Omron Healthcare Blood Pressure Monitor HEM 907XL User Manual |
INSTRUCTION MANUAL
IntelliSense™ Blood Pressure Monitor
ModelHEM-907XL
Table of Contents
Be Sure to Read This Section
S
Y
S
Exemptions ........................................2
m
Notes on Safety .................................3
m
H
g
D
I
A
Know Your Unit
m
m
P
U
H
g
Features of the Product .....................7
Components of the Product...............8
Options ...........................................9
Features and Functions ...................10
Names of the Parts ......................10
Functions and setting
L
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8
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while the unit is in use..................12
K
2
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0
S
T
O
P
Preparations before Measurement
How to Apply the Cuff ......................14
How to Use the Power Source ........16
How to Use the AC Adapter............16
Installation and Replacement
X
A
M
X
E
D
N
I
of Battery Pack.............................17
How to Measure Blood Pressure
List of Measurement Modes ............19
SINGLE Mode ..............................20
AVG Mode ....................................22
MANU Mode.................................24
How to Check Pressure Accuracy..26
How to Clean the Unit after Use........27
List of Error Codes...........................28
Troubleshooting................................29
Thank you for purchasing the OMRON
IntelliSense™ Blood Pressure Monitor.
Please thoroughly read this Instruction Manual
before using this monitor to ensure safe and
accurate use.
Specifications
Caution.............................................30
Five Year Limited Warranty..............31
Specifications...................................31
Please keep this manual near the monitor all
the time for future reference.
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EXEMPTIONS
NOTES ON SAFETY
• The warning signs and the sample icons shown here are listed to insure safe and accurate use.
• The icons and meanings are as follows.
OMRON does not accept liability and warranty becomes void under the following
circumstances:
Warning sign
Contents
1. When persons, not authorized by OMRON, perform repairs or modifications of this
product.
Indicates matters in which death or severe bodily damage may arise as a result
of incorrect handling.
Indicates matters in which bodily harm or material damage* may arise as a
result of incorrect handling.
2. When use and/or operation of this device is adversely effected by a device not
manufactured by OMRON.
* Material damage refers to a wide range of damage involving your house, household goods, domestic animals, and pets.
3. When use and/or operation of this device is adversely effected by use of parts, not
authorized by OMRON, to repair or modify this product.
Examples of signs
The
icon indicates caution (including warning and danger).
4. When Notes on Safety or Instructions for Use contained in this manual are not followed.
Matters involving actual caution are indicated by text or pictures in or near
The pictured icon refers to "caution for flammability".
.
5. When use and/or operation of this device is effected by an act of God, such as fire,
earthquake, flood or other natural disasters.
The
icon indicates prohibitions (what you cannot do).
Matters involving actual prohibitions are indicated by text or pictures in or near
The pictured 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 pictured icon refers to "unplugging the power source plug".
.
Self diagnosis of measured results or treatment is dangerous. Please follow
the instruction of the doctor or healthcare provider.
If cuff inflation does not stop, remove the cuff or pull out the air tube from the
main unit.
If battery fluid gets into your eye or comes in contact with skin, wash the effected
area with water repeatedly. Immediately consult a doctor for treatment.
Do not wrap the cuff over an arm to which intravenous injection or transfusion
is being conducted, or when otherwise contraindicated.
Do not connect the air tube or the cuff to other equipment which is connected
to an intracorporeal organ. Air embolisms may result.
Do not use this unit in the presence of flammable gas or anesthetics or in a
high pressure oxygen room or oxygen tent.
1. The product and contents of this Instruction Manual may be changed without prior notice.
2. We have prepared the contents of this Instruction Manual thoroughly. However, if an
inadequate description or error is found, please let us know.
Do not use the battery pack for devices other than for this unit.
Do not disassemble the battery pack.
3. Reproducing or copying any or all of this Instruction Manual without OMRON’s written
consent is prohibited.
Do not touch the AC adapter with wet hands.
2
3
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NOTES ON SAFETY
NOTES ON SAFETY
Do not use a cellular phone near this unit.
Unplug the AC adapter from the electric outlet if this unit is unused for an
extended period of time.
Do not use this unit in a vehicle.
Unplug the AC adapter from the electric outlet when installing, removing, or
cleaning the unit.
Do not install the parts and/or instruments not specified for this unit.
Do not use a broken power cord or AC adapter.
Do not install or store this unit where it may come in contact with water or
liquid medication.
Confirm readings with a stethoscope when an irregular pulse wave is
displayed or when the measured value is questionable or erratic.
This is a Class II device with double isolation. Earth pin is not for protective
purposes.
Use an AC adapter indicated for use with a power supply of 110 VAC.
