Manuale Uso I Tech Physio 4 MNPG178

OPERATING MANUAL
MNPG178 Rev.4 of 29/06/16
I-TECH
PHYSIO 4/EMG
Contents
Contents 2
Technical information 3
Manufacturer 3
Declaration of conformity 3
Classifications 3
Purpose and scope 3
Technical specifications 4
Description of the controls 5
Labels 6
Contents of the pack 7
Purpose 7
Warnings 7
Side effects 8
Contraindications 8
Electromagnetic interference 9
Instructions on use for electrotherapy treatments 9
Instructions on use for electromyography (EMG) treatments36
Handling and care 43

Charging the battery 43
Cleaning the equipment 43
Operation, transport and storage 44
Information on disposal 44
Maintenance and troubleshooting 44
Assistance 44
Spare parts 44
Warranty 45
EMC tables 46
IACER Srl 2 MNPG178-04

Technical
information
Manufacturer
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE)
Tel. +39 041.5401356 • Fax +39 041.5402684
IACER S.r.l. is an Italian manufacturer of medical devices (CE certificate n° MED24021 released by
the Notified Body n°0476 Cermet).
Declaration of conformity
IACER S.r.l., headquartered in Italy, via S. Pertini 24/A 30030 Martellago (VE), declares that the I-TECH
PHYSIO 4/4/EMG device is manufactured in conformity with Council Directive 93/42/EEC (MDD)
dated 14 June 1993 (Italian Legislative Decree 46/97 dated 24 February 1997 “Attuazione della Direttiva
93/42/CEE concernente i dispositivi medici”), Annex II as amended by Directive 2007/47/EC dated 5
September 2007 (Italian Legislative Decree 37/2010 dated 25 January 2010)
Notified body: Cermet, Via di Cadriano 23 – 40057 Cadriano di Granarolo (BO) ITALY
I-TECH PHYSIO 4/4/EMG is Class IIa equipment, with reference to Directive 93/42/EEC
(MDD), annex IX rules 9 and 10 (and subsequent amendments).
Certification channel: Annex II (excluding paragraph 4)
Martellago, 01/09/2014 The legal representative

Mario Caprara
Classifications
The I-TECH PHYSIO 4/EMG device has the following classification:

 Class IIa equipment (Directive 93/42/EEC, annex IX, rules 9 and 10 and subsequent
amendments);
 Class II with BF type applied part (Classif. IEC EN 60601-1);
 Equipment unsuitable for use in the presence of a flammable anaesthetic mixture containing air,
oxygen or nitrous oxide;
 Equipment suitable for continuous operation;
 Equipment unsuitable for use outdoors.
Purpose and scope
Clinical scope: Therapeutic
Purpose: Outpatient care/Hospital care

The medical device is intended for use by a therapist, a fitness coach at a public/private centre or
clinic, or professional operators in general.
The I-TECH PHYSIO 4 and I-TECH PHYSIO EMG are intended in particular for muscular
rehabilitation in general, muscular cool-down, muscle strengthening, beauty treatments (firming and
drainage), pain therapy (analgesic and muscular atrophy programs) and functional recovery of muscles
after trauma or an accident, specific programs for ionophoresis, incontinence and the treatment of
denervated muscles.
It is possible, therefore, to treat a wide range of both chronic and acute pathologies.
The I-TECH PHYSIO 4/EMG model permits the non-invasive registration of surface
electromyographic (sEMG) signals taken in single differential mode and detected with electrodes
placed on the skin. The user must be familiar with sEMG techniques in order to put the I-TECH
PHYSIO 4/EMG to correct use.
The CE0476 marking on the device applies exclusively to medical programs and does not cover,
therefore, any programs relating to beauty treatments. Refer to the details of the various programs for
further information.
Technical specifications
Characteristic Specification
Power supply NiMH 7.2V 2000mAh (6xAA Size) pack of rechargeable
batteries.
EA1018G-12V battery charger, 100/240VAC 1.0A
50/60Hz input, 12VDC 2.0A output. Non-replaceable
2A 250VAC fuse.
Max absorbed current 1.6 A
Insulation class (IEC EN 60601-1) II
Applied part (IEC EN 60601-1) BF
Dimensions (length x width x 180x110x50
height) (mm)
IP protection IP20. Device protected against the infiltration of solid
bodies measuring more than 12.5mm in diameter.
Device not protected against the infiltration of liquids.
Electrotherapy (models 4 and 4/EMG)
Number of programs A total of 86 programs divided as follows:

26 -
TENS/ANALGESIC/IONOPHORESIS
(diadynamic, faradic, Kotz and interferential
currents).
- 25 REHAB (denervated muscles,
incontinence, pains)
- 17 EMS (strengthening, heating, muscular
cool-down and for beauty treatments).
- 18 Customisable.
Max out 160Vpp with a load of 1000 Ohm
Frequency Between 0.5 and 40kHz
Impulse Between 20 microseconds and 400 milliseconds
Duration of therapy Preset programs, free memories of up to 60 minutes
Electromyography (model 4/EMG only)
4/EMG input dynamics 0 to 4.16 mVpp
4/EMG bandwidth 16 to 402 Hz
4/EMG input level of noise < 3 VRMS
Gain 794 V/V
Input impedance > 100 G over the whole band
CMRR >100 dB
Output dynamics 0 to 3.3 V
Resolution 10 bit
Sampling frequency 1024 Hz
The device has a useful life of 10-year.
Description of the controls
Channel intensity increase/decrease

buttons
Program and parameter

selection/confirmation buttons
Patient 2 selection button
Patient 1 selection button
USB input
Channel 1/2
output
Channel 3/4
output
4/EMG input
Battery charger
ON/OFF button connector

Labels
Label on the back of the device
Model I-TECH PHYSIO 4/EMG Model I-TECH PHYSIO 4
Follow the instructions on use
WEEE directive
Class II device
BF type applied part
In compliance with MDD 93/42/EEC (and subsequent amendments to Dir.

2007/47/EC concerning medical devices)
CE marking
Production data (month-year)
Serial number
Permitted temperatures (temperature range for storage, on the pack)
Relative humidity (relative humidity for storage, on the pack)
Manufacturer data
Device not protected against the infiltration of liquids, keep it dry.
Device able to supply current at above 10mA with a load of 1KOhm
EXT
External power supply unit: EA1018G-12V battery charger, 100/240VAC 50/60Hz
POWER
input, 12VDC 2 A output
SUPPLY

Contents of the pack
The I-TECH PHYSIO 4/EMG pack contains:
 1 x I-TECH PHYSIO 4/EMG device;
 1 x EA1018G-1E battery charger;
 2 x electrotherapy connection cables (yellow/blue and white/red) with 2 mm female
connector, about 2.5m in length;
 2 x ionophoresis connection cables (red and blue) with 2mm female connector, about
2.5m in length;
 1 x EMS connection cable (blue) for tip with 2mm female connector, about 2.5m in
length;
 1 x connection cable with EMG amplifier, about 2m in length (only for the I-TECH
PHYSIO EMG version);
 2 x packs of rectangular single-patient electrotherapy electrodes;
 2 x packs of square single-patient electrotherapy electrodes jack connection;
 1 x pack of round single-patient electrotherapy electrodes jack connection;
 1 x pack of square single-patient electrotherapy electrodes clip (snap) connection(only
for the I-TECH PHYSIO EMG version);
 1 x pack of round single-patient EMG electrodes (only for the I-TECH PHYSIO EMG
version);
 1 x ionophoresis kit (elastic belt, 2 silicon electrodes, 2 sponges);
 1 x tip for EMS stimulation, cable about 2m in length.
Purpose
Warnings
The device was designed and created for use with rechargeable internal batteries and with the battery
charger included in supply.
• The long-term effects of stimulation are not known
• For external use only
• It is forbidden to position the electrodes on the carotid sinuses, especially those of patients known to have
hypersensitive carotid sinuses.
• Do not carry out stimulation on the thyroid, neck or mouth because this could trigger muscle spasms that
can obstruct the airways and cause breathing difficulties and heart rhythm disorders and excessive arterial
pressure.
• It is forbidden to position the electrodes in such a way that the current crosses the heart area (e.g. a black
electrode on the chest and a red electrode on the shoulder blade); however, electrodes can be positioned
along the muscular fascia of the heart area, as for pectoral strengthening. Danger of cardiac arrhythmia.
• Do not carry out stimulation with the patient connected to high frequency surgical devices as this could
cause scalding and skin injuries under the electrodes and problems with the stimulator.
• Do not use the device with short-wave or micro-wave electrosurgical or therapy equipment that sends
electrical impulses to the body as this could cause problems with the stimulator.
• It is forbidden to use the device near flammable substances or in environments where there is a high
concentration of oxygen, in the presence of aerosol devices or in very damp environments (do not use it in
the bathroom or when having a shower/bath).
• It is forbidden to position the electrodes near the eyes; make sure that the current delivered does not cross
the eyeball (one electrode diametrically opposite to the other in relation to the eye); keep a distance of at
least 3cm from the eyeball.
• Do not use it in the area of the genitals
• Do not use it in areas of the body of little sensitivity.
• Do not allow the equipment to be used by people with emotional disorders or who are even only
temporarily incapacitated or have insufficient mental ability.
• Apply the electrodes only on clean, unblemished skin.
• Keep the electrodes separate during operation: electrodes in contact can cause inappropriate stimulation
or skin injuries.
• Keep out of the reach of children.
• Consult your doctor if you have any doubts about using the device.
• Use of the device is prohibited in the presence of signs of deterioration of the device itself and of the
electrodes and cables. Always check the condition of the device before use.
• In the case of metal osteosynthesis implants, consult a doctor before using the device.
Make sure that the plug and battery charger are intact. Should one of these parts show any sign of damage,
suspend use of the battery charger immediately and contact the retailer or manufacturer.
Only use battery chargers supplied by the manufacturer; the use of battery chargers not supplied by the
manufacturer will free the same from any responsibility related to damage to the equipment or user and
expose the user to potential risks like short circuits and fire.
• The device must be used with care for patients with suspected heart problems
• Some patients may suffer skin irritation or hypersensitivity due to treatment or the gel. Suspend treatment
and consult a doctor if the problem persists.
• The intensity of stimulation and the position of the electrodes should be based on the indications of the
prescribing doctor.
• The effectiveness of treatment depends largely on the selection of patients suited to treatment by qualified
personnel.
• Ensure good contact between the skin and the electrode. Prolonged use can cause irritation of the skin in
the area where the electrodes are applied.
• If the intensity of stimulation is uncomfortable or becomes inadequate, reduce the intensity to an
adequate level. Consult your doctor if the problem persists.
• Do not use the device when driving a vehicle or when handling and controlling equipment/machinery.
• Do not confuse the connection cables with the cables of headsets or other devices, and do not connect
the cables/electrodes to other equipment.
• Do not use sharp or pointed objects on the device's keyboard.
• Use only accessories provided by the manufacturer.
Warning: the equipment delivers current in excess of 10mA.
The manufacturer assumes responsibility for the quality, efficiency and safety of the equipment only when:
 any additions, modifications and/or repairs are carried out by authorised personnel;
 the equipment is used observing the instructions on use in this manual.
WARNING: it is forbidden to tamper with this equipment in any way.
Side effects
No significant side effects are known. Some particularly sensitive people have reported skin redness in the
area where the electrodes were positioned: redness normally vanishes a few minutes after treatment. Should
the redness persist please consult a doctor.
In rare cases, stimulation carried out in the evening can cause some people to experience difficulty in falling
asleep. Suspend treatment and consult a doctor if this occurs.
Contraindications
Do not use the device when there are cancerous lesions in the area of treatment. Stimulation must not be
carried out in areas that are infected, swollen or inflamed, or when there are skin eruptions (phlebitis,
thrombophlebitis, etc.).
This device must not be used by people with a pace-maker, epileptics, pregnant women, anxious people or
people suffering from serious illnesses or inguinal or abdominal hernias.
Do not use the device if the cause of pain is not known or not diagnosed. Use the device only after
diagnosing the cause. In the event of injury, muscle stress or any other health problem use the device only
under medical supervision.

