Compex MINI PL-029K5BL User manual

Version 1.0
COMPEX MINI

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TABLE OF CONTENTS
Introduction.........................................................................................................................................................................................................................4
Indications for Use.........................................................................................................................................................................................................4
Safety Warning................................................................................................................................................................................................................4
Contraindications...........................................................................................................................................................................................................5
Warnings..............................................................................................................................................................................................................................5
Precautions.........................................................................................................................................................................................................................6
Adverse Reactions........................................................................................................................................................................................................8
Symbol and Title............................................................................................................................................................................................................8
Environmental Condition for Transport and Storage......................................................................................................................10
How the Device Works............................................................................................................................................................................................14
Setup......................................................................................................................................................................................................................................15
Operating Instruction................................................................................................................................................................................................16
Performance Specifications..............................................................................................................................................................................20
Electrode Maintenance.........................................................................................................................................................................................20
Trouble Shooting..........................................................................................................................................................................................................21
Recommended Use Positions..........................................................................................................................................................................22
Contact Information..................................................................................................................................................................................................25

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INTRODUCTION
Compex® Mini delivers electric pulses generated to the user’s skin through the electrodes. The
portable and compact device has 6 modes of different pulse frequencies, covering Electrical Muscle
Stimulation (EMS) and Transcutaneous Electrical Nerve Stimulation (TENS). It includes operating
elements of ON/ OFF button, intensity increase, intensity decrease, mode selection button, and can
be attached and detached to the electrode through the connector and lead wire. One end of the lead
wire is connected to the device and the other end of the lead wire is connected to the electrode pad.
INDICATIONS FOR USE
Transcutaneous Electrical Nerve Stimulation (TENS) for relief of pain associated with muscle strain,
chronic pain and arthritis pain.
Electrical Muscle Stimulation (EMS) to improve and facilitate muscle performance.
CONSULT ACCOMPANYING DOCUMENTS

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SAFETYWARNING
CONTRAINDICATIONS
»Do not use this device on persons who have a cardiac pacemaker, implanted defibrillator, or other
implanted metallic or electronic devices because this may cause electric shock, burns, electrical
interference, or death.
»Do not use this device on people whose pain syndromes are undiagnosed.
»Not to be used by children or incapacitated persons.
WARNINGS
»Use carefully. May cause serious burns. Do not use over sensitive skin areas or areas with poor
circulation. To reduce the risk of burns, electric shock, and fire, this device must be used in accor-
dance with the instructions.
»Do not crush the device and its electrodes and avoid sharp folds.
»Carefully examine the device and its electrodes, and do not use if they show any sign of
deterioration.
»Do not tamper with this device and its electrodes in any way. There are no user serviceable parts. If
for any reason they do not function satisfactorily, return to the authorized service center at address
given.
»The long-term effects of chronic electrical stimulation are unknown.
»Stimulation should not be applied over the carotid sinus nerves, particularly in persons with a
known sensitivity to the carotid sinus reflex. Carotid sinus is located on both sides of the neck.
»Stimulation should not be applied over the front neck or mouth. Severe spasm of the laryngeal
and pharyngeal muscles may occur and the contractions may be strong enough to close the airway
or cause difficulty in breathing. Stimulation over the neck can also cause adverse effects on heart
rhythm or blood pressure.
»Do not apply stimulation across the user’s chest contralaterally, because the introduction of
electrical current into the chest may cause rhythm disturbances to the user’s heart, which could be
lethal.

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SAFETYWARNING
»Since the effects of stimulation of the brain are unknown, stimulation should not be applied across
the head, and electrodes should not be placed on opposite sides of head.
»Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, e.g.,
phlebitis, thrombophlebitis, varicose veins, etc.
»Stimulation should not be applied over, or in proximity to cancerous lesions.
PRECAUTIONS
»Caution should be used for persons with suspected or diagnosed heart problems.
»Caution should be used for persons with suspected or diagnosed epilepsy.
»Caution should be used if you have any of the following:
• if you have a tendency to bleed internally following an injury;
• if you recently had surgery, or have ever had surgery on your back;
• if areas of skin lack normal sensations, such as skin that is numb.
»Consult with your physician before use over the menstrual uterus.
»You may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical
conductive medium. The irritation can usually be reduced by using an alternate electrode placement.
»Do not use this device while driving, operating machinery, or during any activity in which involuntary
muscle contractions may put the user at undue risk of injury.
»Keep this device out of reach of children.
»Do not use this device in high humidity areas such as a bathroom.
»Stop using this device at once if you feel discomfort, dizziness ornausea, and consult your physician.
»Do not attempt to move the electrodes while the device is operating.