Do not share an electric outlet with other unit or electric appliance.
General advice
Do not place or put anything on this unit.
Do not drop this unit.
After cleaning this unit, dry it well before plugging the AC adapter in the
electric outlet.
Turn off power to the unit and unplug the AC adapter from the electric outlet before moving
the unit.
If this unit fails to perform as indicated, discontinue use, turn off the unit,
unplug the AC adapter from the electric outlet, and contact OMRON’s repair
department.
Read the instruction manual of the other devices to be used at the same time with this unit, to
understand and be aware of the interaction between the devices.
When using the unit
• Do not inflate the cuff without being wrapped over the arm.
• Do not use a damaged cuff.
Do not disassemble or modify this unit.
• Be sure that patients do not touch the Buttons of this unit.
Do not use any cuff other than the models exclusive for this unit.
Do not use this unit on infants.
After using the unit
• Do not disinfect this unit by autoclave or gas sterilization (EtO, gluteraldehyde, or high
concentration ozone).
Do not use this unit on patients using a pump oxygenator.
Do not use an AC adapter or battery pack not specified for this unit.
Do not install or store this unit in the following places.
• Under the direct sunlight,
• Dusty or salty environment,
• Places having slope, vibration, and/or shock,
• Storage of chemicals or where combustable gas may be generated,
• Under high temperature and high humidity.
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NOTES ON SAFETY
Maintenance and inspection
FEATURES OF THE PRODUCT
OMRON IntelliSense™ Blood Pressure unit, Model HEM-907XL is developed to measure blood
pressure and pulse rate accurately and simply in a doctor's office, examination room,
or patient bedside.
1. Check the unit operation on regular basis.
2. If this unit has not been used for more than three months, be sure to check that this unit
operates normally and safely before use.
• One-button operation
Simply wrap the cuff and push the START Button. Blood pressure and pulse rate are automatically
measured by the oscillometric method.
• Automatic pressure setting
Troubleshooting
When the P-SET (Pressure Setting) Knob is set to "AUTO," the unit will automatically inflate the
cuff to the optimal pressure according to each patient's blood pressure. Pre-setting inflation level
is not necessary.
If device error 9 (Er9) occurs, take the following procedure promptly:
(1) Remove the cuff from the patient's arm.
• Noiseless operation
(2) Turn off the power of the unit and unplug the AC adapter from the electric outlet.
(3) Display "Out of use" on this unit so that it cannot be used.
(4) Contact Omron for repair service (1-877-216-1336).
This unit operates so quietly that it can be used in the patient room at night.
• Average Mode (AVG Mode)
In the AVG Mode, this unit will automatically measure for two or three times. The average of
systolic and diastolic blood pressures and pulse rate are displayed. Each measurement can also
be shown individually. The number of measurements, waiting time before first measurement, and
the interval can be changed.
• Auscultation Mode (MANU Mode)
You can measure auscultatory blood pressure by using a stethoscope, with automatic cuff inflation
and deflation by this unit. Because the cuff pressures during deflation are displayed digitally and
synchronized with the heart beat, they can be read with accuracy. After taking systolic reading
you can accelerate cuff deflation to shorten measurement time.
• Large and easy to read display
Large and easy to read figures are displayed on the LCD display.
The IntelliSenseTM Monitor inflates the cuff to the ideal level with each use. No adjustments are
required by the user to select an inflation level. This is especially convenient for hypertensive users
and for people with certain arrhythmia or heart disorders, because their blood pressure is likely to
fluctuate. The advantage is Personalized Inflation for maximum comfort.
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7
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COMPONENTS OF THE PRODUCT
COMPONENTS OF THE PRODUCT
Main unit
(not included)
Options
IntelliSense™ Blood Pressure
Monitor, Model HEM-907XL
Cuffs without bladder *
Bladders *
Extra Large Bladder
For use with the
HEM-907XL only.
Extra Large Cuff
For use with the
HEM-907XL only.
Model:HEM-907-CUFFX
Model: HEM-907-BLDRX
Large Cuff
Model:HEM-907-CUFFL
Large Bladder
Model: HEM-907-BLDRL
Medium Cuff
Model: HEM-907-CUFFM
Medium Bladder
Model: HEM-907-BLDRM
Small Cuff
Model: HEM-907-CUFFS
Small Bladder
Model: HEM-907-BLDRS
Accessories
(Included and also available separately)
Cuff / bladder set Large
(with built-in bladder) *
Model: HEM-907-CL19
Applicable arm circumference:
13" to 17" ( 32 to 42 cm)
Air tube 1.3 m (51 1/6")*
Model: HEM-TUBE-130
Cuff / bladder set Medium
(with built-in bladder) *
Model: HEM-907-CR19
Applicable arm circumference:
Cuff / bladder set Extra Large
(with built-in bladder) *
Model: HEM-907-CX19
For use with the HEM-907XL
unit only.
