iReliev ET-9090 Parts list manual

Instruction & Operating Manual
Read Before Using
MODEL # ET-9090

IMPORTANT INFORMATION
The iReliev®Back Pain Relief System is particularly safe and user-
friendly. When the Wrap is fastened and the electrode pads are in
contact with the skin, the intensity of the iReliev®TENS device may
be adjusted.
iReliev®Back Pain Relief System
Model # ET-9090
Table of Contents
2
Introduction ................................................................................................................................................................... 3
Safety Information .............................................................................................................................................. 4
Battery Safety Information ................................................................................................................. 5
Cautions & Contraindications ....................................................................................................... 5
Package Contents ............................................................................................................................................... 6
Parts Diagram/Features ............................................................................................................................. 7
Inserting/Changing the Batteries ................................................................................................ 8
Putting on the Wrap ........................................................................................................................................ 9
Turning on the Device .................................................................................................................................. 10
Turning off the Device ................................................................................................................................. 10
Selecting Treatment Time .................................................................................................................. 11
Selecting the Program ............................................................................................................................... 11
Selecting the Therapy Intensity Level .............................................................................. 11
Special Features .................................................................................................................................................... 11
Care & Maintenance ........................................................................................................................................ 12
Disposal ................................................................................................................................................................................ 12
Troubleshooting ..................................................................................................................................................... 13
Technical Specifications .................................................................................................................. 14 -18
Warranty ............................................................................................................................................................................. 19
Contact ................................................................................................................................................................................. 19

3
The iReliev®BACK PAIN RELIEF SYSTEM has been designed for people who
suffer from muscular tension and pain in their back. It provides a natural, drug-
free alternative that treats back pain the natural way with no side effects.
Your iReliev®BACK PAIN RELIEF SYSTEM is a Transcutaneous Electrical Nerve
Stimulation (TENS) device. It delivers electrotherapy treatment in the low fre-
quency range. When using this method, electrical impulses are dispersed onto
the skin using two or four electrodes.
This stimulates muscles, nerve fibers and acupuncture meridians in order to
activate your body’s own pain relief mechanisms.
Chronic pain can be treated with different methods such as medication, in-
jections, surgical procedures or with alternative treatment methods such as
acupuncture or TENS.
Electrotherapy treatment can block pain signals by interrupting the transmis-
sion of impulses through the skin by means of electrical impulses. As a result,
the signal interpreted as “pain” is not transmitted to the brain and thus not felt
or greatly reduced.
Furthermore, it will work with the body’s own pain inhibitors as gentle electric
currents from the device stimulates the release of endorphins that function as
a pain reducer. The pain is therefore reduced or eased.
Electrical stimulation cannot remove the causes of pain or cure a disease, but
it could help ease or block pain.
In order to achieve all the benefits from the iReliev®BACK PAIN RELIEF SYSTEM,
carefully read the following safety information and warnings before use.

Use this device only according to its intended purpose as specified in this
instruction and operating manual. The warranty will be invalidated if the
device is used for other than its intended purpose.
Do not use the device if it is not operating correctly, or if it has fallen into
water or has been damaged.
Do not attempt to repair the device yourself in the event of a malfunc-
tion; this will invalidate the warranty.
Do not operate this device near high-frequency transmitters, such as mi-
crowaves, short wave transmitters or radio transmitters. This may impair
the device’s ability to function.
Do not turn on the device until wrap has been snugly secured on the
body.
Do not use the device while taking a bath or a shower.
Do not use this device while sleeping.
Do not use this device while driving a car or another kind of vehicle or
while operating machinery or heavy equipment.
Protect the device from moisture. If liquid should get into the device, re-
move the battery immediately and discontinue use. Should this happen,
contact iReliev®at 855-723-2582.
Never use the device in rooms where aerosols (sprays) are used or med-
ical grade oxygen is being administered.
Do not use with any creams, lotions or gels.
Do not use with heating pad or any other electrical device.
4
Safety Information

