Instructions Manual

NEURODYN
AUSSIE Sport
Manufactured by
Ibramed - Indústria Brasileira de Equipamentos Médicos EIRELI
Made in Brazil
3st edition (Rev. 09/2014)
TABLE OF CONTENTS
SYMBOL DEFINITIONS.................................................3 PREPARING THE EQUIPMENT...........................21
LIST OF SYMBOLS......................................................4 PROGRAMMING THE EQUIPMENT...............................23
CARTON...........................................................4 PROTECTION MESSAGE...............................................25
LIST OF ABBREVIATIONS............................................4 USING THE PROG/MENU BUTTON...............................26
LIST OF FIGURES.....................................................5 PROGRAMMING USER PROTOCOLS.......................27
FOREWORD.................................................................6 PRE-PROGRAMMED PROTOCOLS...................................28
PRODUCT DESCRIPTION...............................................6 DIRECTIONS ABOUT THE ELECTRODES........................33
ESSENTIAL PERFORMANCE..................................6 POSIOTING OF THE ELECTRODES......................35
RESPONSIBILITY FOR USE ELECTROMEDICAL REFERENCES..........................................................36
EQUIPMENT.......................................................7 ELECTROMAGNETIC COMPATIBILITY.............................38
SAFETY PRECAUTIONS.................................................8 ENVIRONMENTAL PROTECTION.....................................45
PRECAUTIONARY DEFINITIONS.............................8 ENVIRONMENTAL INFLUENCES............................45
INDICATIONS AND CONTRAINDICATIONS...................11 ACCESSORIES ACCOMPANYING NEURODYN AUSSIE
PRECAUTIONS AND ADVERSE REACTIONS...................12 SPORT......................................................................46
PATIENT AND USER PROFILE AND TREATMENT AREAS REPLACEMENT ACCESSORIES............................47
.......................................................................13 TROUBLESHOOTING...................................................48
GENERAL CARE WITH THE EQUIPMENT...................14 MAINTENANCE, WARRANTY AND TECHNICAL SUPPORT..48
TRANSPORT DAMAGES......................................14 CEFAI – IBRAMED CENTER FOR EDUCATION AND ADVANCED
INSTALLATION, CARES AND CLEANSING.............14 TRAINING................................................................52
CONTROLS, INDICATORS AND CONNECTIONS.....16
NOMENCLATURE.......................................................16
DEFINITION OF SYMBOLS.........................................18
SPECIFICATIONS .....................................................19
SYSTEM SPECIFICATIONS...................................19
AUSSIE CURRENT..............................................20
ACCESSORIES USED..................................................21
OPERATING INSTRUCTIONS........................................21
SYMBOL DEFINITIONS

Below are the deficitions 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.

Caution! Refer to user manual. Off switch.

On switch.
TYPE BF Electrical equipment.

Voltage in AC (Alternating Current).

Dangerous voltage.

Electrical Network in AC (Alternating Current).

CLASS II Electrical equipment.

Refer to the instructions manual/brochure.

Not protected against the harmful effects
Note: follow the instructions of use.
of water penetration.

Sensitivity against electrostatic discharge. CARTON

Start treatment. Brazilian certification seal.

Stop treatment. Serial number.

3
LIST OF SYMBOLS LIST OF ABBREVIATIONS

CARTON
Hz Hertz (pulses per second)
kHz Kilohertz
Fragile. mA Milliampere
µA Microampere
This side up. VA Volt Ampere
RISE Time of Increase Gradient
Limits of temperature for storage and
ON Time of Muscular Contraction
packaging in °C (Celsius Degrees).
DECAY Time of Decrease Gradient
OFF Time of Muscular Relaxation
Keep away from the rain. CNT Continuous
SYC Synchronous
REC Reciprocal
Stacking up.

Do not use if the packaging is damaged.

Refer to operating instructions for

correct product use.

Manufacturer’s name and address.

4
LIST OF FIGURES

Figure 1. Upper View..................................................24

Figure 2. Rear View.................................................24
Figure 3. Frontal View...................................................24
Figure 4. Bottom Up View..........................................24
Figure 5. A, banana pin connectors (2 mm) channels: 1
–orange, 2 – black, 3 – blue, 4 – green; B, conductive rubber
electrodes; and C, neutral conductive gel....................29
Figure 6. A. and B. Introduction messages; C. NEURODYN
AUSSIE Sport Default screen..................................30
Figure 7. Electrode placement technique.......................34
Figure 8. Approximated positions of some motor points:
A, anterior face of the arm; B, posterior face of the
arm; C, anterior trunk; D, posterior trunk; E, anterior
face of the leg and F, posterior face of the leg......35
Figure 9. Language selection message......................37
Figure 10. Selection of programmed protocols: Protocol 1 –
Muscle Strengthening in Athletes.................................37
Figure 11. Selection of private protocols: - Private
Protocol 1.................................................................38

5
FOREWORD PRODUCT DESCRIPTION

ESSENTIAL PERFORMANCE
• This user manual allows the user to efficiently use the
NEURODYN AUSSIE Sport Electro Stimulator. It also gives NEURODYN AUSSIE Sport transcutaneous
suggestions for treatment protocols so that you can use your neuromuscular stimulator is a four-channel stimulator
equipment to its full potential. with independent controls for current therapy used in
• Consult other resources for additional information regarding AUSSIE CURRENT (Burst Modulated Medium Frequency).
the uses of electrotherapy before attempting any treatment
on a patient.
• Users must read, understand and follow the information in
this manual for each mode of treatment available, as well as
the indications, contraindications, warnings and precautions.
• The specifications and instructions in this manual are in
effect at the time of its publication. These instructions may
be updated at any time at the manufacturer’s discretion. Visit
our website for updates.

6
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.

7
SAFETY PRECAUTIONS

PRECAUTIONARY DEFINITIONS

The precautionary instructions found in this section and

throughout this manual are indicated by specific symbols.
• Read, understand, and practice the precautionary and
Understand these symbols and their definitions before
operating instructions. Know the limitations and hazards
operating this equipment.
associated with the use of any electrical stimulation. Observe
the precautionary and operational labels placed on the unit.
• DO NOT operate this unit in an environment where other
devices intentionally radiate electromagnetic energy in an
Text with a “CAUTION” indicator refers to potential safety unshielded manner.
infractions that could cause minor to moderate injury or • This unit should be operated, transported and stored at
damage to equipment. temperatures between 41°F and 122°F (5°C and 50°C);
Avoid damp and dusty environments.
• Check cables and associated connectors before each use.
• The NEURODYN AUSSIE Sport Electro Stimulator is not
Text with a “WARNING” indicator refers to potential safety designed to prevent the infiltration of water or other liquids.
infractions that could cause serious injury and equipment The infiltration of water or other liquids could cause malfunction
damage. of internal components of the system and therefore create a
risk of injury to the patient.
• Disconnect the power plug from the outlet when left unused
for long periods of time.
Text with a “DANGER” indicator refers to potential safety
infractions that represent immediately life threatening
situations that would result in death or serious injury.

