3.1 T
• T
to deflate the wrist cuff.
• DO NOT use this monitor with other medical electrical (ME)
equipment simultaneouslyn
of the monitor and/or cause an inaccurate reading.
• Remain still and DO NOT talk while taking a measurement.
1. Press the [ST
All symbols appear on the display before starting the
measurement.
2. Remain still and d or talk until the entire
measurement process is completed.
As the r
ideal inflation level. This monitor detects your blood pressure
and pulse rate during inflation.
The “ ” symbol flashes at every heartbeat.
• The “ ” symbol appears if the wrist cuff is wrapped
around the wrist correctly
• When the “ ” symbol is displayed, the wrist cuff is not
applied correctly
your monitor off, then apply the cuff correctly
After your your blood
rate, the cuff automatically deflates. Y
pulse rate are displayed.
3. Press the [STn
• Y
• Weasurements. The wait time
allows the arteries to decompress and return
measurement form. Y
depending on your individual physiological char
Y stores the last reading.
4.1 Viewi
1. Press the button.
The last reading is displayed.
• If there are no readings stored in the
memory
5.1 Deleting the Readings S
1. Press the button, then the “ ” symbol appears.
2. While holding th button down, press and hold the
[ST
3. Using Y
4. Using Memory Function
5. Other Settings
In case of any of the below problems occur during measurement,
first check that no other electrical device is within 3the
problem persists, please refer to the table below
7.1 Mainten
Tns
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.
7.2 Storag
• S
Do not store your monitor:
• If your monitor is wet.
• In locations exposed to extreme temperatures, humidity
sunlight, dust or corrosive vapors su
• In locations exposed to vibrations or shocks.
7.3 Cleaning
• Do not use any abrasive or volatile cleaners.
• Use a soft dry cloth or a soft cloth moistened with neutral soap to
clean your monitor and wrist cuff, and then wipe them with a dry
cloth.
• Do not wash or immerse your monitor and wrist cuff in water
• Do not use gasoline, thinners or similar solvents to clean your
monitor and wrist cuff.
7.4 Calibratio
• The accuracy of this blood pressure monitor has been carefully
tested and is designed for a long
• It is generally recommended to have the unit inspected every two
years to ensure correct functioning and accut
your authorised
at the address given on the packaging or attached literature.
6. Error Messages and T
Display/
Problem
Possible Cause Solution
appears or the
wrist cuff does
not inflate.
The wrist cuff is not
applied correctly
Apply the wrist cuff
correctly
another measurement.
Refer to section 2.3.
Air is leaking from the
wrist cuff.
Contact your OMRON
retail outlet or
distributor
appears
The wrist cuff is
overinflated exceeding
300 mmHg.
Do not touch the wrist
cuff while taking a
measurement.
appears
Y
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 wrist cuff
correctly
another measurement.
Refer to section 2.3.
Remain still and sit
correctly during a
measurement.
If the “ ” symbol
continues
recommend you to
consult with your
physician.
appears
appears
appears
The monitor is
malfunctioned.
Press the [ST
STOP] button again. If
“Er” still appears,
contact your OMRON
retail outlet or
distributor
flashes
Batteries are low
Replacing all batteries
with 2 new alkaline
batteries is
recommended.
section 2.1.
appears or the
monitor is
turned off
unexpectedly
during a
measurement
Batteries are depleted.
Immediately replace all
batteries with 2 new
alkaline
to section 2.1.
No power
Nothing
appears on the
display of the
monitor
Batteries
depleted.
Battery
properly aligned.
Check the battery
installation for proper
placement. Refer to
section 2.1.
Readings
appear
or too low
Blood pressure varies constantly
including stress, time of day
apply the wrist cuff, may affect your blood
pressure. Review sections 2.2 - 2.4 a
3.
Any other
problems occur
Press the [ST
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
7. Mainte
• These specifications are subject to change without notice.
• In the clinical validation studyor
determination of diastolic blood pressure.
• This monitor is clinically investigated according to the
requirements of ISO 81060-2:2013.
• IP classification is protection provided res i
accordance with IEC 60529. This monitor is protected
solid foreign objects of 12.5 mm diameter and greater such as a
fingerng water drops which may cause
issues during a normal operation.
