Gima 49902 El kitabı

Kategori
Kan basıncı birimleri
Tip
El kitabı
M2 (HEM-7143-E)
IM1-HEM-7143-E-01-10/2020
5674676-0A
Instruction Manual
Read Instruction manual and before use.
For symbols information, refer to “Symbols Description” on the back side of
the another “Instruction manual ”.
Automatic Upper Arm Blood Pressure Monitor
English
G
H
I
D
F
E
A
B
C
A
B
C
D
E
F
G
H
I
Display
[Memory] button
[START/STOP] button
Battery compartment
AC adapter jack
Air jack
Arm cu
Air plug
Air tube
Thank you for purchasing the M2 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.
Safety Instructions
This instruction manual provides you with important information
about the M2 Automatic Upper Arm Blood Pressure Monitor. To
ensure the safe and proper use of this monitor, READ and
UNDERSTAND all of these 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.
Intended Use
This device is a digital monitor intended for use in measuring blood
pressure and pulse rate in adult patient population. This monitor
detects the appearance of irregular heartbeats during measurement
and indicates this via a symbol with readings. It is mainly designed for
general household use.
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.
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.
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.
Battery Handling and Usage
•Keep batteries out of the reach of infants, toddlers and
children.
Caution
Indicates a potentially hazardous
situation which, if not avoided, may
result in minor or moderate injury to
the user or patient, or cause damage to
the equipment or other property.
Stop using this monitor and consult with your physician if you
experience skin irritation or discomfort.
Consult with your physician before using this monitor on an
arm where intravascular access or therapy, or an arteriovenous
(A-V) shunt, is present because of temporary interference to
blood flow and could result in injury.
Consult with your physician before using this monitor if you
have had a mastectomy.
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 30cm 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 3.
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 devices 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
2hours 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 3.
DO NOT use this monitor after the durable period has ended.
Refer to section 3.
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.
Introduction
Important Safety Information
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 6 of
instruction manualfor additional information.
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.
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.
•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.
•To stop a measurement, press the [START/STOP] button while
taking a measurement.
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.
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.
1. Error Messages and Troubleshooting
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 4 of
instruction
manual.
Air is leaking from the
arm cuff.
Replace the arm cuff
to the new one. Refer
to section 10 of
instruction
manual.
appears or a
measurement
cannot be complete
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 6 of
instruction
manual.
Due to the systolic
pressure is above
210mmHg, 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 6 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 4 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
2.1 Maintenance
To protect your monitor from damage, follow the directions below:
Caution
DO NOT disassemble or attempt to repair this monitor or other
components. This may cause an inaccurate reading.
2.2 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.
Do not store your monitor and other components:
2.3 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.
2.4 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.
Note
•These specifications are subject to change without notice.
•This monitor is clinically investigated according to the
requirements of EN ISO81060-2:2014 and complies with
ENISO81060-2:2014 and EN ISO81060-2:2019+A1:2020
(excluding pregnant and pre-eclampsia patients). In the clinical
validation study, K5 was used on 85 subjects for determination of
diastolic blood pressure.
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.
Operation mode classification complies with IEC 60601-1.
appears
The monitor has
malfunctioned.
Press the [START/STOP]
button again.
If “Erstill 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.
and
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.
Batteries are
depleted.
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 problems
occur.
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.
Display/
Problem Possible Cause Solution
2. Maintenance
Changes or modifications not approved by the manufacturer
will void the user warranty.
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.
3. Specifications
Product categoryElectronic Sphygmomanometers
Product description Automatic Upper Arm Blood
Pressure Monitor
Model (Code)M2 (HEM-7143-E)
DisplayLCD digital display
Cuff pressure range 0 to 299 mmHg
Blood pressure measurement
range
SYS: 60 to 260 mmHg
DIA: 40 to 215 mmHg
Pulse measurement range 40 to 180 beats / min.
AccuracyPressure: ±3 mmHg
Pulse: ±5% of display reading
Inflation Automatic by electric pump
Deflation Automatic pressure release valve
Measurement method Oscillometric method
Operation mode Continuous operation
IP classification
Monitor: IP20
Optional AC adapter: IP21 for
HHP-CM01, IP22 for HHP-BFH01
Rating DC6 V 4 W
Power source
4AAbatteries 1.5 V or optional
AC adapter (INPUT AC 100 - 240 V
50 - 60 Hz 0.12-0.065 A)
Battery life
Approximately 900 measurements
(Using new alkaline batteries and
included arm cuff. Depending on
the type of battery and arm cuff.)
