Easy@Home EBP-095 User manual

Blood Pressure Monitor EBP-095
version:1.0
To use the monitor correctly and safely, please read the manual thoroughly.
Please keep this manual in order to reference in future.
Arm Type
Thank you very much for selecting Blood Pressure Monitor
EBP-095.
EASY AT HOME MEDICAL,LLC
Any questions,please call toll-free :
1-855-822-6999 M-F 9 a.m.-5 p.m. CST
E-MAIL:[email protected]
User Manual

1
CATALOGUE CATALOGUE
INTRODUCTION...................................................................................................................2
General Description
Safety Information
LCD Display Signal
Monitor Components
BEFORE YOU START...........................................................................................................6
The Choice of Power Supply
Installing and Replacing the Batteries
Setting Date, Time and Measurement Unit
MEASUREMENT...................................................................................................................9
Tie the Cuff
Start the Measurement
DATA MANAGEMENT..........................................................................................................11
Recall the Records
Delete the Records
INFORMATION FOR USER................................................................................................14
Tips for measurement
Maintenances
ABOUT BLOOD PRESSURE..............................................................................................16
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure fluctuate throughout the day?
Why do I get a different blood pressure at home compared to the hospital??
Is the result the same if measuring on the right arm?
TROUBLESHOOTING........................................................................................................18
SPECIFICATIONS...............................................................................................................19
AUTHORIZED COMPONENTS ..........................................................................................20
CONTACT INFORMATION..................................................................................................20
COMPLIED STANDARDS LIST...........................................................................................21
FCC STATEMENT...............................................................................................................21
EMC GUIDANCE.................................................................................................................22
Table of Contents

2 3
INTRODUCTION INTRODUCTION
Thank you for selecting arm type blood pressure Monitor
(EBP-095). The monitor features blood pressure measurement, pulse rate
measurement and the result storage. The design provides you with two
years of reliable service.
Readings taken by the EBP-095 are equivalent to those obtained by a
trained observer using the cuff and stethoscope auscultation method.
This manual contains important safety and care information, and
provides step by step instructions for using the product.
Read the manual thoroughly before using the product.
The signs below might be in the user manual, labeling or other component.
They are the requirement of standard and using.
Safety Information
Features:
60mm*80mm Digital LCD display
Maximum 60 records
Measuring during inflation technology
General Description
This device is intended for adult use only.
This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is
not intended for use on extremities other than the wrist or for functions other than obtaining a blood
pressure measurement.
Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood
pressure.Do not begin or end medical treatment without asking a physician for treatment advice.
If you are taking medication,consult your physician to determine the most appropriate time to
measure your blood pressure. Never change a prescribed medication without consulting your
physician.
If the cuff pressure exceeds 40 kPa (300 mmHg),the unit will automatically deflate. Should the cuff
not deflate when pressures exceeds 40 kPa (300 mmHg),detach the cuff from the arm and press
the START/STOP button to stop inflation.
To avoid measurement errors, carefully read this manual before using the product.
The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable
anesthetic mixture with air of with oxygen or nitrous oxide.
The operator shall not touch output of batteries/AC adapter and the patient simultaneously.
Do not wind air tube in the neck.
CAUTION
This device may provide contradictory results for any female subject who may be suspected of, or
is pregnant. Besides providing inaccurate readings, the effects of this device on the fetus are
unknown.
The device has been evaluated clinically using manual cuff/stethoscope auscultation as the
reference. Blood pressure measurements determined with this device are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultatory method, within the limits
prescribed by the American National Standard, Manual, electronic, or automated
sphygmomanometers.”
If you have any problems with this device, such as setting up, maintaining or using, please
contact the SERVICE PERSONNEL of . Don’t open or repair the device by yourself.
Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE.
Otherwise, it may cause damage to the unit or danger to the user/patients.
Please note that Luer lock connectors are not used on the product and please DO NOT change
any provided connectors.
Manufacturer will make available on request circuit diagrams, component parts list etc.
WARNING: No modifications of this equipment is allowed.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
Otherwise, the patient’s arm and fingers will become anaesthetic, swollen, and even purple due to a
lack of blood.
Please use the device under the environment which was provided in the user manual. Otherwise,
the performance and lifetime of the device will be impacted and reduced.
During use, the patient will be in contact with the cuff. The materials of the cuff have been tested
and found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause
any potential alergic reaction or contact injury.
The device doesn’t need to be calibrated within the two years of reliable service.
Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the
local guidelines.
When the device was used to measure patients who have common arrhythmias such as atrial or
ventricular premature beats or atrial fibrillation, the best result may occur with deviation.
T1A/250V Φ3.6*10CCC
F1
For indoor use only
Symbol for “MANUFACTURER”
Symbol for “SERIAL NUMBER”
Symbol for “TYPE B APPLIED
PARTS”
Symbol for “ENVIRONMENT
PROTECTION – Electrical waste
products should not be disposed of
with household waste. Please follow
local guidelines.”
Symbol for “DIRECT CURRENT”
Symbol for “Class II Equipment”
Symbol for “THE OPERATION
GUIDE MUST BE READ”
Symbol for “MANUFACTURE
DATE”
Please report to if any unexpected operation or events occur.

