Microwave

2450P

Users manual

Doornstraat 87-89 B-2650 Edegem

Tel. +32 3 457 66 76 Fax. +32 3 457 55 38
Email: info@fysiomed.com URL: www.fysiomed.com
 User's manual - Microwave 2450P

1. INTRODUction...............................................................................................................................2
2. INSTALLATION.............................................................................................................................2
3. SAFETY AND MAINTENANCE...................................................................................................2
3.1. ORDINARY MAINTENANCE...........................................................................................................2
3.2. Periodic maintenance by T.A.S...........................................................................................................3
3.3. Immediate maintenance procedure by T.A.S.....................................................................................3
4. specification tag and symbols.........................................................................................................4
I.................................................................................................................................................................................4
IPX1......................................................................................................................................................................4
5. PRECAUTIONS AND RISKS........................................................................................................4
5.1. microwave safety..................................................................................................................................6
6. PRECAUTIONS FOR THE OPERATOR.....................................................................................7
7. GUARANTEE.................................................................................................................................7
8. MANUFACTURER RESPONSIBILITY.......................................................................................7
9. directives and rules..........................................................................................................................8
10. Classification.................................................................................................................................8
11. WORKING AND STORING CONDITIONS...............................................................................9
12. destination......................................................................................................................................9
13. DESCRIPTION OF THE UNIT..................................................................................................9
14. CABLE CONNECTION.............................................................................................................10
15. CONTROLS DESCRIPTION.....................................................................................................10
15.1. back of the unit.................................................................................................................................11
16. APPLICATORS...........................................................................................................................11
17. HOW TO SET UP A WORKING SESSION..............................................................................12
17.1. MANUAL SETTING.......................................................................................................................12
17.2. STANDARD PATHOLOGIES.......................................................................................................14
17.3. ENTER A SPECIAL TREATMENT INTO THE MEMORY......................................................15
17.4. USE THE PRE-SET MEMORIES..................................................................................................15
17.5. DELETE A PRE-SET MEMORY..................................................................................................16
18. WARNING MESSAGES.............................................................................................................16
19. technical features .......................................................................................................................17
20. Periodic maintenance form ........................................................................................................18

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1. INTRODUCTION
This handbook gives all necessary information for a correct and safe use of MICROWAVE 2450P.
The manufacturer works following to its own certified quality system according to the UNI EN ISO 9001 & UNI CEI
EN 13485 rules.

2. INSTALLATION
Before using the unit the first time we suggest to carry out a safety test and a working test, in order to check the
integrity of the unit after the carriage.
As far as particular installation procedure is concerned, read the following paragraphs.

3. SAFETY AND MAINTENANCE

Our tests as well as our strict quality control are essential pre-requisites in order to meet all the security conditions
imposed by the laws in force as far as electro-medical equipment are taken into consideration.
However, don't forget that according to the laws in force, the reliability and the efficiency of an electro-medical unit can
be guaranteed only if:
installation, new settings and repairs are carried out only by the manufacturer or authorised technical staff;
the electrical installation in the treatment room complies with the laws in force;
the unit is used in accordance with the operating instructions;
only original accessories are used.
All the electro-medical units have to be kept in good condition by regularly checking them and doing the necessary
repairs. This preventive maintenance should avoid possible breakdowns and guarantee:
a correct functioning;
the safety of both the patient and the user, as well as of the room in which the treatment is performed;
the best performance of the unit.
Preventive maintenance must be made by the operator, whereas the periodic controls and repairs must be carried out by
the Technical Assistance Service (T.A.S.).
The manufacturer undertakes to give, when required, electric diagrams, components lists, calibration procedures or
everything other could need to the Technical Service department authorised by the manufacturer itself, in order to repair
parts that the manufacturer considers the customer can repair.

3.1. ORDINARY MAINTENANCE

It has to be carried out by the operator within the suggested time.