Durable period (Service life)Monitor: 5 years
Arm cuff: 5 years
Optional AC adapter: 5 years
Operating conditions +10 to +40°C / 15 to 90% RH (non-
condensing) / 800 to 1060 hPa
Storage / Transport conditions -20 to +60°C / 10 to 90% RH (non-
condensing)
Weight
Monitor: approximately 250 g
(not including batteries)
Arm cuff: approximately 110g
Dimensions (approximately
value)
Monitor: 103 mm (W) × 82mm (H)
× 140 mm (L)
Arm cuff: 146 mm × 466 mm (air
tube: 610mm)
Cuff circumference applicable
to the monitor
17 to 42 cm (included arm cuff:
22 to 32 cm)
MemoryStores up to 30 readings
Contents
Monitor, arm cuff (HEM-CR24),
4AAbatteries, storage case,
Instruction Manual and
Protection against electric
shock
Internally powered ME equipment
(when using only batteries)
Class II ME equipment (optional AC
adapter)
Applied part Type BF (arm cuff)
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.
•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.
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.
Important information regarding Electromagnetic
Compatibility (EMC)
Correct Disposal of This Product (Waste Electrical
& Electronic Equipment)
4. Limited Warranty
5. Guidance and Manufacturer’s
Declaration
HEM-7143-E manufactured by OMRON HEALTHCARE Co., Ltd.
conforms 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-7143-E on the website.
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.
Issue Date:
Date de publication :
Ausgabedatum:
Data di pubblicazione:
Fecha de publicación:
2021-05-17
Symbols Description
Description des symboles
Beschreibung der Symbole
Descrizione dei simboli
Descripción de los símbolos
Beschrijving van symbolen
Описание символов
Simgelerin ıklaması
ίϭϣέϟ΍ Ρέη
FR
DE
IT
ES
NL
RU
TR
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 Stromschgen (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
ectricas (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 paa - Tip BF Elektrik
çarpmasına karşı koruma derecesi
(kaçak akım)
ΕΎϣΩλϟ΍ Ωο ΔϳΎϣΣϟ΍ ΔΟέΩ :ϖΑρϣϟ΍ ˯ίΟϟ΍ AR
BF ωϭϧϠϟ (ΏέγΗϣϟ΍ έΎϳΗϟ΍) Δϳ΋ΎΑέϬϛϟ΍
CE Marking
FR
ES
Marquage CE
CE-Kennzeichnung
Contrassegno CE
Marcado CE
CE-merkteken
Знак соответствия директиве ЕС
CE İşareti
(CE) ΔϳΑϭέϭϷ΍ ΔϧΟϠϟ΍ ϊϣ ϖϓ΍ϭΗϟ΍ Δϣϼϋ
Class II equipment. Protection
against electric shock
FR Équipement de classe II. Protection
contre les chocs électriques
DE Gerät der Klasse II. Schutz vor
Stromschgen
IT Apparecchiatura di Classe II.
Protezione contro le folgorazioni
ES Equipo de Clase II. Protección
contra descargas ectricas
NL Apparatuur van Klasse II.
Bescherming tegen elektrische
schokken
RU Изделие класса II Защита от
поражения электрическим током
TRnıf II ünite. Elektrik çarpmasına
karşı koruma
ΕΎϣΩλϟ΍ Ωο ΔϳΎϣΣϟ΍ .II Δ΋ϔϟ΍ ϥϣ ίΎϬΟ AR
Δϳ΋ΎΑέϬϛϟ΍
Ingress protection degree provided
by IEC 60529
FR Degré de protection selon
CEI60529
DE Grad des Eindringschutzes gemäß
IEC60529
IT Livello di protezione IP in base a
IEC60529
ES Grado de protección según la
norma internacional IEC60529
NL Beschermingsgraad tegen
binnendringing volgens IEC 60529
RU Степень защиты, обеспечиваемая
оболочкой, в соответствии со
стандартом IEC 60529
TR Su girmesine karşı koruma derecesi
IEC 60529 tarandan verilmiştir
