Villa Rotograph Plus U.M PDF

ROTOGRAPH PLUS 0434
User's manual
Release 22 November 2002 (Rev. 2)
USER'S MANUAL
Revision history
Revision history
Rev. Date Page/s Modification description
0 21.07.98 - First release

1 30.03.01 All New "ST" version.
New rotating arm without bellows.
General improvement of text and picture.
(Ref. RDM 5016, RDM 5018, RDM 5082)
2 22.11.02 10, 45 New intensifying screens.

(Ref. RDM 5419)
3
4
(Rev. 2) RTG PLUS - CE

USER'S MANUAL
Contents
THIS PAGE IS INTENTIONALLY LEFT BLANK
RTG PLUS - CE (Rev. 2)

USER'S MANUAL
Contents
Contents
1. INTRODUCTION 1
1.1 Icons appearing in the manual ............................................................... 1
2. SAFETY INFORMATION 2
2.1 Warnings ................................................................................................ 3
2.2 Environmental risk and disposal ............................................................ 4
2.3 Symbols used ......................................................................................... 5
3. CLEANING AND DISINFECTING PROCEDURES 6
4. DESCRIPTION 7
4.1 Identification labels ................................................................................ 7
4.2 Description ............................................................................................. 9
5. TECHNICAL FEATURES 11
5.1 Standards and regulation ..................................................................... 14
5.2 X-ray tubehead curves.......................................................................... 15
5.3 Technical factors measuring method .................................................... 16
5.4 Overall dimension................................................................................. 17
6. OPERATING INSTRUCTIONS 18
6.1 Switching on the equipment ................................................................. 18
6.2 Panoramic X-ray examination ............................................................... 19
6.2.1 Preparing the equipment (refer to Figure 8 and Figure 9) ....................19
6.2.2 Programmed/Manual exposure ..........................................................20
6.2.2.1 Programmed exposure (refer to Figure 9) ...............................20
6.2.2.2 Manual exposure (refer to Figure 9).......................................21
6.2.3 Preparing the patient (refer to Figure 2 and Figure 3)..........................22
6.2.4 Making the exposure (refer to Figure 9) ..............................................24
6.3 TMJ examination (not available on "ST" version)................................... 26
6.3.1 Performing the TMJ1 examination......................................................27
6.3.1.1 Preparing the equipment.......................................................27
6.3.1.2 Programmed/Manual exposure .............................................27
6.3.1.3 Preparing the patient (refer to Figure 4).................................28
6.3.1.4 Performing the exposure (refer to Figure 9) ............................30
6.3.2 Performing the TMJ2 examination......................................................31
6.3.2.1 Preparing the equipment.......................................................31
6.3.2.2 Preparing the patient (refer to Figure 5).................................32
6.3.2.3 Performing the exposure (refer to Figure 9) ............................34
(Rev. 1) i RTG PLUS - CE

USER'S MANUAL
Contents
6.4 Sinus examination ................................................................................ 36

6.4.1 Preparing the equipment ................................................................... 36
6.4.2 Programmed/Manual exposure .......................................................... 36
6.4.3 Preparing the patient......................................................................... 36
6.4.4 Performing the exposure .................................................................... 36
6.5 Ceph examination (not available on "ST" version).................................. 37
6.5.1 Preparing the equipment ................................................................... 37
6.5.2 Programmed/Manual exposure .......................................................... 38
6.5.2.1 Programmed exposure (Latero-Lateral) (refer to Figure 9)....... 38
6.5.2.2 Manual exposure (refer to Figure 9) ...................................... 39
6.5.3 Preparing the patient (refer to Figure 10)............................................ 40
6.5.4 Performing the exposure (refer to Figure 9)......................................... 42
6.6 Messages on display (refer to Figure 8 and Figure 9)............................. 44
6.7 Identification and correction of defects in dental
radiographs exposure ........................................................................... 46
6.7.1 Defects due to wrong patient positioning ............................................ 46
6.7.2 Defects due to wrong setting of radiological data and dark room ......... 47
6.7.3 Defects in the film due to equipment.................................................. 48
7. MAINTENANCE 55
This publication can only be reproduced, transmitted, transcribed, or translated

into any human or computer language with the written consent of VILLA SISTEMI
MEDICALI S.p.a.
This manual in English is the original version.
RTG PLUS - CE ii (Rev. 1)

