JOLLY 4 Technical Manual

BMI Biomedical International srl
Via E. Fermi 52 Q/R

24035 Curno (BG)
ITALIA
Technical Manual
JOLLY 4
ref. TM8904
Device compliant with the medical equipment directive 93/42/CEE 0051
Prepared: Approved:
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Revision register
REV DATE Modified REASON FOR REVISION

0 20/03/06 First issue
1 07/11/06 Review of graphic layout
Review of graphic layout and arrangement of
2 16/06/07
information
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Indice
1 MANUFACTURER......................................................................................................... 5
2 HOW TO USE THIS MANUAL ................................................................................... 6
2.1 Graphic symbols ...................................................................................................................................6
3 GENERAL WARNINGS AND INFORMATION......................................................... 7
3.1 Declarations...........................................................................................................................................7
3.2 Warranty ................................................................................................................................................7
3.3 Return modality ....................................................................................................................................7
3.4 Directives and applicable standards .................................................................................................7
3.5 Assistance centers................................................................................................................................7
4 SAFETY ........................................................................................................................... 8
4.1 General information.............................................................................................................................8
4.2 Protection against radiations .............................................................................................................9
4.3 Electric safety...................................................................................................................................... 10
4.4 Environment........................................................................................................................................ 10
5 PRESENTATION OF THE PRODUCT ..................................................................... 11
5.1 Main parts............................................................................................................................................ 11
5.2 Control desk panel............................................................................................................................ 12
1. ON BUTTON ............................................................................................................... 12
5.3 Block diagram ..................................................................................................................................... 13
5.4 Labels.................................................................................................................................................... 15
6 INSTALLATION .......................................................................................................... 16
6.1 Storage and shipment ....................................................................................................................... 16
6.2 Shipment and Transportation......................................................................................................... 16
6.3 Connecting and starting up the equipment................................................................................. 17
6.4 Disposal of the machine................................................................................................................... 17
7 CONFIGURATION...................................................................................................... 17
7.1 When to configure the equipment................................................................................................ 17
7.2 Entering the configuration modality.............................................................................................. 17
7.3 Exiting the configuration modality................................................................................................. 17
7.4 Function of keys in configuration modality.................................................................................. 17
7.5 Setting the data .................................................................................................................................. 17
8 ADJUSTMENT.............................................................................................................. 20
8.1 When to adjust the equipment ...................................................................................................... 20
8.2 mA adjustment ................................................................................................................................... 20
8.3 kV adjustment..................................................................................................................................... 22
8.4 Times adjustment .............................................................................................................................. 23
9 INSTALLING THE SOFTWARE................................................................................ 24
9.1 When to load the software............................................................................................................. 24
9.2 Loading or updating the software.................................................................................................. 24
10 FORMATION OF THE MONOBLOC...................................................................... 27
11 MAINTENANCE AND PERIODICAL CONTROLS................................................. 28
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11.1 Visual controls.................................................................................................................................... 28

Table 8 – Visual controls ............................................................................................................................ 28
11.2 Functional controls – mechanical adjustments ........................................................................... 28
11.3 Controls Part 1(collimator) ............................................................................................................ 29
11.3.1 Controls Part 2 (monobloc).....................................................................................................................29
11.3.2 Controls part 3 (arm) ................................................................................................................................30
11.3.3 Controls part 4 (transportation handle) ...............................................................................................31
11.3.4 Controls part 5 (wheels)...........................................................................................................................32
11.4 Controlli funzionali elettrici ............................................................................................................ 33
11.5 mAs control........................................................................................................................................ 33
11.6 kV control ........................................................................................................................................... 34
11.7 mA control.......................................................................................................................................... 34
11.8 X-ray times control........................................................................................................................... 34
11.9 Cleaning ............................................................................................................................................... 35
12 SPARE PARTS AND REPLACING............................................................................. 36
12.1 Mechanical parts ................................................................................................................................ 36
12.2 Electronic parts .................................................................................................................................. 37
12.2.1 Electronics rack F07S04.............................................................................................................................38
12.2.2 Jolly Keyboard F07S13 ...............................................................................................................................39
12.2.3 Monobloc.......................................................................................................................................................39
13 DIAGNOSTICS AND DATA RESETTING ............................................................... 40
13.1 Error messages................................................................................................................................... 40
14 INDICE DELLE FIGURE E TABELLE ........................................................................ 44
14.1 Figure.................................................................................................................................................... 44
14.2 Tabelle.................................................................................................................................................. 44
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1 MANUFACTURER
Manufactur by: SMAM srl
Manufactur for : BMI Biomedical International srl
Adress: Via E. Fermi 52 Q/R 24035 Curno (BG) - ITALY
Telephono: +39 035.4376381
Fax: +39 035.4376401
Web: www.bmibiomedical.it
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2 HOW TO USE THIS MANUAL
2.1 Graphic symbols

The indications below are used, if necessary, to highlight specific instructions.
DANGER: This symbol is used to identify conditions or actions for which

specific dangers are known to exist, which, if the instructions are
ignored, will certainly generate serious personal injuries, death or
substantial damages to the equipment.
WARNING: This symbol is sued to identify conditions or actions for which

specific dangers are known to exist, which, if the instructions
are ignored, will certainly generate serious personal injuries,
death or substantial damages to the equipment.
WARNING: This symbol is used to identify conditions or actions for which

dangers may arise which, if the instructions are ignored, could
generate personal minor injuries or damages to the
equipment.
NOTE: a Note gives information that may be useful. The notes contain specific information
concerning instruments or special techniques, elements to control before starting up the
equipment or factors to consider relating to a concept or activity.
Underlined italics: Reference to a paragraph inside this manual
Bold italics character: Reference to a document not included in this manual
COURIER character: Text shown on the display of the control desk panel
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3 GENERAL WARNINGS AND INFORMATION
3.1 Declarations
This device is covered by a conformity declaration for the medical devices directive 93/42/CEE.
The original declaration, as per law, is available at the manufacturer’s premises.
3.2 Warranty
For the warranty conditions related to this device, refer to the document Doc SG001 Warranty
Certificate.
3.3 Return modality

To return equipment: wrap in a packaging similar to the original one. We suggest keeping the
original packaging. Damages to the packaging or incorrect transportation make this warranty void.
Usually the qualified assistance centers are certified to disassemble and return the components of
the equipment.
For period covered by the warranty, the parts of the device shall be replaced after returning the
broken component.
3.4 Directives and applicable standards

