I-Tech UT1 User manual

MNPG116 Rev.0 01-08-2013

USER MANUAL
INDEX
USER MANUAL ..................................................................................................... 3
SAFETY INFORMATION .......................................................................................... 3
USE ...................................................................................................................... 5
CONDITIONS OF USE and EQUIPMENT ................................................................... 5
DEVICE DESCRIPTION ............................................................................................ 6
INSTALLATION ...................................................................................................... 9
PRELIMINARY OPERATIONS .................................................................................. 9
ULTRASOUND TREATMENT .................................................................................. 10
CLEANING MAINTENANCE AND STORAGE ............................................................ 16
OPERATION TROUBLES ........................................................................................ 16
ENVIRONMENT PROTECTION ............................................................................... 17
TECHNICAL FEATURES .......................................................................................... 17
SYMBOLS ............................................................................................................ 18
EM COMPATIBILITY – EMC TABLES ....................................................................... 18
WARRANTY ......................................................................................................... 20

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U
US SE ER R M MA AN NU UA AL L
This manual is a resse to:
- machine user;
- owner;
- managers;
- han ling personnel;
- installers;
- users;
- maintenance personnel.
It contains general information on the operation, precautionary practices, an
maintenance information of the evice I-TECH UT1.
This is an essential reference gui e for users. It is essential to rea the manual
carefully before installing an using the evice an to keep it at han for quick
reference.
Partial or complete non-observance of the recommen ations may lea to
malfunction an amage of the evice, an therefore the warranty will no longer be
vali .
Following the provisions an the recommen ations supplie by the manufacturer
scrupulously is the only way of achieving the best results an to benefit from a quick
an efficient technical assistance if nee e .
The limits of this manual:
- the user manual cannot replace actual user experience;
- for particularly eman ing operations, this instruction manual only represents a
remain er of the main operations.
This user manual must be consi ere an integral part of the equipment an must be
preserve for future reference until the evice is ismantle . The instruction manual
must be available for reference at the place of use of the evice an preserve
carefully.
This manual reflects the current state of machine technology an shall not be
consi ere obsolete solely because up ate at a later ate on the basis of acquire
experience.
The manufacturer reserves the right to up ate the pro uction an the manuals with
no obligation to up ate previous versions.
The manufacturer eclines all responsibility for:
- improper use of the machine;
- use contrary to specific national laws;
- incorrect installation;
- efective power supply;
- improper maintenance;
- unauthorise mo ifications an interventions;
- use of material or spare parts that are not specific for the mo el;
- partial or complete non-observance of the instructions supplie ;
- exceptional events.
To get further information, consult the fabricant.
S
SA AF FE ET TY Y I IN NF FO OR RM MA AT TI IO ON N
Cautions
-Rea carefully the contrain ications.
-Respect the limitations an hazar s associate with the use of the evice. Pay attention to
the labels an symbols place on the unit. Always follow your prescribing
octor's or therapist's recommen ations.
-Do not operate this unit in an environment where other evices are use that
intentionally ra iates electromagnetic energy in an unshiel e manner.
-Do not use sharp objects such as pencil point or ballpoint pen to operate the buttons on
the control panel.
-Before each use inspect applicators an cables integrity.
-The evice shoul not be place next to or on top of other evices. Shoul it prove
necessary to place it next to or on top of other evices, supervision is essential at all times
to control its normal functioning.
-Precautions must be taken regar ing the electromagnetic compatibility of the evice,
which must be installe an commissione in compliance with the EMC provi e in this
manual.

