DENAS PCM 6 User manual

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TABLE OF CONTENT
PART 1 –Technical Passport
1. SAFETY REGULATIONS
Part 1. Technical Passport
1. Safety rules.................................................................
2. Purpose.......................................................................
3. Technical parameters .................................................
4. Package contents .......................................................
5. Elements of the device ...............................................
6. Sequences using the device.......................................
7. Using themenu...........................................................
8. Maintenance ...............................................................
9. Battery replacement procedure..................................
10. Troubleshooting ..........................................................
11. Manufacturer’s warranty.............................................
Part 2. Application instructions
1. Conducting treatment procedures ................................
Annex A. Accessories
Annex B.
Zone Atlas for using programs menu................................
Alphabetical index of programs.........................................
Alphabetical listof diseases..............................................
Annex C.
Zone Atlas for using frequency menu................................
Thank you for buying DENAS-PCM device!
For efficient and safe use of the device, it is necessary to read all the chapters of this Operating Manual.
The Information contained in this Operating Manual is important for your safety and correct
use and maintenance of the device.
The device is safe in service as it uses low voltage current source isolated from the applied part (B type
item with F type applied part).
It is not allowed to use the device for treatment of patients with implanted electronic devices (such as a
heart pacemaker) or patients with idiosyncrasy of electric current.
It is prohibited to apply the device in direct projection of the heart in the front.
It is not advisable to connect the patient to any other high frequency electrical devices during the
stimulation. Simultaneous application of the device with another electrical equipment may lead to burns
or possible damage of the device.
If the device is used near short wave or microwave equipment, it may result in instability of the device
output parameters.
It is prohibited to connect the device to any other devices except for external electrodes produced by the
manufacturer.
It is prohibited to use external mains supply. Any partial or full dismantling of the device, as well as any
modifications in the device are prohibited.
The device contains fragile elements. Keeprotect it from shocks.
Keep the device away from continuous direct sunlight at high ambient temperature (above 25 °C). Keep
the device away from heating appliances.

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2. PURPOSE
The device is not waterproof. Keep it away from humidity
Specialists qualified by the manufacturer only should perform any repair works of the devices. Any
partial or full dismantling of the device, as well as any modification in the device are prohibited
Transport Conditions: temperature of 50°С below zero to 50°С above zero, and atmospheric pressure of 70 to
106 kPa (525-to795 mm Hg).
Storage Conditions: temperature of 50°С below zero to 40°С above zero, and atmospheric pressure of 70 to 106
kPa (525-to795 mm Hg).
Operating Conditions: temperature of 10°С above zero to 35°С above zero, and atmospheric pressure of 70 to
106 kPa (525-to795 mm Hg).
Attention! If the device has been stored at temperature 10°С below the ambient air temperature, leave it at a
temperature of application environment for a minimum of two hours before using.
Relative air humidity of 30 to 93 %.
Waste Disposal: packaging materials do not have adverse impact on the environment; they could be
recycled.
The device and batteries should be disposed of according to the established disposal rules for electronic
devices.
The device contains valuable materials, which could be used after recycling subject to environment
protection requirements. They should be taken to specialized waste collection and disposal centers
(consult the relevant agencies at your region).
It is technically feasible to dispose of the device. The device does not pose any hazard to life or health
of people or to environment after the expiry of its service (product) life and it does not require any
special measures to prepare or send its components for disposing.
DENAS-PCM Multipurpose Transcutaneous Electrical Stimulator is designed to exert general regulating impact on
physiological systems of human body and to treat functional disorders of a wide range of illnesses. Application of electric
current impulses on biologically active points and zones of human body perform dynamic electrical nerve stimulation. The
device also allows to select an individual treatment program or to choose among the existing programs. The device has
in-built electrode and a connector for external therapeutic electrodes*.
DENAS-PCM device can be used at healthcare centers and at home according to doctor’s instructions.
*The device should only be connected to external electrodes produced by the manufacturer (see Annex A).