8
SAFETY PRECAUTIONS

• To protect against the risk of fire, only use replacement • Stimulation should not be applied over the anterior neck or
fuses of the same types and ratings. mouth.
• Be sure the unit is grounded by connecting it to a grounded • Severe spasm of the laryngeal and pharyngeal muscles
electrical outlet compliant with the applicable national and may occur and the contractions may be strong enough to
local electrical codes. close the airway or cause breathing difficulties.
• Stimulation should not be applied transthoracically to avoid
• Powered muscle stimulators should be used only with
the introduction of electrical current into the heart which may
the lead wires and electrodes recommended for use by the
cause cardiac arrhythmia.
manufacturer.
• Stimulation should not be applied over swollen, infected,
• Prior to patient treatment become familiar with the operating
and inflamed areas or skin eruptions such as phlebitis,
procedures for each mode of treatment available, as well as
thrombophlebitis, varicose veins, etc.
the indications, contraindications, warnings and precautions.
• Stimulation should not be applied on or near cancerous
Consult other resources for additional information regarding
lesions.
the applications of Electrotherapy.
• Output current density depends on the electrode size.
• To prevent electrical shock, disconnect the unit from the Improper application may result in patient injury. For
power source before performing any maintenance task. any question related to the correct electrode size. The
• Keep electrodes separated during treatment. Electrodes in size of the electrodes and the density of current used
contact with each other could result in improper stimulation during Therapy must respect IEC 60601-2-10, that is,
or skin burns. the density of current per area of the electrode must not
exceed 2 mA/cm2. Follow the manufacturer’s instructions.

9
SAFETY PRECAUTIONS

• Patients with an implanted neurostimulation device must

not be treated with or be in close range of any shortwave
diathermy, microwave diathermy, therapeutic ultrasound
diathermy or laser diathermy anywhere on their body. Energy
from diathermy (shortwave, microwave, ultrasound and laser)
can be transferred through the implanted neurostimulation
system, can cause tissue damage, and can result in severe
injury or death. Injury, damage or death can occur during
diathermy therapy even if the implanted neurostimulation
system is powered “off.”
• Equipment not suitable for use in the presence of a
flammable anesthetic mixture with air, oxygen or nitrous
oxide.

10
INDICATIONS AND CONTRAINDICATIONS

INDICATIONS FOR USE

• The stimulation must not be applied over the cranial
• Prevention or retardation of disuse atrophy. bone.
• Motor reeducation. • The stimulation must not be applied over or next to
• Increase in muscle torque. cancerous lesions.
• Maintaining or increasing range of motion. • The stimulation must not be applied over infected or
• Symptomatic relief of untreatable chronic pain, post- inflamed areas or over skin eruptions, such as phlebitis,
traumatic acute pain and post-operative acute pain. thrombophlebitis.
• Relaxation of muscle spasms. • The stimulation must not be applied over caliber varicose
• Increasing local blood circulation. because of the risk of dislocation of the thrombus.
• The stimulation must not be applied on patients with
CONTRAINDICATIONS acute deep venous thrombosis (DVT).
• The stimulation must not be applied in the presence of
• Powered muscle stimulators should not be used on patients electronically controlled equipment (for example, cardiac
with cardiac demand pacemakers. monitors, ECG alarms), which may malfunction when the
• This device should not be used for symptomatic local pain electrical stimulation device is in use.
relief unless etiology is established or unless a pain syndrome
has been diagnosed.
• The stimulation must not be applied over the
nerves of the carotid sinus, particularly in patients
with altered sensitivity to the carotid reflex.
• The stimulation must not be applied over the cardiac
area, because it may cause cardiac arrhythmia.

11
PRECAUTIONS AND ADVERSE REACTIONS

PRECAUTIONS
the conductor wires and electrodes recommended by the
• The safety of use of neuromuscular stimulators during manufacturers.
pregnancy has not been established.
• Care must be taken with patients suspected of cardiac ADVERSE REACTIONS
conditions or conditions previously diagnosed.
• The stimulation must be applied carefully over the neck • Patients may present skin irritation or hypersensitivity
area, and the application is contraindicated over the carotid caused by electrical stimulation or electrically conductive
area. Spasms of the muscles of the larynx and pharynx may medium. The irritation can usually be reduced
occur, and the contractions may promote blockage of the with the use of an alternative conductor medium
upper airways or cause breathing difficulties. or with the placement of an alternative electrode.
• Care must be taken when treating patients suspected of • Patients may present burns under the stimulation
suffering from or diagnosed with epilepsy. electrodes if the application is not correctly
• Care must be taken with electrical stimulation in the carried out or if the electrodes are worn out.
presence of the following:
a. When there is tendency of hemorrages after acute
trauma or fracture;
b. Following recent surgical procedures, when muscle
contraction may disturb the healing process;
c. Over the abdomen during pregnancy;
d. Over skin areas with sensitivity deficit.
• The placement of the electrodes and the stimulation
configurations must be in accordance with the directions
prescribed by the health professional.
• Neuromuscular stimulators must be kept out of the reach
of children.
• The neuromuscular stimulators must be used only with
12
PATIENT AND USER PROFILE AND TREATMENT AREAS

PATIENT PROFILE
• The user must follow the information contained in these
• Patients with diagnosed painful musculoskeletal conditions. user instructions for each mode of treatment available, as
• Patients with muscle weakness and/or atrophy. well as the indications, contraindications, warnings and
precautions.
• Patients with arthrogenic inhibition.
• The user must have his cognitive functions preserved.
• Patients with edema of the limbs.
• The user must have the necessary motor functions for using
• Patients with muscle spasms.
the equipment intact.
• Patients with decreased articular mobility. • Regarding mobility, this equipment is considered a portable
• Patients must be at least 12 years old, under this age the
device.
device must be used solely under medical or physiotherapeutic
prescription. PART OF THE BODY OR TISSUE ON WHICH IT
• Patients must weigh more than 35 kg, under this weight only IS APPLIED OR WITH WHICH IT INTERACTS
under medical or physiotherapeutic prescription.
Areas of the trunk (except precordial area), upper and lower
• Patients must have their level of consciousness preserved.
limbs. The current interacts with the skin, nerves and muscles
of the treated area. The skin under the electrode must be
USER PROFILE intact.

• The device must be used only under prescription and

supervision of a licensed health professional.
• The device does not require specialized training; however,
the device user must read, understand and practise the
instructions of precaution and operation.
• The user must know the limitations and dangers associated
with the use of any electrical stimulation and observe
the precaution and operation labels placed on the unit.