Clean the unit and the accessories: (every day)

The unit and its accessories must be cleaned every day if you want to be sure you can use your unit as long as
possible. After disconnecting the unit from the power supply, you can easily clean everything with a small sponge
soaked in water and soap. Then dry everything with a piece of dry cloth.
Control the state of cables and the applicators: (once a month)
Remember that damaged cables and applicators can cause troubles to the patient or operator during the treatment
and also seriously jeopardise the correct working of the unit.
Clean and disinfect the applied parts that have to be put in contact with the patient: (after every treatment)
We suggest disinfecting with accuracy the applied parts that have be put in contact with the patient, before carrying
out the treatment.
Control of the antenna alarm: (once a week)
Disconnect the HF cable from the unit, or from the antenna, with the unit in STOP mode, and check whether the
LCD shows the proper message and that an acoustic signal is emitted.

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WARNING
If the unit is not usual cleaned, or if wrong solvent is used, the paint and the serigraphs
of the unit could be damaged.
Check very often the wear and tear of all the cables used. Only power cables with
quality mark are supplied.

3.2. PERIODIC MAINTENANCE BY T.A.S.

The proposed maintenance program is in accordance with the booklet 1276 G published by CEI in November 1989. The
aim is to check if the unit complies with both the general laws of IEC 601-1 and the particular laws IEC 601-2-5. Such
program consists in:
checking the integrity of all the cables, the isolations, the coverings etc. designed to avoid access to parts under
voltage (EVERY TWO YEARS);
running the unit in order to check if it works properly (ONCE A YEAR);
measuring the leakage currents (EVERY TWO YEARS);
checking the resistance between ground and each accessible conductive part that has to be connected to the ground
(EVERY TWO YEARS);
checking you still have the handbook.

If the unit is used more intensively and for much more prolonged periods, we suggest you should check it at least once a
year. Only following this simple suggestion, your unit will function effectively.
After each periodic control, the T.A.S technician will write down the new data in the card enclosed at the end of this
handbook (See paragraph 20).

3.3. IMMEDIATE MAINTENANCE PROCEDURE BY T.A.S.

The operator must request immediate maintenance of the unit if:
the unit has gone through external mechanical stress (i.e. bad falling);
the unit has come into prolonged contact with liquids without any protection;
the unit has gone through overheating (i.e. direct sunlight, fire etc.);
the functionality of the unit seems altered;
parts of the covering have been broken or removed;
some connectors or cables seem worn-out.

WARNING
A whole electric security test must be carried out after any repair of the unit.

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4. SPECIFICATION TAG AND SYMBOLS

On the back of each unit there is the specification tag, according to the IEC 601-1 rule article 6, with the following data:
manufacturers name, model of the unit, serial number, IEC 601-1 classification, fuses, power supply voltage and
frequency, input power, production year, output features, symbols with reference to the following table.
In front of the unit, the CE mark must be present, together with the code of the Notified Body.

The meaning of the symbols placed outside and inside the unit is (with reference to the IEC 601-1 rule II ed. 1989,
Appendix D, the IEC 601-2-22 Appendix D and the IEC 825-1 fig. 14):

Symbols Meaning Short Electro Ultrasound Laser Magneto Traction Micro

wave therapy therapy wave
Warning, read the user manual before using
the system (Tab. D I-Symbol 14)
X X X X X X X
BF type applied part
(Tab. D II - Symbol 1)
X X X X X X
B type applied part
(Tab. D II-Symbol 1)
X
Non ionising radiation emission
(Tab. D II-Symbol 8)
X X X
High voltage
(Tab. D II-Symbol 6)
X X

Alternating current power supply
(Tab. D I - Symbol 1)
X X X X X X X
On: connected to the power supply
I (Tab. D I Symbol 16)
X X X X X X X
Off: disconnected from the power supply
0 (Tab. D I Symbol 15)
X X X X X X X
Protected against the dripping
IPX1 (Tab. D I Symbol 11)
X
Waterproof
IPX7 (Tab. D I Symbol 13)
X
Laser beam warning label
(IEC 825-1 fig. 14)
X
Remote interlock connector
(IEC 601-2-22 Tab. D I Symbol 115)
X

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5. PRECAUTIONS AND RISKS

Before using the unit, be sure the operating voltage of your unit corresponds to that of the power supply.
As long as the plug is in the socket, the unit is not disconnected from power supply.
Do not pull the cable when you want to disconnect the unit from power supply.

Do not place anything onto the unit.