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3. SPECIFICATIONS
3.1 Electric impulse of the device have following output parameters :
3.1.1 Without load = 20 KOhm
Capacity (in standard units)
Minimum*
Maximum**
1
99
Amplitude of phase 1, B
≤ 40
≤ 40
Duration of phase 1, ms
6,0 ± 1,5
400 ± 100
Amplitude of phase 2, B
9,0 ± 2,5
450 ± 113
*The above stated parameters apply to treatment mode impulses and do not apply to test impulses. Parameters should be measured when Therapy
without Contact Control Function is enabled.
**Parameters should be measured when Children’s Doctor Function is disabled.
3.1.2 Relation of the impulse shape to load resistance with medium and maximal capacitylevel.
3.1.3 Dependence of impulse form from load resistance at average and maximum powerlevels.
10 units
99 units
2 kOhm
20 kOhm
Z1
R1 82±5% kOhm
R2 2±5% kOhm
C1 3300±20% pF

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Z2
R1 56±5% kOhm
R2 470±5% kOhm
C1 6200±20% pF
3.2 The device allows setting the following impulse frequencies, Hz :
3.2.1 Range 1 : 1.0 to 9.9 with pitch of 0.1±0.05.
3.2.2 Range 2 :
— 10±1, including MED (preventive treatment) and Screening modes and Programs Menu;
—20±2; 15
—60±2;
—77±3;
— 77±3 and 10±2 modulated with frequency of 2±0.1 (frequency «7710»);
— 77±3 with amplitude modulation (frequency «77_»);
—77±3 (2,0±1,0 s) _ 20±2 (3,0±1,5 s) (frequency «7720»);
—125±4;
—140±5;
—200±5.
3.3 Special stimulation programs.
Program name
Application zone / frequency / duration
Age
ALLERGY
Zone 1 : «7710» (5 min) + 3,8 Hz (5 min)
Zone 2 : 77 Hz (5 min) + 1,7 Hz (5 min) + 3,8 Hz (5 min)
over 7 years
PAIN
Zone 1 : Impulses with quasirandom repetition frequency charge with in the
range of 75 to 135 Hz (15 min)
over 1 year
INTENSE PAIN
Zone 1 : Impuls packets with repetition frequency of 77 Hz and variable
duration and carrier frequency: from 2.5 msec and 27 _Hz at minimum
power level up to 1.0 msec and 2.8 kHz at maximum power level (15 min)
over 7 years
BLOATING
Zone 1 : «7710» (5 min) + 125 Hz (5 min)
any age
DYSTONIA
Zone 1 : «7710» (10 min) + 10 Hz (5 min) + 2,5 Hz (5 min)
over 4 years
GYNECOLOGICAL
PAIN
Zone 1 : «7710» (5 min) + 3,8 Hz (5 min) + 4,0 Hz (5 min)
over 13 years
GYNECOLOGY
Zone 1 : 2,5 Hz (5 min) + 4,0 Hz (5 min) + 9,4 Hz (5 min)
Zone 2 : «7710» (15 min)
Zone 3 : 10 Hz (5 min) + 20 Hz (5 min)
over 13 years
HYPERTENSION
Zone 1 : «7710» (5 min)
Zone 2 : «7710» (5 min)
over 7 years
HYPOTONIA
Zone 1 : «77AM» (15 min)
over 7 years
HEAD
Zone 1 : 60 Hz (5 min)
Zone 2 : 60 Hz (5 min)
Zone 3 : 60 Hz (5 min)
over 7 years
THROAT
Zone 1 : 60 Hz (10 min)
Zone 2 : 77 Hz (10 min)
over 4 years
DIARRHEA
Zone 1 : 125 Hz (10 min)
Zone 2 : 20 Hz (5 min)
any age
ABDOMINAL PAIN
Zone 1 : «7710» (5 min) + 3,8 Hz (5 min) + 5,9 Hz (5 min)
over 4 years
CONSTIPATION
Zone 1 : 125 Hz (10 min)
Zone 2 : 20 Hz (5 min)
any age
COUGH
Zone 1 : «7710» (5 min)
Zone 2 : 60 Hz (10 min)
over 1 year