This device was designed and built in compliance with the following directives and product
standards:
Directive 93/42/CEE of Council, of June 14, 1993, concerning medical devices

and following integrations and amendments
Legislative Decree 46/97 Acknowledgment of directive 93/42/CEE concerning medical devices and
following integrations and amendments
CEI EN 60601-1.............: Medical electric equipment Part 1: General requirements for basic
safety
CEI EN 60601-1-2.........: Medical electric equipment Part 1: General requirements for basic
safety – Collateral standard: Electromagnetic compatibility –
Requirements and tests
CEI EN 60601-1-3.........: Medical electric equipment Part 1: General requirements for basic
safety 3: Additional standard: General requirements for radiation
protection in diagnostic X-ray equipment
CEI EN 60601-2-7.........: Medical electric equipment Part 2: Particular requirements for the
safety of high-voltage generators of diagnostic X-ray generators
CEI EN 60601-2-28.......: Medical electric equipment Part 2: Particular requirements for the
safety of X-ray source assemblies and X-ray tube assemblies for
medical diagnosis
CEI EN 60601-2-32.......: Medical electric equipment Part 2: Particular requirements for the
safety of associated equipment of X-ray equipment
3.5 Assistance centers

Directly contact the dealer or manufacturer for assistance.
DANGER: The user is not authorized to open the unit’s guards or

disconnect the components.
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4 SAFETY
4.1 General information
WARNING: The legally binding version of this document is the one in

Italian. The translations in other languages, even though
controlled and approved by the manufacturer, are supplied
only to help the operator, but they do not present the
necessary accuracy for juridical purposes.
WARNING: This X-ray unit may be dangerous for the patient and the
operator, if the safe exposure factors, operating instructions
and maintenance plans are not observed. Only authorized
personnel can operate the unit.
WARNING: Electric shock hazard. To avoid any possible electric sparks, do

not insert the fingers in the external connectors. Refer to
Figure 2 for more information on the position of the
connectors.
WARNING: It is important to know the unit to recognize any unusual

operation that may be dangerous. In case of unusual operation
or if any safety problem should arise, isolate the unit from
operation and do not use until the problem is solved by
qualified personnel.
ATTENZIONE: This device is connected to an earth protection during

operation. For the safety of the patient and of the operator,
next to this unit, use only devices with certificate compliant
with the proper safety standards for medical equipment and in
perfect operating conditions.
ATTENZIONE: THIS SYSTEM IS NOT DESIGNED TO BE USED BY A

DEFIBRILLATOR!
Never use a defibrillator on a patient in contact with a part of
the mobile X-ray unit. This system must be treated as a
conductive surface and positioned far away from a patient
before defibrillation. If any part of the equipment is in contact
with a patient when a defibrillator is being discharged, the
voltage may pass through the body of the patient and transfer
to the system. This may be dangerous for anybody in contact
with the system and may damage the unit itself. Always read
the instructions for use of any defibrillator used on a patient
exposed to X-rays with this digital mobile unit.
WARNING: THIS EQUIPMENT IS NOT SUITABLE FOR USE NEAR

FLAMMABLE GASES.
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WARNING: If the mobile unit is used in a fixed station, the operator is

responsible for supplying the audio and video communication
between the operator and the patient.
WARNING: If you think there could be electromagnetic interferences that

may affect or are generated by the unit, ask for assistance.
Mobile RF communication equipment may change the medical
electric equipment.
4.2 Protection against radiations

This device emits ionizing radiations for medical purposes.
WARNING: Laws limit the operation of this device to doctors or

authorized people as per law.
The type of X-ray exposure produced with this unit can be divided into two categories:
professional, for operators
diagnostic, for patients subjected to an examination.
Comply with all the necessary safety requirements needed and comply with the national
regulations on protection against radiations, because radiations have harmful effects on the human
body.
While performing X-rays, there is always a dispersion of radiations; this means it is necessary to
provide for protection against these radiations. Before performing the examination, make sure
the doctor knows whether a patient is pregnant or not. If the patient must be assisted by
somebody, this person needs to wear the proper protection equipment.
It is possible to obtain a further protection against the dispersion of radiations, by using the
manual X-ray switch at a distance of 2 meters from the X-ray beams. The cable of the manual
switch is about 4 meters long when completely stretched out.
If the X-ray equipment is not used properly, it may cause injuries. Consequently, these
instructions must be carefully read before operating the equipment. The Manufacturer will be glad
to offer assistance and cooperate to start-up the equipment.
Even though this equipment offers a high level of protection against X-rays, besides the operating
beams, no operating measure can assure a complete protection. The operator shall be
responsible for taking all the necessary safety measures to prevent risks, personal and to others,
resulting from an incorrect or excessive exposure to radiations.
All the operators must receive proper training and take the appropriate safety measures to avoid
injuries.
The equipment is sold with the following condition: the Manufacturer, agents and representatives
cannot be held responsible for damages or injuries that could be caused by the incorrect use of
this equipment.
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Various materials and personal protection equipment are available on the market. We highly
recommend using them.
WARNING: The X-ray beam can pass through the main protective shield.
Use X-ray cassettes or digital receivers with lead support. Do
not stand behind the receiver and/or in line with the X-ray
beam.
WARNING: The patient is the only person who has to be present in the
examination room during the X-ray exposure. According to
the cases, if another person needs to be in the room during
possible X-ray exposures, this person must wear a lead apron
in compliance with the safety practices in force.
WARNING: Use the biggest distance possible between the focus point and
the skin so that the patient absorbs the lowest dose possible.
WARNING: This X-ray unit may be dangerous for the patient and the
operator, if the exposure factors and the correct operating
instructions are not observed.
WARNING: Always use the appropriate X-ray protection on the patient

and operator while using X-ray equipment.
4.3 Electric safety

The user must use only qualified personnel (manufacturer’s specialized technicians or technicians
of an assistance service with equivalent training) for all electrical maintenance interventions on the
equipment.
The connections between the various parts of the device, calibration and tests must be
performed by the manufacturer’s qualified technicians.
WARNING: Only properly trained and qualified personnel can access the
internal parts of the unit or disassembled parts.
4.4 Environment
This symbol indicates that the waste resulting from electric and electronic equipment must not be
disposed of as domestic waste, but they have to be collected separately. For information on the
recycling regulations of the equipment out of service, contact an authorized representative of the
manufacturer.
Figure 1 – Recycling symbol for equipment
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5 PRESENTATION OF THE PRODUCT
5.1 Main parts
This device includes:

