Omron Healthcare Blood Pressure Monitor HEM 907 User Manual

INSTRUCTION MANUAL

SYS

DIA

OMRON

mmHg

Digital Automatic Blood Pressure Monitor

BPM

HID

STA

Model

MOD

VG.

220

CHE

260

280

INDEX

HEM-907

Table of Contents

Thank you very much for purchasing the

OMRON Digital Automatic Blood Pressure

Monitor.

Intended use................................................. 2

Exemptions................................................... 3

Names and Functions of the Parts...............4

Notes on Safety............................................ 8

Components of the Product ....................... 12

Options....................................................... 12

How to Apply the Arm Cuff......................... 13

How to Use the Power Source

(AC Adapter)........................................... 14

How to Measure Blood Pressure ............... 15

SINGLE Mode........................................ 16

AVG. Mode............................................. 17

MANU. Mode.......................................... 18

CHECK Mode......................................... 19

Installation and Replacement of

Requests from OMRON to the

operators and the persons

responsible for maintenance

Please read thoroughly the “Notes on Safety”

of this Instruction Manual before using this unit

so that you can use it safely and correctly after

suf[cient understanding.

After reading this Instruction Manual, please

keep it near the unit all the times for future

reference.

Battery Pack...........................................20

How to Clean the Unit after Use................. 21

List of Error Codes .....................................22

Troubleshooting..........................................23

Speci[cations............................................. 24

= Read the instruction manual carefully

IM-HEM-907-E7-03-01/2012

5329412-4C

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 speci[ed 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 speci[ed 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 [re, earthquake, \ood, 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.

Names and Functions of the Parts

Main unit

1. LCD display

SYS

6. ON/OFF

(power) Button

2. HIDE (non-display) Button

mmHg

DIA

7. START Button

mmHg

PULSE

ON/OFF

BPM

DC8V

8. DEFLATION

(de\ation

control) Button

HIDE

START

SET

3. DC jack

MODE

SINGLE

VG.

220

9. Arm Cuff

Connector

MANU.

CHECK

AUTO

260

280

4. P-SET (pressure

setting) Volume

10. STOP Button

5. MODE Selector

Names and Functions of the Parts

Ready to Measure

Display

Pulse level / Number of

irregular pulse waves

Number of irregular pulse waves:

The pulse wave having a difference

of more than 25% from the average

interval of pulse waves is determined

as irregular. Number of irregular pulse

waves are displayed up to three times.

SYS

Systolic blood

pressure

mmHg

Example of display

No. of arrhythmias

DIA

Diastolic blood

pressure

mmHg

BPM

PULSE

Battery level

Displays

for the usable level.

for the low level.

HIDE

Displays

for the unusable level.

Contents when the AVG.

Mode is selected

Pulse rate

AVG. : Mean value

1st : First measurement

2nd : Second measurement

3rd : Third measurement

Charging

Displays

when the battery

pack is being charged.

External power source

Displays AC when the unit is con-

nected to the AC adapter.

Names and Functions of the Parts

Explanation of Functions

P SET

(1) Pressure setting function

In\ation 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 in\ation and automatically in\ates to the proper value.

Target value setting: The monitor in\ates to the target value.Pressure value is set to 30 to 40 mmHg above the expected

systolic pressure.

HIDE

(2) Non-display function

ON/OFF

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

However, the pressure values during the measurement are displayed.

START

HIDE

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

(average) Mode is selected.

SET

MODE

SINGLE

140

180

AVG.

MANU.

CHECK

220

260

100

STOP

AUTO

280

(3) Manual de\ation control function

ON/OFF

A function to accelerate the de\ation speed by pushing a DEFLATION Button

during de\ation.

START

HIDE

This function can be used when MANU. (auscultation) Mode is selected.

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

260

100

STOP

AUTO

280

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

Number of measurements

Waiting time until the start of measurement

Measurement interval time

2 times, 3 times

0 sec, 3 min, 5 min, 10 min.

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

Setting Change Mode.

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

260

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

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

100

STOP

AUTO

280

List of Functions for each Mode

Measurement

Single measure-

ment (SINGLE)

Average

(AVG.)