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MUSCLES
Zone 1 : Impuls packets with duration of 380±38 msec, repetition frequency
of 1 Hz, and carrier frequency of 125 Hz. The duration of the first phase of
the impulse is variable (15 min)
over 1 year
MUSCLES
Zone 1 : 10 Hz (10 min)
Zone 2 : «7720» (10 min)
any age
POTENCY
Zone 1 : 2,6 Hz (5 min) + 4,0 Hz (5 min) + 9,4 Hz (5 min)
Zone 2 : «7710» (15 min)
Zone 3 : 10 Hz (5 min) + 20 Hz (5 min)
over 13 years
KIDNEYS
Zone 1 : 77 Hz (10 min) + 20 Hz (10 min)
Zone 2 : 2,8 Hz (5 min) + 8,1 Hz (5 min) + «7710» (5 min)
over 7 years
BACK
Zone 1 : 140 Hz (5 min) + 77 Hz (5 min) + 20 Hz (5 min)
over 4 years
JOINTS
Zone 1 : 140 Hz (5 min) + 77 Hz (5 min) + 20 Hz (5 min) + 1,6 Hz (5 min)
Zone 2 : «7710» (10 min)
over 7 years
NAUSEA
Zone 1 : «7710» (10 min)
over 4 years
TRAUMA
Zone 1 : 200 Hz (5 min) + 140 Hz (5 min) + 77 Hz (5 min)
over 1 year
ASPHYXIA
Zone 1 : «7710» (10 min)
Zone 2 : 1,0 Hz (3 min) + 8,0 Hz (3 min) + 3,6 Hz (3 min)
any age
3.4 Maximum consumption current (with supply voltage of 3 V) is not more than 300 mA.
3.5 Power supply source: batteries of LR6/ type, 2 pieces with voltage of 1.5 V. It is allowed to use the relevant storage
batteries with voltage of 1.2 V*.
3.6 The device weighs not more than 0.35 kg.
3.7 The overall dimensions of the device are not more than 165x65x65 mm.
3.8 The device automatically switches off not later than 5 minutes after one of its keys (except for key) has lastbeen
pressed, after the electrodes have been released from skin, or after the stimulation period has finished.
*Operation procedure (recharger types, recharge methods) is described in the storage battery instruction manual. Duration of the device service when
used with storage batteries depends on characteristics of the batteries.
3.9 Electromagnetic Radiation
Test
Conformity to IEC 60601-1-2
Conditions of Use
Radiofrequency
radiation
CISPR 11
Class B
DENAS-PCM Electrical Stimulator can be used in all types of
institutions and at home as well
Group 1
DENAS-PCM emits very little radio-frequency radiation that
cannot lead to failure of electronic equipment located nearby
3.10 Resistance to radio-frequency radiation
Test
IEC 60601-1-2 test conditions
Acceptable level
IEC 61000-4-6
3 Vrms oТ 150 kHz Дo 80 MHz
3 Vrms
IEC 61000-4-3
3 V/m oТ 80 MHz Дo 2,5 GHz
3 V/m
3.11 Resistance to electromagnetic fields.
Magnetic fields
Test level
Conformity level
Conditions of Use
Electrostatic discharge
(ESD) IEC
61000-4-2
±6 kV contact;
±8 kV air
±4 kV contact;
±8 kV air
The floor should be made of wood, concrete or
ceramic tiles. If the floor is covered with synthetic
material, the relative air humidity should be not less
than 40%.
Magnetic fields IEC
61000-4-8
3 A/m
3 A/m
Magnetic field parameters should be within the
normal values for commercial buildings and
healthcare facilities.

