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Instruction Manual 1
Automatic Upper Arm Blood Pressure Monitor
ω΍έΫϟ΍ϰϠϋ΄ΑΕϳΑΛΗϠϟϝΑΎϘϟ΍ϲϟϵ΍ϡΩϟ΍ρϐοαΎϳϗίΎϬΟ
M3 Comfort (HEM-7155-E)
Εέϭϔϣϭϛ3ϡ·
X3 Comfort (HEM-7155-EO)
Εέϭϔϣϭϛ3αϛ΍
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
indicates this via a symbol with the measurement results. It is mainly
designed for general household use.
1.3 Receiving and Inspection
Remove this monitor from the packaging and inspect for damage. If
this monitor is damaged, DO NOT USE and consult with your OMRON
retail outlet or distributor.
2. Important Safety Information
Read the Important Safety Information in this instruction manual
before using this monitor. Follow this instruction manual thoroughly
for your safety.
Keep for future reference. For specific information about your own
blood pressure, CONSULT WITH YOUR PHYSICIAN.
2.1 Warning Indicates a potentially hazardous
situation which, if not avoided, could
result in death or serious injury.
DO NOT use this monitor on infants, toddlers, children or persons
who cannot express themselves.
DO NOT adjust medication based on readings from this blood pressure
monitor. Take medication as prescribed by your physician. ONLY a
physician is qualified to diagnose and treat high blood pressure.
DO NOT use this monitor on an injured arm or an arm under medical
treatment.
DO NOT apply the arm cuff on your arm while on an intravenous
drip or blood transfusion.
DO NOT use this monitor in areas containing high frequency (HF)
surgical equipment, magnetic resonance imaging (MRI) equipment,
computerized tomography (CT) scanners. This may result in incorrect
operation of the monitor and/or cause an inaccurate reading.
DO NOT use this monitor in oxygen rich environments or near
flammable gas.
Consult with your physician before using this monitor if you have
common arrhythmias such as atrial or ventricular premature beats
or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes;
pregnancy; pre-eclampsia or renal disease. NOTE that any of these
conditions in addition to patient motion, trembling, or shivering
may affect the measurement reading.
NEVER diagnose or treat yourself based on your readings. ALWAYS
consult with your physician.
To help avoid strangulation, keep the air tube and AC adapter cable
away from infants, toddlers and children.
This product contains small parts that may cause a choking hazard if
swallowed by infants, toddlers and children.
AC Adapter (optional accessory) Handling and Usage
DO NOT use the AC adapter if this monitor or the AC adapter cable is
damaged. If this monitor or the cable is damaged, turn off the power
and unplug the AC adapter immediately.
Plug the AC adapter into the appropriate voltage outlet. DO NOT
use in a multi-outlet plug.
NEVER plug in or unplug the AC adapter from the electric outlet
with wet hands.
DO NOT disassemble or attempt to repair the AC adapter.
EN2
EN
Battery Handling and Usage
Keep batteries out of the reach of infants, toddlers and children.
2.2 Caution
Indicates a potentially hazardous situation
which, if not avoided, may result in minor
or moderate injury to the user or patient or
damage to the equipment or other property.
Stop using this monitor and consult with your physician if you
experience skin irritation or discomfort.
Consult with your physician before using this monitor on an arm
where intravascular access or therapy, or an arteriovenous (A-V)
shunt, is present because of temporary interference to blood flow
and could result in injury.
Consult with your physician before using this monitor if you have
had a mastectomy.
Consult with your physician before using this monitor if you have severe
blood flow problems or blood disorders as cuff inflation can cause bruising.
DO NOT take measurements more often than necessary because
bruising, due to blood flow interference, may occur.
ONLY inflate the arm cuff when it is applied on your upper arm.
Remove the arm cuff if it does not start deflating during a measurement.
DO NOT use this monitor for any purpose other than measuring
blood pressure.
During measurement, make sure that no mobile device or any other
electrical device that emit electromagnetic fields is within 30 cm of
this monitor. This may result in incorrect operation of the monitor
and/or cause an inaccurate reading.
DO NOT disassemble or attempt to repair this monitor or other
components. This may cause an inaccurate reading.
DO NOT use in a location where there is moisture or a risk of water
splashing this monitor. This may damage this monitor.
DO NOT use this monitor in a moving vehicle such as in a car or on
an aircraft.
DO NOT drop or subject this monitor to strong shocks or vibrations.
DO NOT use this monitor in places with high or low humidity or high
or low temperatures. Refer to section 6.
During measurement, observe the arm to ensure that the monitor is
not causing prolonged impairment to blood circulation.
DO NOT use this monitor in high-use environments such as medical
clinics or physician offices.
DO NOT use this monitor with other medical electrical (ME)
equipment simultaneously. This may result in incorrect operation
and/or cause an inaccurate reading.
Avoid bathing, drinking alcohol or caffeine, smoking, exercising and
eating for at least 30 minutes before taking a measurement.
Rest for at least 5 minutes before taking a measurement.
Remove tight-fitting or thick clothing from your arm while taking a
measurement.
Remain still and DO NOT talk while taking a measurement.
ONLY use the arm cuff on persons whose arm circumference is
within the specified range of the cuff.
Ensure that this monitor has acclimated to room temperature before
taking a measurement. Taking a measurement after an extreme
temperature change could lead to an inaccurate reading. OMRON
recommends waiting for approximately 2 hours for the monitor to
warm up or cool down when the monitor is used in an environment
within the temperature specified as operating conditions after
it is stored either at the maximum or at the minimum storage
temperature. For additional information on operating and storage/
transport temperature, refer to section 6.
DO NOT use this monitor after the durable period has ended. Refer
to section 6.
DO NOT crease the arm cuff or the air tube excessively.
DO NOT fold or kink the air tube while taking a measurement. This
may cause an injury by interrupting blood flow.
To unplug the air plug, pull on the plastic air plug at the base of the
tube, not the tube itself.
ONLY use the AC adapter, arm cuff, batteries and accessories specified
for this monitor. Use of unsupported AC adapters, arm cuffs and
batteries may damage and/or may be hazardous to this monitor.
ONLY use the approved arm cuff for this monitor. Use of other arm
cuffs may result in incorrect readings.
Inflating to a higher pressure than necessary may result in bruising
of the arm where the cuff is applied. NOTE: refer to “If your systolic
pressure is more than 210mmHg in section 13 of instruction
manual for additional information.
Read and follow the “Correct Disposal of This Product” in section 7 when
disposing of the device and any used accessories or optional parts.
EN3
AC Adapter (optional accessory) Handling and Usage
Fully insert the AC adapter into the outlet.
When unplugging the AC adapter from the outlet, be sure to safely
pull from the AC adapter. DO NOT pull from the AC adapter cable.
When handling the AC adapter cable:
Do not damage it. / Do not break it. / Do not tamper with it.
DO NOT pinch it. / Do not forcibly bend or pull it. / Do not twist it.
DO NOT use it if it is gathered in a bundle.
DO NOT place it under heavy objects.
Wipe any dust off of the AC adapter.
Unplug the AC adapter when not in use.
Unplug the AC adapter before cleaning this monitor.