START
STOP
4 5
INTRODUCTION INTRODUCTION
LCD Display Signal
SYMBOL DESCRIPTION
Systolic blood pressure High pressure result
Diastolic blood pressure Low pressure result
EXPLANATION
Pulse Pulse/minute
Deflating CUFF air is exhausting of deflating
Current Time Time(year:month:day:hour:minute)
Memory If “MEM” shows, the displayed
measurement values is from the memory.
Measurement unit Measurement Unit of the blood pressure
Low battery Batteries are low and need to be replaced
Irregular heartbeat DectionIrregular heartbeat
Grade
Heartbeat Heartbeat detection during measurement
The grade of the blood pressure
Component list of
pressure measuring system
1 Cuff
2 Air pipe
3 PCBA
4 Pump
5 Valve
Monitor Components
BATTERY COMPARTMENT
CUFF
AIR HOSE
AIR CONNECTOR PLUG
LCD DISPLAY
MEM/UP BUTTON
START/STOP BUTTON
SET/DOWN BUTTON
List
1. Blood Pressure Monitor
(EBP-095)
4. User manual
3. 4*AA Batteries
2. Cuff (22cm~32cm)
( )
(Type B applied part)
(1mmHg=0.133kPa) (1kPa=7.5mmHg)
Shocking reminder Shocking will result in inaccurate
Start measurement for user 1 and save the
measuring result automatically
Recall the recordsData Enquiry Mode
Start measurement for user 2 and save the
measuring result automatically
User 1
User 2
START
STOP
8~
/
3
”
412 /
1
”
2

7
6
BEFORE YOU START BEFORE YOU START
The Choice of Power Supply
In order to get the best effect and protect your monitor,please
use the right battery and special power adaptor.
1.Slide off the battery cover.
2.Install the batteries by matching
the correct polarity, as shown.
3.Replace the cover.
1.Battery powered mode:
6VDC 4*AA batteries
2.This unit has an optional AC Power
adaptor which is available as an
accessory.Only use AC adaptor with
below specification (not included).
Installing and Replacing the Batteries
CAUTION
Remove batteries if the device is not likely to be used for some time.
The old batteries are harmful to the environment, so please do not dispose with other
daily trash.
Remove the old batteries from the device and follow your local recycling guidelines.
Do not dispose of batteries in fire. Batteries may explode or leak.
CAUTION
Replace the batteries whenever the below happen
The shows
The display dims
The display does not light up
Setting Date, Time and Measurement Unit
It is important to set the clock before using your blood pressure
monitor, so that a time stamp can be assigned to each record that
is stored in the memory. (year :2011—2050 time format:12 H)
1.When the unit is off,
hold “SET” for 3
seconds to enter the
mode for year setting.
2.Press the “MEM” to
change the [YEAR].
Each press will
increase the numeral
by one in a cycling
manner.
3.When you get the right
year, press “SET” to
confirm, and it will divert
to the [MONTH] setting.
Right picture is the hole in for power adaptor.
Input：100-240VAC 50/60Hz 0.3A Max
Output：6V 1000mA
( Conforms to UL certificate )