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4. COMPLETE SET
5. ELEMENTS OF THE DEVICE
3.12 Recommendations for determining the necessary distance between DENAS-PCM Electrical Stimulator and radio
equipment.
Label maximum output
capacity of the
transmitter P (W)
Radiation frequency and formula to determine the distance d (m)
150 kHz –80 MHz
d = 1,2√P
150 kHz –800 MHz
d = 1,2√P
800 MHz –2,5 GHz
d = 2,3√P
0,01
0,12
0,12
0,23
0,1
0,38
0,38
0,73
1
1,2
1,2
2,3
10
3,8
3,8
7,3
100
12
12
23
3.13 Conditions of Use.
3.13.1 Connection of external electrodes not-authorized by the manufacturer (including other cable length, cable type,
electrode construction) may lead to increase of electromagnetic radiation level and/or to reduction of resistance of the
device to external effects.
3.13.2 DENAS-PCM device uses electromagnetic power for its internal functions only; therefore, the deviceemits
minimum radiation and does not affect the electronic equipment located nearby.
3.13.3 Recommendations for User
Electrostatic discharge (ESD). User should not wear clothes made of synthetic materials during the treatment session.
Radio-frequency radiation. Personnel (User) should take the following safety measures: minimum distance from the
device to mobile communicating devices (mobile phones, wireless phones) should 3 meters if the output capacity of these
devices is more than 2 W.
ITEM
QUANTITY
DENAS-PCM Electro Stimulator
1
Operations manual (EN)
1
Consumer packaging
1
Battery of LR6/AA type
2
Promo CD*
1
*Supplied under a separate request
Figure 1 —DENAS-PCM device (top view)

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Attention! External therapeutic electrodes can only be used for Frequency and Programs modes
Figure 2 —DENAS-PCM device (bottom view)
The device can be connected to external therapeutic electrodes of manufacturer’s model 27 range (see Annex ).
In order to improve the contact you can moisture skin with water or with Malavtilin cream or with Baby-DENS cream for
children before applying the electrodes.
5.1 Indicator view in different modes.
5.1.1 Symbols and main menu items.
5.1.2 Timer Setting

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5.1.3 Clock and Alarm Clock Settings
5.1.4 Stimulation Mode
5.1.5 Intensity level settings
5.1.6 MED and Screening Modes

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6. SEQUENCES USING THE DEVICE
6.1 Switching on.
Press button . After playing the sound signal and startup screen the device shows:
- Main Menu if Last Settings Recording Function is disabled;
- the last mode that was active when the device has been switched off if Last Settings Recording Function is enabled.
6.2 Selecting mode or function.
Use the navigation keys to select the necessary program, mode or function and press to openit.
6.3 Return to menu
In order to return to previous menu use key . In order to open Main Menu use key .
6.4 Switching off.
Press key holding it down for 3 seconds. «Good Health» message will appear on the display and the device will switch
off after the sound signal.
7. USING THE MENU
7.1 Menu Structure
7.2 Selecting Menu item
Programs Menu
1
Use navigation and keys to select Programs in the Menu and confirm your choice
by pressing .

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1.1
Choose the necessary program by using and keys in the opened section.
1.1.1
The device will show the chosen mode. On the display will appear recommended zone for
application.
1.1.2
The device will show the chosen mode, for safety reasons electric stimulation will be at
the minimum intensity level. Set the necessary intensity with and keys. Detailed
description of the device operation in Programs mode is given in the Operating Manual,
Part II, Application Instructions.
Frequency Menu
2
Select Frequency in Main Menu by using and navigation keys and confirm your
choice by pressing .
2.1
Choose the necessary frequency by using and keys in the opened section. Make
your choice and press .
2.1.1
If you choose infralow frequencies (1.0 –9.9 Hz) the device will show the settings menu
of infralow frequencies. Set the necessary frequency with navigation keys (set theintegral
value first, then the decimal value) and press in order to confirm the selected
frequency (see item 1.1.1).
2.1.2
The device will show the chosen mode. Set the necessary intensity with and keys.
Detailed description of the device operation in Programs mode is given in the Operating
Manual, Part II. Application Instructions.