Electromagnetic interference
The device doesn’t produce or receive electromagnetic interference from other devices. However it is
recommended to keep a distance of at least 3 metres from televisions, monitors, mobile phones or other
electronic devices.
The equipment must not be used near or on top of other equipment. If this is not avoidable, the operator
must monitor normal operation of the equipment in its current configuration.
Please refer to the EMC tables annexed to this manual for further details.
Instructions on use for electrotherapy treatments

Before using I-TECH PHYSIO 4/EMG clean the skin of the area to be treated; with the cable
disconnected from I-TECH PHYSIO 4/EMG, connect the electrostimulation cable jacks to the self-
adhesive electrodes; position the self-adhesive electrodes on the skin (see photographs of electrode
positions); connect the impulse transmission cables to the relative jacks (Channel 1 and/or Channel 2), then
turn on the device.
Instructions on use for a single patient.

1. Turn on the I-TECH PHYSIO 4/EMG by pressing the ON/OFF switch on the small rear panel of the
device.
2. Select single mode and press the OK key to confirm
3. Select the program group: Wave, Rehab, EMS or Mem, using the left and/or right arrow keys .
4. Select the program using the up/down arrow buttons (e.g. E03 basic strength).
5. Select male or female with the left/right arrow buttons (when applicable) .
Select Select
male female
6. Select the muscle group with the up/down arrow buttons.
arms, male trunk, legs, male arms, female trunk, legs, female
male female
7. Press the OK key to start stimulation and the relative text appears on the screen; place the electrodes on
the skin, connect the cables, and increase the intensity; the type of cable required for the selected type of
treatment also appears on the screen. To start the work session, press the Up arrow key of at least one of
the channels used for electrostimulation, and increase the intensity of the output current; the I-TECH
PHYSIO 4/EMG opens the work screen automatically, displaying the name of the selected program.
8. Press the up arrow button for each channel in use to increase current intensity until the personal
tolerance level is reached.

A bar indicating the start and end of a contraction will appear on the display while the electronic stimulator
is working. The periods of muscular contraction (bold bar) and the periods of recovery (dotted or striped
bar) are graphically visualised under the bar with a cursor. This enables the user to know exactly when a
contraction starts.
9. At the end of the first phase, the I-TECH PHYSIO 4/EMG cancels the previously selected intensity,
and warns the user with an intermittent signal; to continue with the program, increase the intensity again.
Three sound signals will advise of the end of the program.
At the end of the program, switch off the I-TECH PHYSIO 4/EMG and remove the cables. Attach the
electrodes to the transparent films and put them in their original packaging.
Option to simultaneously increase the intensity on all 4 channels:

Select the desired program as instructed above.
Increase the intensity of all the channels up to at least 1 by pressing the relative keys, and then press
the Up arrow keys to increase the intensity for all 4 channels. To decrease the intensity, press the
Down arrow keys.
Skip phase control:

Press the right arrow button during normal program operation to skip to the next phase.
Pause/stop program control:

During normal program operation, press the OK button once to momentarily pause the normal work
cycle. Press the OK button again to restart the program.
Press the OK button twice consecutively to stop the program.
Instructions on use for two patients.

1. Turn on the I-TECH PHYSIO 4/EMG by pressing the ON/OFF switch on the small rear panel of the
device.
2. Select two patient mode and press the OK key to confirm.
3. Next, select the program required for patient 1 following the instructions above.
4. Press key 2 to set the program and make the relative adjustments for patient 2.

During therapy, it is possible to switch between patient 1 and patient 2 at any time by pressing key 1 or 2
on the keyboard.
Electrostimulation and stimulation intensities.

Electrostimulation consists of the transmission of electric micro-impulses from the I-TECH PHYSIO
4/EMG to the human body.
The fields of application of electrostimulation are: pain therapy, recovery of muscle trophism after
injury or a surgical operation, athletic preparation and beauty treatments.
Specific electric impulses are used for every one of these applications.
The stimulation intensity is shown for each channel, on a scale of 0 to 120mA, on the screen of the I-
TECH PHYSIO 4/EMG. For Sport and Beauty programs, the intensity differs according to the type
of muscle or the program in use. The following description helps the user to choose the correct
intensity according to impulse.
Impulse categories are:
Tens impulse: for tens programs, the intensity should be set at a level between the thresholds of
perception and pain. The maximum limit is reached when the muscles surrounding the area treated
begin to contract. It is best to stay below that limit.
Micro-current impulse: the maximum adjustable intensity is 12, so very low.It can be set between 6
and 12 and may be barely perceivable: this is not a fault, but quite normal for the program.
Ionophoresis impulse: the intensity must be strong enough to produce a relevant perception, near
pain, till the muscles surrounding the area treated begin to contract. Maximum adjustable intensity: 50.
EMS impulse: in this case the intensity is raised a little at a time to stimulate and gradually increase
the metabolism of the treated muscle. A comparison could be drawn with a car: the engine needs to
warm up before it can be run at maximum speed.
Toning, training and atrophying contraction impulse:the muscle treated must visibly contract
during a training impulse.The fact that the muscle tends to stiffen and increase in volume will be
visible to the naked eye. Intensity should be increased gradually (in the first contraction) to enable you
to identify the right level of stimulation comfort. Intensity can be increased up to the personal
tolerance threshold during the second training contraction; this operation is then repeated during each
contraction until the workload reaches the level of intensity recommended in the description of the
single programs. We recommend that you record the level of intensity reached in order to try to
improve the level of stimulation and consequently your performance.
Massage, winding down, active recovery impulse: the intensity must be adjusted gradually to
massage the treated muscle. The level of intensity should be sufficient to obtain a comfortable
massage. Bear in mind that there is no need to endure high levels of intensity in this case as it is meant
to be a massage, meaning that intensity can be increased gradually and not to an excessive degree.
Capillarisation impulse: increase the intensity gradually to produce constant, visible stimulation of
the treated area; a medium stimulation threshold is recommended, always below the pain threshold.
Lipolysis/drainage impulse: the “pump” effect is produced by sequential tonic contractions. The
intensity must be sufficient to produce these contractions: the greater the contraction, the greater the
induced pump effect. There is no benefit to be gained from enduring intensity high enough to cause
pain. The first electrostimulation sessions should be carried out at a low intensity to allow the
organism to get used to new sensations. In this way intensity can be increased gradually without
causing any trauma.
Other impulses: see program details.

WAVE programs.
WARNING!
It must be remembered that an electronic stimulator is a very effective analgesic instrument and that
pain can indicate various types of medical condition!
Most of the programs described in this section are analgesic. You are advised to read the manual
carefully before using the I-TECH PHYSIO 4/EMG.
TENS, an acronym standing for “transcutaneous electrical nerve stimulation”, is a therapeutic

technique mainly used for analgesic purposes to counter the effects (usually pain) of a wide variety of
medical conditions: cervical pans, arthritis, myalgia, neuritis, back pains, periarthritis, heaviness in the
legs and muscular weakness, to mention but a few.
On an academic level, TENS can be divided into various categories according to the mechanism used
to reduce the pain. The main types are: conventional TENS (or fast analgesic), electro acupuncture
training TENS (or delayed analgesic), TENS sequential where stimulation parameters are modified
automatically by the program itself during the treatment, TENS at maximum values with antidromic
action and consequently an immediate local anaesthetic effect, TENS burst that combines
conventional and electro acupuncture training TENS.
The rehabilitative action of TENS is represented by its power to reduce pain thereby restoring
physiological conditions; more often than not this allows the patient to regain normal motor function.
Consider a patient suffering from irritating periarthritis; they either resort to using analgesics or learn
to live with the pain that often makes even the simplest movements impossible. Immobility reduces
metabolic activity making it impossible to eliminate algogenic substances. So a vicious circle begins. In
addition to relieving pain, TENS causes induced muscle stimulation increasing metabolic activity and
blood flow and improving tissue oxygenation with an intake of nutritional substances. So the positive
effect can be amplified by combining TENS with muscle stimulation of the area concerned.
Position of electrodes and intensity levels.