Auscultation

(MANU.)

Check

(CHECK)

Mode

Function

Pressure setting

function

Non-display

function

Manual de\ation

control function

Setting mode

change function

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

•^t^T^o^h^pere^ic^voennst^a^thⁿ^e^d^r^m^is^e^k^a^annⁱⁿ^d^g^t^s^he^ar^d^e^a^a^m^s^a^f^g^o^e^llo^to^w.^{you and others from happening.}

Warning sign

Contents

Indicates matters in which death or sever bodily damage may arise as a result of incorrect

handling.

Warning

Indicates matters in which bodily harm or material damage* may arise as a result of incorrect

handling.

Caution

* 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-

. The left icon refers to “prohibition to disassemble”.

cated by text or pictures in or near

The

icon indicates something that is compulsory (always follow). Matters involving actual compul-

sory actions are indicated by text or pictures in or near

source plug”.

. The left icon refers to “pulling the power

Warning

If any abnormal matter occurs during the measurement such as in\ation 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 in\ammable gas, such as highly in\ammable 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.}

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 [re 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, con[rm 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 [re ignition.}

If you [nd 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 [re ignition.}

Do not disassemble or remodel the unit.

•^{You may suffer electric shock, or there may be short circuit or [re 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 speci[ed for this unit.

•^{It may cause [re 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 speci[ed 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 [re 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 [re because of deteriorated insulation.}

Notes on Safety

Caution

Be sure to use the power supply of 230 VAC.

•^{It may cause [re or electric shock.}

Do not share an electric outlet with other unit or electric appliance.

•It may cause [re 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 [re 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 con[rm that all cords and tubes are connected correctly and completely before use.}

•^{Inspect the Buttons and so on to con[rm that the unit operates normally before use.}

•^{When using a battery pack, be sure to con[rm that the voltage is suf[cient before use. If you are not going to use the}

unit for a long period of time, remove the battery pack.

•^{Do not in\ate 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

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 con[rm that the unit operates normally and safely before use

Durability

The durability of this unit is [ve 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

Components of the Product

Main unit

Accessories

Medium size arm cuff (with built-in air bag)

Model: HEM-9CMC

Instruction Manual

(with guarantee card)

Art.no.: 4928640-0

Air tube (1 m)

Art.no.: 4928647-8

Applicable arm circumference: 22 to 32 cm

MIN

RANGE

MAX

ON/OFF

HIDE

START

MODE

260

280

AC adapter

Battery pack

(48H907N-E)

Model: HEM-9BAT

Art.no.: 1098391-0

(80230H907S)

Model: HEM-9ADAP

Art.no.: 1098200-0

Options

Large size arm cuff

Model: HEM-9CLC

Art.no.: 4928654-0

Applicable arm

Medium size arm cuff

Small size adult arm cuff

Model: HEM-9CSC

Art.no.: 4928639-7

Applicable arm

Model: HEM-9CMC

Art.no.: 4928640-0

Applicable arm

circumference:

32 to 42 cm

22 to 32 cm

17 to 22 cm

MIN

RANGE

MIN

MAX

RANGE

MAX

MIN

RANGE

MAX

Air tube (1.3 m)

Model: HEM-9T1.3

Art.no.: 4928648-6

Stand exclusive

for this unit

Model: HEM-9ST

Art.no.: 4928649-4

Wall-hanging kit

Model: HEM-9WM

Art.no.: 4928650-8

Pole-mounting kit

Model: HEM-9PM

Art.no.: 4928651-6

How to Apply the Arm Cuff

Requests from OMRON

Warning

•^{Do not use the unit to the patient using a pump oxy-}

Do not apply the arm cuff during the intravenous

injection or transfusion.

•^g^D^eonⁿ^a^o^to^t^rⁱ^.^{n\ate the unit without applying the arm cuff.}

• Intravenous injection or transfusion is impossible.

