4. Error Messages and T roubleshooting
4.1 Error Messages
4.2 T roubleshooting
5. Maintenance and S torage
5.1 Maintenance
T o protect your device from damage , please observe the following:
• S tore the device and the components in a clean, safe
location.
• Do not use any abrasive or volatile cleaners.
• Do not wash the device and any component s or immerse
them in water .
• Do not use gasoline, thinners or similar solvents to cle an the
device.
• Use a soft and dry cloth, or a soft and m oistened clo th and
neutral soap to clean on the monitor and the arm cuff.
• Changes or modificatio n not approved by the manufa cturer
will void the user warranty . Do not disassemble or attempt to
repair the d evice or components. Co nsult Customer Service.
5.2 Storage
1. Unplug the air plug from the air jack.
2. Gently fold the air tube into the arm cuff.
Note: Do not bend or crease the air tube
excessively .
Do not store the device in the following situation s:
•If the device is wet.
•Locations exposed to extreme temperatures, humidity , direct sunlight, dust or
corrosive vapors such as bleach.
•Locations exposed to vibrations, shocks or where it will be at an angle.
5.3 Optional Medical Accessories
Using the Optional AC Adapter
1. Insert the AC adap ter plug
into the AC adapter jack on
the rear side of the monitor .
2. Plug the AC adapter in to an
electrical outlet.
T o disconnect the AC adapter , unplug the AC adapter from t he electrical outlet
first, and then remove the AC adapter plug from the mo nitor .
6. Specificati ons
Notes :
• These specifications are subject to change without notice.
• In the clinical validation study , the 5th phase was used on 85 subjects for
determination of diastolic blood pressure.
• This device has not been validated for use on pregnant patients.
7. FCC St atement
FCC CAUTION
Changes or modifications not expressly approved by the party responsible for
compliance could void the user ’s authority to operate the equipment.
Note:
This equipment 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 r esidential
installation. This equipment generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the instr uctions, may cause
harmful interference to radio communicatio ns. However , there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause
harmful interference to radio or television reception, which can be determined by
turning the equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment and receive r .
• Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected.
• Consult the dealer or an experienced radio/TV technician fo r help.
8. Limited W arranty
Y our BP742N Automatic Blood Pressure Monitor , excluding the arm cuff and
batteries, is warranted to be free from defects in materials and workm anship
appearing within 2 years fr om the date of purchase, when used in accordance with
the instructions provided with the monitor . The arm cuff is warranted to be free from
defects in materials and workmanship appearing within 1 year from the date of
purchase when the monitor is used in accordance with the instructions provided
with the monitor . The above warranty extends only to the original retail purchaser .
We will, at our option, replace without charge any monitor or arm cuff covered by the
above warranty . Replacement is our only responsibility and your only remedy under
the above warranty .
T o obtain warranty service contact Customer Service by calling 1-800-634-4350 for
the address of the inspection center and the return shipping and handling fee.
Enclose the original printed receipt. Include a letter, with your name, address, phone
number , and description of the specific problem. Pack the product carefully to
prevent damage in transit. Because of possible loss in transit, we r ecommend
insuring the product with return receipt requested.
THE FOREGOING IS THE SOLE W ARRANTY PROVIDED BY OMRON IN
CONNECTION WITH THIS PRODUCT , AND OMR ON HEREBY DISCLAIMS ANY
OTHER W ARRANTIES, EXPRESS OR IMPLIED, INCLUDING IMPLIED
W ARRANTIES OF MERCHANT ABILITY AND FITNESS FOR A P ARTICULAR
PURPOSE. IMPLIED W ARRANTIES AND OTHER TERMS THA T MA Y BE
IMPOSED BY LAW , IF ANY , ARE LIMITED IN DURA TION TO THE PERIOD OF
THE ABOVE EXPRESS W ARRANTY .
OMRON SHALL NOT BE LIABLE FOR LOSS OF USE OR ANY OTHER SPECIAL,
INCIDENT AL, CONSEQUENTIAL OR INDIRECT COSTS, EXPENSES OR
DAMAGES.