Battery Handling and Usage
DO NOT insert batteries with their polarities incorrectly aligned.
ONLY use 4 AA” alkaline or manganese batteries with this monitor.
DO NOT use other types of batteries. DO NOT use new and used
batteries together. DO NOT use different brands of batteries
together.
Remove batteries if this monitor will not be used for a long period of
time.
If battery fluid should get in your eyes, immediately rinse with
plenty of clean water. Consult with your physician immediately.
If battery fluid should get on your skin, wash your skin immediately
with plenty of clean, lukewarm water. If irritation, injury or pain
persists, consult with your physician.
DO NOT use batteries after their expiration date.
Periodically check batteries to ensure they are in good working
condition.
2.3 General Precautions
To stop a measurement, press the [START/STOP] button while taking
a measurement.
When you take a measurement on the right arm, the air tube should
be at the side of your elbow. Be careful not to rest your arm on the
air tube.
Blood pressure may differ between the right and left arm, and
may result in a different measurement value. Always use the same
arm for measurements. If the values between both arms differ
substantially, check with your physician on which arm to use for
your measurements.
When using an optional AC adapter, make sure not to place your
monitor in a location where it is difficult to plug and unplug the
ACadapter.
Battery Handling and Usage
Disposal of used batteries should be carried out in accordance with
local regulations.
The supplied batteries may have a shorter life span than new
batteries.
Remember to have a record of your blood pressure and pulse
readings for your physician. A single measurement does not provide
an accurate indication of your true blood pressure.
Please use the Blood Pressure Diary to keep records of several
readings over a certain period of time. To download PDF files of the
diary, visit www.omron-healthcare.com.
EN4
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 5 of instruction manual .
Air is leaking from the arm cuff. Replace the arm cuff to the new one. Refer to section 12 of
instruction manual .
appears or a
measurement
cannot be
completed after the
arm cuff inflates.
You move or talk during a measurement
and the arm cuff does not inflate
sufficiently.
Remain still and do not talk during a measurement. If “E2”
appears repeatedly, inflate the arm cuff manually until the
systolic pressure is 30 to 40 mmHg above your previous
readings. Refer to section 11 of instruction manual .
Due to the systolic pressure is above
210mmHg, a measurement cannot
be taken.
appears
The arm cuff is inflated exceeding the
maximum allowable pressure.
Do not touch the arm cuff and/or bend the air tube while taking
a measurement. If inflating the arm cuff manually, refer to
section 11 of instruction manual .
appears You move or talk during a measurement.
Vibrations disrupt a measurement.
Remain still and do not talk during a measurement.
appears The pulse rate is not detected correctly. Apply the arm cuff correctly, then take another measurement.
Refer to section 5 of instruction manual . Remain still and
sit correctly during a measurement.
If the symbol continues to appear, we recommend you to
consult with your physician.
//
appears
does not flash during
a measurement
EN5
Display/Problem Possible Cause Solution
appears The monitor has malfunctioned. Press the [START/STOP] button again. If “Er still appears, contact
your OMRON retail outlet or distributor.
flashes Batteries are low. Replacing all 4 batteries with new ones is recommended. Refer
to section 3 of instruction manual .
appears or the
monitor is turned
off unexpectedly
during a
measurement
Batteries are depleted. Immediately replace all 4 batteries with new ones. Refer to
section 3 of instruction manual .
Nothing appears on the
display of the monitor. Battery polarities are not properly
aligned.
Check the battery installation for proper placement. Refer to
section 3 of instruction manual .
Readings appear too high or
too low.
Blood pressure varies constantly. Many factors including stress, time of day, and/or how you apply the arm
cuff, may affect your blood pressure. Review section 2 of instruction manual .
Any other problem occurs.
Press the [START/STOP] button to turn the monitor off, then press it again to take a measurement.
If the problem continues, remove all batteries and wait for 30 seconds. Then re-install batteries.
If the problem still persists, contact your OMRON retail outlet or distributor.
EN6
EN
4. Limited Warranty
Thank you for buying an OMRON product. This product is constructed of high quality materials and great care has been taken in its manufacturing.
It is designed to give you every satisfaction, provided that it is properly operated and maintained as described in the instruction manual.
This product is warranted by OMRON for a period of 5 years after the date of purchase. The proper construction, workmanship and materials of
this product is warranted by OMRON. During this period of warranty OMRON will, without charge for labour or parts, repair or replace the defect
product or any defective parts.
The warranty does not cover any of the following:
A. Transport costs and risks of transport.
B. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.
C. Periodic check-ups and maintenance.
D. Failure or wear of optional parts or other attachments other than the main device itself, unless explicitly warranted above.
E. Costs arising due to non-acceptance of a claim (those will be charged for).
F. Damages of any kind including personal caused accidentally or from misuse.
G. Calibration service is not included within the warranty.
H. Optional parts have a one (1) year warranty from date of purchase. Optional parts include, but are not limited to the following items: cuff and
cuff tube.
Should warranty service be required please apply to the dealer whom the product was purchased from or an authorised OMRON distributor. For
the address refer to the product packaging / literature or to your specialised retailer. If you have difficulties in finding OMRON customer services,
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) M3 Comfort (HEM-7155-E)
X3 Comfort (HEM-7155-EO)
Display LCD digital display
Cuff pressure range 0 to 299mmHg
Pulse measurement range
40 to 180 beats / min.
Blood pressure measurement range
SYS: 60 to 260mmHg / DIA: 40 to 215mmHg
Accuracy Pressure: ±3mmHg / Pulse: ±5% of display reading
Inflation Automatic by electric pump Deflation
Automatic pressure release valve
Measurement method Oscillometric method Operating mode Continuous operation
IP classification Monitor: IP20 / Optional AC adapter: IP21 (HHP-CM01) or IP22 (HHP-BFH01)
Rating DC6 V 4.0W Applied part Type BF (arm cuff)
Power source
4 AA batteries 1.5V or optional AC adapter (INPUT AC 100 - 240V 50 - 60Hz 0.12 - 0.065A)
Battery life Approximately 1000 measurements (using new alkaline batteries)
Durable period (Service life) Monitor: 5 years / Cuff: 5 years / Optional AC adapter: 5 years
Operating conditions +10 to +40°C / 15 to 90% RH (non-condensing) / 800 to 1060hPa
Storage / Transport conditions -20 to +60°C / 10 to 90% RH (non-condensing)
Contents Monitor, arm cuff (HEM-FL31), 4 AA batteries, storage case, Instruction Manual and
Protection against electric shock Internally powered ME equipment (when using only batteries)
Class II ME equipment (optional AC adapter)
Weight Monitor: approximately 337g (not including batteries) / Arm cuff: approximately 163g
Dimensions (approximately value) Monitor: 105mm (W) × 85mm (H) × 152mm (L)
Arm cuff: 145mm × 532mm (air tube: 750mm)
Memory Stores up to 60 readings per user
EN9
Note
These specifications are subject to change without notice.