•^{Do not use the damaged cuff.}

MIN

RANGE

MAX

1. Select the arm cuff according to the arm circumference of the patient.

Arm circumference

17 - 22 cm

22 - 32 cm

32 - 42 cm

Name of the arm cuff

Small size adult arm cuff (option)

Adult arm cuff

MIN

RANGE

MAX

Large size adult arm cuff (option)

MIN

RANGE

MAX

•^{Be sure to use the arm cuff suitable for the size of the patient’s arm.}

•^{If an arm cuff not suitable for the size of the arm is used, blood pressure}

may not be measured correctly.

Cuff side

Air tube

side

2. Securely connect the air tube.

•^{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

the patient with the palm

of hand facing upward.

5. Place the arm cuff over the patient’s

arm by matching the mark indicating

the artery position

ART.

to the brachial artery.

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}

•^mTh^ee^asa^urm^redcu^cf^of^rw^rera^ctp^lyp^.ed diagonally along the shape of the arm does not affect the measurement value.

1-2 cm

How to Apply the Arm Cuff

(cont.)

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

[1] and the electric outlet [2].

Warning

Do not use the unit in the place where in\amma-

ble gas, such as highly in\ammable 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.

•^{You may suffer electric shock.}

[2]

[1]

Caution

Be sure to use the power supply of 230 VAC.

•^{It may cause [re or electric shock.}

Do not install or store the unit where it may be

sprayed with water or medication.

•You may suffer electric shock.

•When using an optional battery pack, the AC adapter

functions as the charger also.

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

•^c^Inasup^t^e^iocn^t^s^th^b^e^ef^B^o^u^re^tto^uⁿ^s^s^e.^{to con[rm that the unit operates}

normally before use.

How to Measure Blood Pressure

Warning

Caution

If any abnormal matter occurs during the mea-

surement such as the in\ation does not stop,

remove the arm cuff or pull the air tube from the

main unit.

In the following case, con[rm the measurement

with the stethoscope.

(1) When an irregular pulse wave is displayed

· An error may be displayed when an external vibra-

tion 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 vibra-

tion is applied or the patient moves his/her body.

· An error may be generated in the measured valueor

the blood pressure may not be able to measure for

the patient having peripheral circulatory disturbance

or extreme hypotension.

ꢁ

You may suffer peripheral neuropathy.

Requests from OMRON

ꢁ

Be sure that the patient should not touch the unit.

ꢁ

Be sure to monitor all the time that the unit and the

patient are not abnormal.

ꢁ

Do not use the unit in a vehicle.

· 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

Refer to Page

To measure

only once

SINGLE Mode

16.

To measure three

times

Refer to Page

AVG. Mode

(or two times)

consecutively

17.

To measure

by using a

Refer to Page

MANU. Mode

18.

stethoscope

To con[rm the

Refer to Page

accuracy of

CHECK Mode

19.

pressure display

How to Measure Blood Pressure

(in SINGLE Mode)

1. Wrap the arm cuff over the

patient’s arm.

2. Push the ON/OFF (power)

Button to turn on the power.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

260

100

STOP

AUTO

280

3. Set the MODE Selector to

“SINGLE”.

4. Set the P-SET (pressure set-

ting) Volume to “AUTO” or the

target in\ation value.

ON/OFF

START

HIDE

•^{When setting the P-SET to}

SET

180

MODE

SINGLE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

AVG.

MANU.

CHECK

220

260

220

260

100

“AUTO”, turn the Volume

STOP

AUTO

280

AUTO

280

counterclockwise as far as it

goes until you can hear the

•^c^W^li^h^ck^en^so^th^u^e^nd^{sy. stolic pressure is}

expected to exceed 220 mmHg,

proper in\ation may not be pos-

sible in “AUTO” setting.

Set the target in\ation value to

30 to 40 mmHg higher than the

expected systolic pressure.

6. Measured results are dis-

played.

5. Push the START Button to start

the measurement.

SYS

ON/OFF

mmHg

DIA

START

•^{If the in\ation is determined}

HIDE

insuf[cient, the unit may start

mmHg

BPM

SET

180

MODE

SINGLE

140

PULSE

AVG.

MANU.

CHECK

220

100

•ⁱ^Iⁿ^f^\^y^a^o^t^u^io^wⁿ^a^ang^t^a^toⁱⁿ^s^a^to^u^p^to^m^m^e^a^a^tic^su^a^r^ll^e^y^-^.

ment, push the STOP Button.