The electrodes should be positioned to form a square surrounding the painful area using Channel 1
and Channel 2 as shown in figure 1 (positioning of the red electrode at the top/black one at the
bottom is irrespective of the type of therapy, refer to the manual of electrode positions) Intensity
adjusted to a level between the thresholds of perception and pain: the maximum intensity level is the
moment in which the muscles surrounding the area treated begin to contract; over this limit
stimulation does not become more effective, just more irritating, so it is best to stop before that point.
Figure 1
IMPORTANT
Create a square area with the

electrodes, over the painful zone.
Keep the electrodes a minimum of
4cm apart.
W01 • Rapid TENS. (Medical program).

Program also called conventional tens, used for analgesic purposes; its purpose is to induce the
organism into blocking pain at the spine, in accordance with the “Gate Control Theory” by Melzack
and Wall. Pain impulses leave part of the body (for example the hand) and run along the nerve tracts
(through small-diameter nerve fibres) until they reach the central nervous system where the impulses
are interpreted as pain. Conventional tens activates large-diameter nerve fibres, blocking the path of

small-diameter nerve fibres at the spine. It therefore acts mainly on the symptom: to simplify it
further, the wire transmitting pain information is obstructed.
Treatment duration should be no less than 30/40 minutes. Conventional tens is a current that can be
used to treat general everyday pain. The first benefits can be seen after an average of 12 to 15
treatments carried out on a daily basis (there are no contraindications for up to double this amount).
The program has a duration of 30 minutes in a single phase. The program can be repeated at the end
of the session for particularly persistent pain.
Position of electrodes: form a square above the painful area as shown in figure 1.
Intensity adjusted to a level between the thresholds of perception and pain: the maximum intensity
level is the moment in which the muscles surrounding the area treated begin to contract (over this
limit stimulation does not become more effective, just more irritating, so it is best to stop before that
point).
W02 • Endorphinic TENS 0.5 Hz Frequency. (Medical program).

This type of stimulation produces two effects in relation to the position of the electrodes: positioning
the electrodes in the dorsal region, see photograph 08 in the positions manual, promotes the
endogenous production of morphine-like substances capable of raising the pain perception threshold;
positioning the electrodes to form a square above the painful area as shown in figure 1 produces a
vascularising effect. Vascularisation increases arterial flow and consequently aids the removal of
algogenic substances and helps to restore normal physiological conditions.
Treatment duration 20 minutes in a single phase, daily frequency.
Do not position the electrodes close to inflamed areas.
Intensity adjusted for good solicitation of the part stimulated (1530), the sensation must be similar to
that of a massage.
W03 • Endorphinic TENS 1 Hz Frequency. (Medical program).

See previous program description, but with 1 Hz frequency.
W04 • Endorphinic TENS 2 Hz Frequency. (Medical program).

See previous program description, but with 2Hz frequency.
W05 • TENS sequential. (Medical program).

The action of this program is very similar to that of the W01 program. During stimulation, this program
modifies the frequency and impulse width in order to prevent inurement to the stimulation (no need to
continuously adjust the intensity value). Select the intensity at the beginning of the program and maintain it
until the end of the program: set it in order to produce a slight tingling effect in the treated area. If the
perception of current decreases a lot during the program, do not increase the intensity value and wait until
the end of therapy. The TENS program is working properly.
Program duration: 20 minutes for each phase. Intensity: set above the threshold of perception.
Position of electrodes: form a square on the painful area as shown in figure 1 or see photographs 25 to 33.
W06 • TENS at maximum values. (Medical program).

Very short duration, 3 minutes. Blocks pain impulses peripherally creating a proper anaesthetising effect in
the area treated. This type of stimulation is suitable for injuries or bruises when rapid action is required. The
intensity selected is the maximum tolerable value (well in excess of conventional tens, and therefore with
considerable contraction of the muscles surrounding the area treated). That is the reason why such
stimulation is undoubtedly the least tolerated but is extremely effective. This type of stimulation is not
recommended for particularly sensitive people and in any case the electrodes should not be positioned in
sensitive areas such as the face and genitals or close to wounds.
Position of electrodes: form a square on the painful area as shown in figure 1 or see photographs 25 to 33.

W07 • TENS Burst impulse. (Medical program).
This program produces a training effect using the frequencies of conventional TENS. Useful for pain
therapy. The action is similar to the one of endorphinic TENS, with a treatment time of 15 minutes
for a phase.
Position of electrodes: form a square on the painful area as shown in figure 1.
Intensity adjusted for good solicitation of the part stimulated (1530mA), the sensation must be
similar to that of a massage.
W08 • Microcurrent (MENS). (Medical program).

MENS releases a very low and barely perceivable current. The main features of MENS are:
correct body bioelectric currents when they have been altered by diseases;
analgesic action;
ATP production (ATP production promotes proteins synthesis and faster healing of wounds);
reduction of oedema: MENS is able to reduce vascular permeability with an improvement of
lymphatic activity.
It is a program suitable for more delicate parts of the body (face, close to genitals, inflamed areas) or
for people that don’t tolerate conventional TENS very well. Program duration: 30 minutes. Maximum
intensity limited to 12. We recommend to set the intensity level between 6 and 12.
Table of correspondences adjusted/effective current:
Adjusted intensity displayed on screen Effective current

0.5 0.15 mA
1 0.30 mA
3 0.90 mA
5 1.5 mA
9 2.7 mA
12 3.6 mA
W09-W10 • Ionophoresis 1 / Ionophoresis 2. (Medical program).

Ionophoresis is an electrotherapeutic technique that uses continuous current to carry drugs into a
painful area or contracture area. Ionophoresis means "transfer of ions": a continuous current transfers
active pharmacologic ions through the skin. The electric current favours the penetration of the drug
into the cells, and at the same time it stimulates the elimination of metabolic slag.
The drug can have negative polarity, positive polarity or double polarity. The current induces the drug
to run from one pole to the other, crossing the painful area and releasing the specific active ingredient.
WARNING: before starting the therapy, wet the sponge electrodes and wring them to avoid dripping,
then put the drug on the electrode as follows:
Drugs with positive polarity: dissolve this type of drug on the electrode connected to the positive pole
(red connector).
Drugs with negative polarity: dissolve this type of drug on the electrode
connected to the negative pole (black connector).
Two-pole drugs: these can be dissolved on either the positive pole or
the negative pole.
Position the electrode with the drug on the painful area, and the other
electrode on the other side.
Program duration: 20 minutes. Select channel 1 or channel 2 (select
both channels only if you need to stimulate two different areas).
Position the electrodes (positive and negative) horizontally to the
treatment area. Channels 3 and 4 are disconnected. Set an intensity

value to create the tingling effect in the treatment area. At the end of the program, the skin could turn
slightly red; any reddening usually vanishes a few minutes after the end of the program.
Program 1 works at 1000 Hz frequency, program 2 at 1500 Hz. Program 2 has a higher transfer
capacity than program 1, but also involves a higher probability of reddening of the skin. Do not use
the ionophoresis program near metallic prostheses!
W09 and W10 programs differ only in terms of the level of frequency. The second program works at a
frequency higher than the first so it is better at transferring active principles. On the other hand, this
aspect can cause greater irritability of the skin. In the case of the W10 program, it is advisable to check
for reddening of the skin 5 minutes into treatment (stop the program and remove the electrodes to
check the skin): in the case of excessive reddening, use program W09 instead.
Ionophoresis is also used for the treatment of diseases affecting the urogenital male apparatus, like
IPP (Induratio Penis Plastica) or La Peyronie disease.
Consult a specialist before starting the therapy.
Contact the manufacturer for other information.
W11 • Haematomas. (Medical program).

Consult a doctor before using this program to treat haematomas. Total program duration: 20 minutes
in a single phase. Few applications carried out within a few hours of the bruise. A combination of
various types of square-wave impulses has a graduated draining effect on the area to be treated
(impulses at different frequencies drain the area at different depths). Intensity: should be adjusted to a
level between the thresholds of perception and pain.
Position of electrodes: form a square above the area to be treated as shown in figure 1 page 12.
W12 • Oedema. (Medical program).

Consult a doctor before using this program to treat oedemas. Total program duration: 15 minutes in a
single phase. A combination of various types of square-wave impulses has a graduated draining effect
on the area to be treated (impulses at different frequencies drain the area at different depths).
Intensity: should be adjusted to a level between the thresholds of perception and pain.
DIADYNAMIC CURRENTS
Diadynamic currents are composed of waves with unidirectional and always positive impulses. These
kind of waves derive from electrical sine waves (low frequency) that have been previously combined
and modulated.
Diadynamic currents are indicated for the treatment of tendinitis (of the elbow, wrist, shoulders, knee
and ankle), articular traumas, acute and chronic articular diseases and muscular pains.
W13 • MF Diadynamic. (Medical program).

It is a sinusoidal single-phase current with pulse trains of 10ms and a 10ms pause at 50 Hz. The main
effect of this kind of current is an excitomotor action on striated muscle and on motor nerves, but it
also has an analgesic, tonic and vasodilatory effect. The analgesic effect is delayed and continuous.
Indications: It is indicated as therapy for painful non-spastic conditions and to improve the tonicity of
the connective tissue of muscles. Total program duration: 15 minutes in a single phase. Intensity:
should be adjusted to a level between the thresholds of perception and pain.
W14 • MFSR Diadynamic. (Medical program).

