IDL01526

English

Short-wave therapy
Code 5T06

0476

REV. DATA
02 18/10/2006
 IDL01526

INDEX

GETTING STARTED
INTRODUCTION: SCOPE OF APPLICATION ............................................................................................................ 4
WARNINGS ....................................................................................................................................................... 4
MANUFACTURER ‘S RESPONSIBILITY .................................................................................................................. 5
SYMBOLS USED ON THE APPARATUS .................................................................................................................. 6
INSTALLATION................................................................................................................................................... 6
MECHANICAL INSTALLATION .............................................................................................................................. 7
GENERAL INFORMATION .................................................................................................................................... 8
PRECAUTIONS TO BE ADOPTED DURING TREATMENT ........................................................................................... 9
DISC ELECTRODES ....................................................................................................................................... 9
PLATE ELECTRODES ..................................................................................................................................... 9
INDICATIONS AND CONTRAINDICATIONS. ......................................................................................................... 12

BASIC OPERATION
DESCRIPTION OF CONTROLS, INDICATIONS AND DEVICES OF THE APPARATUS..................................................... 13
MAIN MENU AND MODES OF OPERATION ........................................................................................................... 14
PATIENTS ................................................................................................................................................ 15
CREATING A PATIENTS’ FILE ..................................................................................................................... 15
ENTERING THE PATIENT’S DATA ................................................................................................................ 16
PATIENT’S PERSONAL CARD ..................................................................................................................... 16
THERAPIES ............................................................................................................................................. 18
RESIDENT PROGRAM FILE................................................................................................................................ 19
CHECKING CABLES AND APPLICATORS .......................................................................................................... 20
RESIDENT PROGRAM OUTPUT NOT ACTIVE .................................................................................................... 20
RESIDENT PROGRAM OUTPUT ACTIVE ........................................................................................................... 21
FREE OPERATION ........................................................................................................................................... 22
SETTING THE FREE PROGRAM PARAMETER ................................................................................................... 22
FREE PROGRAM OUTPUT ACTIVE .................................................................................................................. 23
INFORMATION ........................................................................................................................................ 24
GENERAL FEATURES ............................................................................................................................... 24
ELECTRODE POSITIONING ........................................................................................................................ 25

MODALITIES OF APPLICATION
PREPARING THE PATIENT. ............................................................................................................................... 26

MAINTENANCE AND CLEANING

MAINTENANCE ................................................................................................................................................ 27
CLEANING. ..................................................................................................................................................... 27

MALFUNCTIONS ............................................................................................................................................ 28

SPECIFICATIONS AND TECHNICAL DATA

SPECIFICATIONS ............................................................................................................................................. 29
TECHNICAL DATA ............................................................................................................................................ 30

PACKAGE CONTENT
ORDERING THE ACCESSORIES......................................................................................................................... 31

DISPOSAL ...................................................................................................................................................... 32

ANNEX 1
INDICATIONS FOR THE INSTALLATION OF THE TUBE ............................................................................................ 33

ANNEX 2
TABLE OF TREATMENT PROGRAMS ................................................................................................................... 35

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[2]

[5]
[7]

[1]

[3]

[6]

[A]

[B]
[4]

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GETTING STARTED

Introduction: scope of application

The SW500 apparatus is a short-wave generator (frequency 27.120 MHz) designed for use in the field of
diathermic therapy and non-thermal therapy applications.

The primary indications for short-wave therapy include: analgesic treatments, muscle contractures and
inflammatory states.

The apparatus can be used only by specially trained personnel (physicians, physiotherapists) and should be
installed exclusively in environments specially equipped for this purpose (hospitals, clinics and surgeries).

The unit allows short waves to be delivered either in continuous mode or in pulsed mode (pulse packets).

The apparatus is supplied complete with two standard applicators consisting in 150-mm diameter circular
capacitive electrodes (Schliephake), but it can also be used with other types of inductive or capacitive
electrodes supplied as options.

The SW500 unit features an automatic tuning system which search the best tuning between generator and
patient, enabling a wide range of therapeutic applications.

The applicators are applied in close proximity to the patient’s skin without contact. Where contact is required
(rubber inductive electrodes), a cotton cloth or felt should be interposed between the applicator and the
patient’s skin.