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-Portable RF evices can affect the functioning of the evice. Do not use mobile phones or
other evices that emit electromagnetic fiel s nearby. This may result in incorrect
operation of the unit.
-Only use the evice for the recommen e applications.
-Do not use the evice in presence of inflammable anesthetic mixture an in environments
with high concentrations of oxygen. I.A.C.E.R. will not be hel responsible for any acci ent
if the above instructions are not complie with in full.
-
Warnings
-Make sure of the evice connection to an electrical system in conformity with the current
National laws.
-Care must be taken when operating this equipment aroun other equipment. Potential
electromagnetic or other interference coul occur to this or to the other equipment. Try
to minimize this interference by not using other equipment in conjunction with I-TECH
UT1.
-Before a ministering any treatment to a patient you shoul become acquainte with the
operating proce ures for each mo e of treatment available, as well as the in ications,
contrain ications, warnings an precautions. Consult other resources for a itional
information regar ing the application of Ultrasoun .
-To avoi the risk of electric shock isconnect the evice from the electrical system before
maintenance service.
-Use of accessories, trans ucers an cables other than those specifie here (even as
internal spare parts) may result in EM immunity re uction or in EM emissions increase.
-The evice must not be use in the same environment where magnetic resonance evices
are working or are installe .
Contraindications
-Ultrasoun therapy must not be performe near the uterus on pregnant women or those
who suspect they might be pregnant. Therefore the ultrasoun beam shoul not be use
in this area without ensuring that the patient is not pregnant.
-This evice shoul not be use over the thoracic area if the patient is using a car iac
pacemaker in or er to avoi interferences between the ultrasoun evice an the
pacemaker.
- Do not irect the beam towar s or near the eyes.
-This evice shoul not be use over car iac area.
-This evice shoul not be use over neoplastic lesions.
-Do not use near testicles not to increase their temperature.
-The treatment with ultrasoun s shoul be avoi e in those areas affecte by
thrombophlebitis not to make the thrombus move. Avoi treating patients with eep vein
thrombosis, embolism or arteriosclerosis..
-Tissues that have previously been treate with X rays or other ra iations shoul not be
treate with ultrasoun s.
-Using ultrasoun s on the stellate ganglion, on the spinal column after a laminectomy, on
the area surroun ing the main nerves or the cranium shoul be avoi e .
-This evice shoul not be use on ischemic tissues in in ivi uals with vascular isease
where the bloo supply woul be unable to follow the increase in metabolic eman an
tissue necrosis might result.
-This evice shoul not be use over a healing fracture.
-Avoi using ultrasoun s near bone growth centres in ki s/growing chil ren.
Precautions
-Ultrasoun s shoul not be use on areas with re uce sensitivity or circulation. Patients
experiencing re uce sensitivity may not be able to warn their therapist/ octor when the
ultrasoun is too intense. Patients experiencing circulation problems may suffer from an
excessive increase of temperature in the treate area.
-If the patient feels a eep an sharp pain uring the treatment, the intensity must be
re uce to a comfortable level.
-The ten ency to blee is increase by the heat as more bloo flows in the area. Be careful
when treating patients with blee ing isor ers.
-We a vise moving the hea if the intensity is more than 0,5 W/ sq cm.
-Avoi heating or overheating the capsule in cases of acute an subacute arthritis.
-This evice shoul not be use for symptomatic local pain relief unless etiology is
establishe or unless a pain syn rome has been iagnose .
-This evice shoul not be use when cancerous lesions are present in the treatment area.
-Cautions shoul be use for patients affecte by the following iseases: areas of the spinal
column which un erwent a laminectomy, anesthesise areas, patients with blee ing
isor ers.
-Ultrasoun shoul be routinely checke before each use to etermine that all controls
function normally, especially that the intensity control oes properly a just the intensity
of the ultrasonic power output in stable manner. Also, etermine that the treatment time
control oes actually terminate ultrasonic power output when the timer reaches zero.
-Han le the han piece with care to preserve its characteristics.
-Before using the evice pay attention to the appllicators an hea integrity in or er to
avoi the ingress of liqui s.
-The ultrasoun therapy controls unit is not esigne to prevent the ingress of water or
liqui s. Ingress of water of liqui s coul cause malfunction of internal components of
system an therefore create risk of injury to the patient/user.
Unwanted effects
-In case of un esire effects, suspen the therapy, stop using the evice straight away an
contact your octor.
-Follow the instructions in or er to minimise the un esire effects of the ultrasoun
therapy.

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-If the han piece moves too slowly the patient may experience sharp an /or eep
peripheral pain. If it moves too quickly, or if the han piece is not hel correctly, the
therapeutic effects of the ultrasoun might be re uce .
-Some patients might be particularly sensitive to ultrasoun an might therefore
experience un esire reactions such as hot flushes in the treate area. Check the treate
area before, uring an after the treatment an suspen it in case of un esire effects.
-Make sure that the han piece is in contact with the skin using a specific ultrasoun gel.
Any substance use for this purpose must be highly con uctive. Air is a terrible con uctor
of ultrasoun waves.
U
US SE E
I-TECH UT1 is a evice for ultrasoun therapy.
Ultrasoun treatment is in icate for several chronic an sub-chronic treatments as:
•Muscle pains an contractures
•Contractures
•Capsulitis
•Bursitis
•Myositis
•Soft tissues iseases
•Ten initis
•Ten inosis
Use: hospital an omestic use. it is recommen e the use only by seasone
professional.
Expecte lifetime (time after which we suggest sen ing the evice to the
manufacturer for safety checks): 2 years.
C
CO ON ND DI IT TI IO ON NS S O OF F U US SE E a an nd d E EQ QU UI IP PM ME EN NT T
Environmental con itions for use:
-Environment temperature: from +10° to +40°C;
-Relative humi ity: from 30% to 85% without con ensation;
-avoi irect sunlight, chemical pro ucts an vibrations.
The evice is equippe with the following accessories:
Description
Kit
1
Power supply
15V 3A
1
piece
2
Power supply cable
1
piece
3
Ultrasoun hea
with
5cmq
a
rea
1
piece
4
User manual
1
piece
5
Ultrasoun gel
1
piece
All accessories are available on eman as spare parts.
Moreover the ultrasoun hea with 1 cmq area is available on eman .

