HF IBRAMED

HF IBRAMED
HF IBRAMED
Manufactured by IBRAMED
Indústria Brasileira de Equipamentos Médicos EIRELI
Made in Brazil
ANVISA Nº: 10360310020
2th edition (REV_03/2012)
TABLE OF CONTENTS
fIGURES GLOSSARY.....................................................3
SYMBOL DEFINITIONS.................................................4
PREFACE....................................................................5
PRODUCT DESCRIPTION...............................................5
PRECAUTIONARY DEFINITIONS.............................6
SAFETY PRECAUTIONS.................................................6
INDICATIONS AND CONTRAINDICATIONS.......................8
PATIENT PROFILE, USERS PROFILE AND TREATMENT AREA...9
RESPONSIBILITY FOR USE ELECTROMEDICAL EQUIPMENT...10
ENVIRONMENTAL PROTECTION....................................11
ELECTROMAGNETIC COMPATIBILITY GUIDANCE.............12
ELECTROMAGNETIC COMPATIBILITY.............................13
NOMENCLATURE........................................................19
SYSTEM SPECIFICATIONS..................................20
SPECIFICATIONS.......................................................20
HF IBRAMED - ELECTRICAL POWER FEED......................21
HF - HIGH FREQUENCY...............................................21
DIRECTIONS FOR TREATMENT PERFORMANCE...............22
GLASS ELECTRODES - APPLICATORS HIGH FREQUENCY..23
TURNING ON THE HF IBRAMED....................................25
ACCESSORIES WHICH ACCOMPANY HF IBRAMED...........26
TROUBLESHOOTING...................................................27
MAINTENANCE, WARRANTY terms AND TECHNICAL
SUPPORT..................................................................28
CEFAI – IBRAMED Center for Education and
Advanced Training................................................30
FIGURES GLOSSARY
Figure 1. HF Ibramed Pen............................................21
Figure 2. A: larger spherical type electrode used in direct
sparkling or fluxation. Before attaching the spherical electrode
to the patient, place one fingertip on the extremity of the
pen, and only remove it when the electrode is in contact with
the patients skin. B: Comb glass electrode used for capillary
treatment.................................................................23
Figure 3. A: small spherical glass electrode used in direct
sparkling or fluxation. Before attaching the spherical
glass electrode to the patient, place one fingertip on the
extremity of the pen and only remove it when the electrode
is in contact with the patient’s skin................................23
Figure 4. Fork glass electrode used in direct sparkling or
fluxation in curved treatment areas such as neck, arms,
breasts, armpits, etc.....................................................23
Figure 5. Saturator glass electrode used in indirect sparkling.
It increases the vascularization of the skin. It is normally
applied with oils and skin nutrition creams......................23
Figure 6. Correct position for the patient to hold the
saturator glass electrode while the therapist performs
manual
stimulation
on
the
treatment
area.....24
Figure 7. Cauterizing glass electrode used in direct sparkling
for acne hemostasis.....................................................24
3
SYMBOL DEFINITIONS
BELOW ARE THE DEFINITIONS OF THE SYMBOLS USED ON THE EQUIPMENT AND THROUGHOUT THE INSTRUCTIONS
FOUND IN THIS MANUAL. UNDERSTAND THESE SYMBOLS AND THEIR DEFINITIONS BEFORE OPERATING THIS
EQUIPMENT.
Keep away from the rain.
Caution! Refer to user manual.
Voltage in AC (Alternating Current).
Stacking up.
Fragile.
This side up.
Limits of temperature for storage and
packaging in °C (Celsius Degrees).
4
PREFACE
PRODUCT DESCRIPTION
These instructions of use allow the user to use the Ibramed
HF Pen efficiently. Users must read, understand and follow the information present in these instructions of use
for each possible treatment mode as well as indications,
contraindications, warnings and precautions. The specifications and instructions present in these instructions of
use are applicable on the date of its publication. These instructions of use can be visualized at any given time, under
the manufacturer criterion. Visit our webpage for updates.
HF Ibramed is a portable high frequency piece of equipment
for facial, body, capillary and podology application. The
application frequency is monopolar, that is, only one electrode
is used. The function of the gas inside the electrode is to
induce the current flow. This gas is excited through the
passage of electric current and produces a light, whose color
depends on the type of gas used. The gas is then ionized by
the high tension, making the glass bulb fluorescent.