The SW500 units contains a series of resident programs for the most common pathologies. Each resident
program indicates the treatment mode, either continuous or pulsed, the pulse frequency and the treatment
time. It will be the operator’s care to adjust the output level according to the patient’s thermal sensation.

The SW500 also allows customised programs to be created and stored.

In addition to this, the unit features a patients’ file directly manageable via a touch-screen.

It is the user's responsibility to ensure that the apparatus is installed in compliance with current safety
regulations and that all suitable measures are adopted to prevent any accidents.

Warnings
Please ensure this manual is always readily available to all personnel authorised to operate the apparatus.

Before using the SW500 unit, the operator should read carefully the instructions contained in this manual.

The operator should read carefully all warning plates and labels applied on the apparatus and ensure that he
fully understands their meaning in relation to their specific location.

Before performing any treatment, the operator should get familiar with the apparatus operating modes and
be aware of all indications and contraindications for the use of the unit.

The SW500 apparatus can interfere with or be affected by other electronic equipment. For this reason, the
use of other electrical or electronic devices (including walkie-talkies and radiotelephones) within the therapy
room, is prohibited when the SW500 is operated.
To ensure compliance with this prescription, it is recommended that a warning notice be posted at the
entrance of the room.

Do not attempt to remove any parts of the apparatus, as this not only may cause a potential danger, but may
also compromise proper operation of the unit resulting in automatic cancellation of the warranty.

Any repair or service operation on the unit, should be performed solely and exclusively by authorised

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GETTING STARTED
personnel.

Manufacturer ‘s responsibility
Emildue s.r.l. will answer for the safety, reliability and performance of the apparatus only when the following
conditions are complied with:
• The installation, repair and overhaul of the apparatus are performed by authorised personnel.
• The environment where the apparatus is used meets the prescribed safety standards.
• The apparatus is used in compliance with the indications contained in this manual.
• The apparatus is used with the original accessories.

Emildue s.r.l. will not be held responsible for therapy effects resulting from improper use of the apparatus.

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GETTING STARTED

Symbols used on the apparatus

Caution: consult the attached documents.

The apparatus emits non-ionising radiations.

BF-type applied part.

Product to be disposed of as special waste at the end-of-life stage.

Installation

• Before connecting the apparatus to the power line, make sure the mains voltage and frequency
correspond to the values indicated on the identification plate.

• Ensure the mains outlet connected to the apparatus is properly grounded: use only the power cable
supplied with the equipment.
• Use of the apparatus is allowed only in premises intended for medical use (CEI 64-8 standard, Part 7,
Section 710: premises for medical use).

• Do not expose the apparatus to excessive pressure, humidity, direct sunlight, mechanical vibrations or
dust.

• Adopt suitable measures to prevent the penetration of liquids into the apparatus: if this should occur,
disconnect immediately the unit from the mains and contact the after-sales service.

• The unit cannot be used in explosion-hazardous environments or hydrotherapy rooms. Do not use
oxidising or flammable anaesthetic gases, such as oxygen or nitric oxide (N2O), while performing a
short-wave treatment.

WARNING:
The apparatus requires special electromagnetic compatibility (EMC) precautions.

Portable and mobile radio communication units may affect the apparatus operation.

THE UNIT IS TRANSPORTED AND DELIVERED WITH THE TUBE REMOVED. INSTALLATION OF THE
TUBE SHOULD BE CARRIED OUT EXCLUSIVELY BY QUALIFIED PERSONNEL.

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GETTING STARTED

Mechanical installation
Fix the articulated arm to the unit using the four screws included in the package. To tighten the screws use
the wrench supplied with the equipment (fig. 1).

Fig.1

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GETTING STARTED
General information
The patient should be positioned solely and exclusively on wooden beds or chairs without uncovered
metallic parts.

Patients with hearing aids are recommended to switch off or, better yet, to remove the device before starting
the treatment, to avoid annoying interferences.

WARNING:
Patients with pacemakers cannot be subjected to short-wave therapy and should be kept away from
the area of operation of the unit.

