3.4 T urning “OFF” Bluetooth
®
T ur n of f the Bluet ooth
®
in your monitor in the following areas where use
of wireless equipment is prohibited.
• On aircraft • I n hospitals • While abroad
Y our blood press ure monitor comes with the Bluetooth
®
already turned
on.
1. Tu rn y our monitor power o f f if it is turned on.
2. Press and hold the conne ction butt on for more than
10 se conds.
3. Relea se the co nnection butt on when “ ” appea rs on
the disp lay .
4. Press th e [ST ART/STOP] button to turn the monitor off.
Note: The monitor will aut o maticall y turn o f f after 2 minutes.
How to turn “ON” Bluetooth
®
Operate the following step when t he power has been of f.
Press and hold t he connection button f or more than 2 seconds and
then release the connection button w hen
“” appears on t he
display .
3.5 Restoring Y our Monitor to the Default Settings
T o delete all the information stored in your monitor , f ollow the instructions
below . Make sure that your monitor is turned off. It will be of f when the
screen is not showing numbers or symbols.
1. Whil e holding th e connec tion button down, the Connec tion
symbol “ ” and “P ” appear on the display , and th en press
the [ST ART/STOP] b utton for more th an 5 seconds .
2. When the “Clr” symbol appears on t he display , releas e the
connec tion button and [ST ART/STOP] button .
The “Clr” will appear on t h e display when your monitor settings have
reverted back to their original.
3. Press th e [ST ART/STOP] button to turn the monitor off.
Notes:
• The monitor will aut om atically turn off after 2 minutes.
• Reverting to initial settings of this monitor will not delete the information
in the app.
• When using this monitor again, please delet e the registration of the
monitor in the app first, and t hen pair your monitor .
4. Error Messages and T roubleshooting
4.1 Error Messages
4.2 T roubleshooting
5. Maintenance and St orage
5.1 Maintenance
T o protec t your device f rom damage, please follow the directio ns below:
• S tore the device and the components in a clean, safe location.
• Do not use any abrasive or volat ile cleaners.
• Do not wash t he device and any com ponents or immerse them in water .
• Do not use gasoline, thinners or si milar solvents to clean the d evice.
• Use a soft dry cloth, or a soft cloth m oistened with neutral soap to c lean
on the monitor and the arm cuf f, and then wipe it with a dry cloth.
• Changes or m odification not approved by the manufacturer will void t he
user warrant y . Do not disassemble or attempt t o repair the device or
components.
Calibration and Service
• The accuracy of this blood pressure monitor has been carefully tested
and is designed for a long service lif e.
• It is ge nerally recommended to have the device inspected every 2 years
to ensure correct functioning and accuracy . Please consult your OMRON
retail outlet or distributor .
5.2 Storage
Do not s tore the devi ce in the foll owing situati ons:
• If the device is wet.
• Locations exposed to extreme tempe ratures, humidity , direc t sunlight,
dust or corr osive vapors such as bleach.
• Locations exposed to vibrations, s hocks or where it will be at an angle.
6. Spec ifications
Notes:
• These specifications are subject to change without notice.
• In the clinical validation study , K5 was used on 85 subjects for determination of
diastolic blood press ure.
• This device is clinically investigated according to the requirements of
ISO81060-2:2013.
• This device has not been validated for use on p regnant pati e nts.
• IP classification is degrees of protection provided by enclosures in accordance
with IEC 60529. T his device is protected agains t solid foreign objects of 12 mm
diameter and greater such as a finger , and against oblique falling water drops
which may c ause issues during a normal operation.
• This device fulfils the provisions of EC direc tive 93/42/EEC (Medical Device
Directive).
• This blood pressure monitor is designed according to t he European S tandard
EN1060, Non-invasive sphygmom anometers Part 1: General Requirements
and Part 3: Supplementary requirements for electromechanical blood pressure
measuring syst ems.
• Hereby , OMRON HEAL THCARE Co., Ltd., declares that the radio equipment
type EVOL V (HE M-7600T -E) is in compliance with Directive 2014/53/EU.
The full text of the EU declaration of c onformity is available at the following
internet address: ww w . omron-healthcare.com
• This OMRON product is produced under the strict quality system of OMRON
HEAL TH CARE Co., Ltd., Japan. The Core component for OM RON blood
pressure monitors, which is the Press ure Sensor , is produced in Japan.
Use this monitor only in the member countries of EU or the country you
purchased it in. If you use it el sewhere, you may violate t he radio laws or
regulations of that cou ntry .
