Jamr Technology BC31L User manual

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Fully Automatic Upper Arm
Model Number: BC31L/BC31LT
USER’S MANUAL
Blood Pressure Monitor
Shenzhen Jamr Technology Co., Ltd.
A101-301, D101-201, Jamr Science & Technology Park, No. 2
Guiyuan Road, Guixiang Community, Guanlan Street, Longhua
District, Shenzhen 518100, PEOPLE'S REPUBLIC OF CHINA
Shanghai International Holding Corp. GmbH (Europe)
Eiffestrasse 80, 20537 Hamburg, Germany.
[email protected]
Version Number:1.0


1.Introduction and Intended Use..........................................................
2.Important Information on Blood Pressure and its Measurement.......
3. Components of Your Blood Pressure Monitor..................................
4. Using Your Monitor for the First Time...............................................
5.Measurement Procedure....................................................................
6.Care and Maintenance.......................................................................
7. Warranty/service...............................................................................
8. Certifications.....................................................................................
9. Technical Specifications...................................................................
10. FCC Statement...............................................................................
11. EMC Declaration.............................................................................
2
5
6
8
10
17
18
18
18
19
19
CONTENTS

1.Introduction and Intended Use
This device is a fully automatic digital blood pressure measuring device,it
is intended to measure systolic and diastolic blood pressure as well as the
pulse by wrapping around the upper arm with cuff circumference ranging
from 22cm to 42cm .
The device is used for adult that age is more than 12 years old ,and the
intended populations are the patients with hypertension or need blood
pressure monitoring. The device can be used in medical facilities or at
home,and only for indoor use.
Contraindication: The device is not used for patients under dialysis
therapy or on anticoagulant, antiplatelets, or steroids.
Before using, please read this instruction manual carefully and then keep
it in a safe place.
1.1 Remember…
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measurements.
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before prescribing or making adjustments to any medications used to
control hypertension. Under no circumstances should YOU alter the
dosages of any drugs prirately unless you have the permission of
physician.
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before using this instrument on a child.
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instrument should only be evaluated after consultation with a physician.
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with local regulations after reaching the life cycle.
Warning: The use of other accessories other than those specified or
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electromagnetic radiation to increase or decrease
electromagnetic immunity resulting in operational failure
Warning: This system may fail to yield specified measurement accuracy if
operated or stored in temperature or humidity conditions outside
the limits stated in the specifications section of this manual.
Warning:
Warning:
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Do not use the AC adapter if the unit or the power cord is
damaged.Turn off the power and unplug the power cord
immediately.
Warning: 7KHXVHUPXVWFKHFNWKDWWKHHTXLSPHQWIXQFWLRQVVDIHO\DQG
see that it is in proper working condition before being used.
Warning:
Warning:
Warning:
Warning:
Use of power adapters
1.Adapter: input 100-240V, 50/60hz output d.c. 5V 1A
2.Do not be prone to water leakage, high temperature, moisture,
direct sunlight and more or more corrosive gas environment. And
Do not use this product in the above environment.
Warning: The device is not suitable for use in the presence of flammable
anesthetic mixtures with air or with oxygen or nitrous oxide.
Warning: If the patient is an intended operator, the functions of monitoring
blood pressure and pulse rate can be safely used by patient. The
routine clean and changing batteries can be performed by the
patient.
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Caution: To avoid any possibility of accidental strangulation, keep this
device away from children and do not drape tubing around your
neck.
1.2 Warnings and Precautions
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to blood flow interference.
Don’t place the cuff over wound part.
Pressurization of the CUFF can temporarily cause loss of function
of simultaneously used monitoring ME EQUIPMENT on the same
limb.