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D
DE EV VI IC CE E D DE ES SC CR RI IP PT TI IO ON N
1. Program selection button
2. Frequency selection button 1/3MHz
3. Duty cycle selection button
4. Timer selection button
5. LCD isplay
6. STOP button
7. Intensity selection knob an PAUSE
8. Han le socket (5 cmq an 1 cmq)
9. Power supply socket
10.ON/OFF button

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DISPLAY LCD
MANIPOLI
1. Program in icator
2. Frequency in icator 1/3MHz
3. Duty cycle in icator
4. Timer in icator
5. Output intensity/power in icator
6. Ultrasoun hea etector
7. PAUSE therapy in icator
1. Ultrasoun hea
2. LED for ultrasoun hea etector
3. Han le applicator

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LABELS
ON /OFF button
Polarity of Power Supply
Stop treatment
Start/Pause button
Protecte against the effects of immersion: for ultrasoun
han le
WEE Regulations
Applie part type BF
Pro uct in compliance with Directive 93/42/EEC (MDD)
Ultrasoun intensity
Ultrasoun applicator state (contact hea /skin)
In icator of connection socket of treatment hea
Ultrasoun output intensity
Ultrasoun output power
Treatment time
Fabricant name an a ress
Manufacturing ate (month/year)
I-TECH UT1

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Attention. Consult operating instructions
Ultrasoun han le lot
Serial number of ultrasoun han le
I
IN NS ST TA AL LL LA AT TI IO ON N
Remove the evice an all accessories from shipping cartons. Check the evice
equipment.
Before the installation an the connection of the evice to the mains supply, check
that the voltage an frequency correspon with the available mains supply an
in icate in this user manual. We recommen that you use the MPU50-160 type
power supply.
Follow the instructions below for a correct installation:
•Connect the power supply cable to the power supply
•Connect the power supply to the evice connector
•Connect the power supply plug to the wall socket
Press on ON/OFF button to switch on the evice.
If it is connecte correctly, isplay will show the picture below.
If it is connecte in wrong way, isplay will show the picture below.
P
PR RE EL LI IM MI IN NA AR RY Y O OP PE ER RA AT TI IO ON NS S
Imme iately after switching on, the evice carries out a self-test. At the en of the
self-test a beep is hear an isplay shows the picture as escribe in previous
paragraph. When an error is foun an error co e will appear on the isplay: please
rea the paragraph “Operation troubles” to get more etails.
Before starting treatment please pay attention to the following suggestions:
•Put the patient in a comfortable position. The area to be treate shoul be
properly supporte an expose an perfectly relaxe .
•Inform the patient on the purpose of the treatment an the sensation he will
perceive uring the treatment.
•Ensure there are no contrain ications to treatment.
•Inspect the patient's skin accurately for any abrasions, inflammation, surface
veins etc.
•Clean the area to be treate with a 70% alcohol or soap.
•It is suggeste to shave areas of excessive hair-growth.
Durante il trattamento:
1. The ultrasoun -hea has to be move constantly when intensity is higher
than 0,5 W/cmq.
2. Ask the patient about his/her sensation uring the treatment. If necessary
a just ultrasoun intensity, by re ucing it if the treatment is not
comfortable.
3. In case of in ications of wrong contact, it is recommen e to a the contact
gel or reposition the ultrasoun -hea .
4. During the treatment if the ultrasoun hea works correctly, the applicator
LED will light; if there is no contact , the applicator LED will blink light. When
the treatment is in PAUSE, the applicator LED will be turne off an the
count own will also be stoppe .
LOT
SN