• Monobloc with X-ray tube
• Control desk
• Mobile unit
Figure 2 - Main parts

1. X-ray monobloc
2. Collimator
3. Transportation handle
4. Control desk panel
5. ON/OFF switch
6. Manual preparation/ray switch
7. Power cable
8. Cassette holder
9. Arm unlock handle
10. Potter connector
11. DAP connector
12. Monobloc sheath 4
9 3
6
7 5
10
8
11
12
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5.2 Control desk panel
1. ON BUTTON
2. OFF button
3. Anatomic techniques memorization key
4. X-ray parameters increase and decrease button (kVp, mA, sec, mAs)
5. X-ray parameters selection buttons (kVp, mA, sec, mAs)
6. Selection button for 2 point (kV, mAs) and 3 point (kV, mA, sec) technique
7. Collimator lamp on/off switch
8. Potter Bucky selection button
9. Automatic radioscopy selection button (not active)
10. Automatic exposure selection button (optional)
11. Reset exposure timer (not enabled)
12. Anatomic techniques selection button
13. Graphic or exposure modality selection button (not enabled)
14. Display for x-ray parameters and anatomic techniques
15. X-ray ready indicator
16. X-ray exposure indicator
17. Read instructions for use
18. Danger ionizing radiations
Figure 3 – Control desk panel
15 16 17 18 1 2
14
6 7 8 9 4
3
5 5
10 11 12 13 4
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5.3 Block diagram
The equipment can be divided into the following macro-blocks:
X-ray monobloc
Collimator
Accessories
Manual prep/X- Potter
ray button Mobile unit:
Control desk AEC

+
Power supply
DAP
Figure 4 – Main block diagram
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Mobile unit
Control desk
Keyboard
J4 – JP1
Manual prep/X- CPU
ray button
JP2– J1
Rack
Cond
PR4
312Vdc
CPU Interf.
Logic CTRL
Filament
Inverter
220Vac
PSU
Feedback KV,mA
LC
Sic.Termica
Filament
Collimator
PR5
Potter
Monobloc
Potter
Collimator
Figure 5 – Wiring block diagram
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5.4 Labels
Position of identification labels on equipment.
Machine label
Monobloc label
Figure 6 – Position of identification labels
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6 INSTALLATION
6.1 Storage and shipment

Temperature: from –10°C to + 50°C
Humidity: maximum 75% without condensate
Altitude: 12.000 m
6.2 Shipment and Transportation

The equipment is normally shipped in cellophane.
If the equipment is shipped in a box, inside it is wrapped in pluriball sheets and fixed using wood
beams to prevent the equipment from moving during transportation. For returns it may necessary
to wrap the product as it was originally shipped
A shockwatch label and the handling and destination instructions are

applied on the outside of the box.
To unpack the equipment follow the procedure as indicated in the following photos:
1. Open the box by removing the front panel identified by the label
2. Remove the platform and the beams, removing the screws visible
from the outside of the box
3. Position the slide, inside the box and slide out the equipment
Figure 7 – Sequence for unpacking the equipment
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6.3 Connecting and starting up the equipment

The equipment does not need any particular installation, component connection, calibration or
data entry operation before use.
6.4 Disposal of the machine

This product is an electronic unit subject to legislative decree 151/05, acknowledging the
European Directives 2002/95/CE – 2002/96/CE – 2003/108/CE; The equipment cannot be
disposed of in the European territory as urban waste. It must be returned to the manufacturer or
distributor from whom it was purchased. This operation does not entail any extra costs for the
user.
For the extra-EC markets, comply with the standards in force considering the product contains:
Dielectric oil
Lead
Electronic components
Glass
Iron, aluminum and copper alloys
Tungsten, molybdenum, rhenium, nickel copper, silver
7 CONFIGURATION
7.1 When to configure the equipment

The equipment is sold with default configuration.
Repeat configuration after:
1. Replacing the CPU board (see paragraph 12 Spare parts and replacing)
2. Software updating if clearly indicated
7.2 Entering the configuration modality

Switch on the unit using the magneto-thermal switch SW1 and at the same time press the key 2
(see Figure 3 – Control desk panel pag.12) wait for the green LED of the key to flash, then release
key 2 and quickly press in sequence the keys 4 arrow down, 5 right arrow, then press the key
1, to enter the set-up modality.
7.3 Exiting the configuration modality

After changing and confirming the relating parameter, exit the configuration modality without
changing any other parameter by switching the machine using key 2.
7.4 Function of keys in configuration modality

(see Figure 3 – Control desk panel pag.12)
Keys 4: they are used to increase or decrease the adjustment values.
Keys 5: they are used to select the paragraph in the setup, for example the type of generator
Key 3: it is used to memorize the selected paragraphs and to select the set-up functions
7.5 Setting the data