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2.Important Information on Blood Pressure
and its Measurement
2.1. How does high or low blood pressure arise?
Your level of blood pressure is determined in the circulatory center of the brain
and adjusts to a variety of situations through feedback from the nervous
system. To adjust blood pressure, the strength and speed of the heart (Pulse),
as well as the width of circulatory blood vessels is altered.Blood vessel width
is controlled by fine muscles in the blood vessel walls.
Your level of arterial blood pressure changes periodically during heart activity:
During the “blood ejection” (Systole) the value is highest (systolic blood
pressure value). At the end of the heart’s “rest period” (Diastole) pressure is
lowest (diastolic blood pressure value).
2.2. Which values are normal?
Please refer to the diagram below(Picture-01)
Note: This device contains sensitive electronic components. Avoid
strong electrical or electromagnetic fields in the direct vicinity of
the device (e.g. mobile telephones, microwave ovens) during use.
These can lead to erratic results.
Note: Do not attempt to service or repair this device yourself. Should a
malfunction occur, refer to local distributor or the manufacturer.
Caution: To avoid damaging the device, keep this unit away from children
and pets.
Caution: The standard material used for the bladder and tubing is latex-free.
Attention: The device is intended for monitoring,and not for a diagnsis.
Unusual values must always be discussed with a physician.
Under no circumstances should you alter the dosages of any
drugs prescribed by a physician.
Attention: The device cannot be used to substitute the professional ECG
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Attention: In cases of irregular heartbeat, measurements made with this
instrument should only be evaluated after consultation with a
physician.
Note: To obtain the greatest accuracy from your blood pressure
instrument, it is recommended that the instrument be used within
the specified temperature and the relative humidity, please see
the Technical Specifications.
Note: The cuff is defined as the applied part.The user should contact
the manufacturer for assistance, if needed, replace, or
maintaining the device.


3. Components of your blood pressure monitor
There are six grids in the display of device. Please refer to the picture-01-01.
Different grids represent different interval scales of WHO.
Picture-02
Picture-03
3.3 Features of Model
3.2 The symbols on the LED display
2. Double users: 2 x 120 sets memory
4. Irregular heartbeat checking
6. Low battery display
8. Auto power-off
10. Volume adjustment
1. Voice function
3. Cuff self-checking function
5. Average value function
7. WHO function
9. External power adapter support
11. Date/time display
Note: Arm circumference should be measured with a measuring tape in the
middle of the relaxed upper arm. Do not force cuff connection into the
opening. Make sure the cuff connection is not pushed into the AC adapter
port.
START/STOP
button
Memory
button
AC Adapter Port
Mute
button
Users Switch
button
LED Display
1.USER 1
3.Bluetooth symbol
5.Cuff wrap error symbol
7.Low battery symbol
9.Pulse display / Memory number
11.Memory symbol
13.Movement error symbol
15.Systolic blood pressure
17.WHO function symbol
2.USER 2
4.Cuff wrap correct symbol
6.Mute symbol
8.Date/Time display
10.Heartbeat symbol number
12.Irregular heartbeat symbol
14.Average value symbol
16.Diastolic blood pressure
1 2 3 4 5 6 7
8
9
1011
12
1314151617
Cuff Connector Port

A.Setting the voice.
In some states that need to play voice, the voice can be turned on or off by
pressing the ( ) button.

4. Using your Monitor for the First Time
The battery is built-in chargeable Lithium battery.
Press the START/STOP button, if the Low battery symbol is blinking and the
device speaks “battery low power, please recharge it” . It means the battery
power is low and you cannot take any further measurements,it need tobe
recharged.
During the charging process, the charging indicator on the display screen
blinks. When the charging indicator stops blinking. it means the battery
power is fully recharged.
4.1 Battery Power checking
Picture-04
Insert the cuff tube into the opening on the left side of the monitor ( As shown
in picture-05)
4.3. Cuff tube connection
Before setting, ensure that the battery power is enough.
4.2. System Settings
Setting the Year:
When the year display is flashing, press the Users button continuously and it
will increase continuously 1 by 1 until 2049, and then return the original year,
press the Mute button continuously and it will reduce continuously 1 by 1, once
the year set is OK, press the Memory button to confirm.
C.Setting the User ID/Year/Month/Date/ hour system/Time/Volume:
With the unit off,Long press the Memory button for more than 3s, and then you
can start to set.
B.Setting the User ID(1 or 2):
With the unit off,Press the Users button and then you can set the User ID user
by pressing the Users button.
Setting Month/Date:
Initial Month/Date is 1/01, when the Month display is flashing, press the
Users button continuously, the month will increase continuously 1 by 1 ,press
the Mute button continuously and it will reduce continuously 1 by 1, press the
Memory button to confirm, and do in the same way to set the date, press the
Memory button to confirm.
Setting hour system：
Initial hour system is 12 hour ,press the Users button or Mute button and
then you can switch 12 or 24 hour system ,press the Memory button to
confirm.
Setting Time :
When the hour display is flashing, press the Users button continuously, the
hour will increase continuously 1 by 1, press the Mute button continuously and
it will reduce continuously 1 by 1,press the Memory button to confirm, and do
in the same way to set the minute. Press the Memory button to confirm.
Setting Volume:
When display with VOL is flashing, press the Users button or Mute button to
switch volume 1,volume 2, volume 3 or OFF. Press the Memory button to
confirm.After the setting is completed, the device switches off automatically
and save the setting result.


