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USER MANUAL
MNPG71 Rev. 03 del 12/09/16
Ultrasound
Mio-Sonic
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I.A.C.E.R. Srl
Via S. Pertini 24/A – 30030
Martellago (VE) ITALY
Tel. +39 041 5401356 – Fax +39 041 5402684
e-mail: iacer@iacer.it - http://www.itechmedicaldivision.com
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Summary
Summary.................................................................................... 3
Introduction .............................................................................. 4
Warnings ................................................................................... 6
Contraindications ...................................................................... 6
Side effects ................................................................................. 7
Accessories and device description .......................................... 7
Technical features ..................................................................... 7
Labeling ..................................................................................... 8
Symbols description .................................................................. 9
Specifications ............................................................................ 9
Purpose ...................................................................................... 9
Kit contents .............................................................................. 10
How to use Mio Sonic .............................................................. 10
Analgesic and decontracting treatments ........................................... 11
Beauty treatments ................................................................................ 12
Cleaning ................................................................................... 17
Carriage and storage ................................................................ 17
Disposal .................................................................................... 18
Electromagnetic interferences and device safety .................... 18
Assistance ................................................................................. 18
Spare parts ................................................................................ 19
Warranty ................................................................................... 19
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Introduction
Mio-Sonic is an innovative and advanced medical device for
ultrasound treatment. Thanks to its practicity it’s ideal for home use.
The sound is given by a body vibration that expands in the air with a
specific frequency and finally it reaches the ear. Sound frequency is
measured in Hertz (Hz) and it is the number of oscillations (pressure
variations) per second. The human ear can nominally hear sounds in
a range from 20 Hz to 20000 Hz. Wavelength is the spatial period of
the wave in a complete oscillation.
Ultrasounds are mechanical sound waves with frequencies higher
than frequencies audible by the human ear.
Ultrasounds mechanical waves, generated by piezoelectric elements,
are used in different industrial fields for years.
Thanks to the study of ultrasound waves in human application new
diagnostic medical instrumentation has been built and they are
widely used in gynecology, gastroenterology, hagiology and
cardiology.
These instrumentations uses back-echo resulting from ultrasound
beam that spreads in the human body and it is decelerated in
different ways by anatomic structures. Each tissue has a specific
acoustic impedance so ultrasound wave crossing through anatomic
structures provokes different biological effects. Thermal Effect is the
first effect that has a pain-killer function in orthopedics, sport
medicine and in aesthetic fields for cellulite and adipose tissue
treatment.
How do ultrasound waves generate heat?
Ultrasound waves loss energy when they
cross through the tissues. The delivered
energy is given to the crossed anatomic
structure. Then energy to heat conversion
increases significantly local temperature, in
particular between tissues with different
acoustic impedance (for example bone/soft tissues), and increases
microcirculation. The bloodstream helps to dissipate the increased
heat.
There are also Not Thermal Effects in ultrasound waves
propagation.
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The first are the Mechanical Effects caused by the ultrasound
waves force on the cells that move toward low-pressure zones. As a
consequence cells torsions and rotations with small vortexes happen
in interstitial fluids (streaming).
These pressure variations can provoke permeability alterations of
cells membranes (biochemical and biological effects). In case of
adipose cells pressure variations promotes complex molecules
liberation as fats that are released in circulatory system and
subsequently they are eliminated through lymphatic system and
micro-circulation.
Another aspect related to biochemical effect is the Phonophoresis,
a technique that introduces drugs in tissues through the ultrasounds.
A non – thermal effect is the Cavitation.
In therapeutic field the ultrasounds are obtained in an artificial way.
In fact some mineral crystals are able to dilate and condense when
they are subjected to electric field action. Ultrasound irradiation
creates some vibrations and a consequent intensive micro-massage
on tissues in depth and as a consequence heat is generated
(ultrasounds interaction with biological tissues has mechanical,
thermal, chemical and cavitation effects).
Ultrasounds therapy is particularly
indicated for locomotor apparatus
pathologies in order to obtain an
analgesic effect, in sciatic pain and
neuritis, in periarticular calcifications, in
Duplay’s disease, in Dupuytren’s
disease, in hematomas and in heal
tissues, in tendinitis, in muscle
contractures. The ultrasounds can be
used also in cellulite treatment by activating local circulation and by
decreasing orange-peel effect. They promotes active substances
penetration like essential oils, liposolubil vitamins (for example
vitamin A and E) and water-soluble agents through skin by relaxing
the tissues with great results in wrinkles treatment.