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SAFETYWARNING
»Do not apply stimulation of this device in the following conditions:
• Contralaterally across the chest because the introduction of electrical current into the chest may
cause rhythm disturbances to the heart, which could be lethal;
• over open wounds or rashes, or over swollen, red, infected, or inflamed areas or skin eruptions
(e.g., phlebitis, thrombophlebitis, varicose veins);
• in the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms);
• on children or incapacitated persons.
»Be aware of the following:
• consult with your physician before using this device;
• this device is not effective for pain associated with Central Pain Syndromes, such as headaches;
• this device is not a substitute for pain medications and other pain management therapies;
• this device is a symptomatic treatment and, as such, suppresses the sensation of pain that
would otherwise serve as a protective mechanism;
• stop using the device if the device does not provide pain relief;
• use this device only with the electrodes, and accessories recommended for use by the
manufacturer.
»Store the device away from high-temperature and direct-sunlight. Storage outside of stated
storage temperature may result in measurement error or device malfunction.
»Do not share the use of the electrodes with others; electrodes are intended for single person use.
»Do not use the device while it’s charging.
»This device contains a lithium battery. If overheating of the device occurred during the charging,
stop the charging or operation immediately and contact customer support.
»Dispose of this battery-containing device according to the local, state, or federal laws.
»Skin burns may occur, and check the skin under the electrode periodically.

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SAFETYWARNING
ADVERSE REACTIONS
»You may experience skin irritation and burns beneath the stimulation electrodes applied to the
skin; check skin under electrodes frequently.
»You should stop using the device and should consult with your physicians if you experience
adverse reactions from the device.
SYMBOLAND TITLE
Information essential for proper use shall be indicated by using the corresponding symbols. The
following symbols may be seen on the device and labeling.
CE mark with notify body number
Symbol for “authorized representative in
the european community”
Consult instructions for use
Caution, consult accompanying
documents
Use by date
Date of manufacture
Batch code

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SAFETYWARNING
Catalogue number
Manufacturer
Temperature limitation
Humidity limitation
Non-sterile
MR Unsafe - keep away from magnetic
resonance imaging (MRI) equipment
Fragile, handle with care
Keep away from rain
Product packaging is able to be recycled

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SAFETYWARNING
ENVIRONMENTAL CONDITION FORTRANSPORTAND STORAGE
Normal working ambient temperature: 5~40°C
Normal working ambient humidity: 15~90%
Store and transport ambient temperature: -25 ~70°C
Store and transport ambient humidity: 0~90%
Atmospheric pressure: 70~106kPa
Fragile; handle with care
Keep away from rain
Product packaging is able to be recycled
Non-sterile
ENVIRONMENTAL CONDITION FOR TRANSPORT AND STORAGE
1) This product needs special precautions regarding electromagnetic compatibility (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 radio frequency (RF) communications equipment.
15%
90%
90%
0%
70°C
-25°C
5°C
40°C

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SAFETYWARNING
2) Do not use other devices that emit electromagnetic fields, near the unit. This may result in
incorrect operation of the unit.
3) Caution: This device should not be used adjacent to or stacked with other equipment and that if
adjacent or stacked use is necessary, this device should be observed to verify normal operation in
the configuration in which it will be used.
This unit has been thoroughly tested and inspected to assure proper performance and
operation.
GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC EMISSION
The device is intended for use in the electromagnetic environment specied below. The customer of the user or the device
should assure that it is used in such an environment.
EMISSION TEST COMPLIANCE ELECTROMAGNETIC ENVIRONMENT – GUIDANCE
RF emissions
CISPR 11 Group 1 The device uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emission
CISPR 11 Class B The device is suitable for use in all establishments, including
domestic establishments and those directly connected to
the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2 Class A
Voltage uctuations/ icker
emissions IEC 61000-3-3 Complies