5
Battery Safety Information
Keep away from children
Do not recharge
Do not short-circuit
Do not throw in a fire
Please recycle. Do not dispose of old batteries with your household waste.
Dispose of batteries safely at an acceptable recycling center
Caution, the device should not be used by patients with:
Pacemakers, defibrillators or extreme cardiac irregularities
Metal implants or electronic auxiliary devices
Diabetes or abnormally high blood pressure
A tendency toward internal bleeding
Pregnant women
Therapy with the iReliev®BACK PAIN RELIEF SYSTEM is a proven and natural way of fighting
pain; however, it does not replace medical diagnosis or treatment. If you are not sure, con-
sult your doctor before using this device.
Consult your doctor always before use, if you suffer from epilepsy or certain disabilities.
People whose sensitivity is disturbed or impaired should only apply this device under
supervision of your physician.
Do not use this device if suffering from menstrual pains.
Do not use this device if your skin burns or is numb.
Operation of this device should only be carried out under the careful supervision and
instruction of a doctor or physical therapist.
Do not treat parts of the body that are swollen, burned, inflamed, peeling skin, wounds
or other sensitive points.
In case of doubt, consult a doctor or medical professional for instructions and guidance
or contact iReliev for additional operating instruction.
Keep out of reach of children.
Treatment should be monitored if used on or near children or persons who are handi-
capped.
If you feel pain or have an unpleasant feeling, stop treatment and consult your doctor.

Package Contents
Before using this accessory, make sure that you have all components.
The iReliev®Conductive Back Wrap Includes:
1. 1 iReliev®Conductive Back Wrap
2. 1 iReliev®TENS Control Unit
3. 1 Clip Holster
4. 2 Lead Wires
5. 3 AAA Batteries
6. 1 Conductive Gel Tube
7. 1 Portable Storage Bag
8. 1 Conductive Back Wrap Extension
9. 1 Operating & Instruction Manual
10. 1 Quick Start Guide
The packaging can be reused or recycled. Please dispose of properly if no longer required.
If you notice any damage from shipping, please contact the store in which you pur-
chased the BACK PAIN RELIEF SYSTEM or ExcelHealth Inc. at 855-723-2582.
6
1
2356
7
8910
WARNING
:
:Do not use this system if you have cardiac pacemaker,
implant defibrillator or any other
implanted metallic/electronic device.
:If pregnant, consult a physician prior to use.
:Do not use the iReliev™
system if you have undiag-nosed chronic pain.system if you have undiag-nosed chronic pain.
DO NOT TOUCH ELECTRODE (S) AFTER
TURNING ON
When you are familiar with the operation of
your iReliev™ device, use the following steps
as a quick reference guide to operate.
For more information, refer to the
Operating & Instruction Manual
Step 1. Insert 3 AAA batteries, taking
care to match up the symbols.
Step 3. Correctly position the
Conductive Back Wrap around the area
to be treated. Adjust the Wrap so it fits
comfortably.
Step 4. The belt may be tightened or
loosened as shown by adjusting the
hook and loop closure.
Step 5. Attach the connector plugs on
the Conductive Back Wrap into the
sockets at the top of the unit.
Step 6. Turn on the unit. Select your
treatment program, timer and intensity
level.
Step 2. Before use, dampen the
integrated silicon electrodes with water.
IMPORTANT
: Steps 1-4 should be performed with the device turned OFF.
Once the iReliev™ unit has been turned ON, do not remove electrodes without first turning
OFF the unit.
4

7
Parts Diagram/Features
1.) Lead Wire Cables (Coiled Type)
2.) Conductive Silicone Pads
3.) iReliev®Conductive Back Wrap
4.) Hook and Loop Closure
5.) Power On/Adjust, Increase Key
6.) Power Off/Adjust, Decrease Key
7.) Program Mode/Therapy Time Selection
8.) CH 1 (Channel 1) Key
9.) CH 2 (Channel 2) Key
10.) Program Number
11.) Therapy Time Remaining
12.) CH 1 Intensity Level
13.) CH 2 Intensity Level
14.) Therapy Duration Status
15.) Lock Status Indicator
16.) Battery Status Indicator
17.) Battery Compartment
18.) Battery Cover