It is a sinusoidal single-phase current with pulse trains of 10ms and a 10ms pause, with 2 seconds of
action and a 1 second pause at 50 Hz. The main effect of this kind of current is an excitomotor action
on striated muscle and on motor nerves, but it also has an analgesic, tonic and vasodilatory effect. The
analgesic effect is delayed and continuous. Indications: It is indicated as therapy for painful non-

spastic conditions and to improve the tonicity of the connective tissue of muscles. Total program
duration: 15 minutes in a single phase. Intensity: should be adjusted to a level between the thresholds
of perception and pain.
W15 • MFSL Diadynamic. (Medical program).

It is a sinusoidal single-phase current with pulse trains of 10ms and a 10ms pause, with 5 seconds of
action and a 2 second pause at 50 Hz. The main effect of this kind of current is an excitomotor action
on striated muscle and on motor nerves, but it also has an analgesic, tonic and vasodilatory effect. The
analgesic effect is delayed and continuous. Indications: It is indicated as therapy for painful non-
spastic conditions and to improve the tonicity of the connective tissue of muscles. Total program
duration: 15 minutes in a single phase. Intensity: should be adjusted to a level between the thresholds
of perception and pain.
W16 •DF Diadynamic. (Medical program).

It is a sinusoidal single-phase current with pulse trains of 10ms and a 0ms pause at 100 Hz. Current
sensibility is of course lower than MF Diadynamic thanks to its higher frequency. So its passage is
more pleasant and less perceived. Physiological effects: The main action of the DF current is reduced
sensibility that provokes an analgesic effect. However, the inhibitory action is hindered by rapid
inurement. Moreover, it causes vasodilatation, has a sedative effect on the sympathetic nervous system
and a great effect of functional and motor recovery of the muscle. Indications: It is indicated as
therapy for painful non-spastic conditions and to improve the tonicity of the connective tissue of
muscles. Total program duration: 15 minutes in a single phase. Intensity: should be adjusted to a level
between the thresholds of perception and pain.
W17 • DFSR Diadynamic. (Medical program).

It’s a diadynamic biphasic current with 2 seconds of action and a 1 second pause at 100 Hz. The main
W18 • DFSL Diadynamic. (Medical program).

It is a diadynamic biphasic current with 5 seconds of action and a 2 second pause at 100 Hz. The main
W19 • CP Current. (Medical program).

It is composed of alternated single-phase (3 seconds) and biphasic (3 seconds) waveforms. The short
term current has an essentially dynamogenic effect. This action promotes contraction of the striated
muscles, improves the nutritional status of the tissue and facilitates the re-absorption of post-
traumatic oedemas. Frequency alternating current is clearly perceptible: the DF current produces a
light tremble while the MF current produces a strong pulsation.
Physiological effects: This kind of current has a strong dynamogenic effect (or trophic effect) and a
great analgesic effect, especially in the case of chronic pain. Moreover, the CP current is particularly
effective with regard to the re-absorption of haematomas and oedemas. Indications: It is used in the
short term to treat pain resulting from the inflammation of tendons, articular capsule and soft tissues

(tendinitis, bursitis, rheumatoid arthritis and trauma in general). Total program duration: 15 minutes in
a single phase. Intensity: should be adjusted to a level between the thresholds of perception and pain.
W20 • LP Current. (Medical program).

It is composed of alternated single-phase (10 seconds) and biphasic (5 seconds) waveforms. The long
term current has essentially an inhibiting action on muscle and sensibility: as a consequence it
produces analgesia and relaxation of the striated muscles.
Total program duration: 15 minutes in a single phase. Intensity: should be adjusted to a level between
the thresholds of perception and pain.
W21 • HVPC. (Medical program).

HVPC can be used for the reconstruction of tissue, the re-absorption of oedemas and the reduction
of pain.
For repairing tissue, place a sterile gauze dampened with a saline solution on the wound: if the anode
(positive electrode) is placed over the wound, the migration of vascular cells and the synthesis of
collagen occur, increasing the speed of recovery. If the cathode (negative electrode) is placed over the
wound, a bactericide effect occurs and the growth of pathogenic microorganisms is delayed.
W22 • Kotz Current. (Medical program)

The Kotz current was discovered by Y. M. Kotz in the 1970s. It is a middle-frequency current and is
used for the strengthening of normally innervated muscle. A 2.5 kHz interrupted carrier current is
used. It is characterised by 10ms packages with 10ms pauses in between; therefore 50 packages of
impulses are supplied per second. The program consists of 10 seconds of stimulation (with the
aforementioned parameters) and 20 seconds of rest. Total program duration: 10 minutes.
The Kotz excitomotor effect occurs in deep muscles because of their lower resistance. In fact it has
been demonstrated that the electrical impedance skin decreases with an increase in frequency.
Intensity: adjusted in order to produce good contractions of muscles stimulated at the pain threshold.
Maximum adjustable intensity: 50. The intensity is adjustable only during the 10 seconds of the supply
of impulses and not during the OFF phase.
Active channels: Ch1 and Ch2.
Position of electrodes: see photographs 01 to 22.
NEOFARADIC CURRENT
The neofaradic current is used for the stimulation of normal muscle. It is suitable for treating
muscular hypotrophy, and the contraction of muscles also has a positive effect on bones and articular
circulation.
The programs W23, W24 and W25 are composed of 2 phases:
The first phase lasts 33 seconds and is for selecting the intensity of contraction. When the desired
level is reached, press the RIGHT ARROW key to confirm. Next, press the intensity increase key of
any channel: phase 2 will begin automatically at the selected intensity (90% first turn, 95% second
turn, 100% third turn).
The second phase lasts 15 minutes and it alternates 10 seconds of recovery with 5 seconds of
contraction.
W23, W24, W25 Neofaradic 20, 50, 100 Hz Total program duration: 15 min 33 sec
Position of electrodes: photographs 01 to 22
Phase 1 Phase 2
Test phase duration 33 seconds Work duration 15 minutes

W23 • Neofaradic 20 Hz. (Medical program)
It is a low frequency (20 Hz) current that is used to produce individual muscular contractions. It
consists of 5 seconds of stimulation and a 10 second pause.
Intensity: adjusted for good contraction of the muscles stimulated.

It is a middle frequency current (50 Hz) used to obtain muscular tetanus; it consists of 5 seconds of
stimulation and a 10 second pause.
Intensity: adjusted in order to produce good contractions of muscles stimulated almost at the pain
threshold.

It is a high frequency current (100 Hz) used to obtain muscular tetanus; it consists of 5 seconds of
stimulation and a 10 second pause.
Intensity: adjusted in order to produce good contractions of muscles stimulated at the pain threshold.
W26 • Interferential. (Medical program)

Interferential therapy is based on the interference of two sinusoidal currents at different frequencies
applied to the patient; the resultant current, endogenously generated, is a new kind of current. Its
frequencies are respectively the difference and the sum of the two initial frequencies and their
multiples.
There are several advantages to this current: easy transfer through the skin, no sensation of pain for
the patient, an excellent therapeutic effect in depth, no electrolytic effects.
Position of electrodes: see following figure.
Intensity: adjusted in order to produce a good tingling, not painful.
REHAB programs.
R01 • Denervated. (Medical program)
This program is specifically indicated for the treatment of denervated muscles, i.e. with complete
rupturing of the peripheral nerve. In this case it is not possible to stimulate the muscle through its
nerve fibres: it is necessary, instead, to stimulate the muscle fibres directly.
Impulses have a longer duration (calculated in milliseconds and not in microseconds as in the case of
normal innervated muscle) and a much lower frequency.
The recommended intensity should be adjusted to stimulate the muscle with a short contraction every
2 seconds. Program duration: 20 minutes in a single phase.
Position of electrodes: use 2 big electrodes, better if wet and in a sponge, placed at the two ends of the
muscle to be treated.

R02 • Partially denervated. (Medical program)
This program is specifically indicated for the treatment of partially denervated muscles, i.e. with partial
rupturing of the peripheral nerve. The purpose of the program is to stimulate the healthy innervated
part of the muscle. The intensity should be adjusted in order to produce a good contraction of the
treated muscle.
Program duration: 20 minutes in a single phase.
WARNING: In the case of the programs R01 and R02 we recommend rectangular electrodes
(measuring 50x90 mm) for medium-high intensities. With smaller electrodes, the device could
generate an alarm and, therefore, not perform the treatment correctly.
R03 • Stress Incontinence. (Medical program).

Program duration 13 minutes, intensity set above the threshold of perception to produce light internal
stimulation.
This program, for which no photographs are provided regarding the position of the electrodes,
requires the use of appropriate internal stimulation probes, supplied separately together with the
relative instructions.
We recommend that you consult your doctor before using this program and during the treatment.
R04 • Urgency Incontinence. (Medical program).

stimulation.
R05 • Mixed Incontinence. (Medical program).

stimulation.
WARNING: in the case of the programs R03, R04 and R05, we recommend certified probes (class IIa
medical devices). The datasheet of the probes must contain information on use, storage and cleaning
precautions and any other useful information.
R06 • Anti-inflammatory. (Medical program).

Program recommended for inflammatory conditions. Apply until the inflammatory state is reduced.
Up to 2 treatments daily if required. Intensity adjusted just above the threshold of perception. Identify
the area to be treated and position the electrodes as shown in figure 1 page 12.
R07 • Neck pain / Headache. (Medical program).

Specific program for the treatment of pain in the neck area.
level is the moment in which the muscles surrounding the area treated begin to contract. The first
benefits can be seen after 10 to 12 treatments carried out on a daily basis; proceed with the treatment
until the symptoms pass.

R07 Neck pain/Headache Total program duration: 33 minutes
Position of electrodes: cervical (see photograph 25).
Phase 1 Phase 2
Short width Tens impulse 30 min. De-contracting 3 min.
R08 • Backache/Sciatic pain. (Medical program).

