HEM-907-E_B_M03_111006.

pdf

INSTRUCTION MANUAL
SYS

OMRON DIA
mmHg

Digital Automatic Blood Pressure Monitor

mm
PULS Hg
E

ON/O
BPM FF

Model
HIDE
STA
P-SE
RT
T
140

HEM-907
100 180
MO
DE
AVG. SING AV DE F
220 LE G . LA T I
/1 s O
MAN t /2 n N
AU d / 3r d
TO U.
260 CHEC
280 K

STO
P

X
A
M

X
DE
IN

T.
AR

Thank you very much for purchasing the Table of Contents

OMRON Digital Automatic Blood Pressure Intended use................................................. 2
Monitor. Exemptions................................................... 3
Requests from OMRON to the Names and Functions of the Parts............... 4
Notes on Safety ............................................ 8
operators and the persons Components of the Product ....................... 12
responsible for maintenance Options ....................................................... 12
How to Apply the Arm Cuff......................... 13
Please read thoroughly the “Notes on Safety” How to Use the Power Source
of this Instruction Manual before using this unit (AC Adapter)........................................... 14
so that you can use it safely and correctly after How to Measure Blood Pressure ............... 15
sufficient understanding. SINGLE Mode ........................................ 16
AVG. Mode ............................................. 17
After reading this Instruction Manual, please MANU. Mode.......................................... 18
keep it near the unit all the times for future CHECK Mode......................................... 19
Installation and Replacement of
reference. Battery Pack ........................................... 20
How to Clean the Unit after Use ................ 21
List of Error Codes ..................................... 22
= Read the instruction manual carefully Troubleshooting .......................................... 23
Specifications ............................................. 24

IM-HEM-907-E7-04-01/2018
5329412-4D
1

18A0183
 Intended Use
Medical Purpose This is a medical device that measures the brachial blood
pressure in a non-invasive manner.
Intended User Legally certified: such as doctor, nurse and medical expert.
Patient Population It is used on adult patients only.
Environment The instrument is used in physicians’ offices, hospitals, clinics
and other medical facilities.
Measurement Parameter ■ Non-invasive Blood Pressure
■ Pulse rate
Precautions for use Warnings and cautions described in the instruction manual
should be observed.

2
 Exemptions
OMRON will not bear any responsibilities on the following matters.
1. When a problem or damage occurs caused by the maintenance and/or repair con-
ducted 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 manu-
facturer 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
lightening

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 (com-
pany), it cannot be used without getting OMRON’s permission from the standpoint
of the Copyright Law.

3
 Names and Functions of the Parts
Main unit

1. LCD display

SYS
6. ON/OFF
2. HIDE (non-display) Button (power) Button
mmH
g
DIA

7. START Button
mm
PUL
SE
Hg

ON/O
DC BPM
AC
FF
8. DEFLATION
8V
(deflation
HID
E
control) Button
STA
P-S
RT
3. DC jack 100
140
ET
180
MO
D
E
220 AVG SINGL
. E AV D E F
G. L AT
/1 s ION 9. Arm Cuff
Connector
MA t /2n
d /3rd
AU NU
4. P-SET (pressure
TO 260 .
CHE
280 CK

setting) Volume
STO
P

10. STOP Button

5. MODE Selector

4
 Names and Functions of the Parts
Ready to Measure
Display

Pulse level / Number of

irregular pulse waves
SYS Number of irregular pulse waves:
The pulse wave having a difference
Systolic blood of more than ±25% from the average
interval of pulse waves is determined
pressure
as irregular. Number of irregular pulse
mmHg waves are displayed up to three times.

DIA Example of display

No. of arrhythmias
Diastolic blood 1 2 3
pressure
mmHg
PULSE

BPM AC Battery level

Displays for the usable level.

HIDE Displays for the low level.

Displays for the unusable level.

Contents when the AVG.
Mode is selected Pulse rate
AVG. : Mean value
1st : First measurement
Charging
2nd : Second measurement
Displays when the battery
3rd : Third measurement
pack is being charged.

External power source

Displays AC when the unit is con-
nected to the AC adapter.

5
 Names and Functions of the Parts
Explanation of Functions

(1) Pressure setting function P-SET

Inflation can be set by AUTO (automatic setting) or the target value.

AUTO (automatic setting): In the SINGLE (single measurement), AVG. (average), and MANU. (auscultation) Modes, the
monitor estimates the systolic blood pressure value during inflation and automatically inflates to the proper value.
Target value setting: The monitor inflates to the target value.Pressure value is set to 30 to 40 mmHg above the expected
systolic pressure.

(2) Non-display function HIDE

A function not to display the results of measured blood pressures.