USER'S MANUAL
Introduction
1. INTRODUCTION
NOTE:
* The present manual is updated for the product it is sold with in order to
grant an adequate reference to use properly and safely the product.
The manual may not reflect changes to the product not impacting
operating modes or safety.
This manual is fully applicable for units having serial number
≥01036406.
ROTOGRAPH PLUS, manufactured by Villa Sistemi Medicali, is a

radiological device which allows to carry out radiological examinations of
the dento maxillo facial complex.
ROTOGRAPH PLUS is available in the following version:

• For PANORAMIC examination only (ST version)
• For PANORAMIC examination and examination of the Temporo-
Mandibular Joint (TMJ)
• The latter is also available with the CEPHALOMETRIC device in order
to carry out CEPHALOMETRIC (CEPH) examination.
This manual provides to the operator the instructions for proper and safe
use of the appliance.
The appliance must be used strictly following the procedures described
in this manual and never for activities other than those for which it was
designed.
Before using the appliance, we recommend to read carefully this manual.
Keep it in a safe place near the unit for future reference.
ROTOGRAPH PLUS is an electromedical appliance and may be used only
under medical supervision, i.e. with the supervision of highly qualified
persons with the necessary know-how regarding X-ray protection.
The user is responsible for complying with the legal requirements
regarding the installation and operation of the equipment.
1.1 Icons appearing in the manual
Indicates a “NOTE”; the utmost attention shall be devoted to the

* reading of paragraphs marked by this icon.
Indicates a “WARNING”; paragraphs marked with this icon cover

, patient and/or operator safety aspects.
(Rev. 1) 1 RTG PLUS - CE

USER'S MANUAL
Safety information
2. SAFETY INFORMATION
, WARNING:
Read this chapter very carefully.
VILLA SISTEMI MEDICALI designs and manufactures equipment in

compliance with safety requirements; moreover, it provides all the
necessary information for correct utilization as well as warnings related
to risks associated to X-ray generators.
Villa Sistemi Medicali shall not be responsible for:
• any use of the ROTOGRAPH PLUS different from that for which it
has been designed,
• any damage to the equipment, the operator or the patient caused
either by incorrect installation and maintenance not compliant with
the procedures contained in the relevant user’s and installation
manuals provided with the equipment, or by incorrect operation
techniques,
• any mechanical and/or electrical changes effected during or after
installation, different from those reported in the service manual.
Only qualified service personnel, authorized by VILLA SISTEMI

MEDICALI is allowed to perform technical interventions on the
equipment.
Only authorized personnel is allowed to remove the tubehead from

its support and access the internal components.
RTG PLUS - CE 2 (Rev. 1)

USER'S MANUAL
Safety information
2.1 Warnings
The system has not been designed to be used in presence of vapours,

anaesthetic mixtures that are flammable with air, or oxigen or nitrous
oxide.
Ensure that water or other liquids do not get into the machine so as to
prevent short-circuits and corrosion.
Always disconnect from mains before cleaning the machine.
Where necessary, accessories such as lead-sealed aprons must be used

to protect the patient from radiations.
Only the patient and the operator may remain in the room during the
execution of the radiography examination.
ROTOGRAPH PLUS has been developed for continuous use with

intermittent load. The prescribed operating cycles to allow the heat
accumulated by the radiogenic source to be discharged must be
observed.
Although the appliance has been designed to have a reasonable degree of

protection from electromagnetic interference, it must be installed at a
certain distance from electricity transformer rooms, static continuity
unit, portable two-way hand radios and cellular phones. The latter may
only be used at a distance of over 1.5 meters from all elements of the
machine.
All instruments or equipment for professional use and used near the
machine must be in conformance to the electromagnetic compatibility
standards.
Nonconforming instruments whose low immunity to electromagnetic
fields is known must be installed at least 3 meters away from the
ROTOGRAPH PLUS and be powered via an independent electric line.
ROTOGRAPH PLUS must be switched off during the entire period of use
of ESU (Electro Surgery Units) units or similar equipment.
Clean or eventually disinfect the chin support, positioning handles,

temples clamp support, nose rest and any other part that may come in
touch with the patient.
At the end of the examination, replace the bite and the ear rods.