9" to 13" (22 to 32 cm)
The air tube is available for the large,
medium or small size cuff.
It is NOT for use with the extra-large
cuff size.
Applicable arm circumference:
17" to 20" ( 42 to 50 cm)
Cuff / bladder set Small
(with built-in bladder) *
Model: HEM-907-CS19
Applicable arm circumference:
7” to 9" (17 to 22 cm)
Exclusive Stand
Model: HEM-907-STAND
Wall-hanging kit
Model: HEM-907-WKIT
Pole-mounting kit
Model: HEM-907-PKIT
AC adapter
Model: HEM-AC-J
Air tube 1.0m (39 1/3") *
Model: HEM-TUBE-100X
Battery pack (48H907N)
Instruction Manual
Model: HEM-907-PBAT
Items identified
with an asterisk (*)
are consumables
and not covered by
the guarantee.
Accessories and
options are subject
to change without
prior notice.
The air tube is available for the
large, medium or small cuff size.
It is NOT for use with the
extra-large cuff size.
Items identified with an asterisk (*) are consumables and not covered by the guarantee.
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FEATURES AND FUNCTIONS
FEATURES AND FUNCTIONS
Names of the Parts
Display
Main unit
1. Display
Systolic blood pressure
(See Page 11 for detail)
SYS
6. ON/OFF (power)
Button
Ready to Measure /
Pulse synchronization
2. HIDE (non-display) Button
m m Hg
DIA
Diastolic blood pressure
Pulse level /
Number of irregular pulses
Number of irregular pulse waves: The pulse
wave having a difference of more than 25%
from the average interval of pulse waves is
determined irregular. Number of irregular
pulse waves is displayed up to three times.
7. START Button
m m Hg
PULSE
SYS
ON/OFF
BPM
DC8V
AC
8. DEFLATION
(deflation control)
/Measurement
Result Display
Switch Button
HIDE
m m Hg
m m Hg
START
Example of display
P
-
SET
3. DC jack
DIA
1
40
1
80
1
00
No. of irregular pulses
MODE
SINGLE
VG.
D
A
A
E
/
220
F
1
2
3
V
L
A
T
n
G
9. Air Connector
.
I
d
O
/
N
1
s
t
/
MANU.
CHECK
2
3
r
d
AUTO
4. P-SET (pressure
setting) Knob
260
280
ST
OP
PULSE
10. STOP Button
BPM AC
Battery level
Displays
5. MODE Selector
for the operable level.
1. Display: Displays blood pressure and, pulse rate readings, and oscillation pulse level.
2. HIDE Button: Switches display and non-display of measured results.
3. DC jack: Connects the AC adapter.
HIDE
Blinks
for a low charged
level
4. P-SET (pressure setting) Knob: In the AUTO position, inflation level is automatically set.
Otherwise, inflation level can optionally be set manually between 100 and 280 mmHg.
5. MODE Selector: Selects the operation mode.
Displays
for the inoperable
level.
Contents when the AVG
Mode is selected
AVG. : Mean value
Pulse rate
• One-time Measurement Mode (SINGLE Mode): Measurement with automatic inflation.
• Average Mode (AVG Mode): Automatically measures two (or three) times consecutively.
• Auscultation Mode (MANU Mode): Automatic inflation, automatic deflation, and pressure display for auscultation (does
not measure blood pressure).
1st : First reading
2nd : Second reading
3rd : Third reading
Charging
Displays
when the battery
pack is being charged.
• Check Mode (CHECK Mode): Checks the accuracy of pressure display. Displays only pressure.
External power source
Displays AC when the unit is connected
to the external power source via the AC
adapter.
6. ON/OFF (power) Button: Turns on or off the unit.
7. START Button: Starts the measurement.
8. DEFLATION (deflation control) /Measurement Result Display Switch Button:
• In the MANU Mode, deflates the cuff by approximately 5 to 10 mmHg with each push during deflation.
• In the AVG Mode, switches the display of average values and the measurement results with each push.
9. Air Connector: Connects the air tube.
10. STOP Button: Stops the measurement and deflates air rapidly.
10
11
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FEATURES AND FUNCTIONS
Functions setting
FEATURES AND FUNCTIONS
List of Functions for each Mode
Measurement
Single (SINGLE)
Mode
Average
(AVG) Mode
Auscultation
(MANU) Mode
Check
(CHECK) Mode
Mode
Function
-
P SET
(1) Inflation level setting
Inflation level set-
ting
AUTO (Automatic setting): Can be used when the SINGLE, AVG, or MANU Mode is selected.