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Minimum effective dose (MED)
3
Select MED mode in Main Menu by using navigation keys and confirm your choice
by pressing .
3.1
The device will show MED mode. Set the necessary intensity with and keys.
Detailed description of the device operation in MED mode is given in the Operating
Manual, Part II. Application Instructions.
Screening Diagnostic Mode
4
Select Screening mode in the Main Menu by using and navigation keys andconfirm
your choice by pressing .
4.1
The device will show Screening mode, electric stimulation will be at fixed intensity level. It
is not possible to change the intensity in Screening mode.
4.2
If you make measuring for the second time, the previous value will appear in the lower
right corner.
Detailed description of the device operation in Screening mode is given in the Operating
Manual, Part II. Application Instructions.
Children’s Doctor Function
5
Select Children’s Doctor section in Main Menu byusing and navigation keys and
confirm your choice by pressing .

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5.1
The device has a function of limiting the intensity for sessions with the children. Set the
child’s age by using and keys and confirm your choice by pressing . If you press
or key instead of key or if you power off the device, Children’s Doctor settings
will return to earlier saved settings. If Children’s Doctor function is enabled, symbol will
appear in the status bar.
Sound Menu
6
Select Settings section in Main Menu or Stimulation Window by using and
navigation keys and confirm your choice by pressing . The number of items in
SETTINGS menu depends on the current status of the device.
6.1
Select Sound in Settings Menu by using and keys and confirm your choice by pressing
6.1.1
The device will show Sound Settings Menu: general device sound, skin contactsound,
key pressing sound. Select one of the changeable parameters by using and keys and
confirm your choice by pressing .
6.1.1.1
The device has three volume levels for adjusting the general device sound : mute,
minimal and maximal levels indicated as 0, 1 and 2 correspondently.
Select one of the volume levels by using and keys and confirm your choice by
pressing . If you press or keyinstead of key or if you power off thedevice,
Sound settings will return to earlier saved settings.
Attention! The volume of sound signals depends on the set volume level. If Mute level is
set there will be no sound signals.
6.1.2.1
The contact of electrodes with the skin can be confirmed with a sound signal under the
relevant settings. Enable or disable this function by using and keys and confirm
your choice by pressing . If you press or key instead of key or if you power off
the device, Sound settings will return to earlier saved settings.
6.1.3.1
Navigation around the Menu can be accompanied with sounds. Enable or disable this
function by using and keys and confirm your choice by pressing . If you press
or key instead of key or if you power off the device, Sound settings will return to
earlier saved settings.
6.1.3.2
Indication of volume level
Mute, level 0;
Volume on, level 1 or 2.

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Brightness Menu (Display Brightness adjustment)
6
Select Settings section in Main Menu by using and navigation keys and confirm
your choice by pressing .
6.2
Select Brightness in Settings Menu by using and keys and confirm your choice by
pressing .
6.2.1
The device has brightness adjustment option within the range of 5 to 100 with a pitch of 5.
Select the comfortable brightness level using and keys. And confirm your choice by
pressing . If you press or key instead of key or if you power off the device,
Brightness settings will return to earlier saved settings.
Attention! If you use increased backlit brightness it may lead to increase of current
consumption and earlier change of batteries. If you use the minimal backlit brightness, it
will allow prolonging the service of the installed batteries.
Economy Menu (Economical use of batteries)
6
Select Settings section in Main Menu by using and navigation keys and confirm
your choice by pressing .
6.3
Select Economy in Settings Menu by using and keys and confirm your choice by
pressing .
6.3.1
The device will show Economy mode, which allows selecting Economical Use of Batteries
function: activating lower energy consumption mode by reducing backlit duration
(notwithstanding the set brightness level). Enable or disable this function by using and
keys and confirm your choice by pressing . If you press or key instead of
key or if you power off the device, Economy Mode settings will return to earliersaved
settings.