ON/OFF

However, the pressure values during the measurement are displayed.

START

This function can be used when SINGLE (single measurement) or AVG.

HIDE

(average) Mode is selected.

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

(3) Manual deflation control function

A function to accelerate the deflation speed by pushing a DEFLATION Button ON/OFF

during deflation.
This function can be used when MANU. (auscultation) Mode is selected.
START
HIDE

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

6
 Names and Functions of the Parts
(4) Setting mode change function
You can set the number of times to measure, the waiting time until the start of measurement, and the interval between
measurements.

Items to set Set value

F1 Number of measurements 2 times, 3 times
F2 Waiting time until the start of measurement 0 sec, 3 min, 5 min, 10 min.
F3 Measurement interval time 5 sec, 30 sec, 1 min, 2 min, 3 min.

Procedure to change the set values

ON/OFF

1) When the power is off, press the ON/OFF Button for more than three
seconds while holding the START Button and change the mode to the HIDE
START

Setting Change Mode. DEF

AVG L AT I O r d
N
. /1st / 2nd / 3
P-SET MODE

2) Press the START Button to select the item from F1 to F3.

140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260

3) Press the DEFLATION Button to change the set values.

AUTO 280

List of Functions for each Mode

Measurement Single measure- Average Auscultation Check
Mode
Function ment (SINGLE) (AVG.) (MANU.) (CHECK)

Pressure setting
function
Non-display
function
Manual deflation
control function
Setting mode
change function

7
 Notes on Safety
• The warning signs and the sample icons shown here are listed for you to use the product safely and correctly as well as
to prevent the risk and the damage to you and others from happening.
• The icons and meanings are as follow.
Warning sign Contents
Indicates matters in which death or sever bodily damage may arise as a result of incorrect
Warning handling.

Indicates matters in which bodily harm or material damage* may arise as a result of incorrect
Caution handling.
* Material damage refers to a wide range of damage involving your house, household goods, domestic animals, and pets.

Examples of signs

The icon indicates caution (including warning and danger). Matters involving actual caution are
indicated by text or pictures in or near . The left icon refers to “caution for ignition”.

The icon indicates prohibitions (what you cannot do). Matters involving actual prohibitions are indi-
cated by text or pictures in or near . The left icon refers to “prohibition to disassemble”.

The icon indicates something that is compulsory (always follow). Matters involving actual compul-
sory actions are indicated by text or pictures in or near . The left icon refers to “pulling the power
source plug”.

Warning
If any abnormal matter occurs during the measurement such as inflation does not stop, remove the arm
cuff or pull out the air tube from the main unit.
• You may suffer peripheral neuropathy.

Do not wrap the arm cuff over the arm to which intravenous injection or transfusion is being conducted.
• Intravenous injection or transfusion is impossible.

Do not use the unit in the place where inflammable gas, such as highly inflammable anesthetic, may be
generated or in a high pressure oxygen room or an oxygen tent.
• It may cause ignition and explosion.

Do not touch the AC adapter with wet hands.

• You may suffer electric shock.

8
 Notes on Safety
Caution
When you are not going to use the unit for a long period of time, be sure to remove the AC adapter
from the electric outlet.
• You may suffer electric shock, or electric leak or fire may arise because of deteriorated insulation.
Be sure to remove the AC adapter from the electric outlet when installing, removing, or cleaning the
part.
• You may suffer electric shock or injure yourself.
Pull the AC adapter from the electric outlet when cleaning the unit.
• You may suffer electric shock.
In the following case, confirm the measurement with the stethoscope.
(1) When an irregular pulse wave is displayed
· An error may be displayed when an external vibration is applied or the patient moves his/her body.
(2) When an error is generated or the measured value is doubtful
· An error may be displayed when an external vibration is applied or the patient moves his/her body.
· An error may be generated in the measured value or the blood pressure may not be able to measure for the
patient having peripheral circulatory disturbance or extreme hypotension.
· An error may be generated in the measured value or the blood pressure may not be able to measure for the
patient having short variation of blood pressure such as arrhythmia.
After cleaning the unit, dry it well, then insert the AC adapter to the electric outlet.
• You may suffer electric shock.
Insert the AC adapter to the electric outlet as far as it goes.
Wipe off the dust on the AC adapter.
• You may suffer electric shock, or there may be short circuit or fire ignition.
If you find any trouble with this unit, immediately stop using it, turn off the power, pull out the AC
adapter from the electric outlet, then contact the repair department.
• You may suffer electric shock, or there may be short circuit or fire ignition.

Do not disassemble or remodel the unit.

• You may suffer electric shock, or there may be short circuit or fire ignition.

Do not use the unit to the patient using a pump oxygenator.

