User manual
PG219 Rev 00 Editi 250316
Pressotherapy model
I-PRESS 4
I.A.C.E.R. Srl
Via S. Pertini 24/A – 30030
Martellago (VE) ITALY
Tel. 041.5401356 • Fax 041.5402684
e-mail: iacer@iacer.it - www.itechmedicaldivision.com
Summary
Summary 3
Pressotherapy 4
Machine body and accessories 5
Accessories size 5
Configurations 7
Specifications 8
Technical Specifications 8
Purpose 8
Labels 9
Working instructions 11
Troubleshooting 15
Warnings 16
Cleaning 18
Maintenance, carriage and storage 19
Disposal 20
Assistance 20
Spare parts 20
Warranty 20
EMC Tables 21
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Pressotherapy
Compressive limbs therapy is able to promote a right venous circulation
by decreasing muscle tension caused by stress or chronic and acute
pains: thanks to its pump action it favorites venous return by increasing
tissues blood circulation and finally their physiological renewal.
Compressive limbs therapy can solve blood stagnation problem in
damaged sanguine vessels or in body zones not correctly bedewed.
External compression allows excess interstitial fluids to return in
circulatory system in order to be quickly removed.
Most common applications are:
• Body massage increase;
• Blood flow promotion thanks to a slow and progressive
pressure;
• Lymphatic drainage;
• Lower limbs relief and comfort;
• Substances stagnation prevention in peripheral tissues;
• Blood insufficiency prevention caused by an inadequate pump
action;
• Muscle tone loss in disabled or paralyzed patients.
Compressive limbs therapy substitutes the manual massage for
trophic purposes.
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OUTPUT
Machine body and accessories
(8)
PRESSURE
PLANTARS
(1)
ON/OFF
(2)
TIMER
LEGGINGS
(6)
CONNECTION TUBE
(3)
AIR DISCHARGE
(5)
PRESSURE
(4)
ELECTRIC
CABLE
(10)
1 DERIVATION
CONNECTION TUBE
(12)
ABDOMINAL
BAND
(9)
2 DERIVATIONS
FOR LEGGINGS
SPECIAL SPLITTER FOR SIMULTANEOUS THERAPY ON BOTH LEGS AND
(13)
ABDOMINAL BAND
ADJUSTEMENT
(7)
EXTENSIONS
FOR LEGGINGS
(11)
ARMBAND
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Accessories size
Legging:
• Length around 76 cm (from upper side to heel)
• Thigh circumference around 65
• Ankle circumference around 38 cm
Armband:
• Max. length around 86 cm
• Biceps circumference around 50 cm
• Wrist circumference around 36 cm
Abdominal band:
• Abdominal around 136 cm
• Height around 46 cm
• Velcro height around 31 cm
Extensions:
• Max. width around 13 cm
• Min. width around 6 cm
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Configurations
I-PRESS 4 can be supplied in 5 different versions:
I-PRESS 4 TOT – compressive limb therapy system comprising
machine body, double legging (6), 2 derivations connection tube
(9), 2 pressure plantars (8), armband (11), abdominal band (12), 1
derivation connection tube (10), special connector for
simultaneous therapy on both legs and abdominal band (13).
I-PRESS 4 LEG2-ABD – compressive limb therapy system
comprising machine body, double legging (6), 2 derivations
connection tube (9), 2 pressure plantars (8), abdominal band (12),
1 derivation connection tube (10), special connector for
simultaneous therapy on both legs and abdominal band (13).
I-PRESS 4 LEG2 – compressive limb therapy system comprising
machine body, double legging (6), 2 derivations connection tube
(9), 2 pressure plantars (8).
I-PRESS 4 LEG1 – compressive limb therapy system comprising
machine body, single legging (6), 1 derivation connection tube
(10).
I-PRESS 4 ARM1 – compressive limb therapy system comprising
machine body, armband (11), 1 derivation connection tube (10).
Extensions for wide legs (7) and special connector for simultaneous
therapy on both legs and abdominal band (13) are available as
accessories.
Single accessories are available as optional to complete I-PRESS 4
content and potentiality.