9
8
BEFORE YOU START MEASUREMENT
Rest For 5 minutes before
measuring.
Wait at least 3 minutes between
measurements. This allows your
blood circulation to recover.
For a meaningful comparison,
try to measure under similar
conditions. For example, take daily
measurements at approximately
the same time, on the same wrist,
or as directed by a physician.
Tie the Cuff
1.Tie the cuff on your upper arm,
then position the tube off-center
toward the inner side of arm in
line with the little finger.
2.The cuff should be snug but not
too tight. You should be able to
insert one finger between the
cuff and your arm.
3.Sit comfortably with your arm
resting on a flat surface.
2~3cm
4.Patients with Hypertension should
sit with correct posture.
- Bare your arm or wear tights only
when starting measurement.
- Sit comfortably with legs
uncrossed, feet flat on the floor,
back and arm supported.
The center of the cuff should be at
the same level as the right atrium
of the heart.
4.Repeat steps 2 and 3 to
set the [MONTH] and
[DAY].
5.Repeat steps 2 and 3 to
set the [HOUR] and
[MINUTE].
7.After the [MEASUREMENT UNIT] is
set,the LCD will display “dOnE”, and
then turn off.
6.Repeat steps 2 and 3 to set
the [MEASUREMENT
UNIT].
(0.8”~1.2”)

11
10
MEASUREMENT
1.After selecting the user, press the “START/STOP” to
start measurement, and it will finish the whole
measurement for the selected user.
Take User 1 for example.
Adjust the zero .
LCD display
Inflating and measuring. Display and save the results. The
corresponding backlight shows
according to the grade of blood
pressure.
Start the Measurement
2.Press “SET”, “MEM” or
“START/STOP” button to
power off, otherwise it will turn
off within 1 minute.
DATA MANAGEMENT
Recall the Records
Date,time will be
shown under the
Pulse by turns.
Before you start the measurement, please press the SET button to choose
either User 1 or User 2 as the User ID. When the desired User ID is shown,
press START/STOP button to confirm the User ID. 1. When the monitor is off, please press the
“MEM” to show the average value of the
latest three records.
2. Press MEM button or SET button to rotate the records. Up to 60
records will be stored under each user ID.
There are 8 records.
The current is the No.1.
The corresponding
time is A.M.10:35.
The corresponding
date is 16th October.
A.M.

13
12
The most recent record (1) is shown first. Each new measurement
is assigned to the first (1) record. All other records are pushed back
one digit (e.g., 2 becomes 3, and so on), and the last record (60) is
dropped from the list.
CAUTION
DATA MANAGEMENT
1.Hold “MEM” for 3
seconds when the
monitor is in the
memory mode ,then
“dEL ALL” will show.
2.Press “MEM” to
confirm deleting and
the monitor will turn
off.
3.If you don’t want to delete the
records, press “START/STOP”
button or “SET” button to
escape.
If you did not get the correct measurement, you can delete all
results for the selected user by the following steps below.
Delete the Records
4. If there is no record.
the right display will
show when recalling
the record.
3. If you want to check another user’s records, press
START/STOP button to turn off the monitor when it is in the
memory recall mode. Then press SET button, the user icon
will be shown, press “SET” button to select the desired user
ID, press “MEM” button to review the selected user’s records.
4. Press the START/STOP button to turn off the monitor.
Otherwise, the monitor will shut off within 1 minute after last
operation.
DATA MANAGEMENT

15
14
Tips for Measurement
wait at least 1 hour after dinner or drinking
Wait at least 20 minutes after taking a bath
In a very cold environment
Immediate measurement
after tea, coffee, smoking
When talking or moving your fingers
When you want to discharge urine
Measurements may be inaccurate if taken in the following
circumstances.
INFORMATION FOR USER INFORMATION FOR USER
START
STOP
START
STOP
START
STOP
START
STOP
START
STOP
Maintenance
In order to get the best performance, please follow the instructions
below.
Put in a dry place and avoid the sunshine
Avoid intense shaking and collisions
Use wet cloths to remove dirt
Avoid touching water,
clean it with a dry cloth in case.
Avoid dusty and unstable
temperature environment
Avoid washing the cuff