1. Open the battery compartment [17] at the back of the device by pushing the battery cover
[18] labeled “Open” downward (this area features raised marks for easy identification).
2. Insert 3 AAA (1.5 V) batteries in the battery compartment; make sure to match up the sym-
bols (+/–).
3. Close the battery cover by carefully placing the stud into the slot in the rear area and sliding
it upward, applying slight pressure.
4. Follow the same procedure when replacing the battery at a later date.
▲NOTE: Always use only 3 x 1.5V (AAA) batteries. Please refer to “Battery Safety Information,”
for important precautions regarding the batteries.
Inserting/Changing the Batteries
8

Putting on the iReliev®Conductive Back Wrap
1. Before putting on the Conductive Back Wrap, remove any residue on skin, cream or oint-
ment. Make sure that your skin is clean. Do not place the wrap on injured or inflamed areas of
the skin, such as wounds, sores, rashes or reddening.
2. Before use, apply iReliev®Conductive Gel. Or you may dampen the integrated silicone elec-
trodes with water but use extreme caution to not oversaturate.
3. Position the Conductive Back Wrap so that the electrode pads are on the area of the body
to be treated. If your lower back aches at waist level, position the wrap so that the middle of
the wrap sits approximately 1 to 2 inches below the waist. The Wrap should fit very snugly
around your body as follows:
4. When the wrap has been placed in the correct position, bring the two ends of the neo-
prene straps together and fasten with the built-in hook and loop closure so that it is snug.
5. The wrap may be tightened or loosened as shown by adjusting the hook and loop closure.
(See diagram below)
▲NOTE/CAUTION: Subjective perception of the electric current may alter with changing fre-
quencies or pulse widths. Lower the intensity as soon as the application becomes unpleas-
ant or the pleasant prickling sensation is not felt for a long period of time.
Please ensure that iReliev®Conductive Gel has been applied over the silicone pads to allow
for optimal conductive impulse dispersion. If this step is not completed, impulse sensation
may feel like a prickling sensation and may be uncomfortable.
9

10
Turning On the Device
1. Press and hold the ON+ button [5]* for two (2) seconds
to turn on the device.
2. The most recently selected treatment time and pro-
gram will flash when the unit is turned on.
▲NOTE: Do not turn the device on until Back Wrap is
properly attached.
Turning Off the Device
1. The device turns off automatically after the therapy
session time has elapsed.
2. To turn the unit off manually, press the OFF- button
[6]* for three (3) seconds. The display will be blank and
the device will turn off.
In an emergency, you may also pull the connector(s)
from the device and then remove the belt.
▲NOTE: To prevent unpleasant electric shocks, never
remove the device while it is still turned on.
Selecting the Treatment Program Mode
The iReliev stimulator device (Model # ET-9090/ET-1313/ET-7070) offers eight preset
treatment program modes. The programs differ with respect to varying pulse
widths and frequencies. The user may choose suitable stimulation mode depend-
ing on their personal condition as indicated in the following steps:
1. Start from P1: only change each mode after a couple of seconds after sensing
the stimulation of that mode.
2. Choose the suitable mode in which you feel most comfortable. Set the device
on that mode.
3. In the case you don’t feel certain about the appropriate mode, repeat steps 1 & 2.
Selecting the Therapy Intensity Level
1. Intensity is adjustable according to the channel selected. Select the channel you
wish to adjust by pressing CH1 or CH2. “CH1” or “CH2” will flash on the display.
2. To increase or decrease intensity, press ON + (to increase) or OFF – (to decrease)
repeatedly until the desired intensity level flashes on the display.
▲NOTE: You will feel the intensity increase or decrease as you select the intensity
level.

