Omron Blood Pressure Monitor HBP 1300 User Manual

Professional Blood Pressure Monitor  
HBP-1300  
• Instruction Manual  
• Mode d’emploi  
• Gebrauchsanweisung  
• Manuale di istruzioni  
• Manual de instrucciones  
• Gebruiksaanwijzing  
EN  
FR  
DE  
IT  
ES  
NL  
RU  
TR  
AR  
VYꢂTHTJWXHT ꢀT ꢁꢂWꢀQYFXF\NN  
• Kullanꢃm Kꢃlavuzu  
Thank you for purchasing this OMRON Professional Blood Pressure Monitor.  
Please completely read this Instruction Manual before using the monitor for the first time.  
Read this manual to ensure the safe and accurate use of the monitor.  
IM-HBP-1300-E-01-02/2013  
5337346-6A  
 
Introduction  
Intended Use  
Medical Purpose  
The device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult and  
pediatric patient population with arm circumference ranging from 12 cm to 50 cm (from 5 inches to  
20 inches).  
Intended User  
This device should be used by a medical professional.  
Patient Population  
This device is intended for use on adults and children of age 3 years and older.  
Environment  
The instrument is designed for use in physicians’ offices, 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 at all times.  
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 specified 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 specified 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  
EN  
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 fire, earthquake, flood, or  
lightning  
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.  
1
 
Notes on Safety  
The warning signs and symbol examples indicated below are intended to ensure safe use of the  
product and prevent damage and injury to you and others. The signs and symbols are explained below.  
Safety Symbols used in this Instruction Manual  
Indicates the matters in which death or severe bodily damage may arise as a result  
of incorrect handling.  
Warning  
Indicates the matters in which bodily harm or material damage may arise as a result  
of incorrect handling.  
Caution  
General Information  
Indicates general information to keep in mind when using the unit and other useful information.  
Note:  
2
 
Warnings and Cautions  
Usage warnings and cautions  
Setup  
Warning  
Do not use the cuff or AC adapter to lift the unit, it can also cause the unit to malfunction.  
If the unit has broken down, contact OMRON HEALTHCARE.  
Do not use in combination with a hyperbaric oxygen therapy device, or in an environment where  
combustible gas may be generated.  
Do not use in combination with magnetic resonance imaging (MRI) equipment. If MRI is to be  
performed, remove cuff connected to the unit from the patient.  
Do not use with a defibrillator.  
Do not install the unit in the following locations:  
- Locations subject to vibration such as ambulances and emergency helicopters.  
- A location where there is gas or flame.  
- A location where there is water or steam.  
- A location where chemicals are stored.  
Do not use at extremely high temperature, high humidity, or high altitude. Use only within the required  
ambient conditions.  
Do not subject the unit to intense shock.  
Do not place heavy objects on the AC adapter cable, or allow the unit to sit on the cord.  
Clinical testing has not been conducted on newborn infants and pregnant women. Do not use on  
newborn infants and pregnant women.  
Do not plug in or unplug the AC adapter with wet hands.  
Caution  
EN  
Do not install the unit in the following locations:  
- Locations with dust, salt, or sulfur.  
- Locations directly exposed to sunlight for extended periods of time (in particular, do not leave in  
direct sunlight or near a source of ultraviolet light for extended periods, as ultraviolet light will cause  
deterioration of the LCD).  
- Locations subject to vibration or shock.  
- Near heaters.  
Do not use the unit near large equipment that uses a switching relay for power ON/OFF.  
3
 
Before use / during use  
Warning  
The unit complies with the EMC standard (IEC60601-1-2). As such, it can be used simultaneously  
with multiple medical instruments. However, if instruments that generate noise such as an electric  
scalpel or a microwave therapy device are near the unit, check the operation of the unit during and  
after use of these instruments.  
If an error occurs or a measurement result is questionable, check the vital signs of the patient by  
auscultation or palpation. Avoid relying solely on the measurement results of the unit when judging  
the patient’s condition.  
Only trained healthcare providers should use this device. Do not allow patients to operate this  
device.  
Properly connect the connectors and AC adapter cable.  
Do not place objects or liquids on top of this unit.  
Check the following before using the unit:  
- Make sure the AC adapter cable is not damaged (wires are not exposed or broken), and the  
connections are firm.  
For the AC adapter connected to the unit, supplies, and optional devices, use only the standard  
accessories or OMRON-specified products.  
Do not use in a location with moisture, or a location where water may splash on the unit.  
This unit is intended for use in physicians’ office, hospitals, clinics and other medical facilities.  
Do not use the unit if it emits smoke, an abnormal odor, or abnormal noise.  
Do not bring cellular telephones or transceivers into the room where the unit is installed or being  
used.  
Do not connect multiple monitors to the same patient.  
Do not connect the unit to a power outlet that is controlled by a wall switch.  
4
 
Caution  
Before using the unit, verify that none of the following apply to the patient:  
- Poor peripheral circulation, noticeably low blood pressure, or low body temperature (there will be  
low blood flow to the measurement position)  
- The patient uses an artificial heart and lung (there will be no pulse)  
- An SpO sensor and the cuff are attached to the same arm  
2
- The patient has an aneurysm  
- The patient has frequent arrhythmia  
- Body motions such as convulsions, arterial pulsations, or trembling (cardiac massage in progress,  
minute continuous vibrations, rheumatism, etc.)  
Before use, visually inspect the unit to make sure there are no deformations due to falling, and that  
there is no dirt or moisture on the unit.  
When the unit has not been used for an extended period of time, always verify that it operates  
normally and safely before use.  
Do not use in a location where the unit may easily fall. In the event that the unit falls, verify that it  
operates normally and safely.  
EN  
5
 
Cleaning  
Warning  
When cleaning the unit, turn off the power and disconnect the AC adapter from the unit.  
After cleaning the unit, make sure it is completely dry before connecting to a power outlet.  
Do not spray, pour, or spill liquids into or onto the unit, accessories, connectors, buttons, or openings  
in the housing.  
Caution  
Do not use thinner, benzene, or other solvents to clean the unit.  
Do not sterilize by autoclave or gas sterilization (EOG, formaldehyde gas, high-concentration ozone,  
etc.).  
If using an antiseptic solution for cleaning, follow the instructions of the manufacturer.  
Clean the unit regularly.  
Maintenance and inspection  
Warning  
To use the unity safely and correctly, always inspect the unit when starting work.  
Unauthorized modification is prohibited by law. Do not attempt to disassemble or modify the unit.  
6
 