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Last Settings Recording Menu (Recording of last settings)
6
Select Settings section in Main Menu by using and keys and confirm your choice by
pressing .
6.4
Select Recording in Settings Menu by using and keys and confirm your choice by
pressing .
6.4.1
The device will show Last Settings Back-up Menu. In this section, you can change status
of the Last Settings Recording Function. If this function is enabled the device will switch
on in the same treatment mode that was active when the device has last been switched
off. If this function is disabled, the device will go into Main Menu after switching on.
Enable or disable this function by using and keys and confirm your choice by
pressing . If you press or keyinstead of key or if you power off the device,
Last Settings Recording settings will return to earlier saved settings.
Clock Menu (time adjustment)
6
Select Settings section in Main Menu by using and keys and confirm your choice by
pressing .
6.5
Select Clock in Settings Menu by using and keys and confirm your choice by
pressing .
6.5.1
When setting the time you can set the current time, in order to do that set the cursor on
the changed area by using and keys, change the values in correspondence with
their true values by using and keys and confirm your choice by pressing . If you
press or key instead of key or if you power off the device, the current time values
will not change.

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Alarm Clock Menu (Alarm Clock Settings)
6
Select Settings section in Main Menu by using and keys and confirm your choice by
pressing .
6.6
Select Alarm Clock in Settings Menu by using and keys and confirm your choice by
pressing .
6.6.1
The device will show Alarm Clock Menu where you can set the periodicity of alarm clock
signal and alarm clock time. Select one of the changeable items in the Menu by using
and keys and confirm your choice by pressing .
6.6.1.1
In order to set the periodicity of the alarm clock, use keys and to select one of
operation modes : disabled, one time or every day. Press to save the selected mode. If
you press or key instead of key or if you power off the device the current alarm
clock settings will not change.
If alarm clock is enabled, symbol will appear in the status bar. In order to turn offthe
alarm clock when it goes off press button one time.
6.6.2.1
In order to set the signal time of the alarm clock, use keys and to set the cursor on
the changeable area, and change the values according to the desired values by using
and keys and confirm your choice by pressing . Switch off the device. If you press
or key instead of key or if you power off the device the current alarm clock
settings will not change.
Language Menu
6
Select Settings section in Main Menu by using and keys and confirm your choice by
pressing .
6.7
Select Language in Settings Menu by using and keys and confirm your choice by
pressing .

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6.7.1
The user interface of the device is available in five languages: Russian, English, German,
Italian, and French. Use and keys to select the necessary language in Language
Menu and confirm your choice by pressing key. If you press key or instead of
key or you turn off the power, the language setting will return to the previously savedone.
Colour Menu
6
Select Settings section in Main Menu by using and keys and confirm your choice by
pressing .
6.8
Select Colour in Settings Menu by using and keys and confirm your choice by
pressing .
6.8.1
The user interface of the device is available in four colour themes: Turquoise, Winter,
Bronze, and Night. Use and keys to select the necessary colour theme inColour
Menu and confirm your choice by pressing key. If you press key or instead of
key or you turn off the power, the colour setting will return to the previously savedone.
Contact Menu (Therapy without Contact Control Function is available for Programs and Frequency
modes only except for Muscles Program)
7
Contact Menu allows operating Therapy without Contact Control Function, which makes it
possible to generate electrical impulses notwithstanding the quality of contact or whether
the electrodes contact the skin. When Therapy without Contact Control Function is
enabled, the device does not produce any signal if electrodes stop contacting the skin.
Therapy without Contact Control Function can be enabled by using navigation keys in
Stimulation Window (Programs, Frequency). Select Contact Menu in Stimulation Window
(Programs, Frequency) by using and keys and confirm your choice by pressing
key.
7.1
The device will show Contact Menu . Enable or disable this function by using and
keys and confirm your choice by pressing key. If you press key instead of key in
order to close Therapy without Contact Control Function its settings will notchange.
Contact status indication :
indication is on without interruption –electrodes contact the skin, Therapywithout
Contact Control Function is disabled;
electrodes do not contact the skin; it is recommended to slightly moisture the skin for
better contact or to enable Therapy without Contact Control Function;
indication flashes on and off –Therapy without Contact Control Function is enabled.