This warranty provides you with specific legal rights, and you may have other rights
that vary by jurisdiction. Because of special local requirements, some of the above
limitations and exclusions may not apply to you.
9. Guidance and Manufacturer ’ s Declaration
OMRON Automatic Blood Pressure Monitor
Information for accompanying documents in the scope of IEC60601-1-2:2007
Model: BP742N including AC-adapter
Error Display Cause Solution
Irregular heartbeats are
detected.
Remove the arm cuff. W ait 2 - 3
minutes and then take another
measurement. Repeat the steps
in section 3.3. If this error
continues to appear , contact
your physician.
Movement during measurement.
Carefully read and repeat the
steps in section 3.3.
The batteries are low .
Y ou sho uld replace the batteries
with new ones ahead of time.
Refer to section 2.1.
The batteries are exhausted.
Y ou sho uld replace the batteries
with new ones at once.
Refer to section 2.1.
Air plug disconnected.
Insert the plug securely .
Refer to section 3.1.
Arm cuff is applied too loosely .
Apply the arm cuff tighter .
Refer to section 3.1.
Air is leaking from the arm cuff.
Replace the arm cuff with a new
one.
Refer to section 5.3.
Movement during measurement
and the arm cuff has not been
inflated sufficiently .
Repeat measurement. Remain
still and do not talk during
measurement.
Refer to section 3.3.
If “E2” appears repeatedly ,
inflate the arm cuff manually
until it is 30 to 40 mmHg above
your previous measurement
result.
Refer to section 3.3.
The arm cuff was inflated
exceeding the maximum
allowable pressure, and then
deflated automatically when
inflating the arm cuff manually .
Do not touch the arm cuff and/or
bend the air tube while taking a
measurement. Do not inflate the
arm cuff more than necessary .
Refer to section 3.3.
Movement during measurement.
Repeat measurement. Remain
still and do not talk during
measurement.
Refer to section 3.3.
Clothing is interfering with the
arm cuff.
Remove any clothing interfering
with the arm cuff.
Refer to section 3.1.
Device error . Contact Customer Service.
Problem Cause and Solution
No power .
No display appears on the monitor .
Replace all batteries with new ones.
Check the battery installation for proper
placement of the battery polarities.
Refer to section 2.1.
Measurement values appear too high or
too low .
Blood pressure varies constantly . Many
factors including stress, time of day , and
how you wrap the cuff, may affect your
blood pressure. Review the section 1.2
and section 3.3.
Arm cuff AC Adapter
Arm circumference
9” - 17” (22 - 42 cm)
CD-WR17
(Model: HEM-RML31)
HEM-ADPTW5
Model BP742N (HEM-7131-Z)
Display LCD digital display
Measurement range Pressure: 0 to 299 mmHg
Pulse: 40 to 180 beat s / min.
Accuracy Pressure: 3 mmHg or 2% of reading
Pulse: 5% of display reading
Inflation Fuzzy-logic controlled by electric pump
Deflation Automatic pressure release valve
Measurement method Oscillometric method
IP classif ication IP 20
Power source
4 “AA” ba tterie s 1.5V or opt ional AC ad apter (I NPUT AC10 0-240V
50/60Hz 0.12 A)
Battery life Approximately 1000 measur ements (using n ew alkaline batteries)
Operating temperature
/ humidity
50°F to 104°F (10°C to 40°C) / 15 to 90% RH
Storag e temperatur e /
humidity / air pre ssure
-4°F to 140°F (-20°C to 60°C) / 10 to 95% RH / 700 to 106 0hPa
Weig ht Monitor : Approximately 10 5/8 oz. (300 g) not including batteries
Arm cuff : Approximately 6 oz. (17 0 g)
Dimensions Monitor : Approximately 4 1/4” (w) 3 1/8” (h) 5 1/2” (l )
(107mm 79mm 141mm)
Arm cuff : Approximately 5 3/4 ” 23 1/2” (air tub e: 29 1/2”)
(145 mm 594 mm (air tube: 750 mm))
Cuff circ umfere nce 9” to 17” (220 to 420 mm)
Memory Up to 50 per user
Contents
Monitor , arm cuff , battery set, instruction manual, quick st art guide
FOR CUSTOMER SER VICE
Visit our web site at: www .omronhealthcare.com
Call toll free: 1-800-634-4350
Important information regarding Elect ro Magnetic Compatibility (EMC)
With the increased number of electronic de vices such as PC’s and mobile (cellular)
telephones, medica l devices in use may be susceptib le to electromagnetic interf erence from
other devices. Electromagnetic int erference may result in incorrect oper ation of the medical
device and create a potentially unsafe situat ion. Medical devices shou ld also not interfere with
other devices.