Ultrasounds result very efficacious in anti-inflammatory process
that re-generate tissues in case of acne, in fats movement for tissue
metabolism promotion, with positive effects also on vascularization
and lymphatic drainage.
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Warnings
The device doesn’t produce or receive electromagnetic
interferences from other devices. However it’s recommended to
keep a distance of at least 3 meters from televisions, monitor,
mobile phones or other electronic devices.
The device must not be used in the presence of patient monitoring
equipment.
Do not use the device with electrosurgical or shortwave or
microwave therapy equipment.
Use of the device is prohibited to persons known to be of unsound
mind.
Use of the device is prohibited in hyposensitive zones and on
carotid sinus. Avoid neck and mouth treatment.
Use of the device is prohibited to persons temporarily disabled
unless assisted by qualified personnel (e.g. a doctor or therapist).
Use of the device is prohibited in the presence of signs of
deterioration of the device itself.
Should any foreign matters penetrate the device contact the retailer
or manufacturer immediately.
If dropped, check that the housing is not cracked or damaged in
any way; if so, contact the retailer or manufacturer.
Should you notice any changes in the device’s performance during
treatment, interrupt the treatment immediately and consult the
retailer or manufacturer (patients being treated in a centre must
also be informed of the event).
Use of the device is prohibited in combination with other medical
devices.
Use of the device is prohibited close to flammable substances or in
environments with high concentrations of oxygen.
Consult a doctor before using Mio-Sonic with metallic
osteosynthesis devices.
Contraindications
Use of the device is prohibited to persons with a pace-maker,
cardiopathic subjects, epileptics, pregnant women, anxious people
or people suffering from heart disease, phlebitis, thrombophlebitis
or serious illnesses.
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Use of the device is prohibited to persons persons suffering from
serious cardiovascular problems, tuberculosis, vertebral column
diseases, malignant tumour, neoplasia or with metallic prosthesis
carriers (different medical prescriptions excepted), acute infections,
vein thrombosis, serious osteoporosis, arteriopathies,
inflammations and to persons younger than 12 years old.
In the event of injury, muscle stress or any other health problem
use the device only under medical supervision.
Avoid to position the device in a way that ultrasound beam hits the
eye area or in presence of glands, near uterus and abdomen, or in
thrombophlebitis and inflammation area.
Side effects
With ultrasound therapy inflammation temporary increases can happen
in treatment area, and so pain temporary increase, traumas due to more
dosage, nervous system reactions, sanguine coagulation. If this occurs,
suspend the treatment and consult a doctor.
Accessories and device
description
(1) Treatment time led
(2) Treatment time selector
(3) Switching on led
(4) Intensity indicator led
(5) Intensity selector
(6) ON/OFF
(7) Ultrasound head
(8) Power supply connector
Technical features
Power supply
100-240VAC, 50-60 Hz with UE24WCP150120SPA power supply, output
15VDC 1.2A
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Model: Mio-Sonic
Power supply: DC 15V/1.2A max RBN (Max): 5.0
Acoustic frequency: 1.0 MHz Beam type: Collimated
Waveform: pulsed Ie:1.6W/cm²
Modulation shape: 100 Hz P:6.4W
IPX7 (only for treatment head) AER:4.0cm²
I.A.C.E.R. Srl – Via S. Pertini 24/a, 30030 Martellago (VE) - ITALY
year/month
Insulation class (CEI EN
60601-1)
II
Applied part (CEI EN 60601-1)
BF
Dimensions (mm)
200x50x70
Maximum absorption
9.6 W ± 20% peak value (6.4 W ± 20%
medium)
Effective absorption
2.4 W/cm2 ± 20% peak value (1.6 W/cm2
± 20% medium)
Ultrasound frequency
1MHz ±10%
Modulation waveform
100Hz ±10%
Waveform
Pulsed
Ultrasound intensity levels
Adjustable on 3 levels L-M-H (5-50-100
% duty cycle)
Ultrasound head dimensions
5 cm²
Radiant area
4 cm² ± 10%
Type of ultrasound beam
Collimated
Ultrasound head (material)
Aluminum
Labeling
Work frequency
Waveform
Modulation
frequency
Power/area
ration
Type of
beam
Maximum
intensity
Maximum
absorption
Radiant area
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Symbols description
Attention. Please read annex documents
Product subject to WEEE regulations concerning
separate waste collection of electronic equipment
Class II equipment
Applied part type BF
0476
Product in compliance with Directive 93/42/EEC
(MDD) (and following modifications Dir. 2007/47/EC)
Manufacturing date (month/year)
S/N xxxxxx
Serial number
Specifications
Mio Sonic has the following specifications:
Class IIa equipment (Directive 93/42/CEE, Annexed IX, rule 9
and following modifications);
Class II applied part type BF (Classif. EN 60601-1);
Equipment not protected against liquid penetration; IPX7 only for
ultrasound head. NOT INDICATED FOR IMMERSION
TREATMENTS.
