Omron HEM-907 Owner Manual

HEM-907-E_B_M03_111006.pdf

INSTRUCTION MANUAL

OMRON

Digital Automatic Blood Pressure Monitor

Model

HEM-907

M

AX

INDEX

Thank you very much for purchasing the

OMRON Digital Automatic Blood Pressure

Monitor.

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 suffi cient understanding.

After reading this Instruction Manual, please keep it near the unit all the times for future reference.

= Read the instruction manual carefully

SYS

DIA mmHg

PULS

E mmHg

BPM

ON/OF

F

HIDE

100

AUTO

180

220

280

260

AVG.

MO

DE

SING

LE

MAN

U.

CHE

CK

STA

RT

AV

G

DE

./1 st

/2nd /3rd

STOP

A

R

T

.

Table of Contents

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

AVG.

MANU.

CHECK ......................................... 19

Installation and Replacement of

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

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

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

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

Specifi cations ............................................. 24

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

5329412-4C

1

2

Intended Use

Medical Purpose

Intended User

Patient Population

Environment

This is a medical device that measures the brachial blood pressure in a non-invasive manner.

Legally certifi ed: such as doctor, nurse and medical expert.

It is used on adult patients only.

The instrument is used in physicians’ offi ces, 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.

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 conducted by a person other than OMRON or the dealer specifi ed 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 specifi 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 fi re, earthquake, fl 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 (company), it cannot be used without getting OMRON’s permission from the standpoint of the Copyright Law.

3

4

Names and Functions of the Parts

Main unit

1. LCD display

2. HIDE (non-display) Button

SYS

DIA mmHg

3. DC jack

4. P-SET (pressure setting) Volume

DC8V

PULS

E mmHg

BPM

AC

HIDE

100

AUT

O

P-SET

140

180

220

280

260

AVG.

MOD

SINGLE

E

MAN

U.

CHE

CK

ON/O

FF

START

AV

D

EF

G./1

L ATIO

N

STOP

5. MODE Selector

6. ON/OFF

(power) Button

7. START Button

8. DEFLATION

(defl ation control) Button

9. Arm Cuff

Connector

10. STOP Button

Display

SYS

Systolic blood pressure

DIA mmHg

Diastolic blood pressure

PULSE

mmHg

BPM AC

HIDE

Contents when the AVG.

Mode is selected

AVG. : Mean value

1st : First measurement

2nd : Second measurement

3rd : Third measurement

Pulse rate


Ready to Measure

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.

Example of display

1

No. of arrhythmias

2 3

Battery level

Displays for the usable level.

Displays

Displays

for the low level.

for the unusable level.

Charging

Displays when the battery pack is being charged.

External power source

Displays AC when the unit is connected to the AC adapter.

5

6


Explanation of Functions

(1) Pressure setting function

P-SET

Infl 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 infl ation and automatically infl ates to the proper value.

Target value setting: The monitor infl ates 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.

However, the pressure values during the measurement are displayed.

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

(average) Mode is selected.

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

(3) Manual defl ation control function

A function to accelerate the defl ation speed by pushing a DEFLATION Button during defl ation.

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

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP


(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.

F1

F2

F3

Items to set

Number of measurements

Waiting time until the start of measurement

Measurement interval time

Set value

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

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.

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

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

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

List of Functions for each Mode

Measurement

Mode

Function

Single measurement (SINGLE)

Pressure setting function

Non-display function

Manual defl ation control function

Setting mode change function

Average

(AVG.)

Auscultation

(MANU.)

Check

(CHECK)

7

8

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

Warning

Contents

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

Caution

Indicates matters in which bodily harm or material damage* may arise as a result of incorrect 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 indicated 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 compulsory 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 infl 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 infl ammable gas, such as highly infl 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 fi 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.


In the following case, confi 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 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.


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 fi re ignition.

If you fi 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.


•

Do not disassemble or remodel the unit.


•

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 specifi ed for this unit.

It may cause fi 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 specifi 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.

•


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 fi re because of deteriorated insulation.

9

10

Notes on Safety

Caution

•

•

Be sure to use the power supply of 230 VAC.


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

•

It may cause fi 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 fi re or electric shock.

•

Do not install or store the unit where it may be sprayed with water or medication.


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 confi rm that all cords and tubes are connected correctly and completely before use.

•

Inspect the Buttons and so on to confi rm that the unit operates normally before use.

•

When using a battery pack, be sure to confi rm that the voltage is suffi cient before use. If you are not going to use the unit for a long period of time, remove the battery pack.

•

Do not infl 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.

2.

Be sure to inspect the unit on regular basis. Check accuracy on a 1 year interval.

If the unit has not been used for a while, be sure to confi rm that the unit operates normally and safely before use

Durability

The durability of this unit is fi 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.

