NL
Houd de voeten plat, benen niet gekruist, zit stil en praat niet.
RU
Поставьте ноги ровно, не перекрещивая их, не двигайтесь и не разговаривайте.
TR
Ayaklarınızı düz, bacaklarınızı açık tutun, hareketsiz kalın ve konuşmayın.
ΙΩΣΗΗϻϭϙΗΎΑΛϰϠϋυϓΎΣϭΩϋΎΑΗϣϊοϭϲϓϙϳϗΎγϭ΢
˷
ργϣϊοϭϲϓϙϳϣΩϗϝόΟ΍
AR
6
Setting Date and Time Manually
FR
Réglage manuel de la date et de l’heure
NL
Datum en tijd handmatig instellen
DE
Manuelles Einstellen von Datum und Uhrzeit
RU
Установка даты и времени вручную
IT
Impostazione manuale di data e ora
TR
Tarih ve Saatin Manuel Olarak Ayarlanması
ES
Ajuste manual de la fecha y la hora
Ύ
˱
ϳϭΩϳΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑο
AR
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.
FR
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.
DE
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.
IT
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.
ES
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.
NL
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.
RU
Если прибор синхронизирован со смарт-устройством, дата и время устанавливаются автоматически.
Если необходимо установить их вручную, выберите год > месяц > день > час > минута.
TR
Ölçüm cihazınız akıllı cihazınızla eşleştirilmişse tarih ve saat otomatik olarak ayarlanır. Bunları manuel
olarak ayarlamanız gerektiğinde, yıl > ay > gün > saat > dakika değerini ayarlayın.
ρΑο΍ˬΎ
˱
ϳϭΩϳΎϣϬρΑοϰϟ·ΔΟΎΣϟ΍ΩϧϋΎ
˱
ϳ΋ΎϘϠΗΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑοϡΗϳˬϲϛΫϟ΍ίΎϬΟϟΎΑϙΑιΎΧϟ΍αΎϳϘϟ΍ίΎϬΟϥ΍έϗ·ϝΎΣϲϓ
AR
ΔϘϳϗΩϟ΍PLQXWHΔϋΎγϟ΍KRXUϡϭϳϟ΍dayέϬηϟ΍PRQWKΔϧγϟ΍\HDU
Year
Month
Day
Hour
Minute
Back / Forward
FR
Arrière / Avant
DE
Zurück / Vorwärts
IT
Indietro / Avanti
ES
Atrás / Adelante
NL
Terug / vooruit
RU
Назад / Вперед
TR
İleri / Geri
ϡΩϘΗϟ΍ωϭΟέϟ΍
AR
1
Instruction Manual
Instruction Manual
3.
11
Checking Readings
FR
Vérication des résultats
NL
Metingen bekijken
DE
Prüfen der Messwerte
RU
Проверка результатов
IT
Controllo dei risultati
TR
Ölçüm Değerlerini Kontrol Etme
ES
Comprobación de lecturas
Ε΍˯΍έϘϟ΍ϥϣϖϘΣΗϟ΍
AR
1
2
3
4
1
Appears if “SYS is 135 mmHg or above
and/or “DIA is 85 mmHg* or above.
FR
S’affiche si «SYS» est égale ou supérieure à
135mmHg et/ou «DIA» égale ou supérieure
à 85mmHg*.
DE
Wird angezeigt, wenn „SYS“ 135mmHg oder
mehr beträgt und/oder wenn „DIA“ 85mmHg*
oder mehr beträgt.
IT
Viene visualizzato se la pressione sistolica
“SYS” è pari o superiore a 135 mmHg e/o la
pressione diastolica “DIA” è pari o superiore
a 85 mmHg*.
ES
Aparece si “SYS es 135mmHg o superior
y/o “DIA es 85mmHg* o superior.
NL
Verschijnt als “SYS” 135 mmHg of hoger is
en/of “DIA 85 mmHg* of hoger is.
RU
Отображается, если «SYS» 135 мм.рт.ст. и
выше и/или «DIA» 85 мм.рт.ст.* и выше.
TR
“SYS” 135 mmHg ya da üstünde olduğunda
ve/veya “DIA” 85 mmHg* ya da üstünde
olduğunda görünür.