NOTE: Verify that the data match the board FRP11/L attached to the supplier’s documentation.
• GENERATOR TYPE SELECTION: use key 3 to enter the generator selection mode 4kW
12kW 15kW 30kW 40kW. Use the keys 5 and confirm pressing key 3.
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• TUBE SELECTION: press the key 3, the display shows the type of X-ray tubes that can be
used on the equipment, select the one being used and confirm.
• TIME TABLE SELECTION: press the key 3, the display shows four different pairs of values
the minimum and maximum exposure time, select and confirm.
• AUTOMATIC EXPOSURE CONTROL UNIT: press the key 3 the display shows
ENABLE/DISABLE. Select ENABLE to use the automatic exposure meter or select
DISABLE if it will not be used, and confirm pressing key 3.
• POTTER BUCKY SELECTION: press the key 3, the display shows ENABLE/DISABLE.
Select ENABLE to use the potter bucky, or select DISABLE if it will not be used, and confirm
pressing key 3
• FLUORO SELECTION: press the key 3, the display shows ENABLE/DISABLE. Select
DISABLE and confirm pressing key 3
• AUTO/PULS FLUORO SELECTION: press the key 3, the display shows
ENABLE/DISABLE. Select DISABLE confirm pressing key 3
• LANGUAGE SELECTION: press the key 3, the display shows the possible languages. Select
the desired language and confirm pressing key 3.
• ANATOMIC PARTS SELECTION: press the key 3, the display shows HUMAN – PET –
HORSE – PET TH – AUTO PET TH. Select the HUMAN anatomic part and confirm
pressing key 3.
• STARTER SELECTION: press the key 3, the display shows ENABLE/DISABLE. select
ENABLE to enable the safety mode for the anode rotation. Confirm pressing key 3.
• MODE 3P SELECTION: press key 3 the display shows ENABLE/DISABLE. Select
DISABLE (only 2P technique is possible). Confirm by pressing key 3
• DISPLAY REAL mAs AT X-RAY END: press key 3 the display shows
ENABLE/DISABLE. Select DISABLE if you don’t want to show the real mAs values on the
display after the X-ray exposure or select ENABLE to show values and confirm by pressing
key 3
• KV LIMIT: press key 3 the display shows ENABLE/DISABLE. Select DISABLE and confirm
by pressing key 3. Selecting DISABLE limits voltage to 99kV.
• DISPLAY TOTAL EXPOSURE MAKE: press key 3 the display shows the number of
exposures performed by the operator. To reset press the key 4 arrow up, or confirm
pressing key 3
• WARM UP LARGE FOCUS: press the key 3, the display shows the number matching the
pre-starting value of the large focus of the x-ray tube; set value at 1200 which corresponds
to a reference voltage of 2.17 V, measured with the multimeter on the ends of the diode
DZ2 (see topographic diagram of the sheet E68S33401). Confirm by pressing key 3
• WARM UP SMALL FOCUS: press the key 3, the display shows the number matching the
pre-starting value of the small focus of the x-ray tube; set value at 1200 which corresponds
to a reference voltage of 2.17 V, measured with the multimeter on the ends of the diode
DZ2 (see topographic diagram of the sheet E68S33401). Confirm by pressing key 3
• kV 1st STEP RANGE: press the key 3, the display shows the number matching the value of
the reference voltage (1V/20kV) equal to 2V (measured between TP29 and mass TP12) used
by the logic board to pilot the X-ray tube with a voltage of 40 kV. Confirm by pressing key 3
• kV 2st STEP RANGE: press the key 3, the display shows the number matching the value of
the reference voltage (1V/20kV) equal to 5.5V (measured between TP29 and mass TP12) used
by the logic board to pilot the X-ray tube with a voltage of 110 kV. Confirm by pressing key
3
• X-RAY VALUE mA ADJUST: adjustment sequence of mA described in paragraph 8.2, page
20
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Cliente / Customer
Apparecchiatura tipo / Unit type Codice / Code N° Serie / Serial N°

________________________ ______________________ ________________________
Generator type selection: 4kW 12kW 15kW 30kW 40kW

Tube selection: X22 E7846 OX125M5 RTM77H SV11-30 OX110/15
Time table (ms) selection: 3/6300 10/6300 3/5000 10/1000
Automatic exposure control unit: Enable Disable
Potter Bucky selection: Enable Disable
Fluoro selection: Enable Disable
Auto fluoro selection: Enable Disable
Language: English Italian French German Spanish
Anatomic parts selection: Human Pet Horse Pet TH AutoPet TH
Starter selection: Enable Disable
Mode 3 p selection: Enable Disable
Display real mAs at X-RAY End: Enable Disable
KV Limit: Enable Disable
Display total exposure make:
Warm up Large Focus Adjust: 1200 Warm up Small Focus Adjust: 1200
kV First step range Adjust: kV Second step range Adjust:
Table 1 – Summary of configuration data Form FRP11/L
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8 ADJUSTMENT
8.1 When to adjust the equipment

The equipment is sold with default adjustment.
During the yearly control, repeat the adjustment after:
1. Replacing the monobloc
2. Replacing the CPU board (see paragraph 12 Spare parts and replacing)
3. Replacing the Filament Board (see paragraph 12 Spare parts and replacing)
4. Replacing the Logic Board (see paragraph 12 Spare parts and replacing)
5. Software updating if clearly indicated
8.2 mA adjustment
WARNING: do not adjust mA values if the equipment hasn’t warmed up.

Remember to bring the monobloc in temperature by running a
pre-heating cycle.
Perform 6 exposures in the sequence indicated below (total time 2 minutes):
kVp mAs Esp Intervallo

60 4 1 20 sec
60 10 1 20 sec
80 4 1 20 sec
80 10 1 20 sec
100 4 1 20 sec
100 10 1 20 sec
Table 2 – Monobloc pre-heating cycle
WARNING : If the microprocessor board is new or has lost the data, it is not
possible to run a pre-heating cycle. Complete the configuration
and adjustment procedure.
Switch off the machine and wait for at least an hour and a half.
Switch the machine on and run the pre-heating cycle.
Repeat the mA adjustment procedure.
Instruments to use:
1. mA value shown on the equipment’s display
in addition we suggest using the following control instruments
2. mAs meter (ex. KEITHLEY 35035).
3. kilovoltmeter (PMX-I/R)
4. oscilloscope, or a mA meter and/or kilovoltmeter
Make sure the equipment is switched off.

Remove jumper JP2 on the Logic Board S100015 and connect the prods of the mAs meter.
Make sure the equipment is set on mAs.
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Position the kilovoltmeter in axis with the X-ray beams at a meter form the focus. Open
collimator to light up the sensor of the kilovoltmeter.
Connect the probes of the oscilloscope to the following test points of the Logic Board:
• TP18, to measure the mA; 1V corresponds to 20mA of current to tube.
• TP20, to measure the kV; 1V corresponds to 20kVp to tube.
• Take reference mass from TP12.
Suggested configuration of oscilloscope:

1. TP20, time base 10 msec/div, amplitude 1V/div
2. TP18, time base 10 msec/div, amplitude 1V/div
The exposure time is pre-set at 60msec. The kV and mA values are set as indicated in the
following Table 4 and Table 5.
Switch on the unit using the magneto-thermal switch SW1 and at the same time press the key 2
wait for the red LED of the key to flash, then quickly press in sequence the keys 4 arrow down, 5
right arrow, then press the key 1, to enter the configuration modality (see paragraph 7.2 pag. 17).
To save even just one figure it is necessary to complete the entire cycle confirming the
adjustment values. Otherwise the values are not saved.
Press button 3 until the following message appears X-RAY VALUE 01 mA ADJUST. Press
ENTER, to show:
1. INITIALIZATION (only at first adjustment)
2. interval of 15 sec
3. CHARGE IN PROGRESS …
At the end of the capacitor loading phase the following appears:

kV=0040 (pre-set kVp value), mA=0025, ADJUST= adjustment value to enter.
Press the first X-ray step, wait at least 3 seconds for the filament of the tube to reach a constant
and repeatable temperature, then press the 2nd X-ray step. At the end of the exposure, by
keeping the X-ray button pressed, the display will show three mA values (Min AVG Max). The
average value AVG represents the mA tube value to refer to, read from the return line of the
monobloc. By releasing the X-ray button the machine shows kV-mA-ADJUST again. During the
first adjustment, the initial value in ADJUST is equal to the value entered in WARM UP LARGE
FOCUS.
If the values read in AVG, oscilloscope, mAs meters, kilovoltmeter do not fall within a ±5%
tolerance range compared to the pre-set values, follow this procedure:
1. for kV, use the potentiometer P4 on the Logic Board. This adjustment increases or
decreases the kV on the entire kV range.
2. for mA, use the ADJUST parameters, increasing or decreasing the value in relation to the
number displayed or written on the module FRP11/L attached to the device.
Repeat the exposure and verify values.
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WARNING : An excessive increase in the ADJUST value may cause an over-