Warnings and cautions for safe measurement  
Rechargeable battery  
Warning  
If battery fluid comes in contact with the eye, immediately flush with copious amounts of water. Do not  
rub. Seek medical attention immediately.  
Do not use the battery pack in any other device besides this unit. Do not throw into flame,  
disassemble, or heat.  
Always disconnect the AC adapter from the unit before removing or installing a battery.  
If the unit will not be used for a month or longer, remove the battery from the unit and store. Charge  
the battery once every 6 months. (Storage conditions for the battery are a temperature of -20 to 30°C  
(-4 to 86°F) and a humidity of 65 20%.)  
Before use, always charge the battery.  
Do not attempt to disassemble or modify the battery.  
Do not apply pressure to and deform the battery. Do not throw, pound, drop, bend, or hit the battery.  
The battery has positive/negative polarity. If the battery does not connect well to the unit, do not  
forcibly connect it.  
Do not connect the positive and negative terminals of the battery with a wire or other metal object. Do  
not carry or store a battery with metal necklaces, hairpins, or other metal objects.  
Use only the specified type of battery.  
Caution  
Do not touch the positive and negative terminals of the battery pack with a wire or other metal object.  
If battery fluid comes into contact with the skin or clothes, immediately rinse with water.  
EN  
7
 
Non-Invasive Blood Pressure (NIBP) measurement  
Warning  
If a cuff is used on a patient with an infection, treat the cuff as medical waste, or disinfect before  
reuse.  
If frequently performing NIBP measurement using a cuff over an extended period of time, periodically  
check the patient’s circulation. In addition, wrap the cuff as indicated in the cautionary points in this  
manual.  
Do not connect the NIBP cuff or cuff joint to a luer lock adapter.  
Do not bend cuff tube during inflation and deflation, particularly after a change of body position.  
Do not wrap the cuff on the following parts:  
- An upper arm on which intravenous drip or a blood transfusion is being performed.  
- An upper arm on which an SpO sensor, IBP catheter, or other instrument is attached.  
2
- An upper arm with a shunt for hemodialysis  
If measuring blood pressure with the cuff wrapped on the arm on the side of the body where a  
mastectomy was performed, check the patient’s condition.  
Caution  
NIBP measurement should be performed on the upper arm.  
During NIBP, stop excessive body movement by the patient and minimize trembling.  
If a doctor has indicated that the patient has hemorrhagic diathesis or hypercoagulability, check the  
condition of the arm after measurement.  
Use the appropriate cuff size to ensure correct measurements. If too large a cuff is used, the  
measured blood pressure value tends to be lower than the actual blood pressure. If too small a cuff is  
used, the measured blood pressure value tends to be higher.  
Before and during measurement, verify that none of the following apply to the patient:  
- The part where the cuff is wrapped is at a different height than the heart.  
(A difference of 10 cm (4 inches) in height may cause a variation in the blood pressure value of up  
to 7 or 8 mmHg.)  
- Body movement or conversing during measurement.  
- Cuff wrapped over thick clothing.  
- Pressure on the arm due to a rolled up sleeve.  
In the case of a cuff for adults, the cuff should be wrapped to a tightness that allows two fingers to be  
inserted in between the cuff and the arm.  
The accuracy of a flashing measurement value that is out of the measurement range cannot be  
guaranteed. Always check the patient’s condition before deciding what steps to take.  
Do not use the cuff if it is damaged or has holes.  
Only OMRON GS CUFF can be used with this device.  
8
 
Note:  
Setup  
• Read and understand the manual for each optional accessory. This manual does not contain  
cautionary information for optional accessory.  
• Exercise caution with the cables and arrange so that the patient does not become entangled or  
bound.  
Before use / during use  
• Check the following after turning on the power:  
- No smoke, abnormal odor, or abnormal noise is emitted.  
- Press each button and verify that it operates.  
- For functions that cause icons to light or flash, verify that the icons light or flash (page 13).  
- Measurement can be performed normally, and measurement error is within the tolerance value.  
• If the screen is not displayed normally, do not use the unit.  
• When recycling or disposing of parts (including batteries) of the unit, follow local government rules  
and regulations.  
Cleaning  
• For cleaning, see page 24.  
Rechargeable battery  
To prevent accidents, keep batteries out of reach of infants and small children.  
• If you sense that something is wrong with a battery, immediately move it to a safe location and contact  
the administrator responsible for the unit or OMRON HEALTHCARE.  
• If the battery voltage is low, operation by battery may not be possible.  
Non-Invasive Blood Pressure (NIBP) measurement  
• If the patient has acute inflammation, a pyogenic ailment, or an external wound at the location where  
the cuff is to be wrapped, follow the instructions of the doctor.  
• Non-Invasive Blood Pressure measurement (NIBP) is performed by compressing the upper arm.  
Some people may experience intense pain, or transient spotting caused by subcutaneous  
hemorrhaging (bruising) may appear. The spotting will disappear with time; however, it may be  
appropriate to inform patients for whom this may be a concern that spotting sometimes occurs, and if  
necessary, refrain from measurement.  
To measure correctly, it is recommended that the patient relax and not talk during measurement.  
To measure correctly, it is recommended that the patient rest quietly for 5 minutes before  
measurement.  
EN  
9
 
Using the Unit  
Components of the Product  
Before using the unit, make sure that no accessories are missing and that the unit and accessories are  
not damaged. If an accessory is missing or there is damage, please contact OMRON HEALTHCARE.  
Main unit  
Standard Medical Accessories  
GS CUFF L (32 - 42 cm)/M (22 - 32 cm)  
• AC adapter  
Others  
• Battery pack  
• Instruction Manual (this paper)  
Options  
Optional Accessory  
Battery pack  
HXA-BAT-2000  
(9065797-0)  
10  
 