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8. TECHNICAL MAINTENANCE
Attention! If the batteries are removed from the device for more than 5 minutes, User’s individual settings
and any set reminders will clear off and information about current time will be lost as well.
9. BATTERY REPLACEMENT PROCEDURE
Timer Menu
8
Timer Function is necessary when it is not possible to control the time of stimulation (in
case of electrical stimulation of hard-to-reach zones) or when the time of stimulation is
strictly specified. When this function is enabled the stimulation time will be counted in the
form of a countdown timer. When this function is disabled the maximum session time is
30 minutes. Timer function settings are available in Frequency Menu. The time in
Programs, MED, and Screening Menus is fixed.
Use and navigation keys to select Timer item and confirm your choice by pressing
key.
8.1
The device will show Timer Menu. Use and keys to set the desired timer value from
1 to 30 minutes (with pith of 1 minute) and confirm your choice by pressing . If you
press key instead of key in order to close the timer its settings will not change. If
timer is set on 0 minutes this function will be disabled and there will be direct timing of
sessions in stimulation modes.
If Timer function is ON it will appear symbol in status bar.
8.1 Daily maintenance include the following operations :
- visual inspection of the device;
- disinfection of electrodes.
Use standard disinfection means (such as 3% penozone) and soft napless diapers for cleansing of electrodes.
8.2 Operability of the device is checked according to recommendations stipulated in Section 6.
8.3 If you are supposedly not going to use the device for a long time, remove the set of batteries from the batterycase
(see Section 9).
8.4 If the battery symbol flashes and the device generates intermittent alarm sound it is necessary to replace the setof
batteries of the device (see Section 9).
Replacement of the set* of batteries :
- open battery case (1) and remove the batteries;
- place new batteries** respecting the polarity (2);
- close the battery case (3).
*The set consists of two batteries.
**Place only those batteries, which are designed for this type of the device: LR6/AA type with nominal voltage of 1.5 V or relevant storage batteries with
nominal voltage of 1.2 V.