supply of current to the tube which may seriously damage the
tube.
Confirm the ADJUST value by pressing ENTER. The device will show the next adjustment step.
ADJUST value suggested at the beginning of the

mA tube
adjustment
25 1900
32 1930
40 1960
63 2000
80 2050
Table 3 – mA adjustment; initial ADJUST values
Confirm the ADJUST value by pressing button 3.
Real values
Pre-set values
mAs meter kilovoltmeter TP 18 TP 20
Focus singular
Measure 1 40kV 25mA 1.5 mAs 40 1.25 V 2 V

Measure 2 40kV 32mA 1.92 mAs 40 1.6 V 2V
Measure 3 40kV 40mA 2.4 mAs 40 2V 2V
Table 4 – mA adjustment: pre-set values for Jolly 4
At the end of the adjustment procedure, the display will show “END SETUP”. Switch off the
machine.
N.B. Remenber to disconnect the mAs meter and riconnect the wire 4 on the PR1.
8.3 kV adjustment
Instrument to use: kilovoltmeter (PMX-I/R).
Modality: position the instrument perpendicular to the radioactive source centering it on the
collimator’s cross at a distance of 100 cm from the focus, measured using the meter of the
collimator itself.
Perform x-ray exposures using the parameters in the table
60 kV 20 mAs 80 kV 20 mAs 90 kV 20 mAs

Table 5 – kV adjustment: exposure parameters
If the values do not fall within a 5% tolerance range, adjust the trimmer P4 of the Logic Board
S100015 to bring them back within the range This adjustment affects the entire kV range. If the
values to adjust refer to the high or low values, see the instructions in paragraph 7 (kV I° step
range adjust and kV II° step range adjust).
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8.4 Times adjustment

Instrument to use: oscilloscope.
Modality: on the Logic Board S100015
1. Connect probe to test point TP20
2. Take the mass from test point TP12
Suggested configuration of oscilloscope:

1. TP20, times base 1 msec/div, amplitude 1V/div, for exposures up to 0,006 s
2. TP20, times base 2 msec/div, amplitude 1V/div, for exposures at 0,012 s
3. TP20, times base 5 msec/div, amplitude 1V/div, for exposures at 0,040 s
Power the unit. Perform x-ray exposures using the parameters in the table.
60 kV 0,5 mAs
80 kV 0,5 mAs
60 kV 1,3 mAs
75 kV 1,3 mAs
60 kV 2,5 mAs
75 kV 2,5 mAs
60 kV 8 mAs
75 kV 8 mAs
Table 6 – Times control: exposure parameters
Verify the times on the oscilloscope, counting the beginning of the beams starting from 75% of
the amplitude value read on the TP20. If the values do not fall within a 5% tolerance range,
replace the CPU board.
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9 INSTALLING THE SOFTWARE
9.1 When to load the software

The equipment is sold with the most updated software version loaded and operative.
Load the software after:
• Replacing the CPU
• Updating the software
9.2 Loading or updating the software

Instruments to use:
1. Personal Computer with USB port and Windows operative ystem
2. USB cable / 9 pin serial+ cable 9 pin tray/10 poles flat
3. Communication software for PC, AVR Bootloader
4. Control software (ref. SW0001.HEX)
Verify that the magnetoswtich of the machine is off. Connect the cable from one USB port of the
PC to connector COM1 of the CPU card, under the keyboard. Install the AVR Bootloader
program on the PC. The following window appears.
Figure 8 – Initial window
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Follow the operations below:
1. Select the USB port used on the PC in the field ComPortSelection field.
(Figure 8 point 1 pag.24)
2. Select number 38400 in the BaudRateSelection field (Figure 8 point 2)
3. Press Browse and select the file SW0001.HEX (Figure 8 point 3)
4. Switch on ONLY the magnetoswitch of the machine and then, within 5 seconds, select
Start Download of Figure 8 point 4
At this point transmission will start and Figure 9 pag. 25 will appear which shows the progress of
the process. It will show the end when it reaches zero.
Progress Status
Figure 9 – Data transmission
If the communication fails switch off the magnetoswitch and run the previous procedure again. At
the end of a successful communication a window like the one in Figure 10 pag.26will appear:
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Status=0
Figure 10 – Successful transmission
the end of communication
Switch off the magnetoswtich SW1, disconnect the serial cable from COM1 and the USB from the PC.
At this point perform the configuration.
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10 FORMATION OF THE MONOBLOC

If the unit hasn’t been used for more than 3 months, run the formation cycle indicated below.
Perform the following exposures in the sequence indicated below (total time 1h):
kVp mAs Esp Intervallo

40 6.3 3 20 sec
pausa 120 sec
50 6.3 3 20 sec
pausa 120 sec
60 6.3 3 20 sec
pausa 120 sec
70 6.3 3 20 sec
pausa 120 sec
80 6.3 3 20 sec
pausa 120 sec
90 6.3 3 20 sec
pausa 120 sec
100 6.3 3 20 sec
pausa 30 min
40 20 1 180 sec
50 20 1 180 sec
60 20 1 180 sec
70 20 1 180 sec
80 20 1 180 sec
Table 7 – Monobloc formation cycle
If there are no errors the equipment is ready for ordinary operation.
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11 MAINTENANCE AND PERIODICAL CONTROLS
WARNING The installation, the updating and the repairs of the X-ray
equipment, must be carried out by personnel authorized by the
manufacturer and in any case by technicians aware of the safety
regulations on medical electrical equipment.
This paragraph explains the list of preventive maintenance controls performed by technical
assistance.
11.1 Visual controls

We suggest carrying out the below controls every year.
Part Control
• Power cable • Visual control for good condition (no cuts, abrasions, cracks)
• Labels ( Figure 6 – page 16) • Visual control for integrity and clarity
• X-ray monobloc (Figure 2 page 11, • Visual control for oil leaks.
point 1) • Functional control for anode rotation (unusual noise during
preparation phase)
• Collimator • Follow maintenance plan indicated in the manufacturer’s manual
• Control desk panel • Visual control for panel integrity.
• Clarity of symbols and characters on display.
• Wheels • Visual control for integrity
• Fairing • Visual control for good condition (no cuts, abrasions, cracks, dents,
fixing)
Table 8 – Visual controls
11.2 Functional controls – mechanical adjustments

