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Hem 907
Hem 907
SYS
OMRON DIA
mmHg
ON/O
BPM FF
Model
HIDE
STA
P-SE
RT
T
140
100 180
MO
DE
220 AVG. SINGLE AV DE F
G . LA T I
/1 s O
MAN t /2 n N
AU d / 3r d
TO U.
260 CHEC
280 K
HEM-907
STO
P
X
A
M
X
DE
IN
T.
AR
Thank you very much for purchasing the Table of Contents
OMRON Digital Automatic Blood Pressure Intended use................................................. 2
Monitor. Exemptions................................................... 3
Requests from OMRON to the Names and Functions of the Parts ............... 4
Notes on Safety ............................................ 8
operators and the persons Components of the Product ....................... 12
responsible for maintenance Options ....................................................... 12
How to Apply the Arm Cuff......................... 13
Please read thoroughly the “Notes on Safety” How to Use the Power Source
of this Instruction Manual before using this unit (AC Adapter)........................................... 14
so that you can use it safely and correctly after How to Measure Blood Pressure ............... 15
sufcient understanding. SINGLE Mode ........................................ 16
AVG. Mode ............................................. 17
After reading this Instruction Manual, please MANU. Mode.......................................... 18
keep it near the unit all the times for future CHECK Mode......................................... 19
Installation and Replacement of
reference. Battery Pack ........................................... 20
How to Clean the Unit after Use................. 21
List of Error Codes ..................................... 22
= Read the instruction manual carefully Troubleshooting .......................................... 23
Specications ............................................. 24
IM-HEM-907-E7-03-01/2012
5329412-4C
1
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.
1. LCD display
SYS
6. ON/OFF
2. HIDE (non-display) Button (power) Button
mmH
g
DIA
7. START Button
mm
PUL
S
Hg
E
ON/O
DC BPM
AC
FF
8. DEFLATION
8V
(deation
HID
E
control) Button
STA
P-S
RT
ET
3. DC jack 100
140
180
MO
D E
AVG SINGL AV D E F
220 . E
MA
G. L AT
/1 s
t /2n
ION 9. Arm Cuff
d /3rd
4. P-SET (pressure
AU
TO
280
260
NU
CHE
.
CK
Connector
setting) Volume
STO
P
HIDE
(2) Non-display function
A function not to display the results of measured blood pressures.
ON/OFF
This function can be used when SINGLE (single measurement) or AVG. DEF N
AVG L AT I O r d
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
during deation.
START
This function can be used when MANU. (auscultation) Mode is selected. HIDE
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
1) When the power is off, press the ON/OFF Button for more than three
seconds while holding the START Button and change the mode to the HIDE
START
STOP
260
AUTO 280
Pressure setting
function
Non-display
function
Manual deation
control function
Setting mode
change function
Indicates matters in which bodily harm or material damage* may arise as a result of incorrect
Caution handling.
* Material damage refers to a wide range of damage involving your house, household goods, domestic animals, and pets.
Examples of signs
The icon indicates caution (including warning and danger). Matters involving actual caution are
indicated by text or pictures in or near . The left icon refers to “caution for ignition”.
The icon indicates prohibitions (what you cannot do). Matters involving actual prohibitions are indi-
cated by text or pictures in or near . The left icon refers to “prohibition to disassemble”.
The icon indicates something that is compulsory (always follow). Matters involving actual compul-
sory actions are indicated by text or pictures in or near . The left icon refers to “pulling the power
source plug”.
Warning
If any abnormal matter occurs during the measurement such as ination 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 inammable gas, such as highly inammable anesthetic, may be
generated or in a high pressure oxygen room or an oxygen tent.
• It may cause ignition and explosion.
10
Durability
The durability of this unit is ve years. (Arm cuff is a consumable.)
11
EX
IND
ON/O
FF ")
m(9"~13
22~32c
ART.
-CR19
REF
HEM
HIDE
STA
P-S
RT
ET
140
100 180
MO
E D
220 AVG. SINGLE AV D E F
G . L AT I
/1 s ON
STO
P (80230H907S) (48H907N-E)
Model: HEM-9ADAP Model: HEM-9BAT
Art.no.: 1098200-0 Art.no.: 1098391-0
Options
Large size arm cuff Medium size arm cuff Small size adult arm cuff
Model: HEM-9CLC Model: HEM-9CMC Model: HEM-9CSC
Art.no.: 4928654-0 Art.no.: 4928640-0 Art.no.: 4928639-7
Applicable arm Applicable arm Applicable arm
circumference: circumference: circumference:
32 to 42 cm 22 to 32 cm 17 to 22 cm
MIN RANGE MAX MIN RANGE MAX
3") 9")
m(9"~1 17~22cm(7"~
22~32c
(13"~17")
32~42cm ART. ART.
REF HEM-CS19
R19
REF
HEM-C
9 ART.
REF HEM-CL1
12
Do not apply the arm cuff during the intravenous • Do not use the unit to the patient using a pump oxy-
injection or transfusion. genator.
• Intravenous injection or transfusion is impossible. • Do not inate the unit without applying the arm cuff.
• Do not use the damaged cuff.
1. Select the arm cuff according to the arm circumference of the patient. INDEX
MIN RANGE MAX
REF HEM-CL
19
)
ART.
cm(9"
~13")
22~32
R19
REF
HEM-C
• Be sure to use the arm cuff suitable for the size of the patient’s arm.