Avoid installing or leaving the unit:
- near source heat, i.e. radiators, air ducts or heaters;
- directly exposed to sunlight;
- exposed to rain or humidity;
- exposed to dust or dirt.
If the above mentioned conditions are not followed, the unit could be seriously damaged.
Do not touch any uncovered part of cables or antennae while the unit is working: there is risk of burns.
In order to avoid interference handy telephones shouldn't be used in the same room where the unit is working.
Should any solid object or liquid penetrate into the unit, disconnect it immediately and call qualified personnel
before using it again.
Place the unit so that there is a good aeration toward the back of the cabinet, because when the unit is working it
needs air-cooling.
In order to adjust the arm position closed to the body (in wheeled units), do not draw the arm without keeping the
cabinet of the unit, because that last one could overturn and fall down. Moreover, to move the unit, use the proper
handles.

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WARNING
Operating close to short-wave units can lead to outputs instability. The working of high-
frequency units can interfere with the functioning of electrical units. Therefore, when used
simultaneously in the same room, a minimum safety-distance should be observed. In most cases
1,5 meter distances is enough.
Before treating patients with implanted heart pacemakers or with cochlea transplant,
consult a specialist. The energy delivered by these devices could cause troubles to this kind of
prosthesis.
Particular attention should be paid to all the other types of endoprothesis, which shouldn't be
thus treated.
Before treating patients with lower limb ischemia, cardiovascular disease, epilepsy or pregnant
women, consult a physician.
Before carrying out each treatment, disinfect the applied parts that have to be put in
contact with the patient.
Do not put any applied part onto skin lesions or inflamed/infected parts of the body.

WARNING
Any physical therapy treatment must be carried out on conscious patients. Furthermore pay always
attention to the patients sensation while the output energy (electrical, mechanical, high frequency,,
energy) is increasing.

If you have any question or problem, not sufficiently dealt in this handbook, please consult your authorised dealer.

5.1. MICROWAVE SAFETY

WARNING
The output power must not be enable during the positioning of the applicator before
carrying out the treatment.
Do not point the applicator directly at eyes and testicles.
Microwaves energy doesnt be delivered to patients with metallic objects, such as jewels,
buttons, threads etc.
Parts of the body with metallic equipment (for instance intramedullary) must not be
treated without any specialist authorisation.
When small parts of the body has to be treated (for instance the wrist), the applicator
must be placed so that sensory area (for instance eyes and testicles) are not on the radiation
beam not intercepted by the part under treatment (wrist).
Operators and people not under treatment must stay at 1.5m from the applicator at least.
Handle the applicators with care; directional features could change after shock.
Patients with low thermal sensitivity in the treatment area must not be treated with
microwaves.
Do not carry out short weave therapy on ischemic areas, malignant tumour, tubercular
infection, areas recently treated with X-rays therapy.
Do not place the unit closed to inflammables, but keep 1m as minimum-security
distance at least.

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6. PRECAUTIONS FOR THE OPERATOR

The operator should keep an inventory or register for all the units he uses, in which instructions and any other relevant
information are recorded, as required by IEC 601-1 law. Moreover, maintenance and controls should be made regularly
at fixed times. Do not forget, the units should be used only by trained and skilful operators who can guarantee an
appropriate use.

WARNING
Should any serious accident happen, inform your dealer immediately.

7. GUARANTEE
The guarantee covers all the defects of materials and workmanship for one year, starting from the purchase date, if not
differently agreed.
If the unit did not work properly during the guaranteed time, we will repair it. No charge is made for repair; in fact, the
guarantee includes the cost of spare parts and labour, expect for the following conditions:
Guarantee is valid only if the identification data (model, mark and technical features, etc) are present on the unit.
We will repair only breakdowns. Costs and risks during removal, transport and installation aren't covered by the
guarantee.
Or technical assistance centres authorised by the manufacturer must make all repairs. If non-authorised personnel
carry out repairs, guarantee is automatically invalid.
Guarantee does not cover periodic checks, calibrations, maintenance and modifications.
Guarantee isn't valid when:
- damages have been caused by accidents, carelessness, modifications, use of non original spare parts and/or
accessories;
- cables, electrodes and any other accessory subject to deterioration.
The manufacturer reserves the right to introduce changes or improvements without being obliged to modify any unit
produced previously.

