Omron HBP-1100 User manual

Professional Blood Pressure Monitor
HBP-1100









Thank you for purchasing this OMRON Professional Blood Pressure Monitor.

Read this manual to ensure the safe and accurate use of the monitor.
IM-HBP-1100-E-01-08/2013
2294509-7A
13E1306
EN
FR
DE

ES
NL
RU

AR



Intended Use .........................................................................................1
Exemptions............................................................................................2
Notes on Safety.....................................................................................3

Components of the Product ..................................................................9
Options ..................................................................................................9
Features of the Product.......................................................................10
Features / Functions of Unit ................................................................ 11
Installing the Batteries ........................................................................13
Connecting the AC Adapter ................................................................13
Cuff Selection and Connection........................................................... 14
Applying the Cuff to the Patient ..........................................................15
Zero Indicator Function ....................................................................... 17

Measurement in “Normal Mode”.........................................................18
Measurement in “Auscultation Mode”.................................................20
Stopping the Measurement.................................................................21
Non-Invasive Pressure Measurement Principles ...............................22

Maintenance Inspection and Safety Management.............................23
Cleaning of the Device........................................................................23
Accessory Care...................................................................................23
Check before Use ...............................................................................24
Checking Pressure Accuracy..............................................................25
Troubleshooting...................................................................................26
List of Error Codes ..............................................................................29
Disposal...............................................................................................31

...................................................32
Manufacturer’s Declaration.................................................................35

1
EN



The device is a digital monitor intended for use in measuring blood
pressure and pulse rate in adult and pediatric patient population with arm
circumference ranging from 12 cm to 50 cm (from 5 inches to 20 inches).

This device should be used by a medical professional.

This device is intended for use on adults and children of age 3-years and older.

The instrument is designed for use in physicians’ offices, hospitals,
clinics and other medical facilities.




Warnings and cautions described in the instruction manual should be
observed at all times.

2


1. When a problem or damage occurs caused by the maintenance and/or repair
conducted by a person other than OMRON or the dealer specified by OMRON
2. The problem or damage of OMRON product caused by the product
of other manufacturer not delivered by OMRON
3. The problem and damage caused by the maintenance and/or repair
using the repair parts not specified by OMRON
4. The problem and damage caused by the results not observing the Notes
on Safety or the operational method mentioned in this Instruction Manual
5. Under the circumstances not within the operating conditions of this
unit including the power source or the setting environment mentioned
in this Instruction Manual
6. The problem and damage caused by the result(s) of remodeling or
improper repair of this product
7. The problem and damage caused by act of god such as fire,
earthquake, flood, or lightning
1. The contents of this Instruction Manual may be changed without prior
notice.
2. We have thoroughly reviewed the contents of this Instruction Manual.
However, if an inadequate description or error is found, please let us
know.
3. It is prohibited to copy a part of or the entire Instruction Manual
without getting OMRON’s permission. Unless this Instruction Manual
is used by an individual (company), it cannot be used without getting
OMRON’s permission from the standpoint of the Copyright Law.

3
EN

The warning signs and symbol examples indicated below are intended to
ensure safe use of the product and prevent damage and injury to you and
others. The signs and symbols are explained below.

 Indicates the matters in which death or severe bodily
damage may arise as a result of incorrect handling.
 Indicates the matters in which bodily harm or material
damage may arise as a result of incorrect handling.

Note:
Indicates general information to keep in mind when using the unit and
other useful information.



unit to malfunction.

distributor.

in an environment where combustible gas may be generated.

equipment. If MRI is to be performed, remove cuff connected to the unit
from the patient.


- Locations subject to vibration such as ambulances and emergency
helicopters.
- A location where there is gas or flame.
- A location where there is water or steam.
- A location where chemicals are stored.

altitude. Use only within the required ambient conditions.


sit on the cord.

pregnant women. Do not use on newborn infants and pregnant women.


