нструкция импловит.en
нструкция импловит.en
нструкция импловит.en
The purpose of the device and its safety. This will allow you to optimally use the
unique capabilities of the device for the treatment and prevention of a wide range
of diseases, both in physiotherapy departments, medical and preventive institutions,
and by patients themselves at home.
Conditions recommended by a doctor.
ATTENTION! Please keep the user manual throughout the entire service life of the
device. When transferring the device to third parties, the user manual must also be trans-
ferred. Performing procedures by the patient at home does not require special prepara-
tion or skills. To effectively use the device, study the user manual and correctly perform
the treatment methods.
ATTENTION! In case of any questions regarding the use of the device, please
call the toll-free hotline of the factory at 8 800 5509001 or consult a physiotherapist in
your area.
CONTENTS
Symbols on the device. 2
Safety instructions. 3
Principle of operation . 4
Contraindications 5
Side effects. 6
Methodological recommendations . . 8
Technical Maintenance . 1 7
Appendix A 1 9
Acceptance Certificate 2 1
Manufacturer's Warranty 2 2
OPERATING MANUAL
SYMBOLS ON THE DEVICE AND IN THE MANUAL
On the device:
Information Symbol
SN
Serial number;
Year of production;
Electromagnetic radiation;
On the coils:
Information Symbol
(())
Electromagnetic radiation;
2 OPERATING MANUAL
SAFETY INSTRUCTIONS
Perform procedures in locations convenient for plugging the power cord into
a power outlet, avoiding tension on the power cord and
of the emitter cables, otherwise use industrial extension cords. The device
should only be plugged into a functioning power outlet with a working network
voltage of ~ 220V / 50Hz.
Lifting, moving, or pulling the device out of the socket by the power cord is
prohibited.
To avoid damaging the device, keep it away from unsupervised
access by children.
Do not allow moisture to enter the control unit and inductors when treating
their surfaces with disinfectant solutions. Protect the device from moisture, vi-
brations, and impacts.
Protect the device from direct sunlight and high temperatures.
Do not twist or bend the cables. Store the device after use in consumer
packaging.
Do not place the connected device (within 0.5m) near magnetic storage
media (floppy disks, credit cards, video recordings, mobile storage devices).
Disclaimer: The manufacturer is not responsible for damages that occur due to non-
compliance with the instructions provided.
above.
OPERATING MANUAL 3
Medical devices should also not interfere with the functioning of other devices. In order
to regulate the requirements for EMC (electromagnetic compatibility) to prevent the
occurrence of unsafe situations related to the use of products, the standard GOST R IEC 6
0601-1-2 and GOST R 51318.11 was put into effect. This standard defines levels of immunity
to electromagnetic interference, as well as maximum levels of electromagnetic radiation
applicable to medical equipment. This medical device, manufactured by YUKOND company, meets
the requirements of the standard regarding immunity to interference and emitted
radiation.
Make sure the equipment is functioning correctly if the conditions differ from those listed
in Appendix A! Special requirements for ensuring electromagnetic compatibility are pre-
sented in Appendix A.
OPERATING PRINCIPLE
home and medical settings through transcutaneous electrical stimulation with a frequency
of up to 400 kHz.
It produces sustainable therapeutic effects:
•
improvement of blood circulation and tissue nutrition;
•
oxygen saturation of cells;
.
venous blood and lymphatic drainage;
•
activation of local immunity;
•
reduced pain sensitivity;
.
The device, using coils, provides therapeutic effects on the patient through a high-frequency
alternating electric field (up to 400 kHz), but with low voltage (up to 10 V) and low
output current on the coil (up to 0.3 A).