Specific program for the treatment of pain in the lumbar area or along the sciatic nerve, or both.
level is the moment in which the muscles surrounding the area treated begin to contract; over this
limit stimulation does not become more effective, just more irritating, so it is best to stop before that
point. The first benefits can be seen after 12 to 15 treatments carried out on a daily basis; proceed
with the treatment until the symptoms pass.
R08 Backache/Sciatic pain Total program duration: 35 minutes

Position of electrodes: dorsal/paravertebral (photograph 10), lumbar area (photograph 27), sciatic area
(photograph 28).
Phase 1 Phase 2
Short width Tens impulse 30 min. Tens Burst impulse 5 min.
R09 • Sprains / Bruises. (Medical program).

The program effectively inhibits localised pain caused by this type of injury. Intensity: should be
adjusted to a level between the thresholds of perception and pain.
Number of treatments: until pain is lessened, on a daily basis (even 2/3 times a day).
R09 Sprains/Bruises Total program duration: 30 minutes

Position of electrodes: ankle (see photograph 32).
Phase 1 Phase 2
Tens rapid 15 min. Emathoma impulse 15 min.
R10 • Hand and wrist pain. (Medical program).

This program is suitable for all types of hand and wrist pain (for example Carpal Tunnel Syndrome).
level is the moment in which the muscles surrounding the area treated begin to contract. Intensity has
to be adjusted 3 times, for each starting phase. Impulses at different frequencies stimulate different
sized nerve fibres promoting an inhibitory action at spinal level.
R10 Hand and wrist pain Total program duration: 40 minutes

Phase 1 Phase 2 Phase 3
Tens 70Hz, 15 min Tens 90Hz, 15 min Tens 110Hz, 10 min
R11 • Plantar stimulation. (Not medical program)

This program has a relaxing and draining effect on the limb stimulated. It is ideal for people suffering
from a sense of “heaviness in the legs”.
Duration: 40 minutes. Intensity: set above the threshold of perception.
Position of electrodes: 2 electrodes (one positive, the other negative) on the sole of the foot, one
close to the toes, the other under the heel.
R11 Plantar stimulation Total program duration: 40 minutes


R12 • Epicondylitis. (Medical Program).
Also known as “tennis elbow”, it is an insertional tendinopathy concerning insertion of the elbow
bone into the epicondylar muscles, those enabling finger and wrist extension (bending backwards). 15
applications once a day (even twice), until the symptoms pass. We recommend that you consult your
doctor to identify the precise cause of the pain in order to prevent the condition from reoccurring.
Program duration 40 minutes, intensity adjusted above the threshold of perception.
R12 Epicondylitis Total program duration: 40 minutes

Position of electrodes: see photograph 29.
R13 • Epitroclea. (Medical program).

Also known as “golfing elbow”, it affects golfers but also those who carry out repetitive tasks or tasks
involving frequent intense strain (for example carrying a particularly heavy suitcase). It causes pain in
the flexor and pronator tendons inserted in the epitroclea. Pain is felt when bending or straightening
the wrist against resistance, or when clenching a hard rubber ball in the hand. 15 applications once a
day (even twice), until the symptoms pass. We recommend that you consult your doctor to identify
the precise cause of the pain in order to prevent the condition from reoccurring.
Program duration 40 minutes, intensity adjusted above the threshold of perception.
R13 Epitroclea Total program duration: 40 minutes

Position of electrodes: photograph 29 with electrodes moved towards the inside of the arm (rotated by
90°).
Phase 1 Phase 2
Tens 90Hz, 20 min Tens 70Hz, 20 min
R14 • Periarthritis. (Medical program).

Scapulo-humeral periarthritis is an inflammatory condition affecting the fibrous tissues surrounding
joints: tendons, serous sacs and connective tissue. These appear altered and can break into fragments
and calcify. If neglected, this condition can become heavily crippling. For this reason, after carrying
out a cycle of 15/20 applications once a day, we recommend that you consult your doctor for a cycle
of specific rehabilitation exercises to reduce the pain.
The R14 program consists of various phases including Tens and muscle stimulation aimed at
improving the tone of the muscles surrounding the joint.
Program duration 41 minutes, intensity set above the threshold of perception with small muscle
contractions at the end of the program (10 minutes before the end).
R14 Periarthritis Total program duration: 41 minutes

Position of electrodes: periarthritis (see photograph 26).
Tens 150Hz, 1 min Tens 90Hz, 30 min EMS 10 min
R15 • Neuralgias. (Medical program)

Neuralgia Program, single-phase, 30 minutes of duration. Intensity adjusted just above the threshold
of perception. Two treatments daily for 10/12 days.
R16 • Menstrual pains. (Medical program).

R16 Menstrual pains Total program duration: 35 minutes
Position of electrodes: 2 electrodes of the channel 1 on lower abdomen.
Phase 1 Phase 2
Tens 90Hz, 30 min Tens Burst, 5 min
Intensity: adjusted in order to produce a light tingling, not painful.
R17 • Carpal tunnel. (Medical program).

Program duration: 30 minutes in a single phase. Position of electrodes: see photograph 33.
R18 • Tendinitis. (Medical program).

Program duration: 20 minutes in a single phase. Position of electrodes: 2 electrodes of channel 1 on
painful area.
R19 • Strain. (Medical program).

treated area.
Intensity: adjusted between 6 and 12. The maximum adjustable intensity is 12.
R20 • Muscular tears. (Medical program).

treated area.
Intensity: adjusted between 6 and 12. The maximum adjustable intensity is 12.
R21 • Herpes Zoster. (Medical program).

Program duration: 30 minutes in a single phase. Position of electrodes: use channels 1 and 2 and form
a square as shown in figure 1 page 12.
R22 • Wounds/healing. (Medical program).

Position of electrodes: use the 2 electrodes of channel 1. Use rubber and buckskin electrodes or
conductive rubber sponge-covered electrodes.
For repairing tissue, place sterile gauze dampened with a saline solution on the wound: the positive
electrode is placed on the wound, and the negative electrode is placed distally or (if the treated zone is
too thick) at 10 cm of distance. This causes migration of the vascular cells and the synthesis of
collagen, increasing the speed of recovery. Total program duration: 15 minutes in a single phase.
Intensity: should be adjusted to a level between the thresholds of perception and pain.
R23 • Wounds/bactericide. (Medical program).

Position of electrodes: use the 2 electrodes of channel 1. Use rubber and buckskin electrodes or
conductive rubber sponge-covered electrodes.
Place a sterile gauze dampened with a saline solution on the wound to kill any bacteria. Cathode
(positive electrode, red plug) is placed on the wound and negative electrode is placed distally or ( if the
treated zone is too thick) at a distance of 10 cm. This provokes a bactericide effect and consequently
the growth of pathogenic microorganisms is delayed.
R24 • Venous insufficiency. (Medical program).

The program is indicated for the treatment of venous insufficiency. Position the 2 electrodes of
channel 1 on the left calf and the 2 electrodes of channel 2 on the right calf. It is possible to use
square or rectangular electrodes according to the size of the calf and the comfort of the patient. Start
the program by selecting an intensity able to produce a good (not painful) muscular contraction.

R25 • Superficial osteogenesis. (Medical program).

A study of the healing of fractures was carried out in 1968 in Japan and the United States. This study
consists of two main techniques:
1. The implanting of sharp needle electrodes near the bone to be calcified (invasive
technique).
2. The positioning of self-adhesive electrodes on the external surface near the bone.
We consider the second technique for the treatment of fractures, in particular when the bone to be
stimulated is in a superficial position (vertebral column, wrist, kneecap, ankle, etc.). This technique is
not suitable if the bone is in a deep position (femur, humerus, radius, etc.).
2 electrodes of channel 1 have to be positioned 10 cm apart near the bone to be treated.
The program lasts 60 minutes and it can be repeated several times a day (up to 4/5 times).
The maximum adjustable intensity is 30.
For the treatment of the vertebral column use 2 rectangular electrodes measuring 50x90mm. To treat
smaller zones (for example the wrist), use electrodes measuring 48x48mm.
Table of current density with electrodes measuring 48x48mm:

Value displayed on screen Current density mA/cm² Current density μA/cm²
5 0.034 34
10* 0.068 68
20 0.137 137
30 0.205 205
Table of current density with electrodes measuring 50x90mm:

Value displayed on screen Current density mA/cm² Current density μA/cm²
5 0.0175 17.5
10* 0.035 35
20* 0.07 70
30 0.105 105
* The recommended intensity ranges are in bold.
EMS programs.
IMPORTANT. Intensity of stimulation: EMS programs (Firming up and Toning up, Strength,
Endurance, Agonist/Antagonist) are divided in 3 phases: warm up phase, work phase, recovery phase.
During the warm up phase (phase 1) the intensity of stimulation has to be set in order to produce
reasonable solicitation of the muscle and warm it up without causing fatigue (1830mA). During the
work phases (the middle phases of each program), T-ONE alternates contraction impulses with active
recovery impulses. The two intensities must be selected separately: the contraction intensity (shown by
a full bar on the display) should be set at 2030 for not very trained people, 3050mA for trained
people, over 50mA for well trained people.
We suggest that you set the recovery intensity value (between one contraction and another) at about
1015% less than the contraction intensity value. During the last recovery phase, the intensity value
has to be set for good massaging of the stimulated part, without producing pain (1830).
E01 • Firming up.

Indicated for firming up muscles in the arms and bust, or the legs; working mainly on slow-twitch
fibres. Treatment frequency: 3/4 times in a week.
The intensity must be sufficient to produce good but not painful muscle contractions (15 as an initial
value) increasing it gradually week by week.

Programs and muscle groups of interest with electrodes position photograph as reference:
E01 Firming up Total program duration: 30 minutes

Biceps (photograph 02/15), Triceps (photograph 03/16), Hand Extensors (photograph
04), Hand Flexors (photograph 05), Deltoid (photograph 06).
Abdominals (photograph 01/20), Pectoral/Breast (photograph 07/17), Trapezius

(photograph 08), Large dorsal (photograph 09), Gluteus (photograph 19).
Quadriceps/thighs (photograph 11/18), Biceps femoris (photograph 12), Calves

(photograph 13), Anterior tibial (photograph 14).