13
GENERAL CARE WITH THE EQUIPMENT

TRANSPORT DAMAGES INSTALLATION, CARE AND CLEANSING

• The electrical stimulator NEURODYN AUSSIE Sport is Installation instructions

delivered complete to the client, inside a box. Upon receiving 1. Connect the line cord to the back of the NEURODYN
it, inspect the box and the equipment to Check for potential AUSSIE Sport Electro Stimulator.
damage. 2. Plug the line cord into a grounded wall outlet (100/240V
• In case of damage, keep all the transport materials, - 50/60 Hz).
including the packaging and contact the agents in charge of 3. Plug the electrode cables into the electrode cable
the delivery of the unit. All complaints regarding transport connections.
damage should be presented directly to them. 4. Switch on your equipment.
• The manufacturer does not take responsibility for
any damage during transport; it will not perform minor Equipment storage and care
adjustments unless a formal complaint is presented by the
receiver against the transport agent. • Avoid places subject to vibration.
• The box in which your electrical stimulator NEURODYN • Install the device on a firm and flat surface.
AUSSIE Sport was delivered is specially designed to protect • Do not block ventilation.
the equipment during transport. • Avoid humid, warm and dusty environments.
• Keep the transport packaging in case you need to return your • Make sure the area surrounding the electrical feed cable is
equipment for maintenance. We suggest that the packaging free.
is kept for the warranty period. • Do not introduce any objects into the orifices of the
device.
• Temperature range during transport and storage: 5 - 50°
C/ 41 - 122° F.

14
GENERAL CARE WITH THE EQUIPMENT

Care and storage of the stimulation cables Equipment and stimulation cable cleansing

• Avoid places subject to vibration.

• Disconnect the equipment from the electrical feed source.
• Avoid humid, warm and dusty environments.
• Clean the equipment and the stimulation cables with alcohol
• Make sure the area surrounding the stimulation cable is
chlorhexidine at 0.5% and dry them with a paper towel.
free.
• The cleansing procedure must be performed whenever
• Temperature range during transport and storage: 5 - 50°
necessary. Ibramed suggests a weekly cleansing of the
C/ 41 - 122° F.
equipment, and the stimulation cables should be cleaned
after each session.
• Do not immerse the equipment or the stimulation cables in
Care and storage of electrodes liquids.

• Avoid humid, warm and dusty environments.

• Temperature range during transport and storage: 5 - 50°C/ Electrode cleansing
41 - 122°F.
• Do not leave residues of conductive gel on the electrodes • Remove the residues of conductive gel after the therapy.
after use. • Wash the electrodes in running water.
• Store the electrodes in a dry place, appropriate and protected • Clean the electrodes with alcohol chlorhexidine at 0.5%
from environmental aggression for their longer durability. and dry them with a paper towel.
• The cleansing procedure must be performed whenever
necessary. Ibramed suggests the electrodes are cleaned after
each treatment session.

15
NOMENCLATURE

CONTROLS, INDICATORS AND CONNECTIONS

1
13
5

12 11 10
3 14
8 Figure 2. Rear Access Panel.
4

6
2
Figure 4. Lower Access Panel.
Figure 1. Upper Access Panel.

Figure 3. Front Access Panel.

16
NOMENCLATURE

1- Power ON/OFF Switch. 8. UP and DOWN control key.

9. Outlet connections cables to patient.

2- Power On Indicator LED.

10. Connection to power cable.

3- SELECT control key.

11. Protection fuse.

4- SET control key.
12. General technical information.

5- Alphanumerical LCD display.

13. Label with technical characteristics.

6- START/STOP control key.

14. Serial number.

7- PROG/MENU control key PROG: selection of 15. LED indicators of current output of channels 1, 2, 3 and
pre-programmed protocols; MENU: language selection. 4.

17
SYMBOL DEFINITIONS

Read and Understand these symbols and their definitions before operating this equipment.

PROG/MENU: Double Function Key:

PROG – Selection of pre-programmed
protocols and private protocols;
MENU – Selection of language (Portuguese,
English or Spanish).

START/STOP: Button used to start or stop

the treatment. Always press the center key. UP or DOWN Intensity: Channel 1, 2, 3 and 4. Note the
colors related to channels.
Observe the colors relating to the channels.

SET key: selection of the values of the

parameters.

SELECT key: selection of the current

parameters.

18
SPECIFICATIONS

SYSTEM SPECIFICATIONS
Temperature Range During Transport and Storage:
DIMENSIONS 5 - 50°C/ 41 - 122°F.
Width: 26.4 cm (10.4 in) ± 5%
Environment operating temperature range:
Depth: 26.1 cm (10.3 in) ± 5%
Height: 11.6 cm (4.6 in) ± 5% 5 - 45 °C/ 41- 113 °F.

Standard Weight
(without accessories): 1.5 kg ± 5%

Power
Input: 100 / 240V~ 50/60 Hz
Input Power: 100 VA
Fuses: 5A 250V~ (20AG)
Electrical Class: CLASS II
Electrotherapy: TYPE BF

REGULATORY COMPLIANCE
IEC 60601-1
IEC 60601-1-2
IEC 60601-2-10
IEC 60601-1-6
IEC 60601-1-4

19
SPECIFICATIONS

AUSSIE CURRENT
Output Mode: Electrodes
Aussie current (Australian Current) is an alternating medium Output Intensity: (CC*): 0-180 mA**
frequency current liberated in short bursts (1 kHz/duration
Current Modes:
of burst of 2 ms or 4 kHz/duration of burst of 4 ms) used to
Continuous: CNT (1, 2, 3 & 4 channel)
produce maximum muscle torque or analgesia, respectively,
without significant discomfort for the patient. Synchronous: SYN (1, 2, 3 & 4 channel)
Reciprocal: REC (1 & 3, 2 & 4 channel)
Burst Duration: 2 or 4 ms
Carrier Frequency: 1 or 4 kHz
Burst Frequency: 1-120 Hz
Ramp
Rise (Time of Increase Gradient): 1-20 s
On (Time of Muscular Contraction): 1-60 s
Decay (Time of Decrease Gradient): 1-20 s
1 kHz/2 ms
Off (Time of Muscular Relaxation): 1-60 s

Treatment Time: 1-60 min

Set Intensity: Individual Channel Intensity Setting
Available on Channels: 1, 2, 3 or 4.

CC*= Constant current

**Impedance charge rate for these parameters: 900 - 1100
Ohms.
4 kHz/4 ms
20
ACCESSORIES USED OPERATING INSTRUCTIONS

AUSSIE CURRENT: banana pin connection cables (2 mm) PREPARING THE EQUIPMENT
channel 1 –orange, 2 – black, 3 – blue, 4 – green (each
As soon as the ON/OFF key is pressed to the ON position, the
connector contains two stimulation channels), conductive
display will show the introduction message for a few seconds,
rubber electrodes and neutral conductive gel (Figure 5).
A. followed by the default screen of the device (Figure 6).