11
Selecting the Treatment Time
Press MODE [7]*. The preset (default) treatment time will flash on the display.
To increase or decrease the treatment time, press the button ON + (to increase) or the button OFF –
(to decrease) repeatedly until the desired duration appears on the display.
Press MODE [7]* again to save your selection. The treatment time you selected will appear on the
display the next time you turn the device on.
▲NOTE: If you change programs during the course of a therapy session, the treatment time will not
reset unless you manually reset it by performing the steps described above.
Selecting the Therapy Intensity Level
Intensity is adjustable according to the channel selected. Select the channel you wish to adjust by
pressing CH1 or CH2. “CH1” or “CH2” will flash on the display.
To increase or decrease the intensity, press ON + (to increase) or OFF – (to decrease) repeatedly until
the desired intensity level flashes on the display.
Note: You will feel the intensity increase or decrease as you select the intensity level. You can use
this as a guide to select a level that is comfortable for you.
Press MODE to save your selection.
Special Features
Therapy Time
The device offers 12 preset therapy times: 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 minutes.
The therapy time will countdown on the display in 1-minute increments for the duration of your
session.
• The device turns off automatically when the therapy time has elapsed.
• The most recently set therapy time is stored.
• If you alter the program mode during your therapy, the therapy time won’t restart unless you
reset the therapy time.
• The last treatment program used will appear on the display when the device is turned on.
• To change the program, press ON + or OFF – repeatedly until the desired program appears on the
display.
• Press MODE to save selection. The program selected will appear on the display the next time you
turn on the program.
Lock Function
If you have turned on the device but have not pressed any button for 20 seconds, the device will
automatically lock.
Press and hold the ON + and OFF – keys simultaneously for 1 second to unlock the device.
Automatic Shut-Off
The device automatically turns off when no button is pressed for 60 seconds. The device automati-
cally turns off when the time for your therapy session has elapsed.
Intensity Level Reset
For your safety and comfort, the intensity level will reset to 0 each time the device turns off, includ-
ing after therapy sessions.
Low Battery Status Indicator
The battery status indicator will light whenever the battery is low. This means the batteries will soon
need to be changed.

12
Care and Maintenance
iReliev®TENS Device:
The iReliev®stimulator device may be wiped clean with a small amount of soapy
water on a clean cloth. Do not submerge the device in liquids or expose to large
amounts of water.
Never use aggressive cleaning products or stiff brushes to clean the device.
Remove the batteries before cleaning the device.
Do not use the device again until completely dry.
Do not expose the device to direct sunlight and protect it from dirt and moisture.
iReliev®Conductive Back Wrap:
If the wrap has become damp during use, let it dry naturally before using again.
Do not wash the wrap in water. Do not wash the wrap in the washing machine.
Lay the wrap out flat or hang it up to dry naturally. Do not tumble dry. The wrap may
be cleaned using a lightly dampened sponge.
Do not use bleach when washing the wrap.
Do not dry clean your wrap. Do not dry it over anything hot (e.g. a radiator) as it con-
tains plastic parts. Ensure the wrap is completely dry before using it again. The wrap
should never be ironed.
Always detach the lead wires from snap and the unit from the lead wires. Do not pull
on the lead wire cables but on the connectors attached to the ends of the cables.
Do not expose the device to direct sunlight and protect it from dirt and moisture.
How to Store Your iReliev®System:
1. Store your iReliev®system at room temperature in a dry place, out of the reach of chil-
dren.
2. If the iReliev®stimulator will not be used for more than a week, remove the batteries
from the stimulator.
Disposal
Follow all laws and regulations regarding the proper disposal of batteries and electronic
devices that are relevant in your area. Consult your municipal authorities or your iReliev®
dealer for information about proper disposal.

DEFECT
The device does
not turn on.
The device turns on
and then off again.
The device turns
on, but does not
generate electric
pulses.
The unit does not
turn on even though
new batteries have
been inserted.
REMEDY
Replace batteries.
Insert battery again.
Replace battery.
Contact ExcelHealth at
855-723-2582.
Reconnect lead wires to
device & wrap.
Connect cable properly
and power on.
Securely fasten wrap
on body.
Contact ExcelHealth at
855-723-2582.
CAUSE
No battery or bad battery.
Battery not inserted
properly.
Battery life expired.
Lead wires not connected.
Cable not connected
properly or treatment time
has expired.
Wrap not securely fastened.
Troubleshooting
Always check the unit and accessories before use to prevent damage and defects; these
are some of the simple checks:
1.) Make sure the battery has sufficient charge and is not corroded.
2.) Make sure the cables fit tightly into the connection sockets of the device. The table below
shows some common defects. If you cannot remedy the defects as described, contact
ExcelHealth or an authorized iReliev®Dealer.
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Use only iReliev®parts. The following iReliev®replacement parts are available:
ET-1616 Conductive Back Wrap
ET-4949 Clip Holster
AC-0005 Carrying Case
CM-5050-BK Electrode Pads, 2’’ x 2’’
CM-4848 Lead Wires
The sensation is
uncomfortable and feels
like a “prickling” sensation.
Electrode pads are not
moistened.
Apply iReliev®Conductive
Gel for optimal dispersion
of electrical current.