Optional Medical Accessories  
(within the scope of EC Medical Device Directive 93/42/EEC)  
GS CUFF XL  
GS CUFF L  
GS CUFF M  
GS CUFF S  
HXA-GCUFF-XLLB  
(9065802-0)  
HXA-GCUFF-LLB  
(9065798-9)  
HXA-GCUFF-MLB  
(9065799-7)  
HXA-GCUFF-SLB  
(9065800-4)  
CUFF HOSE No.1  
(3.5m)  
HBP-CUFFH-BLU35  
(9968171-8)  
CUFF HOSE No.2  
(1.5m)  
HBP-CUFFF-BLU15  
(9968172-6)  
AC adapter*  
AC ADAPTER-E1600  
(9063658-2)  
GS CUFF SS  
HXA-GCUFF-SSLB  
(9065801-2)  
* UK plug type  
AC ADAPTER-UK1600  
(9994843-9)  
Caution  
Only OMRON GS CUFF can be used with this device.  
EN  
Features of the Product  
The OMRON HBP-1300 is an affordable professional blood pressure unit that is clinically proven  
accurate and provides fast, reliable results and is easy to use.  
Key features, benefits, look  
• 5 cuffs available - (SS: 12 to 18 cm, S: 17 to 22 cm, M: 22 to 32 cm, L: 32 to 42 cm, XL: 42 to 50 cm)  
(12 to 50 cm arm circumference range)  
• Designed to be used on a table  
• Motion stop function (When body movement is detected, the device stops deflation for 5 seconds.)  
• Irregular pulse Indicator - Helps identify changes in heart rate, rhythm, or pulse which may be caused  
by heart disease or other serious health issues.  
• Inflation Pressure Setting - 4 options: Auto, 220 mmHg, 250 mmHg, 280 mmHg  
• Last reading display function  
• Auto-Off  
• Custom Rechargeable battery  
• Large, easy-to-read backlight display  
11  
 
Features / Functions of Unit  
Front and back of unit  
4
6
5
2
3
1
7
Power ON / Measure blood pressure  
Press when the power is off to turn on the power and start  
blood pressure measurement. During inflation or  
measurement, press to stop.  
[START/STOP] button  
(Power ON/OFF)  
1
Power OFF  
Hold down at least 3 seconds to turn off the power.  
Press to enter “Menu Mode” and configure various settings.  
If held down at least 3 seconds when a measurement result  
is displayed, the measured data is cleared without being  
stored in memory.  
2
3
[MODE] button  
Displays the system settings (page 16) and the last reading  
(page 23). When using “Auscultation Mode”, inflates and  
deflates the cuff.  
[
] [  
] button  
4
5
6
7
Alarm lamp  
NIBP connector  
DC jack  
Lights up or flashes when an alarm occurs (page 28).  
Connects the cuff tube.  
Connects the AC adapter.  
Battery cover  
Open to install or replace the battery.  
Meaning of the Symbols  
Symbol Description  
Symbol Description  
This shows the Type BF applied part.  
Consult the instruction manual.  
Class II (AC Adapter)  
12  
 
LCD Display  
1
2
4
3
8
5
6
7
9
10  
1
2
3
SYS  
Displays systolic blood pressure.  
Displays diastolic blood pressure.  
Displays the pulse rate.  
DIA  
Pulse  
Pulse  
synchronization icon  
Flashes in synchronization with the pulse during  
measurement.  
4
5
6
Lights in the measurement result display and memory  
display if the pulse wave interval was irregular or there  
was body movement during measurement (page 23).  
Irregular pulse wave  
icon  
EN  
Lights while the previous data are being displayed  
(page 23).  
Memory icon  
Charge icon*  
Flashes during charging. Solid colored light displays  
when charging is finished.  
7
8
9
Battery charge level  
icon*  
Displays how much charge the battery has (page 14).  
Lights when “Auscultation Mode” is ON (page 16).  
Auscultation icon  
10  
Inflation setting icon  
The set initial Inflation pressure value lights (page 16).  
* Only when the battery is installed.  
13  
 
Installing the Battery Pack  
Warning  
• If battery fluid comes in contact with the eye, immediately flush with copious amounts of water.  
Do not rub. Seek medical attention immediately.  
• Do not use the battery pack in any other device besides this unit. Do not throw into flame,  
disassemble, or heat.  
Caution  
Do not short the positive and negative terminals of the battery pack with a wire or other metal object. If  
battery fluid comes into contact with the skin or clothes, immediately rinse with water.  
1. Make sure the AC adapter has been disconnected.  
2. Remove the two screws from the top of the rear  
unit cover, and remove the battery cover.  
3. Connect the battery pack to the connector on the  
monitor, and insert the battery pack into the  
compartment so that the triangle mark on the  
battery pack is aligned with the triangle mark on  
the monitor.  
4. Replace the battery cover and secure with screws.  
Take care not to pinch the wires when replacing the cover.  
5. Connect the AC adapter to the unit and charge the battery pack.  
When using the battery pack for the first time, be sure to fully charge (about 4 hours) before using.  
Battery life  
• About 300 measurements are possible with one charge.  
• A general guideline for replacement of the battery pack is about one year, however, the usage time  
per charge may grow shorter depending on usage conditions. If you find that the usage time after  
each charge has grown shorter and the  
icon frequently appears, replace the battery pack.  
Charging time  
• Charging automatically starts after the AC adapter is connected.  
When a new battery pack or a battery pack that has not been used for a long time is used, some time  
may elapse before charging starts.  
• The  
icon flashes during charging.  
• Charging is completed in about 4 hours.  
Low battery  
When the  
icon starts flashing, promptly charge the battery pack.  
When the icon changes to  
battery.  
, the battery is too low for blood pressure measurement. Charge the  
Auto Power Off  
• When the unit is powered by the battery pack, the power automatically turns off after the set time  
elapses if you forget to turn off the power.  
• When the unit is used with the AC adapter connected, the “Auto Power Off” setting does not operate.  
14  
 
Battery charging  
State  
LCD contents and operations  
The icon flashes.  
Icon  
Charging  
Fully charged  
(Charging completed)  
The icon is lit.  
Problem with the  
battery  
Error message is displayed.  
-
Battery level  
Battery level  
LCD contents and operations  
Icon  
The icon is lit.  
The unit can be used.  
Fully charged  
The icon flashes (E40 error not displayed).  
The unit can be used.  
Battery level is 20%.  
The icon flashes (E40 error displayed).  
The unit cannot be used.  
If the unit is being continuously used, the power will be  
automatically turned off in 30 seconds.  
-
Battery level is 5%.  
Connecting the AC Adapter  
AC power  
Verify that the power outlet supplies the specified voltage and frequency (100 - 240 V AC, 50/60 Hz).  
EN  
Connect the AC adapter to the DC jack on the unit and the power outlet.  
Note:  
When the battery pack is installed  
If there is no problem with the following.  
- AC adapter  
- DC jack  
- Power outlet  
- Battery  
And the  
icon does not flash, contact OMRON HEALTHCARE.  
15  
 