A.
B. E

Figure 5. A, banana pin connectors (2 mm) channels: 1 –

orange, 2 – black, 3 – blue, 4 – green; B, conductive rubber
electrode and C, conductive neutral gel.

• To start the therapy, the screws of the connector of B.

the stimulation cable must be firmly fixed onto the
equipment and the banana pins of the cables must
be introduced in the conductive rubber electrodes.
• After the end of the therapy, to remove the banana pin of the
electrodes from the stimulation cables it is necessary to pill
them by their protective cap. Never pull them by the cable.
To remove the stimulation cables you must turn the screws
of the cable connectors to release them from the device.
21
OPERATING INSTRUCTIONS

C. Patient preparation
Prepare the patient for therapy as described and read about
the use of electrodes.

Start treatment
Press the START button to begin therapy
session.

Stop treatment
Press the STOP key to stop the treatment.
Figure 6. A and B, LCD Messages; C. NEURODYN
AUSSIE Sport Electro Stimulator Default Screen.
Current Intensity

Editing current parameters The current intensity may be increased or decreased at any
time during the session. Press the intensity button (UP or
The SELECT button allow you to select the parameters DOWN).
required for the treatment. Press the cursor keys to move to
the next parameter or rewind the cursor back to the previous
setting.
The SET buttons allow you to select the values of each
parameter required for the treatment.

Treatment time
Set the session time. At the end of the scheduled time, you
will hear a beep indicating that the emission current has been
interrupted. Press the STOP button, the sound signal turns off
and the equipment goes back to the programming status.

22
PROGRAMMING EQUIPMENT

Example 1: Suppose that to treat a specific pathology, Selection of current frequency (Carrier):
you need to select the following parameters:

Current Mode: Synchronous

Frequency of Current (carrier) = 1 kHz
Frequency of Burst = 50 Hz
Duration of Burst= 2 ms
Rise = 2 s
On = 10 s
Decay = 2 s
Selection of Burst duration:
Off = 10 s
Treatment time = 15 min

1. Turn the equipment on to start the standard

program described above. Observe the parameter of
the chosen current and the values of intensity blinking.

Selection of Mode:

2. Using the SELECT and SET keys scroll the other

parameters and select the values shown in the example
bellow: Selection of frequency of current (carrier):
23
PROGRAMMING EQUIPMENT

Selection of Burst frequency: Selection of ramp down (Decay):

Selection of up ramp time (Rise): Selection of muscle relaxation time (Off):

Selection of muscle contraction (On): Selection of treatment time (Timer):

24
PROGRAMMING THE EQUIPMENT PROTECTION MESSAGE

OVERLOAD
3. Now press the START key to start the treatment.
The protection message OVERLOAD will appear on the screen
4. Press the UP or DOWN keys of the channels in use to of the equipment when there is overcurrent in the output
select the quantity of current necessary for the treatment. circuit, that is, in case there is excessive consumption of
electrical current or the stimulation cable is short-circuited.
Note: The adjustment of intensity must be made after The equipment will emit a sound signal and the message
pressing the START key, according to the therapeutic
OVERLOAD will appear on the display, as described below:
objective (sensory or motor threshold) and to the patient’s
tolerance.

5. At the end of the programmed time, the emission of

current is interrupted and a sound beep will signal the end of
treatment.

6. Press the STOP key to stop the sound beep. The equipment
can be turned off, the same program can be reused again or
a new program can be used.

When the OVERLOAD image appears on the screen, the

user must press the START/STOP key to return to the
programming screen. If the message OVERLOAD appears
on the screen too often, the user must contact authorized
technical assistance.

25
USING THE PROG/MENU BUTTON

USING THE MENU BUTTON

This is the first equipment to offer a choice of Treatment
The MENU/PROG button is used to select the language. Protocols.
Press MENU/PROG until you hear three “beeps.” Select the
desired language: ‘Português’, ‘Español or ‘English’. Short
press MENU/PROG to set the chosen language.

Figure 10. Selection of Treatment Protocols; 1- Strengthening

in athletes.
Figure 9. LCD displays the selected language.
Use the SET button to select another protocol. If this is the
USING THE PROG BUTTON protocol chosen, press the PROG key once again. The LCD
Connect the equipment as described above. Briefly press displays the parameters of the equipment scheduled for the
PROG and the following information will appear on the LCD. selected protocol.
Then simply press the START button and select the desired
current density.

Proceed the same way to select any of the protocols available.

Simply follow the steps above.

26
USING THE PROG/MENU BUTTON

PROGRAMMING USER PROTOCOLS

To program new protocols, briefly press the key PROG and

press the SET button to select USER protocols. With the
SET button choose one of the 20 available user protocols.
Enter the parameters according to therapeutic needs and
press START. The last set parameters will be recorded in
the device memory. To access Protocols saved by the user,
simply select the PROG key and the SET key to choose the
protocol number desired.

Figure 11. Parameters of the Pre-Programmed Protocol.

27
PRE-PROGRAMMED PROTOCOLS

Prog 1: Muscle Parameters values Prog 2: Increase of Parameters values

Strengthening in Athlete Muscle Torque

Description: Increase of the

Description: Increase of
muscular strength in health
muscle force production
individuals
Mode Sync (Synchronous)
Mode Sync (Synchronous)
Carrier Frequency 1 kHz
Carrier Frequency 1 kHz
Burst duration 2 ms
Burst duration 2 ms
Burst Frequency 70 Hz
Burst Frequency 50 Hz
Rise 2s
Rise 1s
On 20 s
On 9s
Decay 2s
Decay 1s
Off 20 s
Off 50 s
Treatment time 15 min or the number of
Treatment time 15 min or the number of
required contractions
required contractions
Intensity 0 - 180*
Intensity 0 - 180*
Positioning of electrodes Myoenergy technique or
Positioning of electrodes On the motor muscular
motor point
point

*The manufacturer does not indicate the necessary intensity in the protocol, because it must be adjusted by the therapist
according to the clinical needs of each patient.

28
PRE-PROGRAMMED PROTOCOLS

Prog 3: Motor Re- Parameters values Prog 4: Strengthening Parameters values

education Disuse Atrophy

Description: For motor Description: For patients

facilitation and motor that present muscular
relearning atrophy due to lack of use.
Mode Sync (Synchronous) Mode Sync (Synchronous)
Carrier Frequency 1 kHz Carrier Frequency 1 kHz
Burst duration 2 ms Burst duration 2 ms
Burst Frequency 50 Hz Burst Frequency 15 Hz
Rise 1s Rise 1s
On 3s On 3s
Decay 1s Decay 1s
Off 3s Off 3s
Treatment time 20 min Treatment time 20 min
Intensity 0 - 180* Intensity 0 - 180*
Positioning of electrodes Myoenergy technique or Positioning of electrodes Myoenergy technique or
motor point motor point

*The manufacturer does not indicate the necessary intensity in the protocol, because it must be adjusted by the therapist
according to the clinical needs of each patient.