έΛϛ΃ϭ΃Ύ
˱
ϳϘΑ΋ί΍
˱
έΗϣϳϠϠϣ˺˼˾ώϠΑϳSYSϥΎϛϝΎΣϲϓέϬυΗ
AR
έΛϛ΃ϭ΃Ύ
˱
ϳϘΑ΋ί΍
˱
έΗϣϳϠϠϣ́˾DIAϭ΃ϭ
2
Appears when an irregular rhythm** is detected during a measurement.
If it appears repeatedly, OMRON recommends to consult your physician.
FR
S’affiche lorsqu’un rythme irrégulier** est détecté pendant une mesure. S’il s’affiche à
plusieurs reprises, OMRON recommande de consulter votre médecin.
DE
Wird angezeigt, wenn während einer Messung ein unregelmäßiger Herzschlag** festgestellt
wird. Wird das Symbol wiederholt angezeigt, empfiehlt OMRON, sich an Ihren Arzt zu wenden.
IT
Viene visualizzato se nel corso di una misurazione viene rilevato un ritmo cardiaco irregolare**.
Se il simbolo appare ripetutamente, OMRON consiglia di consultare il medico curante.
ES
Aparece cuando se detecta un ritmo irregular** durante una medición. Si aparece varias veces,
OMRON recomienda que consulte a su médico.
NL
Verschijnt wanneer tijdens een meting een onregelmatig ritme** wordt gedetecteerd. Als dit
herhaaldelijk verschijnt, raadt OMRON aan om uw arts te raadplegen.
RU
Отображается, если при измерении определяется нерегулярный ритм**. Если этот символ
отображается неоднократно, компания OMRON рекомендует обратиться к лечащему врачу.
TR
Bir ölçüm esnasında düzensiz ritim** saptandığında görünür. Tekrarlı şekilde görünürse
OMRON doktorunuza danışmanızı önerir.
ϙΑϳΑρΓέΎηΗγΎΑOMRONϲλϭΗˬέέϛΗϣϝϛηΑΎϫέϭϬυΩϧϋαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓΏϠϘϟ΍ΕΎΑέοϡΎυΗϧ΍ϡΩϋϑΎηΗϛ΍ΩϧϋέϬυΗ
AR
3
Appears when your body moves during a measurement. Remove the
arm cu, wait 2-3 minutes and try again.
FR
S’affiche si vous bougez pendant une mesure. Retirer le brassard, attendre 2 à 3minutes et essayer à nouveau.
DE
Wird angezeigt, wenn Sie sich während der Messung bewegen. Nehmen Sie die Manschette ab, warten Sie
2–3Minuten und versuchen Sie es erneut.
IT
Viene visualizzato se l’utilizzatore si muove durante la misurazione. Rimuovere il bracciale, attendere 2-3 minuti e riprovare.
ES
Aparece cuando se mueve el cuerpo durante una medición. Retire el manguito, espere unos 2 o 3minutos e
inténtelo de nuevo.
NL
Verschijnt wanneer uw lichaam tijdens een meting beweegt. Verwijder de armmanchet, wacht 2-3 minuten
en probeer het opnieuw.
RU
Отображается при движении тела во время измерения. Снимите манжету, подождите 2-3 минуты и
попробуйте еще раз.
TR
Bir ölçüm esnasında vücudunuz hareket ettiğinde görünür. Kolluğu çıkarın, 2-3 dakika bekleyip tekrar deneyin.
ϯέΧ΃ΓέϣΔϟϭΎΣϣϟ΍ϭϖ΋ΎϗΩ˼ϰϟ·˻ϥϣέΎυΗϧϻ΍ϭω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍Δϟ΍ίΈΑϡϗαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϙϣγΟϙέΣΗΩϧϋέϬυΗ
AR
4
Cu is tight enough.
FR
Le brassard est suffisamment serré.
DE
Manschette sitzt ausreichend straff.
IT
Il bracciale è stretto a sufficienza.
ES
El manguito está lo suficientemente prieto.
NL
Manchet zit strak genoeg.
RU
Манжета затянута достаточно туго.
TR
Kolluk yeterince sıkıdır.
ϲϔϛϳΎϣΑϡϛΣϣρϏΎοϟ΍ρϳέηϟ΍
AR
4
Apply cu again MORE TIGHTLY.
FR
Poser le brassard en le serrant davantage.
DE
Manschette STRAFFER ziehen.
IT
Applicare di nuovo il bracciale
STRINGENDOLO DI PIÙ.
ES
Vuelva a poner el manguito MÁS PRIETO.
