Transtek Medical Electronics TMB1014BT BLOOD PRESSURE MONITOR User Manual
Guangdong Transtek Medical Electronics Co.,Ltd BLOOD PRESSURE MONITOR
Contents
- 1. User Manual
- 2. Users Manual
Users Manual
User Manual
Blood Pressure Monitor TMB-1014-BT
To use the monitor correctly and safely, please read the manual
thoroughly.
Thank you very much for selecting TRANSTEK Blood Pressure Monitor
TMB-1014-BT.
Please well keep this manual in order to reference in future.
Zhongshan Transtek Electronics Co., Ltd
Jin’an Road, Minzhong, Zhongshan 528441, Guangdong, China
Wrist Type
Version:1.0
CATALOGUE INTRODUCTION
INTRODUCTION 1
Safety information
LCD display signal
Monitor components
BEFORE YOU START 4
The Choice of power supply
Installing and replacing the batteries
Setting Date, time and measurement unit
MEASUREMENT 7
Tie the cuff
Strat a measurement
THE OPERATION OF RECALLING RECORDS 9
Recall the records
Delete the records
INFORMATION FOR USER 11
Tips for operation
Maintenances
ABOUT BLOOD PRESSURE 13
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure fluctuate throughout the day?
Why the blood pressure I get from the hospital is different from
home?
If the result is the same if measuring on the right wrist?
TROUBLESHOOTING 15
SPECIFICATIONS 16
CONTACT INFORMATION 17
The below signs might be in the user manual, labeling or other component.
They are the requirement of standard and using.
Safety information
This device is intended for adult use only.
This device is intended for no-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 based solely 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.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
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 wrist 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 the battery and the patient simultaneously.
The user must check that the equipment functions safely and see that it is in proper working
condition before being used.
The manufacturer does not require such preventive inspections by other persons.
The Max. temperature of apply part can be achieved is 42.5℃ under the environmental
temperature of 40℃.
Manufacture will make available on request circuit diagrams, component part list, etc.
CAUTION
Caution:Consult accompanying
documents
CE Mark: conforms to
essential requirements of the
Medical Device Directive
93/42/EEC.
Manufacturer
Specifies serial number
Type B applied part
Direct current
DI SP OS AL: Do n ot d is p os e th is
product as unsorted municipal waste.
Collection of such waste separately
for special treatment is necessary.
Authorized Representative in
the European Community
EC REP
Thank you for selecting TRANSTEK wrist blood pressure Monitor (TMB-1014-BT).
The monitor features blood pressure measurement, pulse rate measurement and
auto-save the result. The design provides you with many years of reliable service.
Reading taken by the TMB-1014-BT 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 instruction for using the product.
Read the manual thoroughly before using the product.
Features:
Systolic blood pressure
Diastolic blood pressure
Pulse rate
Historic record of up to 60 measurements
LCD DISPLAY
SYSTOLIC
DIASTOLIC
MEM/UP
BUTTON
SET/DOWN
BUTTON
START/OFF BUTTON
CUFF
(Type B applied part)
PULSE RATE
GRADE
TIME
BATTERY
COMPARTMENT
INTRODUCTION INTRODUCTION
Monitor components
LCD display signal
6 < 0 % 2 / ' ( 6 & 5 ,3 7 ,2 1 ( ; 3 /$ 1 $ 7 ,2 1
Systolic
blood pressure High pressure result
Diastolic
blood pressure Low pressure result
Pulse Pulse/minute
mmHg Measurement unit the blood pressure
Time Currently time
Low battery
Batteries are low and need to be replaced
Error
User
Recalling
Blood pressure monitor has detected
error
The current selected user
The erecords will be showed
Bluetooth Bluetooth is in an open position
Grade The grade of the blood pressure
For instructions,refer to Page 13
Arrhythmia Arrhythmia is detected
BEFORE YOU STARTBEFORE YOU START
Slide off the battery cover.
Install the batteries by matching the correct polarity, as shown
below. Always use the correct battery type (2 alkaline LR03AAA-size).
Replace the cover.
The installment and replacement of battery 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. In sure the “lock” key is glided to the
unlock mode.(year :2010—2050; time:24 H))
Remove batteries if the device is not likely to be used for some time.
The old battery is harmful to the environment, so please disposal with other daily trash.
Remove the old battery from the device and follow your local recycling guidelines.
CAUTION
Replace the batteries whenever the below happen
The shows
The display dims
The display does not light up
2.Press the “MEM” to
change the [Hour].
1.Pressing “SET” for
3 seconds to enter
the mode for [Hour]
setting.
3.When you get the right [Hour],
press “SET” to set down and
turn to next step automatically.