In order to regulate the requ irements for EMC (Electro Magnetic Compatibility) with the aim to
prevent unsafe product situations, the IEC60601-1-2 sta ndard has been implemented. This
standard def ines the levels of immunity to electromagnet ic interferences as well a s maximum
levels of electromagnet ic emissions for medica l devices.
Medical devices manufactured by OMRON Healthcare conform to this I EC60601-1-2:2007
standard for both immunity and emissions.
Nevertheless, special precautions need to be observed:
• The use of accessories and cables other than those specified by OMRON, with the exception
of cables sold by OMRON as replacement p arts for internal compon ents, may result in
increased emission or decreased immunity of the device.
• The medical devices shou ld not be used adjacent to or stacked with other equipment.
In case ad jacent or st acked use is necessary , the medical device should be observed to
verify normal operation in the configuration in which it will be used.
• Refer to further guidance below regarding the EMC environment in which the devi ce should
be used.
• The MEDICAL ELECTRICAL EQUIPMENT BP742 N including AC-adapter needs special
precautions regarding EMC and needs to be installed and put into service according to the
EMC information pr ovided in this document ations.
• The Essential Performance of the BP742N including AC-adapter is to measure a blood
pressure and a pulse rate and using the memory function.
The BP742N including AC-adap ter may be interfered with by other equipment, even if that
other equipment complies with CISPR EMISSION requirements .
Guidance and manufacturer ’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the elect romagnetic environment
specified below . The customer or the user of this OMRON BP742N inclu ding AC-adapter should
assure that it is used in such environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 1 1
Group 1
The OMRON BP742N including AC-adapter uses RF
energy only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions
CISPR 1 1
Class B
The OMRON BP742N including AC-adapter is suitable for
use in all establishments, including domestic
establishments and those directly connected to the public
low-voltage power supply network that supplies buildings
used for domestic purposes.
Harmonic
emissions
IEC 61000-3-2
Class A
V oltage
fluctuations/
flicker emissions
IEC61000-3-3
Complies
Guidance and manufacturer ’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the elect romagnetic environment
specified below . The customer or the user of this OMRON BP742N inclu ding AC-adapter should
assure that it is used in such environment.
Immunity test
IEC 60601 test
level
Compliance level
Electromagnetic environment -
guidance
Electrostatic discharge
(ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floor should be wood, concrete,
or ceramic tile. If floors are
covered with synthetic material,
the relative humidity should be at
least 30 %.
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for power
supply lines
±1 kV for
input/output lines
±2 kV for power
supply lines
±1 kV for
input/output lines
Mains power quality should be
that of a typical commercial
and/or hospital environment.
Surge
IEC 61000-4-5
±1 kV line(s) to
line(s)
±2 kV line(s) to
earth
±1 kV line(s) to
line(s)
±2 kV line(s) to
earth
Mains power quality should be
that of a typical commercial
and/or hospital environment.
V oltage dips, short
interruptions and
voltage variations on
power supply inputlines
IEC 61000-4-1 1
<5 % U
T (>95 % dip
in U
T)
for 0.5 cycle
<5 % U
T (>95 % dip
in U
T)
for 0.5 cycle
Mains power quality should be
that of a typical commercial
and/or hospital environment. If the
user of the OMRON BP742N
including AC-adapter requires
continued operation during power
mains interruption, it is
recommended that the OMRON
BP742N including AC-adapter be
powered from an uninterruptible
power supply .