• Position the HF Pen cable in such a way that it is free,
away from places where it might be treated on, and do not
place any piece of furniture over it.
• The HF application electrodes are made of glass. Incorrect
handling may break them or affect their characteristics.
Therefore, avoid ‘impact or mechanical chocks’.”.
• Do not introduce object in the orifices on the equipment
and do not lean any recipients containing liquid on the
equipment.
• Do not use volatile substances (benzene, alcohol, and
solvents in general) to clean the Ibramed HF Application
Pen. They may damage the equipment cover. Use only a
clean, dry and soft cloth.
5
SAFETY PRECAUTIONS
PRECAUTIONARY DEFINITIONS
The precautionary instructions found in this section and
• Read, understand, and practice the precautionary and
throughout this manual are indicated by specific symbols.
operating instructions. Know the limitations and hazards
Understand these symbols and their definitions before
associated with the use of any electrical stimulation.
operating this equipment prior to therapy session.
• Observe the precautionary and operational labels placed
on the unit.
• DO NOT operate this unit in an environment where other
Text with a “CAUTION” indicator refers to potential safety
devices intentionally radiate electromagnetic energy in an
infractions that could cause minor to moderate injury or
unshielded manner.
damage to equipment.
This unit should be transported and stored at temperatures
between 41°F and 122°F (5°C and 50°C); Avoid damp and
dusty environments.
Text with a “WARNING” indicator refers to potential safety
• Check cables and associated connectors before each use.
infractions that could cause serious injury and equipment
• The HF IBRAMED Electro Stimulator is not designed
damage.
to prevent the infiltration of water or other liquids. The
infiltration of water or other liquids could cause malfunction
of internal components of the system and therefore create a
Text with a “DANGER” indicator refers to potential safety
risk of injury to the patient.
infractions that represent immediately life threatening
• Disconnect the power plug from the outlet when left unused
situations that would result in death or serious injury.
for long periods of time.
6
SAFETY PRECAUTIONS
• Be sure the unit is grounded by connecting it to a grounded
• Patients with an implanted electrical device should not be
treated with high frequency.
electrical outlet compliant with the applicable national and
local electrical codes.
• Prior to patient treatment become familiar with the
operating procedures for each mode of treatment available,
as well as the indications, contraindications, warnings
and precautions. Consult other resources for additional
information regarding the applications of
Electrotherapy.
• To prevent electrical shock, disconnect the unit from the
power source before performing any maintenance task.
• Stimulation should not be applied on or near cancerous
lesions.
7
INDICATIONS AND CONTRAINDICATIONS
INDICATIONS OF USE
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
Facial, capillary and podology treatments
Acne skin and podal lesion treatments
Cauterization of skin following pustule extraction
Facilitation in permeation of an active
Skin rejuvenation and hydration protocols
Disinfection of scalp in case of seborrhea
Facial and capillary blood circulation stimulation
Post depilation
Solution of skin continuity (ulcers of pressure and open
wounds)
• Sore wounds following extraction of nail bed cuticle
GENERAL CONTRAINDICATIONS
Local tumor
Unbalanced diabetes or hypertension
Allergy to current
Infection processes
Epilepsy
Kidney or cardiac insufficiency
Patients with diagnosis for deep venous thrombosis
• Do not use as an adjuvant flammable or alcoholic nature
products.
• Remove all metal accessories of the patient
• Pregnancy or intention to become pregnant
• IMPLANTED ELECTRONIC DEVICES – We recommend
that a patient with an implanted electronic device (ex:
pacemaker) is not subjected to electrostimulation therapy,
unless a medical authorization has been previously given.
• HEARING AIDES – hearing aides must be removed during
sessions. If subjected to electrical stimulation, the hearing
aides might undergo damage and present malfunction.
8
PATIENT PROFILE, USERS PROFILE AND TREATMENT AREA
PATIENT PROFILE
USERS PROFILE
• Patients must be over twelve years of age, under that age
• Este dispositivo debe ser usado solamente bajo prescripción
only by medical or physiotherapeutic prescription.
y supervisión de un profesional de la salud diplomado.
• Patients must weigh more than 35 kg, under that weight only
• Este dispositivo no necesita de capacitación especializada,
by medical or physiotherapeutic prescription.
sin embargo, el usuario de este dispositivo debe leer,
• There are no restrictions regarding nationality.
comprender y practicar las instrucciones de precaución y
• Patients must have their level of consciousness preserved.
funcionamiento.