System Settings  
The system settings are divided into two modes, “Menu Mode” and “Utility Mode”.  
Menu Mode  
“Menu Mode” allows you to configure the “Initial Inflation Pressure Value” and “Auscultation Mode” settings.  
Initial Inflation  
Pressure Value  
Auscultation Mode  
1. Press the [MODE] button.  
The “Initial Inflation Pressure Value” setting screen appears.  
2. Press the [ ] or [ ] button to change the setting.  
• Press the [ ] button to change the setting in the order “280”, “250”, “220”, “AUTO”, “280”...  
• Press the [ ] button to change the setting in the order “220”, “250”, “280”, “AUTO”, “220”...  
When the “Initial Inflation Pressure Value” is set, inflation takes place at a fixed speed to the set  
value and thus is quicker.  
“AUTO” estimates the systolic blood pressure during inflation and automatically inflates the cuff to a  
suitable value.  
When using “220”, “250”, or “280” mmHg, select the value that is 30 to 40 mmHg higher than the  
estimated systolic blood pressure.  
3. When you have completed the “Initial Inflation Pressure Value” setting,  
press the [MODE] button.  
The “Auscultation Mode” settings screen appears.  
“ON” or “OFF”  
appears.  
4. Press the [ ] or [ ] button to set to “ON” or “OFF”.  
When set to “ON”, SYS and DIA can be recorded using auscultation measurement.  
For information on auscultation measurement, see page 22.  
5. When you have completed the “Auscultation Mode” setting, press the  
[MODE] button.  
“0” appears.  
To start blood pressure measurement, press the [START/STOP] button.  
Note:  
• The body movement detection function is disabled while “Auscultation Mode” is in use.  
• If the power is turned off, the settings revert to the factory settings.  
“Initial Inflation Pressure Value” changes to “AUTO”, and “Auscultation Mode” changes to “OFF”.  
16  
 
Utility Mode  
“Utility Mode” allows you to configure the “Auto Power Off” and “Pressure Accuracy Confirmation” setting.  
1. Confirm that the device is switched off.  
If the power is on, hold down the [START/STOP] button for at least 3 seconds to  
turn off the power.  
2. Hold down the [MODE] button until the “Auto Power Off”  
setting screen appears.  
The “Initial Inflation Pressure Value” setting screen appears, and changes to the  
“Auto Power Off” setting screen appears.  
3. Press the [ ] or [ ] button to change the auto power off  
setting.  
“5” or “10”  
appears.  
The “5 min.” or “10 min.” setting is entered.  
When the unit is powered by the battery pack and is not used for the set time (“5 min.” or “10 min.”),  
the power automatically turns off to save battery power.  
If a mid-priority alarm other than a low battery error (E40 error) has occurred, the power does not  
turn off automatically.  
4.When you have completed the “Auto Power Off” setting, press the [MODE]  
button.  
EN  
The “Pressure Accuracy Confirmation” screen appears. “0” appears.  
“0” appears.  
5. Check the Pressure Accuracy.  
Add pressure externally as explained on page 24.  
Compare with the displayed value and verify that there is no problem.  
6. When you have completed “Pressure Accuracy Confirmation”, press the  
[START/STOP] button.  
The power turns off.  
17  
 
Non-Invasive Blood Pressure (NIBP) Measurement  
Non-Invasive Pressure Measurement Principles  
Oscillometric method  
The beat in the pulsation generated by the contraction of the heart is captured as the pressure inside  
the cuff to measure the blood pressure. If the cuff wrapped around the upper arm is pressurized  
sufficiently, the blood flow stops, but the beat of the pulsation is present and the pressure inside the cuff  
receives this and oscillates. Next, as the pressure inside the cuff gradually decreases, the oscillation of  
the pressure within the cuff gradually increases and reaches a peak. As the pressure within the cuff  
decreases further, the oscillation decreases from its peak.  
The pressure within the cuff and the relationship with the increase and decrease of the oscillation within  
the cuff in this series of processes are stored into memory, calculations are carried out, and the blood  
pressure value is determined.  
The pressure within the cuff when the oscillation increases drastically is the systolic pressure and the  
pressure within the cuff when the oscillation decreases drastically is the diastolic pressure. Also, the  
pressure within the cuff when the oscillation peaks is taken as the average pulsation pressure.  
The oscillometric method does not determine the blood pressure value instantly like a microphone type  
automatic blood pressure gauge with the auscultation method, but rather determines it from the series  
of change curves as explained above. Therefore, it is not easily affected by external noise, an electric  
scalpel or other electro surgical instruments.  
KOROTKOV SOUNDS  
CUFF  
PRESSURE  
OSCILLATIONS IN CUFF PRESSURE  
RADIAL PULSE  
5 SEC  
Comparison between the auscultatory, oscillometric and  
palpatory methods of measuring blood pressure.  
L.A. Geddes,  
“The Direct and Indirect Measurement of Blood Pressure”, Year Book Medical Publishers, Inc. 1970  
18  
 
Cuff Selection and Connection  
Selecting the cuff  
Warning  
If a cuff is used on a patient with an infection, treat the cuff as medical waste, or disinfect before  
reuse.  
Caution  
• Do not use the cuff if it is damaged or has holes.  
• Use the appropriate cuff size to ensure correct measurements. If a cuff that is too large is used, the  
measured blood pressure value tends to be lower than the actual blood pressure. If a cuff that is too  
small is used, the measured blood pressure value tends to be higher.  
Note:  
It is important to use the correct sized cuff for a patient in order to get an accurate reading.  
Measure the circumference of the patient’s arm and select the cuff size  
that is appropriate for the circumference.  
Select the cuff that is suitable for the patient from the cuffs below.  
Arm circumference  
Cuff name  
(cm)  
(inch)  
17-20  
13-17  
9-13  
7-9  
GS CUFF XL*  
GS CUFF L  
42 - 50  
32 - 42  
22 - 32  
17 - 22  
12 - 18  
GS CUFF M  
GS CUFF S*  
GS CUFF SS*  
5-7  
* Available as an optional accessory.  
EN  
Connecting the cuff  
Connect the cuff tube to the NIBP connector on the unit and turn  
clockwise to lock.  
Caution  
Only OMRON GS CUFF can be used with this device.  
Note:  
• If the cuff tube is too short, the optional 3.5 m or 1.5 m CUFF HOSE can be connected to lengthen the  
cuff tube. Do not extend other than the optional 3.5 m or 1.5 m CUFF HOSE, as this will affect  
measurement accuracy.  
• Make sure the connections are tight.  
19  
 