We suggest carrying out the below controls every year.
Part Control
1. Collimator A. Functional control for light operation.
B. Functional control for collimator rotation.
C. Functional control for fixing of monobloc to flange.
D. Functional control for light field-X-ray filed matching
2. X-ray monobloc A. Functional control for stability of position on the rotation axis and its
(Figure 2 Pag.11, point 1) maximum rotation.
B. Functional control for fastening of positioning handle.
3. Arm A. Functional control for vertical stability and maximum height.
B. Functional control for fastening of locking block.
4. Transportation handle A. Functional control for brake operation (engagement/disengagement)
(Figure 2 Pag.11, point 3)
5. Wheels A. Proper operation of rotation of front wheels on axis
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11.3 Controls Part 1(collimator)

Control A:
Switch on the machine, press key 7 (see Figure 3 pag.12) and verify the operation of the light.
If the light does not work see the manufacturer’s manual.
Control B:
The collimator can rotate +/- 90° around the axis of the x-ray
beam. The collimator’s rotation travel is limited by a
mechanical stopper.
If the collimator does not rotate contact the dealer of the
machine,
Control C:
Verify that the collimator fixed to the monobloc does not move in other ways than those
foreseen. If so, work on the fastening nuts on the collimator (see collimator manual
Control D:
Verify that the light field matches the X-ray field following the instructions indicated on the
collimator manual.
11.3.1 Controls Part 2 (monobloc)

Control A:
The rotation of the monobloc group on the horizontal axis is ±180°
If the monobloc does not stay in the desired position work on the ring
nut (detail indicated by arrow) placed on the fork support to adjust the
friction.
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The rotation of the monobloc group on the vertical axis is 0° ÷ +90°.

If the monobloc does not stay in the desired position work on the ring nut
(detail indicated by arrow) placed on the fork support to adjust the friction
Control B:
Verify that the handle does not move from its seat. If it moves tighten the nuts and the fastening
screws.
11.3.2 Controls part 3 (arm)

Control A:
Verify that the arms keeps the vertical position for the entire travel up to the maximum height
foreseen (2 meters).
If the arm does not keep the set vertical position, work
on the spring-balance group inside the column. After
removing the protection cover of the column, work on
the indicated nut to adjust the strength of the spring.
An effective adjustment procedure is when the arm is
steady at 90°.
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Control B:
Verify that the arm lock keeps the arm hooked onto the column. If the
arm does not stay hooked onto the column it means the components are
deteriorated and need to be replaced (Photo 1–2 Par. 12.1 Mechanical
parts pag.36).
11.3.3 Controls part 4 (transportation handle)

Control A:
Verify that the equipment does not move with the transportation
handle (Figure 2 - Main parts) while in rest position and vice versa that
it moves by exercising a slight pressure downwards on the handle
itself.
If the above conditions do not take place, probably the brake ropes are
broken (Photo 5 Par. 12.1 Mechanical parts pag.36).
To replace the brake ropes remove nut

A, slide out the ring screw from its seat,
slide an end of the rope into the ring B,
fix the other end to the brake C. Re- C
insert the ring screw into its seat, tighten
the nuts A and D to increase the
tensioning of the rope until the operation
B of the brake is restored.
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11.3.4 Controls part 5 (wheels)

Control A:
Verify that the movement of the front wheels (turning and rotation) and of the back wheels
(turning) is smooth. If this is not the case, it might be necessary to replace the wheels (Photo 5
Par. 12.1 Mechanical parts pag.36).
To replace the front wheels remove the four

socket head screws.
Remove the wheel cover and slide the wheel

out of its seat to replace the back wheels.
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11.4 Controlli funzionali elettrici

Part Control
• Power cable • Earth connection impendence
• Leakage current
• Control desk panel • Functional, increase and decrease in the following values:
• kVp, mA, sec, mAs, anatomic techniques.
• Functional for keys.
• Functional for leds.
• Magnetothermal • Functional, on and off
( point 5)
• mAs • Stability – see par. 11.5
• kV • Stability – see par. 11.6
• mA • Stability – see par. 11.7
• RX time exposure • Stability – see par. 11.8
11.5 mAs control

Instrument to use: mAs meter d.c. (es. KEITHLEY 35035).
Disconnect the wire 4 of the PR1 of the Logic Board S100015 and connect it to the mAs meter;
connect the port 4 of the PRI to the positive out of the mAs meter. Make sure the mAs meter
is set on the mAs measurement.
Perform an x-ray exposure using the parameters in the table
Values Set values

60 kV 4 mAs
60 kV 10 mAs
60 kV 20 mAs
80 kV 4 mAs
80 kV 10 mAs
80 kV 20 mAs
90 kV 4 mAs
90 kV 10 mAs
90 kV 32 mAs
If the values do not fall within a 10% tolerance range, verify the adjustment of the (see paragraph
8.2).
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11.6 kV control
Instrument to use: kilovoltmeter (PMX-I/R).
Modality: position the instrument perpendicular to the radioactive source centering it on the
collimator’s cross at a distance of 100 cm from the focus, measured using the collimators meter.
60 kV 10 mAs 80 kV 10 mAs 90 kV 10 mAs

If the values do not fall within a 5% tolerance range, adjust the trimmer P4 of the Logic Board
S100015 to bring them back within the range. This adjustment affects the entire kV range. If the
values to adjust refer to the high or low values, see the CONFIGURATION instructions (kV I°
step range adjust and kV II° step range adjust).
11.7 mA control
Instrument to use: mAs d.c. meter (es. KEITHLEY 35035).
Disconnect the wire 4 of the PR1 of the Logic Board S100015 and connect it to the mAs
meter; connect the port 4 of the PRI to the positive out of the mAs meter. Make sure the
mAs meter is set on the mA measurement.