• El usuario debe conocer las limitaciones y peligros asociados
PART OF THE BODY OR TISSUE ON WHICH IT
IS APPLIED OR WITH WHICH IT INTERACTS
con el uso de dispositivos electrónicos y observar las etiquetas
Areas of the torso ( except precordial region), upper and lower
limbs, face, neck and décolleté (except thyroid region).
• El usuario debe seguir las informaciones contenidas en
de precaución y operacionales colocadas en esta unidad.
estas instrucciones de uso para la modalidad de tratamiento
disponible, así como las indicaciones, contraindicaciones,
advertencias y precauciones.
• El usuario debe tener íntegras sus funciones cognitivas.
• El usuario debe tener íntegras las funciones motoras
necesarias para el manejo de este equipo.
• En relación a la movilidad, este equipo es considerado en
equipo portátil.
9
RESPONSIBILITY FOR USE ELECTROMEDICAL EQUIPMENT
The use of electromedical equipment is restricted to a physician or under his command, the physical therapists or health
professionals properly licensed.
The professional will be responsible for properly licensed use and operation of the equipment. IBRAMED makes no representations
regarding laws and federal, state or local laws that may apply to the use and operation of
any electromedical equipment.
The physician or under his command, also the physical therapist or other professional health care licensed assumes total and full
commitment to contact the local certifying agencies to determine any credential required by law for clinical use and operation of
this equipment.
The use of electromedical equipment must comply with the local, state and federal country.
10
ENVIRONMENTAL PROTECTION
HF IBRAMED is an electronic device and has heavy metal parts such as lead. So, there are risks of contamination to the
environment associated with the discharge of this device and its accessories at the end of their service life. HF IBRAMED, its
parts and the accessories must not be disposed of as urban residues. Contact the local distributor to obtain information about
norms and laws relative to the elimination of electrical residues, electronic equipment and their accessories.
The device and its consumable parts must be eliminated at the
end of their shelf-life, according to the federal norms and/or
state norms and/or local norms of each country.
11
ELECTROMAGNETIC COMPATIBILITY GUIDANCE
Medical Electrical Devices require special attention regarding Electromagnetic Compatibility (EMC) and must be installed and
put into service according to the EMC information provided in the following tables.
Portable and Mobile Radio Frequency (RF) communications equipment can affect Medical Electrical Devices.
The use of accessories, other than those listed, except when supplied or sold by Ibramed Indústria Brasileira de Equipamentos
Médicos Ltda as replacement parts for internal or external components, may result in increased emission or decreased immunity
of the HF IBRAMED Electro Stimulator.
12
ELECTROMAGNETIC COMPATIBILITY
Directions and Manufacturer’s Statement – electromagnetic emissions
The HF IBRAMED electro-stimulator is destined for use in the electromagnetic environment specified below. The user of the
equipment must ensure that it is used in such an environment.
Emission Essay Compliance
RF Emissions
Group 1
NBR IEC CISPR 11
IEC CISPR 11
RF Emissions
Harmonics Emission
Class A
Emissions due to tension
fluctuation/scintillation
IEC 61000-3-3
HF IBRAMED stimulator uses RF energy only for its internal
functions. However, its RF emissions are very low and unlikely to
cause any interference in nearby electronic equipment.
Class A
NBR IEC CISPR 11
IEC CISPR 11
IEC 61000-3-2
Electromagnetic Environment directions
HF IBRAMED electrostimulator is adequate for use in all
premises which are not residential and not directly connected
to the public low tension electric power distribution line which
supplies buildings appropriate for domestic use.
Class A
13
ELECTROMAGNETIC COMPATIBILITY
Directions and Manufacturer’s Statement - electromagnetic immunity
The HF IBRAMED electro-stimulator is destined for use in the electromagnetic environment specified below. The user of the
equipment must ensure that it is used in such an environment.
Immunity Trial
Electrostatic
Discharge
(ESD)
IEC 61000-4-2
Rapid electric
transitory / train
pulse
(Burst)
IEC 61000-4-4
Surges
IEC 61000-4-5
Level of the trial
IEC 60601
± 6 kV per
contact
± 8 kV by air
± 2 kV in the
Power lines
± 1 kV in the
input /output
lines
± 1 kV differential
mode
± 2 kV regular mode
Level of Conformity
± 6 kV per contact
± 8 kV by air
Electromagnetic Environment - directions
The flooring must be either wooden, concrete or
ceramic. If the flooring is covered with synthetic
material, the humidity must be of least 30%.