This monitor is clinically investigated according to the requirements of EN ISO 81060-2:2014 and complies with EN ISO 81060-2:2014 and
EN ISO 81060-2:2019 + A1:2020. In the clinical validation study, K5 was used on 85subjects for determination of diastolic blood pressure.
This device has been validated for use on pregnant and pre-eclampsia patients according to the Modified European Society of Hypertension
Protocol*.
This device has been validated for use on diabetic (Type II) population**.
IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This monitor and optional AC adapter are
protected against solid foreign objects of 12.5 mm diameter and greater such as a finger. The optional AC adapter HHP-CM01 is protected
against vertically falling water drops which may cause issues during a normal operation. The optional AC adapter HHP-BFH01 is protected
against oblique falling water drops which may cause issues during a normal operation.
* Topouchian J et al. Vascular Health and Risk Management 2018:14 189–197
** Chahine M.N. et al. Medical Devices: Evidence and Research 2018:11 11–20
7. Correct Disposal of This Product (Waste Electrical & Electronic Equipment)
This marking shown on the product or its literature, indicates that it should not be disposed of, with other household wastes at the
end of its working life.
To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate this product from
other types of wastes and recycle it responsibly to promote the sustainable reuse of material resources.
Household users should contact either the retailer where they purchased this product, or their local government office, for details of
where and how they can return this item for environmentally safe recycling.
Business users should contact their supplier and check the terms and conditions of the purchase contract. This product should not be mixed with
other commercial waste for disposal.
8. Important Information Regarding Electromagnetic Compatibility (EMC)
HEM-7155-E and HEM-7155-EO conform to EN60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at
www.omron-healthcare.com
Refer to the EMC information for HEM-7155-E and HEM-7155-EO on the website.
9. Guidance and Manufacturer’s Declaration
This blood pressure monitor is designed according to the European Standard EN1060, Non-invasive sphygmomanometers Part 1: General
Requirements and Part 3: Supplementary requirements for electromechanical blood pressure measuring systems.
This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan. The Core component for OMRON
blood pressure monitors, which is the Pressure Sensor, is produced in Japan.
Please report to the manufacturer and the competent authority of the Member State in which you are established about any serious incident
that has occurred in relation to this device.
EN10
EN
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
CEΔϳΑϭέϭϷ΍
SD2
UKCA marking
FR Marquage UKCA
DE UKCA-Kennzeichnung
IT Marchio UKCA
ES Marcado UKCA
NL UKCA-markering
RU Маркировка UKCA
TR UKCA işareti
ιΎΧϟ΍ϖϓ΍ϭΗϟ΍ϡϳϳϘΗΔϣϼϋ AR
ΓΩΣΗϣϟ΍ΔϛϠϣϣϟΎΑ
Serial number
FR Numéro de série
DE Seriennummer
IT Numero di serie
ES Número de serie
NL Serienummer
RU Серийный номер
TR Seri numarası
ϝγϠγΗϣϟ΍ϡϗέϟ΍ AR
LOT number
FR Numéro de LOT
DE LOT-Nummer
IT Numero di lotto
ES Número de lote
NL Partijnummer
RU Код (номер) партии
TR Parti numarası
ΔϠϳϐηΗϟ΍ϡϗέ AR
UDI Unique device identifier
FR Identifiant unique des
dispositifs
DE Produktidentifizie-
rungsnummer
IT Identificatore univoco
del dispositivo
ES Identificador único del
producto
NL Unieke apparaat-ID
RU Уникальный
идентификатор устройства
TR Benzersiz cihaz
tanımlayıcısı
Ωϳέϔϟ΍ίΎϬΟϟ΍ϑ ˷
έόϣ AR
Medical device
FR Dispositif médical
DE Medizinprodukt
IT Dispositivo medico
ES Producto sanitario
NL Medisch apparaat
RU Медицинский прибор
TR Tıbbi cihaz
ϲΑρίΎϬΟ AR
Temperature limitation
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
SD3
For indoor use only
FR Pour un usage à
l’intérieur uniquement
DE Nur für die Nutzung in
Innenbereichen
IT Solo per uso in interni
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΍
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΍
SD4
,
Manufacturer’s quality control mark
FR Marque de contrôle de
la qualité du fabricant
DE Qualitätskontroll-
zeichen des Herstellers
IT Contrassegno controllo
qualità del produttore
ES Marca del control de
calidad del fabricante
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
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΍
SD5
Need for the user to follow this instruction
manual thoroughly for your safety.
FR L’utilisateur doit suivre
attentivement ce mode
d’emploi pour votre sécurité.
DE Damit die Sicherheit
gewährleistet ist, muss
der Benutzer diese
Gebrauchsanweisung
sorgfältig befolgen.
IT Per la propria sicurezza,
l’utente deve seguire
attentamente il presente
manuale di istruzioni.
ES Es necesario que el
usuario siga rigurosamente
este manual de instrucciones
para su seguridad.
NL Noodzaak voor de
gebruiker om zich voor de
eigen veiligheid zorgvuldig
aan deze gebruiksaanwijzing
te houden.
RU В целях обеспечения
безопасности строго
следуйте указаниям в
данном руководстве по
эксплуатации.
TR Güvenlik açısından
kullanıcının bu kullanım
kılavuzuna dikkatle uyması
gerekir.
ωΎΑΗ΍ϰϟ·ϡΩΧΗγϣϟ΍ΔΟΎΣ AR
ϝϳϟΩϲϓΓΩέ΍ϭϟ΍Ε΍ΩΎηέϹ΍
υΎϔΣϠϟ΍ΫϫϝϣΎϛϟΎΑΕ΍ΩΎηέϹ΍
Δϣϼγϟ΍ϰϠϋ
Direct current
FR Courant continu
DE Gleichstrom
IT Corrente diretta
ES Corriente directa
NL Gelijkstroom
RU Постоянный ток
TR Doğru akım
έηΎΑϣϟ΍έΎϳΗϟ΍ AR
Alternating current
FR Courant alternatif
DE Wechselstrom
IT Corrente alternata
ES Corriente alterna
NL Wisselstroom
RU Переменный ток
TR Alternatif akım
ΏϭΎϧΗϣϟ΍έΎϳΗϟ΍ AR
Date of manufacture
FR Date de fabrication
DE Herstellungsdatum
IT Data di fabbricazione
ES Fecha de fabricación
NL Productiedatum
RU Дата изготовления
TR Üretim tarihi
ϊϳϧλΗϟ΍ΦϳέΎΗ AR
Prohibited action
FR Action interdite
DE Verbotene Aktion
IT Operazione proibita
ES Acción prohibida
NL Verboden handeling
RU
Запрещенные действия
TR Yasaklanmış eylem
έϭυΣϣ˯΍έΟ· AR
SD6
Issue Date:
2022-05-25
Date de publication:
Ausgabedatum:
Data di pubblicazione:
Fecha de publicación:
Uitgiftedatum:
Дата выпуска:
Teslim Tarihi:
έ΍ΩλϹ΍ΦϳέΎΗ
IM1-HEM-7155-E-05-01/2022
2870433-4D
IM2-HEM-7155-E-05-01/2022
2870434-2D
Instruction Manual 2
1
Instruction Manual
Instruction Manual
2.3
Automatic Upper Arm Blood Pressure Monitor
ω΍έΫϟ΍ϰϠϋ΄ΑΕϳΑΛΗϠϟϝΑΎϘϟ΍ϲϟϵ΍ϡΩϟ΍ρϐοαΎϳϗίΎϬΟ
M3 Comfort (HEM-7155-E)
Εέϭϔϣϭϛ3ϡ·
X3 Comfort (HEM-7155-EO)
Εέϭϔϣϭϛ3αϛ΍
Read Instruction manual and before use.
FR Lire le mode d’emploi et avant l’utilisation.
DE Lesen Sie vor der Verwendung die Gebrauchsanweisung und .
IT Leggere il manuale di istruzioni e prima dell’uso.
ES Lea el manual de instrucciones y antes del uso.
NL Lees de gebruiksaanwijzing en voor gebruik.
RU
Прочтите руководство по эксплуатации и перед использованием.
TR Kullanmadan önce, kullanım kılavuzu ve 'yi okuyun.
ϡ΍ΩΧΗγϻ΍ϝΑϗ ϭ Ε΍ΩΎηέϹ΍ϝϳϟΩ΃έϗ΍
AR
1Package Contents
FR Contenu de l’emballage NL Inhoud van de verpakking
DE Packungsinhalt RUКомплект поставки
IT Contenuto della confezione TR Paketin İçindekiler
ES Contenido del envase ΓϭΑόϟ΍ΕΎϳϭΗΣϣ 
AR
1
Instruction Manual
Instruction Manual2
2Preparing for a Measurement
FR Préparation d’une mesure NL Een meting voorbereiden
DE Vorbereiten einer Messung RUПодготовка 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
RUЗа 30 минут до
TR 30 dakika önce
ΔϘϳϗΩ˼˹ώϠΑΗ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.
RUЗа 5 минут до: расслабьтесь и отдохните.
TR 5 dakika önce: Gevşeyin ve dinlenin.
˶ΥέΗγ΍ϭΡέΗγ΍ϖ΋ΎϗΩ˾ώϠΑΗΓΩϣΑαΎϳϘϟ΍ϝΑϗ
AR
5Applying the Cuff on the Left Arm
FR Pose du brassard sur le bras gauche NL De manchet op de linkerarm aanbrengen
DE Anbringen der Manschette am linken Arm RUРасположение 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