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ATTENTION:
- The treatment shoul be performer with a regular movement of the ultrasoun
hea , not too slow to avoi in ucing heat, not too fast to prevent a ba contact
which woul re uce the effectiveness of the treatment.
- if it is nee e to replace the han le, turn the power switch off an isconnect
the evice from power supply.
After the treatment clean the skin of the treate area as well as the ultrasoun hea
by using a ry towel. The ultrasoun -hea shoul be cleane up with a 70% alcohol
solution. Check the patient con itions an the treate area (pain, circulation, etc.).
The patient shoul reveal any complaint/reaction before starting the treatment after.
U
UL LT TR RA AS SO OU UN ND D T TR RE EA AT TM ME EN NT T
After performing the preliminary operations liste in the previous paragraph,
start the session making sure to follow these steps:
1. Press PROGRAM keys to select the program: scroll up/ own the
programmes with the arrows.
2. Select the frequency 1 or 3 MHz by pressing the button FREQUEN. .
3. Select uty cycle (10-100%) by pressing the buttons DUTY CYCLE
(up arrow an own arrow)
4. Select therapy time (1-30 minutes) by pressing the buttons TIME ( up
arrow an own arrow.
5. Put a goo quantity of con uctive gel on the area to be treate . It is
recommen e to use a CE con uctive gel CE
6. Regulate the intensity of the treatment using the knob (7). Press any of the
PROGRAM, FREQUEN., DUTY CYCLE or TIME buttons uring the treatment to
visualise W (Watts) or W/cm² (Watt/sq cm).
7. Keep the hea in constant contact with the skin an make sure that the part is
covere in gel so that the therapy is effective. The green LED locate next to the
hea on the han piece lights up when the evice is working.
8. The evice has a hea /skin coupling system for safety reasons. If the contact is
not correct an if the intensity is set above 0,5W, the LED on the han piece an
the symbol on the isplay will start flashing. The system is not
available on the 1cm hea because of the re uce contact area: the evice emits
an ultrasoun beam even if the hea is not in contact with the skin. This is not a
efect but rather a technical choice, as it woul be impossible to perform
therapies on small an irregular areas like toes or fingers with such a system.
9. It’s possible to stop temporary the therapy at any time pressing the knob (7).
Press again the knob to continue the treatment.
10. Press the orange button to stop imme iately the treatment in progress.
We a vise han ling the han pieces with care in or er to preserve them.
In or er to ensure efficient transfer of energy, a contact means is require between
the ultrasoun hea an the bo y. Air causes virtually total reflection of the
ultrasoun energy. The best means for the transfer of ultrasoun energy is the
ultrasoun gel.

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Put a quantity of con uctive gel on the area to be treate . Move the ultrasoun hea
uring therapy session in a circular motion. The treate area shoul be twice the
ultrasoun hea area.
If the bo y surface is very irregular, making it ifficult to obtain goo contact
between the ultrasoun hea an the bo y, or if irect contact must be avoi e (e.g.
ue to pain), the affecte area may be treate un er water (subaqual metho ). The
water shoul be egasse (by previous boiling ) in or er to prevent air bubbles that
coul ecrease the effectiveness of the treatment.
ATTENTION. The han piece an its cable are the only parts protecte against water
amage with a IPX7 gra e.
ATTENTION. Never apply the gel to the ultrasoun hea . The treatment hea will
register this as contact an may emit ultrasoun energy, which coul amage the
ultrasoun hea . Always use the gel certificate with the requirements of the
me ical, such as with CE mark.
Programs features and main applications.
Make reference to the following table for programs features. All parameters are
a justable by the user.
PROG. FREQ. DUTY CYCLE TIME SUGGESTED INT.
U-01 1MHz 80% 10 min. 1.0W/cm²
U-02 1MHz 50% 10 min. 1.0W/cm²
U-03 1MHz 50% 20 min. 1.5W/cm²
U-04 1MHz 50% 15 min. 1.0W/cm²
1.5W/cm²
2.0W/cm²
U-05 3MHz 80% 15 min. 1.0W/cm²
U-06 1MHz 30% 15 min. 1.5W/cm²
U-07 1MHz 80% 15 min. 1.0W/cm²
1.5W/cm²
U-08 1MHz 80% 8 min. 1.5W/cm²
U-09 1MHz 50% 12 min. 1.5W/cm²
U-10 3MHz 80% 10 min. 1.0W/cm²

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TREATMENT PRG
HANDLE POSITION
FREQ DUTY CYCLE TIME HEAD SUGGESTED INTENSITY APPLICATIONS
NUMBERS
Acne
U
-
01/10
Affecte area
3MHz
30%
15 min
5 cmq
1,5W/cm²
Free
Muscle fatigue
U
-
01/10
Affecte area
1MHz
70%
20 min.
5 cmq
2 W/cm²
2
-
3
Algo ystrophy
U
-
01/10
Affecte area
1MHz
50%
10 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Anti
-
i
nflammatory
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Arthritis
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Fingers arthritis
U
-
01/10
Han fingers
1MHz
40%
15 min.
1 cmq
1.5W/cm²
-
2W/cm²
10
-
15
Arthrosis
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.5W/cm²
-
2W/cm²
10
-
15
Bursitis
U
-
01/10
Affecte area
1MHz
30%
15 min.
5 cmq
2W/cm²
10
-
15
Brachialgia
U
-
01/10
Trapezium an arm
1MHz
30%
15 min.
5 cmq
2W/cm²
10
-
15
Capsulitis
U
-
01/10
Shoul er
1MHz
30%
15 min.
5 cmq
2W/cm²
10
-
15
Cavitations
U
-
01/10
Affecte area
1MHz
70%
20
min.
5 cmq
2W/cm²
-
3W/cm²
20
-
30
T
-
T hea ache
U
-
01/10
Cervical area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
T
-
T hea ache
U
-
01/10
Massetere
1MHz
50%
15 min.
5 cmq
1.5W/cm²
10
-
15
Cervicalgias
U
-
01/10
Cervical area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Whiplash
U
-
01/10
Cervical an orsal +
front zone
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Con ropathy
U
-
01/10
Affecte area
1MHz
60%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Muscle contractures
U
-
01/10
Affecte area
1MHz
70%
20 min.
5 cmq
2W/cm²
4
-
6