MIN RANGE MAX
INDEX
~ 9")
17~22cm(7"
ART.
REF HEM-CS19
• 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
2. Securely connect the air tube. side
• If you connect the attached 1m air tube, the air tube can be used with the
entire length of 1.2 m.
4. Place the right hand of 5. Place the arm cuff over the patient’s ART.
the patient with the palm arm by matching the mark indicating
of hand facing upward. the artery position MIN
ART. RANGE
MAX
~13")
22~32cm(9"
-CR19
REF HEM ART.
6. Wrap the arm cuff snugly using both hands and securely fasten it with the Velcro tape. At this time, the lower
edge of the arm cuff must be placed 1 to 2 cm above the inner side of elbow joint.
• If the arm cuff is not wrapped snugly, patient may feel numbness on his/her arm, or blood pressure may not be
measured correctly.
• The arm cuff wrapped diagonally along the shape of the arm does not affect the measurement value.
1-2 cm
MIN
MIN
RANGE RANGE
EX
IND
"~13")
22~32cm(9
-CR19
REF HEM ART.
ART.
13
RANGE INDEX
RANGE
22~32cm (9"~13")
REF HEM-CR1
9
ART.
ART.
7. Adjust the level of the arm cuff to the level of the heart.
• Keep the level of the arm cuff at the same level as the heart during the measure-
ment.
How to use the Power Source (AC adapter exclusive for this unit)
Connect the AC adapter to the DC jack of the main unit
Warning [1] and the electric outlet [2].
Do not use the unit in the place where inamma-
ble gas, such as highly inammable anesthetic,
may be generated, or in the high pressure
oxygen room or the oxygen tent.
• It may cause ignition and explosion.
Do not touch the AC adapter with wet hands. [2]
• You may suffer electric shock.
Caution [1] DC
8V
14
To measure three
times Refer to Page
AVG. Mode
(or two times) 17.
consecutively
15
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
P-SET MODE
SINGLE
DEF
AVG L AT I O r d
N
. /1st / 2nd / 3 • When setting the P-SET to P-SET MODE
SINGLE
DEF
AVG L AT I O r d
N
. /1st / 2nd / 3
5. Push the START Button to start 6. Measured results are dis- SYS
ON/OFF
STOP
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
16
START
HIDE
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
“AVG.”.
ON/OFF
START
target ination value. START
HIDE
DEF N
DEF N AVG L AT I O r d
AVG L AT I O r d . /1st / 2nd / 3
. /1st / 2nd / 3
AUTO 280
260
STOP
terclockwise as far as it goes AUTO
260
280
STOP
the measurement.
ON/OFF
displayed.
• Set the unit to the start time of START
• After the measurement is DIA
mmHg
STOP
260
BPM
7. Push the ON/OFF (power) To stop the measurement during the measurement:
Button to turn off the power.
ON/OFF
STOP
260
AUTO 280
17
ON/OFF
START
HIDE
D EF N
AVG L AT I O r d
. /1 st /2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
“MANU.”.
ON/OFF
DEF N
DEF N AVG L AT I O r d
AVG L AT I O r d . /1st / 2nd / 3
. /1st / 2nd / 3
P-SET MODE
P-SET MODE
140 180 SINGLE
140 180 SINGLE
AVG. MANU.
AVG. MANU.
100 220 CHECK
100 220 CHECK
STOP STOP
260
260
AUTO 280
AUTO 280
DEF N
stops ination at the pres- DEF
AVG L AT I O r d
N
sure considered to be 30 to
AVG L AT I O r d . /1st / 2nd / 3
. /1st / 2nd / 3
P-SET MODE P-SET MODE
220
AVG.
SINGLE
MANU.
CHECK
DEF N
AVG L AT I O r d
. /1st / 2nd / 3
P-SET MODE
140 180 SINGLE
AVG. MANU.
100 220 CHECK
STOP
260
AUTO 280
18
power. BPM
AC
ON/OF
F
“CHECK”. P-SE
140
T
T
180 MODE
100 D
STO
P
object.
5. Close the air release valve
of rubber ball and inate
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 deate.
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
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 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.
• If a mark is displayed, the battery is low. Please charge the battery.
20
AC adapter.
HIDE
STAR
T
STOP
21
22
Is the level of the brachium to which the Keep the level of the brachium to which
arm cuff is wrapped at the same level as the arm cuff is wrapped at the same level
the heart? as the heart, then measure again.
23
* Please understand that specications may be changed without prior notice. = Type B
= Class II
This blood pressure monitor fulls the requirements of the EC directive 93/42 EC directive 93/42/EEC (Medical Device
Directive). It also conforms to the European standard EN 1060, Non-invasive Sphygmomanometers. Part 1: General
Requirements an Part 3: Additional Requirements for Electromechanical Blood Pressure Measuring Systems.
24
25
With the increased number of electronic devices such as PC.s and mobile
(cellular) telephones, medical devices in use may be susceptible to
electromagnetic interference from other devices. Electromagnetic interfer-
ence may result in incorrect operation of the medical device and create a
potentially unsafe situation.
Important information for users Medical devices should also not interfere with other devices.
Household users should contact either the retailer where they purchased
this product, or their local government ofce, 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.
26