iReliev®(Model # ET-9090, ET-1313, and ET-7070) Stimulator Technical Specifications
Channel: Dual, isolated between channels.
Pulse Amplitude: Adjustable 0 – 80mA peak into 500Ωload each channel.
Pulse Rate: As pre-programming operation mode.
Pulse Width: As pre-programming operation mode.
Software Ramp Up Feature: Pulse width ramp up when changing mode.
Timer: 5~60 min. selectable.
LCD: Show modes, pulse rate, pulse width, timer, CH1/CH2, intensity level.
Program Modes:
Wave Form: Symmetrical Bi-Phasic square pulse.
Max Charge per Pulse: 20.8 micro-coulombs maximum.
Power Source : 3 x AAA / 4.5 Volt batteries
All electrical specifications are ±20% at 500Ωload.
Description of Symbols:
(i) There are a number of technical symbols on your iReliev®unit explained as follows:
Program Max. Phase duration Rate Function mode Wave form Type
P1 80mA 260uS 15Hz Constant A
P5 80mA 260~150uS 60Hz Modulated A
P2 80mA 260uS 60Hz Modulated A
P6 80mA 260uS 7 <->60Hz Modulated C
P3 80mA 260uS 60Hz Constant A
P7 80mA 260~156uS 60Hz Modulated A
P4 80mA 260~150uS 2 ~ 60Hz Modulated B
P8 80mA P1 ~P7 Cycle A/B/C
This symbols means “Serial number.“
This symbols means “Attention” consult the
accompanying documents.
This symbols means “Manufacturer.“
This symbol means “used before”, represented as “YYYY-MM” (for year and
month).
This symbol means type BF equipment; this device offers protection
against electrical shock by standard compliance to leakage currents of
electrode pad.
(ii) Package of electrode pads are labeled as
follows:
14

Electromagnetic Compatibility
• The device complies with current specifications with regards to electromagnetic
compatibility and is suitable for use in all premises, including those designated for
private residential purposes. The radio frequency emissions of the device are ex-
tremely low and in all probability do not cause any interference with other devices in
the proximity.
• It is recommended that you do not place the device on top of or close to other elec-
tronic devices. Should you notice any interference with other electrical devices, move
the device or connect it to a different socket.
• Radio equipment may affect the operation of this device.
Electromagnetic Compatibility Information
Guidance and manufacturer’s declaration – electromagnetic emissions
The ET-9090/ET-1313/ET-7070 is intended for use in the electromagnetic environment
specified below. The customer or the user of the ET-9090/ET-1313/ET-7070 should
assure that it is used in such an environment.
Emissions
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage fluctu-
ations/ flicker
emissions IEC
61000-3-3
Compliance
Group 1
Class B
Class C
Complies
Electromagnetic environment - guidance
The ET-9090/ET-1313/ET-7070 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 ET-9090/ET-1313/ET-7070 is suitable for use
in all establishments, including domestic estab-
lishments and those directly connected to the
public low-voltage power supply network that
supplies buildings used for domestic purposes.
15

Guidance and manufacturer’s declaration – electromagnetic immunity
NOTE: UT is the a.c. mains voltage prior to application of the test level
The ET-9090/ET-1313/ET-7070 is intended for use in the electromagnetic environ-
ment specified below. The customer or the user of the ET-9090/ET-1313/ET-7070
should assure that it is used in such an environment.
Immunity test
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
Power frequency
(50/60 Hz) mag-
netic field IEC
61000-4-8
Compliance level
± 6 kV contact
± 8 kV air
± 2 kV for power
supply lines
± 1 kV line(s)
and neutral
<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 5s
Not applicable.
IEC 60601
test level
± 6 kV contact
± 8 kV air
± 2 kV for power
supply lines
± 1 kV line(s)
and neutral
<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 5s
3 A/m
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%.
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
ET-9090/ET-1313/ET-7070 requires
continued operation
during power mains interruptions, it
is recommended that the
ET-9090/ET-1313/ET-7070 be pow-
ered from an uninterruptible power
supply or a battery.
Not applicable.
16