The unit de\ates fast.

STOP

260

280

AUTO

HIDE

7. Push the ON/OFF (power)

Button to turn off the power.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

100

STOP

260

280

AUTO

How to Measure Blood Pressure

(in AVG. Mode)

1. Wrap the arm cuff over the

patient’s arm.

2. Push the ON/OFF (power)

Button to turn on the power.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

260

100

STOP

AUTO

280

4. Set the P-SET (pressure set-

ting) Volume to “AUTO” or the

target in\ation value.

3. Set the MODE Selector to

“AVG.”.

ON/OFF

START

HIDE

•^{When setting the P-SET to}

“AUTO”, turn the Volume coun-

terclockwise as far as it goes

until you can hear the click

SET

180

MODE

SINGLE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

AVG.

MANU.

CHECK

220

260

100

220

260

100

STOP

AUTO

280

AUTO

280

•^s^W^o^h^u^eⁿ^{nd.the systolic pressure is}

expected to exceed 220 mmHg,

proper in\ation may not be pos-

sible in “AUTO” setting.

Set the target in\ation value to

30 to 40 mmHg higher than the

expected systolic pressure.

6. Measured results are

displayed.

5. Push the START Button to start

the measurement.

SYS

ON/OFF

mmHg

•^{After the measurement is}

completed, average values are

displayed.

•^{Set the unit to the start time of}

the [rst measurement, then the

unit starts measurement auto-

matically.

DIA

START

HIDE

mmHg

BPM

SET

180

MODE

SINGLE

PULSE

140

AVG.

MANU.

CHECK

220

100

•^{Each time a DEFLATION}

(de\ation control) Button is

pushed, the measurement

results for each time are

displayed.

STOP

260

280

AUTO

•^{After displaying the results of}

[rst measurement, the unit will

measure blood pressure in the

set number of times automati-

HIDE

•^c^F^a^o^l^r^ly^thbe^y^s^ta^e^k^ttiiⁿⁿ^g^g^a^o^{nf ti}^hⁿ^e^teⁿ^rv^u^a^m^l^{.ber of}

measurements, the waiting time

before start of measurement,

and the interval time, refer to

Page 7.

7. Push the ON/OFF (power)

Button to turn off the power.

To stop the measurement during the measurement:

Push the STOP Button.

To start the stopped measurement again:

Push the START Button.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

100

STOP

260

280

AUTO

How to Measure Blood Pressure

(in MANU. Mode)

1. Wrap the arm cuff over the

patient’s arm.

2. Place the stethoscope on the

patient’s arm.

ON/OFF

START

HIDE

P-SET

40 80

MODE

SINGLE

MANU.

CHECK

220

260

STOP

AUTO

280

4. Set the MODE Selector to

“MANU.”.

3. Push the ON/OFF (power)

Button to turn on the power.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

AVG.

MANU.

CHECK

220

260

100

220

260

100

STOP

AUTO

280

AUTO

280

6. Push the START Button to

start the measurement.

5. Set the P-SET (pressure set-

ting) Volume to “AUTO” or the

target in\ation value.

ON/OFF

•^{In the “AUTO” setting, the unit}

START

HIDE

stops in\ation at the pres-

•^{When setting the P-SET to}

“AUTO”, turn the Volume coun-

terclockwise as far as it goes un-

•^t^W^il^h^yo^e^uⁿ^c^th^a^eⁿ^shy^e^s^a^to^r^l^t^ic^he^pr^c^e^li^s^c^sku^s^re^ou^is^nd.

expected to exceed 220 mmHg,

proper in\ation may not be pos-

sible in “AUTO” setting.

SET

180

MODE

SINGLE

SET

180

MODE

SINGLE

sure considered to be 30 to

40 mmHg above the expected

systolic pressure, then start

140

AVG.

MANU.

CHECK

AVG.

MANU.