8. MANUFACTURER RESPONSIBILITY
The manufacturer is responsible about safety, reliability, and performance only whether:
assembly, new settings, adjustments, modifies and repairs are carried out only by the manufacturer or authorised
technical staff;
the electrical installation in the treatment room complies with the laws in force;
the unit is used in accordance with the operating instructions;
only original accessories are used.

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9. DIRECTIVES AND RULES

Our appliances for physical therapy have been designed and manufactured in compliance with the 93/42/EEC Directive
dated on 14/06/93. In particular:
1. the Enclosure I (essential requirements) of the 93/42/EEC Directive has been satisfied;
2. the whole production process is made according to the Enclosure II of the 93/42/EEC Directive (Complete Quality
System1), for class IIa and IIb units;
3. the declaration of conformity has been drown up following the enclosure VII procedure of the 93/42/EEC Directive,
for class I units.
Furthermore it has been made in compliance with the IEC 601-1 rules (II ed.1989) and the special rules (see the
following table), and according to the EMC 89/336/EEC Directive dated on 04/12/92, thus it complies the IEC 601-1-2
rule (I ed.1991).

Kind of device Particular IEC 601 rules

Short wave IEC 601-2-3
Electrotherapy IEC 601-2-10
Laser IEC 601-2-22
Ultrasound IEC 601-2-5
Microwave IEC 601-2-6

10. CLASSIFICATION
Short wave Electro Ultrasound Laser Magneto Microwave Traction
therapy therapy
Protection against Class I Class I Class I Class I Class I Class I Class I
electrical hazards for (Roland
devices supplied by series)
external electric source
(ref. IEC 601-1 art. Class II
5.1.a.) (Excel
series)
Protection against Type BF Type BF Type BF Type BF Type BF Type B Type BF
direct and indirect applied part applied part applied part applied part applied part applied part applied part
contacts (ref. IEC 601-
1 art. 5.2.)
Protection against Common, Common, Cover Common, Common, Common, Common,
liquids penetration (ref. cover not cover not protected cover not cover not cover not cover not
IEC 601-1 art. 5.3.) protected protected (IPX1). protected protected protected protected
Water-
proofed
head
(IPX7).
Security use with Not suitable Not suitable Not suitable Not suitable Not suitable Not suitable Not suitable
inflammable using these using these using these using these using these using these using these
anaesthetic mixtures kind of kind of kind of kind of kind of kind of kind of
with air or oxygen or material material material material material material material
nitrogen oxide (ref.
IEC 601-1 art. 5.5.)
Kind of working (ref. Continuous Continuous Continuous Continuous Continuous Continuous Continuous
IEC 601-1 art. 5.6.)
Directive 93/42/EEC IIa IIa IIa IIb IIa IIb IIb
classification
(Enclosure IX - Rule 9)

1 Made according to the UNI EN ISO 9001 & ISO CEI EN 46001 Rules.

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11. WORKING AND STORING CONDITIONS

Temperature during work: from 10C to 40C
in store: from 0C to 45C
Humidity during work: from 30% to 75% RH (not condensed)
in store: from 20% to 80% RH (not condensed)
Pressure during work: from 700hPa to 1060hPa
in store: from 700hPa to 1060hPa

12. DESTINATION
Microwave units are used in physical therapy and rehabilitation Centre. Traditionally the microwave therapy consists in
the heat-based irradiation of the body with electromagnetic waves, in the microwave frequency band. The microwaves,
owing to their peculiar wave-length, differ in the range of high-frequency electromagnetic waves of the classic
diathermy, since: they penetrate deeper than IR radiation emitted by incandescent heat sources and they are selectively
absorbed by soft tissues (with a rich blood flow). The main biological action of the heat-based treatment with
microwaves consists in the activation of the cell metabolism owing to the increased temperature of the tissues and the
phenomenon of induced vasodilatation of capillaries and arteries. In general all the traumatic and inflammatory
affections that take advantage from the anti-inflammatory, antalgic and myorelaxing action associated with the
absorption of microwaves find a sound indications to the treatment. The mainly indicated fields are the disorders of the
locomotion system with a special attention to the treatment of traumatic and rheumatic conditions affecting the soft
tissues and the more superficial joints.