Position the applicators only on uncovered parts: the treatment should not be performed on persons wearing
metallic objects or garments with metallic materials (buttons, buckles, wires etc.).

Do not treat parts of the patient’s body with metallic implants (prostheses) without the authorisation of a
specialist.

Do not perform treatments on areas with large quantities of adipose tissue.

Before starting the treatment ensure the patient’s skin is perfectly dry.

When treating the axillary area or the hand and foot finger areas, interpose a cotton cloth between the
applicator and the skin to prevent the formation of sweat.

When using the rubber inductive electrodes, place the cotton felt provided with the equipment between the
electrode and the patient’s skin.

The applicators should always be positioned in such a way as to minimise radiations on other parts of the
body.

The applicators should never come in contact the patient’s skin, but should be held at a distance of 1 cm to
prevent the formation of sweat and the consequent risk of skin burns.

The RF cables should never be placed in contact with the patient’s skin nor with energy conducting or
absorbing objects.

WARNING:
PLATE ELECTRODES should never be applied in direct contact with the patient’s skin; a
biocompatible material should be interposed between the two surfaces to prevent allergic reactions
or skin irritations. The most suitable materials include cotton gauzes and the cellulose paper
commonly used to cover examination couches, which are readily available at chemist’s and medical
supply shops. The piece of material used should be large enough to cover entirely the part of skin in
contact with the electrode.

WARNING:
Check regularly the condition of both the applicators and RF cables. Any damage to insulation may
cause serious electric shocks to both the patient and operator.

WARNING:
NEVER disconnect the RF cables or the applicators during the treatment.
Always switch off the unit before replacing the applicators or the RF cables.
Non-compliance with the above safety prescriptions may result in serious electric shocks to both
patient and operator.

WARNING:
Do not subject the units to shocks or bumps when the tube is still hot.

WARNING:
Use of accessories, transducers and cables other than those specified in Emildue catalogue may
result in increased electromagnetic EMISSIONS or reduced apparatus IMMUNITY.

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GETTING STARTED

Precautions to be adopted during treatment

During short-wave applications special care should be taken to avoid overdosage which may result in both
surface or deep burns, in particular:
- Ensure there are no contraindications to the treatment.
- Assess the patient’s thermal sensation (for treatments in continuous mode).
- Do not treat bony prominences, as the absence of soft tissue, along with wave reflection on the bony
structure and the reduced effect of vasodilatation, may cause an overdosage. If the treatment of such
parts cannot be avoided, increase the distance of the applicator from the skin.
- Make sure the skin is perfectly dry both before and during the treatment (disc electrodes).
When treating the axillary area, interpose an absorbing medium between the applicator and the patient’s
skin (the same should be done when treating hands and feet applying the absorbing medium between
the fingers).
- Treat only uncovered parts of the body, if this is not possible, remove any wet or synthetic garments.
- Align accurately the electrodes on the area to be treated in order to obtain the optimum heating pattern.
- Do not treat parts of the body with metallic prostheses.
- If the patients wears a hearing aid, it is advisable to turn it off before starting the treatment to avoid
annoying interferences.
- Inform the patient of the thermal sensation he should perceive.
- For medical-legal purposes, the operator should stress the risk of burns that may result from lack of
cooperation from the patient.

The operator should refrain from treating the patient, when this is connected to other devices.

The position of the patient varies according to the area to be treated; he may be either seated or lying, but in
any case he should be always positioned on wooden chairs or beds without metallic parts.

To avoid an excessive concentration of high-frequency current that may increase the heat intensity in the
tissue, causing burns, the patient is required to take off all metal objects (chains, rings, watches, hooks,
metallic prostheses etc.), even if they are located at some distance from the area to be treated.

The type and dimension of the electrodes, as well as their positioning, influence significantly the efficacy of
the therapy. Here we will limit to provide some general indications; it will be up to the operator to select the
most appropriate features for the kind of treatment to be performed, based on his knowledge and clinical
experience.

Schliephake condenser electrodes (disc electrodes) should be held at a distance of 3 to 5 mm from the skin
to allow air circulation, thus favouring the evaporation of the sweat caused by local heating.