CHECK

220

100

220

260

100

STOP

260

280

AUTO

280

•^d^T^e^h^\^e^a^u^ti^noiⁿ^t^.^{can be re-in\ated}

only while the START Button is

•^p^T^u^h^s^e^h^per^de.^{ssure display is syn-}

Set the target in\ation value to

30 to 40 mmHg higher than the

expected systolic pressure.

chronized with the pulse rate

•^a^Eⁿ^a^d^ch^re^tⁿ^im^e^e^we^th^d^e^.^DEFLATION

(de\ation control) Button is

pushed, the unit de\ates by

•⁵^W^~^h¹^e0n^m^y^m^ou^H^p^gr.^{ess the STOP But-}

ton, the unit de\ates fast and

ends the operation.

7. Push the ON/OFF (power)

Button to turn off the power.

ON/OFF

START

HIDE

SET

180

MODE

SINGLE

140

AVG.

MANU.

CHECK

220

260

100

STOP

AUTO

280

How to Measure Blood Pressure

Display of pressure can be con[rmed by the CHECK Mode (yearly procedure).

What you need to prepare

(in CHECK Mode)

(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 insuf[cient 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

the Figure.

mmH

DIA

ULS

2. Push the ON/OFF (power)

Button to turn on the

power.

mmHg

3. Set the MODE Selector to

IDE

“CHECK”.

SET

MOD

SING

220

4. Tightly wrap the arm cuff

over a sturdy cylindrical

object.

CHEC

260

280

5. Close the air release valve

of rubber ball and in\ate

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 de\ate.

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.

Installation and Replacement of Battery Pack

Warning

Caution

Do not disassemble or modify the battery pack.

Do not throw the battery pack into [re or heat it.

Do not charge the battery pack by using equip-

ment other than this unit.

Do not short the polarities of battery using metal

object such as the wire.

If the \uid in the battery is stained on your skin

or cloth, immediately wash off the \uid with

water.

If the \uid in the battery pack gets into your

eye, wash the eye with suf[cient water without

rubbing the eye. Then immediately consult the

doctor for treatment.

•^{You may suffer injury, or battery \uid may leak,}

or battery may heat, ignite [re, or explode.

•^{You may suffer injury, or battery \uid may leak,}

or battery may heat, ignite [re, 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 [ve 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}

•^{If a}

mark starts to \ash, you can use the battery for twenty to thirty measurements. However it is

better to charge the battery as soon as possible.

mark is displayed, the battery is low. Please charge the battery.

How to Clean the Unit after Use

Requests from OMRON

Caution

Pull the AC adapter from the electric outlet when

cleaning the unit.

•^{You may suffer electric shock.}

•^{Do not clean the unit with gasoline, thinner, or high}

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

Chlorhexizin

Amphoteric surface active agent

0.01 - 0.2 w/v%

0.05 - 0.5 w/v%

0.01 - 0.2 w/v%

•^{When cleaning or disinfecting the unit, do not wipe the}

ON/OFF

AC adapter.

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

MODE

List of Error Codes

Error code

Cause

How to correct

In\ation error

•If the connector of rubber tube connecting the

arm cuff and the main unit is loose, connect them

correctly, then measure.

Er1

•^{When the pressure does not exceed 15}

mmHg after operating a pump for 15 seconds

•^f^W^ro^h^m^en^th^t^e^he^stⁱ^aⁿ^r^\ta^o^ti^foiⁿ^n\^dao^t^e^io^sⁿ^{not reach the set}

pressure of the arm cuff within the speci[ed

time after starting the in\ation

•^{If the rubber tube connecting the arm cuff and the}

main unit is bent, stretch it, then measure.

•^{If the arm cuff is wrapped loosely, wrap it correctly,}

then measure.

De\ation error

Er2

•^{When the de\ation speed is too fast during}

•^t^W^he^he^m^net^a^h^seu^d^re^e^m^\a^e^tⁿ^io^t^{n speed is too slow during}

•^t^W^he^he^m^net^a^h^seu^m^re^e^m^a^e^sⁿ^u^t^{rement does not end}

within the speci[ed time after starting the

•^m^W^e^h^a^e^snutr^h^e^e^m^per^net^{ssure is applied more than 5}

minutes

Overpressure error

•If the rubber tube connecting the arm cuff and the

main unit is bent, stretch it, then measure.