NL
Breng de manchet STRAKKER aan.
RU
Наложите манжету еще раз БОЛЕЕ ТУГО.
TR
Kolluğu tekrar, DAHA SIKI bir şekilde takın.
Ύ
˱
ϣΎϛΣ·έΛϛ΃ϝϛηΑϯέΧ΃ΓέϣρϏΎοϟ΍ρϳέηϟ΍ϑϟ
AR
Error messages or other problems? Refer to:
FR
Messages d’erreur ou autres problèmes? Voir:
DE
Weitere Fehlermeldungen oder Probleme siehe:
IT
Messaggi di errore o altri problemi? Fare riferimento a:
ES
¿Hay mensajes de error u otros problemas? Consulte:
NL
Foutmeldingen of andere problemen? Raadpleeg:
RU
Сообщения об ошибках или другие неисправности? См:
TR
Hata mesajları veya başka sorunlar mı var? Bkz:
ϰϟ·ϊΟέ΍ˮϯέΧϷ΍Εϼϛηϣϟ΍ϭ΃΄ρΧϟ΍ϝ΋Ύγέ
AR
*The high blood pressure definition is based on the 2018 ESH/ESC Guidelines.
FR
*La définition de l’hypertension est basée sur les recommandations ESH/ESC 2018.
DE
*Die Definition für Bluthochdruck basiert auf den 2018 ESH/ESC Richtlinien.
IT
*La definizione di alta pressione arteriosa si basa sulle linee guida 2018 di ESH/ESC.
ES
*La definición de presión arterial alta se basa en las guías 2018 ESH/ESC.
NL
*De definitie van hoge bloeddruk is gebaseerd op de ESH/ESC-richtlijnen uit 2018.
RU
*Определение высокого артериального давления основано на Рекомендациях 2018 ESH/ESC.
TR
*Yüksek kan basıncı tanımı, 2018 ESH/ESC Kılavuzlarını temel alır.
.2018ϡΎόϟESCΏϠϘϟ΍ΏρϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍ESHϡΩϟ΍ρϐορέϔϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍Ε΍ΩΎηέ·ϰϟ·ΩϧΗγϳϊϔΗέϣϟ΍ϡΩϟ΍ρϐοϑϳέόΗ
AR
** An irregular heart beat rhythm is defined as a rhythm that is 25% less or 25%
more than the average rhythm detected during a measurement.
FR
** Un rythme cardiaque irrégulier est défini comme un rythme inférieur ou supérieur de 25% au
rythme moyen détecté durant une mesure.
DE
** Ein unregelmäßiger Herzschlag ist definiert als ein Herzrhythmus, der weniger als 25% oder mehr
als 25% des mittleren Herzrhythmus beträgt, der während der Blutdruckmessung erkannt wird.
IT
** Si definisce ritmo cardiaco irregolare un ritmo cardiaco inferiore del 25% o superiore del 25%
rispetto al ritmo medio rilevato durante una misurazione.
ES
** Latido arrítmico se define como un ritmo que es un 25% menor o un 25% mayor que el ritmo
medio detectado durante una medición.
NL
** Een onregelmatig hartslagritme wordt gedefinieerd als een ritme dat 25% lager of 25% hoger is dan
het gemiddelde ritme dat tijdens een meting wordt gedetecteerd.
RU
** Нерегулярный ритм сердцебиения — это ритм, который на 25% медленнее или быстрее
измеренного среднего ритма.
TR
** Düzensiz kalp atışı ritmi, bir ölçüm sırasında saptanan ortalamadan %25 daha düşük veya %25 daha
yüksek ritim olarak tanımlanır.
̃˻˾ϝΩόϣΑϪϧϣέΛϛ΃ϭ΃̃˻˾ϝΩόϣΑαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϪϓΎηΗϛ΍ϡΗϳϱΫϟ΍ϲόϳΑρϟ΍ϡ
˸
υϧϟ΍ϥϣϝϗ΃ϡ
˸
υϧϪϧ΄ΑΏϠϘϟ΍ΕΎΑέοΏ΍έρο΍ϑέό
˵
ϳ
AR
12
Using Memory Functions
FR
Utilisation des fonctions de mémoire
NL
Geheugenfuncties gebruiken
DE
Verwendung der Speicherfunktionen
RU
Использование функции памяти
IT
Uso delle funzioni di memoria
TR
Hafıza Fonksiyonunun Kullanılması
ES
Uso de las funciones de memoria
Γέϛ΍Ϋϟ΍ϑ΋Ύυϭϡ΍ΩΧΗγ΍
AR
Before using memory functions, select your user ID.