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GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY
The stimulator is intended for use in the electromagnetic environment specied below. The customer or the user of the stimulator
should assure that it is used in such an environment.
IMMUNITY TEST IEC 60601 TEST LEVEL COMPLIANCE LEVEL ELECTROMAGNETIC
ENVIRONMENT - GUIDANCE
Electrostatic
discharge (ESD) IEC
61000-4-2
±8kV contact
±15kV air
±8kV contact
±15kV air
Floors should be wood, concrete or
ceramic tile. If oors are covered
with synthetic material, the relative
humidity should be at least 30%.
Electrical fast
transient/burst IEC
61000-4-4
±2kV for power supply lines
±1kV for input/output lines
±2kV for power supply lines Mains power quality should be that
of a typical commercial or hospital
environment
Surge
IEC 61000-4-5
±1kV Line to Line
±2kV line(s) to earth
±1kV dierential mode Mains power quality should be that
of a typical commercial or hospital
environment.
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
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
Mains power quality should be
that of a typical commercial or
hospital environment. If the user of the
stimulator requires continued operation
during power mains interruptions, it is
recommended that the stimulator be
powered from an uninterrupted power
supply or a battery.
Power frequency
(50/60Hz) magnetic
eld IEC 61000-4-8
30 A/m 30 A/m Power frequency magnetic elds
should be at levels characteristic of a
typical location in a typical
commercial or hospital environment.
SAFETYWARNING
UT is the a.c mains voltage prior to application of the test level.

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SAFETYWARNING
GUIDANCE AND MANUFACTURE’S DECLARATION – ELECTROMAGNETIC IMMUNITY
The device is intended for use in the electromagnetic environment specied below. The user should assure that it is used
in such an environment.
IMMUNITY TEST IEC 60601 TEST LEVEL COMPLIANCE LEVEL ELECTROMAGNETIC
ENVIRONMENT – GUIDANCE
Conducted RF
IEC 61000-4-6
Radiated RF IEC
61000-4-3
3 Vrms
150 kHz to 80 MHz
10 V/m
80 MHz to 2.5 GHz
3 Vrms
10 V/m
Portable and mobile RF communications
equipment should be used no closer to any
part of the device, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency
of the transmitter. Recommended separation
distance
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 xed RF
transmitters, as determined by an
electromagnetic site survey,a should be less
than the compliance level in each frequency
range.b
Interference may occur in the vicinity of
equipment marked with the
following symbol:

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SAFETYWARNING
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 aected by absorption and
reection from structures, objects and people.
a) Field strengths from xed 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 xed RF transmitters, an electromagnetic site survey
should be considered. If the measured eld 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.
b) Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.
Recommended separation distances between portable and mobile RF communications equipment and the device.
The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The
customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the device as recommended below,
according to the maximum output power of the communications equipment.
Rated maximum output
power of transmitter (W) Separation distance according to frequency of transmitter (m)
150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
11.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23

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SAFETYWARNING
* Note: These programs have 5 min of 3 Hz at the end, and that is why the total time is 5 min more than the
work time.
HOWTHE DEVICE WORKS
The device has 6 programs, the details of which are listed in the table below.
Program Contraction
Frequency (Hz) Contraction Time (sec) Rest Frequency (Hz) Rest Time (sec) Work Time (min) Total Time (min)
Program 1:
Pre-Warm Up 8 Hz 25 min 3 sec
Program 2:
Endurance* 10 8 3 2 45 50
Program 3:
Resistance* 50 7 5 7 18 23
Program 4:
Active Recovery 9 Hz for 2 min, 8 Hz for 2 min, 7 Hz for 2 min, 6 Hz for 3 min, 5 Hz for 3 min, 4 Hz for 3 min, 3 Hz for 24 min
Program 5: Muscle
Relaxation 1 Hz 20 min 3 sec
Program 6: Relief 160 10 0 2 30 30 min
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in metres (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.

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SETUP
Remove the 2 devices and accessories from the box. The accessories include electrodes, lead wires
and a USB cable. The USB cable should be used to charge both units.
1. There are two devices included. The device marked “1” on its side is the master device, and the
device marked “2” is the affiliation device. The master device and the affiliation device are paired as
received. Therefore, after turning on the devices, you can use them directly out of the box.
Note: If the devices unpair, you can pair the mother device with the affiliation device manually. Use
a pin to press the PAIR (RESET) hole on the back of the devices. Press and release the reset hole of
the affiliation device first (beeping twice (0.5s per beeping) and the LED lights keep flashing), mean-
ing the affiliation device is ready for pairing; then press and release the reset hole of the mother de-
vice (beeping and flashing once, 0.5s per beeping/flashing) to send the pairing signal to the affiliation
device. When the pairing is successful, the affiliation device will beep once (0.5s per beeping) and its
LED lights becomes steadily on. Pressing the reset hole for more than 2 seconds could unpair the
affiliation device, indicated by the flashing/beeping twice (0.2s per beeping/flashing).
2. Intensity levels +/- can only be increased or decreased via puck 1 (master device).
3. Alternatively, the phone application can automatically pair with the master device and operate it
via Bluetooth. Simultaneously, the master device controls the affiliation device via the radio
frequency. If using one device make sure it is the master device which is marked “1” on its side.
Note: Cannot independently use puck #2
PIN HOLE