MEM
SET
MEM
SET
MEM
SET
BEFORE YOU START BEFORE YOU START
Bluetooth phones’ test software
1.Open the Bluetooth 4.0 special test
mobile phones after electrify blood
pressure monitor.
2.After operating Bluetooth Test program
(It is about 8 m from mobile to blood
pressure monitor), the “discovered
device” column will remind “searching
for device”...
3.Long press the "START" button after
power off the blood pressure monitor,
it’ll show moving "o”.
4.At this moment, the “discovered device”
column of mobile will display devices
list.
5.Choose detected device from the list.
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4.Repeat the 2 and 3 to
set the [Minute].
5.Repeat the 2 and 3 to
set th e [ YEA R],
[MONTH] and [DAY].
7.After the unit is set,
the right picture will
show, then it turn off
automatically.
MEM
SET
MEM
SET
MEM
SET
Positioning the wrist cuff
1.Remove all accessories (watch, bracelet, etc) from your left wrist. If your
physician has diagnosed you with poor circulation in your left wrist, use your
right wrist.
2.Roll or push up your sleeve to expose the skin.
3.Apply the cuff to your left wrist with your palm facing up.
4.Position the edge of the cuff about 1-1.5cm.
5.Fasten the wrist cuff around your wrist, leaving no extra room between the cuff
and your skin. If the cuff is too loose, the measurement will not be accurate.
6.When the blood pressure monitor show
“[ ]”, it means matching successfully;
When it display”E1”, it indicates
matching unsuccessfully.
7.If matching successfully, it will show the
lately measuring record on the “receive
data” column.
8.Choose “Bloodpressure Record” to view
the history record.
9.Click “back” to return main interface of
testing software and go on testing next
blood pressure monitor.
Resting 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.
BEFORE YOU START MEASUREMENT
START
STOP
START
STOP
1.Press the START/STOP, it will
finish the whole measurement
automatically.
Adjust the zero automatically.
Please press the SET to choose the user 1 or user 2 when the blood pressure monitor
turn off
Inflating and measuring
automatically.
Display and save the
results automatically.
Start the Measurement
4.Press the ST AR T/S TO P t o
power off, otherwise it will turn
off automatically within 1 minute.
2.After meas uring ，
it’ll disp lay t he
movin g “o” and
send data at the
same time.
3.If da ta is sent succ essfu lly,
go ba ck to disp lay t he
inter face of me asuri ng
resul ts.
If the data failed to send，go back
to display the interface of measuring
results after display “E9”.
MEASUREMENT MEASUREMENT
THE OPERATION OF
RECALLING RECORDS
Recalling the records
1.Press the “MEM” to show
the last 3 average of the
record.
2. Press the “MEM”
or “SET” to get the
record you want.
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
UP
DOWN
MEM
SET
MEM
SET
If you did not get the correct measurement, you can delete all
results by following below steps.
Deleting a measurement record from memory
1.Hold pressing “MEM” for 3
seconds, when the memory is
shown.
2.When flash “Delete all”, press the
“SET” to delete the memory.
3.If you don’t want to delete the
records, press
“START /STOP ” to escape.
4.If there is no record. the
right display will show.
MEM
SET
THE OPERATION OF
RECALLING RECORDS
MEM
SET
Tips for measurement
INFORMATION FOR USER
Wait at least 1 hour
after dinner or drinking
Wait at least 20 minutes
after taking a bath
In a very cold enviroment
Immediate measurement
after tea, coffee, smoking
When talking or moving your fingers
When you want to discharge urine
INFORMATION
It can cause incorrectness if the measurement are taken in the
following circumstances.
Maintenance
In order to get the best performance, please follow the below
instructions.
Put in a dry place and avoid the sunshine
Avoid the intense shaking
and collision
Using the wet clothing to remove the dirt
Avoid touching water,
clean it with a dry cloth in case.
Avoid the dusty and unstable-
temperature environment
Avoid washing the cuff
Clean the cuff with a soft dry cloth. Do not use any abrasive or volatile cleaners.
In order to reduce the pollution of the environment, please return to the
manufacture when the product is close to the end of life.
Instructions for correct replacement of interchangeable or detachable parts
specified by MANUFACTURER as replaceable by SERVICE PERSONNEL.
Please calibrate the blood pressure monitor in specific institute once every
two years to ensure the precise measurement。In order to get the best
performance, please follow the below instructions for storage.
ABOUT BLOOD PRESSURE
1. Individual blood pressure varies
every in one day, it also affected by the
w ay y o u t i e you r cuf f and t he y o u r
measurement position, so please take
the measurement at the same condition.
2.The varies of the pressure is
greater if the person take medicine.
3.Waiting at least 4-5 minutes for
another measurement.
Why my blood pressure
is varies even in one
day?
If the result is the same
i f m e a s u r i n g o n t h e
right wrist?