7. T rademarks
The Bluetooth
®
Smart word m ark and logos are registered
trademarks owned by Bluetooth SIG , Inc. and any use of
such marks by OMRON HEAL THCARE C o., Ltd. is under
license. Other trademarks and trade names are those of
their respective owne rs.
Apple and t he Apple logo are trademarks of Apple Inc., registered in the U.S.
and other countries. App S tore is a service mark of Apple Inc.
Android, the Google Play logo are trademarks of Google Inc.
8. Limited W arranty
Thank yo u for buying an O MRON product. This pr oduct is construc ted of high
quality mate rials and great care h as been taken in its manufacturing. It is
designed to give you every satisfaction, provided that it is properly ope rated and
maintained as described in the instruction manual.
This product is guaranteed by OMRON for a period of 3 years af te r the date of
purchase . The proper construction, workmanship and mat erials of this product is
guaranteed by OMRON. During this per iod of guarantee OMRON will, without
charge for labour or part s , repair or repla ce the defect product or any def ective
parts.
The guarantee does not cover any of the following:
a. T ransport costs and risks of t ransport.
b. Costs for repairs and / or def ect s resulting from repairs done by unau thorised
persons.
c. Periodic ch eck-ups and maintenance .
d. Failure or wear of optional p arts or other attachments other than the main
device itself, unless explicitly g uaranteed above.
e. Costs arising due to non -acceptance of a claim (those will be charged f or).
f. Damages of any kind including personal caused accidentally or f rom misuse.
g. Calibration service is not included within the guarantee.
Should guarantee service be required please apply to the dealer whom the
product was purc hased from or an authorised OMRO N distributor . For the
address refer to the product packaging / literature or to your specialised ret a iler .
If you have difficulties in finding OMRON cus tomer services, contact us for
information.
omron-healthcar e.com
Repair or replacement under the guarantee does not give rise to any extension
or renewal of the guarantee period.
The guarantee will be granted only if the co mplete product is r eturned together
with the original invoice / cash t icket issued to the consum er by the retailer .
9. Some Useful Information about Blood Pressure
What is Blood Pressure?
Blood pressure is a measure of t he force of blood flowing against t he walls of the
arteries. Arterial blood pressure is cons t antly changing during the c ourse of the
heart’s cycle.
The highest pres sure in the c ycle is called the Sy stolic Blood Pressur e; the
lowest is the Diastolic Blood Pressure. Both pressures, the Systolic and
Diastolic, are neces sary to enable a ph ysician to evaluate t he status of a
patient’s blood p ressure.
What is Arr hythmia?
Arrhythmia is a condition where the heartbeat rhythm is abnormal due to flaws in
the bio-electrical sy stem that drives the heartbeat. T ypical sy mptoms are
skipped heartbeats, premature contract ion, an abnormally rapid (t ac hycardia) or
slow (bradycar dia) pulse.
Why is it a Good Thing to measure Blood Pressure at
Home ?
Many factors such as physical act ivity ,
anxiety , or the time of day , can influence
your blood pres sure. A single
measurement may not be suffi c ient for an
accurate diagnosis.
Thus it is best to try and measure your
blood pressure at the same time each
day , to get an accurate indication of any
changes in blood pressure. Blood pressure is typically low in the morning and
increases from afternoon to evening. It is lower in the summer and higher in the
win ter .
How is Hypertension related to S troke?
Hypertension (high blood pressure) is the key risk factor for S troke .
It is estimated that amongst hypertensive patients, ef fective treatment would
prevent 1 in 4 haemorrhagic str okes (bleeding around the brain).
Hypertension guidelines have endorsed the us e of Home Blood Pressure
Monitoring in addition to the measurements in ph ysicians’ offices to help manage
hypertension effectively .
References to above medical claims are available upon request.
Error Display Cause S olution
Irregular heartbeat is
detected.
Remove the arm cuff. W ait
2 - 3 minutes and then take
another measurement.
Repeat the steps in s ection
3.1. If this error continues to
appear , contact your
physician.
Movement du ring
measurement.
Carefully read and repeat the
steps in section 3.3.
Arm cuff is applied
too loosely .
Apply the arm cuff t ight er .
Refer to section 3.1.
The batteries are
low .
Recommend replacement of
all 4 batteries with new ones .
Refer to section 2.1.
The batteries are
depleted or battery
polarities are not
properly aligned.
Immediately replace
4 batteries with new ones.