29
PRE-PROGRAMMED PROTOCOLS

Prog 5: FES after Stroke Parameters values Parameters values

Prog 6: Edema Reduction
Description:Electrical functional
Description: To control and
stimulation after stroke to reduce the edema as well
prevent muscular atrophy due to as for lymphatic drainage
lack of use, prevent the shoulder procedures
subluxation after stroke and to Mode Sync (Synchronous)
facilitate the motor re-learning. Carrier Frequency 4 kHz
Mode Sync (Synchronous) Burst duration 4 ms
Carrier Frequency 1 kHz Burst Frequency 35 Hz
Burst duration 2 ms Rise 1s
Burst Frequency 15 Hz On 5s
Rise 1s Decay 1s
On 9s Off 4s
Decay 1s Treatment time 20 min
Off 9s Intensity 0 - 180*
Treatment time 20 min Positioning of electrodes On the belly of the muscle,
Intensity 0 - 180* which correlates to the edema
Positioning of electrodes Myoenergy technique or or the track of the lymphatic
motor point vessels.

*The manufacturer does not indicate the necessary intensity in the protocol, because it must be adjusted by the therapist
according to the clinical needs of each patient.

30
PRE-PROGRAMMED PROTOCOLS

Prog 7: Acute Pain Prog 8: Chronic Pain

Parameters values Parameters values
(Gate Control Theory) (Endorphin Release)
Description: Modulation of Description: Modulation of
pain through activation of pain through activation of
the ascending mechanism the descending mechanism
to promote analgesia by to promote the analgesia by
activation of the pain gate release of endorphins
Mode Cont (Continuos) Mode Cont (Continuous)
Carrier Frequency 4 kHz Carrier Frequency 4 kHz
Burst duration 4 ms Burst duration 4 ms
Burst Frequency 100 Hz Burst Frequency 10 Hz
Treatment time 30 min Treatment time 30 min
Intensity 0 - 180* Intensity 0 - 180*
Positioning of electrodes On the dermatomes Positioning of electrodes One pair of electrodes
positioned on the pain point
and another pair on the
corresponding neural root.

*The manufacturer does not indicate the necessary intensity in the protocol, because it must be adjusted by the therapist
according to the clinical needs of each patient.

31
PRE-PROGRAMMED PROTOCOLS

Prog 9: Postoperative Prog 10: Postoperative

Functional Recovery Initial Parameter Values Functional Recovery Parameter Values
Phase Advanced Phase
Description: Muscle recovery Description: postoperative
in postoperative period – muscular recovery –
initial phase of treatment. advanced treatment phase
Mode Sync (Synchronous) Mode Sync (Synchronous)
Frequency of current 1 kHz Frequency of current 1 kHz
Duration of Burst 2 ms Duration of Burst 2 ms
Frequency of Burst 30 Hz Frequency of Burst 50 Hz
Rise 3s Rise 1s
On 20 s On 20 s
Decay 3s Decay 1s
Off 30 s Off 20 s
Treatment Time 10 min Treatment Time 20 min
Intensity 0 - 180* Intensity 0 - 180*
Positioning of electrodes Myoenergy technique or Positioning of electrodes Myoenergy technique or
motor point motor point

*The manufacturer does not indicate the necessary intensity in the protocol, because it must be adjusted by the therapist
according to the clinical needs of each patient.

32
ELECTRODE GUIDELINE

PATIENT PREPARATION DIRECTIONS ABOUT THE ELECTRODES

• The electrode placement can be performed using the Electrode placement technique
bipolar or monopolar techniques. The adequate placement
The electrode placement technique is carried out to provide
and contact will assure comfort and the efficiency of the
stimulation of muscle groups or to provide analgesia. In the
treatment.
case of muscle stimulation, electrodes of the same size are
• Examine the skin and clean the treatment area, disinfecting
positioned over the muscle or muscle group (Myoenergy
with medical use alcohol.
technique or bipolar technique). For analgesia, electrodes of
• Conductive rubber electrodes need neutral gel as a
the same size are positioned over the pain area or on the
conductive medium.
corresponding dermatome. For treatment, it is necessary to
Self-adherent electrodes can be placed directly on the skin.
connect the conductive rubber electrodes to the banana pin
• Make sure the surface of the electrode is in contact with the
connector cables, and then apply neutral conductive gel on
skin of the patient, pressing it on place.
the face of the electrode in contact with the skin and then fix
• Check the contact of the electrode regularly during
the electrodes onto the skin using micropore tape or adhesive
treatment.
tape, as demonstrated below:
• Examine the skin again after the treatment.

• ELECTRODES - BIOCOMPATIBILITY (ISO 10993-1):

Ibramed declares that the electrodes supplied with the
equipment do not cause allergic reactions.
These electrodes must be positioned only on the integral
surface of the skin, respecting a limit period of time for this
contact of up to 24 hours..

Figure 7. Electrode placement technique

33
ELECTRODE GUIDELINE

Size of the electrodes and density of current

• The size of the electrodes and the density of current used during the Therapy must be in compliance with the IEC 60601-2-10,
that is, the density of current per area of the electrode must not exceed 2 mA/cm2.

Wear and tear of the electrodes

• The electrodes suffer wear and tear with use, and must be replaced whenever they present an aspect of dryness or every
6 (six) months.

The placement of the electrodes near the cardiac

area may increase the risk of cardiac fibrillation.

34
ELECTRODE GUIDELINE

POSIOTING OF THE ELECTRODES

Map of the main treatment areas and their respective motor points
The electrodes can be positioned over the motor points of the muscles (monopolar technique) located in the treatment area. In
the figure below are the locations of the motor points of the main treatment areas.
A B C D E F

Figure 8. Approximate positions of some motor points: A, anterior face of the arm; B, face posterior face of the arm; C, anterior
of trunk; D, posterior of trunk; E, anterior face of the leg and F, posterior face of the leg.

35
REFERENCES

Ward AR, Robertson VJ. Sensory, motor and alternating pain Ozcan J, Ward AR, Robertson VJ. A comparison of true and
thresholds for stimulation with medium frequency premodulated interferential currents. Archives of Physical
current. Archives of Physical Medicine & Rehabilitation. Medicine and Rehabilitation. 2004; 85(3): 409-415.
1998a; 79(3): 273-278.
Ward AR, Robertson VJ, Ioannou H. The effect of and
Ward AR, Robertson VJ. The variation in torque production frequency on muscle torque production using kHz frequency
with frequency using medium frequency alternating current. range alternating current. Medical Engineering and Physics.
Archives of Physical Medicine and Rehabilitation. 1998b; 2004; 26(7): 569-579.
79(11): 1399-1404.
McManus FJ, Ward AR, Robertson VJ. The analgesic effects
Ward AR, Robertson VJ. The variation in fatigue rate with of interferential therapy on two experimental pain models:
frequency using kHz frequency alternating current. Medical cold and mechanically induced pain. Physiotherapy. 2006;
Engineering and Physics. 2000; 22(9): 637-646. 92: 95-102.