Equipment and accessories not subjected to sterilization;
Use of the equipment is prohibited close to flammable
substances or in environments with high concentrations of
oxygen or nitrogen protoxide;
Continuous operating mode equipment;
Equipment not suited to be used in external.
Purpose
Clinical purpose: Therapeutic and aesthetic
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Use: Clinic and domestic use
Mio Sonic is indicated for the treatment of muscular and nervous
pathologies, for traumas recovery and also for chronic and acute
pathologies.
Ultrasound therapy is particularly indicated for analgesic treatment
and for contracted muscle relaxation, and in neuritis, sciatalgy,
articular calcification, tendinitis, hematomas and contractures
treatments.
Ultrasound therapy is also indicated for treatments in aesthetic field
like for example in cellulite treatment, tissues regeneration,
vascularization and lymphatic drainage.
Please read chapter “How to use Mio-Sonic” to get all
information about treatments, applications details and
programs.
Read and follow carefully user manual instructions for a secure
and safe use of the device.
Kit contents
Mio Sonic
Medical Power Supply
Ultrasound gel
User manual
Carriage bag
How to use Mio Sonic
Before and after using Mio Sonic clean and disinfect ultrasound head
with a disinfectant solution.
Instructions
1. Connect the power supply plug to the device.
2. Put a good quantity of ultrasound gel on the area to be
treated. The gel is an important factor in order to guarantee a
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right combination between the treated zone and the
ultrasound head so finally the therapy efficacy.
3. Move the on ON/OFF switch on ON position: PWR led and L
(low intensity) led will be switched on.
4. Put the ultrasound head on the area to be treated.
5. Select the intensity using the button MODE: middle intensity
led (M) and high intensity led (H) will light up sequentially.
6. Select the treatment time using the button TIME: 5-10-15 leds
will light up sequentially and the device will start to work.
ATTENTION: in ultrasound treatment we recommend an
adjusted intensity equal to M. If you use intensities equal to H
pay attention to keep ultrasound head in continuous movement.
Intensity equal to L corresponds to 0,08 W/cm2, M corresponds
to 0,90 W/cm2 and H corresponds to 1,6 W/cm2.
ATTENTION: the device is equipped with a right combination
detector between the ultrasound head and patient skin in order
to guarantee patient safety. In case of wrong combination the
treatment time led starts flashing.
ATTENTION: it’s important to keep in continuous movement
ultrasound head on the treated area during the therapy with
slow and circular or vertical (at least of 7-8 cm) movements. It’s
forbidden to keep ultrasound head fixed in a point during the
treatment.
Analgesic and decontracting treatments
In the imagines pain zones are illustrated by the red color and
trigger points by the blue color.
Make reference to the figures in the attached table PAIN ZONES
AND TRIGGER POINTS in order to get details and suggestions
about treatable pathologies.
Pain zones could be different from trigger points as it’s illustrated in
the figures.
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First we recommend a daily treatment of 10 minutes for a period
of 21 days. If the pain persists we suggest a therapy interruption
of 7 days and eventually you can start a new therapy cycle of 21
days.
Patholgy
Ultras.