USER'S MANUAL
Safety information
Although the X-ray dosage supplied by dental radiology appliances is on

average low and distributed over a relatively small surface, the operator
must take the necessary precautions and/or follow the safety procedures
for both himself and the patient during an exposure. We recommend
that the X-ray activation always be commanded from an X-ray protected
area via remote control. If it is necessary to operate the exposure near
the patient, remain at the maximum distance allowed by the remote
control cable in the direction opposite to the emission of the rays, at a
distance of at least 2 meters (6.6 feet) from both the radiation source and
patient.
2.2 Environmental risk and disposal
A number of machine parts contain materials and liquids that upon

completion of the machine’s life cycle must be disposed of at recovery
centers established by the local health units.
The machine contains the following materials and/or components:

• Tubehead: dielectric oil, lead, copper, iron, aluminum, glass,
tungsten, beryllium
• Control box and remote control: iron, copper, glass resin, non-
biodegradable plastic casings
• Column, rotating arm, extensions: iron, lead, aluminum, copper,
non-biodegradable plastic materials, glass resin.
NOTE:
* Disassembling part of the unit must be performed by Villa Sistemi
Medicali personnel or by authorized technical people.
NOTE:
* VILLA SISTEMI MEDICALI or its representative will not be responsible
for the disposal of dismissed machines by the user and relative costs.

USER'S MANUAL
Safety information
2.3 Symbols used
Symbol Description
Equipment with Type B applied parts (according to

IEC 601-1)
∼ Alternating Current
N Connection to neutral conductor
L Connection to line conductor
Protection ground
Functional ground
OFF ; equipment not connected to power line
 ON ; equipment connected to power line
Warning: read the documentation provided with the

unit
Conformity to the CE 93/42 Directive

USER'S MANUAL
Cleaning and disinfecting
3. CLEANING AND DISINFECTING

PROCEDURES
In order to guarantee a careful hygiene and cleaning it is advisable to
follow scrupulously the procedures hereunder reported:
WARNING:
, Disconnect from the mains before cleaning the unit.
• Do not allow liquids and water to enter inside the unit, to prevent
from shortcircuits and corrosion of inner parts.
• Clean the painted surfaces, the accessories and the connection

cables using only a damp cloth and neutral detergents. Take care to
dry the parts with a dry cloth. Do not use corrosive or abrasive
solvents (alcohol, gasoline, “trielina”).
• The bite rod, the centering bite and the ear centering pins must be
replaced after each examination where they have been used. In
addition, the bite must be disinfected by using a 2% Glutharaldeid
solution, following the rules provided by the manufactures of the
cleaning solution itself.
• The chin support, the patient positioning handles, the nose rest and
the temple-clamp must be carefully cleaned and disinfected with a
2% Glutharaldeid solution or similar (find out what is available; e.g.
Milton) after each examination where they have been used.

USER'S MANUAL
Description
4. DESCRIPTION
4.1 Identification labels
ROTOGRAPH PLUS is labeled with a set of labels identifying different

components according to the requirements of the international
standards.
The following picture shows the position of the different labels:

USER'S MANUAL
Description
1 2
ROTOGRAPH PLUS label Tubehead label
3a 3b
Diaphgram label Diaphgram label
(not present on “ST” version) (not present on “ST” version)
4 5
Collimator label CEPH device label
6
Remote control label

USER'S MANUAL
Description
4.2 Description
ROTOGRAPH PLUS has been designed to perform the following

examinations:
• Panoramic examination (all versions)

• "SINUS" examination of the paranasal sinus (all versions)
• Examination of the Temporo-Mandibular Joints (TMJ) with open or
closed mouth on a single film (not available on "ST" version)
• Cephalometric examinations (CEPH) of the skull (if equipped with
the cephalometric optional device; not available on "ST" version) with
1.65 mt. (65 inches) focus-film distance and 1.5 mt. (59 inches)
focus-patient distance.
All the allowed examination may be made with different parameters

according to the setting of the remote-control (please refer to the specific
chapter of this manual).
ROTOGRAPH PLUS is controlled by a soft touch console and equipped