The unit estimates the systolic blood pressure during inflation and inflates to a proper cuff pressure
(approximately 30-40 mmHg above the patient’s systolic pressure).
Non-display func-
tion
Manual deflation
control
Manual level setting: Inflation level can be set manually between 100 and 280 mmHg. Set the
level to 30 to 40 mmHg higher than the expected systolic pressure.
(4) AVG Function setting
You can set the number of measurements, the waiting time until the 1st measurement, and the
measurement interval for the AVG Mode.
• To set the P-SET to "AUTO," turn the P-SET Knob counterclockwise as far as it goes until you can hear a click.
• In the "AUTO" setting, inflation level may not be set automatically when the systolic blood pressure is more than
220 mmHg. Use the unit in the manual setting.
• If the cuff has not been inflated to the necessary level, it may be re-inflated automatically.
Items to set
Set value
2 times or 3 times
Function #
F1
Number of measurements
Waiting time until the start of 1st measurement
Measurement interval
F2
F3
0 sec, 3 min, 5 min, or 10 min.
5 sec, 30 sec, 1 min, or 2 min.
HIDE
Note: The bold letters represent the factory-set values.
(2) Non-display function
ON/OFF
Use to prohibit the display of measurement results. However,
XL
Procedure to change the set values
the cuff pressure during measurement is displayed.
This function can be used in the SINGLE and AVG Modes.
START
HIDE
1) When the power is OFF, push the ON/OFF (power) Button
for more than three seconds while holding the START Button;
F1 is displayed.
-
ON/OFF
P
SET
MODE
SINGLE
HIDE
140
180
By pushing the
Button, display or non-display of status
AVG.
MANU.
CHECK
220
260
100
AC
START
AUTO
280
is switched alternatingly.
HIDE
A
/
-
P
SET
180
MODE
SINGLE
140
AVG.
MANU.
220
260
CHECK
100
STOP
SYS
AUTO
280
m m Hg
2) Push the START Button and select the function to set from
F1 to F3. Each time you push the START Button, the func-
Display
Non-display
DIA
XL
tions change in the order of
.
m m Hg
PULSE
BPM AC
AC
ON/OFF
AC
START
HIDE
A
/
-
P
SET
180
MODE
SINGLE
140
AVG.
MANU.
220
260
CHECK
100
STOP
3) Push the DEFLATION (deflation control)/Measurement
Result Display Switch Button and change the set values.
AUTO
280
(3) Manual deflation control
ON/OFF
Accelerate deflation by pushing the DEFLATION (deflation
control) / Measurement Result Display Switch Button during
deflation in the measurement by the MANU Mode.
XL
START
HIDE
A
/
-
P
SET
MODE
SINGLE
140
180
AVG.
MANU.
CHECK
220
100
With each push of the
Button, cuff is deflated rapidly
min
sec
STOP
ON/OFF
260
280
AUTO
in increments of 5 to 10 mmHg.
AC
4) When the setting is finished, push the ON/OFF (power)
Button to turn off the power. The setting is changed.
START
HIDE
A
/
-
P
SET
180
MODE
SINGLE
140
AVG.
MANU.
CHECK
220
100
STOP
260
280
AUTO
12
13
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HOW TO APPLY THE CUFF
The cuff of OMRON IntelliSense™ Blood Pressure Monitor HEM-907XL plays an important role of
collecting the information on blood vessels. Please wrap the cuff according to the procedure, below.
HOW TO APPLY THE CUFF
3. Place the right or left hand of the patient
with the palm of hand facing upward.
Do not wrap the cuff over an arm to which
intravenous injection or transfusion is being
conducted, or when otherwise contraindicated.
4. Align the Artery Position Mark
with the brachial artery.
Do not connect the air tube or the cuff to other
equipment which is connected to intracorporeal
organ. Air embolisms may result.
General advice
• Do not inflate the cuff without being wrapped over
the arm.
• Do not use a damaged cuff.
5. Wrap the cuff snugly using both hands
and securely fasten it with the Velcro™
tape. At this time, the lower edge of
the cuff must be placed 1/2" to 1"
1. Select the cuff according to the arm size
above the inner side of elbow joint.
Arm circumference Name of the cuff
(7" - 9") 17-22 cm HEM-907-CS19 (Small)
(9" - 13") 22-32 cm HEM-907-CR19 (Medium)
(13" - 17") 32-42 cm HEM-907-CL19 (Large)
(17" - 20") 42-50 cm HEM-907-CX19 (Extra Large)
Cuff
• If the INDEX is positioned outside the RANGE, select the cuff suitable for the
patient's arm circumference and wrap it again.