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Power Supply
220-240 VAC,
Therapy time
Impostabile 0÷30
Current
0,2 A
Max pressure
300 mm Hg
Max output
50 VA Weight
2 Kg
Specifications
I-PRESS 4 has the following specifications:
• Class IIa equipment (Directive 93/42/EEC, annexed IX, rule 9);
• Class II, applied part type BF (Classif. CEI EN 60601-1);
• CE0476 certificate;
• Equipment not protected against liquids penetration;
• 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;
• Continuous operating mode equipment;
• Equipment not suited to be used in external.
Technical Specifications
power
Purpose
Compressive limbs therapy device designed for the treatment of
vascular system diseases. It promotes the blood flow and prevents
thrombosis and/or vessels obstructions.
Clinical Purpose: Therapeutic
Use: Clinic and domestic use
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50-60 Hz
min.
(±10%)
Compressible Limb Therapy
Labels
Model I-PRESS 4
System
Voltage AC220~240V Frequency 50/60Hz
Maximum output
power
50VA
Maximum
pressure
300mmHg±10%
I.A.C.E.R srl
Via Sandro Pertini 24/A
30030 Martellago (VE), Italy
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Warning
Product subject to WEEE regulations concerning separate
waste collection of electronic equipment
Applied part type BF
Class II equipment
Compliance with Directive 93/42/EEC
Manufacturing date
Attention, consult operating instructions
Instructions for use
Device with IP21 level protection
Not protected against liquids entrance, keep dry.
Relative humidity for product storage
Temperature range for product storage
Pushing prohibited
Sitting prohibited
Stepping prohibited
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Working instructions
1) Connect cable to the domestic plug 220-240 VAC, then turn ON (1)
the ON/OFF switch (1);
2) Wear the applicators
a) Leggings use
i) Wear the leggings (or single legging) and close the zip up
to the end, then close the retaining Velcro straps; in case of
wide circumferences legs, connect the extensions available
as accessories;
ZIP
VELCRO
CONNECTION
PLUGS
i) Insert the pressure plantars under the feet (available only
with double leggings);
ii) When wearing the leggings pay attention to position the
tubes connection cables in the internal side of each
legging; in single legging version connection cables
position is not important;
iii) Connect 4 tubes to the 4 plugs positioned on each legging,
paying attention to connect the longer tube to the higher
position connector (darker color) of legging (thigh);
PRESSURE PLANTARS
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iv) After connecting the tubes to the relatives leggings,
connect the tubes to the air discharge output (5).
b) Abdominal band use
i) Wear the band and connect the tubes to the band plugs,
paying attention to connect the longer tube to the higher
position connector on abdominal band;
ii) After connecting the tubes to the band, connect the tubes
to the air discharge output (5).
b) Simultaneous use of double leggings and abdominal band
i) Connect the
special splitter for
simultaneous
therapy (13) to
the air discharge
output (5). Then
connect double
leggings and
abdominal band
connectors to the
splitter;
CONNECTION
PLUGS
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ii) Wear the leggings (or single legging) and close the zip up
to the end, then close the retaining Velcro straps; in case of
wide circumferences legs, connect the extensions available
as accessories;
iii) Insert the pressure plantars under the feet (available only
with double leggings);
iii) When wearing the leggings pay attention to position the
tubes connection cables in the internal side of each
legging; in single legging version connection cables
position is not important;
iv) Connect 4 tubes to the 4 plugs positioned on each legging,
paying attention to connect the longer tube to the higher
position connector (darker color) of legging (thigh);
iv) After connecting the tubes to the relatives leggings,
connect the tube to the splitter connected to the air
discharge output (13);
v) Wear the band and connect the tubes to the band plugs,
paying attention to connect the longer tube to the higher
position connector on abdominal band;
vi) After connecting the tubes to the band, connect the tubes
to the splitter connected to the air discharge output (13).
c) Armband use
i) Wear the armband and
connect the tubes to the
armband plugs, paying
attention to connect the
longer tube to the higher
position connector
(darker color) on
armband;
ii) After connecting the
tubes to the armband
connect the tubes to the
air discharge output (5).