13. DESCRIPTION OF THE UNIT

These electrotherapy units are innovative systems produced following the most sophisticated techniques.
Thanks to the large liquid crystal display (LCD) showing all functions and function keys, as well as the help function on
line, these units can be easily used.

The Microwave units have a microprocessor control that allows them to have important peculiarities, such as flexibility
and performance, not shared by the common electrotherapy appliances available on the market. The unit can work both
in continuous and pulsed mode. The top output power of the 2450P is maximum 250W.

The 2450P is equipped with function keys F#, the function of which is always shown on the LCD.
This large LCD visualises all the parameters and the help function making the operation of the unit very easy.
The operator can store up to 80 different personalised treatments, which can be memorised as alphanumeric codes, the
name of patient or disease. Each programming operation is made up of five different types of currents that will be
delivered in sequence. Moreover, the operator can also use a large number of pre-set treatments, already largely used in
many physical therapy centres.

The Microwave 2450P has the IMQ quality mark.

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14. CABLE CONNECTION

In order to fasten the cable to the output of the unit, after connecting the cable connector one has to rotate it clockwise.
To disconnect the cable, one has to rotate it anticlockwise:

connection

disconnection

15. CONTROLS DESCRIPTION

1) LCD
The back lighted display consists in 15360 optical points that are controlled by the processor.
The LCD shows all the therapy parameters as follows:
the model or function indication, at the top;
the application time in the middle, on the right;
the duty cycle and the number of impulses per second (Peak rate from 1 to 4) indication in the middle, under the
application time;
the power indication (Peak power and Average power) in the middle, on the left;
the graphic indications for each function key (F1, F2, F3, F4, F5, F6) in the last line.

2) Control panel
The control panel is made up of a knob and a keyboard with its LED indicators.

3) Function keys (F1, F2, F3, F4, F5, and F6)

The function of each key changes according to the mode or the program set: the varying functions are always clearly
shown in the last line of the LCD.
If you want to regulate any value (for instance: intensity, frequency, emission, pause, etc.), all you have to do is to turn
the knob, after pressing the proper function key.

4) START key
Once you have chosen the application time, press the START key to begin the therapy. The operator starts thus giving
off energy, as indicated by the small light, which is on, just near the key.

5) STOP key
This key allows the operator to stop his work before the fixed time or to stop the acoustic signal at the end of the
treatment. The LED signals when the unit isn't working anymore.

6) MENU key
With this key, the operator selects the menu that precedes the one shown on the display.

8) NEXT key
It allows looking up in the pre-set pathologies list.

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9) Knob
This knob determines the value of each parameter on the display, after selecting them with the above mentioned
function keys. After pressing the START key, it allows to adjust the output power from 0 to the top value.

15.1. BACK OF THE UNIT

10) ON/OFF
By means of the main switch the unit is turned on and off; a green light shows when the unit is on.

11) Fuses
Two fuses (2xT3.15A) are placed between the ON/OFF key and the supply power connector. After disconnecting the
supply power plug from the unit, you can open the case containing the fuses and thus substitute them according to the
type shown among the technical data.

12) Power supply

The power supply cable must be plugged into this socket. Remember that power supply amounts to 220V (10%)
50Hz.

13) Air cooling grid

Be sure the ventilation grid isn't obstructed during the treatment.

16. APPLICATORS
Applicator Dimensions Use Top
[mm] power
[W]
small rectangular 100x50 localised treatment (wrist, ankle, etc.) 250
big rectangular 470x120 spine 250
large field 460x180x200 lumbar region, knees, shoulders 250
cone shaped 170 generic (standard radiator) 250

WARNING
When small parts of the body have to be treated (for instance the wrist), the applicator must be placed
so that sensory area (for instance eyes and testicles) are not intercepted by the radiation beam.

Only original applicators must be used.

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 17. HOW TO SET UP A WORKING SESSION
Connect the unit to the nearest power supply socket (220V - 50Hz) by using the power cable.
Check the microwave radiator, suitable for the therapy, is well connected to the unit by the proper HF cable.
Start the unit by switching on the key at the back of the unit itself, just near the supply socket. The unit makes a
rapid inner control and is immediately ready for use.