3.

4.

Turn off the power and pull the AC adapter from the electric outlet. If an optional battery pack is used, remove it also.

Display “Trouble” on the unit so that it cannot be used.

Contact the dealer where you purchased the unit or the nearest OMRON dealer

11

12

Components of the Product

Main unit Accessories

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

Model: HEM-9CMC

Art.no.: 4928640-0

Applicable arm circumference: 22 to 32 cm

MIN RANGE

MAX

IND

EX

22~3

2cm

(9"~1

3")

REF

ART.

ON/OFF

HIDE

100

140

P-SE

T

180

220

MODE

AVG

.

SING

LE

AUTO

280

260 CHE

CK

STA

RT

DE

G./

FLA

1st /2

TION nd/3rd

STOP

AC adapter

(80230H907S)

Model: HEM-9ADAP

Art.no.: 1098200-0

Instruction Manual

(with guarantee card)

Air tube (1 m)

Art.no.: 4928647-8

Battery pack

(48H907N-E)

Model: HEM-9BAT

Art.no.: 1098391-0

Options

Large size arm cuff

Model: HEM-9CLC

Art.no.: 4928654-0

Applicable arm circumference:

32 to 42 cm

MIN RANGE MAX

IND

EX

32~42 cm(13 "~17"

REF HE

M-CL19 ART.

Air tube (1.3 m)

Model: HEM-9T1.3

Art.no.: 4928648-6

Medium size arm cuff

Model: HEM-9CMC

Art.no.: 4928640-0


22 to 32 cm

MIN RANGE

MAX

INDE

X

22~3 2cm

(9"~1 3")

REF H EM-C

R19

ART.

Stand exclusive for this unit

Model: HEM-9ST

Art.no.: 4928649-4

Small size adult arm cuff

Model: HEM-9CSC

Art.no.: 4928639-7


17 to 22 cm

MIN RANGE MAX

IND EX cm(7" ~ 9")

REF HEM

-CS19 ART.

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

Warning Requests from OMRON

1.

Do not apply the arm cuff during the intravenous

•

injection or transfusion.

Intravenous injection or transfusion is impossible.

•

•

•

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

Do not infl ate the unit without applying the arm cuff.

Do not use the damaged cuff.

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

Arm circumference Name of the arm cuff

17 - 22 cm

22 - 32 cm

32 - 42 cm

Small size adult arm cuff (option)

Adult arm cuff

Large size adult arm cuff (option)

•

•

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.

32~42 cm(13 "~17"

REF H

EM-CL

19

IND EX

22~3 2cm

(9"~1

3")

EM-C

REF H

R19

IND

EX

17~22 cm(7" ~ 9")

REF HE

M-CS1

MIN

MIN

RANGE

ART.

RANGE

ART.

MAX

MIN RANGE MAX

ART.

MAX

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.

Cuff side Air tube side

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 to the brachial artery.

ART.

IND

EX

22~32

~13")

REF HE

M-CR19

ART.

MIN

RANGE

MAX

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

INDEX cm(9"

~13")

REF HE

M-CR1

9

MIN

RANGE

ART.

MIN

RANGE

ART.

13

How to Apply the Arm Cuff

(cont.)

RANGE

RANGE

ART.

INDEX

22~32cm(9"~13")

REF HEM-CR19

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 measurement.

14

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 infl ammable gas, such as highly infl 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.


[2]

Caution

•

Be sure to use the power supply of 230 VAC.


Do not install or store the unit where it may be

• sprayed with water or medication.



•

•

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 confi rm that the unit operates normally before use.

[1]

DC

8V

•

When using an optional battery pack, the AC adapter functions as the charger also.

Warning

If any abnormal matter occurs during the measurement such as the infl ation does not stop, remove the arm cuff or pull the air tube from the main unit.

●

You may suffer peripheral neuropathy.


●

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.

How to Measure Blood Pressure

Caution

In the following case, confi rm the measurement with the stethoscope.

(1) When an irregular pulse wave is displayed


(2) When an error is generated or the measured value is doubtful


· 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.

· 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 only once

To measure three times

(or two times) consecutively

To measure by using a stethoscope

To confi rm the accuracy of pressure display

SINGLE Mode

AVG. Mode

MANU. Mode

CHECK Mode

Refer to Page

16.

Refer to Page

17.

Refer to Page

18.

Refer to Page

19.

15

16


(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.

3.

Set the MODE Selector to

“SINGLE”.

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

5.

•

•

Push the START Button to start the measurement.

If the infl ation is determined insuffi cient, the unit may start infl ation again automatically.

If you want to stop measurement, push the STOP Button.

The unit defl ates fast.

HIDE

ON/OFF

START

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

7.


Button to turn off the power.

ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

4.

•

•

Set the P-SET (pressure setting) Volume to “AUTO” or the target infl ation value.

When setting the P-SET to

“AUTO”, turn the Volume counterclockwise as far as it goes until you can hear the click sound.

When the systolic pressure is expected to exceed 220 mmHg, proper infl ation may not be possible in “AUTO” setting.

Set the target infl ation value to

30 to 40 mmHg higher than the expected systolic pressure.

ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

6.

Measured results are displayed.

SYS

DIA mmHg

PULSE mmHg

BPM

HIDE

1.



(in AVG. Mode)

2.



ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

3.


“AVG.”.

ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

5.

•

•

•

Push the START Button to start the measurement.

Set the unit to the start time of the fi rst measurement, then the unit starts measurement automatically.

After displaying the results of fi rst measurement, the unit will measure blood pressure in the set number of times automatically 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.

HIDE

ON/OFF

START

100

AUTO

P-SET

140 180

220

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

7.



ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

4.

•

•

Set the P-SET (pressure setting) Volume to “AUTO” or the target infl ation value.






ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

6.

•

•

Measured results are displayed.

After the measurement is completed, average values are displayed.

Each time a DEFLATION

(defl ation control) Button is pushed, the measurement results for each time are displayed.

SYS

DIA mmHg

PULSE mmHg

BPM

HIDE

To stop the measurement during the measurement:

Push the STOP Button.

To start the stopped measurement again:

Push the START Button.

17

18


(in MANU. Mode)

1.


2.

Place the stethoscope on the patient’s arm.

ON/OFF

HIDE

START

100

140 P-SET 180

220 AVG.

SINGLE MODE

CHECK MANU.

280

260

AUTO

STOP

3.



ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

4.


“MANU.”.

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

5.

•

Set the P-SET (pressure setting) Volume to “AUTO” or the

•

target infl ation value.






ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

MODE

AVG.

SINGLE

MANU.

CHECK

STOP

6.

Push the START Button to

•

•

•

•

•

start the measurement.

In the “AUTO” setting, the unit stops infl ation at the pressure considered to be 30 to

40 mmHg above the expected systolic pressure, then start defl ation.

The unit can be re-infl ated only while the START Button is pushed.

The pressure display is synchronized with the pulse rate and renewed.

Each time the DEFLATION

(defl ation control) Button is pushed, the unit defl ates by

5~10 mmHg.

When you press the STOP Button, the unit defl ates fast and ends the operation.

ON/OFF

START

HIDE

100

P-SET

140 180

220

AUTO

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP

7.



ON/OFF

START

HIDE

100

AUTO

P-SET

140 180

220

260

280

AVG.

MODE

SINGLE

MANU.

CHECK

STOP


(in CHECK Mode)

Display of pressure can be confi rmed 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 insuffi cient amount of mercury in the mercury, dirty glass tube, or clogged glass tube cap.

How to use the blood pressure monitor

1.

2.

3.

4.

5.

6.

7.

Connect the mercury blood pressure monitor, rubber ball, and this unit with the

T-shaped tube as shown in the Figure.




“CHECK”.

Tightly wrap the arm cuff over a sturdy cylindrical object.

Close the air release valve of rubber ball and infl ate the monitor to a certain value (pressure to be checked).

SYS

DIA mmHg

PULSE mmHg

BPM

AC

HIDE

100

P-SET

140

180

AUTO

220

280

260

AVG.

MODE

SINGLE

MANU

.

CHEC

K

ON/OFF

START

AV

DE

G./1

FLATION st /2nd/3rd

STOP

Compare the value displayed on this monitor and that on the mercury.

Open the air release valve of rubber ball to defl 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.

19

20

Installation and Replacement of Battery Pack

Warning

Do not disassemble or modify the battery pack.

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

Do not charge the battery pack by using equipment other than this unit.

If the fl uid in the battery pack gets into your eye, wash the eye with suffi cient water without rubbing the eye. Then immediately consult the

• doctor for treatment.

You may suffer injury, or battery fl uid may leak, or battery may heat, ignite fi 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.

Caution

Do not short the polarities of battery using metal object such as the wire.

If the fl uid in the battery is stained on your skin or cloth, immediately wash off the fl uid with

• water.

You may suffer injury, or battery fl uid may leak, or battery may heat, ignite fi re, or explode.

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 fi 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 fl 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.

Caution

Pull the AC adapter from the electric outlet when

• cleaning the unit.


After cleaning the unit, dry it well, then insert the

•

AC adapter to the electric outlet.


How to Clean the Unit after Use


•

Do not clean the unit with gasoline, thinner, or high concentration alcohol.

•

Do not sterilize the unit by autoclave or gas sterilization

(EOG, formaldehyde, or high concentration ozone.)