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3) Therapy time (selector (2) on machine body)
a) Therapy time can be adjusted from 0 to 30 minutes: pump
motor of main body will start operating;
b) The air will fill up in applicator chambers in 2 minutes.
Attention: The time selector cannot be moved counterclockwise
during the treatment. Please wait the session end to adjust a new
therapy time
4) Pressure regulator (selector (3) on machine body)
c) Air pressure in compression chambers can be adjusted from 0
to maximum pressure (around 300 mmHg ± 20%) by rotating
the knob in clockwise;
a) Start the treatment with a middle pressure and increase it
progressively according to your needs.
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Troubleshooting
Problem Solution
I-PRESS 4 doesn’t
switch on
I-PRESS 4 emits a
strange sound like
air leakage
There is no
pressure or the air
doesn’t go into the
applicators
Air goes into the
compression
chambers and/or
an air leakage is
present in the
applicators
ATTENTION: with I-PRESS 4 double leggings version, always connect
both leggings to the connection tube even if you use only one legging
during the treatment.
• Check the connection to the domestic
plug
• Check the ON/OFF button
• Check the power supply status (no sign
of damages)
• Check if there are any damages and/or
holes in the tubes and connectors
• Check the applicators right connection to
the main body
• Check if the tubes are pressed or bent
• Check the applicator right connection to
the main body
• Check if the tubes are pressed or bent
• Check if the compression chambers
swell up in a progressive way
• Check if there are any holes or
damages in the compression chambers.
If there are not any air leakages, switch
off the device then switch on it and recheck the right working
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Warnings
The following warnings guarantee user safety and prevention against
damages and/or lesions.
Please read it carefully before using I-PRESS 4.
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Cleaning
Clean the device and its accessories using a soft cloth.
Resistant stains can be removed using a sponge soaked in solution of
water and mild soap.
Wait for the complete drying before using the device and its
accessories.
Do not use chemical substances, solvents or cleaners to avoid device
and accessories damage.
Maintenance, carriage and storage
If it is used in accordance with the instructions of the user manual, the
device does not need a particular regular maintenance.
Carriage precautions
It doesn’t need any particular carriage precautions: however we
recommend to put away I-PRESS 4 and its accessories in their own box
after every treatment.
Storage precautions
I-PRESS 4 is protected till following environmental conditions.
Outside of the packaging
temperature from +5 to + 40 °C
humidity from 30 to 80%
pressure from 500 to 1060 hPa
Inside of the packaging
temperature from –10 to +55 °C
humidity from 10 to 90%
pressure from 500 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.
Assistance
Every intervention on device must be performed by manufacturer. For
any assistance intervention contact the national distributor or:
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE) -ITALY
Tel. 041.5401356 • Fax 041.5402684
You can get any technical documentation on spare parts but only prior
business authorization.
Spare parts
Contact the distributor or the fabricant for original spare parts at
following address:
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE)
Tel. 041.5401356 • Fax 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).
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Guidance and MANUFACTURER’S declaration
– ELECTROMAGNETIC EMISSIONS
Emission test
Compliance
Electromagnetic environment
–
Guidance and MANUFACTURER’S declaration
– ELECTROMAGNETIC IMMUNITY
Immunity test
Test level EN
Compli
ance level
Electromagnetic
±
±
EMC Tables
I-PRESS S 4 is intended for use in the electromagnetic environment specified below.
The customer or the user of the I-PRESS 4 should assure that it is used in such an
environment.
RF emissions
Cispr 11
RF emissions
Cispr 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
– FOR ALL THE EQUIPMENT AND THE SYSTEMS
Group 1
Class B I-PRESS 4 is suitable for use in all
Class A
Complies
Complies
I-PRESS 4 uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network that supplies
buildings used for domestic purposes.
The I-PRESS 4 is suitable for use in all
establishments, other than domestic
establishments and those directly
connected to the public low voltage
power supply network that supplies
buildings used for domestic purposes
guidance
I-PRESS 4 is intended for use in the electromagnetic environment specified below.
The customer or the user of I-PRESS 4 should assure that is used in such
environment.