5. Measurement Procedure
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measurement. These factors influence the measurement result. Find time to
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before taking a measurement.
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5.1. Before measurement:
Please refer to picture-05
a) Wrap the cuff around your upper left arm. The rubber tube should be on
the inside of your arm extending downward to your hand. Make certain the
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edge of the cuff (Artery Mark) must lie over the artery which runs down the
inner side of the arm.
b) To secure the cuff, wrap it around your arm and press the hook and loop
closure together.
c) There should be little free space between your arm and the cuff. You
should be able to fit 2 fingers between your arm and the cuff. Cuffs that don’t
fit properly result in false measurement values. Measure your arm
circumference if you are not sure of proper fit.
d) Lay your arm on a table (palm upward) so the cuff is at the same height as
your heart. Make sure the tube is not kinked.
5.2. Fitting the Cuff
Picture-05
a) Press the START/STOP button and then turn the device on ,all symbols
appear on the display.The pump begins to inflate the cuff. In the display, the
increasing cuff pressure is continually displayed.
NOTE:
If the voice is playing,you can turn off the voice by pressing the ( ) button
before the pump begins to inflate the cuff.
b) After automatically reaching an individual pressure, the pump stops and the
pressure slowly falls. The cuff pressure is displayed during the measurement.
c) When the device has detected your pulse, the heart symbol in the display
begins to blink.
d) When the measurement has been concluded, the measured systolic and
diastolic blood pressure values, as well as the pulse will be displayed.
e) The measurement results are displayed until you turn the device off by
pressing the START/STOP button .If no button is pressed for 60 seconds,
the device switches off automatically.
f) Cuff self-checking symbol ( )
The cuff correct symbol( ) will be displayed if the cuff position is correct,
otherwise the wrong symbol( ) will be displayed. Please check again the
cuff if the wrong symbol( ) is displayed.
5.3. Measure Procedure
Refer to picture-06
1. Sit comfortably in a chair with your feet flat on the floor.
2. Select your User ID (1 or 2).
3. Stretch your arm forward on the desk and keep relaxing, make sure the
palm of hand is upturned. Make sure arm is in correct position, to avoid
body movement. Sit still and do not talk or move during the measurement.
After the cuff has been appropriately positioned on the arm and connected
to the blood pressure monitor, the measurement can begin:
1) Operate via the App on smart phone with Bluetooth (No Bluetooth models
do not have this step )
a) Install the App from Google play store or Apple app store.
Open Bluetooth on smart phone, and then Turn on the App.
b) Bluetooth pairing for the first time
Press the Memory button and the Bluetooth symbol will flash，Then operate
bluetooth pairing according to the Settings on the APP,The bluetooth symbol
(will stop flashing after the connection is successful).
c)Bluetooth paired successfully
Bluetooth will be automatically searched and connected when it is powered on.
The device is designed to take measurements and store the measurement
values in memory for two people using User ID 1 and User ID 2.
Operate on the device


Patient Position:
1) Comfortably seated 2) Legs uncrossed
3) Feet flat on the floor 4) Back and arm supported
5) Middle of the CUFF at the level of the right atrium of the heart
NOTE:
This symbol( ) - indicates that certain pulse irregularities were detected
during the measurement.
In this case, the result may deviate from your normal basal blood pressure –
repeat the measurement.
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Heartbeat Symbol.
This instrument is an oscillometric blood pressure monitor device that also
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tested.
If pulse irregularities occur during measurement, the irregular heartbeat
symbol is displayed after the measurement. If the symbol appears more
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if it suddenly appears more often than usual, we recommend the patient to
seek medical advice. The instrument does not replace a cardiac examination,
but serves to detect pulse irregularities at an early stage.
5.4. Irregular Heartbeat Detector
5.5. Error Indicates
Picture-06
The following symbol will appear on the display when measuring abnormal
Er 1
SYMBOL
No display
appears
Weak battery or improper
placement
Sensor abnormal
Replace both batteries with new ones.
Check the battery installation for proper
placement of the battery polarities.
CAUSE CORRECTION
Er 2
Er 3
Er 4
Er 5
Er 6
Er 7
Er 8
Check if the pump is working or not. If it
is working, then the problem is sensor
abnormal. Please send it to the local
distributor.
start the measurement again.If the error is
still displayed, please send it to local
distributor
start the measurement again.If the error is
still displayed, please send it to local
distributor
Occasionally-measure for one more time/
Always - send it to local distributor
Tie the cuff correctly and make sure the air
plug is properly inserted in the unit
Correct it and make the measurement again
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Please send back to the local distributor
Monitor could not detect pulse
wave or cannot calculate the
blood pressure data
Measurement result is abnormal
Too loose cuff or air leakage
The air tube is crimped
The sensor is sensing great
fluctuation in the pressure
The pressure that the sensor
sensing is over the limit
The demarcation is incorrect or the
device has not been demarcated
g) Movement error symbol ( )
The Movement Error Symbol ( ) is displayed if you move your body
during the measurement. Please remove the cuff, and wait 2-3 minutes.
Reapply the cuff and take another measurement.