• The unit can not measure correctly. The unit cannot measure when it cannot detect any beat.
Do not use the AC adapter and the battery pack not specified for this unit.
• It may cause fire or electric shock.
Do not use a portable phone near the unit.
• The unit may malfunction.
Do not install the parts and/or instrument not specified for this unit.
• It may cause damage to the unit.
Do not use the damaged power cord or AC adapter, or loose electric outlet.
• You may suffer electric shock, or there may be short circuit or fire ignition.
Do not damage the power cord of the AC adapter by placing heavy thing on it or pinching it, or modify,
forcibly bend, pull, twist, or bundle it.
• You may suffer electric shock or there may be electric leak and fire because of deteriorated insulation.

9
 Notes on Safety
Caution
Be sure to use the power supply of 230 VAC.
• It may cause fire or electric shock.
Do not share an electric outlet with other unit or electric appliance.
• It may cause fire or electric leak.
Do not pull the power cord when pulling out the AC adapter from the electric outlet.
• The power cord will be disconnected or shorted and may cause fire or electric shock.
Do not install or store the unit where it may be sprayed with water or medication.
• You may suffer electric shock.

Requests from OMRON

• Do not place or put anything on the unit.

• Do not apply strong shock to or drop the unit.
• When you move the unit, be sure to turn off the power and remove the connected AC adapter.
• When using this unit concurrently with other unit, be sure to read the Instruction Manual of the other unit to be used
concurrently and understand the warnings and cautions before use.
• Be sure to confirm that all cords and tubes are connected correctly and completely before use.
• Inspect the Buttons and so on to confirm that the unit operates normally before use.
• When using a battery pack, be sure to confirm that the voltage is sufficient before use. If you are not going to use the
unit for a long period of time, remove the battery pack.
• Do not inflate the arm cuff without being wrapped over the arm.
• Do not use a damaged arm cuff.
• Do not use the unit in a vehicle.
• Be sure to monitor all the time that the unit and the patient are not abnormal.
• Please keep the unit out of the reach of patient.
• Clean and store the unit and accessories after each use.
• Do not clean the unit with gasoline, thinner, or high concentration alcohol.
• Do not disinfect the unit by autoclave or gas sterilization (EOG, formaldehyde, or high concentration ozone.)
• Do not store the unit in the following places.
· Under the direct sunshine
· Dusty or salty environment
· Places which slope, vibrate, and/or are prone to shocks
· Storage of chemicals or where gas may be generated
· Under high temperature and high humidity

10
 Notes on Safety
Maintenance
1. Be sure to inspect the unit on regular basis. Check accuracy on a 1 year interval.
2. If the unit has not been used for a while, be sure to confirm that the unit operates normally and safely before use

Durability
The durability of this unit is five years. (Arm cuff is a consumable.)

Measures to take at the time of trouble or accident

If a device error (Er9) occurs, take the following procedure promptly.
1. Remove the arm cuff from the patient’s arm.
2. Turn off the power and pull the AC adapter from the electric outlet. If an optional battery pack is used, remove it also.
3. Display “Trouble” on the unit so that it cannot be used.
4. Contact the dealer where you purchased the unit or the nearest OMRON dealer

11
 Components of the Product
Main unit Accessories
Medium size arm cuff (with built-in air bag) Instruction Manual (with guarantee card)
Model: HEM-CR19 Model: HEM-TUBE-100CE
Art.no.: 9523006-1 Air tube (1 m)
Applicable arm circumference: 22 to 32 cm Art.no.: 9523008-8
MIN RANGE MAX

EX
IND

ON/O
FF ")
m(9"~13
22~32c
ART.

-CR19
REF
HEM

HIDE
STA
P-S
RT
ET
140

AC adapter Battery pack

100 180
MO
E D
220 AVG. SINGLE AV D E F
G . L AT I
/1 s ON
MAN t / 2n

Model: HBP-ACCA907E (48H907N-E)

AU d / 3rd
TO U.
260 CHEC
280 K

Art.no.: 2815964-6 Model: HEM-9BAT

STO
P

or Art.no.: 1098391-0
Model: HBP-ACCA907UK
Art.no.: 2815965-4

Options
Large size arm cuff Medium size arm cuff Small size adult arm cuff
Model: HEM-CL19 Model: HEM-CR19 Model: HEM-CS19
Art.no.: 9523005-3 Art.no.: 9523006-1 Art.no.: 9523007-0
Applicable arm circumference: Applicable arm circumference: Applicable arm circumference:
32 to 42 cm 22 to 32 cm 17 to 22 cm
MIN RANGE MAX MIN RANGE MAX