Rubber flexible electrodes (plate electrodes) which are usually held in place via rubber bands, should never
be positioned in such a way as to favour the accumulation of sweat which could cause burns.

INTERPOSE BETWEEN THE PATIENT SKIN AND THE PLATE ELECTRODES THE SEPARATION
MATERIAL SPECIALLY PROVIDED (see “General Information”).

The electrode connection cables should never cross. They should possibly be held at the same distance as
between the cable entry bushes.
The cables should be arranged in such a way as to avoid contact with conductive parts. The operator should
also prevent the patient from contacting cables or any metallic parts of the equipment.

Disc Electrodes
They are available in various sizes: Ø 100 mm, Ø 140 mm (standard).
The position of the inside metal disc can be adjusted with respect to the hard cover.

Plate Electrodes
They are available in the following dimensions: 90x120 mm and 130x190 mm.
The metal plate is incorporated into a flexible rubber cover which enables it to adapt itself to the various
parts of the body.

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GETTING STARTED
Electrodes should NEVER touch each other.

NO!

NO!

Cables should NEVER cross.

NO! NO!

NO!

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GETTING STARTED

Electrodes should NEVER come in contact with cables

NO!

NEVER position electrodes face-to-face while they are emitting short waves.

NO!

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GETTING STARTED

Indications and contraindications.

Hereunder are mentioned some of the indications and contraindications for the use of the unit.
For more detailed information please refer to the specific bibliography.

Indications:

Continuous short-wave therapy is indicated for the following conditions:

• Arthrosis
• Sequelae of traumas
• Muscle contractures
• Preparation for kinesiotherapy sessions

Pulsed short-wave therapy is indicated for the following conditions:

• Tissue traumas
• Recent injuries
• Synovitis and acute traumatic haematomas
• Sub-acute and chronic infections, such as paranasal sinusitis
• Initial treatment of peripheral nerve lesions
• Treatment of pain due to various conditions such as degenerative arthritis and neurogenic pain
(phantom limb pain, causalgia, Sudek’s atrophy)

Contraindications:

• Metallic implants
• Varicose veins and thrombophlebitis
• Osteoporosis (only continuous wave therapy allowed)
• Obliterating arteriopathies
• Haemorrhage
• Menses
• Obesity
• Presence of pace-makers or hearing aids
• Pregnancy and TBC in the active phase
• Neoplasias
• Cutaneous hypoesthesia
• Ischemic tissues
• Active tuberculotic lesions
• Pyretic patients

Undesired effects:

• Skin burns
In the presence of skin moisture or cutaneous hypoesthesia, SWT can cause skin burns.

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BASIC OPERATION

Description of controls, indications and devices of the apparatus.

The control devices and indications described below refer to the general view of the apparatus and the
relevant panel (see page 3).

[1] Touch screen.

Control panel of the unit.

[2] Pen
The pen is used to select the parameters displayed on the touch screen.

[3] ON-OFF switch

The ON-OFF switch is used to power the apparatus after the cable of the power supply unit has been
plugged into the relevant socket [C].

[4] Data plate

This plate provides the data related to the short-wave unit: manufacturer, model, serial number,
protection degree and power consumption.
Additional features are described further on (see “Specifications” page 29 and “Technical data” page
30).

[5] Cable support arms

[6] RF cables

[7] Electrodes (Schliephake)

[A] SW500 unit

[B] Connector for power supply cable

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BASIC OPERATION

Main menu and modes of operation

SW500

START

• Press SETUP to set the language

• Press START to start the therapy session

After pressing START, three options appear on the display:

• PATIENTS
• THERAPIES
• INFORMATION

Gives access to the

patientsÕfile PATIENTS

Gives access to the

therapeutic section THERAPIES

Gives access to the

short-wave therapy info INFORMATION
section

Returns to the
previous screen

Select the desired option by clicking the corresponding icon.

WARNING:
The treatment of personal data is regulated by the European Directive 95/46/EC of 24 October 1995;
in Italy this matter is governed by the Legislative Decree No. 196 of 30 June 2003 “Personal data
protection code” and its subsequent additions and amendments.
It is the responsibility of the user of the SW500 to treat confidentially all data contained in the
PATIENTS’ file.