Each unit stores 120 sets measurements for 2 users,totally 240 sets (User 1
and 2).Measurements for each user are stored separately. Be certain that
you are viewing the measurements for the correct user.
5.6. Memory
With the unit off, press the Memory button. The monitor will display User ID
and an average value of the last 3 times measurements stored in the unit.( If
measurements are less than 3 sets, directly display the first set )
Each time you press the Memory button, it will display the memory value from
the latest to the oldest in turn.
Each time you press the Users button, it will display the memory value from
the oldest to the latest in turn.
A.View the memory
The following symbols may appear in this manual, on the Digital Blood
Pressure Monitor, or on it's accessories. Some of the symbols represent
standards and compliances associated with the Digital Blood Pressure
Monitor and its use.
SYMBOL DESCRIPTIONS
Authorized Representative in the European Community
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Device Directive 93/42/EEC.
Date of manufacture.
Manufacturer
Specifies serial number
Type BF applied part
Direct current
DISPOSAL: Do not dispose this product as unsorted municipal
waste. Collection of such waste separately for special treatment
is necessary.
Follow instructions for use
B.Delete memory:
In average value memory viewing mode,the average value symbol ( ) is
being displayed, long press the (MEM) button for 3 seconds ,then it will delete
all measurements for the current user.
In single set memory viewing mode,long press the (MEM) button for 3 seconds
,then it will delete only a set measurement being displayed.
Put up
Medical device
Fragile
Afraid of the rain
Fear of the sun
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Temperature range
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Mode of operation: continuous
Trouble removal
Problem
No power
No inflation
Err and stop
working
Cuff leak
Whether the plug broken or leak
Please contact the distributor if you can’t solve the problem, do not
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Whether move the arm when inflate Keep the body peaceful
Check if chatting when measured
Whether the cuff wrap too loose Wrap the cuff tightly
Whether the cuff broken Change a new cuff
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Change a new cuff
Whether the plug insert Insert into the air socket tightly
Check the battery power Replace new one
Installation for proper placement
of the batteries polarities
Check the polarity position
Check Cause and solutions


6.Care and Maintenance
If it is necessary to interrupt a blood pressure measurement for any reason
(e.g the patient feels unwell), the Start/Stop button can be pressed at any
time. The device then immediately lowers the cuff pressure automatically.
5.7. Discontinuing a Measurement
5.8. Using the AC Adapter
When the device is charging by using the AC adapter (output d.c. 5V /1A
with Type c connector),it cannot be turned on and work.
a) Ensure that the AC adapter and cable are not damaged.
b) Plug the adapter cable into the AC adapter port on the right side of the
blood pressure monitor.
c) Plug the adapter into your electrical outlet. When the AC adapter is
connected, The device will be recharged.
Note:
If you decide to delete the all memory, please keep the memory in another
way, incase you need it some days later. Take the battery out won’ t lead to
a memory missing. Wash hands after each time measurement.
If one device is used by different patients, wash hands before and after
each use.
a) Do not expose the device to either extreme temperatures, humidity,
dust or direct sunlight.
b) The cuff contains a sensitive air-tight bubble. Handle this cuff carefully
and avoid all types of stress through twisting or buckling.
c) Clean the device with a soft, dry cloth. Do not use gas, thinners or
similar solvents. Spots on the cuff can be removed carefully with a damp
cloth and soapsuds, if necessary, 70% isopropanol can be used. The cuff
with bladder must not be washed in a dishwasher, clothes washer, or
submerged in water.
d) Handle the tube carefully. Do not pull on it. Do not allow the tubing to
kink and keep it away from sharp edges.
e) Do not drop the monitor or treat it roughly in any way. Avoid strong
vibrations.
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g) Batteries and electronic instruments must be disposed of in accordance
with the locally applicable regulations, not with domestic waste.
6.1. Accuracy test
Sensitive measuring devices must be checked for accuracy from time to
time. We recommend a periodical inspection of your device by an
authorized dealer every 1 year. Please turn to local distributor or the
manufacturer.