Intensity
Frequency
Headache
L
daily
Face pain
L
daily
Mononeuropathy
L-M
daily
Muscle pain
M-H
daily
Cervical Rizopathy
L-M
daily
Neuralgia
M-H
daily
Sciatalgy
M-H
daily
Knee pain
M-H
daily
Trapezius pain
M-H
daily
Lumbalgy
M-H
daily
Thigh pain
M-H
daily
Neck pain
L-M
daily
Shoulder pain
L-M
daily
Elbow pain
L-M
daily
Rheumatic pains
L-M
daily
Intercostal pains
L-M
daily
Menstrual pains
L
daily
Phantom limb pain
L-M
daily
Hip pain
M-H
daily
Knee osteoarthritis pain
M
daily
Beauty treatments
Cavitation
Cavitation is a physical fenomena that consists in the formation of
vapor zones within a fluid. The fluid dissolved gas forms vapor
bubbles or cavities due to ultrasound pressure decrease. Then vapor
bubbles collapses because of movement in high pressure zones.
The delivered energy produces different reactions on the surrounding
areas.
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Cavitation applications
Acoustic waves with frequency from 1 to 16 Mhz are used in medical
field both for diagnosis and dermatoligic purposes. In fact these
waves produces a thermal and analgesic effect and also a cavitation
effect than can be used for kidney stones removal (litotrissia).
Microbubbles collapse destroys kidney stones and it pulverizes solid
substances within the kidney. Moreover cavitation effect is used in
aesthetic medecine in order to decrease or eliminate adiposities.
This technique is called non-surgical liposuction.
Cellulite is a deasese affecting the hypoderma that is a tissue under
the dermal tissue and with an adipose nature. The consequence is
an increase of adipose cells volume, like so hydric retention and
liquids stasis in the inter-cell spaces.
There are three kinds of cellulite desease:
Compact: this type of cellulite causes an oedema that is a
liquids concentration; it appears in adipose tissue in particular
near the ankles, calfs, thighs and it’s present also in persons
with good health conditions and with tonic muscles.
Flaccid: is found in middle-age persons with hypo-tonic
muscles.
Edematous: is the progression of compact cellulite and it
appears in presence of circulatory pathologies.
Cavitation and aesthetic
Aesthetic cavitation consists in low frequency (0,03-3 MHz)
ultrasound waves application that generates vapor bubbles in
adipose tissue. These bubbles rapidly implode delivering energy that
breaks up adipose cell and transform localised fat in a form which
can be easily eliminated by lymphatic system and urinary way and
with the help of a right drainage.
In aesthetic field 3 MHz ultrasounds has been used for years.
Recently new studies induce ultrasound devices manufacturers to
decrease working frequencies since ultrasounds ability to penetrate
in depth in tissues is in inverse proportion to the ultrasound beam
frequency. Nowadays the marketing offers 3MHz,1MHz till 0,03MHz
ultrasound devices.
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Application
Ultrasound head has to work in a uniform way on the area to be
treated in order to avoid adipose anti-aesthetic and solid masses on
non-treated areas.
Ultrasound head has to be in continuous movement in order to
avoid treated zone overheating.
Ultrasound head has to be in continuous contact with the treated
zone through a conductive gel, better if it’s a gel with active
ingredient.
We always recommend to treat a maximum area of 20cmX20cm size
for 10 minutes, afterwards treat an adjacent area in order to treat
finally all interested area.
This kind of treatment can be done with hours or days intervals or
consecutively between the different areas.
Cream or gel use with active ingredients promotes ultrasound action.
In fact ultrasound action promotes substances and active principles
penetration into the tissues (Phonophoresis). As a consequence
ultrasound effect will be amplified if you use a specific active
principle.
Cavitation purpose is to transform adipose cells (fat) in a form
which can be easily eliminated by lymphatic system. After a
cavitation treatment we heartily recommend to do optionally:
a walk at a fast pace for 30/40 minutes
a pressotherapy treatment for 20/30 minutes
swimming for 20/30 minutes
in order to promote “liquid” fat elimination.
Thanks to their effects (thermal, chimical, mechanical, cavitation)
ultrasounds are indicated for:
3MHz beam,
characteristically more
collimated but with
lower tissue
penetration.
1MHz beam,
characteristically less
collimated but with
higher tissue
penetration.