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Coxarthrosis
U
-
01/10
Hip
1MHz
60%
15 min.
5 cmq
2W/cm²
10
-
15
Cramps
U
-
01/10
Affecte area
1MHz
70%
20 min.
5 cmq
2W/cm²
4
-
6
Cruralgy
U
-
01/10
Internal thigh
1MHz
40%
15 min.
5 cmq
2W/cm²
10
-
15
Discopathy
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
S
trains
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Articular pain
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Intercostal pain
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Menstrual pain
U
-
01/10
Ab omen
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Muscle pain
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Rheumatic pain
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Dorsalgy
U
-
01/10
Dorsal area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Drainage
U
-
01/10
Affecte area
1MHz
60%
15 min.
5 cmq
2W/cm²
30
Eczemas
U
-
01/10
Affecte area
3 MHz
50%
15
min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Oe emas
U
-
01/10
Affecte area
1MHz
30%
15 min.
5 cmq
2W/cm²
10
-
15
Hematomas
U
-
01/10
Affecte area
1MHz
40%
15 min.
5 cmq
2W/cm²
-
3W/cm²
10
-
15
Epicon ylitis
U
-
01/10
Elbow
1MHz
40%
15 min.
5 cmq
1.0W/cm²
-
1,2W/cm²
10
-
15
Epitrocleitis
U
-
01/10
Internal elbow
1MHz
40%
15 min.
5 cmq
1.0W/cm²
-
1,2W/cm²
10
-
15
Slippe isc
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Gonarthrosis
U
-
01/10
Knee
1MHz
50%
15 min.
5 cmq
1.5W/cm²
-
2W/cm²
10
-
15

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Ly
mphoe ema
U
-
01/10
Affecte area
1MHz
30%
15 min.
5 cmq
2W/cm²
10
-
15
Lypolisis
U
-
01/10
Affecte area
1MHz
60%
15 min.
5 cmq
2W/cm²
30
Lumbago
U
-
01/10
Lumbar area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Massage
U
-
01/10
Affecte area
1MHz
70%
20 min.
5 cmq
2 W/cm²
Free
Mialgy
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Mononeu
ropathy
U
-
01/10
Pain zone
1MHz
50%
15 min.
5 cmq
1.5W/cm²
12
-
15
Neuralgia
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Periarthritis
U
-
01/10
Shoul er
1MHz
70%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Pubalgy
U
-
01/10
Internal thigh
(upper zone)
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Ra iculitis
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Muscle recovery
U
-
01/10
Affecte area
1MHz
70%
20 min.
5 cmq
2 W/cm²
Free
Rizarthrosis
U
-
01/10
Thumb area
1MHz
30%
15 min.
5 cmq
1,5W/cm²
10
-
15
Rizopathy
U
-
01/10
Dorsal area
1MHz
60%
15 min.
5 cmq
1,5W/cm²
10
-
15
Wrinkle
U
-
01/10
Affecte area
3MHz
30%
15 min
5 cmq
1,5W/cm²
Free
Sciatalgy
U
-
01/10
Affecte area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Stretch marks
U
-
01/10
Affecte area
3MHz
40%
15 min
5 cmq
2W/cm²
Free
Venous stasis
U
-
01/10
Extremities limbs
1MHz
50%
15 min.
5 cmq
2W/cm²
Free
Sprains
U
-
01/10
Affecte area
1MHz
40%
15 min.
5 cmq
2W/cm²
4
-
6
Muscle sprains
U
-
01/10
Affecte area
1MHz
40%
15 min.
5 cmq
2W/cm²
8
-
10

I.A.C.E.R. Srl
15
Tallonitis
U
-
01/10
Heel
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Ten initis
U
-
01/10
Affecte ten ons
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Stiff neck
U
-
01/10
Cervical area
1MHz
50%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Carpal tunnel syn rome
U
-
01/10
Internal wrist
1MHz
40%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
10
-
15
Vascularisation
U
-
01/10
Affecte area
1MHz
60%
15 min.
5 cmq
1.0W/cm²
-
1,5W/cm²
Free
Active principle vehiculation
U
-
01/10
Affecte area
1MHz
60%
15 min.
5 cmq
2W/cm²
Free
In ications regar ing intensity an number of sessions can vary epen ing on the opinion of your personal octor or therapist.
In particular, in ications on intensity o not consi er the wi th of the area to be treate . If it is very wi e, the intensity can be increase by 20% with respect to what in icate an
it can be re uce if it is a small area.
Similarly, the movement on the area must be appropriate to the heat felt by the patient. The slower it moves, the stronger the heat. If the patient complains about the heat, we
a vise re ucing the intensity or moving the hea faster.