The impact is provided by a sinusoidal high-frequency electric field on the body tissues. The
high-frequency electric field (the impact of the magnetic field in the device is minimized) affects
the tissues in such a way that polarization of charged particles and induction of weak eddy
currents occur in the latter. As a result of this process, complex physicochemical transformations
occur in the cells, they are slightly heated, which leads to a calming effect on the -
tissues
4 OPERATING MANUAL
INDICATIONS FOR USE:
•
diseases of the peripheral nervous system;
•
neuralgia;
.
disorders of sensitivity, hypoesthesia, paresthesia;
-
•
osteochondrosis of the spine;
•
consequences of neuritis;
radiculitis;
•
disorders of the central nervous system;
.
neuroses;
•
insomnia;
•
migraine;
•
neurocirculatory dystonia;
•
enuresis;
.
neurodermatitis;
.
varicose vein expansion;
diseases of the ENT organs;
•
inflammation of the oral mucosa; vaso-
motor rhinitis;
•
chronic sinusitis;
•
diseases of the reproductive organs;
prostatitis;
•
inflammatory processes of the female reproductive organs.
•
presence of a cardiac pacemaker;
•
atherosclerosis;
•
hypertension in stage 3;
•
arrhythmias;
.
myocardial infarction;
cardiovascular insufficiency of 2-3 degrees;
•
•
acute cerebrovascular disorder - stroke;
•
thyroid diseases - hyperthyroidism and thyrotoxicosis;
-
•
active tuberculosis;
epilepsy;
.
bleeding and systemic blood disorders;
•
pregnancy.
OPERATING MANUAL 5
SIDE EFFECTS:
•
Risk of congenital pathology development. Exposure to an electrostatic field
may cause chromosomal abnormalities and lead to fetal anomalies.
•
Risk of recurrent stroke. If less than 6 months have passed since the brain
blood circulation disorder, the likelihood of recurrent bleeding increases. The risk is asso-
ciated with increased overall and cerebral blood circulation.
ATTENTION! Before performing the procedure, the patient must remove all metal
wardrobe items and accessories.
1. Visually inspect the power cable of the device for any damage.
2. Connect the device to a 220V power supply.
3. Turn on the device by pressing the 'ON' button.
4. Depending on the patient's condition, select the appropriate treatment procedure (
Guidelines for using the 'Disk' and 'Tor' coils), using the physiotherapeutic device 'IM-
PLOVIT' according to TU 26.60.13-005-40958670-2018.
5. Connect one of the coils included in the kit ('Tor' or 'Disk') to the device, depending on the pro-
cedure (see Fig. 2). Connect the plug of the coil to the device's socket. The coil has a working
surface on both sides.
6. Depending on the procedure, set the desired operating time of the device (see Fig. 1) using
the timer buttons. The LED indicators will indicate the selected mode: 5, 15, 30, 60 minutes.
7. To check if the device is in working condition, use the LED indicator labeled 'NO
FIELD' located on the control panel.
ATTENTION! If the red light indicator 'NO FIELD' does not turn off after connecting
the coil to the device, refer to the table. No. 1 (Common Malfunctions and Their Remedies).
8. Depending on the procedure and the patient's age (see Fig. 1), select the desired power
(50% or 100%).
ATTENTION! Procedures for pediatric patients (1 year to 14 years old) are per-
formed at 50% power and only under adult supervision.
9. After transportation or storage at negative temperatures, the device must be kept in
the transport packaging for at least 8 hours at normal (room) temperature.
6 OPERATING MANUAL
Figure 1
IN
RU
on. DE SS
IA
MA
4 5 K O HD
Power switch, depending on the power (min - 50% or max - 100%)
Tolyatti , the corresponding LED lights up
MAX
power
M I N
no field
minutes
5 1 5 3 0 6 0 Timer buttons: '5 minutes', '15 minutes', '30 minutes', '60 minutes'.
