Transtek Medical Electronics TMB1014BT BLOOD PRESSURE MONITOR User Manual

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User Manual
Blood Pressure Monitor
TMB-1014-BT
Wrist Type
Zhongshan Transtek Electronics Co., Ltd
Jin’an Road, Minzhong, Zhongshan 528441, Guangdong, China
Thank you very much for selecting TRANSTEK Blood Pressure Monitor
TMB-1014-BT.
To use the monitor correctly and safely, please read the manual
thoroughly.
Please well keep this manual in order to reference in future.
CATALOGUE
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
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.
INTRODUCTION
Features:
Systolic blood pressure
Diastolic blood pressure
Pulse rate
Historic record of up to 60 measurements
Safety information
The below signs might be in the user manual, labeling or other component.
They are the requirement of standard and using.
Caution:Consult accompanying
documents
Type B applied part
CE Mark: conforms to
essential requirements of the
Medical Device Directive
93/42/EEC.
DISPOSAL: Do not dispose this
product as unsorted municipal waste.
Collection of such waste separately
for special treatment is necessary.
Manufacturer
Specifies serial number
Direct current
EC
REP
Authorized Representative in
the European Community
CAUTION
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.
INTRODUCTION
INTRODUCTION
LCD display signal
Monitor components
SYSTOLIC
MEM/UP
BUTTON
DIASTOLIC
GRADE
PULSE RATE
LCD DISPLAY
6 < 0 % 2 / ' ( 6 & 5 ,3 7 ,2 1
START/OFF BUTTON
TIME
SET/DOWN
BUTTON
( ; 3 /$ 1 $ 7 ,2 1
Systolic
blood pressure
High pressure result
Diastolic
blood pressure
Low pressure result
Pulse
Pulse/minute
Low battery
Batteries are low and need to be replaced
mmHg
Measurement unit the blood pressure
Grade
The grade of the blood pressure
For instructions,refer to Page 13
Arrhythmia
Arrhythmia is detected
Bluetooth
Bluetooth is in an open position
Error
Blood pressure monitor has detected
error
User
The current selected user
Recalling
The erecords will be showed
Time
Currently time
CUFF
(Type B applied part)
BATTERY
COMPARTMENT
BEFORE YOU START
BEFORE YOU START
The installment and replacement of battery
Setting Date, time and measurement unit
 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.
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))
1.Pressing “SET” for
3 seconds to enter
the mode for [Hour]
setting.
MEM
SET
2.Press the “MEM” to
change the [Hour].
MEM
Replace the batteries whenever the below happen
The
shows
SET
The display dims
The display does not light up
CAUTION
3.When you get the right [Hour],
press “SET” to set down and
turn to next step automatically.
MEM
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.
SET
BEFORE YOU START
BEFORE YOU START
Bluetooth phones’ test software
4.Repeat the 2 and 3 to
set the [Minute].
1.Open the Bluetooth 4.0 special test
MEM
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”...
SET
5.Repeat the 2 and 3 to
set the [YEAR],
[MONTH] and [DAY].
MEM
MEM
3 .Long press the "START" button after
power off the blood pressure monitor,
it’ll show moving "o”.
SET
SET
4.At this moment, the “discovered device”
column of mobile will display devices
list.
7.After the unit is set,
the right picture will
show, then it turn off
automatically.
5.Choose detected device from the list.
7KHUHLV³¼´RQWKHULJKW
BEFORE YOU START
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.
MEASUREMENT
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.
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.
9.Click “back” to return main interface of
testing software and go on testing next
blood pressure monitor.
MEASUREMENT
MEASUREMENT
Start the Measurement
Please press the SET to choose the user 1 or user 2 when the blood pressure monitor
turn off
1.Press the START/STOP, it will
finish the whole measurement
automatically.
Adjust the zero automatically.
Inflating and measuring
automatically.
Display and save the
results automatically.