Verify that at the end of every x-ray exposure the display shows the correct value of the real
mAs.
KV mAs mA
60 kV 5 mAs 50mA
80 kV 5 mAs 40mA
90 kV 5 mAs 40mA
60 kV 10 mAs 50mA
80 kV 10 mAs 40mA
90 kV 10 mAs 40mA
60 kV 20 mAs 50mA
70 kV 20 mAs 40mA
If the values do not fall within a 10% tolerance range, verify the adjustment of the mA to perform
this operation (see paragraph 8.2).
11.8 X-ray times control

Instrument to use: mAs d.c. meter (es. KEITHLEY 35035).
Disconnect the wire 4 of the PR1 of the Logic Board S100015 and connect it to the mAs meter;
connect the port 4 of the PRI to the positive out of the mAs meter. Make sure the mAs meter
is set on the mAs measurement.
At the end of every RX exposition verify on the mAs meter if the measured mAs era correct.
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60 kV 0,5 mAs
80 kV 0,5 mAs
60 kV 1,3 mAs
75 kV 1,3 mAs
60 kV 2,5 mAs
75 kV 2,5 mAs
60 kV 8 mAs
75 kV 8 mAs
If the values do not fall within a 5% tolerance range, verify the adjustament of the mA (see
paragraph 8.2).
11.9 Cleaning
Disconnect the equipment from the mains before any cleaning operation.
Proper cleaning procedures are essential for the good preservation of the equipment.
At least once a month clean the outside surfaces.
Do not use aggressive chemical products (solvents, disinfectants, detergents) that could damage
the surfaces (ex. Cidex).
Never pour the detergent directly on the equipment to avoid damages to the internal circuits.
Use a mild detergent and a damp cloth to clean the equipment.
If a liquid product is accidentally poured onto the equipment, dry and clean immediately.
To disinfect the equipment pour a watery solution with ammonium quaternary salts on a cloth.
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12 SPARE PARTS AND REPLACING
12.1 Mechanical parts
1 2
4
5
Position SMAM code DESCRIPTION

1-2 43A031 HOOK SUPPORT
3 M20C22 JOLLY BACK WHEEL
4 M20C21 JOLLY FRONT WHEEL
5 43A018 BRAKE ROPE
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12.2 Electronic parts
Keyboard group F07S13
Monobloc
Elettronics rack F07S09
Capacitor plate F06S06
Inverter
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12.2.1 Electronics rack F07S04

3 4 5 1 6 8 7
11
9
12 10
Position SMAM Code DESCRIPTION

1 E68SD0 POWER BLOCK S100016
2 E68S30 C.S. BACK PLANE HANDY S1000H1
3 E68S31 C.S. CPU INTERFACE HANDY S1000H2
4 E68SC7 C.S. LOGIC BOARD S100015
5 E68S33 C.S. FILAMENT HANDY S1000H4
6 E68S35 C.S. PSU HANDY S1000H6
7 E60A22 M.T SWITCH ABB BIPOLAR S941N C32
8 E55A30 FILTER FN660B-16/06
9 E58A03 STATIC RELAY RA 4450-D-08-5-04
10 E68S38 C.S.CAP.DISCHARGE S1000H9
11 F05S04 GROUP LC
12 E68SD1 C.S.IGBT DRIVER S100017
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12.2.2 Jolly Keyboard F07S13
3
4
Position SMAM CODE DESCRIPTION

1 E68SC4 C.S. CPU S100012-1
2 E68SC8 C.S. KEYBOARD S100018
3 E68S40 C.S. SCHERMO RF CPU HANDY S1000H0
4 E67A04 FLAT CABLE 90cm. 50 pin
5 E59A12 SEMIFERRITE 28S2011-0M0
12.2.3 Monobloc
Position SMAM CODE DESCRIPTION

F01S25 MONO EURO 1
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13 DIAGNOSTICS AND DATA RESETTING
13.1 Error messages

If there is an error the equipment warns the operator by showing the error message on the
display.
Below is an explanation of:
• The error messages
• Description of the possible cause that generated the error.
• Actions needed to restore the operating conditions of the equipment
MESSAGE CAUSE and SOLUTION

Cause: Ready signal of automatic exposure meter not
available
AEC not ready Action: Verify the connections to the module and the
AEC chamber. Verify the voltages +12Vdc, -12Vdc, +5Vdc
on the AEC module.
Cause: Loss of configuration data
Action: Switch the unit off.
Repeat the reconfiguration procedure (see par.7
Configuration pag.17). Enter the data on the form
FRP11/L drawn up by the Manufacturer.
If the configuration values are lost repeatedly, the cause
CALIBRAZIONE NON
might be electrical due to high voltage discharges coming
ESEGUITA from the X-ray tube or high disturbances coming from the
power cable.
In the first case follow the monobloc formation procedure
(see par.10 pag.27).
In the second case verify that there are no other units nearby
that may disturb the mains.
Loading of capacitors in progress. If after 90 sec the loading has
Loading in progress not been completed, contact technical assistance for help.
kVp, mA parameters or times too long; reduce load values
Maximum load
to tube.
Cause: mA higher than 50% of set value
Action: verify whether led L1 of the Logic Board lights up
during the x-ray exposure.
If the led is on:
• L1 overcurrent: it indicates an over-current in the
primary of the monobloc;
Maximum current Possible causes:
- mA too high, verify the adjustement of the mA (see
par. 8.2 pag. 20)
- The led lights up even with low mA for high voltage
discharges inside the monobloc or in the X-ray tube.
Perform the monobloc formation procedure (see par.10
pag.27). If outcome is negative contact manufacturer.
Cause: mA lower than 50% of set value
Action: Verify the adjustement of the mA (see par. 8.2 pag.
20), verify whether led L1, L2 and L3 of the Logic Board
lights up during the x-ray exposure.
Minimum current If the led is on:
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Possible causes:
par. 8.2 pag. 20)
Perform the monobloc formation procedure (see
par.10 pag.27). If outcome is negative contact
manufacturer.
• L2 overload: indicates an excess current load on the
exposure time.
Possible causes:
par. 8.2 pag. 20)
- Voltage alimentation of the power block below the
minimum value (180Vcc). Verify the value of the line
resistance that could be too high (> 0,4 Ohm).
• L3 kV unbalance: indicates that the positive and negative
kV are unbalanced, or that one of the signals is missing.
Possible causes:
- interruption of a connection cable (see Layout
diagram)
- interruption inside the monobloc
In the second case it is necessary to contact the
manufacturer.
Cause: over current on the primary monobloc
Verify whether led L1 of the Logic Board switches on during
the X-ray exposure.
If the led is on:
• Possible causes:
OVC par. 8.2 pag. 20)
manufacturer.
Cause: Over-current in the monobloc
Action: Verify whether led L2 of the Logic Board
switches on during the X-ray exposure.
• Possible causes:
OVL - mA too high, verify the adjustement of the mA (see
par. 8.2 pag. 20)
Cause: the x-ray signal was interrupted before the end of the
set x-ray time
Action: Verify that the LEDs L1 – L2 – L3 are off before and
during the x-ray exposure
Overcurrent protection If the leds are on:
active • L1 overcurrent: it indicates an over-current in the
Possible causes:
par. 8.2 pag. 20)
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manufacturer.
exposure time.
Possible causes:
par. 8.2 pag. 20)
Possible causes:
diagram)
In the second case it is necessary to contact the manufacturer.
Released 1st step before performing the 2nd X-ray step. Repeat
Release 1st step the exposure
Release 2nd step Released 2nd step before the X-ray time. Repeat the exposure
Cause: The output x-ray signal of the CPU is blocked
Action:
Verify that the leds L1 – L2 – L3 of the Logic Board are on
before the x-ray exposure.
If the leds are on:
Possible causes:
par. 8.2 pag. 20)
manufacturer.
X-ray blocked • L2 overload: indicates an excess current load on the
exposure time.
Possible causes:
par. 8.2 pag. 20)
Possible causes:
diagram)
manufacturer.
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Cause: the converter or the active safety micros are not
powered
Action: Verify the fuses F1 e F2 mounted on the
Cap.Discharger board (par Electronics rack F07S04). Verify
that the leds L1 – L2 – L3 of the Logic Board are on before
the x-ray exposure.
If the leds are on:
• L1 overcurrent: indicates an overcurrent in the primary
of the monobloc;
Possible causes:
- mA too high, verify the adjustment of the , mA (see
par. 8.2 page 20)
Signal 85% not available manufacturer.
exposure time.
Possible causes:
par. 8.2 pag. 20)
Possible causes:
diagram)
manufacturer.
Cause: due to strong interferences on the mains power or to
high voltage discharges inside the monobloc, the system could
have lost the configuration data
System not configured Action: re-configure the unit (see par. 7 page 17)
Perform the monobloc formation procedure (see par. 10 page
27). If outcome is negative contact manufacturer.
Cause: Stop signal of automatic x-ray exposure meter not
Stop X-ray AEC not available
present Action: Verify the connections between the AEC module and
AEC chamber.
Tabella 9 – Error messages
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14 INDEX OF THE FIGURE AND TABLE
14.1 Figure
Figure 1 – Recycling symbol for equipment.................................................................................................................... 10