TIMER BUTTONS
Figure 2
IMPLOVIT
PHYSIOTHERAPY DEVICE
BA
RU
on. DE
SS
IA
Coil 'Tor'
MA
40KOHD
only
M A X
power
MIN
Coil 'Disk'
ONA
no field
minutes
1 5 3 0 6 0
TIMER BUTTONS
OPERATING MANUAL 7
GUIDELINES
The effect is exerted by the coil field of the 'Disk' coil or the 'TOR' coil, de-
pending on the structure of the affected organ. The 'Disk' coil is used to
affect hollow organs (organs of the abdominal cavity, thoracic cavity, and head). The 'TOR
' coil is used to affect musculoskeletal formations (joints, ligaments, muscles, reflex
zones of the body).
The duration of the treatment is set on the device timer (5 minutes, 15 minutes, 30
minutes, 60 minutes). An audible signal is emitted at the beginning and end.
end of session.
During the operation of the "Disk" or "TOR" coil, it is possible to move it within
the impact zone, making stops or performing circular massaging
movements.
The time until complete recovery will depend on the severity of the condition
and may vary from 10 days to 12 months.
80
OPERATING MANUAL
Diseases of the peripheral nervous system (neuralgia, sensory disor-
ders - hypoesthesia, paresthesia, osteochondrosis of the spine, consequences of
neuritis, radiculitis)
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
OPERATING MANUAL 9
Thoracic radiculitis. Act
on zone 1, then on zone 2.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Lumbosacral disorders.
Act on zones 1 located on the back near the spinal column from both sides.
Then on the main zones 2. When pain spreads down to the legs or abdomen, apply treat-
ment on zone 3.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
10 OPERATING MANUAL
Cervical radicular disorders, osteochondrosis. Act on zone
1, then sequentially on the pain spreading zone 2 and zone 3.
Hold the toroid between your palms.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Trigeminal neuralgia
Regardless of the location of the pain, apply pressure to the areas where the facial nerve exits, starting from the
healthy side and then moving to zone 2.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
OPERATING MANUAL 11
Migraine (headache attack) Zone 1: oc-
ciput, Zone 2: temples, Zone 3: base of the skull.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Cellulite, peripheral circulatory disorders, varicose vein expansion. Apply to main zone 1, then
zones 2 and 3.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
12 OPERATING MANUAL
ENT diseases (inflammation of the oral mucosa, vasomotor rhinitis,
chronic sinusitis)
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
OPERATING MANUAL 13
Allergic rhinitis (runny nose)
Target zone 1 - in the temple area, then target zones 2 and 3.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Prostatitis
Target zones 1, 2, and 3 - perineal area.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
14 OPERATING MANUAL
Menstrual Cycle Disorders
Impact on zones.
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
Painful Menstruation
Impact on zone 1, then zone 2.
( 2 ) 2
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
OPERATING MANUAL 15
Gynecological Inflammatory Processes
Upper Genital Tract (Endometritis, Salpingo-oophoritis, Parametritis)
Impact on zone 1, then move to zone 2, and finally zone 3.
3)
(2
Coil torus,
then the disc
Treatment time
- 30-60 minutes
Coil disc
- 15-30 minutes
Coil torus
PACKAGE CONTENTS
Signal Generator . 1
Emitter Coil. . . . . .
.2
User Manual 1
The arrangement and fastening of transport boxes should ensure their stable posi-
tion and absence of displacement during transportation.
Transportation conditions must comply with storage conditions 5 according to
GOST 15150 (at ambient temperature from minus 50 to plus 50 ° C and relative humid-
ity up to 100%).
Storage conditions in the transport packaging at the manufacturer's (consumer's
) warehouses must comply with storage conditions 2 according to GOST 15150.
( at ambient temperatures ranging from minus 40 to plus 50 °C and
relative humidity up to 98% ) .
It is not allowed to store the products in a room where evaporating
liquids and substances that can cause corrosion are present.
16 OPERATING MANUAL
MAINTENANCE
The device and all its components have a complete design and do not
require maintenance throughout the entire shelf life.
Maintenance of the device involves preventive inspection,
dust and dirt cleaning, disinfection, and periodic monitoring of its
operability.