Ύϫέϓϭϳ ϲΗϟ΍ϭ Ω΍ϭϣϟ΍ ϝϭΧΩ ϥϣ ΔϳΎϣΣϟ΍ ΔΟέΩ AR
IEC 60529 έΎϳόϣ
Serial number
Numéro de série
Seriennummer
Numero di serie
mero de serie
Serienummer
Порядковый (серийный) номер
Seri numarası
ϝγϠγΗϣϟ΍ ϡϗέϟ΍
LOT number
Numéro de LOT
LOT-Nummer
Numero di lotto
mero de lote
Partijnummer
Код (номер) партии
Parti numarası
ΔϠϳϐηΗϟ΍ ϡϗέ
Medical device
Dispositif médical
Medizinprodukt
Dispositivo medico
Producto sanitario
Medisch apparaat
Медицинский прибор
bbi cihaz
ϲΑρ ίΎϬΟ
For indoor use only
FR Pour un usage à l’intérieur
uniquement
DE Nur für die Nutzung in
Innenbereichen
NL
Solo per uso in interni
Para uso solo en interiores
Alleen voor gebruik binnenshuis
RU Для использования только
внутри помещений
Sadece mekanda kullanım için
ρϘϓ ΔϘϠϐϣϟ΍ ϖρΎϧϣϟ΍ ϲϓ ϡ΍ΩΧΗγϼϟ ΢ϟΎλ
Temperature limitation
Limitation de temrature
Temperaturbegrenzung
Limite di temperatura
Limitación de la temperatura
Temperatuurbegrenzing
Температурный диапазон
cakk sınırlaması
ΔΑγΎϧϣϟ΍ Γέ΍έΣϟ΍ ΔΟέΩ ΩϭΩΣ
Humidity limitation
Limitation dhumidité
Luftfeuchtigkeitsbegrenzung
Limite di umidità
Limitación de la humedad
Vochtigheidsbegrenzing
Диапазон влажности
Nem sınırlaması
ΔΑγΎϧϣϟ΍ ΔΑϭρέϟ΍ ΩϭΩΣ
Atmospheric pressure limitation
FR Limitation de pression
atmosphérique
Luftdruckbegrenzung
Limite di pressione atmosferica
ES Limitación de la presión
atmosrica
Luchtdrukbegrenzing
RU Ограничение атмосферного
давления
TR Atmosferik bası sınırlaması
ΏγΎϧϣϟ΍ ϱϭΟϟ΍ ρϐοϟ΍ ΩϭΩΣ
DE
IT
NL
RU
TR
AR
IP XX
FR
DE
IT
ES
NL
RU
TR
AR
FR
DE
IT
ES
NL
RU
TR
AR
FR
DE
IT
ES
NL
RU
TR
AR
IT
ES
TR
AR
FR
DE
IT
ES
NL
RU
TR
AR
FR
DE
IT
ES
NL
RU
TR
AR
DE
IT
NL
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
Полярность разъема адаптера
Bağlantı polarite göstergesi
ϝλϭϣϟ΍ ΔϳΑρϘϟ έϳηΗ Δϣϼϋ
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 ΔρϏΎοϟ΍ ρ΋΍έηϟ΍ ΩϳΩΣΗ ΕΎϣϼϋ AR
ίΎϬΟϟ΍ ϊϣ ΔϘϓ΍ϭΗϣϟ΍
OMRONs 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 markateknolojisidir
αΎϳϘϟ OMRON ΔϳέΎΟΗϟ΍ Δϣϼόϟ΍ ΔϳϧϘΗ AR
ϡΩϟ΍ ρϐο
Arm circumference
DE
NL
Circonrence du bras
Armumfang
Circonferenza del braccio
Perímetro de brazo
Armomtrek
Окружность плеча
Kol çevresi
ω΍έΫϟ΍ ρϳΣϣ
Cuff positioning indicator for the left
arm
FR Indicateur de positionnement du
brassard pour le bras gauche
DE Indikator für die
Manschettenposition am linken Arm
IT Indicatore di posizionamento del
bracciale per il braccio sinistro
ES Indicador de posición del manguito
en el brazo izquierdo
NL Indicator voor positionering van de
manchet voor de linkerarm
RU Метка для правильного
расположения манжеты на левой
руке
TR Sol kol için kolluk konumlandırma
göstergesi
ρϏΎοϟ΍ ρϳέηϟ΍ ϊοϭϣΑ ιΎΧϟ΍ έη΅ϣϟ΍ AR
έγϳϷ΍ ω΍έΫϠϟ
Marker on the cuff to be positioned
above the artery
FR Rere 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 расположения
плечевой артерии
TR Kolluk üzerindeki işaretin konumu
arterin üzerine gelmelidir
ΏϭΟϭ ϰϟ· ΓέΎηϺϟ ρϏΎοϟ΍ ρϳέηϟΎΑ Δϣϼϋ AR
ϥΎϳέηϟ΍ ϕϭϓ Ϫόοϭ
Range pointer and brachial artery
alignment position
FR Pointeur de plage et position
dalignement sur l’artère brachiale
DE Bereichsanzeiger und
Ausrichtungsposition mit der
Oberarmarterie
IT Puntatore e posizione di
allineamento dell’arteria brachiale
ES Indicación de las medidas y
posición de alineación con la arteria