Ward AR, Robertson VJ. The variation in motor threshold with Ward AR, Oliver W, Buccella D. Wrist extensor torque
frequency using kHz frequency alternating current. Muscle production and discomfort associated with low frequency and
and Nerve. 2001; 24: 1303-1311. burst modulated kHz frequency currents. Physical Therapy.
2006; 86(10): 1360-1367.
Ward AR, Robertson VJ, Makowski RJ. Optimal frequencies
for electrical stimulation using medium frequency alternating
Shanahan C, Ward AR, Robertson VJ. A Comparison of
current. Archives of Physical Medicine and Rehabilitation.
the analgesic efficacy of interferential therapy and TENS.
2002; 83(7): 1024-1027.
Physiotherapy. 2006; 92: 247-253.

DutyWard AR, Shkuratova N. Russian electrical stimulation: Ward AR, Oliver W. A comparison of the hypoalgesic effectiveness
the early experiments. Physical Therapy. 2002; 82(10): of low frequency and burst modulated kHz frequency currents.
1019-1030. Physical Therapy. 2007; 87(8): 1056-1063.

36
REFERENCES

Ward AR, Lucas-Toumbourou S. Lowering of sensory,

motor and pain-tolerance thresholds with burst
duration using kHz frequency alternating current electrical
stimulation. Archives of Physical Medicine and Rehabilitation.
2007; 88(8): 1036-1041.

Ward AR, Lee Hung Chen W. Lowering of sensory, motor

and pain-tolerance thresholds with burst duration using kHz
frequency alternating current electrical stimulation: part II.
Archives of Physical Medicine and Rehabilitation. 2009; 90:
1619-1627.

Ward AR, Lucas-Toumbourou S, McCarthy B. A comparison

of the analgesic efficacy of medium-frequency alternating
current and TENS. Physiotherapy. 2009; 95: 280-288.
Ward AR. Electrical stimulations using kilohertz-frequency
alternating current. Physical Therapy. 2009; 89 (2):181-
190.

Laufer Y, Tausher H, Esh R., Ward AR. Sensory transcutaneous

electrical stimulation fails to decrease discomfort associated
with neuromuscular electrical stimulation in healthy individuals.
American Journal of Physical Medicine & Rehabilitation. 2011;
90(5): 399-406.

37
ELECTROMAGNETIC COMPATIBILITY

Electromagnetic Compatibility Guidance

Medical Electrical Devices require special attention The use of accessories, other than those listed, except
regarding Electromagnetic Compatibility (EMC) and must when supplied or sold by Ibramed Indústria Brasileita de
be installed and put into service according to the EMC Equipamentos Médicos EIRELI as replacement parts for
information provided in the following tables. internal or external components, may result in increased
Portable and Mobile Radio Frequency (RF) communications emission or decreased immunity of the NEURODYN
equipment can affect Medical Electrical Devices. AUSSIE Sport Electro Stimulator.

38
ELECTROMAGNETIC COMPATIBILITY
Electromedical devices require special attention concerning electromagnetic compatibility and must be installed and put in ser-
vice according to the information about electromagnetic compatibility given in the tables below. Portable and mobile Radiofre-
quency (RF) communication equipment may affect electromedical devices.

Manufacturer’s directions and declarations - electromagnetic emissions

NEURODYN AUSSIE Sport is designed for use in the electromagnetic environment described below. The user of the
equipment must assure it is used in such environment.

Emission assay Conformity Electromagnetic Environment – directions

Emission Assay NEURODYN AUSSIE Sport uses RF energy only for its internal
RF Emissions functions. However, its RF emissions are very low and it is not
Group 1
NBR IEC CISPR 11 probable that they cause interference in nearby equipment.
IEC CISPR 11

RF Emissions
NBR IEC CISPR 11 Class A
IEC CISPR 11

NEURODYN AUSSIE Sport is adjusted for use in all premises

Emission of harmonics which are not residential and which are not directly connected
Class A
IEC 61000-3-2 with the public low tension mains power line which feeds
domestic use buildings.
Emissions due to
tension fluctuation/
Class A
scintillation
IEC 61000-3-3
39
ELETROMAGNECTIC COMPATIBILITY

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity

The NEURODYN AUSSIE Sport is intended for use in the electromagnetic environment specified below. The
customer or the user of the NEURODYN AUSSIE Sport should assure that it is used in such an environment.

IEC 60601
Immunity Test Compliance Level Electromagnetic Environment - Guidance
Test Level

Electrostatic Floors should be wood, concrete or ceramic tile.

6 kV by contact 6 kV by contact
discharge (ESD) If floors are covered with synthetic material, the
8 kV by air 8 kV by air
IEC 61000-4-2 relative humidity should be at least 30%.

2 kV for power 2 kV for power

Electrical fast
supply lines supply lines Mains power quality should be that of a typical
transitories/burst
1 kV for input/ 1 kV for input/ commercial or hospital environment.
IEC 61000-4-4
output lines output lines

1 kV diferencial 1 kV diferencial
Surge mode mode Mains power quality should be that of a typical
IEC 61000-4-5 2 kV common 2 kV common commercial or hospital environment.
mode mode

40
ELETROMAGNECTIC COMPATIBILITY

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity

The NEURODYN AUSSIE Sport is intended for use in the electromagnetic environment specified below. The
customer or the user of the NEURODYN AUSSIE Sport should assure that it is used in such an environment.

IEC 60601
Immunity Test Compliance Level Electromagnetic Environment - Guidance
Test Level

< 5% UT < 5% UT
(> 95% voltage drops (> 95% voltage drops
in UT ) 0,5 by cycle in UT )by 0,5 cycle
Voltage dips, Mains power quality should be that of a typical
40% UT voltage drops 40% UT
short interruptions commercial or hospital environment. If the
in (60% de voltage drops
and voltage (60% UT ) by 5 cycles in UT )by 5 cycles user of the NEURODYN AUSSIE Sport
variations in requires continued operation during power
70% UT 70% UT
power input lines mains interruptions, it is needed that the
(30% voltage drops in (30% voltage drops in
NEURODYN AUSSIE Sport be powered from
IEC 61000-4-11 UT ) by 25 cycles UT ) by 25 cycles
an uninterruptible power supply or battery.
< 5% UT < 5% UT
(> 95% voltage drops (> 95% voltage drops
in UT ) by 5 seconds in UT ) by 5 seconds

Power frequency Power frequency magnetic fields should be at

(50/60 Hz) levels characteristic of a typical location in a
3 A/m 3 A/m
magnetic fild typical commercial or hospital environment.
IEC 61000-4-8

NOTE: UT is the A.C. mains voltage prior to applications of the test level.
41
ELETROMAGNECTIC COMPATIBILITY

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity

The NEURODYN AUSSIE Sport is intended for use in the electromagnetic environment specified below. The
customer or the user of the NEURODYN AUSSIE Sport should assure that it is used in such an environment.