± 2 kV in the
The quality of the power supply should be equivalent
Power lines
± 1 kV in the
input /output lines
to the one of a hospital or a typically commercial
establishment.
± 1 kV differential
mode
± 2 kV regular mode
14
The quality of the power supply should be equivalent
to the one of a hospital or a typically commercial establishment.
ELECTROMAGNETIC COMPATIBILITY
Level of the
trial
IEC 60601
Level
of Conformity
< 5% U T
(> 95% of tension fall
< 5% U T
(> 95% of tension fall
in U ) per 0.5 cycle
Immunity Trial
Voltage falls,
short interruptions
and voltage
variations in the
input power lines
IEC 61000-4-11
in U
T
) per 0.5 cycle
40% U T
(60% of tension fall in
U
T
) per 5 cycles
70% U T
(30% of tension fall in
U
T
) per 25 cycles
< 5% U T
(> 95% of tension
fall in U
seconds
Magnetic Field in
the frequency of
Power feed
(50/60 Hz)
3 A/m
T
) per 5
40% U T
(60% of tension fall in
U
T
) per 5 cycles
70% U T
(30% of tension fall in
U
T
T
The quality of the power supply should be
equivalent to the one of a hospital or a typically
commercial establishment. If the user of the
equipment
requires
continuous
operation
during energy interruption, it is recommended
that the equipment should be fed by a source
of uninterrupted power supply or a battery.
) per 25 cycles
< 5% U T
(> 95% of tension
fall in U
seconds
T
) per 5
Magnetic fields in the frequency of power supply
must be on the same levels characteristic of a
hospital environment or a typically commercial
establishment.
3 A/m
IEC 61000-4-8
NOTE: U
Electromagnetic Environment directions
is the power AC voltage before the application of the trial level.
15
ELECTROMAGNETIC COMPATIBILITY
Directions and Manufacturer’s Statement - electromagnetic immunity
The HF IBRAMED electro-stimulator is destined for use in the electromagnetic environment specified below. The
user of the equipment must ensure that it is used in such an environment.
Level of the trial
Level
Electromagnetic Environment - directions
Immunity Trial
IEC 60601
of Conformity
RF Communication equipment, portable or mobile, must
not be used next to any part of HF IBRAMED, including
cables, with a separation distance of less than the
recommended, calculated from the equation applicable to
the frequency of the transmitter.
RF Conducted
IEC 61000-4-6
3 Vrms
150 kHz to
80 MHz
Separation distance recommended
d = 1.2
3V
d = 0.35 800 MHz up to 800 MHz
d = 0.7 800 MHz up to 2.5 GHz
RF Radiated
IEC 61000-4-3
10 V/m
80 MHz to 2.5 GHz
Where P is the maximum output nominal potency of the
transmitter in watts (W) according to the manufacturer
of the equipment, and d is the separation distance
recommended in meters (m).
It is also recommended that the Field intensity
established by the RF transmitter, as determined by an
electromagnetic inspection at the site should be lower
than the conformity in each frequency band .
Interference around the equipment marked with the
following symbol might occur:
10 V/m
16
ELECTROMAGNETIC COMPATIBILITY
NOTE 1: In 80 MHz and 800 MHz highest frequency band is applied.
NOTE 2: These directions may not be applicable in all situations. The electromagnetic propagation is affected by the absorption
and reflection of structures, objects and people.
The Field intensities established by the fixed transmitters, such as base radio stations, telephone (cellular/wireless) and
mobile terrestrial radios, radio amateur, transmission radio AM and FM and TV transmission cannot be theoretically predicted
with accuracy. To evaluate the electromagnetic environment due to fixed RF, an electromagnetic, it is recommended to check
the local. If the field intensity measurement at location where HF IBRAMED is used, exceeds the level of conformity used
above, the equipment must be observed in order to verify whether the operation is normal. IF an abnormal performance is
observed, additional procedures may be necessary, such as reorientation or the reinstalling of the equipment.
a
b
Above 150 KHz to 80 MHz frequency band, the field intensity should be lower than 10 V/m
17
ELECTROMAGNETIC COMPATIBILITY
Recommended Separation Distances between portable and mobile RF and HF IBRAMED
The HF IBRAMED electro-stimulator is conceived to be used in electromagnetic environments in which RF disturbances
are controlled. The user of the electrostimulator may help to prevent electromagnetic interferences by keeping a minimum
distance between the portable and mobile RF communication equipment (transmitters) and HF IBRAMED, as recommended
below, according to the maximum potency of the communication equipment.