braquial
NL Bereikaanduiding en positie voor
uitlijning met slagader
RU Указатель диапазона и
расположения плечевой артерии
TR Arak işaretçisi ve kol arteri
hizalama konumu
ϊϣ Γ΍ΫΎΣϣϟΎΑ ιΎΧϟ΍ ϊοϭϟ΍ϭ ϕΎρϧϟ΍ έη΅ϣ AR
ϱΩοόϟ΍ ϥΎϳέηϟ΍
Range indicator of arm
circumferences to help selection of
the correct cuff size
FR Indicateur de plage de
circonrence du bras, pour la sélection
de la taille de brassard adaptée
DE Bereichsanzeige für den
Armumfang zur Auswahl der richtigen
Manschettengröße
IT Indicatore degli intervalli di
circonferenze braccio per la scelta della
misura di bracciale corretta
ES Indicador de las medidas del
perímetro de brazo para ayudarle a
seleccionar el tamaño de manguito
correcto
NL Bereikindicator voor armomtrek
om te helpen bij het kiezen van de
juiste manchetmaat
RU Символ диапазона окружности
плеча для помощи при подборе
правильного размера манжеты
TR Doğru kolluk ölçüsünü bulmaya
yardımcı olan kol çevresi arak
göstergesi
ΩϳΩΣΗ ϰϠϋ ΓΩϋΎγϣϠϟ ω΍έΫϟ΍ ρϳΣϣ ϕΎρϧ έη΅ϣ AR
ρϏΎοϟ΍ ρϳέηϠϟ ΢ϳΣλϟ΍ ϡΟΣϟ΍
Necessity for the user to consult this
instruction manual
FR L’utilisateur doit consulter le
présent mode demploi
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 gebruiksaanwijzing te raadplegen
RU Необходимость для
пользователя обратиться к данному
руководству по эксплуатации
TR Kullanıcı, bu kullanım kılavuzuna
başvurmadır
ΕΎϣϭϠόϣϟ΍ ϰϟ· ϡΩΧΗγϣϟ΍ ωϭΟέ Γέϭέο AR
΍Ϋϫ Ε΍ΩΎηέϹ΍ ϝϳϟΩ ϲϓ ΓΩέ΍ϭϟ΍
RU
TR
AR
FR
IT
ES
RU
TR
AR
,
Need for the user to follow this
instruction manual thoroughly for
your safety.
FR L’utilisateur doit suivre
attentivement ce mode demploi pour
votre sécurité.
DE Damit die Sicherheit gewährleistet
ist, muss der Benutzer diese
Gebrauchsanweisung sorgfältig
befolgen.
IT Per la propria sicurezza, lutente
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 Обратитесь к руководству по
эксплуатации.
TR Güvenlik açısından kullanıcının bu
kullanım kılavuzuna dikkatle uyması
gerekir.
ΓΩέ΍ϭϟ΍ Ε΍ΩΎηέϹ΍ ωΎΑΗ΍ ϰϟ· ϡΩΧΗγϣϟ΍ ΔΟΎΣ AR
.Δϣϼγϟ΍ ϰϠϋ υΎϔΣϠϟ ΍Ϋϫ ϝϣΎϛϟΎΑ Ε΍ΩΎηέϹ΍ ϝϳϟΩ ϲϓ
Direct current
Courant continu
DE Gleichstrom
Corrente diretta
Corriente directa
NL Gelijkstroom
Постоянный ток
Doğru akım
έηΎΑϣϟ΍ έΎϳΗϟ΍
Alternating current
Courant alternatif
Wechselstrom
Corrente alternata
Corriente alterna
Wisselstroom
Переменный ток
TR Alternatif akım
ΏϭΎϧΗϣϟ΍ έΎϳΗϟ΍
Date of manufacture
DE
Date de fabrication
Herstellungsdatum
Data di fabbricazione
Fecha de fabricación
Productiedatum
RU Дата изготовления в формате
ГГГГ-ММ-ДД
TR Üretim tarihi
ϊϳϧλΗϟ΍ ΦϳέΎΗ
Manufacturers quality control mark
FR Marque de contrôle de la qualité du
fabricant
DE Qualitätskontrollzeichen des
Herstellers
IT Contrassegno controllo qualità del
produttore
ES Marca del control de calidad del
fabricante
NL Symbool voor kwaliteitscontrole
van fabrikant
RU Отметка производителя о
контроле качества
TR Üreticinin kalite kontrol işareti
ΔλΎΧϟ΍ ΓΩϭΟϟ΍ ϲϓ ϡϛΣΗϟ΍ Δϣϼϋ AR
Δόϧλϣϟ΍ ΔϛέηϟΎΑ
Prohibited action
Action interdite
Verbotene Aktion
Operazione proibita
Acción prohibida
Verboden handeling
Запрещенные действия
Yasaklanmış eylem
έϭυΣϣ ˯΍έΟ·
FR
IT
ES
RU
TR
AR
FR
DE
IT
ES
NL
RU
AR
FR
IT
ES
NL
AR
,
FR
DE
IT
ES
NL
RU
TR
AR
Instruction Manual 2
Read Instruction manual and before use.