Refer to section 2.1.
Confirm the batteries a re
properly inserted with
polarities correctly aligned.
Refer to section 2.1.
Connection failure.
Data is not being
tran smitted.
Refer to “Conn ection failur e.
Data is n ot being
transmitted.” in section 4.2.
Arm cuff is applied
too loosely .
Apply the arm cuff t ight er .
Refer to section 3.1.
The arm cuff was
inflated exceeding
the maximum
allowable pressure,
and then deflated
automatically .
Do not touch the arm cuff
while t aking a measurement.
Refer to section 3.3.
Movement du ring
measurement.
Repeat measurement.
Remain still and do not talk
during measurement.
Refer to section 3.3.
Clothing is interfering
with the arm cuf f.
Remove any clothing
interfering with the arm cuff.
Refer to section 3.1.
* : “XX” will change to
display an error
number , 6 and
higher .
Device error .
Contact y our local OMRON
representative.
Problem Cause and S olution
No power .
No display appears on the
monitor .
Replace all batteries with new o nes.
Check the battery installation f or proper
placement of the battery polarities.
Refer to section 2.1.
Measurement values appear
too high or too low .
Blood pressure v aries constantly . Many
factors including stress, time of day , and h ow
you apply the arm cuff, may affect your blood
pressure.
Review the section, 3.2 and 3.3.
Connection failure. /
Data is not being transmitted.
The blood pressure m onitor might not be
properly placed within the smart device's
transmission range and is too far from t he
smart device. I f there are no causes of data
transmission interference f ound near the
blood pressure monit or , m ove the blood
pressure monitor within 5 m (16 ft.) of the
smart device and try again.
The Bluetoot h feature of the smart device
is turned of f. Turn on the Bl ueto oth feature
of the smart device and your monitor , and t r y
sending the data again.
The Bluetoot h feature of the blood
pressure monitor is turned off.
Refe r to “T o turn “ON” the Bluetooth ” in
“3.4 T urning “OFF” the Bl uetooth ”.
The blood pressure m onitor did not pair
successfully to the smart device. Try to p air
the devices again.
Refer to “P airing Y our Monitor with a Smart
Device” in section 2.2.
For more detail, go to “ Help” in the “OMR ON
connect” app.
The application on the smart device is not
ready . Check the application then try sending
the dat a again.
Refer to “P airing Y our Monitor with a Smart
Device” in sect ion 2.2. If the “Err” sy mbol still
displays after checking t he application,
contact your OMRON retail outlet or
distributor . Confirm your smart device
compatibility wit h this mon itor at
omronconnect.com
Prod uct cate gory
Electroni c S ph ygmomano meters
Prod uct des criptio n
Automatic Upper Arm Blood Pressure Monit o r
Model (code)
EVOL V (H EM-7600 T -E)
Display OLED display
Cuff pr essure range Pressure : 0 to 299 mmHg
Meas urement ra nge Pressure : 40 to 260 m mHg
Pulse: 40 to 180 be ats / min.
Accuracy Pressure : ±3 mmH g
Pulse: ±5% of display reading
Inflatio n Fuzzy-logic controlled by electric pump
Deflatio n Automa tic rapid def lation
Meas urement me thod Oscillometric meth od
T ran smission method
Bluetooth Smart
Wir eless commu nication Frequen cy range: 2 .4 GHz (240 0 - 2483 .5 MHz)
Modulation : GFSK
Effective r adiated po wer: <20 dB m
IP clas sificatio n IP 22
Power s ource
4 “AAA” batteries 1. 5V
Batt ery life Approxim ately 300 m easureme nts
(using new alkal ine batteries )
Durabl e period (Service life) Monito r: 5 years
Operat ing condi tions 10°C to 40°C / 15 to 90% RH ( non-condensi ng) /
800 to 10 60 hPa
Stor age / T ran sport
conditio ns
-20°C to 60°C / 10 to 90% RH (non-con densing)
Wei ght Monito r: Approxima tely 240 g
(not inclu ding batteri es)
Dimens ions Monito r: Approximat ely 85 mm × 120 mm × 20 mm
(no t includ ing the a rm cuf f)
Arm circ umference 22 to 42 cm
Contents Monitor, battery set, instruction manu al, setup ins tructions,
storage ca se
Applied part Ty p e B F
Prote ction ag ainst el ectric
shock
Inte rnall y powere d ME equi pment
Symbol d escripti ons
Please consult this instruction manual
Applied part - T ype BF
Degree of protection against electric shock (leakage
current)
T o indicate generally elevated, potentially hazardous,
levels of non-ionizing radiation, or t o indicate
equipment or syst ems e.g. in th e medical electrical
area that include RF transmitters or that intentionally
apply RF electromagnet ic energy for diagnosis or
treat ment.