• Wrap the cuff so that you can insert only one finger between the cuff and arm.
• Check the following before applying the cuff:
1) The bladder is correctly installed in the cuff.
2) The bladder is not twisted inside the cuff.
1/2"-1"
3) The bladder tube is protruding from the cuff as shown in
Extract the air tube from
.
the Figure on the right.
Air tube
Enlarged figure of
the circled part
Air connector
Air plug
2. Connect the air tube securely.
To use the cuff in small, medium or large size
• Connect the air tube to the main unit by securing
the air plug to the base of the air connector.
• Securely connect the air tube and the cuff/bladder
set by rotating the luer connection as shown in
the Figure on the right.
6. Keep the level of the cuff at the
same level as the heart during the
measurement.
To use the cuff in extra-large size only
The extra-large cuff comes with an air tube with
an integrated air plug. Connect the air plug of the
cuff to the air connector securely when
connecting to the main unit.
Air tube side
Cuff side
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HOW TO USE THE POWER SOURCE
HOW TO USE THE POWER SOURCE
How to use the AC adapter
Installation and Replacement of Battery Pack
If battery fluid gets into your eye or comes in
contact with skin, wash the affected area with
water repeatedly. Immediately consult a doctor
for treatment.
Be sure to use the AC adapter from the
power supply of 110 VAC.
Do not use this unit in the presence of
flammable gas, or anesthetics, or in a high
pressure oxygen room or oxygen tent.
Do not install or store this unit where it may
come in contact with water or liquid medication.
Do not use the battery pack for devices other
than for this unit.
Do not touch the AC adapter with wet hands.
This is a Class II device with double isolation.
Earth pin is not for protective purposes.
Do not disassemble the battery pack.
General advice
1. Remove both screws on the upper portion of
the battery cover of this unit, and remove
the cover.
• Read the instruction manual of the other devices
to be used at the same time with this unit to
understand and be aware of the interaction
between the devices.
2. Disconnect the old battery pack from the
connector and replace with a new one.
3. Install the battery cover and fasten it with both
screws. Be careful not to pinch the lead wire.
4. Connect the main unit to the AC adapter to
charge the new battery. The battery is not
charged when you purchase the monitor. When you use the battery for the first
time, charge it for more than twelve hours before use.
Connect the AC adapter to the DC jack of the main unit [1] and the electric outlet [2].
NOTE: When the AC adapter is connected and the unit is turned off, the AC adapter
charges the installed rechargeable battery.
[2]
[1]
16
17
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HOW TO USE THE POWER SOURCE
HOW TO MEASURE BLOOD PRESSURE
Battery life
• You can use the unit for approximately three hundred measurements with one charge.
• Approximate life of battery is two years. However the battery life from each charging may be
shortened depending on the state of using. If the interval between charging becomes short and
the
icon appears frequently, replace it.
Confirm readings with the stethoscope when
If cuff inflation does not stop, remove the cuff
Charging time
an irregular pulse wave is displayed or when
or pull out the air tube from the main unit.
• At approximately five seconds after connecting the AC adapter, the unit will start battery charging
automatically.
the measured value is questionable or erratic.
• While the battery is being charged, the
• The battery can be completely charged in approximately twelve hours.
icon turns on.
General advice
Do not use a cellular phone near this unit.
• Patients should not touch the unit.
Battery low
• When the
Do not use this unit in a vehicle.
icon starts to blink, twenty to thirty measurements remain on the battery.
However if the Battery Low Mark starts to blink, charge it soon.
• If the
icon is displayed, the battery is low and the unit cannot operate. Please charge
the battery.
Automatic Power Off
• When using the unit with the battery, the unit will turn off automatically after five minutes
of inactivity.
List of Measurement Modes
• While the AC adapter is connected, the Auto Power Off function does not work.
Refer to Page
To measure
only once
SINGLE Mode
20.
To measure two
Refer to Page
times (or three times)
AVG Mode
automatically and
22.
consecutively
To measure by
using a stetho-
scope
Refer to Page
MANU Mode
24.
18
19
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HOW TO MEASURE
BLOOD PRESSURE (IN SINGLE MODE)
HOW TO MEASURE
BLOOD PRESSURE (IN SINGLE MODE)
5. Push the START Button to start the
measurement.
1. Push the ON/OFF (power) Button to
turn on the power.
• Do not push the
START Button without
wrapping the cuff.
• If you want to stop
measurement, push
the STOP Button. The
cuff will rapidly
deflate.
6. The measurement results are
displayed.
2. Set the MODE Selector to "SINGLE".
• While the battery pack is in use, the
monitor will turn off automatically after
five minutes of inactivity and the display
(measurement results) will disappear.