Maximum Nominal
Output potency of
the transmitter
W
Distance of Separation in accordance with the frequency of the transmitter
m
150 KHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
d = 1.2
d = 0.35
d = 0.7
0.01
0.12
0.035
0.07
0.1
0.38
0.11
0.22
1
1.2
0.35
0.7
10
3.8
1.1
2.2
100
12
3.5
7
For transmitters with a maximum nominal output potency not listed above, the separation distance recommended in
meters (m) may be determined by an equation applicable to the frequency of the transmitter, where P is the maximum
nominal output potency in watts (W) according to the manufacturer of the transmitter.
NOTE 1: From 80 MHz to 800 MHz, the distance of separation relative to the highest frequency band is applied.
NOTE 2: These directions may not be applicable in all situations. The electromagnetic propagation is affected by the
absorption and reflection of structures, objects and people.
18
NOMENCLATURE
7
4
1
2
6
3
5
1. HF application pen
2. High Frequency intensity on/off switch
3. HF pen cable
4. Power feeding equipment
5. HF cable output
6. 110/220 volts converter key
7. Connection pins from feeding source to power outlet
19
SPECIFICATIONS
SYSTEM SPECIFICATIONS
Dimensions
Width
7 cm (2.7 in)
Depth
11 cm (4.3 in)
Height
6 cm (2.3 in)
Temperature Range During Transport and Storage:
5 - 50°C/ 41 - 122°F.
Environment operating temperature range:
5 - 45°C/ 41 - 113°F.
Standard Weight (without accessories) 500 g
Power
Input
127/240V ~ 50/60 Hz
Input Power
50 VA
Electrical Class CLASS II
Electrotherapy
TYPE BF
Regulatory Compliance
IEC 60601-1
IEC 60601-1-2
20
HF IBRAMED - ELECTRICAL POWER FEED
HF - HIGH FREQUENCY
In the High Frequency mode, glass electrodes filled with
special gas are used as a conductor mean to electrical
stimulation The equipment generates an alternated current
of some thousands of volts (low current) which is applied
to this glass electrode. The gas inside the electrode is then
excited, producing small ‘electrical sparks’ on the external
face of the glass electrode. During this process of electrical
sparks, ozone is generated, and the properties of ozone
(oxygenating, fungicide, bactericide and viral inactivation)
are used in this type of treatment. The ozone is a reactive
type of oxygen. Oxygen (O2) in nature is composed of only
two atoms, while ozone (O3) is composed of three atoms.
At room temperature, ozone is an invisible gas, with a
characteristic odor. For the treatment, a so-called HF pen is
used. It is to this pen that the glass electrodes are connected.
These electrodes present differentiated shape to adequate
themselves to the treatment areas.
For the treatment, a so-called HF pen is used. It is to this
pen that the glass electrodes are connected.
HF Ibramed is adjusted for a power grid of 220 volts /
50/60 Hz. If necessary, it can be adjusted for 110 volts /
50/60 Hz; just by converting the 110/220 volt key located
on the cabinet rear power feed panel.
The equipment has an internal protection fuse, not
accessible to the user.
NOTE: never open the electrical power feed and/or the
HF application pen in the equipment. There are dangerous
tensions present inside these parts.
Figure 1. HF Ibramed Pen
21
DIRECTIONS FOR TREATMENT PERFORMANCE
1. Clean the skin and apply the electrode on the skin
(fluxation) or brief touches on the skin (direct sparkling)
2.
Demonstrate the technique to the patient before
initiating procedure.
3.
The larger and smaller spherical electrodes may be
used in the fluxation or sparkling techniques, however,
before placing the electrode on the patient, the therapist
must touch the extremity of the electrode with the tip of
the fingers and remove it only after the contact with the
patient’s skin. This avoids the occurrence of an electrical
discharge to the patient, which might frighten the patient.
4.
The fork electrode is used in direct sparkling or neck
fluxation on the arms, neck, breasts, etc. to facilitate the
access to these areas.
Attention: Avoid contact with the HF pen extremity where
it connects to the glass electrode, because dangerously
intense sparks might occur. Always hold the body of the
HF pen. Never hold the pen cable.
Asepsis: Wash the glass electrodes with current water
and soap and then dry them with paper towels. This
type of electrode is self-cleaning the ozone production
itself will provide sterilization.