MIN RANGE MAX

X
INDE
INDEX
INDEX

3") 9")
m(9"~1 17~22cm(7"~
22~32c
(13"~17")
32~42cm ART. ART.
REF HEM-CS19

R19
REF
HEM-C
9 ART.
REF HEM-CL1

Air tube (1.3 m) Stand exclusive for this unit Wall-hanging kit Pole-mounting kit
Model: HEM-TUBE-130CE Model: HEM-9ST Model: HEM-9WM Model: HEM-9PM
Art.no.: 9523010-0 Art.no.: 4928649-4 Art.no.: 4928650-8 Art.no.: 4928651-6

12
 How to Apply the Arm Cuff
Warning Requests from OMRON

Do not apply the arm cuff during the intravenous • Do not use the unit to the patient using a pump oxy-
injection or transfusion. genator.
• Intravenous injection or transfusion is impossible. • Do not inflate the unit without applying the arm cuff.
• Do not use the damaged cuff.
1. Select the arm cuff according to the arm circumference of the patient. MIN RANGE MAX

Arm circumference Name of the arm cuff

INDEX

)
(13"~17"
32~42cm

17 - 22 cm Small size adult arm cuff (option)

19 ART.
REF HEM-CL

22 - 32 cm Adult arm cuff

MIN RANGE MAX

X
INDE

32 - 42 cm Large size adult arm cuff (option)

~13")
cm(9"
22~32
ART.

R19
REF
HEM-C

• Be sure to use the arm cuff suitable for the size of the patient’s arm.
MIN RANGE MAX

INDEX

• If an arm cuff not suitable for the size of the arm is used, blood pressure
~ 9")
17~22cm(7"

ART.
REF HEM-CS19

may not be measured correctly.

Cuff side Air tube
2. Securely connect the air tube. side
• If you connect the attached 1m air tube, the air tube can be used with the
entire length of 1.2 m.

3. Prepare the patient to be ready to wrap the arm cuff.

• Wrap the arm cuff over the right upper arm’s skin as a rule.
• If the arm cuff is wrapped over a thick cloth or by rolling up the jacket or shirt, blood pressure may not be measured
correctly.

4. Place the right hand of 5. Place the arm cuff over the patient’s ART.
the patient with the palm arm by matching the mark indicating
of hand facing upward. the artery position
ART.
MIN
RANGE

to the brachial artery.

MAX

EX
IND

~13")
22~32cm(9"

-CR19
REF HEM ART.

6. Wrap the arm cuff snugly using both hands and securely fasten it with the Velcro tape. At this time, the lower
edge of the arm cuff must be placed 1 to 2 cm above the inner side of elbow joint.
• If the arm cuff is not wrapped snugly, patient may feel numbness on his/her arm, or blood pressure may not be
measured correctly.
• The arm cuff wrapped diagonally along the shape of the arm does not affect the measurement value.

1-2 cm
MIN
MIN
RANGE RANGE

EX
IND

")
22~3 2cm (9"~13

-CR19
REF HEM ART.
ART.

13
 How to Apply the Arm Cuff (cont.)

RANGE INDEX
RANGE

22~32cm (9"~13")

REF HEM-CR1
9

ART.
ART.

7. Adjust the level of the arm cuff to the level of the heart.
• Keep the level of the arm cuff at the same level as the heart during the measure-
ment.

How to use the Power Source (AC adapter exclusive for this unit)
Connect the AC adapter to the DC jack of the main unit
Warning [1] and the electric outlet [2].
Do not use the unit in the place where inflamma-
ble gas, such as highly inflammable anesthetic,
may be generated, or in the high pressure
oxygen room or the oxygen tent.
• It may cause ignition and explosion.
Do not touch the AC adapter with wet hands. [2]
• You may suffer electric shock.

Caution [1] DC
8V

Be sure to use the power supply of 230 VAC.

• It may cause fire or electric shock.
Do not install or store the unit where it may be • When using an optional battery pack, the AC adapter
sprayed with water or medication. functions as the charger also.
• You may suffer electric shock.
Requests from OMRON
• If this unit is used concurrently with other unit, be sure
to read the Instruction Manual of the other unit to be
used concurrently and understand the warnings and
cautions before use.
• Inspect the Buttons to confirm that the unit operates
normally before use.