17
16
ABOUT BLOOD PRESSURE
What are systolic pressure and diastolic pressure?
press
artery vein
blood discharging
Systolic
relax
blood entering
Diastolic
When ventricles contract and pump blood out
of the heart, the blood pressure reaches its
maximum value in the cycle, which is called
systolic pressure. When the ventricles relax,
the blood pressure reaches its minimum value
in the cycle, which is called diastolic pressure.
What is the standard blood pressure classification?
Irregular Heartbeat Detector
CAUTION
The appearance of the IHB icon indicates that a pulse irregularity consistent with an
irregular heartbeat was detected during measurement. Usually this is NOT a cause for
concern. However, if the symbol appears often, we recommend you seek medical
advice. Please note that the device does not replace a cardiac examination, but serves
to detect pulse irregularities at an early stage.
Only a physician can tell your normal BP range. Please contact a physician if your measuring result falls
out of the range. Please note that only a physician can tell whether your blood pressure value has
reached a dangerous point.
The chart on the right is the
standard blood pressure
classification published
by American Heart
Association (AHA).
CAUTION
Blood Pressure Category
Normal
Prehypertension
High Blood Pressure
(Hypertension) Stage 1
High Blood Pressure
(Hypertension) Stage 2
Hypertensive Crisis
(Emergency care needed)
Systolic
mmHg (upper#)
Diastolic
mmHg (lower#)
less than 120
120-139
140-159
160 or higher
Higher than 180
and
or
or
or
or
less than 80
80-89
90-99
100 or higher
Higher than 110
This chart reflects blood pressure categories defined by American Heart Association.
AHA Home Guideline for
Upper Limit of Normal BP
SYS 135 mm Hg
DIA 85 mm Hg
ABOUT BLOOD PRESSURE
1. Individual blood pressure varies
multiple times everyday. It is also
affected by the way you tie your cuff
and your measurement position, so
please take the measurement under the
same conditions.
2.If the person takes medicine, the
pressure will vary more.
3.Wait at least 3 minutes for another
measurement.
Why does my blood
pressure fluctuate
throughout the day?
Is the result the same if
measuring on the right
arm?
It is ok for both arms, but there
will be some different results for
different people. We suggest you
measure the same arm every time.
Why do I get a different
blood pressure at home
compared to the hospital?
The blood pressure is different even
throughout the day due to weather,
emotion, exercise etc, Also, there is the
“white coat” effect, which means blood
pressure usually increases in clinical
settings.
What you need to pay
attention to when you measure
your blood pressure at home:
If the cuff is tied properly.
If the cuff is too tight or too loose.
If the cuff is tied on the upper arm.
If you feel anxious.
Taking 2-3 deep breaths before
beginning will be better for measuring.
Advice: Relax yourself for 4-5
minutes until you calm down.
An irregular heartbeat is detected when a heartbeat rhythm varies while the unit is
measuring the systolic and diastolic blood pressure.During each measurement,
this equipment records the heartbeat intervals and works out the standard deviation.
If the calculated value is larger than or equal to 15,the irregular heartbeat symbol
appears on the symbol when the measurement results are displayed.
Blue
Blue
Yellow
Red
Red
Backlight
on BPM