FR
Avant d’utiliser les fonctions de mémoire, sélectionner votre ID Utilisateur.
DE
Wählen Sie vor dem Verwenden der Speicherfunktionen Ihre Benutzer-ID aus.
IT
Prima di utilizzare le funzioni di memoria selezionare il proprio ID utente.
ES
Antes de usar las funciones de memoria, seleccione su ID de usuario.
NL
Selecteer uw gebruikers-ID voordat u geheugenfuncties gebruikt.
RU
Перед использованием функции памяти выберите идентификатор пользователя.
TR
Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.
ϙΑιΎΧϟ΍ϡΩΧΗγϣϟ΍ϑέόϣΩΩΣˬΓέϛ΍Ϋϟ΍ϑ΋Ύυϭϡ΍ΩΧΗγ΍ϝΑϗ
AR
12.1 Readings Stored in Memory
FR
Mesures stockées en mémoire
DE
Gespeicherte Messungen
IT
Risultati conservati in memoria
ES
Lecturas guardadas en la memoria
NL
Meetwaarden opgeslagen in het geheugen
RU
Сохранение результатов в памяти
TR
Hafızada Saklanan Ölçüm Değerleri
Γέϛ΍Ϋϟ΍ϲϓΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍
AR
Up to 60 readings
arestored.
FR
Jusqu’à 60mesures
sont stockées.
DE
Es werden bis zu
60Messwerte
gespeichert.
IT
Vengono conservati
fino a 60 risultati.
ES
Se almacenan hasta
60lecturas.
NL
Er kunnen tot 60 meetwaar-
den worden opgeslagen.
RU
Сохраняется до
60 результатов.
TR
60 adede kadar ölçüm
değeri saklanır.
ΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ΩΩϋϝλϳ
AR
Γ˯΍έϗ˿˹ϰϟ·
12.2 Average of the Latest 2 or 3 Readings Taken
within a 10 Minute Span
FR
Moyenne des 2 ou 3 dernières mesures prises en l’espace de 10minutes
DE
Mittelwert der letzten 2 oder 3Messwerte, die in einem 10-Minuten-
Zeitrahmen erfasst wurden
IT
Media degli ultimi 2 o 3 risultati ottenuti nell’arco di 10 minuti
ES
Promedio de las 2 o 3últimas lecturas realizadas en un intervalo de 10minutos
NL
Gemiddelde van de laatste 2 of 3 metingen uitgevoerd binnen een
tijdspanne van 10 minuten
RU
Среднее значение из последних 2-х или 3-х результатов
полученных в течение 10 минут
TR
10 Dakika Aralıkta Alınan Son 2 veya 3 Ölçüm Değerinin Ortalaması
ϖ΋ΎϗΩ˺˹ώϠΑΗΔϳϧϣίΓΩϣϲϓΎϬϳϠϋϝϭλΣϟ΍ϡΗΕ΍˯΍έϗ˼ϭ΃ϥϳΗ˯΍έϗέΧ΁ργϭΗϣ
AR
3 sec+
12.3 Deleting All Readings
FR
Suppression de toutes les mesures
DE
Löschen aller Messwerte
IT
Cancellazione di tutti i risultati
ES
Eliminación de todas las lecturas
NL
Alle metingen verwijderen
RU
Удаление всех результатов
TR
Tüm Ölçüm Değerlerini Silme
Ε΍˯΍έϘϟ΍ϊϳϣΟϑΫΣ
AR
4sec+ 4sec+

13
Other Settings
FR
Autres réglages
NL
Andere instellingen
DE
Weitere Einstellungen
RU
Другие настройки
IT
Altre impostazioni
TR
Diğer Ayarlar
ES
Otros ajustes
ϯέΧϷ΍Ε΍Ω΍ΩϋϹ΍
AR
13.1 Disabling/Enabling Bluetooth
FR
Désactivation/activation de Bluetooth
DE
Deaktivieren/Aktivieren der Bluetooth-Funktion
IT
Disattivazione/attivazione della funzione Bluetooth
ES
Activar o desactivar el Bluetooth
NL
Bluetooth uitschakelen/inschakelen
RU
Выключение/включение Bluetooth
TR
Bluetooth’u Devre Dışı Bırakma/Etkinleştirme
%OXHWRRWKΔϳλΎΧϝϳρόΗϥϳϛϣΗ
AR
10 sec+
3 sec+
Bluetooth is enabled
by default.