– FOR ALL THE EQUIPMENT AND THE SYSTEMS
60601-1-2
Electrostatic
discharge (ESD)
EN 61000-4-2
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6kV contact
± 8kV air
6kV contact
± 8kV air
environment –
guidance
Floors should be
wood, concrete or
ceramic tile. If floor
are covered with
synthetic material,
the relative humidity
should be at least
30%
±
±
recommended that
Electrical fast
transient/burst
IEC 61000-4-4
Impulses
EN 61000-4-5
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
Mains power
electromagnetic field
EN 61000-4-8
± 2kV for power
supply lines
1kV differential
mode
< 5% U
T
(>95% dips of UT)
per 0,5 cycles
40% U
T
(60% dips of UT)
per 5 cycles
70% U
T
(30% dips of UT)
per 25 cycles
< 5% U
T
(>95% dips of UT)
per 5 seconds
3 A/m 3 A/m Mains power quality
± 2kV per power
supply lines
1kV differential
mode
< 5% U
T
(>95% dips of UT)
per 0,5 cycles
40% U
T
(60% dips of UT)
per 5 cycles
70% U
T
(30% dips of UT)
per 25 cycles
< 5% U
T
(>95% dips of UT)
per 5 seconds
Mains power quality
should be at that of
a typical commercial
or hospital
environment.
Mains power quality
should be at that of
a typical commercial
or hospital
environment.
Mains power quality
should be at that of
a typical commercial
or hospital
environment.
If the user of the IPRESS 4 requires
continued operation
during power mains
interruptions, it is
I-PRESS 4 be
powered from an
uninterruptible
power supply or a
battery.
should be at that of
a typical commercial
or hospital
environment.
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Guidance and MANUFACTURER’S declarat
ion –
ELECTROMAGNETIC IMMUNITY
–
Immunity test
Test level EN
Compliance
Electromagnetic
Portable and mobile RF
Recommended separation distances between portable and mobile
Rated maximum
Separation distance according to the frequency of the
150kHz to 80MHz
80MHz to 800MHz
800MHz to
FOR ALL THE EQUIPMENT AND THE SYSTEMS
SUPPORTING
THAT ARE NOT LIFE-
I-PRESS 4 is intended for use in the electromagnetic environment specified below. The
customer or the user of I-PRESS 4 should assure that is used in such environment
Conducted RF
EN 61000-4-6
RF Radiata
EN 61000-4-3
60601-1-2
3 Veff from
150kHz to 80MHz
3 Veff from
80MHz to 2,5GHz
level
3 Veff from
150kHz to 80MHz
3 Veff from
80MHz to 2,5GHz
environment – guidance
communications equipment
should be used no closer to
any part of I-PRESS 4,
including cables, than the
recommended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance:
d = 1,2 ⋅√P 150kHz to 80MHz
d = 1,2 ⋅√P 80 MHz to 800
MHz
d = 2,3 ⋅√P 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 strangths from fixed RF transmitters, are determined by an electromagnetic site
survey, should be less than the complicance level in each frequency rage.
Interference may occur in the vicinity of equipment marked with the
following symbol:
I-PRESS 4 is intended for the use in an electromagnetic environment in which radiated RF
communications equipment and the EQUIPMENT
disturbances are controlled. The customer or the user of I-PRESS 4 can help prevent
electromagnetic interferences by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and I-PRESS 4 as recommended
below, according to the maximum output power of the communication equipment.
power of the
transmitter (m)
transmitter (W)
d = 1,2 ⋅√P
0,01 0,12 0,12 0,23
0,1 0,38 0,38 0,73
1 1,2 1,2 2,3
10 3,8 3,8 7,3
100 12 12 23
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d = 1,2 ⋅√P
2GHz
d = 2,3 ⋅√P
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in metres (m) can be estimated using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in Watts (W) according to the transmitter manufacturer.
Note:
(1) At 80 MHz and 800 MHz the separation distance for the higher frequency range
applies.
(2) These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
I-PRESS 4. All rights reserved. I-PRESS 4 and logos are owned by
I.A.C.E.R Srl and are registered.
IACER SRL Page 24 MNPG219-00 25/03/16
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