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BASIC OPERATION
PATIENTS

Select ”PATIENTS” to access the patients’file.

PATIENTS

SURN AME NAME

SURN AME NAME

SURN AME NAME

The patientsÕnames SURN AME NAME
and surnames are
SURN AME NAME
displayed
SURN AME NAME

SURN AME NAME

Enters a n ew
patient
Confirms entry
Returns to of a patient
previous sc reen

Deletes a
patient

Creating a patients’ file

• Press the key to add a patient to the file;

• Enter the patient’s data by filling in the fields displayed on the screen:

Returns to
NAME main menu

SURNAME DATE OF BIRTH

ADDRESS NR OF TR EATMENTS
SCHEDULEDD

Nr. of
ZIP CODE 0 treatments
performed
DATE O F FIRST
Date of first
TOWN
TREATMENT treatment

TEL. PATHOLOGY

Confirms
Returns to treatment
previous screen

• Click a data field (ex. name); an alphameric keyboard will appear to allow the patient’s data to be
entered;

• If you don’t want to save the data entered, press to return to the previous screen;

• To confirm and save the patient’s data in the file, press

• Press to return to the main menu.

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BASIC OPERATION
Entering the patient’s data

Confirms data
Returns to entered
prevous sc reen

• Enter the patient’s data via the alphameric keyboard

• Press to confirm the data entered

• Press to return to previous screen

Patient’s personal card

JOHN SMITH Returns to
DATE OF BIRTH …… main menu
ADDRESS ……

TEL. ……
NR. OF TREATMENTS SCHEDULED ……
DATE OF FIRST TREATMENT …… Gives access
NR. OF TREATMENTS PERFORMED …… to the file to
PATHOLOGY ……
modify data

Returns to Enters a new

previous screen treatment

Gives access to a screen allowing the pain level to be

set for both first and last treatment

• Press to modify the patient’s data

• Press to return to previous screen

• Press to enter a new therapeutic program into the patient’s personal card

The new program will be saved in the patient’s personal card so that it can be accessed directly from the
patients’ file.

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BASIC OPERATION

Returns to
main menu

PAIN LEVEL

Pain level
scale 1 2 3 4 5 6 7 8 9 10

FIRST LAST Sets the pain level

Sets the pain
level for the first TREAT. TREAT. for the last
session
session 0 0

Returns to Confirms data

previous screen

• To set the level of pain to be perceived by the patient during the first session, press “FIRST TREAT.”
and then a number between 1 and 10 for the corresponding pain level.

• To set the level of pain to be perceived by the patient during the last session, press “LAST TREAT.”
and then a number between 1 and 10 for the corresponding pain level.

• Press to save the data entered and return to the patient’s card.

• Press to return to the patient’s card without saving the data entered.

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BASIC OPERATION
THERAPIES

The therapeutic section features three modes of operation:

• PROGRAMS
• FREE OPERATION
• USER PROGRAMS

Gives access to the

resident program file PROGRAMS

Gives access to the

free operation mode
FREE OPERAT.

Gives access to the

user program file USER PROGR.

Returns to
previous screen

Select the desired mode of operation by clicking the corresponding icon.

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BASIC OPERATION

Resident program file

By selecting “PROGRAMS” from the main menu of the “THERAPIES” option, the following screen is
displayed:

Returns to
main menu

Type of applicator ELECTRODE PROGR.

OSTEOARTH. AS
OSTEOARTH. SS
OSTEOARTH. CS
MUSCLE CONT. AS
MUSCLE CONT. SS
CARP. TUNNEL AS
CARP. TUNNEL SS

Returns to
previous screen

Click the desired program to access the output modes (see Annex 2 for resident program parameters).

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BASIC OPERATION
Checking cables and applicators

WARNING:
Before activating the short-wave output, ensure both cables and applicators are correctly positioned
and properly connected.

ENSURE CABLES ARE

PROPERLY
CONNECTED

Confirm
key

Press to continue.

Resident program output not active

Returns to
main menu

Program N. FIBRE RUP. AS Tuning

indicator
Treatment
time 15 : 00
RECOMM.
DOSAGE
Treatment
frequency 60 Hz
I-II

Applicator ELECT.