(Automatic Power Off)
7. Push the ON/OFF (power) Button to
turn off the power.
3. Set the P-SET (inflation level) Knob
to "AUTO" or to the target pressure
value.
4. Measure the patient’s arm size, and
wrap appropriate cuff over the
patient's arm. (Refer to Pages 14
and 15.)
If the monitor determines that the pressure value is not correct,
an error display appears (Er1 to 9). In this case, refer to Page
28 and start the measurement again.
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21
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HOW TO MEASURE
BLOOD PRESSURE (IN AVERAGE MODE)
HOW TO MEASURE
BLOOD PRESSURE (IN AVERAGE MODE)
5. Push the START Button to start the
measurement.
1. Push the ON/OFF (power) Button to
turn on the power.
After the pre-select waiting time, the unit
takes the 1st measurement.
After displaying the results of 1st
measurement, subsequent measures occur
automatically at the specified intervals.
• For setting the number of measurements,
the waiting time until the 1st measurement,
and the interval, refer to Page 13.
• If you want to stop measurement, push the
STOP Button. The unit will rapidly deflate.
• If an error occurs during measurement, the
monitor will automatically start measurement
again. If a second error occurs, measurement
will automatically stop.
2. Set the MODE Selector to "AVG".
The factory-set values are set as follows:
• Do not push the START Button without
wrapping the cuff.
• Number of measurements: 2
• Waiting time until the 1st measurement: 0 sec.
• Interval: 1 min.
To change these factory-set values, refer to
Page 13.
6. The measurement results are displayed.
After all the measurements are finished,
average values will be displayed.
Each time the DEFLATION (deflation control)
/ Measurement Result Display Switch Button
is pushed, the measurement results for each
reading and the average value will be displayed.
3. Set the P-SET (inflation level setting)
Knob to "AUTO" or the target
pressure value.
• While the battery is in use, the monitor will
turn off after five minutes of inactivity and
the display (measurement results) will
disappear. (Automatic Power Off)
7. Push the ON/OFF (power) Button to
turn off the power.
4. Measure the patient’s arm size and
wrap appropriate cuff over the
patient's arm. (Refer to Pages 14
and 15.)
If the monitor determines that the pressure
value is not correct, an error display appears
(Er1 to 9). In this case, refer to Page 28 and
start the measurement again.
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HOW TO MEASURE
BLOOD PRESSURE (IN MANUAL MODE)
HOW TO MEASURE
BLOOD PRESSURE (IN MANUAL MODE)
5. Place the stethoscope on the
patient's arm.
1. Push the ON/OFF (power) Button to
turn on the power.
6. Push the START Button to start the
measurement.
• Do not push the START Button without
wrapping the cuff.
• Do not squeeze or press the cuff during
the measurement.
• If you want to inflate again after the start
of deflation, push the START Button.
• If you want to accelerate deflation after the
start of deflation, push the DEFLATION
(deflation control) / Measurement Results
Display Switch Button. Each time the
Button is pushed, cuff is deflated rapidly in
increments of 5 to 10 mmHg.
2. Set the MODE Selector to "MANU".
7. Take the readings.
8. Push the STOP Button to remove air
inside the cuff.
3. Set the P-SET (inflation level setting)
Knob to "AUTO" or the target
pressure value.
• The unit does not automatically deflate in
the MANU Mode.
9. Push the ON/OFF (power) Button to
turn off the power.
4. Measure the patient’s arm size and
wrap appropriate cuff over the
patient's arm. (Refer to pages 14
and 15.)
If the monitor determines that the pressure
value is not correct, an error display appears
(Er1 to 9). In this case, refer to Page 28 and
start the measurement again.
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HOW TO CHECK
PRESSURE ACCURACY (IN CHECK MODE)
HOW TO CLEAN THE UNIT AFTER USE
General advice
When cleaning this unit, unplug the AC
adapter from the electric outlet.
• Do not clean this unit with gasoline, paint thinner, or
high concentration alcohol.
• Do not disinfect this unit by autoclave or gas steril-
ization (EtO, gluteraldehyde, or high concentration
ozone.)
Accuracy of pressure display can be checked in the CHECK Mode.
After cleaning this unit, dry it well, before
plugging the AC adapter in the electric outlet.
What you need to prepare
(1) Calibrated mercury manometer (including inflation bulb), (2) T-tube, (3) two air tubes, and (4)
a sturdy cylindrical shaped object on which the cuff is wrapped.
HOW TO CLEAN THE UNIT AFTER USE
1. Wipe the monitor with a soft, damp cloth diluted with disinfectant alcohol, or
diluted detergent.