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local sanguine circulation stimulation
skin trophism improvement
cell oxygenation.
Treatments
Ultrasound treatments for drainage/cellulite problems concern the
following body areas:
Thigh
Calfs
Hips (pads)
Ankles
Knees
Gluteus
Arms
Abdomen (with M level as maximum ultrasound intensity)
Cellulite and drainage: each treatment has to be done on a
maximum area 20x20 cm size for 10 minutes. Consequently a thigh
complete treatment will depend on thigh dimension and it will last
from 20 to 30 minutes.
PROGRAMS
ZONE
Intensity
N°
appl.
Frequency
Thighs drainage
M-H
20
daily
Thighs compact cellulite
M-H
30
daily
Thighs flaccid cellulite
M-H
40
daily
Thighs edematous
cellulite
H
40
daily
Calfs drainage
M-H
20
daily
Calfs compact cellulite
M-H
25
daily
Calfs flaccid cellulite
M-H
30
daily
Calfs edematous cellulite
H
30
daily
Pads drainage
M
20
daily
Pads compact cellulite
M
25
daily
Pads flaccid cellulite
M
30
daily
Pads edematous cellulite
M-H
30
daily
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Ankles and knees
drainage
L-H
15
daily
Ankles and knees
compact cellulite
L-H
20
daily
Ankles and knees flaccid
cellulite
L-H
25
daily
Ankles and knees
edematous cellulite
L-H
30
daily
Gluteus drainage
M-H
20
daily
Gluteus compact cellulite
M-H
25
daily
Gluteus flaccid cellulite
M-H
30
daily
Gluteus edematous
cellulite
H
30
daily
Arms drainage
L-M
15
daily
Arms compact cellulite
L-M
20
daily
Arms flaccid cellulite
L-M
20
daily
Arms edematous cellulite
L-M
20
daily
Abdomen drainage
L-M
20
daily
Abdomen compact
cellulite
L-M
25
daily
Abdomen flaccid cellulite
L-M
30
daily
Abdomen edematous
cellulite
M-H
30
daily
Acne / Pimples
L
10/20
daily
ATTENTION:
Keep always in movement ultrasound head
Use a good dose of gel in order to guarantee the contact
Treat a maximum area 20x20cm size during a therapy
session
If the area is bigger than 20x20 cm size do more treatments
in succession on smaller zones
Treat in a uniforme way the interested area
CONTRAINDICATIONS:
Phlogosis
Neoplasia
Pregnancy
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Metal materials near the treated area
Heart area (directly on the chest)
Persons with a pace maker
Arteriopathies
Serious osteoporosis
Thrombophlebitis
Near genital and eyes area
Tumors
Growing bones (younger than 12 years old)
Vertebral column (it’s forbidden to treat area on spinal cord)
Cleaning
Clean the equipment from the dust using a dry soft cloth.
Resistant stains can be removed using a sponge soaked in solution
of water and alcohol.
Carriage and storage
Carriage precautions
MIO-SONIC is a portable device, so it does not need any particular
carriage precautions.
However we recommend to put away MIO-SONIC and its
accessories in their own bag after every treatment.
Storage precautions
Mio-Sonic is protected till following environmental conditions:
Outside of the packaging
temperature from +5 to + 40 °C
humidity from 30 to 85%
pressure from 800 to 1060 hPa
Inside of the packaging
temperature from –10 to +50 °C
humidity from 20 to 93%
pressure from 700 to 1060 hPa
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Disposal
The equipment is subjected to WEEE regulations (see the symbol
on the label) concerning separate waste collection: when
disposing this product, please use the designed areas for disposing
electronic waste or contact the manufacturer.
Electromagnetic interferences and device safety
The device doesn't produce and doesn't receive interferences from
other equipments. However, it’s opportune to use the instrument
keeping it at least at 3 meters from televisions, monitors, cellular
telephones or any other electronic equipment.
The device is manufactured in compliance with EC 60601-12:2001/DIN VDE 0750 Part 1-2.
The device is also in compliance with IEC/EN 60601-1, IEC/EN 606012-5 and IEC/EN 60601-2-10.