20 min. Training
5 min. Warm up 13 sec. recovery 5 min. Recovery
7 sec. Work 30Hz
E02 • Toning up.

The toning up program is suitable for improving trophsim and for the recovery of normal strength in
the treated muscle. This program is indicated after a complete cycle of a minimum of 10 treatments
with the “E01 Firming up” program.
Treatment frequency: 2/3 weekly sessions.
Stimulation intensity has to be middle/high with a contraction between the thresholds of perception
and pain (2030). Benefits can be seen after just 10/15 treatments and these become more definite
after two months of regular treatment.
Programs and muscle groups of interest with photographs showing the position of the electrodes:
E02 Toning up Total program duration: 30 minutes



(photograph 13), Anterior tibial (photograph ).

20 min. Training
7 sec. Work 45Hz
E03 • Basic strength.

The basic strength program is used in sport to develop basic strength which, by definition, is the
maximum tension that a muscle can exert against constant resistance. The contractions alternate with
periods of active recovery during the work phase, allowing the muscle to be trained without subjecting
it to stress and improving oxygenation of the same muscle.
The basic rule for obtaining initial results is as follows: two sessions per week (for each muscle region)
for the first three weeks at increasing intensity (2030), three sessions per week for the next three
weeks at high intensity (3050).
Intensity must be increased gradually treatment by treatment, without overstraining the muscles. In
the event of fatigue, suspend training for a few days and revert to the “E09 Muscle Recovery”
program instead.
WARNING: the program involves an automatic increase in intensity between the second and the
third phase. Consequently it will not be necessary to adjust stimulation intensity between phases but
only press the Up arrow key for any one of the 4 channels. The first work/recovery cycle of phase 3
will start at an intensity of 90% of that set for phase 2; the second work/recovery cycle will go up to
95% of intensity and finally the third work/recovery cycle will go up to 100% of the intensity set for
phase 2.
Programs and muscle groups of interest with electrodes position photographs as reference:
E03 Basic strength Total program duration: 30 minutes



Phase 1 Phase 2 Phase 3 Phase 4

Automatic Increase
10 min. Training 10 min. Training

5 min. Warm up 13 sec. recovery 14 sec. recovery 5 min. Recovery
Intensity
7 sec. Work 50Hz 6 sec. Work 70Hz
E04 • Fast Strength.

This program is designed to increase speed in fast athletes and develop it in athletes lacking the
quality.
The exercise assumes a fast pace and the contraction is short, as is the recovery. It is usually best to
complete a three-week basic strength cycle of increasing intensity before using this program. Then
continue with three weeks of fast strength three times a week at high intensity (3050).
phase 2.

E04 Fast Strength Total program duration: 26 minutes



Automatic
Intensity
Increase
6 sec. work 5 sec. work
E05 • Explosive Strength.

Explosive strength programs increase the explosive power and speed of the muscle mass, with
extremely short, strengthening contractions and very long active recovery times to allow the muscle to
regain strength. It is usually best to complete a three-week basic strength cycle of increasing intensity
before using this program. Then continue with three weeks of explosive strength twice a week. During
the contraction, the intensity must be the highest that can be endured in order to obtain maximum
muscle exertion whilst involving the greatest number of fibres (over 35).
phase 2.
E05 Explosive Strength Total program duration: 28 minutes



Automatic Increase

Intensity


E06 • Resistant Strength.
This program is designed to help increase resistance to physical stress, or rather withstand intense
exertion for a longer amount of time in muscle regions subjected to stimulation. Indicated for sporting
disciplines involving long, intense periods of exertion.
Intensity of stimulation during work: follow the indications mentioned at the beginning of the “EMS
Program” chapter.
phase 2.
E06 Resistant Strength Total program duration: 30 minutes




Automatic

Intensity
Increase

E07 • Endurance.
The Endurance program is used in sports to increase muscle endurance capacity, acting mainly on
slow-twitch fibres.
Program indicated for endurance sports: marathon runners, cross-country runners, ironman, etc.
Program” chapter.
phase 2.

E07 Endurance Total program duration: 50 minutes


Automatic
Intensity
Increase
E08 • Capillarisation.
This program significantly increases arterial flow in the area treated. Prolonged use of this program
develops the intramuscular capillary network of fast-twitch fibres. The effect obtained is an increase in
the capacity of fast-twitch fibres to withstand strain over extended periods of time.
For an athlete with good endurance, the capillarisation program is very useful for recovery after
intense aerobic work, before anaerobic work and when training is not possible (due to bad weather or
an injury). Program duration: 30 minutes / one phase. Recommended intensity of stimulation:
medium (2030).
E09 • Muscle Recovery.

Can be used for all sports, after competitions or the most demanding training sessions, in particular
after long and intense exertion. To be used immediately after exertion. Helps drainage and winding
down, improving muscle oxygenation and helping to discharge synthetic substances produced during
exertion. Program duration: 15 minutes / one phase. Intensity of stimulation: medium-low (1525),
increased during the last 5 minutes.
E10 • Agonist / Antagonist.

The electric stimulator produces alternating contractions on the 4 channels: during the first phase of
warm-up the 4 channels work simultaneously, during the second work phase muscle contractions are
alternated between Channel 1 and 2 (agonist muscles) and Channel 3 and 4 (antagonist muscles). The
program is designed to restore muscle tone to the quadriceps and its antagonist the leg biceps, or the
biceps brachii and the triceps. The work aims at developing strength.
In the second work phase it is necessary to select the intensity 3 times: recovery intensity of four
channels, work intensity of Channels 1 and 2 (agonist muscles) and work intensity of Channels 3 and 4
(antagonist muscles).
Program” chapter. Intensity must be increased gradually treatment by treatment, without overstraining
the muscles. Suspend training for a few days in the event of fatigue and proceed with the “E09 Muscle
Recovery” program.

E10 Agonist / Antagonist Total program duration: 33 minutes
Biceps (CH1+CH2 - photograph 02) / Triceps (CH3+CH4 – photograph 03),
Hand Extensors (CH1+CH2 – photograph 04) / Hand Flexors (CH3+CH4 -
photograph 05).
Quadriceps (CH1+CH2 – photograph 11) / Femoral biceps (CH3+CH4 - photograph
12).
20 min. work alternated over channel pairs:
7sec. work on CH1/CH2 + 7sec. work on CH3/CH4
E11 • Lipolysis.
This program is widely used in the field of beauty treatments to increase micro-circulation and
promote lymphatic activity in areas where there are fatty deposits. This program greatly increases the
local metabolism thanks to its trophic action; it helps to reduce the orange-peel effect when combined
with a low-calorie diet. Treatment sessions can have a daily frequency.
The program produces sequential tonic contractions (first CH1/CH2 then CH3/CH4), reproducing
the typical effect of electronic lymphatic drainage. The logic for application of the electrodes is the
following: CH1/CH2 at the extremities of the limbs (for example the calf or forearm) and CH3/CH4
at the top (for example the thigh or biceps brachii).
Intensity of stimulation: to produce good ( not painful) effects in the stimulated areas (2030).
E11 Lipolysis Total program duration: 30 minutes

Hands Extensors CH1 (photograph 04 with 2 electrodes) / Hands Flexors CH2
Lower (photograph 05 with 2 electrodes);
Muscles: Biceps brachii CH3 (photograph 02 with 2 electrodes) / Triceps CH4 (photograph 03
with 2 electrodes)
Calves CH1 (photograph 13 with 2 electrodes) / Anterior tibial muscles CH2
Lower
(photograph 14 with 2 electrodes); Quadriceps CH3 (photograph 11 with 2 electrodes) /
Muscles:
Femoral biceps CH4 (photograph 12 with 2 electrodes)
20 min. work alternated over channel pairs:
6 sec. recovery
5 min. Warm up 5 min. Recovery
7sec. work on CH1/CH2
7sec. work on CH3/CH4
E12 • Drainage.
The purpose of these programs is to promote drainage, increasing microcirculation inside and around
treated muscular fibres, also creating rhythmic contractions to facilitate the flow of algogenic
substances and lymphatic activity. This program can be useful for elderly people, to aid blood
circulation and lymphatic circulation.
Sequential tonic contractions are carried out during phases 2 and 3 to produce the typical effect of
electronic lymphatic drainage. However, unlike the lipolysis program, the contractions are sequential:
first CH1, then CH2, CH3 and CH4.
There are no real limits to the use of these programs, so they can continue to be used until the desired
result is achieved.
The intensity of stimulation must be such to assure good muscular contractions during treatment, but
not so strong as to generate soreness (2030).
Normally, benefits are discernible after 3/4 weeks with 4/5 treatments a week.
Program and muscle groups of interest with photographs showing the position of the electrodes:

E12 Drainage Total program duration: 25 minutes
Lower Muscles: all the muscles you want to stimulate in sequence. Connect one channel per muscle,
bearing in mind that the contractions are sequential on 4 channels.
3 min. Warm up 20 min. sequential contractions on 4 channels 2 min. Recovery
E13 • Microlifting.
The following program, with a duration of 15 minutes, is used to tone facial muscles using a special
impulse to improve both the appearance and the dynamism of facial muscles.
The position of the electrodes is shown in the photographs of electrode positions (photograph 24).
N.B. a minimum distance of 3cm. must be kept between the electrode and the eyeball.
IMPORTANT: take care when adjusting the intensity as facial muscles are particularly sensitive;
intensity should be increased gradually, starting with a very low level of stimulation (for example 310)
and increasing it with extreme care until you reach a good level of stimulation, represented by good
muscle activation.
IMPORTANT: it is not necessary to reach levels of intensity capable of causing discomfort! The
equation “more pain = more gain” is completely misleading and counterproductive.
Great and significant results are obtained through consistency and patience.
E14 • Atrophy prevention. (Medical program).