19
18
TROUBLESHOOTING
This section includes a list of error messages and frequently
asked questions for problems you may encounter with your blood
pressure monitor. If the products not operating as you think it
should, check here before arranging for servicing.
PROBLEM SYMPTOM CHECK THIS REMEDY
No power
Low
batteries
Error
massage
Display is dim or
will not light up.
Batteries are exhausted. Replace with new batteries
Insert the batteries correctly
Replace with new batteries
Batteries are inserted
incorrectly.
Show on the display
Batteries are low.
E 1 shows The cuff is not
secure.
Refasten the cuff and then
measure again.
E 2 shows The cuff is very tight Refasten the cuff and then
measure again.
E 3 shows The pressure of the
cuff is excess.
Relax for a moment
and then measure again.
E 10 or E11
shows
The monitor detected
motion while measuring.
Movement can affect the
measurement.Relax for a
moment and then measure
again.
E20 shows
EExx,shows on
the display.
A calibration error
occurred.
Retake the measurement.If
the problem persists,contact
the retailer or our customer
service department for
further assistance.
Refer to the warranty for
contact information and
return instructions.
AC adaptor is inserted
incorrectly.
Insert the AC adaptor
tightly
The measurement
process does not detect
the pulse signal.
Loosen the clothing on the
arm and then measure
again
E21 shows The treatment of the
measurement failed.
Relax for a moment and
then measure again.
SPECIFICATIONS
Power supply
Battery powered mode:
6VDC 4*AA batteries
AC adaptor powered mode:
(INPUT: 100-240VAC 50/60Hz 0.3A Max
OUTPUT: 6V 1000mA)(Not Included)
Display mode
Digital LCD V.A.60mm*80mm（2.36’’*3.15’’）
Measurement mode
Oscillographic testing mode
Measurement range
Accuracy
Normal working condition
Storage & transportation
condition
Measurement perimeter
of the upper arm
About 22cm~32cm（ ）
Net Weight
Approx.388g(13.69oz)(Excluding the batteries)
External dimensions
Attachment
Approx.102mm*143mm*73mm (4.02”*5.63”*2.87”)
4*AA batteries, one storage bag, user manual
Mode of operation
Continuous operation
Degree of protection
Software Version
Type B applied part
Protection against
ingress of water
V01
Pressure: 0mmHg~300mmHg(0kPa-40kPa)
pulse value:(40-199)times/minute
IPX0
Pressure:
5℃-40℃(41℉-104℉)within±3mmHg(0.4kPa)
pulse value:±5%
Temperature:5℃to 40℃(41℉ to 104℉)
Relative humidity: ≤85%RH
Atmospheric pressure: 86kPa to 106kPa
Temperature:-20℃-60℃(-4℉ to 140℉)
Relative Humidity: 10%RH-93%RH
Atmospheric Pressure: 50kPa-106 kPa
8-
/
3”
412 /
1”
2

21
20
AUTHORIZED COMPONENTS
Authorized Components
1. please use the
authorized adapter. (Not Included)
Contact Information
Adapter
Input：
100-240VAC 50/60Hz 0.3A Max
Output：6V 1000mA
( Conforms to UL certificate )
For more information about our products, please visit ,
or call Customer 1-866-822-6999 M-F 9 a.m.-5 p.m.CST.usual
problems and customer download, will serve you anytime.
COMPLIED STANDARDS LIST
Complied Standards List
FCC Statement
This device complies with Part 15 of the FCC Rules. Operation is subject
to the following two conditions: (1) this device may not cause harmful
interference, and (2) this device must accept any interference received,
including interference that may cause undesired operation.
Risk management
Labeling
User manual
General Requirements for Safety
Electromagnetic compatibility
Non-invasive Sphygmomanometers
General Requirements
ISO 14971:2007
EN 980:2008
EN 1041: 2008
IEC 60601-1: 2005
IEC 60601-1-2:2007
ASSI/AAMI
SP10:2002/A1:2003/A2:2006/ (R)2008
Software Lifetime EN 62304:2006/AC:2008
2.Storage bag.