14
 How to Measure Blood Pressure
Warning Caution
If any abnormal matter occurs during the mea- In the following case, confirm the measurement
surement such as the inflation does not stop, with the stethoscope.
remove the arm cuff or pull the air tube from the (1) When an irregular pulse wave is displayed
main unit. · An error may be displayed when an external vibra-
● You may suffer peripheral neuropathy. tion is applied or the patient moves his/her body.
(2) When an error is generated or the measured value
is doubtful
Requests from OMRON · An error may be displayed when an external vibra-
tion is applied or the patient moves his/her body.
● Be sure that the patient should not touch the unit. · An error may be generated in the measured valueor
● Be sure to monitor all the time that the unit and the the blood pressure may not be able to measure for
patient are not abnormal. the patient having peripheral circulatory disturbance
● Do not use the unit in a vehicle. or extreme hypotension.
· An error may be generated in the measured valueor
the blood pressure may not be able to measure for
the patient having short variation of blood pressure
such as arrhythmia.
Do not use a portable phone near the unit.
● The unit may malfunction.

List of Measurement Modes

To measure Refer to Page

SINGLE Mode
only once 16.

To measure three
times Refer to Page
AVG. Mode
(or two times) 17.
consecutively

To measure Refer to Page

by using a MANU. Mode
stethoscope 18.

To confirm the Refer to Page

accuracy of CHECK Mode
pressure display 19.

15
 How to Measure Blood Pressure (in SINGLE Mode)
1. Wrap the arm cuff over the 2. Push the ON/OFF (power)
patient’s arm. Button to turn on the power.
ON/OFF

START
HIDE

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

3. Set the MODE Selector to 4. Set the P-SET (pressure set-

“SINGLE”. ting) Volume to “AUTO” or the
ON/OFF ON/OFF

START target inflation value. START

• When setting the P-SET to

HIDE HIDE

DEF N DEF
AVG L AT I O r d AVG L AT I O r d
N
. /1st / 2nd / 3 . /1st / 2nd / 3
P-SET MODE P-SET MODE

“AUTO”, turn the Volume

140 180 SINGLE SINGLE
140 180
AVG. MANU. AVG. MANU.
100 220 CHECK 220 CHECK
100
STOP STOP

counterclockwise as far as it
260 260
AUTO 280 AUTO 280

goes until you can hear the

click sound.
• When the systolic pressure is
expected to exceed 220 mmHg,
proper inflation may not be pos-
sible in “AUTO” setting.
Set the target inflation value to
30 to 40 mmHg higher than the
expected systolic pressure.

5. Push the START Button to start 6. Measured results are dis- SYS

the measurement. played.

ON/OFF

• If the inflation is determined

mmHg
START DIA
HIDE

insufficient, the unit may start P-SET MODE

DEF
AVG L AT I O r d
N
. /1st / 2nd / 3
mmHg

inflation again automatically.

140 180 SINGLE
AVG. MANU. PULSE
100 220 CHECK

• If you want to stop measure-

STOP
260
AUTO 280 BPM

ment, push the STOP Button. HIDE

The unit deflates fast.

7. Push the ON/OFF (power)

Button to turn off the power.
ON/OFF

START
HIDE

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

16
 How to Measure Blood Pressure (in AVG. Mode)
1. Wrap the arm cuff over the 2. Push the ON/OFF (power)
patient’s arm. Button to turn on the power.
ON/OFF

START
HIDE

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

3. Set the MODE Selector to 4. Set the P-SET (pressure set-

“AVG.”. ting) Volume to “AUTO” or the
ON/OFF
ON/OFF

target inflation value. START

• When setting the P-SET to

START HIDE
HIDE

DEF N
DEF AVG L AT I O r d

“AUTO”, turn the Volume coun-

N
AVG L AT I O r d . /1st / 2nd / 3
. /1st / 2nd / 3
P-SET MODE P-SET MODE
140 180 SINGLE
140 180 SINGLE
AVG. MANU.
AVG. MANU.
220 CHECK

terclockwise as far as it goes

220 CHECK 100
100
STOP STOP
260
260
AUTO 280
AUTO 280

until you can hear the click

sound.
• When the systolic pressure is
expected to exceed 220 mmHg,
proper inflation may not be pos-
sible in “AUTO” setting.
Set the target inflation value to
30 to 40 mmHg higher than the
expected systolic pressure.

5. Push the START Button to start 6. Measured results are SYS

the measurement.
ON/OFF
displayed.
• Set the unit to the start time of • After the measurement is DIA
mmHg

completed, average values are

START

the first measurement, then the

HIDE

unit starts measurement auto-

DEF
AVG L AT I O r d
N
. /1st / 2nd / 3
displayed. mmHg

• Each time a DEFLATION

P-SET MODE
140 180 SINGLE PULSE

matically.
AVG. MANU.
100 220 CHECK

STOP

• After displaying the results of (deflation control) Button is

AUTO 280
260
BPM

first measurement, the unit will pushed, the measurement HIDE

measure blood pressure in the results for each time are

set number of times automati- displayed.
cally by taking an interval.
• For the setting of the number of
measurements, the waiting time
before start of measurement,
and the interval time, refer to
Page 7.