It is ok for both wrists, but there
will be some different results for
different person, so suggest you
measure the same wrist every time.
Why the blood pressure
I get from the hospital is
different from home?
The blood pressure is different
even during 24 hour because of the
weather,emotion , exercise etc,
specially the “white coat” in hospital
which makes the results are higher
than the ones at home.
The attention need to pay
when you measure you 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 wrist.
If you feel anxious pressured.
You had better take deep breath 2-3
times before beginning.
Advice:adjust yourself for 4-5 minutes
until you calm down.
ABOUT BLOOD PRESSURE
SYS
DIA
120
80
120~129
80~84
130~139
85~89
140~159
90~99
160~179
100~109
!180
!110
green light yellow
light red light
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PP+J
When ventricles contract and pump blood
out of the heart, blood pressure reaches its
maximum value, the highest pressure in the
cycle is known as systolic pressure. When
the heart relaxes between heartbeats, the
lowest blood pressure is diastolic pressure.
What are systolic pressure and diastolic
pressure?
Below illustrates the blood pressure
classification mode by World Health
Organization (WHO) and International
Society of Hypertension(ISH) in 1999.
What is the standard blood pressure
classification?
Only a physician can tell you your normal blood pressure range and
the point at which you are at risk. Consult your physician to obtain these
values.
If the measurements taken with these products fall outside the range,
consulty.
CAUTION
press
artery vein
blood discharging
Systolic
relax
blood entering
Diastolic
TROUBLESHOOTING SPECIFICATIONS
Power supply 2*AAA alkaline batteries
Display moder Digital LCD V.A.36x41mm
Measurement mode Oscillographic testing mode
Measurement range
Accuracy
Normal working condition
Storage & transportation
condition
Measurement perimeter
of the wrist About 13.5cm-19.5cm
Weight Approx.120g(Excluding the dry cells)
External dimensions
Attachment
Approx.80×65×22mm
2*AAA alkaline batteries,user manual
Mode of operation Continuous operation
Degree of protection Type B applied part
Protection against
ingress of water IPXO
Software version
Device classification
V01
Internally Powered ME Equipment
WARNING: No modification of this equipment is allowed.
Pressure: 0kpa-40kpa（0mmHg-300mmHg）
pulse value:(40-199)times/minute
Pressure:
15ć-25ćwithin±0.4kpa(3mmHg)
10ć-40ć(out of 15ć-25ć)
vithin±0.8kpa(6mmHg)
pulse value:±5%
Temperature:-20ć to 60ć
Relative humidity:10% to 93%
Temperature:5ć to 40ć5HODWLYHKXPLGLW\
Atmospheric pressure: 86kPa to 106kPa
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 Data communication
has failed
Make sure that phone’s
Bluetooth is on or within
the distance range
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 9 shows Product has not been
activated. Reactivated
E 10 or
E 11 shows
The monitor detected
motion while measuring.
movement can affect the
measurement.Relax for a
moment and then
measure again.
E 20 shows
E 21 shows Relax for a moment and
then measure again.
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.
The measurement
process does not detect
the pulse signal.
Loosen the clothing on
the arm and then
measure again.
Measure incorrectly.
CONTACT INFORMATION
For more information about our products, please visit www.transtek.cn.you
can get customer service, usual problems and customer download, transtek
will serve you anytime.
& R Q WDFW,Q IR UP DWLR Q
Authorized European Representative:
Manufactured by: ZHONGSHAN TRANSTEK ELECTRONICES CO.,LTD
Conpany: ZHONGSHAN TRANSTEK ELECTRONICES CO.,LTD
Address: Jin’an Road, Minzhong, Zhongshan,528441,Guangdong, China
Conpany: MDSS - Medical Device Safety Service GmbH
Address: Schiffgraben 41, 30175 Hannover, Germany
Complied European Standards list
Risk management EN/ISO 14971:2007
Labelling EN 980: 2008
User manual EN 1041: 2008
General requirements
for safety
EN 60601-1:1990+A1+A2+A13
Non-invasive
sphygmomanometers
General requirements
EN 1060-1:2001/A1:2002
EN 1060-3:1997/A1:2005
EN 1060-4: 2004
Electromagnetic
compatibility
EN 60601-1-2:2001+A1˖2006
Table 1 Guidance and manufacture’s declaration – electromagnetic emissions-
for all EQUIPMENT and SYSTEMS
Guidance and manufacture’s declaration – electromagnetic emission
Emission test Electromagnetic environment – guidance
RF emissions
CISPR 11 Group 1
Class B
Not applicable
Not applicable
Compliance
The TMB-1014-BT is intended for use in the electromagnetic environment
specified below. The customer of the user of the TMB-1014-BT should assure
that it is used in such and environment.