I.A.C.E.R. Srl
16
C
CL LE EA AN NI IN NG G M MA AI IN NT TE EN NA AN NC CE E A AN ND D S ST TO OR RA AG GE E
Before cleaning switch off the evice an isconnect it from the mains supply.
Disconnect all cables an accessories.
The ust can be remove with a ry cloth. To clean persistent irt use a non-abrasive
liqui househol cleaner (no abrasive, no alcohol content solution). If a more sterile
cleaning is nee e , use a cloth moistene with an antimicrobial cleaner.
ATTENTION.
Do not immerse the evice into liqui s. Shoul the evice acci entally become
submerse , contact the fabricant an / or Authorize Service center imme iately. Do
not attempt to use a system that has been wet insi e until inspecte an teste by
the fabricant or the Service Technician Certifie by Authorize Service center. Do not
allow liqui s to enter the ventilation holes in the optional mo ules.
In case of irritations or re ening, suspen the treatment an consult a octor .
Clean the contact surface imme iately after each treatment using a soft cloth or
paper cloth, lightly wet if nee e . Make sure that no ultrasoun gel remains on the
ultrasoun hea . Aggressive clearing agents coul amage the rubber insulation an
shorten the life of the cables.
Store the han piece/applicators/cables with care at the en of each treatment.
To get more information about the original accessories an spare parts, contact
I.A.C.E.R. Srl authorize centers.
After cleaning the external box, ry all of the parts carefully before turning on the
evice.
Do not isassemble the evice to clean or check it: there is no nee to clean the
insi e of the machine an in any case this operation shoul be performe by skille
technical personnel authorise by I.A.C.E.R. srl.
When not using the evice for a long time, place it together with all its accessories in
a ry place away from ust, irect sunlight an protecte from the weather. Do not
place other objects on top of the evice.
O
OP PE ER RA AT TI IO ON N T TR RO OU UB BL LE ES S
I-TECH UT1was esigne an manufacture using a vance technological solutions
an high-quality components for an efficient an reliable use.
Anyway, shoul there be any problems uring functioning, please refer to this gui e
before contacting an authorise service centre.
PROBLEM POSSIBLE CAUSE SOLUTION
Display oes not
switch on
Wrong/faile connection
with power supply
Check if the mains a apter is
connecte to the evice an to
power supply.
Check the integrity of all
plugs/sockets an connection cables.
Display shows
the following
error
Error uring the self-test Remove any applicators, switch the
apparatus off an on again. If the
problem persists, contact the
fabricant.
Display shows
the following
picture
No han le is connecte Check the connection of applicator/s
to the socket/s. . If the problem
persists, contact the fabricant.

I.A.C.E.R. Srl
17
E
EN NV VI IR RO ON NM ME EN NT T P PR RO OT TE EC CT TI IO ON N
I-TECH MEDICAL DIVISION evices are esigne an manufacture to have minimum
negative impact on the environment in compliance with the functioning an safety
nee s.
We follow the criteria to minimise waste, toxic material, noise, un esire ra iations
an energy consumption.
A careful research on the performance of the evice guarantees a significant
re uction of consumption, in line with the concept of energy saving.
This symbol in icates that the pro uct must not be ispose of with
normal omestic waste.
Please ispose of the evice in accor ance with the irective 2002/ 96/EC WEEE
(Waste Electrical an Electronic Equipment).
T
TE EC CH HN NI IC CA AL L F FE EA AT TU UR RE ES S
Caratteristiche generali
Power supply
Input:
100V
-
240V, 47Hz
-
63Hz, 1.35A
Output: 15VDC, 3A max
Dimensions: 143mmx73mmx40mm
Device
Dimensions: 250mmx185mmx82mm
Environmental con itions for use
Temperature: from 10°C to 40°C
Relative humi ity: 30%-85%
Atmospheric pressure: 800-1060hPa
Environmental con itions for storage
Temperature:
from
-
1
0°C to
55°C
Relative humi ity: 10%-90%
Atmospheric pressure: 700-1060hPa
Maximum a justable therapy time
30 minutes
Timer accuracy
+/
-
3%
Classification EN 60601
-
1
Class I
Applie part
Type BF
Ultrasound features
Ultrasoun wave frequency
1MHz +/
-
10%
3MHz +/-10%
Duty cycle
10%
-
100% a stepping 10%
Working frequency
100Hz+/
-
10%
Therapy time
A justable, max. 30 minutes
Output power (+/
-
20%)
0.5W
-
10.0W, when uty cycle
≥
80% for
5 cmq ultrasoun hea
0.5W-15.0W, when uty cycle ≤ 70% for
5cmq ultrasoun hea
0.1W-2.0W, when uty cycle ≥ 80% for
1cmq ultrasoun hea
0.1W-3.0W, when uty cycle ≤ 70% for
1cmq ultrasoun hea
Effective ra iating area (Aer) (+/
-
20%)
1.0cmq
(optional)
5.0cmq
Effective
intensity
3.0W/cmq +/
-
20%
Accuracy
+/
-
20% (when value > 10% maximum
value )
Rbn (Max)
5.0
Beam type
Collimate
Material of ultrasoun hea
Aluminium
IP Protection
IPX7 only for ultrasoun hea