FR
Bluetooth est activé
par défaut.
DE
Die Bluetooth-Funktion ist
standardmäßig aktiviert.
IT
La funzione Bluetooth è
attiva per impostazione
predefinita.
ES
El Bluetooth está
activado por defecto.
NL
Bluetooth is standaard
ingeschakeld.
RU
Bluetooth включен по
умолчанию.
TR
Bluetooth varsayılan
olarak etkindir.
%OXHWRRWKΔϳλΎΧϥϳϛϣΗϡΗϳ
AR
ϲο΍έΗϓ΍ϝϛηΑ
13.2 Restoring to the Default Settings
FR
Réinitialisation aux réglages par défaut
DE
Wiederherstellen der Standardeinsttellungen
IT
Ripristino delle impostazioni predefinite
ES
Restablecimiento a los ajustes de fábrica
NL
De standaardinstellingen herstellen
RU
Восстановление настроек по умолчанию
TR
Varsayılan Ayarları Geri Yükleme
Δϳο΍έΗϓϻ΍Ε΍Ω΍ΩϋϹ΍ΓΩΎόΗγ΍
AR
4sec+

4sec+
If your systolic pressure is more than 210 mmHg:
After the arm cuff starts to inflate, press and hold the [START/STOP] button until the monitor
inflates 30 to 40 mmHg higher than your expected systolic pressure.
FR
Si votre pression systolique est supérieure à 210mmHg: Lorsque le brassard se gonfle, appuyer sur
le bouton [START/STOP] et le maintenir enfoncé jusqu’à ce que le tensiomètre atteigne une pression de
gonflage supérieure de 30 à 40mmHg à votre pression systolique attendue.
DE
Wenn Ihr systolischer Druck höher ist als 210mmHg: Nachdem die Manschette begonnen hat, sich
aufzupumpen, drücken Sie die [START/STOP]-Taste, und halten Sie sie gedrückt, bis ein Druck von 30 bis
40mmHg über Ihrem erwarteten systolischen Druck erreicht ist.
IT
Se la pressione sistolica è superiore a 210 mmHg: Quando il bracciale inizia a gonfiarsi, premere e
mantenere premuto il pulsante [START/STOP] finché il misuratore non raggiunge una pressione da 30 a
40mmHg superiore rispetto al valore di pressione sistolica atteso.
ES
En caso de que su presión arterial sistólica esté por encima de 210mmHg: Una vez que el manguito
comience a inflarse, mantenga pulsado el botón [START/STOP] hasta que el monitor indique que el inflado
está entre 30 y 40mmHg por encima de la presión arterial sistólica estimada.
NL
Als uw systolische druk hoger is dan 210 mmHg: Zodra de armmanchet wordt opgepompt, houdt u de knop
[START/STOP] ingedrukt totdat de meter 30 tot 40 mmHg hoger aangeeft dan uw verwachte systolische druk.
RU
Если систолическое давление выше 210 мм.рт.ст.: После того, как началось автоматическое нагнетание
воздуха в манжету, нажмите и удерживайте кнопку [START/STOP] до тех пор, пока электронный блок не
поднимет давление до значения, превышающего ожидаемое систолическое давление на 30–40ммрт.ст.
TR
Sistolik basıncınız 210 mmHg’den fazlaysa: Kolluk şişmeye başladıktan sonra, [START/STOP] düğmesine basın
ve ölçüm cihazı beklediğiniz sistolik basınç değerinden 30 ila 40 mmHg daha fazla şişene kadar basılı tutun.