40 % U
T (60 % dip
in U
T)
for 5 cycles
40 % U
T (60 % dip
in U
T)
for 5 cycles
70 % U
T (30 % dip
in U
T)
for 25 cycles
70 % U
T (30 % dip
in U
T)
for 25 cycles
<5 % U
T (95 % dip
in U
T)
for 5 sec.
<5 % U
T (95 % dip
in U
T)
for 5 sec.
Power frequency
(50/60 Hz) magnetic
field
IEC 61000-4-8
3 A/m 3 A/m
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital
environment.
Note: U
T is the A.C. mains voltage prior to application of the test level.
Guidance and manufacturer ’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the elect romagnetic environment
specified below . The customer or the user of this OMRON BP742N inclu ding AC-adapter should
assure that it is used in such environment.
Immunity test
IEC 60601 test
level
Compli
ance
level
Electromagnetic environment - guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 V rms
150 kHz to 80
MHz
3 V/m
80 MHz to 2.5
GHz
3 V rms
3 V/m
Portable and mobile RF communications equipment
should be used no closer to any part of the OMRON
BP742N including AC-adapter including cables, than the
recommended separation distance calculated from the
equation appropriate to the frequency of the transmitter.
Recommend separation distance
d = 1.2 √P
d = 1.2 √P
80 MHz to 800 MHz
d = 2.3 √P
800 MHz to 2.5 GHz
where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters as determined
by an electromagnetic site survey ,
a
should be less than
the compliance level in each frequency range.
b
Interference may occur in the vicinity of equipment
marked with the following symbol:
Note1: At 80 MHz and 800 MHz, the higher frequency range applie s.
Note2: These guidelines may not apply in all situations. Electromagn etic propagation is affected by
absorption and reflection from structures, objects, and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/ cordless) telephones
and land mobile radio, AM and FM radio broadcast, and TV broadcast cannot be predicted
theoretically with accuracy . T o assess the electromagnetic environment due to fixed RF transmitters,
an electromagnetic site survey should be considered. If the measured field strength in the location in
which the OMRON BP742N including AC-adapter is used exceeds the ap plicable RF compliance
level above, the OMRON BP742N including AC-adapter should be obs erved to verify normal
operation. If abnormal performance is observed, additional measures ma y be necessary , such as
reorienting or relocating the OMRON BP742N including AC-adapter.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distance between port able and mobile RF communications
equipment
and the OMRON BP742N including AC-adapter
OMRON BP742N including AC-adapter is intended fo r use in an electromagnetic environment in
which radiated RF disturbances are controlled. The customer or the us er of this OMRON BP742N
including AC-adapter can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and th e OMRON
BP742N including AC-adapter as recommended below, according to the maximum output power of
the communications equipment.
Output Power of T ransmitter in
Wat t
Separation dist ance according to frequency of transmitter
in meter
150 kHz to 80 MHz
d = 1.2 √P
80 MHz to 800 MHz
d = 1.2 √P
800 MHz to 2.5GHz
d = 2.3 √P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, th e recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter , where P is the maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
Note: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note: These guidelines may not apply in all situations. Electromagne tic propagation is affected by
absorption and reflection from structures, objects, and people.
Manufactured for: OMRON HEAL THCARE Co., Ltd.
53, Kunots ubo, T erado-cho, Muko, Kyoto, 617-0002 JAP AN
Distributed by: OMRON HEAL THCARE, INC.
1925 West Field Court Lake Forest, IL 600 45 U.S.A.
www .omronhealthcare.c om
© 2013 OMRON HEAL THCARE, INC.
Made in Vietna m
HEM-7131-Z_B_M.fm 2 ページ 2013 年12月20日 金 曜日 午後12時44 分