T emperature limitation
Humidity limitation
Atmospheric p ressure limitation
Artery mark
Product production d ate is integrated in a Serial or LOT number, which placed
on the Rating Label and sales package: the first 2 digits mean year of
production, the next 2 digits - m onth of production.
Import ant informat ion regarding El ectro Magnet ic Compa tibility (EMC )
With the increased number of electronic devic es such as PC’s and mobile
(cellular) telephones, medical devices in use may be susceptible to
electromagnetic interference from other devices. Electromagnetic
interference may result in incorrect operation of the medical device and create
a potentially unsafe situation.
Medical devices should also not interfere with other devices.
In order to regulate the requirements for EMC (Electro Magnetic
Compatibility) with t he aim to preven t unsafe product sit u ations, the
EN60601-1-2:2007 standard has been implemented. This s tandard defines
the levels of immu nity to electromagnetic interferences as well as m aximum
levels of electromagnetic em issions for medical dev ices.
This medical device m anufactured by OMRON HEAL T HCARE conforms to
this EN60601-1-2:2007 s tandard for both immunity and emissions.
Nevertheless, special pr ecautions need to be observed:
• Do not use mobile (cellular) t elephones and ot he r devices, which generate
strong electrical or electrom agnetic fields, near the medical device. This m ay
result in incorrect operation of the device and create a potentially uns afe
situation. Recomm endation is to keep a minimum distance of 7 m. V erify
correct operation of the device in case the distance is sh orter .
Further documentation in accordance with EN60601-1-2:2007 is available at
OMRON HEAL THCARE EUROPE at the addr ess mentioned in this
instruction manual.
Documentation is also available at om ron-healthcare.com
.
About a w ireless communication interferen ce
This Product operates in the unlicensed ISM band at 2.4GHz. In case this
Product is used around the other w ireless devices including m icrowave and
wireless LAN, which operate same frequency band of this Product, there is a
possibility that interference occurs between this Product and such other
devices. If such interference occurs, please stop the operation of other
devices or r elocate this Product before using this Product or do not use t his
Product around t he other wireless device s.
Correct Disposal of Thi s Product
(W aste Electrical & Electronic Equipment)
This marking s hown on the product or its literature, indicates
that it should not be disposed of, with other household wastes
at the end o f it s working life. T o prevent possible harm to the
environment or human health from uncontrolled waste
disposal, please separate this product fr om other types of
wastes and rec ycle it responsibly t o promote the s ust a inable
reuse of material resources.
Household users should contact either the retailer where t hey purchased this
product, or their local government offi c e, for det ails of where and how they
can return this it em for environmentally safe recycling.
Business users should contact their supplier and check the term s and
conditions of the purchase contract. This pr oduct should not be mixed with
other commercial waste for disposal.
Manufacturer
OMRON HEAL THCARE Co., Ltd.
53, Kun otsubo, T erado- cho, Muko, KYOTO,
617-000 2 JAP AN
EU-representative
OMRON HEAL THCARE EUROPE B.V .
Scorpiu s 33, 2132 LR Hoofd dorp,
THE NETHERLANDS
www.omron-healthca re.com
Product ion facili ty
OMRON HEAL THCARE Co., Ltd.
Matsusak a Factory
1855-37 0, Kubo-cho , Matsusaka-shi,
Mie, 5 15-8503 Japan
Subsid iaries
OMRON HEAL THCARE UK L TD.
Opal Drive, Fox Miln e, Milton K eynes, MK15 0DG , UK
www.omron-healthca re.com
OMRON MEDIZINT ECHNIK HANDELSGESELLSCHAFT mbH
Gottlieb-Da imler-S trasse 10 , 68165 M annheim, GERMANY
www.omron-healthca re.com
OMRON SANTÉ FRANCE SAS
14, rue de Lisbonn e, 93561 Ro sny-sous-B ois Cedex, F RANCE
www.omron-healthca re.com
Made in Ja pan
Example: fluctuation within a day (male, 35 years old)
mmHg
200
150
100
50
61 2 1 8 2 4
Upper curve: systolic blood pressure
Lower curve: diastolic blood pressure
Time of day