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10. TROUBLESHOOTING
DEFECT
PROBABLE REASON
REMEDY
1) The device does not
switch ON after pressing the
key .
Batteries are missing
Place a new set of batteries (see Section 9,
Battery Replacement Procedure)
Voltage of the set of batteries is
less than 2,1 V
Replace the set of batteries (see Section 9,
Battery Replacement Procedure)
2) After switching ON, the
device produces sound
signals and automatically
switches OFF.
Voltage of the set of batteries is
less than 2,1 V
Replace the set of batteries (see Section 9,
Battery Replacement Procedure)
The interval between the device
switching ON and its subsequent
switching OFF is less than 3
seconds
Leave the device when OFF for a minimum of 3
seconds and the switch it ON again
3) The device does not
provide electrical stimulation
when inbuild electrode
contact the skin.
No electric stimulation mode has
been selected.
Open Programs or Frequency Menu and select
the necessary electrical stimulation mode.
The contact area of the inbuild
electrode with the skin is not
sufficient.
Press the electrode tightly to the skin. Slightly
moisten the skin if necessary.
Zero intensity level is set.
Increase the intensity level.
4) The device does not
produce sound signals
(mode switching ON, change
of intensity level, end of the
mode, etc.).
Sound is switched OFF
Increase volume. Go to Settings → Sound →
General
5) The device does not
provide electrical stimulation
when external electrode are
used.
No electric stimulation mode has
been selected.
Open Programs or Frequency Menu and select
the necessary electrical stimulation mode.
The contact area of the external
electrode with the skin is not
sufficient.
Press the external electrode tightly to the skin.
Slightly moisten the skin if necessary.
Zero intensity level is set.
Increase the intensity level.
6) Indicator backlit fades
very fast.
Economical Use of Batteries
Function is enabled.
Disable Economical Use of Batteries Function. Go
to Settings → Economy
7) The device does not
automatically switches OFF
when the electrode stop
contacting the skin or when
the device has not been
used for more than 5
minutes.
Therapy without Contact Control
Function is enabled.
Disable Therapy without Contact Control Function
(see item 7.2.7 Contact Menu)
8) The device switches OFF
or battery symbol flashes
and the device produces
intermittent alarm sound
during the operation.
Voltage of the set of batteries is
less than 2,1V
Replace the set of batteries (see section 9,
Battery Replacement Procedure)
9) The device does not
switch ON in time set for
Alarm Clock.
Alarm Clock is OFF
Switch ON the Alarm Clock. Go to Settings →
Alarm Clock → OFF and select One time of Daily
mode
Voltage of the set of batteries is
less than 2,1 V
Replace the set of batteries (see section 9,
Battery Replacement Procedure)
10) The device switches
OFF without command.
Voltage of the set of batteries is
less than 2,1 V
Replace the set of batteries (see section 9,
Battery Replacement Procedure)
11) Fast consumption of
batteries.
Low-quality batteries
Use high-quality batteries (it is recommended to
use alkaline batteries) or storage batteries of
relevant typical size with voltage not less than
1,5V
Maximal backlit brightness level.
Reduce backlit brightness. Go to Settings →
Brightness
Economical Use of Batteries
Function is disabled.
Enable Economical Use of Batteries Function. Go
to Settings → Economy

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11. MANUFACTURER’S WARRANTY
12) The device does not
provide intensity more than 5
units.
Children’s Doctor Function is
enabled.
Disable Children’s Doctor Function (see item 7.2
Children’s Doctor Function).
13) The Programs Menu
lacks Gynecologic Pain,
Gynecology, Potency.
Children’s Doctor Function is
enabled.
Disable Children’s Doctor Function (see item 7.2
Children’s Doctor Function).
Attention! Any other defects should be remedied by the company-manufacturer.
11.1 The manufacturer guarantees that the device complies with Technical Regulation T_ 9444-009-44148620-2009 on
condition that it is used subject to operation, transportation and storage requirements.
11.2 Product service life is 5 years. The product service life for the designated purpose can exceed the periodstipulated
by the manufacturer considerably if consumer follows all the stipulated operation, transportation and storage
requirements.
11.3 Product warranty period is 12 months after sale.
11.4 If any defects are found within the warranty period the seller (manufacturer) undertakes to satisfy the consumer’s
claim subject to Law of the Russian Federation On Protection of Consumers’ Rights. The seller (manufacturer) or any
organization performing functions of the seller (manufacturer) under the relevant contract will not be responsible for any
defects if they emerge after the product has been delivered to consumer and relate to :
1) violation of operation, transportation and storage requirements stipulated hereto by consumer;
2) mechanical damages;
3) actions of third parties;
4) force-majeure circumstances.
11.5 Product warranty is not valid for the products which sealing marks have been broken.
11.6 If any defect is found within the Product Warranty period or if the delivered device is incomplete, owner of theproduct
should send the product and a request for repair (replacement) to the manufacturer’s address or its representative and
indicate their full name, address, phone number, date and give short description of the defect and conditions under which
it has emerged.
Manufacturer :
«TRONITEK» LLC
Ekaterinburg, 620146, Russia
Academika Postovskogo Str. 15
Ekaterinburg, Russia, 620146
Tel. : [phone]
E-mail : c[email protected]
[email protected]