Assistance
Every intervention on device must be performed by manufacturer or
national distributor. For any assistance intervention contact:
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE) - Italy
Tel. +39 041 5401356 • Fax +39 041 5402684
You can get any technical documentation on spare parts but only
prior business authorization.
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Spare parts
Contact the manufacturer or the national distributor for original spare
parts at following address:
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE) - Italy
Tel. +39 041 5401356 • Fax +39 041 5402684
To preserve product warranty, functionality and product safety we
recommend to use only original spare parts.
Warranty
Make reference to the national laws for any warranty conditions by
contacting the national distributor (or directly the manufacturer
IACER).
logo is owned by I.A.C.E.R Srl and is registered.
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EMC Compliance
Electromagnetic emission
Emission Test
Compliance
Electromagnetic environment
- guidance
RF Emissions
Cispr 11
Group 1
Mio-Sonic device uses RF
Energy only for its internal
function. Therefore its RF
emission are very low and are
not likely to cause any
interference in nearby
electronic equipment.
RF Emissions
Cispr 11
Class B
Mio-Sonic device is suitable
for use in all establishments,
including domestic
establishments and those
directly connected to the public
low-voltage power supply
network that supplies buildings
used for domestic purposes.
Harmonic Emissions
IEC 61000-3-2
Class A
Complies
Voltage Fluctuations /
Flicker emissions
IEC 61000-3-3
Complies
Electromagnetic immunity
Mio-Sonic is intended for use in the electromagnetic environment specified
below. The customer or the user should assure that it is used in such an
environment.
Immunity Test
EN 60601-1-2
Test level
Compliance
Level
Electromagnetic
environment -
guidance
Electrostatic
Discharge (ESD)
EN 61000-4-2
6kV contact
8kV air
6kV contact
8kV air
Floors should be wood,
concrete or ceramic tile.
If floor are covered with
synthetic material, the
relative humidity should
be at least 30%.
Electrical fast
transient /burst
EN 61000-4-4
2kV for
power supply
lines
2kV for power
supply lines
Mains power quality
should be that of a
typical commercial or
hospital environment.
Surge
EN 61000-4-5
1kV
differential
mode
1kV
differential
mode
Mains power quality
should be that of a
typical commercial or
hospital environment.
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Voltage dips,
short
interruptions and
voltage
variations on
power supply
input lines
EN 61000-4-11
< 5% U
T
(>95% dip in
UT)
For 0,5 cycles
40% U
T
(60% dip in
UT)
for 5 cycles
70% U
T
(30% dip in
UT)
for 25 cycles
< 5% U
T
(>95% dip in
UT)
for 5 seconds
< 5% U
T
(>95% dip in
UT)
For 0,5 cycles
40% U
T
(60% dip in UT)
for 5 cycles
70% U
T
(30% dip in UT)
for 25 cycles
< 5% U
T
(>95% dip in
UT)
for 5 seconds
Mains power quality
should be that of a
typical commercial or
hospital environment.
If the user requires
continued operation
during power mains
interruptions, it is
recommended that the
device be powered from
an uninterruptible power
supply or a battery.
Mains frequency
magnetic field
EN 61000-4-8
3 A/m
3 A/m
Mains frequency
magnetic field should be
that of a typical
commercial or hospital
environment.
r.f. Electromagnetic immunity
Mio-Sonic is intended for use in the electromagnetic environment specified
below. The customer or the user should assure that it is used in such an
environment.
Immunity
Test
EN 60601-
1-2
Test level
Compliance
Level
Electromagnetic environment
– guidance
Conducted
RF
EN 61000-46
3 Veff from
150kHz to
80MHz
3 Veff from
150kHz to
80MHz
Portable and mobile RF
communications equipment
should be used no closer to any
part oft he device, including
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RF Radiata
EN 61000-43
3 Veff da
80MHz a
2,5GHz
3 Veff da
80MHz a
2,5GHz
cables, than the recommended
separation distance calculated
from the equation applicable to
the frequency of the transmitter.
Recommended separation
distance
d = 1,2 P from 150kHz to
80MHz
d = 1,2 P from 80 MHz to 800
MHz
d = 2,3 P from 800 MHz to 2,5
GHz where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site survey, should be less than the compliance level in
each frequency range. Interference may occur in the vicinity of equipment
marked with the following symbol:
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