Periodic performance testing is carried out at least once a year. For what purpose is it
necessary:
- position the emitters in such a way that there is access to all the inductors of the
emitters;
- connect the device to the electrical network;
- select any of the four treatment programs;
- start the therapeutic treatment;
- by applying the field indicator to the working surfaces of the inductors, check for
-
the presence of a field in each of them; stop the treatment; turn off the device.
CURRENT REPAIR
Device repair is only carried out by the manufacturer.
It is strictly prohibited to open the device without a representative of the manufacturer.
In case of unauthorized opening and mechanical damage, the manufacturer disclaims
responsibility for warranty obligations specified in these technical conditions.
Table 1.
Measurement tools and instruments Purpose
Lack of voltage
1. The device does not turn on. from the network
Check the network voltage
OPERATING MANUAL 17
Independent opening of the apparatus and carrying out repair work by a person
who is not a representative of the manufacturing company during the warranty period
will result in the termination of warranty obligations.
of the manufacturing company.
After the repair, the device is handed over to the user with the establishment of a war-
ranty period, the beginning of which is calculated from the moment of its transfer.
MAIN TECHNICAL SPECIFICATIONS OF THE DEVICE
Number of Independent Output Channels 1. Connection to either the 'Disk' coil or the 'Tor' coil
from 150 kHz to 400
Frequency Range kHz 0.5-1.5 W not ex-
Nominal Output Power ceeding 12
Output current magnitude on the inductors when connecting the 'Disk' coil not exceeding 0.295A
-
)
Operating mode of the device for conducting a single From 5 minutes to 1 hour
procedure
Establishing the procedure time interval Built-in timer inside the device C
18 OPERATING MANUAL
in the range from 198 toThe device maintains functionality when the network power voltage changes
242 B.
220 ± 22 V, frequency 50 Hz, not exceeding 12 VA. The established value of power consumption, at the power voltage
Time to enter the device's operating mode - not more than 5 seconds.
The device provides a continuous operating mode of at least 8 hours per
day.
The noise level during device operation does not exceed 45 dB.
LIST OF APPLICABLE STANDARDS
GOST R 50267.0-92 (IEC 601-1-88) 'Medical electrical devices.
Part 1 General safety requirements'.
GOST R 51609-2000 'Medical devices, classification according to potential risk of
use'.
APPENDIX A
Appendix A
RF Radiation, CISPR
Class A
11
The devices are suitable for use in all institutions
Harmonic Radia- , except residential premises and institutions
tion Class A directly connected to the communal low-voltage
I EC 61000- 3- 2 power supply network that powers residential
buildings.
Voltage Fluctuations / Os-
cillatory Radiation, IEC 61000 Corresponds to
-3-3
Electrostatic Discharge,
± 6 kV (contact), ± 8 kV (air) ± 6 kV (contact)
IEC 61000-4-2
± 8 kV (air)
OPERATING MANUAL 19
Fast electrical transient
± 2 kV for power lines
processes
or surges ± 1 kV for input/output ± 2 kV for power lines
IEC 61000-4-4 lines
± 1 kV from line(s) to
Overvoltage IEC 61 ±1 kV in differential mode
line(s)
000-4-5 ±2 kV in normal mode
± 2 kV from line(s) to ground < 5
% UT
Electrostatic Discharge,
± 6 kV (contact), ± 8 kV (air) ± 6 kV (contact)
IEC 61000-4-2
± 8 kV (air)
± 1 kV from line(s) to
Overvoltage IEC 61 ±1 kV in differential mode
line(s)
000-4-5 ±2 kV in normal mode
± 2 kV from line(s) to ground < 5
% UT
NOTE: UT refers to the AC mains voltage before applying the test level.