έίϟ΍ϰϠϋέ΍έϣΗγϻ΍ϊϣρϐο΍ˬω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍ΥΎϔΗϧ΍˯ΩΑΩόΑΔϳϘΑ΋ίΕ΍έΗϣϳϠϠϣ˻˺˹ϥϣέΛϛ΃ϲοΎΑϘϧϻ΍ϙϣΩρϐοϥΎϛ΍Ϋ·
AR
ϙϳΩϟΔόϗϭΗϣϟ΍ϲοΎΑϘϧϻ΍ϡΩϟ΍ρϐοΔϣϳϗϥϣϰϠϋ΃Ύ
˱
ϳϘΑ΋ί΍
˱
έΗϣϳϟϝϣ˽˹ϰϟ·˼˹ϥϣΦϔϧϟΎΑίΎϬΟϟ΍ϡϭϘϳϰΗΣϑΎϘϳ·˯ΩΑ>67$576723]
14
Optional Medical Accessories
FR
Accessoires médicaux optionnels
NL
Optionele medische accessoires
DE
Optionales medizinisches Zubehör
RU
Дополнительно принадлежности
IT
Accessori medicali opzionali
TR
Opsiyonel Tıbbi Aksesuarlar
ES
Accesorios médicos opcionales
ΔϳέΎϳΗΧϻ΍ΔϳΑρϟ΍ΕΎϘΣϠϣϟ΍
AR
Arm Cuff
(HEM-FL31)
22 - 42 cm
AC Adapter
(HHP-CM01) (HHP-BFH01)
Do not throw the air plug away. The air
plug can be applicable to the optional cuff.
FR
Ne pas jeter la prise de gonflage. La prise de gonflage
peut être utilisée pour le brassard en option.
DE
Entsorgen Sie den Luftschlauchstecker nicht. Der Luft-
schlauch stecker wird für die optionale Manschette verwendet.
IT
Non gettare via l’attacco del tubo dell’aria. L’attacco del
tubo dell’aria può essere applicato al bracciale opzionale.
ES
No tire el conector para tubo de aire. El conector para tubo
de aire puede ser utilizado con el manguito opcional.
NL
Gooi de plug van de luchtslang niet weg. De
plug van de luchtslang kan worden gebruikt op
de optionele manchet.
RU
Не выбрасывайте воздушный штекер. Он
может подойти к дополнительной манжете.
TR
Hava tıpasını atmayın. Hava tıpası isteğe bağlı
kolluğa uygulanabilir.
ϱέΎϳΗΧϻ΍ρϏΎοϟ΍ρϳέηϟ΍ϊϣ˯΍ϭϬϟ΍ΓΩ΍ΩγϝΎϣόΗγ΍ϥϛϣϳ˯΍ϭϬϟ΍ΓΩ΍Ωγϥϻ
AR
10
Taking a Measurement
FR
Réalisation d’une mesure
NL
Een meting doen
DE
Vornehmen einer Messung
RU
Выполнение измерений
IT
Misurazione
TR
Ölçüm Yapma
ES
Obtención de una lectura
αΎϳϘϟ΍˯΍έΟ·
AR
When the [START/STOP] button is pressed, the measurement is taken and saved
automatically. Open the app to transfer the reading.
FR
Après une pression sur le bouton [START/STOP], la mesure démarre et le résultat est enregistré
automatiquement. Ouvrir l’application pour transférer le résultat.
DE
Beim Drücken der Taste [START/STOP] erfolgt die Messung. Die Messwerte werden automatisch
gespeichert. Öffnen Sie die App, um die Messwerte zu übertragen.
IT
Quando si preme il pulsante [START/STOP], la misurazione viene eseguita e salvata automaticamente.
Aprire la app per trasferire i risultati.
ES
Al pulsar el botón [START/STOP], se obtiene la medición, que se guarda automáticamente. Abra la
aplicación para transferir la lectura.
NL
Wanneer op de knop [START/STOP] wordt gedrukt, wordt de meting automatisch uitgevoerd en
opgeslagen. Open de app om de meting te versturen.
RU
После того, как кнопка [START/STOP] нажата, измерение выполняется и сохраняется
автоматически. Откройте приложение, чтобы передать результаты.
TR
[START/STOP] düğmesine basıldığında ölçüm yapılır ve otomatik olarak kaydedilir. Ölçüm değerini
aktarmak için uygulamayı açın.
Γ˯΍έϘϟ΍ϝϘϧϟϖϳΑρΗϟ΍΢Ηϓ΍Ύ
˱
ϳ΋ΎϘϠΗϪυϔΣϭαΎϳϘϟ΍˯΍έΟ·ϡΗϳˬ>67$576723@έίϰϠϋρϐοϟ΍Ωϧϋ
AR
9
Selecting User ID (1 or 2)
FR
Sélection de l’ID Utilisateur (1 ou 2)
NL
Gebruikers-ID selecteren (1 of 2)
DE
Auswahl der Benutzer-ID (1 oder 2)
RU
Выберите идентификатор
пользователя (1 или 2)
IT
Selezione dell’ID UTENTE (1 o 2)
TR
Kullanıcı Kimliğini Seçme (1 veya 2)
ES
Selección de ID de usuario (1 o 2)
(˻ϭ΃˺ϙΑΔλΎΧϟ΍ϡΩΧΗγϣϟ΍ΔϳϭϫΩϳΩΣΗ
AR
Switching user ID enables you to save readings for 2 people.