Program created to maintain muscle trophism.
This treatment focuses on the toning of muscles, and of slow-twitch fibres in particular. Particularly
indicated for patients recovering from an accident or an operation. Prevents the reduction of muscle
trophism caused by physical inactivity. The muscle area concerned can be stimulated with daily
applications of low intensity; if you increase the intensity, leave a day of rest between applications to
allow the muscles to recover.
phase 2.
E14 Prevention of atrophy Total program duration: 30 minutes

Biceps (photograph 02/15),Triceps (photograph 03/16), Hands Extensors (photograph
04), Hands Flexors (photograph 05), Deltoid (photograph 06).

(photograph 08), Large dorsal (photograph 09), Gluteus (photograph 19), Abdomen
Obliques (photograph 22), Hip (photograph 23).
Quadriceps/thighs (photograph 11/18), Femoral biceps (photograph 12), Calves

(photograph 13), Anterior tibial muscles (photograph 14).

Automatic
Intensity
10 min. 10 min.
Increase


E15 • Atrophy. (Medical program).
This program acts selectively on slow-twitch fibres. Ideal for recovering muscle trophism after a long
period of inactivity or an accident.
Program to be carried out when loss of muscle tone has already occurred. Apply with caution (at low
intensity, enough to produce light muscle contractions) in the first 2/3 weeks. Increase intensity
progressively over the next 3/4 weeks. Application on alternate days.
E15 Atrophy Total program duration: 30 minutes

Biceps (photograph 02/15),Triceps (photograph 03/16), Hands Extensors (photograph
04), Hands Flexors (photograph 05), Deltoid (photograph 06).

(photograph 08), Large dorsal (photograph 09), Gluteus (photograph 19), Abdomen
Obliques (photograph 22), Hip (photograph 23).
Quadriceps/thighs (photograph 11/18), Femoral biceps (photograph 12), Calves

(photograph 13), Anterior tibial muscles (photograph 14).
3 min. Warm up 25 min: 6 sec. recovery + 6 sec. work 2 min. Recovery
E16 • Sequential tonic contractions 1.

This program increases microcirculation within and around the muscle fibres treated creating
rhythmic contractions, promoting better drainage and toning. It can also be applied to older people to
improve blood and lymphatic circulation in the lower limbs (e.g. applying CH1 to the right calf, CH2
to the left calf, CH3 to the right thigh, CH4 to the left thigh).
The programs produce sequential tonic contractions on 4 channels to produce the typical effect of
electronic lymphatic drainage. These programs can be carried out using self-adhesive electrodes. The
intensity of stimulation must be such to assure good muscular contractions during treatment, but not
so strong as to generate soreness (2025). It mainly works on slow-twitch fibres.
E16 Sequential tonic contractions 1 Total program duration: 25 minutes

Lower Muscles: all you want to stimulate in a sequence
20 min. sequential contractions on 4 channels
3 min. Warm up 2 min. Recovery
6 sec duration each
E17 • Sequential tonic contractions 2.

This program produces rhythmic contractions with a stimulation frequency typical of fast-twitch
fibres. Thanks to the high stimulation frequency it is suitable for increasing muscle strength
sequentially.
The programs produce sequential phasic contractions on four channels in phase 2 and 3. These
programs can be carried out using self-adhesive electrodes. The intensity of stimulation must be such
to assure good muscular contractions during treatment, but not so strong as to generate soreness
(2040).

Unlike the previous program, this one uses a higher stimulation frequency during the contraction
phase and therefore works mainly on fast-twitch fibres.
E17 Sequential tonic contractions 2 Total program duration: 25 minutes

Lower Muscles: all you want to stimulate in a sequence
20 min. sequential contractions on 4 .
3 min. Warm up
channels 6 sec duration each 2 min. Recovery
Programmable memories.
M01/M02 • Denervated 1/2. (Medical program).

Stimulation programs for denervated muscle. Active channels: CH1.
Position of electrodes: use 2 big electrodes, better if wet and in a sponge, placed at the two ends of the
muscle to be treated.
Use the left and right arrow keys to scroll through the menu and select the stimulation parameter, and
use the up and down keys to modify the values.
After setting all the stimulation parameters, click on OK to save the program.
To start the saved program, press the OK key.
Three sound signals alert to the end of the program.
In the case of impulses longer than 100ms, set the maximum intensity at 1 Hz.

Table of settable values:
PARAMETER DESCRIPTION MIN MAX
Frequency 0.25 Hertz 2 Hertz
Impulse width 40 milliseconds 400 milliseconds
Total time 1 minute 60 minutes
WARNING: In the case of programs M01 and M02, we recommend the use of rectangular electrodes
(measuring 50x90 mm) for stimulation at medium-high intensity. With smaller electrodes, the device
could generate an alarm and, therefore, not perform the treatment correctly.
M03/M04/M05/M06 • TENS memory 3/4/5/6. (Medical program).

Available programs to set rapid tens, endorphinic tens, maximum values.
Position of electrodes: form a square above the area to be treated as shown in figure 1.

Impulse width 20 microseconds 500 microseconds
M07 • TENS Spyke. (Medical program).

Available programs to set Tens Spyke.
Position of electrodes: form a square above the area to be treated as shown in figure 1.

M08/M09 • EMS 1 second slope.

EMS 1 sec. slope: to set the EMS program with a 1 second impulse slope.
IMPORTANT: 1 second slopes make for a faster contraction, while 2/3 second slopes make for a
more progressive contraction. In the case of memories 12 and 13 in particular, a 3 second slope can be
used to obtain a “triangular” impulse where the impulse parameters are continuously adjusted. This
Use the leftisand
program right arrow
specifically keys tofor
indicated scroll
the through
treatmentthe
ofmenu anddenervated
partially select the stimulation
muscles. parameter, and

Contraction frequency 20 Hertz 120 Hertz
Contraction time 2 seconds 10 seconds
Recovery frequency 0 Hertz 12 Hertz
Recovery time 2 seconds 28 seconds




M14/M15 • FES.
Available programs to set treatments for incontinence prevention and cure.

M16/M17/M18 • Agonist/antagonist 16/17/18.

Available programs to set treatments with alternated contractions on a pair of channels.
Position of electrodes: see the photographs in the position manual.

Instructions on use for electromyography (EMG) treatments
The I-TECH PHYSIO EMG has a biofeedback module based on the analysis of surface
electromyographic (EMG) signals. It was designed to evaluate and record the electrical activity
produced by the human body and provide feedback via two channels.
Bipolar electrodes process the bioelectrical signals. These signals are amplified, filtered, converted into
digital format and displayed on the screen (and saved in the memory when applicable).
The biofeedback is both visual (on the screen) and audible (with an internal buzzer).
The I-TECH PHYSIO EMG allows the user to record different levels of maximum voluntary
contraction of the two muscles and to set different feedback thresholds for each muscle.
To access the functions of the EMG module, simply click on the EMG icon in the main menu of the
I-TECH PHYSIO EMG: the main menu then appears as shown in the figure.
MAIN MENU
Ref. Contraction
Relative Feedback
Working Mode
Edit Target
The work menu of the 4/EMG module is as follows:

Mode Description
Records the level of reference contraction for

Reference Contraction calibrating the measurements in the relative
mode
Enables audible and visual feedback. The level

Relative Feedback of muscle activation is recorded in relation to
the reference contraction
This mode prevents exceeding a set threshold

Under Threshold
for each muscle
Working Mode
This mode is for maintaining a level of
Keep Level contraction expressed as a percentage of the
reference contraction
Permits setting the level of contraction to be

Edit Target
maintained for Keep Level mode
Permits enabling or disabling the channels and

Channel Settings setting the visualisation scale and the alarm
threshold
Saves or loads the settings for the device in one

Save/Load Settings
of the 4 available locations in the memory
Sets the epoch for calculating the width of the

Epoch Size
received signal (0.25 – 0.5 – 1 s)
Settings Permits editing of the identification code to

Filename ID
create the names of files containing the data
Permits editing of the tolerance to attain the

Target Error
level of contraction set in Keep Level mode
Resets the counters used to number the files

Reset Counters
containing the data

To the right in the figure below is the screen that appears when the user selects the mode for
recording the maximum voluntary contraction (MVC).
To the right in the figure below are the two screens that appear when the user selects the Under
Threshold feedback mode (A) instead of Keep Level mode (B).
To the right in the figure below is the screen that appears when the user wishes to select the working
mode.

To the right in the figure below is the screen that appears when the user wishes to select the Target.
The 4 figures below show all the screens that appear in the Setting mode.
Reference Contraction Mode
This functions permits recording of the reference contraction for each channel (each channel is
associated with one pair of electrodes).

In this mode, the instrument provides visual biofeedback in the form of the width of the
electromyographical signal standardised at the maximum acceptable value. The PHYSIO 4/EMG
system automatically records the maximum signal for each of the active channels.
Press "ESC" to exit Reference Contraction mode and return to the main menu; the Up and Down
arrows keys are not used in this mode.
Re-entering Reference contraction mode resets the data ready for reassessment.
In this mode, press OK once to record the course of the signal (when applicable), i.e. the average
rectified values (ARVs) of the current contraction. To close the file, press the OK key again.
Relative Feedback Mode
This functions permits recording of the reference contraction for each channel (each channel is
associated with one pair of electrodes).
In this mode, visual and audible feedback is provided for the patient as a percentage of the reference
contraction for the various channels, which must have been previously recorded for each channel. The
screens differ according to the selected type of mode (Working Mode) selected (Keep Level or Under
Threshold).
The Under Threshold mode is shown in the figure to the left. The system shows 2 dotted vertical bars
that indicate the threshold set for each channel. A horizontal bar increases or decreases its width in
proportion to the level of contraction and keeps within a maximum range relating to the intensity of
the reference contraction.
The Keep Level mode is shown to the right. The two dotted vertical lines indicate the maximum and
minimum strength values within which the user must remain to maintain the level.
The distance between the dotted vertical lines corresponds to the degree of precision required to
maintain the required level. This precision can be modified in the Advanced Settings menu following
the instructions provided further on.
The Target value set in the Keep Level section is calculated as the average of the width of the active
channels. The contraction level, i.e. the ARVs, can be recorded when applicable. Use the Up and
Down arrow keys to edit the value of the target and, therefore, the position of the dotted vertical bars.
In both Relative Feedback modes, press OK to start recording the signals of each active channel and
then press it again to stop recording. The format of the recorded files is described in the next section
of this manual.
Working Mode Function
Use the Up and Down arrow keys in the main window to enter the sub-menu for selecting the relative
working mode of the instrument and setting the required function. Press OK to save the selected
function and use the Left arrow key to return to the previous screen.
Working Mode Function
This parameter is for adjusting the level of deviation from the set maximum and minimum thresholds
of the PHYSIO EMG for the Relative Feedback  Keep Level mode. The target can be set at a value
between 0 and 98% in steps of 2%. Use the Up and Down arrow keys to edit the target deviation
value. Press OK to save the new value and automatically return to the previous screen, and use the
Left arrow key to return to the previous screen without saving the changes.