Starts
Returns to treatment
previous sc reen

Recommended dosage: refers to the thermal sensation the patient should perceive during the treatment:

• I : athermal (the patient does not perceive any heat)

• II : oligothermal (the patient perceives a light heat sensation)
• III : thermal (the patient perceives an agreeable heat sensation)
• IV : hyperthermal (the patient perceives an intense heat sensation, but without discomfort or
pain)

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BASIC OPERATION
Resident program output active

Returns to
main menu

Program OSTHEOARTHR. CS Tuning

indicator
Treatment
time 19 : 36 MAX.

Treatment Graduated
frequency CW scale of power

Applicator ELECT.
MIN.

Stops
Returns to treatment
previous sc reen

To adjust the output power use the and keys.

WARNING:
The value indicated on the graduated scale does not represent an absolute value, but merely
provides a visual indication, therefore the output power should be adjusted according to the
patient’s sensation.

Tuning indicator:

When generator and patient are perfectly tuned, the indicator is yellow. When they are out of tune, the tuning
indicator is blue.

If the indicator remains blue for a while, it means that the unit is not well tuned. In this case, interrupt the
output and reposition the applicators.

Press to stop the output.

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BASIC OPERATION

Free operation
Using the corresponding key, select the desired type of applicator:

Returns to
main menu

MONODE/
DIPLODE

ELECTRODES

Returns to
previous screen

Setting the free program parameter

FREE OPERATION Returns to

Type of
applicator
MON./DIPLODE main menu

Tuning
indicator
Treatment
time 0 : 30

Treatment
frequency CW
Returns to
previous screen

Starts
Saves treatment
program

To adjust the treatment parameters use the and keys located under the indicators.

Press to start output.

Press to save the free program selected; the program will be stored in the user program file.

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BASIC OPERATION
Free program output active

FREE OPERATION Returns to

Type of
applicator
ELECTRODES main menu

Tuning
indicator
Treatment
time 3 : 37 MAX.

Power
graduated
scale
Treatment
frequency 60 Hz

MIN.

Starts
treatment
Saves program

To adjust the output power use the and keys.

WARNING:
The value indicated on the graduated scale does not represent an absolute value, but merely
provides a visual indication, therefore the output power should be adjusted according to the
patient’s sensation.

Tuning indicator:

When generator and patient are perfectly tuned, the indicator is yellow. When they are out of tune, the tuning
indicator is blue.

If the indicator remains blue for a while, it means that the unit is not well tuned. In this case, interrupt the
output and reposition the applicators.

Press to stop the output.

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BASIC OPERATION
INFORMATION

This section provides explanations on the unit operation.

The system displays two types of information:
- GENERAL FEATURES
- ELECTRODE POSITIONING

Gives access to the

general features GENERAL
FEATURES
QuickTime™ e un
decompressore
sono necessari per visualizzare quest'immagine.

Gives access to the

examples of electrode ELECTRODE
positioning
POSITIONING

Returns to
previous screen

Select the desired option by clicking the corresponding icon.

General features

Purpose of this section is to provide both the patient and the operator with information on short-wave
therapy. The section contains the following subjects:
• Short-wave therapy
• Condensing electrodes
• Monode
• Doplode
• Effects
• Treatment instructions
• Recommended dosage
• Therapeutic indications
• Contraindications

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BASIC OPERATION
Electrode positioning

The display shows some practical examples of how electrodes should be positioned.

Examples of electrode positioning on the ankle :

Returns to main
menu

QuickTime™ e un
decompressore
sono necessari per visualizzare quest'immagine.

Returns to
previous screen

Keys for scrolling

images

Other displayable examples:

Positioning of monode on Positioning of disc Positioning of disc

back electrodes on elbow electrodes on wrist

Positioning of disc Positioning of disc

electrodes on knee electrodes on shoulder

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MODALITIES OF APPLICATION

Preparing the patient.

• Make sure there are no contraindications to the therapy.

• Put the patient in a comfortable position. The area to be treated should be properly supported, exposed
and relaxed.

• Inform the patient on the purpose of the treatment and on the sensations he will perceive in the course
of the therapy.