5.
The saturator electrode is used in indirect sparkling.
The application technique is performed by the patient
holding the saturator glass electrode while the therapist
promotes manual stimuli on the treatment area.
6.
The cauterizing electrode is used in direct sparkling
for hemostasis of acne lesions. This electrode concentrates
charge on its tip.
7.
Comb electrode, used for alopecia lesions and other
affected scalp areas. Always apply over dry hair. Comb
the hair with the comb electrode in all directions using the
fluxation technique.
22
GLASS ELECTRODES - APPLICATORS HIGH FREQUENCY
For facial, body capillary and podology treatments, there
are many different types of glass electrodes, making it
difficult to describe all of them here. Below, we describe
the most commonly used types of electrodes:
OPTIONAL GLASS ELECTRODES WHICH MAY
BE USED
GLASS ELECTRODES WHICH ACCOMPANY
HF IBRAMED
Figure 3. A: small spherical glass electrode used in direct
sparkling or fluxation. Before attaching the spherical glass
electrode to the patient, place one fingertip on the extremity
of the pen and only remove it when the electrode is in
contact with the patient’s skin.
A
B
Figure 4. Fork glass electrode used in direct sparkling or
fluxation in curved treatment areas such as neck, arms,
breasts, armpits, etc.
Figure 2. A: larger spherical type electrode used
in direct sparkling or fluxation. Before attaching the
spherical electrode to the patient, place one fingertip
on the extremity of the pen, and only remove it when
the electrode is in contact with the patients skin.
B: Comb glass electrode used for capillary treatment.
Figure 5. Saturator glass electrode used in indirect
sparkling. It increases the vascularization of the skin. It
is normally applied with oils and skin nutrition creams.
23
GLASS ELECTRODES - APPLICATORS HIGH FREQUENCY
Figure 6: Correct position for the patient to hold the
saturator glass electrode while the therapist performs
manual stimulation on the treatment area.
Figure 7: Cauterizing glass electrode used in direct
sparkling for acne hemostasis.
24
TURNING ON THE HF IBRAMED
1.
2.
3.
Before connecting the HF pen, check if the on/off switch and the high frequency intensity key are in the OFF position.
Turn on the HF power feed equipment to the local power line outlet. Read the chapter HF Ibramed – Electrical Feed
before doing so.
Connect the glass high frequency applicator to the tip of the HF pen.
4.
Now, the intensity of the High Frequency can be increased by turning this switch clockwise and it can be decreased by
turning this switch anticlockwise.
5.
At the end of treatment, turn off the equipment turning the intensity control anticlockwise until the position OFF (you will
hear a “CLICK”).
Note: If the HF IBRAMED is not going to be used, remove the electrical power feed from the power line.
25
ACCESSORIES WHICH ACCOMPANY HF IBRAMED
HF IBRAMED contains accessories designed to satisfy the demands of electromagnetic compatibility.
CODE
03026016
03026018
03040004
03026038
QUANTITY
1
1
1
1
PRODUCT
Comb electrode for High Frequency
Large Spherical electrode for High Frequency
IBRAMED Digital User’s Manual 260410
Case for Portable HF Ibramed
26
TROUBLESHOOTING
What may initially look like a problem is rarely a defect. Before calling customer support, please check the items described
below:
SOLUTIONS
PROBLEMS
The equipment does
not turn on 1.
• Is the power cable properly connected?
If not, connect it. Also check the wall socket.
The
equipment
is
turned on but does
not emit current to
patient 1.
• Have you followed the recommendations for correct use the equipment as mentioned in
the instructions?
Check and repeat the steps in the controllers, indications and operation section.
The
equipment
is
turned on but does
not emit current to
patient 2.
• Have you checked the electrodes and the connecting cables to the patient?
Check if the cable plug is adequately inserted in the equipment.
Check if the electrodes are adequately placed on the patient’s body.
The equipment does
not turn on and/or
work properly.
• Is the 110/220v switch key correctly adjusted for the local net?
Check and if necessary adjust this key properly.