A
B
Click
ATube side of the cuff should be 1 - 2 cm above the inside elbow.
FR Le côté tuyau du brassard doit être positionné 1 à 2cm au-dessus de l’intérieur du coude.
DE Das Manschettenstück mit dem Schlauch muss 1 bis 2cm oberhalb des Ellbogens liegen.
IT
Il lato del bracciale con il tubo deve trovarsi al di sopra dell’interno del gomito, a una distanza di circa 1 o 2 cm.
ES El lado del tubo del manguito deberá quedar 1 o 2cm por encima de la parte interna del codo.
NL De kant met de slang van de manchet moet 1 - 2 cm boven de binnenkant van de elleboog liggen.
RUКрай манжеты с трубкой должен находиться на 1–2 см выше локтевого сгиба.
TR Kolluğun boru tarafı, dirsek içinin 1 ila 2 cm üstünde olmalıdır.
ϖϓέϣϟ΍ϥϋϡγ˻ϰϟ·˺ϥϣρϏΎοϟ΍ρϳέηϟ΍ϥϣϡϭρέΧϟ΍ΏϧΎΟϊϔΗέϳϥ΃ΏΟϳ 
AR
BMake sure that air tube is on the inside of your arm and wrap the cuff
securely so it can no longer slip round.
FR 
Assurez-vous que le tuyau à air se trouve du côté intérieur de votre bras et enroulez fermement le brassard de manière qu’il ne puisse plus tourner.
DE 
Stellen Sie sicher, dass der Luftschlauch an der Arminnenseite sitzt, und befestigen Sie die Manschette sicher, so dass sie nicht verrutscht.
IT 
Assicurarsi che il tubo dell’aria si trovi all’interno del braccio e avvolgere il bracciale saldamente in modo che non possa ruotare.
ES 
Asegúrese de que el tubo de aire se encuentra en la cara interna del brazo y enrolle el manguito con firmeza para que no pueda deslizarse.
NL 
Zorg ervoor dat de luchtslang zich aan de binnenkant van uw arm bevindt en wikkel de manchet stevig rond uw
arm zodat deze niet meer kan wegglijden.
RU
Убедитесь, что воздуховодная трубка находится на внутренней поверхности плеча и надежно оберните
манжету, чтобы она не прокручивалась вокруг руки.
TR 
Hava borusunun kolunuzun iç tarafında olduğundan emin olun ve kolluğu kaymayacak şekilde sabit şekilde sarın.
ω΍έΫϟ΍ϝϭΣϖϟίϧϳϻΙϳΣΑϡΎϛΣΈΑρϏΎοϟ΍ρϳέηϟ΍ϑϟϭϙϋ΍έΫϥϣϲϠΧ΍Ωϟ΍ΏϧΎΟϟ΍ϰϠϋ˯΍ϭϬϟ΍ϡϭρέΧϥ΃ϥϣΩϛ΄Η 
AR
3Installing Batteries
FR Mise en place des piles NL Batterijen plaatsen
DE Einsetzen der Batterien RUУстановка элементов питания
IT Installazione delle batterie TR Pillerin Takılması
ES Instalación de las pilas ΕΎϳέΎρΑϟ΍ΏϳϛέΗ
AR
AA, 1.5V × 4
6Sitting Correctly
FR Position assise correcte NL Correct zitten
DE Korrekte Körperhaltung RUСядьте правильно
IT Come sedere nel modo corretto TR Düzgün Oturma
ES Cómo sentarse correctamente ΢ϳΣλϝϛηΑαϭϠΟϟ΍ 
AR
Sit comfortably with your back and arm supported.
FR 
6DVVHRLUFRQIRUWDEOHPHQWGHPDQLqUHjFHTXHOHGRVHWOHEUDVVRLHQWELHQVRXWHQXV
DE 
%HTXHPKLQVHW]HQPLWGHP5FNHQDQOHKQHQXQGGHQ$UPDXIHLQH8QWHUODJHOHJHQ
IT 
6HGHUHFRPRGDPHQWHFRQODVFKLHQDHLOEUDFFLREHQVRVWHQXWL
ES 
6LpQWHVHFyPRGDPHQWHGHPRGRTXHODHVSDOGD\HOEUD]RHVWpQELHQDSR\DGRV
NL 
1HHPHHQFRPIRUWDEHOH]LWSRVLWLHLQPHWXZUXJHQDUPRQGHUVWHXQG
RU
ɋɹɞɶɬɟɭɞɨɛɧɨɱɬɨɛɵɫɩɢɧɚɢɪɭɤɚɨɩɢɪɚɥɢɫɶɧɚɱɬɨɥɢɛɨ
TR 
6ÕUWÕQÕ]YHNROXQX]GHVWHNOHQHUHNUDKDWELUúHNLOGHRWXUXQ
ΩΎϧΗγ΍ϊοϭϲϓω΍έΫϟ΍ϭέϬυϟ΍ϥϭϛϳΙϳΣΑ΢ϳέϣϝϛηΑαϠΟ΍ 
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 8
7Selecting User ID (1 or 2)
FR
Sélection de l’ID Utilisateur (1 ou 2)
NL
Gebruikers-ID selecteren (1 of 2)
DE
Auswahl der Benutzer-ID (1 oder 2)
RU
Выберите идентификатор пользователя (1 или 2)
IT
Selezione dell’ID UTENTE (1 o 2)
TR
Kullanıcı Kimliğini Seçme (1 veya 2)
ES
Selección de ID de usuario (1 o 2)
(˻ϭ΃˺ϙΑΔλΎΧϟ΍ϡΩΧΗγϣϟ΍ΔϳϭϫΩϳΩΣΗ 
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
4Setting Date and Time
FR Réglage de la date et de l’heure NL Datum en tijd instellen
DE Einstellen von Datum und Uhrzeit RUУстановка даты и времени
IT Impostazione di data e ora TR Tarih ve Saatin Ayarlanması
ES Ajuste de la fecha y la hora ΦϳέΎΗϟ΍ϭΕϗϭϟ΍ρΑο AR
Set year > month > day > hour > minute.
FR Réglez l’année > le mois > le jour > les heures > les minutes.