I.A.C.E.R. Srl
18
S
SY YM MB BO OL LS S
ON /OFF button
Polarity of power supply
Stop treatment
Start/Pause button
Protecte against the effects of immersion: for ultrasoun
han le
WEE Regulations
Applie part type BF
Pro uct in compliance with Directive 93/42/EEC (MDD)
Device can supply a current > 10mA r.m.s. or 10V r.m.s. for a
perio of 5 secon s
Fabricant name an a ress
Manufacturing ate (month/year)
Attention. Consult operating instructions
Ultrasoun han le lot
Serial number of ultrasoun han le
E
EM M C CO OM MP PA AT TI IB BI IL LI IT TY Y – – E EM MC C T TA AB BL LE ES S
Use the I-TECH UT1 evice at least 3 metres away from televisions, monitors, mobile
phones, WIFI routers or any other electronic evice as they may affect its functioning.
The evice must be installe an commissione in compliance with the information
on electromagnetic compatibility supplie in this manual. Also see the EMC Charts
paragraph.
Using accessories, trans ucers an cables other than those specifie , except for those
trans ucers an cables sol by the manufacturer as spare parts for internal
components, may result in increase emissions or ecrease immunity of the evice.
The evice shoul not be place next to or on top of other evices. Shoul it prove
necessary to place it next to or on top of other evices, supervision is essential at all
times to control its normal functioning.
Guidance and manufacturer's declaration – electromagnetic emissions
FOR ALL EM DEVICES
The I-TECH UT1 evice is inten e for use in the electromagnetic environment specifie below. The
customer or the user of the I-TECH UT1 shoul assures that it is use in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The I-TECH UT1 evice uses RF energy only for its
internal function. Therefore, its RF emissions are
very low an are not likely to cause any
interference in nearby electronic equipment.
RF emissions
CISPR11
Class B
The I-TECH UT1 evice is suitable for use in all
establishments other than omestic an those
irectly connecte to the public l o w - v o l t a g e
p o w e r s u p p l y network that supplies buil ings
use for omestic purposes.
Harmonic emissions
lEC 61000-3-2
N.A.
Voltage fluctuations /
flicker emissions
lEC 61000-3-3
N.A.
Guidance and manufacturer's declaration-electromagnetic
Immunity
The I-TECH UT1 evice is inten e for use in the electromagnetic environment specifie below. The
customer or the user of the I-TECH UT1 shoul assure that it is use in such an environment.
LOT
SN

I.A.C.E.R. Srl
19
Immunity
test
IEC 60601
test level
Compliance
level
Electromagnetic
environment - guidance
Electrostatic
ischarge
(ESD) lEC 61000-
4-2
±6 kV contact ± 6kV contact
Floors shoul be woo , concrete
or ceramic tile. If floors are
covere with synthetic material,
the relative humi ity shoul
be at least 30 %.
± 8kV air ± 8kV air
Guidance and- manufacturer's declaration. Electromagnetic immunity
FOR EM DEVICES THAT ARE NOT INTENDED FOR LIFE SUPPORT
The I-TECH UT1 evice is inten e for use in. the electromagnetic environment specifie below. The
customer or the user of the I-TECH UT1 shoul assure that it is use in such an environment.
Immunity
test
IEC 60601
test level
Compliance
level
Electromagnetic
environment – guidance
Portable an mobile RF communications equipment shoul be use no closer to any
part of the I-TECH UT1 evice, inclu ing cables, than the recommen e separation istance calculate
from the equation applicable to the frequency of the transmitter.
Electromagnetic
environment - guidance
Con ucte RF lEC
61000-4-6
3V effective
from 150kHz to
80MHz
3V (V
1
)
Portable an mobile RF
communications equipment
shoul be use no closer to any
part of the I-TECH UT1 evice,
inclu ing cables, than the
recommen e separation
istance calculate from the
equation applicable to the
frequency of the transmitter.
Recommen e separation
istance.
= 1,2 ⋅√P from 150kHz to 80MHz
= 1,2 ⋅√P from 80 MHz to 800
MHz
= 2,3 ⋅√P from 800 MHz to 2,5
GHz
where P is the maximum output
power rating of the transmitter In
watts (W) accor ing to the.
Ra iate RF lEC 61000-
4-3
3V/m
from 80MHz to
2,5GHz
3V/m (E
1
)
Transmitter manufacturer an d Is the recommen e separation istance in
meters (m). Fiel strengths from fixe RF transmitters, as etermine by an electromagnetic site
a survey, shoul be less than the compliance level b in each frequency range. Interference may occur
In the vicinity of equipment marke with the following.:
NOTE I At 80 MHz en s 800 MHz. the higher frequency range applies.
NOTE 2 These gui elines may not apply in all situations. Electromagnetic propagation is affecte by
absorption an reflection from structures, objects an people.