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

0.01 - 0.2 w/v%

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.

2.

Then wipe the unit with a soft dry cloth.

ON/OFF

HIDE

100

AUTO

180

220

AVG.

MODE

MANU

.

CHEC

K

START

AV

G./1

FLAT

ION

STOP

21

22

List of Error Codes

Error code

Er1

Er2

Er3

Er4

Er5

Er6

Er7

Er8

Er9

•

•

Cause

•

•

Infl ation error

When the pressure does not exceed 15 mmHg after operating a pump for 15 seconds from the start of infl ation

When the infl ation does not reach the set pressure of the arm cuff within the specifi ed time after starting the infl ation

•

•

•

•

Defl ation error

When the defl ation speed is too fast during the measurement

When the defl ation speed is too slow during the measurement

When the measurement does not end within the specifi ed time after starting the measurement

When the pressure is applied more than 5 minutes

•

Overpressure error

The arm cuff pressure exceeded 299 mmHg.

•

Insuffi cient infl ation error

Blood pressure could not be measured due to insuffi cient infl ation after the measurement ends.

Indeterminable blood pressure error

Blood pressure could not be measured even when the arm cuff pressure reached the specifi ed pressure.

•

Pulse wave small error

Pulse wave was too small.

How to correct

•

If the connector of rubber tube connecting the arm cuff and the main unit is loose, connect them correctly, then measure.

•

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.

•

If the rubber tube connecting the arm cuff and the main unit is bent, stretch it, then measure.

•

If the measurement is made by setting P-SET to

“AUTO”, ask the patient not move his/her arm or body during the infl ation.

•

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.


Measurement error

Relationship between systolic and diastolic pressures was abnormal.

•

Pulse rate error

Pule rate did not stay within the range of 30 to 199 beats/min.

•

Device error

There is a problem with the main unit of the blood pressure monitor.

•

•

•


Do not wrap the arm cuff over a thick cloth or by rolling up the jacket or shirt.

•

Check if the patient has an arrhythmia.

•

Ask the patient not to move his/her arm or body during the measurement.

Contact the dealer where you purchased the unit or the nearest OMRON dealer.

Troubleshooting

If a trouble occurs while using the unit, please check the following.

Problem What to inspect

Is the arm cuff wrapped correctly?

How to correct

Wrap the arm cuff correctly, and measure again.

The unit infl ates to abnormally high (low) pressure.

Is the patient moving his/her arm or body during infl ation?

Does this trouble occur with a specifi c patient?

For patients having arrhythmia, the unit may not infl ate properly

Ask the patient not to move his/her arm or body during measurement, and measure again.

Check the measurement by the stethoscope.

First of all, check the patient’s condition.

After checking the patient with the stethoscope as needed, take a proper measure in accordance with the “list of error codes”.

Is the patient moving his/her arm or body during measurement?

The unit cannot measure blood pressure.

The blood pressure values are extremely high (low).

Does the patient have an arrhythmia?

Ask the patient not to move his/her arm or body during measurement, and measure again.

Check the patient with a stethoscope.

Is the size of the arm cuff and the wrapping of arm cuff correct?

Select the arm cuff in accordance to the circumference of the patient’s arm, wrap it correctly, then measure again.

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.

23

24

Specifi cations

Name : OMRON Digital Automatic Blood Pressure Monitor HEM-907

Measurement Range

Accuracy

Infl ation

Defl ation

Air Release

Power supply

: Pressure; 0 to 299 mmHg

Pulse rate: 30 to 199 beats/min

: Pressure; Within +/-3 mmHg

Pulse rate; Within +/-5% of reading

: Automatic infl ation with pumping

: Automatic defl ation by electromagnetic control valve

: Automatic rapid air release by electromagnetic control valve

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

Electric Shock Protection Method or battery pack (4.8 VDC, 6 W)

: Class II B type

Operating Temperature and Humidity : 10 to 40°C, 30 to 85% RH

Weight of Main Unit

External Dimensions

: Approximately 910 g

: 139 (W) x 203 (H) x 131 (D) mm

Also included in the package

Options

: Adult arm cuff (with built-in air bag), AC adapter, air tube (1 m), Instruction

Manual (with guarantee card)

: 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 specifi cations may be changed without prior notice.

= Class II

= Type B

This blood pressure monitor fulfi 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

EC REP

www.omron-healthcare.com

Subsidiary

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

25

Important information for users

26

EMC & WEEE

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 interference may result in incorrect operation of the medical device and create a potentially unsafe situation.

Medical devices should also not interfere with other devices.

In order to regulate the requirements for EMC (Electro Magnetic Compatibility) with the aim to prevent unsafe product situations, the EN60601-1-2 standard has been implemented. This standard defi 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 fi 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 offi 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.

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