Applying the Cuff to the Patient  
1. Wrap on a bare arm or over thin clothing.  
Wrap the cuff on a bare arm or over thin clothing. Thick clothing or a rolled up sleeve will cause  
inaccurate blood pressure measurements.  
The device can be used on either the right or left arm.  
2. Align the artery mark “INDEX ARTERY” with the brachial artery.  
Run the cuff tube out the peripheral side with no bends (the brachial artery is on the inner side of the  
patient’s upper arm).  
Make sure that “INDEX ARTERY” is within the “RANGE” and the lower edge of the cuff is 1 to 2 cm  
from the inner side of the elbow joint.  
If “INDEX ARTERY” is outside the “RANGE”, error in the blood pressure value will increase. In this  
case, use a different cuff size.  
As a guideline for the tightness of the cuff, It should be possible to insert about two fingers under the  
cuff.  
1.  
2.  
3.  
1 to 2 cm  
3. During measurement, keep the brachial artery on which the cuff is  
wrapped at the same height as the right atrium of the heart.  
20  
 
Caution  
Make sure the cuff is wrapped in the correct arm position and is at the same height as the heart.  
A difference of 10 cm (4 inches) in height may cause a variation in the blood pressure value of up to  
7 - 8 mmHg.  
Note:  
• If measurement is difficult due to arrhythmia, use a different blood pressure measurement method.  
• If the patient has acute inflammation, a pyogenic ailment, or an external wound at the location where  
the cuff is to be wrapped, follow the instructions of the doctor.  
• Non-Invasive Blood Pressure (NIBP) measurement is performed by compressing the upper arm.  
Some people may experience intense pain, or transient spotting caused by subcutaneous hemorrhaging  
may appear. The spotting will disappear over time, however, if it is possible that this will disturb the patient,  
try the following technique:  
- Wrap a thin towel or cloth (one layer) under the cuff.  
If the towel or cloth is too thick, there will be insufficient cuff compression and the blood pressure value  
will measure high.  
• If the patient moves or the cuff is touched, this may be falsely detected as a pulse and over-inflation  
will occur.  
• Do not inflate the cuff when it is not wrapped on the upper arm. This may damage the cuff.  
Taking the Measurement in “Manual Mode”  
1. Press the [START/STOP] button.  
Blood pressure measurement is performed once.  
2. The measurement results are displayed.  
If a measurement value is outside the corresponding range below, the value will flash.  
SYS: 59 mmHg or less, or 251 mmHg or higher.  
DIA: 39 mmHg or less, or 201 mmHg or higher.  
PULSE: 39 bpm or less, or 201 bpm or higher.  
Normal measurement  
Measurement error /  
failure  
EN  
Caution  
The accuracy of a flashing measurement value that is outside the measurement range is not  
guaranteed. Always check the patient’s condition before deciding what steps to take.  
Note:  
If inflation is insufficient, inflation may restart automatically while measurement is in progress.  
21  
 
Irregular pulse wave detection function  
If the pulse wave interval becomes irregular during measurement, the irregular pulse wave detection  
icon will light to notify you.  
Body movement detection function  
If body movement is detected during measurement, deflation stops for 5 seconds. The irregular pulse  
wave icon appears in the measurement result display.  
Deflation stopped  
After 5 seconds, measurement resumes, and an attempt is made to complete measurement in one  
cycle.  
Taking the Measurement in “Auscultation Mode”  
Use a stethoscope to perform measurement.  
When set to “ON”, SYS and DIA can be recorded using auscultation measurement.  
To determine SYS and DIA during measurement, press the [MODE] button.  
SYS is registered the first time and DIA is registered the second time you press the [MODE] button  
during deflation.  
After DIA is determined, the cuff rapidly deflates and SYS and DIA are displayed as the measurement  
results.  
The pulse rate does not appear in the measurement result display.  
During deflation, the [ ] button can be held down to re-inflate, or the [ ] button can be held down to  
deflate faster.  
Stored data that was measured in “Auscultation Mode” is displayed when the auscultation icon is lit.  
During re-inflation  
Note:  
The body movement detection function is disabled while “Auscultation Mode” is in use.  
For Auscultation Mode settings, see page 16.  
22  
 
Stopping the Measurement  
To stop measurement while measurement is in progress, press [START/STOP] button.  
Displaying Last Reading  
The previous measurement value (systolic blood pressure, diastolic blood pressure, and pulse rate)  
and whether or not an irregular pulse wave was detected can be displayed. In the case of auscultation  
measurement, the auscultation icon appears.  
Press the [ ] or [ ] button to display the previous data. This function is also available when the  
device is switched off.  
If an irregular pulse wave or  
body movement was detected,  
the irregular pulse wave icon  
Lights while the previous  
data are being displayed.  
appears.  
When the data was measured  
in “Auscultation Mode”, the  
auscultation icon appears.  
If held down at least 3 seconds when a measurement result is  
displayed, the measured data is cleared without being stored.  
Note:  
When the monitor is left idle for one minute, the backlight will disappear.  
EN  
23  
 