• Position the applicators for treatment following the indications provided in section “Precautions to be
adopted ”.

WARNING:
To avoid burns, the operator should check from time to time the heat sensation perceived by the
patient. He should also seek the patient’s cooperation in order to establish exactly the thermal
sensation perceived by him.

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MAINTENANCE AND CLEANING

Maintenance
The apparatus does not require any special maintenance, but it is essential to check regularly the condition
of both electrodes and connection cables. In case of failures, use always genuine spare parts ( cables,
electrodes, etc.) and avoid makeshift repairs.
To remove dust or foreign bodies use exclusively the compressed-air cans used for computer keyboard
cleaning.

WARNING:
Do not underestimate the importance of the cleaning and maintenance indications.
The penetration of dust or foreign bodies into the short-wave unit could result in a reduction of the
energy actually delivered to the patient, which may compromise the treatment efficacy. It is therefore
advisable to have the device regularly checked at an Emildue authorised centre.
The user is also recommended to keep a record of all the maintenance and repair operations
performed on the apparatus.

The service manual with all the necessary technical descriptions and wiring diagrams is available on request
and can be obtained from any Emildue Authorised Service Centre.

CAUTION:
Check regularly the applicators and RF cables for wear or insulation damage that may cause serious
electric shocks to both patient and operator.

Cleaning.
CAUTION:
Before performing any cleaning operations, switch off the apparatus and disconnect it from the
mains.

• To clean the apparatus, connection cable and electrodes use a soft cloth soaked with lukewarm water
and a non-abrasive, solvent-free detergent.

• Rubber plate electrodes can be cleaned with lukewarm water and disinfected using a 70% alcohol
solution.

CAUTION:
Before putting the unit into operation, make sure the solution used for cleaning and disinfecting the
apparatus have completely evaporated.

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MALFUNCTIONS

During operation, the SW500 performs a series of internal tests designed to ensure that all unit components
of the unit work properly.
In case of failure the treatment is stopped and the system indicates on the display the malfunction detected.

OUTPUT
ERROR

Switch off the apparatus and switch it on again after a few minutes.
If the malfunction does not disappear, contact the nearest service facility.

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SPECIFICATIONS AND TECHNICAL DATA

Specifications

- Number of applicators: 2 disc electrodes, ø 150 mm (Schliephake)

- Generator rated frequency: 27,120 MHz ± 0.6%

- Output modes:
1) Continuous.
- Maximum power: 500 W -30%.

2) Pulsed
- Pulse duration: 400 µs ±30%
- Frequency: 20 ÷ 200 Hz, steps of 20 Hz ±30%
- Peak power: 700 W -30%

- Timer: 0 ÷ 99 min.

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SPECIFICATIONS AND TECHNICAL DATA

Technical data
POWER SUPPLY VOLTAGE
The SW500 can be supplied with a mains supply voltage of either 230 V~ or 110 V~. Before connecting the
unit check the data indicated on the machine plate.

1) Mains voltage 230 V~

- Frequency: 50 - 60 Hz

- Power input: 1300 VA

- Mains fuses: 10A T 250 V

- Weight: 55 Kg

- Overall dimensions: 100x49x45 cm

2) Mains voltage 110 V~

- Frequency: 50 - 60 Hz

- Power input: 1300 VA

- Mains fuses: 20A T 250 V

- Weight: 60 Kg

- Overall dimensions: 100x49x45 cm

- Safety class: Class I, BF-type applied part

- Protection degree: IP20 (Protected against the penetration of solid bodies with diameter ≥ 12mm)

Environmental conditions for use:

Environment temperature: 0 ÷ 50 °C

Relative humidity: 10% ÷ 90%

Atmospheric pressure: 500 ÷ 1060 hPa

Apparatus for continuous duty

Environmental conditions for transport and storage

Environment temperature -10 ÷ +50°C

Relative humidity 10% ÷ 90%

Atmospheric pressure 500 ÷ 1060 hPa

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 IDL01526

PACKAGE CONTENT

4
2

N.1 SW500 short-wave unit 1

N.2 Electrode support arms 2
N.2 Short-wave cables 3
N.2 150-mm diameter disc electrodes (Schliephake) 4

N.1 Power supply cable

N.1 Setscrew wrench size 5
N.1 SW500 User manual
N.1 Warranty certificate

Ordering the accessories.