DE Stellen Sie Jahr > Monat > Tag > Stunde > Minute ein.
IT Impostare anno > mese > giorno > ora > minuti.
ES Ajuste de año > mes > día > hora > minuto.
NL Instellen van jaar > maand > dag > uur > minuut.
RUУстановите год > месяц > день > час > минута.
TR Yıl > ay > gün > saat > dakika ayarlayın.
ΔϘϳϗΩϟ΍ΔϋΎγϟ΍ϡϭϳϟ΍έϬηϟ΍ϡΎόϟ΍ρΑο AR
Year
Month
Day
Hour
Minute
Back / Forward
FR Arrière / Avant
DE Zurück / Vorwärts
IT Indietro / Avanti
ES Atrás / Adelante
NL Terug / vooruit
RUНазад / Вперед
TR İleri / Geri
ϡΩϘΗϟ΍ωϭΟέϟ΍
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
1
Instruction Manual
Instruction Manual
3.
9Checking Readings
FR Vérication des résultats NL Metingen bekijken
DE Prüfen der Messwerte RU 
IT Controllo dei risultati TR Ölçüm Değerlerini Kontrol Etme
ES Comprobación de lecturas Ε΍˯΍έϘϟ΍ϥϣϖϘΣΗϟ΍ 
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
Ɉɬɨɛɪɚɠɚɟɬɫɹɟɫɥɢ©6<6ªɦɦɪɬɫɬ
ɢɜɵɲɟɢɢɥɢ©',$ªɦɦɪɬɫɬɢɜɵɲɟ
TR 
“SYS” 135 mmHg ya da üstünde olduğunda
ve/veya “DIA 85 mmHg* ya da üstünde
olduğunda görünür.
έΛϛ΃ϭ΃Ύ˱ϳϘΑ΋ί΍˱
έΗϣϳϠϠϣ˺˼˾ώϠΑϳ6<6ϥΎϛϝΎΣϲϓέϬυΗ 
AR
έΛϛ΃ϭ΃Ύ˱ϳϘΑ΋ί΍˱
έΗϣϳϠϠϣ́˾',$ϭ΃ϭ
2Appears when an irregular rhythm** is detected during a measurement.
If it appears repeatedly, OMRON recommends to consult your physician.
FR 
S’affiche lorsqu’un rythme irrégulier** est détecté pendant une mesure. S’il s’affiche
àplusieurs reprises, OMRON recommande de consulter votre médecin.
DE
Wird angezeigt, wenn während einer Messung ein unregelmäßiger Herzschlag** festgestellt
wird. Wird das Symbol wiederholt angezeigt, empfiehlt OMRON, sich an Ihren Arzt zu wenden.
IT 
Viene visualizzato se nel corso di una misurazione viene rilevato un ritmo cardiaco irregolare**.
Seil simbolo appare ripetutamente, OMRON consiglia di consultare il medico curante.
ES 
Aparece cuando se detecta un ritmo irregular** durante una medición. Si aparece varias
veces, OMRON recomienda que consulte a su médico.
NL 
Verschijnt wanneer tijdens een meting een onregelmatig ritme** wordt gedetecteerd. Als dit
herhaaldelijk verschijnt, raadt OMRON aan om uw arts te raadplegen.
RU
,      **.   
 ,  OMRON     .
TR 
Bir ölçüm esnasında düzensiz ritim** saptandığında görünür. Tekrarlı şekilde görünürse
OMRON doktorunuza danışmanızı önerir.
ϙΑϳΑρΓέΎηΗγΎΑ20521ϲλϭΗˬέέϛΗϣϝϛηΑΎϫέϭϬυΩϧϋαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓΏϠϘϟ΍ΕΎΑέοϡΎυΗϧ΍ϡΩϋϑΎηΗϛ΍ΩϧϋέϬυΗ
AR
3Appears 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 3minutes et essayer à nouveau.
DE
Wird angezeigt, wenn Sie sich während der Messung bewegen. Nehmen Sie die Manschette ab,
warten Sie 2–3Minuten und versuchen Sie es erneut.
IT 
Viene visualizzato se l’utilizzatore si muove durante la misurazione. Rimuovere il bracciale,
attendere 2-3 minuti e riprovare.
ES 
Aparece cuando se mueve el cuerpo durante una medición. Retire el manguito, espere unos
2o3minutos e inténtelo de nuevo.
NL
Verschijnt wanneer uw lichaam tijdens een meting beweegt. Verwijder de armmanchet,
wacht2-3minuten en probeer het opnieuw.
RU
      .  , 
2-3    .
TR 
Bir ölçüm esnasında vücudunuz hareket ettiğinde görünür. Kolluğu çıkarın, 2-3 dakika bekleyip
tekrar deneyin.
ϯέΧ΃ΓέϣΔϟϭΎΣϣϟ΍ϭϖ΋ΎϗΩ˼ϰϟ·˻ϥϣέΎυΗϧϻ΍ϭω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍Δϟ΍ίΈΑϡϗαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϙϣγΟϙέΣΗΩϧϋέϬυΗ 
AR
4Cu is tight enough.
FR Le brassard est suffisamment serré.
DE Manschette sitzt ausreichend straff.
IT Il bracciale è stretto a sufficienza.
ES El manguito está lo suficientemente prieto.
NL Manchet zit strak genoeg.
RUɆɚɧɠɟɬɚɡɚɬɹɧɭɬɚɞɨɫɬɚɬɨɱɧɨɬɭɝɨ
TR Kolluk yeterince sıkıdır.
ϲϔϛϳΎϣΑϡϛΣϣρϏΎοϟ΍ρϳέηϟ΍ 
AR
4Apply cu again MORE TIGHTLY.
FR 
Poser le brassard en le serrant davantage.
DE 
Manschette STRAFFER ziehen.
IT 
Applicare di nuovo il bracciale
STRINGENDOLO DI PIÙ.
ES