7. Warranty/Service
Your blood pressure monitor is guaranteed for 2 years against manufacturers’
defects for the original purchaser only, from date of purchase. The warranty
does not apply to damage caused by improper handling, accidents,
professional use, not following the operating instructions or alterations made
to the instrument by third parties.
Warranty only applies to the main device and its cuff. All other accessories
are not covered by warranty.
There are no user serviceable parts inside. Batteries or damage from old
batteries is not covered by the warranty.
8. Certifications
Device standard:
This device is manufactured to meet the European blood pressure monitors:
IEC 80601-2-30 / IEC60601-1-11 / IEC60601-1
Electromagnetic compatibility:
Device fulfills the stipulations of the International standard
IEC60601-1-2
9. Technical Specifications 11. EMC Declaration
1) *This product needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided, and
this unit can be affected by portable and mobile RF communications
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2) * Do not use a mobile phone or other devices that emit electromagnetic
fields, near the unit. This may result in incorrect operation of the unit.
3) * Caution: This unit has been thoroughly tested and inspected to assure
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4) * Caution: this machine should not be used adjacent to or stacked with
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machine should be observed to verify normal operation in the configuration in
which it will be used
10. 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.
Measuring method: Oscillometric
Pressure sensor: Resistive
Measuring range: DIA: 40-220mmHg; SYS: 60-260mmHg
Pulse: 40 to 199 per minute
Cuff pressure display range:0-295mmHg
Memory: Automatically stores the last 120 measurements for 2 users (total
240)
Measuring resolution: 1 mmHg
Accuracy: Pressure within ± 3 mmHg / pulse ± 5 % of the reading
Power source: Built-in high capacity lithium battery - 800mAh
b) AC adapter INPUT: a.c. 100-240V= 50/60HZ OUTPUT: d.c. 5V 1A
Accessories: Wide range rigid cuff 8.7” – 16.5” (22 - 42 cm)
Users: Adult
Expected service life of the device and accessories: 5 years
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Model: BC31L/BC31LT
Weight: 259g (battery is not included)
Display: 132×55mm(5.2"×2.17") LED Digital Display
Size: 164(L)×88(W)×69(H) mm(6.46"×3.46"×2.72")
Packaging list: 1×Main Device, 1×Cuff, 1×Users manual,
Operating Conditions: Temperature: 5℃ to 40℃;Humidity: 15% to 93% RH;
Storage And Shipping Conditions:Temperature: -25℃ to 70℃;
+XPLGLW\5+
Atmospheric pressure range: 70kPa~106kPa
IP classification：IP21

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Guidance and manufacture’s declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environment specified below. The customer or
the user of device should assure that it is used in such an environment. 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.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment -
guidance Immunity test IEC 60601 test level Compliance
level Electromagnetic environment - guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
3RZHUIUHTXHQF\
(50Hz/60Hz)
magnetic field IEC
61000-4-8
30 A/m
50/60Hz 30 A/m 50/60Hz 3RZHUIUHTXHQF\PDJQHWLF fields should be at levels
characteristic of a typical
location in a typical commercial
or hospital environment.
0 % UT; 0.5 cycle
at 0°,45°,90°, 135°,
180°, 225°, 270°,
315°
0 % UT ; 1 cycle
70 % UT; 25/30
cycle
0% UT; 250/300
cycle
Not applicable 0DLQVSRZHUTXDOLW\VKRXOGEH
that of a typical commercial or
hospital environment. If the user
RIWKHGHYLFHUHTXLUHVFRQWLQXHG
operation during power mains
interruptions, it is recommended
that the device be powered from
an uninterruptible power supply
or a battery.
±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air
±2 kV for power
supply lines
±1 kV for input/output
lines
± 1 kV line(s) to
line(s)
± 2 kV line(s) to earth
±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air
Not applicable
Not applicable
Floors should be wood, concrete or
ceramic tile. If floor are covered with
synthetic material, the relative
humidity should be at least 30%.
0DLQVSRZHUTXDOLW\VKRXOGEHWKDW
of a typical commercial or hospital
environment.
0DLQVSRZHUTXDOLW\VKRXOGEHWKDW
of a typical commercial or hospital
environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacture’s declaration – electromagnetic immunity
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
10 V/m
80 MHz to 2.7 GHz
80% AM at 1kHz
3 Vrms
150 kHz to 80 MHz
3 V RMS outside the
ISM band, 6 V RMS
in the ISM and
amateur bands
80% AM at 1kHz Not
applicable
10 V/m
80 MHz to
2.7 GHz
80% AM at
1kHz
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should be used no closer to any part of the device,
including cables, than the recommended separation
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IUHTXHQF\RIWKHWUDQVPLWWHU
Recommended separation distance
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G ¥S
80MHz to 800MHz：
G ¥S
800MHzto 2.7GHz：
G ¥S
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.
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site survey, should be less than
WKHFRPSOLDQFHOHYHOLQHDFKIUHTXHQF\UDQJH
,QWHUIHUHQFHPD\RFFXULQWKHYLFLQLW\RIHTXLSPHQW
marked with the following symbol:
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NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
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 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.
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A
B