Guidance and manufacturer’s declaration – electromagnetic immunity
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) tele-
phones 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 ET-9090/ET-1313/ET-7070 is used exceeds the applicable RFcompliance
level above, the ET-9090/ET-1313/ET-7070 should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating
the ET-9090/ET-1313/ET-7070.
b.) Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
The ET-9090/ET-1313/ET-7070 is intended for use in the electromagnetic environ-
ment specified below. The customer or the user of the ET-9090/ET-1313/ET-7070
should assure that it is used in such an environment.
Immunity test
Conducted RF IEC
61000-4-6
Conducted RF IEC
61000-4-6
Compliance level
3 Vrms
3 Vrms
IEC 60601
test level
3 Vrms
150 kHz
to 80 MHz
3 Vrms
150 kHz
to 80 MHz
Electromagnetic environment
— guidance
Portable and mobile RF communi-
cations equipment should be used
no closer to any part of the
ET-9090/ET-1313/ET-7070, including
cables, than the recommended sep-
aration distance calculated from the
equation applicable to the frequency
of the transmitter. Recommended
separation distance
Where P is the maximum output
power rating of the transmitter in
watts (W) according to the trans-
mitter 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:
17

Recommended separation distances between portable and mobile RF communica-
tions equipment and the ET-9090/ET-1313/ET-7070
The ET-9090/ET-1313/ET-7070 is intended for use in an electromagnetic environ-
ment in which radiated RF disturbances are controlled. The customer or the user
of the ET-9090/ET-1313/ET-7070 helps prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communica-
tions equipment (transmitters) and the ET-9090/ET-1313/ET-7070 as recommended
below, according to the maximum output power of the communications
equipment.
For transmitters rated at a maximum output power not listed above, the recom-
mended 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 manu-
facturer.
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 propaga-
tion is affected by absorption and reflection from structures, objects and
people.
Rated maximum
output power of
transmitter
w
150 kHz to 80 MHz
0.12
0.38
1.2
3.8
12
0.01
0.1
1
10
100
Separation distance according to frequency of transmitter
m
80 MHz to 800 MHz
0.12
0.38
1.2
3.8
12
800 MHz to 2.5 GHz
0.23
0.73
2.3
7.3
23
18

Limited One (1) Year Warranty
This item is warranted to be free of defects in materials or workmanship for (1) year
from the date of purchase, provided the product has been used under normal condi-
tions of intended use. If this product is defective, warrantor will replace the product or
refund the purchase price of the product at the place of purchase upon presentation
of sales receipt and original UPC code from packaging. This warranty extends only to
the original purchaser, and excludes any damage to the product resulting from ac-
cident, misuse, abuse, damage caused by operation in ways not recommended or
authorized by these operating and safety instructions. This warranty is voided if the
product is ever used in a commercial or business environment.
There are no warranties beyond this limited warranty. This limited warranty is your
complete and exclusive legal means. Warrantor makes no other warranties, express
or implied, including but not limited to any implied warranty of merchantability or of
fitness for a particular purpose. Warrantor undertakes no responsibility for the quality
of the product except as otherwise provided herein. Warrantor assumes no respon-
sibility that the product will be fit for any particular purpose for which you may be
buying this product. Warrantor expressly disclaims liability for any special, incidental,
indirect, or consequential damages arising out of the purchase or use of this product.
The amount of Warrantor’s liability under this warranty is limited to the amount of
the original purchase price paid for the product by the original retail purchaser. If War-
rantor cannot lawfully disclaim statutory or implied warranties, then all such warran-
ties shall be limited in duration to the duration of this warranty and shall be limited
to the amount of the original purchase price paid for the product by the original retail
purchaser.
This warranty gives you specific legal rights; you may also have other rights that vary
by jurisdiction. This warranty is valid only within the United States of America (USA)
and Canada.
Model # ET-9090
Return to:
ExcelHealth Inc.
1603 Hart St.
Southlake, TX 76092
www.iReliev.com
855-723-2582
©2017 iReliev®, All Rights Reserved
19

ExcelHealth Inc.
www.iReliev.com
1603 Hart St.
Southlake, TX 76092
1-855-723-2582