7. Push the ON/OFF (power) To stop the measurement during the measurement:
Button to turn off the power.
ON/OFF

Push the STOP Button.

HIDE
START
To start the stopped measurement again:
Push the START Button.
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

17
 How to Measure Blood Pressure (in MANU. Mode)
1. Wrap the arm cuff over the 2. Place the stethoscope on the
patient’s arm. patient’s arm.

ON/OFF

START
HIDE

D EF N
AVG L AT I O r d
. /1 st /2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

3. Push the ON/OFF (power) 4. Set the MODE Selector to

Button to turn on the power. “MANU.”.
ON/OFF
ON/OFF

START START
HIDE
HIDE

DEF N
DEF N AVG L AT I O r d
AVG L AT I O r d . /1st / 2nd / 3
. /1st / 2nd / 3
P-SET MODE
P-SET MODE
140 180 SINGLE
140 180 SINGLE
AVG. MANU.
AVG. MANU.
100 220 CHECK
100 220 CHECK

STOP STOP
260
260
AUTO 280
AUTO 280

5. Set the P-SET (pressure set- 6. Push the START Button to

ting) Volume to “AUTO” or the start the measurement.
ON/OFF
ON/OFF

target inflation value. • In the “AUTO” setting, the unit START

• When setting the P-SET to

START

stops inflation at the pres-

HIDE
HIDE

sure considered to be 30 to
DEF N
DEF N AVG L AT I O r d
AVG L AT I O r d . /1st / 2nd / 3

“AUTO”, turn the Volume coun-

. /1st / 2nd / 3
P-SET MODE P-SET MODE
140 180 SINGLE
140 180 SINGLE
AVG. MANU.

40 mmHg above the expected

AVG. MANU.
100 220 CHECK
100 220 CHECK

terclockwise as far as it goes un-

STOP STOP
260
260

systolic pressure, then start

AUTO 280
AUTO 280

til you can hear the click sound.

deflation.
• When the systolic pressure is • The unit can be re-inflated
expected to exceed 220 mmHg, only while the START Button is
proper inflation may not be pos- pushed.
sible in “AUTO” setting. • The pressure display is syn-
Set the target inflation value to chronized with the pulse rate
30 to 40 mmHg higher than the and renewed.
expected systolic pressure. • Each time the DEFLATION
(deflation control) Button is
pushed, the unit deflates by
5~10 mmHg.
• When you press the STOP But-
ton, the unit deflates fast and
ends the operation.
7. Push the ON/OFF (power)
Button to turn off the power.
ON/OFF

START
HIDE

DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK

STOP
260
AUTO 280

18
 How to Measure Blood Pressure (in CHECK Mode)

Display of pressure can be confirmed by the CHECK Mode (yearly procedure).

What you need to prepare

(1) Well-adjusted reference pressure monitor (including rubber ball),
(2) T-shaped tube,
(3) Two rubber tubes, and (4) something in the cylindrical shape to wrap the arm cuff such as the tea container (sturdy one
that will not break or deform with pressure)
* Measurement error may occur even with the mercury blood pressure monitor because of insufficient amount of mercury
in the mercury, dirty glass tube, or clogged glass tube cap.

How to use the blood pressure monitor

1. Connect the mercury blood

pressure monitor, rubber
ball, and this unit with the
T-shaped tube as shown in
SYS

the Figure. DIA

mmHg

2. Push the ON/OFF (power)

Button to turn on the PULS
E
mmHg

power. BPM
AC
ON/OF
F

3. Set the MODE Selector to HIDE

“CHECK”.
STAR
T
P-SE
T
140

4. Tightly wrap the arm cuff

180 MODE
100 D
AV E F L
SINGL G . / AT I O N
220 AVG. E 1st /
2nd / 3rd
MANU
.

over a sturdy cylindrical

CHEC
AU 260 K
TO
280

STO

object.
P

5. Close the air release valve

of rubber ball and inflate
the monitor to a certain
value (pressure to be
checked).
6. Compare the value displayed on this monitor and that on the mercury.
7. Open the air release valve of rubber ball to deflate.

CHECK result
(1) In the measuring rule, the test tolerance of blood pressure monitor (accuracy of pressure when shipped from the
factory) should not exceed 3 mmHg.
(2) If the CHECK result is +/- 3 mmHg or above, contact the dealer where you purchased this unit or the nearest OMRON
dealer.