Patient preparation: Prepare the patient to the treatment and make him stay in a comfortable position, and take off
any clothes from the treatment area. We suggest to test the thermal sensitivity of the patient before starting the
therapy and to inform the patient about the microwave treatment: in order to avoid any burn in the treatment area, he
has to inform the operator if he feels too much heat.
Radiator application: place the microwaves radiator 1-2 cm far from the skin of the patient so that the middle part
of it is parallel to the skin; pay attention not to treat sensitive regions such as eyes and testicles. Treatment of
metallic prostheses must be always avoided, because it could cause overheating of the surrounding regions with
possible burns.
Microwaves irradiation: after pressing the START key, increase very slowly the power using the knob, up to the
patient feels a pleasant sensation of warmth. The therapy stops at the end of the treatment time set before. We
suggest checking quite often the area under treatment, in order to avoid any problem for the patient.

All the following operations will be done by using the keys on the panel of the unit. The keys will react immediately to
a light pressure of your fingers, also delivering a short sound.

17.1. MANUAL SETTING

After switching the unit on, the LCD shows the following menu. In order to select a current manually, press F1 key
(A). Now the LCD will show the parameters for pulsed mode.
The application time is already set at 20 minutes, but if you wish, you can adjust it by the knob. To change it, push
F6. Time from 10 to 30 minutes is usually used; shorter time can be set in order to treat very small regions or acute
disease.

MAIN MENU
A-> Manual setting
B-> Standard pathologies
C-> Memories
_______________________________________
A B C
_______________________________________

F1 F2 F3
 Duty Cycle: is the ratio between the length of the impulse and the period. To adjust it, press the F3 key and rotate
the knob. It can be adjusted from 20% to 80%.
Peak Rate: is the number of impulses per second. In order to adjust it, press the F4 key and rotate the knob. It is
possible to have from 1 to 4 impulses per second.

POWER Time = 20:00

________________________________________
Peak= 0 W Duty cycle= 50%
Average= 0 W Peak rate= 1
________________________________________
CONT
________________________________________

F3 F4 F5 F6

After setting all the parameters, press the START key; the LED placed near the START key itself will light up.
At this point, the operator has to adjust the output power, rotating the knob clockwise; the top value available is
250W.

In any case, pay attention to the patient reaction when the power is increasing. The only general rule is that the
power should be higher in chronic than in acute disease. On the LCD all the parameters set are shown. When the
unit is working in pulsed mode, the average power is shown (top power duty cycle).
 One can set the continuous mode simply pressing the F5 key (CONT on the LCD). The following form will be
shown. The power in continuous mode is equal to the average power of the previous working pulsed emission
mode. In this way, any burn to the patient is avoided. However, if you wish to change the power, it is enough to
rotate the knob. From the continuous mode, it is possible to come back to the pulsed mode, by pushing the F3 key
(PULSE on the LCD).

POWER Time = 20:00

________________________________________
EMISSION Power=0W
CONTINUOUS
________________________________________
PULSE
________________________________________

F3 F6

At the end of the set time, the unit stops the emission an intermittent sound is delivered. In order to stop the therapy
before the end of the time or to stop the end sound, one can press the STOP key.

17.2. STANDARD PATHOLOGIES

From the main menu, press F2 (STANDARD PATHOLOGIES). You will see a list of 5 different pathologies for time
to time of the numerous available pathologies. In order to see the other ones, turn the knob or press the NEXT key.

At the left of each pathology is indicated the relevant function key. When the desired pathology is pointed out, press the
relevant function key. The LCD shows immediately the first current with its parameters. If you want you can change the
value of some parameter, before carrying out the treatment. Press START key in order to start the therapy.

STANDARD PATHOLOGIES
________________________________________
F1-> Spondylarthrosis of back
F2-> Lumbar spondylarthrosis
F3-> Radicualr pathologies degenerative
F4-> Coxarthrosis
F5-> Knee arthrosis
________________________________________

F1 F2 F3 F4 F5 F6
 17.3. ENTER A SPECIAL TREATMENT INTO THE MEMORY
It is possible to store up to 100 different memorised treatments, identifying each file with its own name (for instance the
name of the patient or of the pathology). These programming can be made up by 3 different steps. The programming
remains in memory until you delete them.
Procedure:

Select MEMORY, pushing F3 key. The following menu will appear.