The standard and optional accessories are listed in the Emildue s.r.l. physiotherapy catalogue.

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 IDL01526

DISPOSAL

The symbol of a crossed-out wheeled bin indicates that in the European Union the product
must be disposed of as special waste at the end-of-life stage. The same rule applies to all the
accessories supplied with the apparatus marked with this symbol. These products cannot be
disposed of in the municipal waste but must be collected separately.

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 IDL01526

ANNEX 1

Indications for the installation of the tube

WARNING:
The operations described hereunder must be carried out solely and exclusively by qualified
personnel.

Remove the outer grid using the Allen Remove the inner grid.
wrench.

Fit the tube securely into the relevant socket

Remove the carton support taking care not to

damage the anodic connection.

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 IDL01526

ANNEX 1

Secure the anodic connection as indicated in Make sure the coil present on the anodic
the figure. connection is completely open as shown in the
figure.

Reinstall the inner grid and the rear protection grid.

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 IDL01526

ANNEX 2

Table of treatment programs

The following table provides the list of resident programs. For each program the suggested energy
density is indicated.

It rests with the doctor or therapist to define and adjust the treatment parameters during the
therapy according to the patient's characteristics.

ABBREVIAT. TIME
PATHOLOGY FREQUENCY (Hz) DOSAGE
ON DISPLAY (min)
ACUTE OSTEOARTHRITIS OSTEOARTH. AS 10 CW I-II

SUB-ACUTE OSTEOARTHRITIS OSTEOARTS. SS 15 CW II-III

CHRONIC OSTEOARTHRITIS OSTEOARTS. CS 20 CW III-IV

ACUTE MUSCLE CONTUSION MUSCLE CONT. AS 10 CW I-II

SUB-ACUTE MUSCLE
MUSCLE CONT. SS 15 CW II-III
CONTUSION

ACUTE CARPAL TUNNEL CARP. TUNNEL AS 10 20 -

SUB-ACUTE CARPAL TUNNEL CARP. TUNNEL SS 15 60 -

SUB-ACUTE RHEUMATOID
RHEU. ARTH. SS 15 60 -
ARTHRITIS
CHRONIC RHEUMATOID
RHEU. ARTH. CS 20 200 -
ARTHRITIS

CHRONIC ANNEXITIS ANNEXITIS CS 15 200 -

CHRONIC INFECTION OF
C.I. UR. BLADDER 15 60 -
URINARY BLADDER

SUB-ACUTE EPICONDYLITIS EPICONDYILIT. SS 20 200 -

CHRONIC EPICONDYLITIS EPICONDYLIT. CS 10 20 -

ACUTE FIBROMYALGIA FIBROMYALG. AS 15 60 -

SUB-ACUTE FIBROMYALGIA FIBROMYALG. SS 10 20 -

ACUTE HAEMATOMA HAEMATOMA AS 15 60 -

SUB-ACUTE HAEMATOMA HAEMATOMA SS 10 20 -

ACUTE RUPTURE OF MUSCLE

M. FIBRE RUP. AS 15 60 -
FIBRES
SUB-ACUTE RUPTURE OF
M. FIBRE RUP. SS 10 20 -
MUSCLE FIBRES

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IMPORTANT
In the case of repair requests, the unit must be accompanied by this form, duly
completed in every section.

Applicant’s stamp

Messrs.
EMILDUE s.r.l.
Via Della Canapa, 22
44042 Cento (Ferrara)

Apparatus Mod. SW500, serial number

SUBJECT: AUTHORISATION pursuant to Italian Legislative Decree No. 196 of 30 June

2003 “Personal data protection code”.

In accordance with the above provisions, we hereby authorise the addressee of this
document to view the data contained in the software for the sole purpose of maintenance /
repair.
We therefore relieve the company Emildue s.r.l. of any responsibility pursuant to
Legislative Decree No. 196 of 30 June 2003 on privacy.

Date ____________ Signature

IDL01526