IEC 60601 Compliance

Immunity Test Electromagnetic Environment - Guidance
Test Level Level

Portable and mobile RF communication equipment should

not be used no closer to any part of NEURODYN AUSSIE
Sport, including cable than be separation distance
calculated from the equation applicable to the frequency of
the transmitter.
Conducted RF 3 Vrms
3V
IEC 61000-4-6 150 kHz to 80 MHz Recommended separation distance
d = 1.2 150 kHz to 80 MHz
d = 1.2 80 MHz to 800 MHz

Radiated RF 10 V/m d = 2.3 800 MHz to 2.5 GHz

3 V/m
IEC 61000-4-3 80 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 meters (m).

Field strengths from fixed RF transmitters, as determined

by an electromagnetic site survey,a should be less than the
compliance level in each frequency range.b

42
ELETROMAGNECTIC COMPATIBILITY

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity

The NEURODYN AUSSIE Sport is intended for use in the electromagnetic environment specified below. The
customer or the user of the NEURODYN AUSSIE Sport should assure that it is used in such an environment.

IEC 60601 Compliance

Immunity Test Electromagnetic Environment - Guidance
Test Level Level

Conducted RF 3 Vrms Interference may occur in the vicinity of equipment

3V
IEC 61000-4-6 150 kHz to 80 MHz marked with the following symbol:
Radiated RF 10 V/m
3 V/m
IEC 61000-4-3 80 MHz to 2.5 GHz

NOTE 1: At 80 MHz and 800 MHz the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.

a
Field strengths set by fixed transmitters, such as radio base stations, telephone (cellular/cordless) telephones and land
mobile radios, amateur radio, AM / FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength at the location in which the NEURODYN AUSSIE Sport is used exceeds the
applicable RF compliance level above, the NEURODYN AUSSIE Sport should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be necessary, such as reorientation or relocating the
NEURODYN AUSSIE Sport.

b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
43
ELECTROMAGNETIC COMPATIBILITY

Recommended separation distances between the communication equipment of RF portable and mobile and
NEURODYN AUSSIE Sport

NEURODYN AUSSIE Sport is intended to be used in an electromagnetic environment in which RF disturbances are
controlled. The user of the electro stimulator can help to prevent the electromagnetic interference by maintaining the minimum
distance between the portable communication equipment and mobile RF (transmitters) and, NEURODYN AUSSIE Sport as
recommended below, according to the maximum power of communication equipment.

Maximum rated power Separation distance according to frequency of transmitter

output of the transmitter
m
maximum nominal potency
of transmitter output 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
W d = 1.2 P d = 1.2 P d = 2.3 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

For transmitters with a maximum nominal output power not listed above, the recommended separation distance in meters
(m) can be determined by using the equation applicable to the frequency of the transmitter, where P is the maximum rated
output in watts (W) According to the transmitter manufacturer.
NOTE 1: 80 MHz to 800 MHz, applies to the distance of separation for the higher frequency range.
NOTE 2 These guidelines may not be applicable in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.

44
ENVIRONMENTAL PROTECTION

NEURODYN AUSSIE sport 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.
NEURODYN AUSSIE sport, 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.

ENVIRONMENTAL INFLUENCES

NEURODYN AUSSIE sport must not come into contact with biological material which may suffer degradation from the influence
of bacteria, plants, animals and the like. NEURODYN AUSSIE sport must undergo annual maintenance (calibration), as
specified by the manufacturer in these instructions of use to minimize wear and tear or corrosion which may reduce its mechanical
properties in its useful fife. The useful life period of NEURODYN AUSSIE sport depends on the care by the user and the manner
in which the equipment is handled. The user must respect the instructions regarding cleaning, and storage of the equipment,
cables and electrodes contained in these instructions of use.

CALIBRATION The correct installation of the equipment prevents

safety risks.The device and its consumable parts
The equipment must undergo periodic annual
must be eliminated at the end of their shelf-life,
maintenance to minimize the wear and tear or
according to the federal norms and/or state norms
corrosion which may reduce its mechanical
and/or local norms of each country.
properties in its useful life.

45
ACCESSORIES ACCOMPANYING NEURODYN AUSSIE SPORT

Ibramed NEURODYN AUSSIE Sport contains accessories designed to meet the requirements of electromagnetic comparability
accessories (accessories code 03017006, 03049006 and 03049007) which did not affect the requirements of electromagnetic
compatibility.

CODE QUANTITY ITEM DESCRIPTION

03019012 01 FUSE 20 AG OF 5A
03026009 01 DIAMOND LINE PROTECTION FUSE CARD
03026025 08 RUBBER CONDUCTIVE ELECTRODE 5CM X 5CM
ELECTROSTIMULATION CABLE 38 CABO (BLACK/ORANGE 2 WAYS EACH)
03049006 01
INJECTED
03049007 01 NEURO II 09 CABLE (BLUE/GREEN 2 WAYS EACH) INJECTED
03044001 01 GEL TUBE (100 G.)
03040048 01 DIGITAL OPERATION MANUAL - NEURODYN AUSSIE
03026087 01 BAG SAPPHIRE LINE - BLACK
03017006 01 FEMALE PP CABLE IEC - 2 X 0.75 X 1500MM

NOTE: NEURODYN AUSSIE Sport equipment must be used with neutral conductive gel properly registered in the
national health authority from the country.

46
ACCESSORIES ACCOMPANYING NEURODYN AUSSIE SPORT

REPLACEMENT ACCESSORIES

This list of replacement accessories are designed for use with the NEURODYN AUSSIE Sport Electro Stimulator. When
ordering, provide the respective part numbers, description, and quantity desired.

The use of accessories, cables and electrodes other than those intended for this specific equipment may significantly degrade the
performance of the emissions and immunity. DO NOT USE accessories, cables and electrodes from NEURODYN AUSSIE Sport
equipment on other equipment or medical electro systems.