Vuelva a poner el manguito MÁS PRIETO.
NL 
Breng de manchet STRAKKER aan.
RU

ɇɚɥɨɠɢɬɟɦɚɧɠɟɬɭɟɳɟɪɚɡȻɈɅȿȿɌɍȽɈ
TR

Kolluğu tekrar, DAHA SIKI bir şekilde takın.
Ύ˱ϣΎϛΣ·έΛϛ΃ϝϛηΑϯέΧ΃ΓέϣρϏΎοϟ΍ρϳέηϟ΍ϑϟ 
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*       2018 ESH/ESC.
TR *Yüksek kan basıncı tanımı, 2018 ESH/ESC Kılavuzlarını temel alır.
.ϡΎόϟESCΏϠϘϟ΍ΏρϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍ESHϡΩϟ΍ρϐορέϔϟΔϳΑϭέϭϷ΍ΔϳόϣΟϟ΍Ε΍ΩΎηέ·ϰϟ·ΩϧΗγϳϊϔΗέϣϟ΍ϡΩϟ΍ρϐοϑϳέόΗ 
AR
** An irregular heartbeat rhythm is defined as a rhythm that is 25% less or 25%
more than the average rhythm detected during a measurement.
FR 
** Un rythme cardiaque irrégulier est défini comme un rythme inférieur ou supérieur de 25% au
rythme moyen détecté durant une mesure.
DE 
** Ein unregelmäßiger Herzschlag ist definiert als ein Herzrhythmus, der weniger als 25% oder mehr
als 25% des mittleren Herzrhythmus beträgt, der während der Blutdruckmessung erkannt wird.
IT 
** Si definisce ritmo cardiaco irregolare un ritmo cardiaco inferiore del 25% o superiore del 25%
rispetto al ritmo medio rilevato durante una misurazione.
ES 
** Latido arrítmico se define como un ritmo que es un 25% menor o un 25% mayor que el ritmo
medio detectado durante una medición.
NL 
** Een onregelmatig hartslagritme wordt gedefinieerd als een ritme dat 25% lager of 25% hoger is dan
het gemiddelde ritme dat tijdens een meting wordt gedetecteerd.
RU
**    —  ,   25%   
  .
TR 
** Düzensiz kalp atışı ritmi, bir ölçüm sırasında saptanan ortalamadan %25 daha düşük veya %25 daha
yüksek ritim olarak tanımlanır.
̃˻˾ϝΩόϣΑϪϧϣέΛϛ΃ϭ΃̃˻˾ϝΩόϣΑαΎϳϘϟ΍ΔϳϠϣϋ˯ΎϧΛ΃ϲϓϪϓΎηΗϛ΍ϡΗϳϱΫϟ΍ϲόϳΑρϟ΍ϡ˸υϧϟ΍ϥϣϝϗ΃ϡ˸υϧϪϧ΄ΑΏϠϘϟ΍ΕΎΑέοΏ΍έρο΍ϑέό˵ϳ 
AR
10
Using Memory Functions
FR
Utilisation des fonctions de mémoire NL
Geheugenfuncties gebruiken
DE
Verwendung der Speicherfunktionen RU
  
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

      .
TR
Hafıza fonksiyonunu kullanmadan önce kullanıcı kimliğinizi seçin.
ϙΑιΎΧϟ΍ϡΩΧΗγϣϟ΍ϑέόϣΩΩΣˬΓέϛ΍Ϋϟ΍ϑ΋Ύυϭϡ΍ΩΧΗγ΍ϝΑϗ 
AR
10.1 Readings Stored in Memory
FR Mesures stockées en mémoire
DE Gespeicherte Messungen
IT Risultati conservati in memoria
ES Lecturas guardadas en la memoria
NL Meetwaarden opgeslagen in het geheugen
RU   
TR Hafızada Saklanan Ölçüm Değerleri
Γέϛ΍Ϋϟ΍ϲϓΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ 
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 meetwaarden
worden opgeslagen.
RU
 
60.
TR 
60 adede kadar ölçüm
değeri saklanır.
ΔϧίΧϣϟ΍Ε΍˯΍έϘϟ΍ΩΩϋϝλϳ 
AR
Γ˯΍έϗ˿˹ϰϟ·
10.2
Average of the Latest 2 or 3 Readings Taken
within a 10 Minute Span
FR 
Moyenne des 2 ou 3 dernières mesures prises en l’espace de 10minutes
DE
Mittelwert der letzten 2 oder 3Messwerte, die in einem 10-Minuten-
Zeitrahmen erfasst wurden
IT 
Media degli ultimi 2 o 3 risultati ottenuti nell’arco di 10 minuti
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
    2-  3- ,
   10 
TR 
10 Dakika Aralıkta Alınan Son 2 veya 3 Ölçüm Değerinin Ortalaması
ϖ΋ΎϗΩ˺˹ώϠΑΗΔϳϧϣίΓΩϣϲϓΎϬϳϠϋϝϭλΣϟ΍ϡΗΕ΍˯΍έϗ˼ϭ΃ϥϳΗ˯΍έϗέΧ΁ργϭΗϣ 
AR
3 sec+
10.3 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
  