In order to enter a treatment, select F4 (INS). The LCD shows all the alphanumeric data.

FILE N. 1/0

GO INS DEL
________________________________________

F1 F4 F6

In order to select each character it's necessary to

rotate the knob. When the desired character is selected, press F2 (OK).
When the name, or the code is completed press F5 (END). The currents menu will be shown.
By the F1 and F3 keys you can move left or right the cursor in order to make some correction.

Insert record name

ABC ... XYZ -.0123456789

ok end
________________________________________

F2 F5

Now select the kind of treatment with its relevant parameters.

When all the parameters are selected, press F1 (SAVE).
Pressing the MENU key, you will come back to the MAIN MENU.
If you want to enter another step, repeat the procedure written above; if not press the MENU key.

17.4. USE THE PRE-SET MEMORIES

From the MAIN MENU, press F3 (MEMORY).

Select the desired file by rotating the knob. The number of each file is shown at the bottom of the LCD.
Press F1 key (GO), in order to select the file.
Press START for starting the therapy.
 17.5. DELETE A PRE-SET MEMORY

In order to delete a file, from the MAIN MENU press F3 key (MEMORY). Turn the knob up to the desired file is
shown; then, press F6 key (DEL). The following menu is shown.
Press F1 key (YES) in order to delete the file. Alternatively, press F2 if a mistake has been done.

DELETE FILE N.--/--

DO YOU CONFIRM?
YES NO
___________________________________

F1 F2

18. WARNING MESSAGES

The unit is equipped with a control system based on microprocessor technology that always checks the state of the
apparatus at any time and the correct working.

a. Temperature:
If there is a problem of high temperature inside the unit, an alarm message is shown on LCD:

HIGH TEMPERATURE
Switch off power

The unit must be switched off for about 30 seconds and then switch it on again. If on display the above message is still
present, call your dealer or qualified technical service before using the unit again.

b. Radiator connection:
If the HF cable isn't correctly connected to the radiator or to the unit, a warning message is shown on the LCD. If the
unit is in START mode, in the middle of LCD will be visualised:

'NO OUTPUT CONNECTION'.

it is necessary to switch the unit off, connect correctly the HF cable and then switch it on to carry out the therapy. On
the contrary, if the unit is in STOP mode, the alarm message is visualised in the bottom of the LCD. In that last case, it
is enough to connect correctly the cable without resetting the unit.

c. Circuit fault alarm:

The unit is equipped with a control system that finds out possible faults. In case a fault is present, an alarm message is
shown on LCD:

CIRCUIT FAULT
Switch off power

The unit must be switched off for about 30 seconds and then switch it on again. If on display the above message is still
present, call your dealer or qualified technical service before using the unit.
 19. TECHNICAL FEATURES
Power supply: 220V (+/-10%) - 50Hz
Microprocessor control system
Frequency: 2450 MHz
Emission mode: continuous and pulsed with duty cycle adjustable from 20% to 80%, peak rate from 1 to 4
(continuous and pulsed with duty cycle equal to 25%, 50% or 75% )
Pre-set pathologies
100 available memories
Digital timer adjustable from 0 to 30 minutes
Automatic control device (high magnetron temperature, HF cable not connected well, circuit fault)
Output power: 250W max.
Input power: 500 VA
Fuses: 2 x T3.15A
Standard parts:
- one conic shaped radiator
- one arm support
Dimensions: 400x300x1250mm (wheeled cabinet) - 400x225x325mm (not wheeled cabinet).
Weight: 38 kg (wheeled cabinet) - 24kg (not wheeled cabinet).

The pulse length, frequency and power values are not more than 20% different from the values written on this handbook.

Microwave 2450P has the IMQ quality mark.

Address for after-sales service and technical support:

Technical Assistance Service: FYSIOMED N.V.
(T.A.S.) Doornstraat 87/89
B-2650 Edegem
Belgium
Tel. +32 3 457.66.76
Fax. +32 3 457.55.38
20. PERIODIC MAINTENANCE FORM

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