2. Complete cleaning by wiping the monitor with a soft, dry cloth.
How to check
1. Connect the manometer,
inflation bulb, cuff, and the
monitor with the T-tube as
shown in the figure on
the right.
2. Tightly wrap the cuff over a
sturdy cylinder.
3. Release the valve of inflation
bulb to remove the air inside
the cuff completely.
4. Push the ON/OFF (power) Button to turn on the monitor.
5. Set the MODE Selector to “CHECK”.
6. Close the valve of inflation bulb and inflate the cuff to the
pressure to be checked, based on the manometer read.
7. Compare the pressure values displayed on the monitor to
the one on the manometer.
Check result
Accuracy of the monitor is validated to be ±3 mmHg or 2% of standard manometer reading. If your
result shows a difference exceeding the tolerance, contact Omron repair department (1-877-216-1336).
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LIST OF ERROR CODES
TROUBLESHOOTING
If the unit malfunctions during use, please check the following:
Error code
Explanation
How to correct
Trouble
What to inspect
How to correct
Inflation error
• Confirm that the air tube connecting the cuff and
the main unit is connected securely.
• When the pressure does not exceed 12
mmHg within the set time after the start of
inflation
• When the inflation does not reach the set
cuff pressure within the specified time
after the start of inflation
Wrap the cuff correctly, and
measure again.
• Confirm that the air flow in the air tube
connecting the cuff and the main unit isn’t
being restricted.
Is the cuff wrapped correctly?
(Refer to Page 14 and 15.)
• Confirm that the cuff is wrapped correctly (refer
to pages 14 and 15).
Ask the patient not to move
during measurement, and
measure again.
Is the patient moving during
inflation?
Deflation error
• When the deflation speed is too fast during
the measurement
• When the deflation speed is too slow
during the measurement
The unit inflates to
abnormally high (low)
pressure.
• Check bladder for leaks and, if necessary,
replace the bladder with new one (option).
• When the measurement does not finish
within the specified time after starting the
measurement
Set the P-SET to 30 to 40 mmHg
higher than estimated systolic
pressure of the patient, then
measure.
Does this patient have arrhythmia?
Check the patient's condition.
Overpressure error
• The cuff pressure exceeded 299 mmHg.
• Confirm that air flow in the air tube connecting
the cuff and the main unit isn’t being restricted.
After checking the patient with
the stethoscope refer to the "list
of error codes".
Insufficient inflation error
• Blood pressure could not be measured
due to insufficient inflation level.
• If the measurement is made by setting the P-SET
to "AUTO", ask the patient not to move during
the inflation.
• Confirm that the P-SET is securely set to
"AUTO". Turn the Knob counterclockwise as far
as it goes until you can hear a click sound.
• If the measurement is made by manual inflation
level setting, set the value to 30 to 40 mmHg
higher.
(Refer to Page 28.)
Ask the patient not to move
during measurement, and
measure again.
Is the patient moving during the
measurement?
Indeterminable blood pressure error
• Blood pressure could not be measured
even when the cuff pressure reached the
specified pressure.
The monitor cannot
measure blood
pressure.
Set the P-SET to 30 to 40 mmHg
higher than estimated systolic
pressure of the patient, then
measure.
• Confirm that the cuff is wrapped correctly (refer
to pages 14 and 15).
Does the patient have an
arrhythmia?
Low pulse level error
• Pulse wave was too small.
Measured values are
abnormally high (low).
• Confirm that the cuff is wrapped correctly (refer
to pages 14 and 15).
Select the cuff according to the
patient's arm circumference, wrap
it correctly, then measure again.
(Refer to Pages 14 and 15.)
Is the size of the cuff correct and
is it wrapped correctly?
Blood pressure error
• Relationship between systolic and dias-
tolic pressures was abnormal.
Keep the level of the brachium to
which the cuff is wrapped at the
same level as the heart, then
measure again.
• Ask the patient not to move during the measure-
ment.
Is the level of the brachium to
which the cuff is wrapped at the
same level as the heart?
Pulse rate error
• Check the patient for arrhythmia.
• Pulse rate did not stay within the range of
30 to 199 beats/min.
Device error
• Main unit malfunction.
• Contact Omron’s repair department toll-free at
(1-877-216-1336).
Are the patient’s clothes restricting Remove the clothing and
normal blood flow to the arm?
measure again.
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CAUTION
CAUTION:
Changes or modifications not expressly approved by Omron Healthcare, Inc. could void the user’s authority to
operate this product.