Maintenance  
Maintenance Inspection and Safety Management  
The HBP-1300 must be maintained to ensure functionality and to secure the safety of patients and operators.  
Daily checks and maintenance should be performed by the operator. (page 25)  
In addition, qualified personnel are necessary to maintain the performance and the safety, and to conduct  
periodic inspections. We recommend that the verification test be performed at least once a year.  
Example of connection for pressure accuracy confirmation:  
1. Display the pressure accuracy confirmation screen as explained in  
“Utility Mode” on page 17.  
Display “0” in the pressure accuracy confirmation screen.  
Display the pressure value.  
2. Connect the blood pressure monitor, the calibrated reference pressure  
gauge, and the cuff and inflation bulb.  
3. Check the pressure value of the blood pressure monitor and the  
pressure value of the calibrated reference pressure gauge.  
Note:  
• Make sure that the blood pressure monitor reading is within 3 mmHg compared to the calibrated  
reference pressure gauge.  
To rapidly deflate the cuff, press the [ ] button.  
To repeat “Pressure Accuracy Confirmation”, turn off the power and repeat the procedure from  
step 1 in “Utility Mode” on page 17.  
Cleaning of the Device  
Cleaning and disinfecting should be performed in accordance with your facility’s infection control  
practice.  
Surface cleaning  
Wipe with a cloth that has been moistened with isopropyl alcohol diluted to 50 v/v%, or ethyl alcohol  
(disinfection alcohol) diluted to 80 v/v% or less and wrung out.  
Do not wipe the DC jack or allow it to become wet.  
Removing dust  
Use a moistened cotton bud to remove dust that has accumulated on the vent ports.  
Service  
The device requires no routine service other than cleaning, and visually checking the cuffs, tubing, etc.  
Caution  
• Do not sterilize by autoclave or gas sterilization (EOG, formaldehyde gas, high-concentration ozone, etc.).  
• If using an antiseptic solution for cleaning, follow the instructions of the manufacturer.  
Accessory Care  
Non-Invasive Blood Pressure Measurement (NIBP)  
Cuff  
Wipe clean on the surface of the cuff with a cloth moistened with a 70 v/v% dilution of isopropyl alcohol,  
or a 80 v/v% or less dilution of disinfection ethanol (ethyl alcohol).  
Do not allow any liquids inside the cuff. If a liquid gets in the cuff, dry the inside well.  
24  
 
Check before Use  
Before conducting safety checks, be sure to implement the items in the “Cleaning of the Device” and  
“Accessory Care” sections. (page 24)  
Before turning on the power  
Before turning on the power, check for the following  
External appearance  
The device or accessories are not deformed due to falling or other impact.  
The device is not dirty.  
The device is not wet.  
AC adapter  
The AC adapter is firmly connected to the connector on the device.  
There are no heavy objects lying on the AC adapter cable.  
The AC adapter cable is not damaged (core-wire exposure, breaks, etc.).  
When turning on the power  
When turning on the power, check the following  
Display/lamp  
When the [START/STOP] button is pressed to turn on the power, the screen below appears and the  
alarm lamp lights (page 13).  
The alarm lamp is lit up.  
EN  
After turning on the power  
After turning on the power, check for the following  
External appearance  
There is no smoke or odor coming from the device.  
The device is not making any unusual noises.  
Buttons  
Press each button and check that it works.  
Non-invasive blood pressure (NIBP)  
Make sure that a suitable OMRON GS CUFF is attached (one that fits the circumference of the  
patient’s arm).  
The cuff tube is firmly connected.  
The person checking the cuff should wrap the cuff around arm, perform cuff measurement and check  
to see that blood pressure is in the vicinity of normal measurements.  
While measurement is in progress, bend the relevant arm and move body to halt discharge and  
during this halt check that cuff pressure does not drop.  
25  
 
Troubleshooting  
The power does not turn on  
Cause  
Solution  
If the unit is being powered by the battery, the battery  
is not installed or the charge is depleted.  
Insert battery or replace with a new battery (page 14).  
Disconnect the AC adapter, remove the battery, and  
contact OMRON HEALTHCARE.  
Internal part failure  
• Check if the AC adapter is disconnected or the connection is loose.  
• Check if the AC adapter or battery has failed.  
The unit display does not operate  
Cause / solution  
Stop using the unit and contact OMRON HEALTHCARE.  
The unit becomes hot  
Cause  
Solution  
An object is on top of the unit or right next to the unit. Keep the area around the unit free of objects.  
If the unit becomes too hot to be touched, there may be a problem in the unit. Turn off the unit power,  
disconnect the AC adapter, remove the battery, and contact OMRON HEALTHCARE.  
The unit is connected to a power outlet, but it runs on the the battery pack  
Cause / solution  
If AC power cannot be supplied, the unit will operate by battery only.  
• Check if the AC adapter is properly connected to the unit.  
• Check if AC adapter is connected to a power outlet.  
• Check that the electrical outlet is working by connecting a different device to the same power outlet.  
The cuff does not inflate when the [START/STOP] button is pressed  
Cause  
Solution  
Loose cuff tube connection.  
There is an air leak in the cuff.  
If pressure is displayed, the cuff tube is bent.  
Check the connection.  
Replace the cuff.  
Make sure no part of the cuff tube is bent.  
Measurement was not possible  
Cause / solution  
Check the patient by palpation or other method.  
After checking the patient, check the error code and see “List of Error Codes” (page 28) for Non Invasive  
Blood Pressure (NIBP) measurement.  
26  
 
Abnormal measurement value  
Cause / solution  
The causes below are possible. Check the patient by palpation and then repeat measurement.  
• Body movement (chills or other trembling)  
• Arrhythmia.  
• Noise in the cuff  
- A nearby person touched the patient.  
- Cardiac massage was being performed.  
The measurement value is questionable  
Cause  
Solution  
Deflates quickly  
Check for a loose cuff connection.  
Simultaneously perform measurement with a stethoscope.  
Place the stethoscope and listen while viewing the pressure display of the  
manometer.  
Stethoscope  
Blood pressure may vary widely due to physiological effects.  
The causes below are possible.  
• Emotional excitement or agitation  
- Pain due to cuff wrapping  
- White coat hypertension  
• Cuff size or wrapping method not correct  
• Cuff wrapping position on upper arm not at the same height as the heart  
• Patient’s blood pressure not stable due to pulsus alternans, respiratory changes, or other reason  
Measure circumference or patient’s arm and ensure  
Incorrect cuff size used.  
correct sized cuff is used.  
Ensure cuff is applied to a bare arm, or very thin  
EN  
Cuff wrapped over thick clothing.  
clothing.  
Ensure patient is seated, feet flat on the floor, cuff at  
Patient not seated properly.  
heart level.  
Ensure before measurement taken, patient has not  
Patient ate, drank, or exerted themselves recently.  
had food, caffeinated or alcohol beverages, or  
exerted/exercised in the last 30 minutes.  
27  
 