FR
Changer d’ID Utilisateur permet d’enregistrer les résultats pour 2personnes.
DE
Mit verschiedenen Benutzer-IDs lassen sich Messwerte für 2Personen speichern.
IT
Cambiare ID utente permette di registrare i risultati relativi a 2 persone.
ES
Cambiar de ID de usuario le permite guardar las lecturas de 2personas.
NL
Door het wisselen van gebruikers-ID kunt u metingen voor 2 personen opslaan.
RU
Переключение идентификатора пользователя позволяет сохранять результаты для 2-х людей.
TR
Kullanıcı kimlikleri arasında geçiş yapma, 2 kişi için ölçüm değerlerini kaydetmenizi sağlar.
ϥϳλΧηϟΕ΍˯΍έϘϟ΍υϔΣϡΩΧΗγϣϟ΍ϑέόϣϝϳΩΑΗΔϳϧΎϛϣ·ϙϟ΢ϳΗΗ
AR
https://www.omron-healthcare.com/
Manufacturer
Fabricant
Hersteller
Produttore
Fabricante
Fabrikant
Производитель
Üretici
Δόϧλ
˵
ϣϟ΍Δϛέηϟ΍
OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN
EU-representative
Mandataire dans l’UE
EU-Repräsentant
Rappresentante per l’UE
Representante en la UE
Vertegenwoordiging in de EU
Представитель в ЕС
AB temsilcisi
ϲΑϭέϭϷ΍ΩΎ Σ ΗϻΎΑϝ ϳ Λ ϣ Η ϟ΍ΔϬΟ
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp,
THE NETHERLANDS
www.omron-healthcare.com
Importer in EU
Importateur dans l’UE
Importeur in der EU
Importatore per l’UE
Importador en la UE
Importeur in de EU
Импортер в ЕС
AB’de İthalatçı
ϲΑϭέϭϷ΍ΩΎΣΗϻ΍ϲϓΩέϭΗγϣϟ΍
Production facility
Site de production
Produktionsstätte
Stabilimento di produzione
Planta de producción
Productiefaciliteit
Производственное
подразделение
Üretim Tesisi
ϊϳϧλΗϟ΍Γ΄ηϧϣ
OMRON HEALTHCARE MANUFACTURING
VIETNAM CO., LTD.
No.28 VSIP II, Street 2, Vietnam-Singapore Industrial Park II,
Binh Duong Industry-Services-Urban Complex, Hoa Phu Ward,
Thu Dau Mot City, Binh Duong Province, Vietnam
Subsidiaries
Succursales
Niederlassungen
Consociate
Empresas filiales
Dochteronder-
nemingen
Филиалы
Yan Kuruluşlar
ΔόΑΎΗϟ΍ΕΎϛέηϟ΍
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
www.omron-healthcare.com
OMRON MEDIZINTECHNIK
HANDELSGESELLSCHAFT mbH
Konrad-Zuse-Ring 28, 68163 Mannheim, GERMANY
www.omron-healthcare.com
OMRON SANTÉ FRANCE SAS
3, Parvis de la Gare, 94130 Nogent-sur-Marne, FRANCE
Uniquement pour le marché français:
OMRON Service Après Vente
Vert 0 800 91 43 14
www.omron-healthcare.com
Issue Date / Date de publication / Ausgabedatum/
Datadipubblicazione / Fecha de publicación /
Uitgiftedatum / Дата выпуска / Teslim Tarihi /
έ΍ΩλϹ΍ΦϳέΎΗ
: 2019-07-29
Made in Vietnam / Fabriqué en Vietnam / Hergestellt in Vietnam/
Prodottoin Vietnam / Fabricado en Vietnam / Geproduceerd in Vietnam/
Сделано во Вьетнаме / Vietnam’da Üretilmiştir /
ϡΎϧΗϳϓϲϓϊϧλ
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Omron M4 Intelli IT - HEM-7155T-EBK El manual del propietario

Categoría
Unidades de presión arterial
Tipo
El manual del propietario
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