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OPERATING INSTRUCTION
The following Operating Instructions are used to guide the operation. The step-by-step details are
listed below:
STEP 1 – Check the battery power of the device
The device comes with rechargeable batteries and can be used as received.
If the battery icon is ashing when turned on, it means the battery is running
out of power. Turn o and charge the device with the enclosed USB cable.
The LED light ashes during charging and becomes solid when the device is
charged fully.
Note: When the battery is full, the 3 yellow LED lights are on; when the battery
is running low, only one yellow LED light is on.
STEP 2 - Install the electrode pad onto the device
Snap the enclosed rectangular electrode pad onto the device through the
snap-on connector and use the lead wire to connect the device to the two
square electrode pads. This should be done prior to applying the device onto
the skin of the treatment area.
STEP 3 - Put the electrode pad-installed device on the
stimulation-needed body area
Place the pad-installed device onto the treatment area (such as the bicep).
Press down rmly and ensure a full and rm contact with skin.
Note: The skin should be clean and dry before placing the electrode
pad-installed device.
Battery charging
Electrode pad installation
Place the device on the
body area

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OPERATING INSTRUCTION
STEP 4 - Press the “ON/OFF” to turn on the power
Press and release the ON/OFF button to turn on the device, indicated by the
yellow LED indicators on and beeping once (0.5 second).
STEP 5 - Select one of the stimulation modes
After the device is on, press and release the ON/OFF button to change the
6 programs: The ashing/beeping times of LED indicator represent the cor-
responding programs (0.2s per beeping). For example, 3 timers of ashing/
beeping mean Program 3; 6 timers of ashing/ beeping mean Program 6.
STEP 6 - Adjust the stimulation intensity
Press and release the + or – button to increase or decrease the intensity by
one level (up to 299 levels), indicated by the LED ashing once and beeping
once (0.2s per beeping); holding the + or – button for 1 second could increase
or decrease the intensity by 10 levels, indicated by the LED ashing twice and
beeping twice (0.2s per beeping). After the above mode, time, and intensity
are set up, the stimulation provided by the device will last until the device
until the program is completed.
STEP 7 - Press the “ON/OFF” to turn o the power after done
Hold the ON/OFF button for 1 second to turn o the device, indicated by the
three LED indicators o and beeping twice (0.5s per beeping).
Note: When not in use, store the device and accessory in a cool place, out of
direct sunlight.
Program change
Intensity change
ON / OFF
ON / OFF

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OPERATING INSTRUCTION
Recommended Practice:
• Start from the lowest intensity and gradually adjust the intensity to a comfortable level. Duration
for each skin area is based on the preset timer for each program.
• Good skin care is important for a comfortable use of device. Be sure the treatment area is clean of
dirt and body lotion.
• Keeping the electrode on its backing in the storage bag after use will extend its lifespan. The
electrode pad is disposable and should be replaced when it loses the adhesiveness.To purchase
additional electrodes, please contact the seller.
Electrodes have a shelf life of 2 years, are intended for single person use, and should be replaced
as necessary. If the electrode no longer contacts well with your skin, it is time to replace it. If needed,
you can use a damp and clean cloth to wipe electrodes between uses.
Electrode In Use Direction
1. Clean skin thoroughly prior to each application of electrodes, which will not contact well if any
lotion, make-up, or dirt is left on the skin.
2. Ensure the device is off before applying the electrode to it.
3. Apply the electrode-installed device firmly to the skin.
Electrode Removal and Storage
1. Turn the device off before removing the electrode from the skin.
2. Grab the edge of the electrode and remove from the skin, replace to its backing.
3. When not in use and/or between each use, store the electrode in the re-sealable bag, out of direct
sunlight.
As shown above, the device can be operated independently by pressing its three buttons (ON/OFF
button, intensity increase button, and intensity decrease button).

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OPERATING INSTRUCTION
Alternatively, the phone application interface provides a secondary operation method to wirelessly
realize the functions mentioned above.
At any time you can switch to manually operate the device itself by pressing its three buttons
to deal with any safety issues that may arise.