List of Error Codes  
The alarm lamp flashes when a medium-priority alarm occurs, and lights steadily when a low-priority  
alarm occurs.  
To clear an alarm, press any button.  
If a low-priority alarm and a medium-priority alarm occur at the same time, the medium-priority alarm  
is displayed.  
If the alarms are the same priority level, the error code of the alarm that occurred first is displayed.  
However, to prevent battery consumption when powered by battery, a low battery error (E40 error) is  
always given priority.  
Example: E2  
SYSTEM  
Error  
code  
Priority  
Description  
Points to check  
E9  
Medium Internal hardware error  
Contact OMRON HEALTHCARE.  
NIBP  
Error  
code  
Priority  
Description  
Points to check  
The cuff tube is not connected  
Air is leaking from the cuff.  
Firmly connect the cuff tube.  
E1  
Low  
Replace with an OMRON GS CUFF that  
does not leak.  
Did not inflate properly because the arm Have the patient not move the arm or body,  
or body moved during measurement.  
and repeat measurement.  
Moved body or arm during  
measurement, or talked.  
Have the patient not talk or move, and  
repeat measurement.  
The cuff is not applied correctly.  
Correctly apply the cuff.  
The sleeve is rolled up and is  
compressing the arm.  
Remove the garment and re-wrap the cuff.  
E2  
Low  
The measurement time exceeds the  
expected time, so the measurement was  
ended in order to avoid patient discomfort.  
There is a possibility that measurement is  
being repeated over and over due to air  
leaking from the cuff.  
Measurement time has exceeded  
specified time.  
Specified time: 165 seconds  
28  
 
Other problems  
Error  
Priority  
code  
Cause  
Solution  
When inflating in “Auscultation Mode”,  
release the button when the pressure  
reaches the desired value.  
Inflated the cuff to 300 mmHg or more  
during inflation in “Auscultation Mode”.  
If this occurs during measurement, repeat  
measurement.  
E3  
Low  
Over-inflation occurs  
If this occurs when not performing  
measurement, contact OMRON  
HEALTHCARE.  
Recharge the battery, or replace with a new  
battery. (page 14)  
E40  
E41  
Medium The battery is depleted.  
Medium Battery failed to charge.  
Try charging again. If continues to fail,  
replace with a new battery. (page 14)  
Replace the battery with a new battery. If the  
error continues, contact OMRON  
HEALTHCARE.  
E42  
Medium Battery voltage error  
Disposal  
Description  
As there is a risk of environmental pollution, follow your applicable national and local legal regulations  
regarding disposal or recycling of this equipment and batteries.  
The main constituents of each part are listed in the table below. As there is a risk of infection, do not  
recycle patient attachments such as cuffs, but dispose of them as instructed by your facility’s  
procedures and applicable regulations.  
Item  
Parts  
Material  
Box  
Cushion  
Bag  
Cardboard  
Cardboard  
PE  
Package  
EN  
Enclosure  
Internal parts  
Outer tube  
Cell batteries  
Internal parts  
ABS, PC , SR  
General electronic components  
PVC  
Nickel-metal hydride  
General electronic components  
Main unit and  
accessories  
Battery pack  
29  
 
Specifications  
Factory Default Settings  
Factory default settings and backup are as shown below.  
Backup  
: Setting is retained even if the power is interrupted.  
: Reverts to factory default setting if the power is turned off.  
Setting Pressure Value  
Initial Inflation Pressure Value  
Auscultation Mode  
Settings  
AUTO, 220, 250, 280  
ON, OFF  
Factory Setting  
AUTO  
Backup  
OFF  
Auto Power Off  
5 min, 10 min  
5 min  
Technical Specifications: HBP-1300  
Main unit  
Measurement Parameter  
Dimension  
NIBP, PR  
Main unit: 123 x 201 x 99 (mm) 4.84 x 7.91 x 3.90 (inch) (W x H x D)  
AC adapter: 46 x 66 x 37 (mm) 1.81 x 2.60 x 1.46 (inch) (W x H x D)  
Battery: 54 x 43.5 x 15.4 (mm) 2.13 x 1.71 x 0.61 (inch) (W x H x D)  
Weight  
Main unit: Approx. 0.52 kg (not including accessories and options)  
AC adapter: Approx. 0.2 kg  
Battery: Approx. 0.1 kg  
Display  
7 segment LCD  
Protection Class  
Class II (AC Adapter)  
Internal powered equipment (when operating with battery only)  
Degree of Protection  
Type BF  
MDD Classification  
Power supply  
AC adapter  
Class II a  
Input voltage range: AC 100 V to 240 V  
Frequency: 50/60 Hz  
Output voltage range: DC 6 V 5%  
Rated output current: 1.6 A  
Rechargeable battery  
Type: 3.6 V, 1900 mAh  
Number of operation cycles when fully charged: 300  
Measurement conditions  
• New battery fully charged  
• Ambient temperature of 23°C (73.4°F)  
• Using M-size cuff  
• SYS 120 / DIA 80 / PR 60 (Inflation setting: AUTO)  
• One 5-minute cycle consisting of “cuff measurement time + wait time”  
30  
 
Environmental Conditions  
Operational temperature and  
humidity  
Temperature range: 10 to 40°C (50 to 104°F)  
Humidity range: 30 to 85%RH (not condensed)  
Atmospheric pressure: 700 to 1060hPa  
Storage and transportation  
Temperature range: -20 to 60°C (-4 to 140°F)  
Humidity range: 10 to 95%RH (not condensed)  
Atmospheric pressure: 500 to 1060hPa  
Non-Invasive Blood Pressure (NIBP)  
Measurement technology  
Measurement method  
Oscillometric  
Dynamic Linear Deflation method  
0 to 300 mmHg  
Pressure display range  
Pressure display accuracy  
NIBP measurement range  
Within 3 mmHg  
SYS 60 to 250 mmHg  
DIA 40 to 200 mmHg  
Pulse rate 40 to 200 /min  
NIBP accuracy*  
Maximum mean error within 5mmHg  
Maximum standard deviation within 8mmHg  
Pulse rate accuracy  
Reference standard:  
Within 5 % of reading  
EN1060-1:1995+A2:2009  
EN1060-3:1997+A2:2009  
ISO81060-1:2007  
* Comparison with auscultation method performed by a trained professional.  
DIA determined by the auscultation method is “K5”.  
Note: Specifications may be changed without prior notice.  
EN  
This blood pressure monitor fulfils the requirements of the EC directive 93/42/EEC (Medical Device  
Directive). It also conforms to the European standard EN 1060, Non-invasive Sphygmomanometers  
Part 1: General Requirements and Part 3: Additional Requirements for Electromechanical Blood  
Pressure Measuring Systems.  
31  
 