Lire le mode d’emploi et avant l’utilisation.
Lesen Sie vor der Verwendung Gebrauchsanweisung und .
Leggere il manuale di istruzioni e prima dell’uso.
Lea el manual de instrucciones y antes del uso.
Lees gebruiksaanwijzing en voor gebruik.
Перед использованием прочтите руководства по эксплуатации и .
Kullanmadan önce kullanım kılavuzu ve 'yi okuyun.
Ε΍ΩΎηέϹ΍ ϝϳϟΩ ΃έϗ΍
ϭ .ϡ΍ΩΧΗγϻ΍ ϝΑϗ
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
После того, как кнопка [START/STOP] нажата, измерение выполняется и сохраняется
автоматически.
TR
[START/STOP] düğmesine basıldığında ölçüm yapılır ve otomatik olarak kaydedilir.
AR
] έί ϰϠϋ ρϐοϟ΍ ΩϧϋSTART/STOP.Ύ˱ϳ΋ΎϘϠΗ ϪυϔΣϭ αΎϳϘϟ΍ ˯΍έΟ· ϡΗϳ ˬ[
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.
AR
ϥϣ έΛϛ΃ ϲοΎΑϘϧϻ΍ ϙϣΩ ρϐο ϥΎϛ ΍Ϋ·˻˺˹:ΔϳϘΑ΋ί Ε΍έΗϣϳϠϠϣ
] έίϟ΍ ϰϠϋ έ΍έϣΗγϻ΍ ϊϣ ρϐο΍ ˬω΍έΫϠϟ ρϏΎοϟ΍ ρϳέηϟ΍ ΥΎϔΗϧ΍ ˯ΩΑ ΩόΑSTART/STOP ίΎϬΟϟ΍ ϡϭϘϳ ϰΗΣ (ϑΎϘϳ·/˯ΩΑ) [ ϥϣ ΦϔϧϟΎΑ˼˹ ϰϟ· ˽˹.ϙϳΩϟ ΔόϗϭΗϣϟ΍ ϲοΎΑϘϧϻ΍ ϡΩϟ΍ ρϐο Δϣϳϗ ϥϣ ϰϠϋ΃ Ύ˱ϳϘΑ΋ί ΍˱έΗϣϳϠϠϣ
Automatic Upper Arm
Blood Pressure Monitor
ϲϟϻ΍ ω΍έΫϟ΍ ϰϠϋ΃ ϲϓ ϡΩϟ΍ ρϐο ΔΑϗ΍έϣ ίΎϬΟ
M2 (HEM-7143-E)
(HEM-7143-E) ϡ΍2
IM2-HEM-7143-E-01-10/2020
5674678-6A
1
Package Contents
FRContenu 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
Français
Deutsch
Italiano
Español
Nederlands
Русский
Türkçe
ˬ˴Τȴ̈́Џđ
1
Instruction Manual
1
Instruction Manual
Instruction Manual2
2
Preparing 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
AR
αΎϳϘϟ΍ ΔϳϠϣόϟ ίϳϬΟΗϟ΍
30 minutes before
FR
30minutes avant
DE
30 Minuten vorher
IT
30 minuti prima
ES
30minutos antes
NL
30 minuten ervoor
RU
За 30 минут до
TR
30 dakika önce
AR
ώϠΑΗ ΓΩϣΑ αΎϳϘϟ΍ ϝΑϗ˼˹ΔϘϳϗΩ
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.
AR
ώϠΑΗ ΓΩϣΑ αΎϳϘϟ΍ ϝΑϗ˾.˶ΥέΗγ΍ϭ ΡέΗγ΍ :ϖ΋ΎϗΩ
3
Installing Batteries
FR
Mise en place des piles
NL
Batterijen plaatsen
DE
Einsetzen der Batterien
RU
Установка элементов питания
(приобретаются дополнительно)
IT
Installazione delle batterie
TR
Pillerin Takılması
ES
Instalación de las pilas AR
ΕΎϳέΎρΑϟ΍ ΏϳϛέΗ
AA, 1.5V × 4
12
4
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
ESColocación del manguito en el brazo
izquierdo
AR
ϥϣϳϷ΍ ω΍έΫϟ΍ ϰϠϋ ρϏΎοϟ΍ ρϳέηϟ΍ ϑϟ
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 del gomito interno, 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.