4


- Locations with dust, salt, or sulfur.
- Locations directly exposed to sunlight for extended periods of time (in
particular, do not leave in direct sunlight or near a source of ultraviolet
light for extended periods, as ultraviolet light will cause deterioration
of the LCD).
- Locations subject to vibration or shock.
- Near heaters.

power ON/OFF.



standard (IEC60601-1-2). As such, it can be used simultaneously with
multiple medical instruments. However, if instruments that generate
noise such as an electric scalpel or a microwave therapy device are
near the unit, check the operation of the unit during and after use of
these instruments.

vital signs of the patient by auscultation or palpation. Avoid relying
solely on the measurement results of the unit when judging the patient’s
condition.

patients to operate this device.



- Make sure the AC adapter cable is not damaged (wires are not
exposed or broken), and the connections are firm.

For the AC adapter connected to the unit, supplies, and optional devices,
use only the standard accessories or OMRON-specified products.

splash on the unit.

other medical facilities.


unit is installed or being used.


switch.

5
EN



- Poor peripheral circulation, noticeably low blood pressure, or low body
temperature (there will be low blood flow to the measurement position)
- The patient uses an artificial heart and lung (there will be no pulse)
- An SpO2sensor and the cuff are attached to the same arm
- The patient has an aneurysm
- The patient has frequent arrhythmia
- Body motions such as convulsions, arterial pulsations, or trembling
(cardiac massage in progress, minute continuous vibrations,
rheumatism, etc.)

deformations due to falling, and that there is no dirt or moisture on the
unit.

verify that it operates normally and safely before use.

the unit falls, verify that it operates normally and safely.



adapter from the unit.

to a power outlet.

connectors, buttons, or openings in the housing.





manufacturer.


6



starting work.

disassemble or modify the unit.



with copious amounts of water. Do not rub. Seek medical attention
immediately.


installing a battery.

from the unit and store.


drop, bend, or hit the battery.

their polarities reversed.

wire or other metal object.




rinse with water.

batteries together.



waste, or disinfect before reuse.

extended period of time, periodically check the patient’s circulation.
In addition, wrap the cuff as indicated in the cautionary points in this
manual.



7
EN
change of body position.

- An upper arm on which intravenous drip or a blood transfusion is
being performed.
- An upper arm on which SpO2sensor, IBP catheter, or other instrument
is attached.
- An upper arm with a shunt for hemodialysis.

the side of the body where a mastectomy was performed, check the
patient’s condition.





hypercoagulability, check the condition of the arm after measurement.

large a cuff is used, the measured blood pressure value tends to be
lower than the actual blood pressure. If too small a cuff is used, the
measured blood pressure value tends to be higher.


- The part where the cuff is wrapped is at a different height than
the heart. (A difference of 10 cm (4 inches) in height may cause a
variation in the blood pressure value of up to 7 or 8 mmHg.)
- Body movement or conversing during measurement.
- Cuff wrapped over thick clothing.
- Pressure on the arm due to a rolled up sleeve.

tightness that allows two fingers to be inserted in between the cuff and
the arm.

measurement range cannot be guaranteed. Always check the patient’s
condition before deciding what steps to take.


any other cuff may result in incorrect measurement.

8
Note:


This manual does not contain cautionary information for optional
accessories.

not become entangled or bound.


- No smoke, abnormal odor, or abnormal noise is emitted.
- Press each button and verify that it operates.
- For functions that cause icons to light or flash, verify that the icons
light or flash (page 12).
- Measurement can be performed normally, and measurement error is
within the tolerance value.


follow local government rules and regulations.




wound at the location where the cuff is to be wrapped, follow the
instructions of the doctor.

compressing the upper arm.Some people may experience intense
pain, or transient spotting caused by subcutaneous hemorrhaging
(bruising) may appear. The spotting will disappear with time; however,
it may be appropriate to inform patients for whom this may be a
concern that spotting sometimes occurs, and if necessary, refrain from
measurement.

talk during measurement.

5 minutes before measurement.