Note: Subject to technical modification without prior notice.
Important information regarding Electro Magnetic Compatibility (EMC)
With the increased number of electronic devices 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 the aim to prevent unsafe product situations, the EN60601-1-2:2007
standard has been implemented. This standard defines the levels of immunity to
electromagnetic interferences as well as maximum levels of electromagnetic
emissions for medical devices.
This medical device manufactured by OMRON HEALTHCARE conforms to this
EN60601-1-2:2007 standard for both immunity and emissions.
Nevertheless, special precautions need to be observed:
• Do not use mobile (cellular) telephones and other devices, which generate
strong electrical or electromagnetic fields, near the medical device. This may
result in incorrect operation of the unit and create a potentially unsafe situation.
Recommendation is to keep a minimum distance of 7 m. Verify correct operation
of the device in case the distance is shorter.
Further documentation in accordance with EN60601-1-2:2007 is available at OMRON
HEALTHCARE EUROPE at the address mentioned in this instruction manual.
Documentation is also available at www.omron-healthcare.com.
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
wastes for disposal.
Correct Disposal of This Product
(Waste Electrical & Electronic Equipment)
Made in China
4. Troubleshooting and Maintenance
6. Technical Data
5. Optional Parts
4.1 The Icons and Error Messages
4.3 Maintenance
Calibration and Service
To protect your unit from damage, please observe the following:
• Do not subject the main unit and the cuff to extreme
temperatures, humidity, moisture or direct sunlight.
• Do not fold the cuff or tubing tightly.
• Do not disassemble the unit.
• Do not subject the unit to strong shocks or vibrations
(for example, dropping the unit on the floor).
• Do not use volatile liquids to clean the main unit.
• Do not wash the arm cuff or immerse it in water.
• Do not use petrol, thinners or similar solvents to clean
the arm cuff.
• Do not carry out repairs of any kind yourself. If a defect
occurs, consult your OMRON retail outlet or distributor
as mentioned on the packaging.
• 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.
• The unit should be cleaned with a soft, dry cloth.
• Use a soft, moistened cloth and soap to clean the arm
cuff.
Automatic Blood Pressure Monitor
ProLogic PL100 (HEM-7101-PR)
LCD Digital Display
Oscillometric method
Pressure: 0 to 299 mmHg
Pulse: 40 to 180/min.
Pressure: ±3 mmHg
Pulse: ±5% of display reading
Automatic by electric pump
Automatic pressure release valve
4 “AAA” batteries 1.5V (not included)
Capacity of new alkaline batteries is approx.
300 measurements
= Type B
Internally powered ME equipment
+10°C to +40°C / Maximum: 30 to 85% RH
-20°C to +60°C / Maximum: 10 to 95% RH / 700-1060hPa
Approximately 315g without batteries
Approximately 120g
Approximately 103 (w) mm × 62 (h) mm × 125 (l) mm
Approximately 146 mm × 446 mm (Medium cuff: arm
circumference 22 to 32 cm)
Nylon and polyester
Main unit, cuff, instruction manual
1. Unplug the air tube from the air jack.
2. Gently fold the air tube into the arm cuff.
4.4 Storage
Note:
Do not bend the air tube excessively.
Do not store the unit in the following situations:
• If the unit is wet.
• Locations exposed to extreme temperatures, humidity, direct sunlight,
dust or corrosive vapours.
• Locations exposed to vibrations, shocks or where it will be at an
angle.
Product Description
Model
Display
Measurement Method
Measurement Range
Accuracy
Inflation
Deflation
Power Source
Battery Life
Applied Part
Protection Against
Electric Shock
Operating
temperature/ Humidity
Storage temperature/
Humidity
Console Weight
Cuff Weight
Outer Dimensions
Cuff Dimensions
Cuff Material
Package Content
• This device fulfils the provisions of EC directive 93/42/EEC (Medical Device
Directive).
• 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.
Manufacturer
OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, Kyoto,
617-0002 JAPAN
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes
MK15 0DG, U.K.
OMRON (DALIAN) CO., LTD.
Dalian, CHINA
Distributed by
Production Facility
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp
THE NETHERLANDS
EU-representative
Medium Arm Cuff
Arm circumference
22 - 32 cm
CM2-9513256-6
(Model: HEM-CR24)
Large Arm Cuff
Arm circumference
32 - 42 cm
CL2-9513255-8
(Model: HEM-CL24)
Error Display Cause Remedy
Cuff is under inflated.
Carefully read and repeat the
steps listed under section 3.3.
Movement during
measurement.
Repeat measurement. Remain
still and do not talk during
measurement.
Air plug disconnected.
Insert the air plug securely.
Refer to section 3.1.
Arm cuff not applied
correctly.
Apply the arm cuff correctly.
Refer to section 3.1.
Clothing is interfering
with the arm cuff.
Remove any clothing
interfering with the arm cuff.
Air is leaking from the
arm cuff.
Replace cuff with new one.
Arm cuff has been
inflated above
299 mmHg.
Do not inflate the arm cuff
above 299 mmHg.
Refer to section 3.3.
Battery power is low.
Replace all four “AAA”
batteries with new ones.
Refer to section 2.1.
Device error.
Contact your OMRON retail
outlet or distributor.
Blinks or appears
continuously
Arm cuff deflates too
soon.
The arm cuff is loose.
Apply the cuff correctly
so that it is firmly
wrapped around the
arm.
Refer to section 3.1.
Cannot measure or
readings are too low
or too high.
The arm cuff has not
been inflated
sufficiently.
Inflate the cuff so that it
is 30 to 40 mmHg
above your previous
measurement result.
Refer to section 3.3.
The unit loses power
during measurement.
The batteries are
empty.
Replace the batteries
with new ones.
Nothing happens
when you press the
buttons.
The batteries are
empty.
Replace the batteries
with new ones.
The batteries have
been inserted
incorrectly.
Insert the batteries with
the correct (+/ -)
polarity.
Other problems.
Press the O/I START button and repeat
measurement.
If the problem continues, try replacing the
batteries with new ones.
If this still does not solve the problem, contact
your OMRON retail outlet or distributor.
Arm cuff pressure
does not rise.
The air plug is not
securely inserted into
the main unit.
Make sure that the air
jack is connected
securely.
Refer to section 3.1.
Air is leaking from the
arm cuff.
Replace the arm cuff
with a new one.
4.2 Troubleshooting
Problem Cause Remedy
The reading is
extremely low (or
high).
Arm cuff not applied
correctly.
Apply the arm cuff
correctly.
Refer to section 3.1.
Movement or talking
during measurement.
Remain still and do not
talk during
measurement.
Clothing is interfering
with the arm cuff.
Remove any clothing
interfering with the arm
cuff.
Warranty Statement
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 guaranteed by OMRON for a period of 2 years after the date of
purchase. The proper construction, workmanship and materials of this product
is guaranteed by OMRON. During this period of guarantee OMRON will,
without charge for labour or parts, repair or replace the defect product or any
defective parts.
The guarantee covers only products purchased in the UK
The guarantee 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 accessories or other attachments other than the main
device itself, unless explicitly guaranteed 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 guarantee.
Should guarantee 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.
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 complete product is returned together
with the original invoice / cashticket issued to the consumer by the retailer.