AR
ϥϣ ρϏΎοϟ΍ ρϳέηϟ΍ ϥϣ ϡϭρέΧϟ΍ ΏϧΎΟ ϊϔΗέϳ ϥ΃ ΏΟϳ˺ ϰϟ· ˻.ϖϓέϣϟ΍ ϥϋ ϡγ
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 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.
AR
.ω΍έΫϟ΍ ϝϭΣ ϖϟίϧϳ ϻ ΙϳΣΑ ϡΎϛΣΈΑ ρϏΎοϟ΍ ρϳέηϟ΍ ϑϟϭ ϙϋ΍έΫ ϥϣ ϲϠΧ΍Ωϟ΍ ΏϧΎΟϟ΍ ϰϠϋ ˯΍ϭϬϟ΍ ϡϭρέΧ ϥ΃ ϥϣ Ωϛ΄Η
12
4
Click
1-2 cm
3
3
4
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:
AR
:ϰϟ· ϊΟέ΍ ˬϥϣϳϷ΍ ω΍έΫϟ΍ ϰϠϋ αΎϳϘϟ΍ ˯΍έΟ· ϝΎΣ ϲϓ
Instruction Manual
General Precautions
1
Instruction Manual
1
Instruction Manual
5
Sitting Correctly
FR
Position assise correcte
NL
Correct zitten
DE
Korrekte Körperhaltung RUПравильная поза при измерении
IT
Come sedere nel modo corretto TR Düzgün Oturma
ES
mo sentarse correctamente
AR
΢ϳΣλ ϝϛηΑ αϭϠΟϟ΍
Sit comfortably with your back and arm supported.
FR
S’asseoir confortablement de manière à ce que le dos et le bras soient bien soutenus.
DE
Bequem hinsetzen, mit dem Rücken anlehnen und den Arm auf eine Unterlage legen.
IT
Sedere comodamente con la schiena e il braccio ben sostenuti.
ES
Siéntese cómodamente de modo que la espalda y el brazo estén bien apoyados.
NL
Neem een comfortabele zitpositie in, met uw rug en arm ondersteund.
RU
Сядьте удобно, чтобы спина и рука опирались на что-либо.
TR
Sırtınız ve kolunuz desteklenerek rahat bir şekilde oturun.
AR
.ΩΎϧΗγ΍ ϊοϭ ϲϓ ω΍έΫϟ΍ϭ έϬυϟ΍ ϥϭϛϳ ΙϳΣΑ ΢ϳέϣ ϝϛηΑ αϠΟ΍
Place the arm cuff at the same level as your heart.
FR
Le brassard doit se trouver au même niveau que votre cœur.
DE
Die Manschette auf Herzhöhe platzieren.
IT
Posizionare il bracciale allo stesso livello del cuore.
ES
Coloque el manguito al mismo nivel que el corazón.
NL
Plaats de armmanchet op hetzelfde niveau als uw hart.
RU
Манжета должна находиться на уровне сердца.
TR
Kolluğu kalbinizle aynı düzeye getirin.
AR
.Ϫγϔϧ ΏϠϘϟ΍ ϯϭΗγϣ ϲϓ ω΍έΫϠϟ ρϏΎοϟ΍ ρϳέηϟ΍ ϊο
Keep feet flat, legs uncrossed, remain still and do not talk.
FR
Garder les pieds à plat, les jambes non croisées, ne pas bouger et ne pas parler.
DE
ße 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.
AR
.ΙΩΣΗΗ ϻϭ ϙΗΎΑΛ ϰϠϋ υϓΎΣϭ ΩϋΎΑΗϣ ϊοϭ ϲϓ ϙϳϗΎγϭ ΢˷ργϣ ϊοϭ ϲϓ ϙϳϣΩϗ ϝόΟ΍
1
2
3
1
2
3
6
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
AR
αΎϳϘϟ΍ ˯΍έΟ·
*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/ESClavuzlarını temel alır.
AR
) ϡΩϟ΍ ρϐο ρέϔϟ ΔϳΑϭέϭϷ΍ ΔϳόϣΟϟ΍ Ε΍ΩΎηέ· ϰϟ· ΩϧΗγϳ ϊϔΗέϣϟ΍ ϡΩϟ΍ ρϐο ϑϳέόΗ*ESH Ώρϟ ΔϳΑϭέϭϷ΍ ΔϳόϣΟϟ΍/( ) ΏϠϘϟ΍ESC ϡΎόϟ (2018.
**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 cardíaco irregular 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.