FIVE YEAR LIMITED WARRANTY
Your HEM-907XL IntelliSense™ Automatic Blood Pressure Monitor is warranted to be free from manufacturing defects for a period
of five years under normal use. The five year warranty excludes the monitor cuff. The cuff is warranted for a one year period. This
warranty extends only to the original retail purchaser.
Should repair be needed within the warranty period, ship the unit prepaid to Omron Healthcare, Inc., 300 Lakeview Parkway,
Vernon Hills, IL 60061, Attn: Service Dept., together with $5.00 for return shipping and insurance. Be sure to include the model
number of your unit and your phone number on any correspondence.
NOTE:
We will either repair or replace (at our option) free of charge any parts necessary to correct defects in the materials or workmanship.
POTENTIAL FOR RADIO/TELEVISION INTERFERENCE (for U.S.A. only)
This product has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the
FCC rules.
These limits are designed to provide reasonable protection against harmful interference in a residential installation. The
product generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference
will not occur in a particular installation. If the product does cause harmful interference to radio or television reception,
which can be determined by turning the product on and off, the user is encouraged to try to correct the interference by
one or more of the following measures:
The above warranty is complete and exclusive. The warrantor expressly disclaims liability for incidental, special, or consequential
damages of any nature. (Some states do not allow the exclusion or limitation of incidental or consequential damages, so the above
warranty may not apply to you.)
Any implied warranties arising by the operation of law shall be limited in duration to the term of this warranty. (Some states do not
allow limitations on how long an implied warranty lasts, so the above limitation may not apply to you.)
This warranty gives you specific legal rights, and you may have other rights which vary from state to state. As a condition to operation
of your warranty, the enclosed registration card must be completed and sent to us within 10 days from the date of purchase.
• Reorient or relocate the receiving antenna.
• Increase the separation between the product and receiver.
• Connect the product into an outlet on a circuit different from that to which the receiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.
FOR CUSTOMER SERVICE CALL TOLL FREE:
1-877-216-1336
POTENTIAL FOR RADIO/TELEVISION INTERFERENCE (for Canada only)
This digital apparatus does not exceed the Class B limits for radio noise emissions from digital apparatus as set out in
the interference-causing equipment standard entitled "Digital Apparatus", ICES-003 of the Canadian Department of
Communications.
SPECIFICATIONS
Name:
OMRON Digital Automatic Blood Pressure Monitor
HEM-907XL
Model:
Cet appareil numérique respecte les limites de bruits radioeléctriques applicables aux appareils numériques de Classe
B prescrites dans la norme sur le matériel brouilleur: "Appareils Numériques", NMB-003 èdictée par le ministre des
communications.
Display:
Digital display
Measurement:
Measurement Range:
Oscillometric method
Pressure; 0 to 299 mmHg
Pulse rate; 30 to 199 beats/min
Accuracy:
Pressure; Within ±3 mmHg or 2%
Pulse rate; Within ±5% of reading
Inflation:
Automatic inflation with pumping
Deflation:
Automatic deflation by electromagnetic control valve
Automatic rapid air release by electromagnetic control valve
Electrostatic capacity semi-conductor pressure sensor
AC adapter (120 VAC, 60 Hz, 20 VA) or
Battery pack (4.8 VDC, 6W)
Medical Equipment with respect to electric shock, fire and
mechanical hazards only in accordance with UL 2601-1 and
CAN/CSA C22.2 No. 601.1
Air Release:
Pressure Detection:
Power supply:
Electric Shock Protection Method
:
Class II B type
Operating Temperature and Humidity
:
50°F to 104°F (10 to 40°C), 30 to 85% RH, IPX 0 Rating
Approx. 32 oz (910 g)
Weight of Main Unit:
External Dimensions:
Approx.5 1/2" (W) x 8"(H) x 5 1/6"(D)
139 (W) x 203 (H) x 131 (D) mm
Accessories:
Options:
Cuff / bladder set Extra Large, Cuff / bladder set Large, Cuff / bladder set Medium,
Cuff / bladder set Small,
AC adapter, Battery pack, air tube (1.0 m), Instruction Manual (with guarantee card)
Cuff Extra Large (without bladder), cuff Large (without bladder), cuff Medium
(without bladder), cuff Small (without bladder), Bladder Extra Large, bladder Large,
bladder Medium, bladder Small, air tube 1.3 m (51 1/6"),
Stand exclusive for this unit, wall-hanging kit, pole-mounting kit
* Please note that specifications may be changed without prior notice.
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For Customer Service
Call Toll Free
1-877-216-1336
Manufactured by OMRON
Distributed by:
OMRON HEALTHCARE, INC.
300 Lakeview Parkway
Vernon Hills, Illinois 60061
Copyright © 2003 OMRON HEALTHCARE, INC.
HEM-907XLINST Rev A
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