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions IEC
61000-3-3
RF emission
CISPR 11
The
TMB-1014-BT
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.
The TMB-1014-BT is suitable for use in all
establishments other than domestic and
those directly connected to the public
low-voltage power supply network that
supplies buildings used for domestic
purposes.
1) Caution: This unit has been thoroughly tested and inspected to assure proper performance and
operation!
2) Caution: this machine should not be used adjacent to or stacked with other equipment and that if
adjacent or stacked use is necessary, this machine should be observed to verify normal operation in the
configuration in which it will be used
3) 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 equipment.
4) The guidelines for avoiding or identifying and resolving adverse electromagnetic effects on other
equipment that may result from operation of the ME EQUIPMENT or ME SYSTEM.
5) Each frequency or frequency band of reception; the preferred frequency or frequency band, if applicable,
and the bandwidth of the receiving section of the ME EQUIPMENT or ME SYSTEM in those bands;
6) Warning: the TMB-1014-BT may be interfered with by other equipment, even if that other equipment
complies with CISPR EMISSION requirements.
7) Each frequency or frequency band of transmission, the type and frequency characteristics of the
modulation and the EFFECTIVE RADIATED POWER.
The TMB-
1014-BT
is intended for use in the electromagnetic environment specified
below. The customer or the user of TMB-
1014-BT
should assure that it is used in
such an environment.
Guidance and manufacture’s declaration – electromagnetic immunity
Immunity test
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
±2 kV for
power supply lines
±2kV for
power supply lines
±1 kV line(s)
to line(s)
±1 kV
differential mode
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT)
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
3A/m
NOTE UTis the a.c. mains voltage prior to application of the test level.
Table 2 Guidance and manufacture’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
floor are covered with
synthetic material, the
relative humidity should be
at least 30%.
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.
Mains power quality should
be that of a typical
commercial or hospital
environment. If the user of
the TMB-
1014-BT
requires
continued operation during
power mains interruptions,
it is recommended that the
TMB-
1014-BT
be powered
from an uninterruptible
power supply or a battery.
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
3A/m
Power frequency
(50Hz) 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
Table 4 Guidance and manufacture’s declaration – electromagnetic immunity –
for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacture’s declaration – electromagnetic immunity
Immunity test
3 Vrms
3 V/m
The TMB-
1014-BT
is intended for use in the electromagnetic environment specified
below. The customer or the user should assure that it is used in such an environment.
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 V
rms
150 kHz to
80 MHz
Electromagnetic environment -
guidance
Portable and mobile RF communications
equipment should be used no closer to
any part of the
YS-6100
, including
cables, than the recommended
separation distance calculated from the
equation applicable to the frequency of
the transmitter.
Portable and mobile RF communications
equipment should be used no closer to
any part of the including cables, than the
recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation distance
d = 1.167
d = 1.167
80 MHz to 800 MHz
d
= 2.333
800 MHz to 2.5 GHz
where Pis the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufac-
turer and d is the recommended
separation distance in metres (m).
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey,ashould be
less than the compliance level in each
frequency range.
Interference may occur in the vicinity of
equipment marked with the following
symbol:
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.
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 ELE007839V1 is used exceeds the applicable RF
compliance level above, the ELE007839V1 should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the ELE007839V1.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
0,01
0,1
761.1 761.1
1
096.3096.301
150 kHz to 80 MHz
d = 1.167
80 MHz to 800 MHz
d = 1.167
800 MHz to 2,5 GHz
d = 2.333
Table 6 Recommended separation distances between portable and mobile
RF communications equipment and the EQUIPMENT or SYSTEM –
for ME EQUIPMENT or ME SYSTEM that are not LIFE-SUPPORTING
Recommended separation distances between portable and mobile RF communica-
tions equipment and the ELE007839V1 Fitness Equipment.
The
TMB-
1014-BT is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the
TMB-
1014-
BT can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the
TMB-
1014-BT 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
100
For transmitters rated at a maximum output power not listed above, the recommended
separation distance din meters (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 80 MHz and 800 MHz, 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.
0.167 0.167 0.233
0.369 0.369 0.738
333.2
883.7
11.67 11.67 23.330
This device complies with Part 15 and Part 18 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.
Caution: The user is cautioned that changes or modifications not expressly approved by the party responsible
for compliance could void the user's authority to operate the equipment.
Note: This equipment has been tested and found to comply with the limits for a Class B digital device,
pursuant to part 15 and Part 18 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 guarantee that interference will not occur in a
particular installation. If this equipment does cause harmful interference to radio or television reception, which
can be determined by turning the equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and 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.
This equipment complies with FCC and IC radiation exposure limits set forth for an uncontrolled environment.
End user must follow the specific operating instructions for satisfying RF exposure compliance. This
transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.