19
 Installation and Replacement of Battery Pack
Warning Caution
Do not disassemble or modify the battery pack. Do not short the polarities of battery using metal
Do not throw the battery pack into fire or heat it. object such as the wire.
Do not charge the battery pack by using equip- If the fluid in the battery is stained on your skin
ment other than this unit. or cloth, immediately wash off the fluid with
If the fluid in the battery pack gets into your water.
eye, wash the eye with sufficient water without • You may suffer injury, or battery fluid may leak,
rubbing the eye. Then immediately consult the or battery may heat, ignite fire, or explode.
doctor for treatment.
• You may suffer injury, or battery fluid may leak,
or battery may heat, ignite fire, or explode.

1. Remove the battery cover on the back of the

main unit.

2. Installation: To install the battery pack, connect

the battery pack connector to the connector in the
battery cover.

Replacement: Remove the battery pack from the

connector and replace with a new one.

3. Install the battery cover and fasten it with

screws.

Battery life
• You can use the unit for approximately three hundred measurements.
• If a mark appears frequently even after the battery is charged, replace the battery.
• Approximate battery life is two years.

Charging time
• After inserting the AC adapter, the battery will start to charge automatically in approximately five seconds.
• While the battery is being charged, a mark turns on.
• The battery can be charged in approximately twelve hours.

Battery low

• Even after a mark starts to flash, you can use the battery for twenty to thirty measurements. However it is
better to charge the battery as soon as possible.
• If a mark is displayed, the battery is low. Please charge the battery.

20
 How to Clean the Unit after Use
Caution Requests from OMRON

Pull the AC adapter from the electric outlet when

cleaning the unit. • Do not clean the unit with gasoline, thinner, or high
• You may suffer electric shock. concentration alcohol.
After cleaning the unit, dry it well, then insert the • Do not sterilize the unit by autoclave or gas sterilization
AC adapter to the electric outlet. (EOG, formaldehyde, or high concentration ozone.)
• You may suffer electric shock.

1. Clean the blood pressure monitor,the cuff and the

cables using a cloth dampened with water,diluted
disinfectant alcohol or diluted mild detergent.
• To disinfect, wipe the unit with a soft cloth squeezed
well after moistened with the following disinfectant.

Benzalkonium chloride 0.01 - 0.2 w/v%

Chlorhexizin 0.05 - 0.5 w/v%
Amphoteric surface active agent 0.01 - 0.2 w/v%
• When cleaning or disinfecting the unit, do not wipe the
AC adapter.
ON/OF
F

HIDE
STAR

2. Then wipe the unit with a soft dry cloth.

T
P-SET
140
180
100 MODE
D
AV E F
220 AVG. SINGLE G . L AT I O N
/1 s
t / 2nd
MANU / 3rd
.
AUTO 260 CHEC
K
280

STO
P

21
 List of Error Codes
Error code Cause How to correct
Er1 Inflation error • If the connector of rubber tube connecting the
• When the pressure does not exceed 15 arm cuff and the main unit is loose, connect them
mmHg after operating a pump for 15 seconds correctly, then measure.
from the start of inflation
• When the inflation does not reach the set • If the rubber tube connecting the arm cuff and the
pressure of the arm cuff within the specified main unit is bent, stretch it, then measure.
time after starting the inflation • If the arm cuff is wrapped loosely, wrap it correctly,
then measure.
Er2 Deflation error
• When the deflation speed is too fast during
the measurement
• When the deflation speed is too slow during
the measurement
• When the measurement does not end
within the specified time after starting the
measurement
• When the pressure is applied more than 5
minutes
Er3 Overpressure error • If the rubber tube connecting the arm cuff and the
• The arm cuff pressure exceeded 299 mmHg. main unit is bent, stretch it, then measure.
Er4 Insufficient inflation error • If the measurement is made by setting P-SET to
• Blood pressure could not be measured due “AUTO”, ask the patient not move his/her arm or
to insufficient inflation after the measurement body during the inflation.
ends.
• When setting the P-SET to “AUTO”, turn the Volume
counterclockwise as far as it goes until you can hear
the click sound.
• Set the P-SET to 30 to 40 mmHg higher than the
systolic pressure of the patient, then measure.
Er5 Indeterminable blood pressure error • If the arm cuff is wrapped loosely, wrap it correctly,
• Blood pressure could not be measured even then measure.
when the arm cuff pressure reached the
specified pressure.
Er6 Pulse wave small error • If the arm cuff is wrapped loosely, wrap it correctly,
• Pulse wave was too small. then measure.
• Do not wrap the arm cuff over a thick cloth or by
rolling up the jacket or shirt.
Er7 Measurement error • Check if the patient has an arrhythmia.
• Relationship between systolic and diastolic • Ask the patient not to move his/her arm or body
pressures was abnormal.
during the measurement.
Er8 Pulse rate error
• Pule rate did not stay within the range of 30
to 199 beats/min.
Er9 Device error • Contact the dealer where you purchased the unit or
• There is a problem with the main unit of the the nearest OMRON dealer.
blood pressure monitor.