START
STOP
2.A f te r me as u rin g，
i t’ ll d is pl ay t he
mo v in g “o” a nd
s en d dat a at th e
s ame t ime.
3.If d ata i s s en t s u cc es s fu ll y,
go b ac k to d is p la y th e
i nte rfa c e o f me as uri ng
re su lt s.
If the data failed to send，go back
to display the interface of measuring
results after display “E9”.
4.P re s s the S TA RT/ S TOP to
power off, otherwise it will turn
off automatically within 1 minute.
START
STOP

THE OPERATION OF
RECALLING RECORDS
THE OPERATION OF
RECALLING RECORDS
Recalling the records
1.Press the “MEM” to show
the last 3 average of the
record.
Deleting a measurement record from memory
MEM
If you did not get the correct measurement, you can delete all
results by following below steps.
1.Hold pressing “MEM” for 3
MEM
seconds, when the memory is
SET
shown.
SET
2. Press the “MEM”
or “SET” to get the
record you want.
MEM
UP
2.When flash “Delete all”, press the
“SET” to delete the memory.
MEM
SET
DOWN
SET
CAUTION
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.
3.If you don’t want to delete the
records, press
“S TA R T/ S TOP” to escape.
4.If there is no record. the
right display will show.


INFORMATION
INFORMATION FOR USER
Tips for measurement
Maintenance
It can cause incorrectness if the measurement are taken in the
following circumstances.
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
In order to get the best performance, please follow the below
instructions.
Put in a dry place and avoid the sunshine
Avoid touching water,
clean it with a dry cloth in case.
Avoid the intense shaking
and collision
Avoid the dusty and unstabletemperature environment
Using the wet clothing to remove the dirt
Avoid washing the cuff
When talking or moving your fingers
When you want to discharge urine
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
ABOUT BLOOD PRESSURE
What are systolic pressure and diastolic
pressure?
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.
Systolic
Diastolic
blood discharging
artery
blood entering
vein
press
relax
What is the standard blood pressure
classification?
Why the blood pressure
I get from the hospital is
different from home?
yellow
light
green light
red light
SYS
120
120~129
130~139
140~159
160~179
!180
DIA
80
80~84
85~89
90~99
100~109
!110
CAUTION
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.

1. Individual blood pressure varies
every in one day, it also affected by the
way you tie your cuff and the your
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.
Below illustrates the blood pressure
classification mode by World Health
Organization (WHO) and International
Society of Hypertension(ISH) in 1999.
%ORRG /HYHO
3UHVVXUH
PP+J
Why my blood pressure
is varies even in one
day?
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.
If the result is the same
if measuring on the
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.

SPECIFICATIONS
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
No power
Low
batteries
Error
massage
Display is dim or
will not light up.
REMEDY
Batteries are exhausted. Replace with new batteries
Batteries are inserted
incorrectly.
Show on
Batteries are low.
the display
Display moder
Digital LCD V.A.36x41mm
Measurement mode
Measurement range
correctly
Replace with new batteries
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
movement can affect the
The monitor detected
measurement.Relax for a
motion while measuring. moment and then
measure again.
E 20 shows
The measurement
Loosen the clothing on
process does not detect the arm and then
the pulse signal.
measure again.
E 21 shows
Measure incorrectly.
A calibration error
occurred.
2*AAA alkaline batteries
Insert the batteries
E 1 shows
EExx,shows on
the display.