23
22
EMC Guidance
Table 1 Guidance and MANUFACTURER’s declaration – ELECTROMAGNETIC
EMISSIONS- for all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacturer’sdeclaration – electromagnetic emissions
RF emissions
CISPR 11 Group 1
Class B
Not applicable
Not applicable
Compliance
The device is intended for use in the electromagnetic environment specified
below. The customer or the user of the device should assure that it is used in
such an environment.
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions IEC
61000-3-3
RF emissions
CISPR 11
Emissions test Electromagnetic environment - guidance
The device 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.
Guidance and manufacturer’s declaration – electromagnetic immunity
IMMUNITY test
±6 kV contact
±8 kV air ±6 kV contact
±8 kV air
±2 kV for
power supply lines
±1 kV line(s)
to line(s)
±2 kV line(s)
to earth
<5% U
T
(>95% dip in U
T )
for 0.5 cycle
40% U
T
(60% dip in U
T
)
for5cycles
70% U
T
(30% dip in U
T
)
for 25 cycles
<5% U
T
(>95% dip in U
T
)
for 5 s
3A/m
NOTE U
T
is the a.c. mains voltage prior to application of the test level.
Table 2 Guidance and MANUFACTURER’s declaration – electromagnetic
IMMUNITY – for all ME EQUIPMENT and ME SYSTEMS
IEC 60601 test level Compliance level
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electromagnetic
environment - guidance
Floors should be wood,
concrete or ceramic tile. If
floors are covered with
synthetic material, the
relative humidity should be
at least 30%.
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
3A/m
Power frequency
(50/60Hz)
magnetic field
IEC 61000-4-8
Voltage dips,
short interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
Electrical fast
transient/burst
IEC 61000-4-4
Surge IEC
61000-4-5
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an
environment
±1 kV for
input/output lines
Mains power quality should
be that of a typical
commercial or hospital
environment.
Mains power quality should
be that of a typical
commercial or hospital
environment.
Main power quality should
be that of a typical
commercial or hospital
environment. If the user of
the device requires
continued operation during
power mains interruptions,
it is recommended that the
device be powered from an
uninterruptible power supply
or a battery.
±2 kV for power
supply lines
±1 kV line(s) to
line(s)
<5% U
T
(>95% dip in U
T )
for 0.5 cycle
40% U
T
(60% dip in U
T
)
for5cycles
70% U
T
(30% dip in U
T
)
for 25 cycles
<5% U
T
(>95% dip in U
T
)
for 5 s
EMC GUIDANCE EMC GUIDANCE

24
Table 4 Guidance and MANUFACTURER’s declaration – electromagnetic IMMUNITY –
for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration – electromagnetic immunity
IMMUNITY test
3 Vrms
3 V/m
Compliance
level
IEC 60601
TEST LEVEL
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to
2.5 GHz
3 Vrms
150 kHz to
80 MHz
Electromagnetic environment -
guidance
Portable and mobile RF communications
equipment should be used no closer to
any part of the device, including
cables, than the recommended
separation distance calculated from the
equation applicable to the frequency of
the transmitter.
Recommended separation distance
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment.
where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacturer
and dis the recommended separation
distance in metres (m).
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey, should be
less than the compliance level in each
frequency range.
a
b
Interference may occur in the vicinity of
equipment marked with the following
symbol:
P
=d
P=d 80 MHz t o 800 M Hz
P=d 2.333 800 M Hz to 2, 5 GH z
1.167
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
aField strengths from fixed transmitters, such as base stations for radio (cellular /
cordless) telephones and land mobile radios, amateur radio, AM and FM radio broad-
cast 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 device is used exceeds the applicable RF compliance level above, the device
should be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as re-orienting or relocating the device.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.
b
1.167
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Table 6 Recommended separation distances between portable and mobile
RF communications equipment and the ME EQUIPMENT or ME SYSTEM –
for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances
between portable and mobile RF communications equipment and the device.
The device is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the device
can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmittters) and the
device as recommended below, according to the maximum output power of the
communications equipment.
Rated maximum output
power of transmitter
(W)
Separation distance according to frequency of transmitter(m)
For transmitters rated at a maximum output power not listed above, the recommended
separation distance din metres (m) can be estimated using the equation applicable to
the frequency of the transmitter, where Pis the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80MHz and 800MHz, the separation distance for the higher frequency
range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation
is affected by absorption and reflection from structures, objects and people.
0.01
0.1
1
10
100
0.117 0.117
0.369
1.167
3.690
11.67
0.233
0.738
2.333
7.378
23.33
P=d P=d 1.167 2.333 P=d
0.369
1.167
3.690
11.67
1.167
EMC GUIDANCE EMC GUIDANCE
25