2 0 OPERATING MANUAL
ACCEPTANCE CERTIFICATE: Physio-
OPERATING MANUAL 21
MANUFACTURER'S WARRANTY
The manufacturer guarantees that the quality of the device complies with the requirements of
TU 26.60.13-005-40958670-2018, provided that the consumer complies with the conditions and rules
of transportation, storage, and operation.
The warranty period for the device is 12 months from the date of sale
by the manufacturer.
The warranty period for storing the device in the manufacturer's packaging is 24
months from the date of manufacture.
During the warranty period, the manufacturer undertakes to rectify defects or replace
the malfunctioning device free of charge, provided that the damages are not related to
violation of transportation, storage, installation, and operation rules.
In case of warranty, the user manual is sent to the service center along with
the device. The device without a user manual is accepted for paid repairs only.
For questions regarding product quality and service, please contact the toll-free
hotline at 880055090 01.
REQUIREMENTS FOR DISPOSAL AND ENVIRONMENTAL PROTECTION
Disposal must be carried out in accordance with the rules of collection, registration,
and disposal established by the authorized federal executive body for elec-
tronic devices, as well as SanPiN 2.1.7.2790. It is prohibited to dispose of it as house-
hold waste.
According to SanPiN 2.1.7.2790, the apparatus belongs to class
A - epidemiologically safe waste.
Before disposal, the apparatus must undergo sanitary treatment in accordance
with the guidelines MU - 287-113 dated 30.12.1998.
The apparatus should be disposed of in the following
cases: when the service life expires;
- confirmation of facts and circumstances that pose a threat to life and health of indi-
viduals and indicate non-compliance with the intended purpose.
All packaging, including transportation, should be disposed of.
Paper, polyethylene, and plastic should be disposed of separately.
Disposal should be carried out in accordance with the rules of collection, registration,
and disposal established by the authorized federal executive body for elec-
tronic devices, as well as SanPiN 2.1.7.2790. It is prohibited to dispose of as household
waste.
Electrical and electronic devices should be disposed of through
special organizations specified by local authorities, but not together
with household waste.
22 OPERATING MANUAL
Valid when filled out
WARRANTY CARD
To be completed by the manufacturer of the product
No
Date of issue
year, month
Manufacturer's legal address: P.O. Box 4135, 445046, Tolyatti, Samara Region, Russia
2 0
E - mail : [email protected]
Website: www.jukondmarket.ru/, www.implovit.ru/, www.jukond.ru/
Fills trading enterprises
Workshop Master
the physiotherapy device "IMPLOVIT"
Date of sale
>>
Seller
Seized
signature
Store stamp
Confiscated:
Serial number
Malfunction
OPERATING MANUAL 23
FOR NOTES
2 4 OPERATING MANUAL
Valid when filled out
WARRANTY CARD
To be completed by the manufacturer of the product
No
Date of issue
year, month
E - mail : [email protected]
Website: www.jukondmarket.ru/, www.implovit.ru/, www.jukond.ru/
Fills trading enterprises
Workshop Master
the physiotherapy device "IMPLOVIT"
Date of sale
>>
Seller
Seized
signature
Store stamp
Confiscated:
Serial number
Malfunction
OPERATING MANUAL 25
FOR NOTES
26 OPERATING MANUAL
Valid when filled out
WARRANTY CARD
To be completed by the manufacturer of the product
Physiotherapy device "IMPLOVIT"
according to TU 26.60.13-005-40958670-2018
city TV 26.60.13-005-40958670-2018
No
Date of issue
year, month
stampOTK
The stub of the tear-off ticket for warranty repair by the manufacturer at
E - mail : [email protected]
Website: www.jukondmarket.ru/, www.implovit.ru/, www.jukond.ru/
Fills trading enterprises
Workshop Master
the physiotherapy device "IMPLOVIT"
Date of sale
>>>
Seller
Seized
signature
Store stamp
Confiscated:
Serial number
Malfunction
OPERATING MANUAL 27
FOR NOTES
28 OPERATING MANUAL