47
 MAINTENANCE, WARRANTY AND
TROUBLESHOOTING TECHNICAL SUPPORT

What may initially look like a problem is rarely a defect. MAINTENANCE

Before calling customer support, please check the items
described below: For safe use of the equipment, it is recommended to have it
inspected and undergo preventive maintenance at IBRAMED
PROBLEMS SOLUTIONS or an authorized technical center every 12 months. The
manufacturer IBRAMED only assumes liability for the
The equipment • Is the power cable properly
does not turn on connected? technical features and equipment safety provided the unit
1. If not, connect it. Also check the wall is used according to the instructions for use contained in
socket. the manual, when maintenance, repairs and modifications
The equipment • Have you checked the safety fuse? are undertaken solely by the factory or authorized agents,
does not turn on Check if there is a bad contact. Check and in the event of a breakdown when the components that
2. if the value is correct as stated in the can cause a security risk to the appliance are replaced by
instructions.
original spare parts. If requested, IBRAMED will provide
The equipment • Haveyoufollowedtherecommendations technical documentation (circuit diagrams, lists of parts and
is turned on but for correct use the equipment as
components etc) necessary for the repair of any equipment.
does not emit mentioned in the instructions?
current to patient Check and repeat the steps in the We assume no responsibility for repairs without prior explicit
1. controllers, indications and operation written permission from IBRAMED.
section.
The equipment • Have you checked the electrodes and WARRANTY
is turned on but the connecting cables to the patient?
does not emit Check if the cable plug is adequately
IBRAMED, Indústria Brasileira de Equipamentos Médicos.,
current to patient inserted in the equipment.
2. Check if the electrodes are adequately here identified to the consumer through the following address
placed on the patient’s body. and telephone number: Av. Dr. Carlos Burgos, 2800, Jd Itália,
The equipment • Check if the amount of gel is Amparo/SP; Phone: 55 19 3817 9633 provides product-
does not turn enough. warranty for eighteen (18) months insofar as the conditions
on and/or work • Check if the electrodes are worn set for warranty terms are followed by the user as mentioned
properly. properly.
below.
48
MAINTENANCE, WARRANTY AND TECHNICAL SUPPORT

WARRANTY TERMS
instructions of use contained in this manual;
1)Your IBRAMED product is guaranteed against manufacturing • Due to defects caused by accidents or natural agents
defects, if considered the conditions established by (atmospheric discharges, for example);
this manual 18 consecutive months divided as follows: • When the equipment is connected to an electrical system
a) 03 (first three months) Legal Warranty; with inappropriate voltage and/or subjected to excessive
b) 15 (fifteen) remaining months: Additional warranty fluctuation or overcharge;
provided by IBRAMED - CONTRACTUAL WARRANTY. • In cases of transport accidents.
2) The warranty period will start counting from the date of 4) in the LEGAL WARRANTY period (first three months
purchase (date in which the sale invoice is issued), even if the starting on the purchase date), IBRAMED is responsible for
purchaser, later on, transfers the equipment to a third party. the transport of the equipment to the technical assistance in
The warranty will comprehend the replacement of parts and case of manufacturing defects; however, there is need of a
the labor costs in the repair of the defects found as being previous contact with the company post-sales department,
derived from manufacturing. which in turn will give directions to the Customer about the
3) The LEGAL WARRANTY and the ADDITIONAL/ best manner to ship the product, the location to which it
CONTRACTUAL WARRANTY will cease to be valid in the must be shipped and will issue an authorization for transport.
cases specified below: 5) In case no defect is found in the equipment sent to
• When the identification number (serial number) of the technical assistance in the LEGAL WARRANTY period, all the
equipment is removed or altered; expenses of the transport of that equipment will be charged
• When it is determined that the equipment and/or its to the Customer.
accessories have suffered fall, contact with water or misuse; 6) COVERAGE WITHIN THE LEGAL WARRANTY (03 MONTHS):
• When it is determined that the equipment seal was violated, • Manufacturing defects of the equipment and its
or if it is characterized that the equipment has suffered accessories;
alterations/modifications or repairs by other technicians • Transport of the equipment for repair (following previous
other than the ones certified by IBRAMED; authorization by IBRAMED);
• When the installation or use of the equipment does not 7) COVERAGE WITHIN THE ADDITIONAL/CONTRACTUAL
observe the specifications and recommendations of the (15 MONTHS):
49
MAINTENANCE, WARRANTY AND TECHNICAL SUPPORT

TECHNICAL ASSISTANCE
• Manufacturing defects of the equipment.
8) In the period of ADDITIONAL/CONTRACTUAL If you have any doubts or problems related to the operation
WARRANTY, IBRAMED is not responsible for the transport of
of your equipment please contact our technical department
the equipment to technical assistance, neither is it responsible
in Brazil. Call: +55 19 3817.9633.
for any cost and/or refund of costs from transport.
9) Both in the LEGAL WARRANTY PERIOD and in the
ADDITIONAL/CONTRACTUAL WARRANTY, there is no
coverage of parts subjected to natural wear and tear, such
as command switches, handles, energy cables, patient
connection cables, ultrasound transducer, Support brackets
cabinets, etc. of the equipment.
10) No authorized shop and/or technical assistance is
authorized to alter the conditions mentioned herein or to take
responsibility in the name of IBRAMED.

50
MAINTENANCE, WARRANTY AND TECHNICAL SUPPORT

MAINTENANCE - No change in this equipment is allowed.

- Any unauthorized modification can affect the safety
The user must carry out an annual preventive
use of this equipment.
inspection not the equipment only at IBRAMED or - Never make unauthorized repairs.
at other authorized technical centers. IBRAMED
should not be held responsible for maintenance,
repairs or
modifications which have been performed by agents
or companies not expressly authorized. Company authorization of operation: 103.603-1

Technician in Charge: Maicon Stringhetta

CREA-SP: 5062850975

51
CEFAI – IBRAMED CENTER FOR EDUCATION AND ADVANCED TRAINING

IBRAMED Equipment goes beyond technology. It also provides Special attention is also given to those interested in visiting our
knowledge! Science constitutes our differential value and we structure. Whatever your professional development needs,
effectively take advantage of its benefits in order to ensure we’ll be right by your side to provide you with unconditional
patient safety and thereby maximize results. support.

IBRAMED develops products with scientific support of the We are happy to assist you!
most recent medical studies published in major scientific
journals in the areas of biological, health and exact. Contact – cefai@conexaocefai.com.br
www.conexaocefai.com.br
Access to the knowledge database is guaranteed by CEFAI +55 19 3808. 2348
(IBRAMED Center for Education and Advanced Training)
whose goal is to provide technical and scientific support as Thanks,
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 IBRAMED – A matter of respect!
into account the personal and professional development of all
its partners and customers.

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.

52
 IBRAMED
Indústria Brasileira de Equipamentos Médicos EIRELI
Av. Dr. Carlos Burgos, 2800 - Jd. Itália
13901-080 - Amparo - SP - Brazil
+55 19 3817 9633
www.ibramed.com.br
ibramed@ibramed.com.br

53