• This device has not been validated for use on pregnant patients.
Thank you for buying an OMRON product. This product is
constructed of high quality materials aaken
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
the date of purchase. The proper construction, workma
materials of rranted by riod
of warranty air
replace the defect product or any defective parts.
The warranty does no
A. Tand risks of transport.
B. Costs for repairs and / or defects resulting from repairs done by
unauthorised persons.
C. Periodic check-
D. Failurthan
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
Should warranty service be required ple
whom the product was purchased from or an authorised OM
distributoriterature
or to your specialised retailerdifficulties in finding
OMRON customer services, contact us for information.
www
Repair or replacement under the warranty does not give rise to any
extension or renewal of the warr
The warranty will turned
together with the original invoice / cash ticket issued to the
consumer by the retailer
8. Specifications
Product category Electronic S
Product description Automatic Wrist Blood Pressure Monitor
Model (Code) RS1 (HEM-6160-E)
Display LCD digital display
Cuff pressure range 0 to 299 mmHg
Blood pressure
measurement range
SYS: 60 to 260 mmHg
DIA: 40 to 215 mmHg
Pulse measurement
range
40 to 180 beats / min.
Accuracy
Pressure: ±3 mmHg
Pulse: ±5% of display reading
Inflation Automatic by electric pump
Deflation Automatic rapid deflation
Measurement method Oscillometric method
Operation mode Continuous operation
IP classification IP 22
Rating DC3 V 3.0 W
Power source 2 “AAA” alkaline batteries 1.5V
Battery life
Approximately
new alkaline batteries)
Durable period (Service
life)
5 years
Operating conditions
+10°C to +40°C / 15 to 90% RH (non-
condensing) / 800 to 1060 hPa
S
conditions
-20°C to +60°C / 10 to 90% RH (non-
condensing)
Weight
Approximately 85 g not including
batteries
Dimensions
Approximately 84 mm (w) × 62 mm (h) ×
21 mm (l)
(not including the wrist cuff)
Measurable wrist
circumference
13.5 to 21.5 cm
Memory S
Contents
Monitor
instruction manual
Protection against
electric shock
Internally powered ME equipment
Applied part T
Maximum temperature
of the applied part
Lower than +48°C
9. Limited W
• This device fulfils the provisions of EC directive 93/42/EEC
(Medical Device Directive).
• This blood pressure monitor is desig
European S
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
for OMRON blood pressure monitors, which is the Pr
Sensor
Important
(EMC)
Correct Disposal of This Product (W
Equipment)
10. Guidance and Ma
Symbols description
Applied part - T
Degree of protection against electric
shock (leakage current)
Ingress protection degree provided by
IEC 60529
CE Marking
Serial number
T
Humidity limitation
Atmospheric pressure limitation
Need for the user to consult this
instruction manual.
Indicates the correct positioning for the
monitor on the wrist
Measurable wrist circumference
Battery
Direct current
HEM-6160-E manufactured by OMRON HEALto
EN60601-1-2:2015 Electro Magnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at
www6160-E
website.
This marking shown on the product or itthat it
should not be disposed of, with other household wastes at the end
of its working life.
Tm
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 s
the purchase contract. This product should not be mixed with othe
waste for disposal.
IP XX
Made in Vietnam
Manufacturer
53, Kunotsubo, Terado-cho, Muko, KYOTO,
617-0002 JAPAN
EU-representative OMRON HEALTHCARE EUROPE B.V.
OMRON HEALTHCARE Co., Ltd.
OMRON HEALTHCARE UK LTD.
Scorpius 33, 2132 LR Hoofddorp,
THE NETHERLANDS
www.omron-healthcare.com
Production
facility
Subsidiaries
Opal Drive, Fox Milne, Milton Keynes, MK15
0DG, UK
www.omron-healthcare.com
OMRON MEDIZINTECHNIK
HANDELSGESELLSCHAFT mbH
Konrad-Zuse-Ring 28, 68163 Mannheim,
GERMANY
www.omron-healthcare.com
OMRON SANTÉ FRANCE SAS
14, rue de Lisbonne, 93561 Rosny-sous-Bois
Cedex, FRANCE
www.omron-healthcare.com
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