CHECK THIS
Power supply
Relax for a moment and
then measure again.
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.
Accuracy
Oscillographic testing mode
Pressure: 0kpa-40kpa（0mmHg-300mmHg）
pulse value:(40-199)times/minute
Pressure:
15ć-25ćwithin±0.4kpa(3mmHg)
10ć-40ć(out of 15ć-25ć)
vithinÂą0.8kpa(6mmHg)
pulse value:Âą5%
Normal working condition
Temperature:5ć to 40ć5HODWLYHKXPLGLW\”
Atmospheric pressure: 86kPa to 106kPa
Storage & transportation
condition
Temperature:-20ć to 60ć
Relative humidity:10% to 93%
Measurement perimeter
of the wrist
About 13.5cm-19.5cm
Weight
External dimensions
Attachment
Mode of operation
Degree of protection
Approx.120g(Excluding the dry cells)
Approx.80×65×22mm
2*AAA alkaline batteries,user manual
Continuous operation
Type B applied part
Protection against
ingress of water
IPXO
Software version
V01
Device classification
Internally Powered ME Equipment
WARNING: No modification of this equipment is allowed.

CONTACT INFORMATION
& R Q WDFW,Q IR UP DWLR Q
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.
Manufactured by: ZHONGSHAN TRANSTEK ELECTRONICES CO.,LTD
Conpany: ZHONGSHAN TRANSTEK ELECTRONICES CO.,LTD
Address: Jin’an Road, Minzhong, Zhongshan,528441,Guangdong, China
Authorized European Representative:
Conpany: MDSS - Medical Device Safety Service GmbH
Address: Schiffgraben 41, 30175 Hannover, Germany
Complied European Standards list
Risk management
EN 980: 2008
User manual
EN 1041: 2008
General requirements EN 60601-1:1990+A1+A2+A13
for safety
EN 1060-1:2001/A1:2002
sphygmomanometers EN 1060-3:1997/A1:2005
General requirements
for all EQUIPMENT and SYSTEMS
Guidance and manufacture’s declaration – electromagnetic emission
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.
Emission test
Compliance
Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1
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.
RF emission
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions IEC
61000-3-3
Not applicable
EN/ISO 14971:2007
Labelling
Non-invasive
Table 1 Guidance and manufacture’s declaration – electromagnetic emissions-
EN 1060-4: 2004
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.
Electromagnetic
EN 60601-1-2:2001+A1˖2006
compatibility
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.


Table 2 Guidance and manufacture’s declaration – electromagnetic immunity –
for all ME EQUIPMENT and ME SYSTEMS
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
Guidance and manufacture’s declaration – electromagnetic immunity
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.
Immunity test
IEC 60601 test level Compliance level
Electrostatic
discharge (ESD)
IEC 61000-4-2
Âą6 kV contact
Âą8 kV air
Electrical fast
transient/burst
IEC 61000-4-4
Âą2 kV for
power supply lines
Surge IEC
61000-4-5
Âą1 kV line(s)
to line(s)
Voltage dips,
short
interruptions and
voltage variations
on power supply
input lines IEC
61000-4-11
<5% UT
(>95% dip in UT)
for 0.5 cycle
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
40% UT)
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
Power frequency 3A/m
(50Hz) magnetic
field IEC
61000-4-8
NOTE

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
Âą2kV for
power supply lines be that of a typical
commercial or hospital
environment.
Mains power quality should
Âą1 kV
be that of a typical
differential mode
commercial or hospital
environment.
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.
Immunity test
IEC 60601
test level
Compliance
level
Âą6 kV contact
Âą8 kV air
<5% UT
(>95% dip in UT)
for 5 sec
3A/m
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.
UT is the a.c. mains voltage prior to application of the test level.
Conducted RF 3 Vrms
IEC 61000-4-6 150 kHz to
80 MHz
3 Vrms
Radiated RF
3 V/m 80 MHz
IEC 61000-4-3 to 2.5 GHz
3 V/m
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 P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacturer and d is the recommended
separation distance in metres (m).
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey,a should be
less than the compliance level in each
frequency range.
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.
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 communications 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-1014BT 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 Separation distance according to frequency of transmitter
power of transmitter
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
d = 2.333
d = 1.167
d = 1.167
0,01
0.167
0.167
0.233
0,1
0.369
0.369
0.738
10
1.167
1.167
2.333
3.690
3.690
7.388
100
11.67
11.67
23.330
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 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.


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.


---

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