TR 
Tüm Ölçüm Değerlerini Silme
Ε΍˯΍έϘϟ΍ϊϳϣΟϑΫΣ 
AR
4sec+ 4sec+
  
11
Other Settings
FR
Autres réglages NL
Andere instellingen
DE
Weitere Einstellungen RU
 
IT
Altre impostazioni TR
Diğer Ayarlar
ES
Otros ajustes ϯέΧϷ΍Ε΍Ω΍ΩϋϹ΍ 
AR
11.1 Restoring to the Default Settings
FR Réinitialisation aux réglages par défaut
DE Wiederherstellen der Standardeinstellungen
IT Ripristino delle impostazioni predefinite
ES Restablecimiento a los ajustes de fábrica
NL De standaardinstellingen herstellen
RU   
TR Varsayılan Ayarları Geri Yükleme
Δϳο΍έΗϓϻ΍Ε΍Ω΍ΩϋϹ΍ΓΩΎόΗγ΍
AR
4sec+
 
4sec+
12
Optional Medical Accessories
FR
Accessoires médicaux optionnels NL
Optionele medische accessoires
DE
Optionales medizinisches Zubehör RU
 
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 cu.
FR 
Ne pas jeter la prise de gonflage. La prise de
gonflage peut être utilisée pour le brassard
enoption.
DE 
Entsorgen Sie den Luftschlauchstecker nicht.
Der Luftschlauchstecker wird für die optionale
Manschette verwendet.
IT 
Non gettare via l’attacco del tubo dell’aria.
L’attacco del tubo dell’aria può essere applicato
al bracciale opzionale.
ES 
No tire el conector para tubo de aire. El conec-
tor para tubo de aire puede ser utilizado con el
manguito opcional.
NL 
Gooi de plug van de luchtslang niet weg. De
plug van de luchtslang kan worden gebruikt op
de optionele manchet.
RU
   . 
    .
TR 
Hava tıpasını atmayın. Hava tıpası steğe bağlı
kolluğa uygulanablr.
˯΍ϭϬϟ΍ΓΩ΍ΩγϝΎϣόΗγ΍ϥϛϣϳ˯΍ϭϬϟ΍ΓΩ΍ΩγϥϣιϠΧΗΗϻ
AR
ϱέΎϳΗΧϻ΍ρϏΎοϟ΍ρϳέηϟ΍ϊϣ
Error messages or other problems? Refer to:
FR Messages d’erreur ou autres problèmes? Voir:
DE Weitere Fehlermeldungen oder Probleme siehe:
IT Messaggi di errore o altri problemi? Fare riferimento a:
ES ¿Hay mensajes de error u otros problemas? Consulte:
NL Foutmeldingen of andere problemen? Raadpleeg:
RU
     ? :
TR Hata mesajları veya başka sorunlar mı var? Bkz:
ϰϟ·ϊΟέ΍ˮϯέΧϷ΍Εϼϛηϣϟ΍ϭ΃΄ρΧϟ΍ϝ΋Ύγέ
AR
If your systolic pressure is more than 210 mmHg:
After the arm cuff starts to inflate, press and hold the [START/STOP] button until the monitor
inflates 30 to 40 mmHg higher than your expected systolic pressure.
FR 
Si votre pression systolique est supérieure à 210mmHg: Lorsque le brassard
se gonfle, appuyer sur le bouton [START/STOP] et le maintenir enfoncé jusqu’à ce que
le tensiomètre atteigne une pression de gonflage supérieure de 30 à 40mmHg à votre
pression systolique attendue.
DE 
Wenn Ihr systolischer Druck höher ist als 210mmHg: Nachdem die Manschette
begonnen hat, sich aufzupumpen, drücken Sie die [START/STOP]-Taste, und halten Sie sie
gedrückt, bis ein Druck von 30 bis 40mmHg über Ihrem erwarteten systolischen Druck
erreicht ist.
IT 
Se la pressione sistolica è superiore a 210 mmHg: Quando il bracciale inizia a
gonfiarsi, premere e mantenere premuto il pulsante [START/STOP] finché il misuratore
non raggiunge una pressione da 30 a 40 mmHg superiore rispetto al valore di pressione
sistolica atteso.
ES 
En caso de que su presión arterial sistólica esté por encima de 210mmHg:
Una vez que el manguito comience a inflarse, mantenga pulsado el botón [START/STOP]
hasta que el monitor indique que el inflado está entre 30 y 40mmHg por encima de la
presión arterial sistólica estimada.
NL 
Als uw systolische druk hoger is dan 210 mmHg: Zodra de armmanchet wordt opgepompt,
houdt u de knop [START/STOP] ingedrukt totdat de meter 30 tot 40 mmHg hoger aangeeft
dan uw verwachte systolische druk.
RU
Если систолическое давление выше 210 мм.рт.ст.:  ,  
    ,    
[START/STOP]   ,        ,
     30–40..
TR 
Sistolik basıncınız 210 mmHg'den fazlaysa: Kolluk şişmeye başladıktan sonra,
[START/STOP] düğmesine basın ve ölçüm cihazı beklediğiniz sistolik basınç değerinden
30ila 40 mmHg daha fazla şişene kadar basılı tutun.
ϊϣρϐο΍ˬω΍έΫϠϟρϏΎοϟ΍ρϳέηϟ΍ΥΎϔΗϧ΍˯ΩΑΩόΑΔϳϘΑ΋ίΕ΍έΗϣϳϠϠϣ˻˺˹ϥϣέΛϛ΃ϲοΎΑϘϧϻ΍ϙϣΩρϐοϥΎϛ΍Ϋ·
AR
ϥϣϰϠϋ΃Ύ˱ϳϘΑ΋ί΍ ˱
έΗϣϳϠϠϣ˽˹ϰϟ·˼˹ϥϣΦϔϧϟΎΑίΎϬΟϟ΍ϡϭϘϳϰΗΣϑΎϘϳ·˯ΩΑ>67$576723@έίϟ΍ϰϠϋέ΍έϣΗγϻ΍
ϙϳΩϟΔόϗϭΗϣϟ΍ϲοΎΑϘϧϻ΍ϡΩϟ΍ρϐοΔϣϳϗ
8Taking a Measurement
FR Réalisation d’une mesure NL Een meting doen
DE Vornehmen einer Messung RU 
IT Misurazione TR Ölçüm Yapma
ES Obtención de una lectura αΎϳϘϟ΍˯΍έΟ· 
AR
When the [START/STOP] button is pressed, the measurement is taken and saved
automatically.
FR