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 EN60601-1-2:2007 standard has been implemented. This  
standard defines 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 fields, 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 within this manual, refer to  
section “Manufacturer’s Declaration”.  
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 product 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 office, 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  
contract. 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.  
32  
 
Manufacturer’s Declaration  
The HBP-1300 is intended for use in the electromagnetic environment specified below.  
The customer or the user of the HBP-1300 should assure that it is used in such an environment.  
Electromagnetic Emissions:  
(IEC60601-1-2)  
Emission Test  
RF emission  
CISPR 11  
Compliance  
Electromagnetic Environment  
Group 1  
The HBP-1300 uses RF energy only for internal functions.  
Therefore, this RF emission is extremely weak and there is  
little chance of it creating any kind of interference  
whatsoever with nearby electronic equipment.  
RF emissions  
CISPR 11  
Class B  
Class A  
Complies  
The HBP-1300 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  
Voltage fluctuations/flicker  
IEC 61000-3-3  
Electromagnetic Immunity:  
(IEC60601-1-2)  
IEC60601-1-2  
test level  
Compliance  
level  
Electromagnetic  
environment - guidance  
Immunity test  
Electrostatic discharge  
(ESD)  
IEC 61000-4-2  
6 kV contact  
8 kV air  
6 kV contact  
8 kV air  
Floors should be wood, concrete or  
ceramic tile. If floors are covered with  
synthetic material, the relative  
humidity should be at least 30 %.  
Electric fast transient/  
burst  
2 kV for  
2 kV for  
Mains power quality should be that of  
power supply lines power supply lines a typical commercial or hospital  
IEC 61000-4-4  
1 kV for input/  
1 kV for input/  
environment.  
output lines  
output lines  
EN  
Surge  
IEC 61000-4-5  
1 kV  
differential mode  
2 kV  
1 kV  
differential mode  
2 kV  
Mains power quality should be that of  
a typical commercial or hospital  
environment.  
common mode  
common mode  
Voltage dips, short  
interruptions and  
voltage variations on  
power supply input lines  
IEC 61000-4-11  
<5 % U  
for 0.5 cycle  
<5 % U  
for 0.5 cycle  
Mains power quality should be that of  
a typical commercial or hospital  
environment. If the user of the  
HBP-1300 requires continued  
operation during power mains  
interruptions, it is recommended that  
the HBP-1300 be powered from an  
uninterruptible power supply or a  
battery.  
T
T
40 % U  
40 % U  
T
T
for 5 cycles  
for 5 cycles  
70 % U  
70 % U  
T
T
for 25 cycles  
for 25 cycles  
<5 % U  
for 5 sec.  
<5 % U  
for 5 sec.  
T
T
Power frequency  
(50/60 Hz) magnetic  
field  
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.  
IEC 61000-4-8  
Note: U is the a.c. mains voltage prior to application of the test level.  
T
33  
 
IEC60601-1-2  
test level  
Compliance  
level  
Electromagnetic  
Immunity test  
environment - guidance  
Portable and mobile RF communications  
equipment should be used no closer to any part  
of the HBP-1300, including cables, than the  
recommended separation distance calculated  
from the equation applicable to the frequency of  
the transmitter.  
Recommend separation distance  
P
P
P
d = 1.2  
d = 1.2  
d = 2.3  
150 kHz to 80 MHz  
80 MHz to 800 MHz  
800 MHz to 2.5 GHz  
3 Vrms  
Conducted RF  
IEC 61000-4-6  
150 kHz to  
80 MHz  
3 Vrms  
3 V/m  
80% AM (2Hz)  
where P is the maximum output power rating  
of the transmitter in watts (W) according to he  
transmitter manufacturer and d is the recom-  
mended separation distance in meters (m).  
3 V/m  
Radiated RF  
80 MHz to  
2.5 GHz  
Field strengths from fixed RF transmitters as  
determined by an electromagnetic site  
IEC 61000-4-3  
80% AM (2Hz)  
a
survey , should be less than the compliance  
b
level in each frequency range .  
Interference may occur in the vicinity of  
equipment marked with the following symbol:  
Note1: At 80 MHz and 800 MHz, the higher frequency range applies.  
Note2: These guidelines may not apply in all situations. Electromagnetic 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 radios, amateur radio, AM and FM radio broadcast and TV broadcast  
cannot be predicted theoretically with accuracy. To 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 HBP-1300 is used exceeds the applicable RF  
compliance level above, the HBP-1300 should be observed to verify normal operation. If  
abnormal performance is observed, additional measures may be necessary, such as reorienting  
or relocating the HBP-1300.  
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.  
34  
 
Recommended Separation Distances:  
Recommended separation distance between portable and mobile RF communications equipment  
and the HBP-1300  
The HBP-1300 is intended for use in an electromagnetic environment in which radiated RF disturbances are  
controlled. The customer or the user of the HBP-1300 can help prevent electromagnetic interference by  
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters)  
and the HBP-1300 as recommended below, according to the maximum output power of the communications  
equipment.  
Separation distance according to frequency of transmitter  
m
Rated maximum output  
power of transmitter  
(W)  
150 kHz to 80 MHz  
80 MHz to 800 MHz  
800 MHz to 2.5 GHz  
P
P
P
d = 1.2  
0.12  
0.38  
1.2  
d = 1.2  
0.12  
0.38  
1.2  
d = 2.3  
0.23  
0.73  
2.3  
0.01  
0.1  
1
10  
3.8  
3.8  
7.3  
100  
12  
12  
23  
For transmitters rated at a maximum output power not listed above, the recommended separation  
distance d in metres (m) can be determined 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.  
Note1: At 80MHz and 800MHz, the separation distance for the higher frequency range applies  
Note2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by  
absorption and reflection from structures, objects and people.  
EN  
35  
 
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  
OMRON (DALIAN) CO., LTD.  
Production facility  
Dalian, CHINA  
OMRON HEALTHCARE UK LTD.  
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, U.K.  
OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH  
Gottlieb-Daimler-Strasse 10, 68165 Mannheim, GERMANY  
Subsidiary  
OMRON SANTÉ FRANCE SAS  
14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE  
Made in China  
 

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