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Guidance and manufacture’s declaration – electromagnetic emission
The device is intended for use in the electromagnetic environment specified below. The customer of the
user of the device should assure that it is used in such an environment.
Guidance and manufacturer’s declaration - electromagnetic immunity
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.
Emission test
RF emissions
CISPR 11
Compliance Electromagnetic environment – guidance
Group 1
The device use RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
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The device is suitable for use in all establishments, including
domestic establishments other than domestic and those directly
connected to the public low-voltage power supply network that
supplies buildings used for domestic purposes.
RF emission
CISPR 11 Class B
Harmonic emissions
IEC 61000-3-2 Not applicable
Not applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
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
PDLQWDLQLQJDPLQLPXPGLVWDQFHEHWZHHQSRUWDEOHDQGPRELOH5)FRPPXQLFDWLRQVHTXLSPHQW
(transmitters) and the device as recommended below, according to the maximum output power of the
FRPPXQLFDWLRQVHTXLSPHQW
Rated maximum output
power of transmitter
(W)
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150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.7 GHz
For transmitters rated at a maximum output power not listed above, the recommended separation
GLVWDQFHGLQPHWUHVPFDQEHHVWLPDWHGXVLQJWKHHTXDWLRQDSSOLFDEOHWRWKHIUHTXHQF\RIWKH
transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the
transmitter manufacturer.
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NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
The MANUFACTURER should consider reducing the minimum separation distance, based on RISK
MANAGEMENT, and using higher IMMUNITY TEST LEVELS that are appropriate for the reduced
minimum separation distance. Minimum separation distances for higher IMMUNITY TEST LEVELS
shall be
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NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting
antenna and the ME EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m test distance is
permitted by IEC 61000-4-3.
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E7KHFDUULHUVKDOOEHPRGXODWHGXVLQJDGXW\F\FOHVTXDUHZDYHVLJQDO
c ) As an alternative to FM modulation. 50% pulse modulation at 18 Hz may be used because while it
does not represent actual modulation, it would be worst case.
Where P is the maximum power in W, d is the minimum separation distance in m, and E is the
IMMUNITY
TEST LEVEL in V/m.
Test
IUHTXHQF\
(MHz)
Band
(MHz) Service Modulation
Maximum
power
(w)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
385
450
710
745
780
810
870
930
430-470 GMRS 460,
FRS 460
FM
±5 kHz deviation
1 kHz sine
2
380-390 TETRA 400 Pulse Modulation
18 Hz
1.8 0.3 27
0.3 28
20.328
20.328
20.328
0.2 0.3 9
0.3 9
704-787
800-960
1700-1990
LTE Band 13,
17
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1,3
4,25;UMTS
Pulse
Modulation
18 Hz
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz 0.2
1720
1845
1970
2450 2400-2570
5100-5800
Bluetooth,
WLAN
802.11 b/g/n,
RFID 2450,
LTE Band 7
WLAN 802.11
a/n
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz
5240
5500
5785
a)
b)
b)
b)
b)
b)
b)
c)
a)
a)

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.
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 residential installation. This
equipment generates, uses and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to radio
communications. However, there is no guarant ee 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 receiver.
—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 for help.
Caution: Any changes or modifications not expressly approved by the party responsible
for compliance could void the user's authority to operate the equipment.
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled
environm ent. This transmitter must not be co-located or operating in conjunction with any
other antenna or transmitter.