I.A.C.E.R. Srl
20
*1: Fiel strengths from fixe transmitters, such as base stations for ra io ( cellular / cor less)
telephones an lan mobile ra ios, amateur ra io, AM an FM ra io broa cast an TV broa cast
cannot be pre icte theoretically with accuracy. To assess the electromagnetic environment u to
fixe RF transmitters, an electromagnetic site survey shoul be consi ere . If the measure fiel
strength in the location in which the I-TECH UT1 evice is use excee s the applicable RF compliance
level above, shoul be observe to verify normal operation. If abnormal performance is observe ,
a itional measures may be necessary, such as reorienting or relocating the I-TECH UT1.
*2: Over the frequency range 150 kHz to 80 MHz, fiel strengths shoul be less than [V ] V/m.
Recommended separation distances between portable and mobile
rf communications equipment and the em devices that are not intended for life support
The I-TECH UE evice is inten e for use in an electromagnetic environment in which ra iate RF
isturbances are controlle . The customer or the user of the I-TECH UE evice can help prevent
electromagnetic interference by maintaining a minimum istance between portable an mobile RF
communications equipment (transmitters) an the I-TECH UE as recommen e below, accor ing to
the maximum output power of the communications equipment.
Rated maximum output
power of transmitter (W)
Separation distance according to frequency of transmitter (m)
From 150kHz to
80MHz d = 1,2 ⋅
⋅⋅
⋅√
√√
√P
From 80MHz to
800MHz d = 1,2 ⋅
⋅⋅
⋅√
√√
√P
From 800MHz to 2GHz
d = 2,3 ⋅
⋅⋅
⋅√
√√
√P
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.69 3.69 7.38
100 11.67 11.67 23.33
For transmitters rate at a maximum output power not liste above, the recommen e separation
istance d in meters (m) can be estimate using the equation applicable to the frequency of the
transmitter, where P is the maximum output power rating of the transmitter in watts (W) accor able
to the transmitter manufacturer.
NOTE 1:
At 80 MHz an 800 MHz. the separation istance for the higher frequency range applies.
NOTE 2:
T h e s e g u i e l i n e s m a y n o t a p p l y i n a l l s i t u a t i o n s . E l e c t r o m a g n e t i c p r o p a g
a t i o n i s a f f e c t e b y a b s o r p t i o n a n r e f l e c t i o n f r o m s t r u c t u r e s , o b j e c t s a n
p e o p l e.
W
WA AR RR RA AN NT TY Y
The device has a 2 year warranty starting from the purchase date covering
electric and electronic parts for household use. In case of purchase from
professional operators (purchase with an invoice), the warranty is 12 months.
All of the parts subject to normal wear and tear (ultrasound head) are not
covered by warranty as well as all the parts that are defective due to
negligence, improper maintenance, tampering or repair work carried out by
personnel that has not been authorised by the manufacturer or the authorised
dealer.
The warranty conditions are those described under “Warranty Regulations”.
In accordance with the Medical Devices Directive 93/42/EEC, the manufacturer
must be able to trace the devices at any time in order to intervene promptly in
case of manufacturing faults.
In the event of future repairs under warranty, the equipment must be packaged
to prevent damage during transport and sent to the manufacturer together with
all of the accessories. The purchaser only has the right to repair under
warranty when the equipment is returned to the manufacturer complete with
the receipt or invoice proving the correct origin of the product and purchase
date.
Warranty regulations.
1. In the event f repairs under warranty, the purchaser must include in the package the receipt or
invoicing proving the purchase date.
2. The electronic parts are covered by a 24-months (12 months for professional user) warranty. The
warranty is given through the point of sale or directly from the manufacturer.
3. The warranty covers exclusively product damage causing operational defects.
4. The warranty covers exclusively the repair or replacement free of charge, including labour, of
components found to be defective in terms of manufacture or material.
5. The warranty does not apply to damage caused by neglect or use not complying with the
instructions provided, damage caused by work carried out by unauthorized personnel or damage
caused by accidental causes or the buyer’s negligence, with particular reference to external parts.
6. The warranty does also not apply to damage to the equipment caused by incompatible power
supplies
7. Parts subject to wear after use are excluded from the warranty.
8. The warranty does not include transport costs to be paid by the purchaser in relation to the method
and speed of transport.
9. The warranty empire after 24 months (12 months for professional user).. After such time repair work
will be carried out at the rates currently in force for the parts replaced and the labour and transport
costs.
10. Any controversy will fall within the exclusive jurisdiction of the Venice courts.