Figure 2 - Main parts ............................................................................................................................................................ 11
Figure 3 – Control desk panel ........................................................................................................................................... 12
Figure 4 – Main block diagram ........................................................................................................................................... 13
Figure 5 – Wiring block diagram ....................................................................................................................................... 14
Figure 6 – Position of identification labels....................................................................................................................... 15
Figure 7 – Sequence for unpacking the equipment ....................................................................................................... 16
Figure 8 – Initial window ..................................................................................................................................................... 24
Figure 9 – Data transmission.............................................................................................................................................. 25
Figure 10 – Successful transmission.................................................................................................................................. 26
14.2 Table
Table 1 – Summary of configuration data Form FRP11/L ........................................................................................... 19
Table 2 – Monobloc pre-heating cycle............................................................................................................................. 20
Table 3 – mA adjustment; initial ADJUST values .......................................................................................................... 22
Table 4 – mA adjustment: pre-set values for Jolly 4..................................................................................................... 22
Table 5 – kV adjustment: exposure parameters............................................................................................................ 22
Table 6 – Times control: exposure parameters ............................................................................................................ 23
Table 7 – Monobloc formation cycle ............................................................................................................................... 27
Table 8 – Visual controls..................................................................................................................................................... 28
Tabella 9 – Error messages................................................................................................................................................. 43
EN ISO 9001:00 EN ISO 13485:03
Manufactured by
SMAM Srl
Via Tiziano n. 24
20053 Muggiò MI
ITALY
Technical Manual
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BMI Biomedical International srl

Via E. Fermi 52 Q/R

Device compliant with the medical equipment directive 93/42/CEE 0051

DSQ 20BMI rev. 2 del: 16/06/2007 1 di 44

REV DATE Modified REASON FOR REVISION

11.1 Visual controls.................................................................................................................................... 28

2 HOW TO USE THIS MANUAL

2.1 Graphic symbols

DANGER: This symbol is used to identify conditions or actions for which

WARNING: This symbol is sued to identify conditions or actions for which

WARNING: This symbol is used to identify conditions or actions for which

Underlined italics: Reference to a paragraph inside this manual

Bold italics character: Reference to a document not included in this manual

3 GENERAL WARNINGS AND INFORMATION

3.3 Return modality

3.4 Directives and applicable standards

Directive 93/42/CEE of Council, of June 14, 1993, concerning medical devices

3.5 Assistance centers

DANGER: The user is not authorized to open the unit’s guards or

4.1 General information

WARNING: The legally binding version of this document is the one in

WARNING: Electric shock hazard. To avoid any possible electric sparks, do

WARNING: It is important to know the unit to recognize any unusual

ATTENZIONE: This device is connected to an earth protection during

ATTENZIONE: THIS SYSTEM IS NOT DESIGNED TO BE USED BY A

WARNING: THIS EQUIPMENT IS NOT SUITABLE FOR USE NEAR

WARNING: If the mobile unit is used in a fixed station, the operator is

WARNING: If you think there could be electromagnetic interferences that

4.2 Protection against radiations

WARNING: Laws limit the operation of this device to doctors or

WARNING: Always use the appropriate X-ray protection on the patient

4.3 Electric safety

Figure 1 – Recycling symbol for equipment

5 PRESENTATION OF THE PRODUCT

5.1 Main parts

This device includes:

Figure 2 - Main parts

5.2 Control desk panel

Figure 3 – Control desk panel

5.3 Block diagram

The equipment can be divided into the following macro-blocks:

Control desk AEC

Figure 4 – Main block diagram

Figure 5 – Wiring block diagram

Figure 6 – Position of identification labels

6.1 Storage and shipment

6.2 Shipment and Transportation

A shockwatch label and the handling and destination instructions are

Figure 7 – Sequence for unpacking the equipment

6.3 Connecting and starting up the equipment

6.4 Disposal of the machine

7.1 When to configure the equipment

7.2 Entering the configuration modality

7.3 Exiting the configuration modality

7.4 Function of keys in configuration modality

7.5 Setting the data

Apparecchiatura tipo / Unit type Codice / Code N° Serie / Serial N°

Generator type selection: 4kW 12kW 15kW 30kW 40kW

Table 1 – Summary of configuration data Form FRP11/L

8.1 When to adjust the equipment

WARNING: do not adjust mA values if the equipment hasn’t warmed up.

kVp mAs Esp Intervallo

Make sure the equipment is switched off.