AR
ϝΩόϣΑ αΎϳϘϟ΍ ΔϳϠϣϋ ˯ΎϧΛ΃ ϲϓ ϪϓΎηΗϛ΍ ϡΗϳ ϱΫϟ΍ ϲόϳΑρϟ΍ ϡ˸υϧϟ΍ ϥϣ ϝϗ΃ ϡ˸υϧ Ϫϧ΄Α ΏϠϘϟ΍ ΕΎΑέο Ώ΍έρο΍ ϑέό˵ϳ**˻˾ ϝΩόϣΑ Ϫϧϣ έΛϛ΃ ϭ΃ ̃˻˾.̃
9.1 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
Восстановление настроек по умолчанию
TR
Varsayılan Ayarları Geri Yükleme
AR
Δϳο΍έΗϓϻ΍ Ε΍Ω΍ΩϋϹ΍ ΓΩΎόΗγ΍
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 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.
ESNo 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.
AR
.ϱέΎϳΗΧϻ΍ ρϏΎοϟ΍ ρϳέηϟ΍ ϊϣ ˯΍ϭϬϟ΍ ΓΩ΍Ωγ ϝΎϣόΗγ΍ ϥϛϣϳ .˯΍ϭϬϟ΍ ΓΩ΍Ωγ ϥϣ ιϠΧΗΗ ϻ
7
Checking Readings
FR
Vérification 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΍
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 “SIS” es 135mmHg o superior
y/o “DIA” es 85mmHg* o superior.
NL
Verschijnt als “SYS 135 mmHg of hoger is
en/of “DIA” 85 mmHg* of hoger is.
RU
Отображается, если «SYS»
(Систолическое давление) 135 мм рт.ст.
и выше и/или «DIA» (Диастолическое
давление) 85 мм рт.ст.* и выше.
TR
“SYS” 135mmHg ya da üstünde
olduğunda ve/veya DIA” 85mmHg* ya
da üstünde olduğunda görünür.
AR
" ϥΎϛ ΍Ϋ· έϬυΗSYS ώϠΑϳ "˺˼˾ ϭ΃ Ύ˱ϳϘΑ΋ί ΍˱έΗϣϳϠϠϣ ϭ΃/ϭ έΛϛ΃DIA "́˾.έΛϛ΃ ϭ΃ *Ύ˱ϳϘΑ΋ί ΍˱έΗϣϳϠϠϣ "
Appears when your body moves during a measurement. Remove the arm
cuff, wait 2 - 3 minutes and try again.
FRS’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
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.
AR
ϥϣ έυΗϧ΍ϭ ω΍έΫϠϟ ρϏΎοϟ΍ ρϳέηϟ΍ Δϟ΍ίΈΑ ϡϗ .αΎϳϘϟ΍ ΔϳϠϣϋ ˯ΎϧΛ΃ ϲϓ ϙϣγΟ ϙέΣΗ Ωϧϋ έϬυΗ˻ ϰϟ· ˼.ϯέΧ΃ Γέϣ ϝϭΎΣϭ ϖ΋ΎϗΩ
1
2
3
4
1
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 saffiche 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.
AR
ˬέέϛΗϣ ϝϛηΑ ΎϫέϭϬυ Ωϧϋ .αΎϳϘϟ΍ ΔϳϠϣϋ ˯ΎϧΛ΃ ϲϓ **ΏϠϘϟ΍ ΕΎΑέο ϡΎυΗϧ΍ ϡΩϋ ϑΎηΗϛ΍ Ωϧϋ έϬυΗ
ϲλϭΗOMRON.ϙΑϳΑρ ΓέΎηΗγΎΑ
Cuff 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.
AR
.ϲϔϛϳ ΎϣΑ ϡϛΣϣ ρϏΎοϟ΍ ρϳέηϟ΍
Apply cuff 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.
AR
.Ύ˱ϣΎϛΣ· έΛϛ΃ ϝϛηΑ ϯέΧ΃ Γέϣ ρϏΎοϟ΍ ρϳέηϟ΍ ϑϟ
3
4
4
Error messages or other problems? Refer to:
FR
Messages d’erreur ou autres problèmes? Voir:
Instruction Manual
1.
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:
RUСообщения об ошибках или другие
неисправности? См.
TR
Hata mesajları veya başka sorunlar mı var? Bkz:
AR
:ϰϟ· ϊΟέ΍ ˮϯέΧϷ΍ Εϼϛηϣϟ΍ ϭ΃ ΄ρΧϟ΍ ϝ΋Ύγέ
8
Using Memory Functions
FRUtilisation 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
ESUso de las funciones de memoria AR
Γέϛ΍Ϋϟ΍ ϑ΋Ύυϭ ϡ΍ΩΧΗγ΍
8.1 Readings Stored in Memory
FRMesures stockées en mémoire
DE
Gespeicherte Messwerte
IT Risultati conservati in memoria
ES
Lecturas guardadas en la memoria
NL Metingen opgeslagen in het geheugen
RU
Сохранение результатов в памяти
TR Hafızaya Kaydedilen Değerler
AR
Γέϛ΍Ϋϟ΍ ϲϓ Ε΍˯΍έϘϟ΍ ϥϳίΧΗ ϡΗ
Up to 30 readings are stored.