Settings
This menu enables the user to edit the instrument's settings.
Channel SettingsThis function permits modification of the settings of each channel. Use the arrow
keys to select a parameter and press OK to then scroll through the possible values and edit the
parameter. It is possible to change the status of each channel (ON or OFF), change the gain (x1, x2,
x4 and x8) and change the threshold for Under Threshold mode in steps of 2%.
Save/LoadSettings. This function is for saving new parameters or loading ones already saved.

EpochSize.This parameter is used to calculate ARVs. The basic EMG signal is rectified and average
over time intervals called epochs. The values can be 0.25 s, 0.5 s and 1 s. Increasing the duration of
the epoch increases the stability of the ARVs and also of the feedback signal, but decreases the speed
of response.
Filename ID. the string represents a part of the name of the saved file to which is added a
progressive number incremented for each file.
Target Error. This value determines the precision, as a percentage, for maintaining the set level of
contraction. The value can be set at between 1 and 9%.
Reset Counters. Press OK when this item is selected in the menu to reset the counters for the
progressive numbering of the data files saved on the I-TECH PHYSIO EMG.
Handling
and care
Charging the battery
The display shows when the battery is low:
Batteries fully Batteries partially Batteries fully

charged discharged discharged
BATTERIA SCARICA (battery low) appears on the display when the batteries run low.
In this case, connect the battery charger to the relative connector on the small rear panel of the device.
To replace the battery, please contact the manufacturer or a specialist technical centre. Replace the
battery only with one of the same model provided by the manufacturer.
Cleaning the equipment

Use a soft dry cloth to remove dust.
Use a small sponge dampened with a water and alcohol solution to remove any stubborn stains.
WARNING: never clean the device when it is in operation. Disconnect the device from the battery charger
and disconnect all the connection cables before cleaning the device.

Always observe the recommendations above and contact the manufacturer for information on any other
cleaning/maintenance operations.
Operation, transport and storage
The device is designed to operate in the following ambient conditions:
ambient temperature +0 to + 40 °C
relative humidity 10 to 93%
pressure 700 to 1060 hPa
Precautions for transport

No special precautions need to be taken for transport because the I-TECH PHYSIO 4/EMG is a portable
device.
It is advisable to always put the I-TECH PHYSIO 4/EMG and its accessories back in the carrying
case provided after use.
Precautions for storage
The equipment is designed to withstand the following ambient conditions (with or without the case
provided):
ambient temperature -25 to + 70 °C
relative humidity up to 93%
pressure 700 to 1060 hPa
Information on disposal
The product is subject to the WEEE regulations (as indicated by the symbol on the label)
concerning differentiated waste collection: take the product to an electronic waste recycling centre or
contact the manufacturer.
Maintenance and troubleshooting
The equipment does not require any particular routine maintenance when used in the manner
indicated in this manual.
It is advisable to have the device inspected by the manufacturer once every 24 months in order to
guarantee correct operation and compliance with the requirements concerning safety and efficiency.
If any faults or problems occur during use of the I-TECH PHYSIO 4/EMG, please refer to the
troubleshooting guide below:
 The I-TECH PHYSIO 4 does not turn on. Check that the battery is not dead (refer to the section
"Charging the battery"). If the problem persists please contact the manufacturer.
 The I-TECH PHYSIO 4/EMG does not transmit electrical impulses.Check all the connections,
cables and applicators as indicated in this manual. If the problem persists please contact the
manufacturer.
 The I-TECH PHYSIO 4/EMG turns itself off during operation.Check the battery to see if it is
low, contact the manufacturer.
Assistance
Please contact the manufacturer for all technical assistance regarding the equipment. To request
technical assistance, contact:
I.A.C.E.R. S.r.l.
Tel. +39 041.5401356 • Fax +39 041.5402684
Technical documents concerning repairable parts can be provided only with the consent of the
company and only when the personnel entrusted with maintenance have received appropriate training.
Spare parts
The manufacturer can provide original spare parts for the equipment at any time. To request spare
parts:

I.A.C.E.R. S.r.l.
Tel. +39 041.5401356 • Fax +39 041.5402684
Under the terms of the warranty, and in order to ensure the safety and efficiency of the product, it is
recommended to use only original spare parts provided by the manufacturer (refer also to the section
"Warnings").
Warranty
The I-TECH PHYSIO 4/EMG comes with a 2-year warranty valid from the date of purchase that
covers the electronic parts. The warranty covers the parts prone to wear (like the battery) only in
terms of manufacturing defects. The warranty is rendered null and void if the equipment is tampered
with or serviced by personnel not authorised by the manufacturer or retailer.
In the case of repairs under the terms of the warranty, the equipment must be packed to protect it
against damage during transport and shipped to the manufacturer together with all the accessories.
Under the terms of the warranty, the purchaser must return the equipment to be repaired together
with the receipt or invoice as proof of the provenance and date of purchase of the product.
The manufacturer is obliged, in accordance with the Medical Device Directive 93/42/EEC, to ensure
the traceability of all the equipment supplied in order to promptly fix manufacturing defects when
necessary.
Terms of the warranty.

1. The warranty covers the repair of defective goods only when these are returned together with the
tax receipt or purchase invoice.
2. The warranty covers the electronic parts for a period of 2 (two) years. The warranty is provided
by the retailer/distributor or can be requested directly from the manufacturer.
3. The warranty covers only damage to the product that affects operation. The warranty is valid only
if the product concerned bears the same serial number as that indicated on the tax receipt or
purchase invoice.
4. The warranty covers only the repair or replacement, free of charge and including labour, of any
components found to have manufacturing or material defects.
5. The warranty does not cover damage caused by carelessness or failure to observe the instructions
provided, damage attributable to repairs by unauthorised personnel, damage due to accidental
causes or the negligence of the purchaser, with regard to the external parts in particular.
6. The warranty also does not cover damage to the equipment caused by an inappropriate power
supply.
7. Parts prone to wear due to use are not covered by the warranty.
8. The warranty does not include the cost of transport which can vary according to the mode and
time of transportation and is to be borne by the purchaser.
9. The warranty is valid for 2 years. The purchaser is then billed for the cost of replaced parts,
labour and transport according to the rates in force.
10. All disputes shall fall under the jurisdiction of the Court of Venice.

EMC tables

I-TECH PHYSIO 4/EMG. All rights reserved. I-TECH PHYSIO 4/EMG and the logo
are the sole property of I.A.C.E.R. Srl and are registered.

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OPERATING MANUAL

MNPG178 Rev.4 of 29/06/16

Instructions on use for electromyography (EMG) treatments36

Handling and care 43

IACER Srl 2 MNPG178-04

Via S. Pertini, 24/a • 30030 Martellago (VE)

Tel. +39 041.5401356 • Fax +39 041.5402684

Martellago, 01/09/2014 The legal representative

The I-TECH PHYSIO 4/EMG device has the following classification:

Purpose and scope

Clinical scope: Therapeutic

Purpose: Outpatient care/Hospital care

IACER Srl 3 MNPG178-04

Number of programs A total of 86 programs divided as follows:

The device has a useful life of 10-year.

Description of the controls

Channel intensity increase/decrease

Program and parameter

Patient 2 selection button

Patient 1 selection button

IACER Srl 5 MNPG178-04

Follow the instructions on use

BF type applied part

In compliance with MDD 93/42/EEC (and subsequent amendments to Dir.

Production data (month-year)

Permitted temperatures (temperature range for storage, on the pack)

Relative humidity (relative humidity for storage, on the pack)

Device not protected against the infiltration of liquids, keep it dry.

Device able to supply current at above 10mA with a load of 1KOhm

IACER Srl 6 MNPG178-04

Warning: the equipment delivers current in excess of 10mA.

IACER Srl 8 MNPG178-04

Instructions on use for electrotherapy treatments

Instructions on use for a single patient.

6. Select the muscle group with the up/down arrow buttons.

IACER Srl 9 MNPG178-04

Option to simultaneously increase the intensity on all 4 channels:

Skip phase control:

Pause/stop program control:

Instructions on use for two patients.

IACER Srl 10 MNPG178-04

Electrostimulation and stimulation intensities.

Impulse categories are:

IACER Srl 11 MNPG178-04

TENS, an acronym standing for “transcutaneous electrical nerve stimulation”, is a therapeutic

Position of electrodes and intensity levels.

Create a square area with the

W01 • Rapid TENS. (Medical program).

IACER Srl 12 MNPG178-04

W02 • Endorphinic TENS 0.5 Hz Frequency. (Medical program).

W03 • Endorphinic TENS 1 Hz Frequency. (Medical program).

W04 • Endorphinic TENS 2 Hz Frequency. (Medical program).

W05 • TENS sequential. (Medical program).

W06 • TENS at maximum values. (Medical program).

IACER Srl 13 MNPG178-04

W08 • Microcurrent (MENS). (Medical program).

Table of correspondences adjusted/effective current:

Adjusted intensity displayed on screen Effective current