22
 Troubleshooting
If a trouble occurs while using the unit, please check the following.
Problem What to inspect How to correct
Wrap the arm cuff correctly, and measure
Is the arm cuff wrapped correctly?
again.

Ask the patient not to move his/her arm or

Is the patient moving his/her arm or body
body during measurement, and measure
The unit inflates to abnormally during inflation?
again.
high (low) pressure.

Does this trouble occur with a specific

patient? Check the measurement by the stetho-
For patients having arrhythmia, the unit scope.
may not inflate properly

After checking the patient with the stetho-

scope as needed, take a proper mea-
First of all, check the patient’s condition.
sure in accordance with the “list of error
codes”.

Ask the patient not to move his/her arm or

Is the patient moving his/her arm or body
body during measurement, and measure
during measurement?
The unit cannot measure again.
blood pressure.
The blood pressure values are Does the patient have an arrhythmia? Check the patient with a stethoscope.
extremely high (low).
Select the arm cuff in accordance to the
Is the size of the arm cuff and the wrapping
circumference of the patient’s arm, wrap it
of arm cuff correct?
correctly, then measure again.

Is the level of the brachium to which the Keep the level of the brachium to which
arm cuff is wrapped at the same level as the arm cuff is wrapped at the same level
the heart? as the heart, then measure again.

23
 Specifications
Name : OMRON Digital Automatic Blood Pressure Monitor HEM-907
Model : HEM-907-E / HEM-907-E7
Display : Digital display
Measurement : Oscillometric method
Measurement Range : Pressure; 0 to 299 mmHg
Pulse rate: 30 to 199 beats/min
Accuracy : Pressure; Within +/-3 mmHg
Pulse rate; Within +/-5% of reading
Inflation : Automatic inflation with pumping
Deflation : Automatic deflation by electromagnetic control valve
Air Release : Automatic rapid air release by electromagnetic control valve
Power supply : AC adapter (AC 100 - 240 V, 50 - 60 Hz, 0.2 A)
or battery pack (4.8 VDC, 6 W)
Electric Shock Protection Method : Class II B type
Operating Temperature and Humidity : 10 to 40°C, 30 to 85% RH
Weight of Main Unit : Approximately 910 g
External Dimensions : 139 (W) x 203 (H) x 131 (D) mm
Also included in the package : Adult arm cuff (with built-in air bag), AC adapter, air tube (1 m), Instruction
Manual (with guarantee card)
Options : Large size adult arm cuff, adult arm cuff, small size adult arm cuff, cuff cloth
of each size, air bag of each size, air tube (1.3 m), air tube (1 m), battery pack,
stand exclusive for this unit, wall-hanging kit, pole-mounting kit

* Please understand that specifications may be changed without prior notice. = Type B

= Class II

This blood pressure monitor fulfils the requirements of the EC directive 93/42 EC directive 93/42/EEC (Medical Device
Directive). It also conforms to the European standard EN 1060, Non-invasive Sphygmomanometers. Part 1: General
Requirements an Part 3: Additional Requirements for Electromechanical Blood Pressure Measuring Systems.

24
Manufacturer OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, Kyoto,
617-0002 JAPAN

EU-representative OMRON HEALTHCARE EUROPE B.V.

Scorpius 33, 2132 LR Hoofddorp,
EC REP THE NETHERLANDS
www.omron-healthcare.com
OMRON HEALTHCARE Co., Ltd.
Matsusaka Factory
Production facility
1855-370, Kubo-cho, Matsusaka-shi,
Mie, 515-8503 Japan
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
www.omron-healthcare.com
OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH
Subsidiaries Gottlieb-Daimler-Strasse 10, 68165 Mannheim, GERMANY
www.omron-healthcare.com
OMRON SANTÉ FRANCE SAS
14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE
www.omron-healthcare.com
Made in Japan

25
 English

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 interfer-
ence may result in incorrect operation of the medical device and create a
potentially unsafe situation.
Important information for users Medical devices should also not interfere with other devices.

In order to regulate the requirements for EMC (Electro Magnetic Compat-

ibility) with the aim to prevent unsafe product situations, the EN60601-1-2
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.

Correct Disposal of This Product

(Waste Electrical & Electronic Equipment)

This marking shown on the product or its literature, indicates

that it should not be disposed 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 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 take this item for environmentally safe recycling.

Business users should contact their supplier and check the terms and
conditions of the purchase contact. This product should not be mixed with
other commercial wastes for disposal.

This product does not contain any hazardous substances.

Disposal of used batteries should be carried out in accordance with the

national regulations for the disposal of batteries.

EMC & WEEE

26