FR
Jusqu’à 30mesures sont stockées.
DE Es werden bis zu 30Messwerte gespeichert.
IT
Vengono conservati fino a 30 risultati.
ESSe almacenan hasta 30lecturas.
NL
Er kunnen tot 30 meetwaarden worden opgeslagen.
RUСохраняется до 30 результатов.
TR
30 adede kadar ölçüm değeri saklanır.
AR
ϰϟ· ΔϧίΧϣϟ΍ Ε΍˯΍έϘϟ΍ ΩΩϋ ϝλϳ˼˹.Γ˯΍έϗ
1
Instruction Manual
1
Instruction Manual
9
Other Settings
FR
Autres réglages
NL
Andere instellingen
DE
Weitere Einstellungen
RU
Прочие настройки
IT
Altre impostazioni
TR
Diğer Ayarlar
ES
Otros ajustes
AR
ϯέΧϷ΍ Ε΍Ω΍ΩϋϹ΍
4sec+
23 5
4sec+
4
1
10
Optional Medical Accessories
FR
Accessoires médicaux optionnels
NL
Optionele medische accessoires
DE
Optionales medizinisches Zubehör
RU
Аксессуары, которые пользователь,
при необходимости, может
приобрести отдельно от комплекта
поставки медицинского изделия
IT
Accessori medicali opzionali
TR
Opsiyonel Tıbbi Aksesuarlar
ES
Accesorios médicos opcionales
AR
ΔϳέΎϳΗΧϻ΍ ΔϳΑρϟ΍ ΕΎϘΣϠϣϟ΍
Wide Range Soft Cu
HEM-RML31
22 - 42 cm
Small Cu
HEM-CS24
17 - 22 cm
Medium Cu
HEM-CR24
22 - 32 cm
HHP-CM01 HHP-BFH01
AC Adapter
https://www.omron-healthcare.com/
Manufacturer
Fabricant
Produttore
Fabricante
Fabrikant
Производитель
Üretici
 
ΓΩϭΩΣϣϟ΍έϳϛΙϠϳϫϥϭέϣ΍Δϛέη
    
   
 
 
OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN
ϥΎΑΎϳϟ΍617-0002ϭΗϭϳΎϛˬϭϛϭϣϭηϭΩ΍έΗϭΑϭγΗϭϧϭϛ53
EU-representative
Mandataire dans l’UE
Rappresentante per l’UE
Representante en la UE
Представитель в ЕС
AB temsilcisi
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS
www.omron-healthcare.com
Importer in EU
Importateur dans l’UE
Importatore per l’UE
Importador en la UE
Импортер в ЕС
AB'de İthalatçı
Production Facility
Site de production Planta de producción
Productiefaciliteit
Производственно
е подразделение
Üretim Tesisi
OMRON MEDIZINTECHNIK
HANDELSGESELLSCHAFT mbH
www.omron-healthcare.com/distributors
OMRON SANTÉ FRANCE SAS
www.omron-healthcare.com/distributors
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
www.omron-healthcare.com/distributors
Omron Healthcare Brasil Indústria e
Comércio de Produtos Médicos Ltda
Av. Ain Ata (Lot. M II. P I Logístico),
nº 370 – Lote 12 – Quadra B – Jardim Ermida I
13212-213 – Jundiai – SP – Brazil
Hersteller
EU-Vertreter
Produktionsstätte
Importeur in der EU
 
Issue Date / Date de publication / Ausgabedatum /
Data di pubblicazione / Fecha de publicación /
Uitgiftedatum / Дата выпуска / Teslim Tarihi /
: 2021-05-17
Made In Brazil / Fabriqué au Brésil / Hergestellt in Brasilien /
Fabbricato in Brasile / Fabricado en Brasil / Geproduceerd in Brazilië /
Сделано в Бразилии / Brezilya’da üretilmiştir /
Vertegenwoordiging in de EU
Importeur in de EU
Stabilimento di produzione
Subsidiaries
Consociate
Niederlassungen
Succursales Филиалы
Yan Kuruluşlar
Importer in the United
Kingdom and UK
responsible person
Dochterondernemingen
Empresas liales
  
  • Page 1 1
  • Page 2 2
  • Page 3 3

Gima 49902 El kitabı

Kategori
Kan basıncı birimleri
Tip
El kitabı

İlgili Makaleler