Er3

Er4

•^{The arm cuff pressure exceeded 299 mmHg.}

Insuf[cient in\ation error

•If the measurement is made by setting P-SET to

“AUTO”, ask the patient not move his/her arm or

body during the in\ation.

•^{Blood pressure could not be measured due}

to insuf[cient in\ation after the measurement

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.

Indeterminable blood pressure error

•^{Blood pressure could not be measured even}

when the arm cuff pressure reached the

speci[ed pressure.

•If the arm cuff is wrapped loosely, wrap it correctly,

Er5

Er6

then measure.

Pulse wave small error

•^{Pulse wave was too small.}

•If the arm cuff is wrapped loosely, wrap it correctly,

•^t^D^h^o^en^no^m^t^e^w^a^r^s^a^u^p^re^th^.^{e arm cuff over a thick cloth or by}

rolling up the jacket or shirt.

Measurement error

•Check if the patient has an arrhythmia.

Er7

Er8

Er9

•^{Relationship between systolic and diastolic}

•^{Ask the patient not to move his/her arm or body}

pressures was abnormal.

during the measurement.

Pulse rate error

•^{Pule rate did not stay within the range of 30}

to 199 beats/min.

Device error

•Contact the dealer where you purchased the unit or

the nearest OMRON dealer.

•^{There is a problem with the main unit of the}

blood pressure monitor.

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

again.

Is the arm cuff wrapped correctly?

Ask the patient not to move his/her arm or

body during measurement, and measure

again.

Is the patient moving his/her arm or body

The unit in\ates to abnormally during in\ation?

high (low) pressure.

Does this trouble occur with a speci[c

patient?

Check the measurement by the stetho-

scope.

For patients having arrhythmia, the unit

may not in\ate properly

After checking the patient with the stetho-

scope as needed, take a proper mea-

sure in accordance with the “list of error

codes”.

First of all, check the patient’s condition.

Ask the patient not to move his/her arm or

body during measurement, and measure

again.

Is the patient moving his/her arm or body

during measurement?

The unit cannot measure

blood pressure.

Does the patient have an arrhythmia?

Check the patient with a stethoscope.

The blood pressure values are

extremely high (low).

Select the arm cuff in accordance to the

circumference of the patient’s arm, wrap it

correctly, then measure again.

Is the size of the arm cuff and the wrapping

of arm cuff correct?

Is the level of the brachium to which the

arm cuff is wrapped at the same level as

the heart?

Keep the level of the brachium to which

the arm cuff is wrapped at the same level

as the heart, then measure again.

Speci[cations

Name

OMRON Digital Automatic Blood Pressure Monitor HEM-907

HEM-907-E / HEM-907-E7

Model

Display

Digital display

Measurement

Measurement Range

Oscillometric method

Pressure; 0 to 299 mmHg

Pulse rate: 30 to 199 beats/min

Pressure; Within +/-3 mmHg

Accuracy

Pulse rate; Within +/-5% of reading

Automatic in\ation with pumping

Automatic de\ation by electromagnetic control valve

Automatic rapid air release by electromagnetic control valve

AC adapter (230 VAC, 50 Hz. 20 VA)

or battery pack (4.8 VDC, 6 W)

Class II B type

In\ation

De\ation

Air Release

Power supply

Electric Shock Protection Method

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 speci[cations may be changed without prior notice.

= Class II

= Type B

This blood pressure monitor ful[ls 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.

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, THE NETHERLANDS

www.omron-healthcare.com

REP

OMRON HEALTHCARE Co., Ltd.

Production facility

Subsidiary

Mie, JAPAN

OMRON HEALTHCARE UK LTD.

Opal Drive

Fox Milne, Milton Keynes, MK15 0DG, U.K.

OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH

John-Deere-Str. 81a, 68163 Mannheim, GERMANY

www.omron-medizintechnik.de

OMRON SANTÉ FRANCE SAS

14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE

Made in Japan

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.

Medical devices should also not interfere with other devices.

Important information for users

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 de[nes 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 [elds, 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 of[ce, 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

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