27
MAINTENANCE, WARRANTY terms AND TECHNICAL SUPPORT
MAINTENANCE
WARRANTY TERMS
We suggest that you make an inspection and preventive
maintenance at IBRAMED or authorized technical center
allowed every 12 months for use of equipment. As a
manufacturer, IBRAMED is liable for the technical features
and of the safety equipment only in cases where the unit
was used according to the instructions for use contained in
the manual, where maintenance, repairs and modifications
have been made by the factory or authorized agents, and
where the components that can cause security risks and the
appliance has been replaced in the event of a breakdown by
original the spare parts. If requested, IBRAMED can make the
technical documentation (circuit diagrams, lists of parts and
components etc) necessary for the repair of any equipment.
We assume no responsability for the repairs without our
explicit written permission.
1)
IBRAMED product is warranted against defects in manufacturing, if considered the established conditions by this
manual for 18 consecutive months.
2) The warranty period shall start from the date of purchase
of the first owner, even if the product is transferred to
third parties. It will involve the replacement of parts and
repairing of the defects when certified that the problems
have occurred.
3) The warranty service shall be exclusively made by the
sales center representing IBRAMED, by IBRAMED itself or
any other specifically designated by the manufacturer.
4) The warranty does not include damages that the product
may suffer as a result of:
a) During the installation or use, the recommendations of
these specifications and instructions are not followed.
b) Accidents or natural agents, connection of electrical
systems with inappropriate voltages and / or subjected to
excessive fluctuations or overloading.
WARRANTY
IBRAMED, Indústria Brasileira de Equipamentos Médicos
Ltda., here identified to consumers by the phone and address
: 2800, Dr. Carlos Burgos Ave., Jd Itália, CEP: 13.901-080,
Amparo SP; phone +55 19 3817 9633, warranties this product
for a period of eighteen (18) months under the terms of the
warranty below.
28
MAINTENANCE, WARRANTY terms AND TECHNICAL SUPPORT
TECHNICAL ASSISTANCE
c) The unit has been used carelessly or has received
changes, modifications or repairs made by unauthorized
persons or technical centers.
d) There is removal or alteration of the serial number of
the device.
e) Transportation accidents.
Any question or malfunction with your equipment,
please
contact
our
technical
department.
Call : +55 19 3817 9633
- No change in this equipment is allowed. Any
unauthorized modification can affect the safety
use of this equipment.
- Never make unauthorized repairs.
5) The statutory warranty does not include: installation
cost of the product, shipping of the product to the factory
or authorized retailer, cost of labor, materials, parts and
adjustments necessary for the local preparation for the
installation of the equipment such as the main power line,
masonry, hydraulic network, grounding and adaptations.
6) The warranty does not include parts subjected to natural
wear, such as, command control keys, handles and moving
parts, power cords, connecting cables to the patient,
conductive rubber electrodes, glass electrodes, tips , pen
body, holders and cabinets of the equipment.
Company authorization of operation: 103.603-1
Technician in Charge: Maicon Stringhetta
7) No sales representative is authorized to change the
conditions mentioned or commitments on behalf of
IBRAMED.
CREA-SP: 5062850975
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CEFAI – IBRAMED Center for Education and Advanced Training
Special attention is also given to those interested in visiting
our structure. Whatever your professional development
needs, we’ll be right by your side to provide you with
unconditional support.
IBRAMED Equipment goes beyond technology. It also
provides knowledge! Science constitutes our differential
value and we effectively take advantage of its benefits
in order to ensure patient safety and thereby maximize
results.
We are happy to assist you!
IBRAMED develops products with scientific support of the
most recent medical studies published in major scientific
journals in the areas of biological, health and exact.
Contact – [email protected]
www.conexaocefai.com.br
+55 19 3808 2348
Access to the knowledge database is guaranteed by CEFAI
(IBRAMED Center for Education and Advanced Training)
whose goal is to provide technical and scientific support as
well as current literature on therapies and their applicability
while our treatment choices are always thoroughly selected
according to the best and latest clinical criteria. CEFAI takes
into account the personal and professional development of
all its partners and customers.
Thanks,
IBRAMED – A matter of respect!
CEFAI invites both students and professionals in the
fields of Physical Rehabilitation, Esthetics, Physiotherapy,
Dermatology and Esthetic Medicine to take part in free
courses, workshops, and the best Postgraduate Lato
Sensu courses in the areas of physical rehabilitation and
esthetics.
30
Manufactured by:
IBRAMED
Indústria Brasileira de Equipamentos Médicos EIRELI
Av. Dr. Carlos Burgos, 2800 - Jd. Itália
13901-080 - Amparo - SP - Brazil
phone: +55 19 3817 9633
www.ibramed.com.br
[email protected]
31
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