Après une pression sur le bouton [START/STOP], la mesure démarre et le résultat est enregistré automatiquement.
DE
Beim Drücken der Taste [START/STOP] erfolgt die Messung. Die Messwerte werden automatisch gespeichert.
IT 
Quando si preme il pulsante [START/STOP], la misurazione viene eseguita e salvata automaticamente.
ES 
Al pulsar el botón [START/STOP], se obtiene la medición, que se guarda automáticamente.
NL
Wanneer op de knop [START/STOP] wordt gedrukt, wordt de meting automatisch uitgevoerd en opgeslagen.
RU
 ,   [START/STOP] ,     .
TR 
[START/STOP] düğmesine basıldığında ölçüm yapılır ve otomatik olarak kaydedilir.
Ύ˱ϳ΋ΎϘϠΗϪυϔΣϭαΎϳϘϟ΍˯΍έΟ·ϡΗϳˬ>67$576723@έίϰϠϋρϐοϟ΍Ωϧϋ 
AR
Taking a measurement in guest mode
FR Réalisation d’une mesure en mode Invité
DE Vornehmen einer Messung im Gast-Modus
IT Misurazione in modalità Ospite
ES
Obtención de una lectura en modo de invitado
NL Een meting in gastmodus afnemen
RU     
TR Konuk modunda ölçüm yapma
ϑϳοϟ΍ϊοϭϡ΍ΩΧΗγΎΑαΎϳϘϟ΍˯΍έΟ·
AR
The guest mode can be used to take a single measurement for another user.
Noreadings are stored in the memory.
FR
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.
DE
Soll eine einzelne Messung bei einem anderen
Benutzer durchgeführt werden, kann dafür der
Gast-Modus aktiviert werden. Im Gast-Modus
werden keine Messwerte gespeichert.
IT
La modalità Ospite può essere utilizzata
per eseguire una singola misurazione su un
diverso utente. I risultati ottenuti non vengono
memorizzati.
ES
Para realizar una única medición para otro
usuario, se puede utilizar el modo de invitado.
Cuando se selecciona el modo de invitado,
nose guardan lecturas.
NL De gastmodus kan worden gebruikt om
één enkele meting uit te voeren voor een
andere gebruiker. Er worden geen metingen
opgeslagen in het geheugen.
RU    
  
   .  
 ,   
  .
TR Konuk modu, başka br kş çn tek br ölçüm
yapmak üzere kullanılablr. Konuk modu
seçldğnde, ölçüm değerler hafızada saklanmaz.
ΓΩΣ΍ϭαΎϳϗΔϳϠϣϋ˯΍έΟϹϑϳοϟ΍ϊοϭϡ΍ΩΧΗγ΍ϥϛϣϳϭ
AR
ϥ΃ΎϣϛΓέϛ΍Ϋϟ΍ϝΧ΍ΩΓ˯΍έϗϱ΃ϥϳίΧΗϡΗϳϻέΧ΁ϡΩΧΗγϣϟ
3 sec+
https://www.omron-healthcare.com/
Manufacturer
Fabricant
Hersteller
Produttore
Fabricante
Fabrikant

Üretici
Δόϧλ˵ϣϟ΍Δϛέηϟ΍
OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN
ΓΩϭΩΣϣϟ΍έϳϛΙϠϳϫϥϭέϣ΍Δϛέη
ϭηϭΩ΍έΗϭΑϭγΗϭϧϭϛ
ϭΗϭϳΎϛˬϭϛϭϣ
ϥΎΑΎϳϟ΍
EU-representative
Mandataire dans l’UE
EU-Repräsentant
Rappresentante per l’UE
Representante en la UE
Vertegenwoordiging in de EU
  
AB temsilcisi
ϲΑϭέϭϷ΍ΩΎ ΣΗϻΎΑϝ ϳΛ ϣΗϟ΍Δ ϬΟ
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp,
THE NETHERLANDS
www.omron-healthcare.com
Importer in EU
Importateur dans l’UE
Importeur in der EU
Importatore per l’UE
Importador en la UE
Importeur in de EU
  
AB’de İthalatçı
ϲΑϭέϭϷ΍ΩΎΣΗϻ΍ϲϓΩέϭΗγϣϟ΍
Production facility
Site de
production
Produktionsstätte
Stabilimento di produzione
Planta de producción
Productiefaciliteit


Üretim Tesisi
ϊϳϧλΗϟ΍Γ΄ηϧϣ
OMRON HEALTHCARE MANUFACTURING
VIETNAM CO., LTD.
No.28 VSIP II, Street 2, Vietnam-Singapore Industrial Park II,
Binh Duong Industry-Services-Urban Complex, Hoa Phu Ward,
Thu Dau Mot City, Binh Duong Province, Vietnam
Subsidiaries
Succursales
Niederlassungen
Consociate
Empresas filiales
Dochteronder-
nemingen

Yan Kuruluşlar
ΔόΑΎΗϟ΍ΕΎϛέηϟ΍
Importer in the United Kingdom and UK responsible person
Importateur au Royaume-Uni et la personne responsable au Royaume-Uni
Importeur im Vereinigten Königreich und Verantwortliche Person für UK
Importatore per il Regno Unito e Responsabile in UK
Importador en el Reino Unido y persona responsable en el RU
Importeur voor het Verenigd Koninkrijk en verantwoordelijke in het VK
Импортер в Великобританию и ответственное лицо в Великобритании
Birleşik Krallık’taki İthalatçı ve Birleşik Krallık sorumlusu
ΓΩΣΗϣϟ΍ΔϛϠϣϣϟ΍ϲϓϝϭ΅γϣϟ΍ιΧηϟ΍ϭΓΩΣΗϣϟ΍ΔϛϠϣϣϟ΍ϲϓΓΩέϭΗγϣϟ΍ΔϬΟϟ΍
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
www.omron-healthcare.com/distributors
OMRON MEDIZINTECHNIK
HANDELSGESELLSCHAFT mbH
www.omron-healthcare.com/distributors
OMRON SANTÉ FRANCE SAS
www.omron-healthcare.com/distributors
Issue Date / Date de publication / Ausgabedatum/
Datadipubblicazione / Fecha de publicación /
Uitgiftedatum /   / Teslim Tarihi / έ΍ΩλϹ΍ΦϳέΎΗ
: 2022-05-25
Made in Vietnam / Fabriqué en Vietnam / Hergestellt in Vietnam/
Prodottoin Vietnam / Fabricado en Vietnam / Geproduceerd in Vietnam/
   / Vietnam'da Üretilmiştir /
ϡΎϧΗϳϓϲϓϊϧλ
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