with an alphanumeric digital display for a clear indication of the working
parameters and operative messages. The operative cycle is entirely run
by a microprocessor, controlling its different modes : from programming
of the emission parameters according to the chosen examination and
the patient's size, to the voltage fluctuation and to the notification of
possible anomalies, failures or errors.
The excellent quality radiographs thus obtained is the result of a clever

design based upon the pseudo-elliptic rotation system, the original light
beam-luminous cross pattern centering system, the use of green emiting
Rare Earth Intensifying screens and most of all the small dimension of
the focal spot.
This particular rotation system allows an orthogonal imaging of all teeth
and wide image layer with an optimum focused zone of 10 mm for the
incisors and 20 mm for the molars.
ROTOGRAPH PLUS, besides operating in the programmed mode, can

also operate in the manual personalized mode by modification of the
parameters, as described in chapter 6.
In the Panoramic and TMJ modes, with all interlock enabled, it is

possible to activate the TEST push button (31) (see Figure 9 at the end of
the manual).
The TEST functioning mode allows the operator to check the

functionality of the selected examination cycle or to show to the patient
the examination he will undergo (including all movements of the
machine) without emitting X-rays.

USER'S MANUAL
Description
The TEST push button as X-RAY button are a “dead man” buttons,
which means thus if they are released during the examination cycle, the
latter is interrupted stopping the movements in progress. To re-start the
cycle first reset the unit by means of the key 32 (Figure 9), than start
again the function which was interrupted.
The following intensifying screen - film combinations are recommended

in order to obtain good quality images:
Intensifying screens Films

Type Supplier Type Supplier
KR II KONIKA MG KONIKA
KR II KONIKA MGH KONIKA
Lanex
KODAK T-MAT G/RA KODAK
Regular
Curix Ortho
AGFA T-MAT G/RA KODAK
Regular
T 16 3M / IMATION XDA 3M / IMATION
Medium AGFA HTA AGFA
G8 FUJI HR-G FUJI
The above listed intensifying screens are all of the Green Rare Earth
emitting type.
Use of screens and films different from those stated on the table above
requires system recalibration by an Authorized Technician.
The calibration of the above mentioned combination has only an

indicative value. The effective adjustment depends on different factors,
such as the real dose emitted by the unit, the film development system
and the user predilection for more or less devise images.
The good quality of the image does not exclusively depend on

ROTOGRAPH PLUS but a great importance is to be given to the film
developer; and dark room techniques.
Therefore, it is necessary:
• to perform developer maintenance as indicated by the manufacturer
instructions;
• to check regularly the level of the used chemical substances,
substituting them at time intervals as indicated by the manufacturer
instructions, usually a direct function of the number of radiographs
developed and chemicals concentration.

USER'S MANUAL
Technical features
5. TECHNICAL FEATURES
General characteristics
Equipment ROTOGRAPH PLUS

Manufacturer VILLA SISTEMI MEDICALI
Buccinasco (MI) Italy
Class Class I with type B applied parts
according to IEC.
Degree of protection IP20

Rated line voltage 220/230/240V∼
Line frequency 50Hz
Max line current at nominal voltage 5A rms momentary; 0.5A stand-by
Maximum power 1.15 kVA @ 230V
Power fuse 6.25A T
Command fuse 0.5A T
Filament fuse 0.315A F
Compensation of the mains voltage automatic
fluctuation
Apparent line resistance 0.5 Ω max
High voltage 60-85 kV (5 kV steps)
KV accuracy ± 10% @ nominal voltage ± 10%
Anodic current 10 mA
Anodic current accuracy ± 10% @ nominal voltage ± 10%
Exposure time (Panoramic) 17s adult
14s child
(with deceleration ramp) 15s child
Exposure time (TMJ1 + TMJ2) 10.4s adult
(see note 1) 9.4s child
Exposure interval (PAN & TMJ) 240s (1:16 duty cycle)
Film size (PAN & TMJ) 12.7x30 cm (5"x12")
Image mean enlargement (PAN & TMJ) 1.2 : 1
Inherent filtration of the PAN cassette 1mm Al eq @ 70 kV
Exposure time (Cephalometric) 0.2 ÷ 3s in 19 position
(see note 1)

USER'S MANUAL
Technical features
General characteristics
Exposure time accuracy (CEPH) ± 10ms for times ≤ 0.33s0

± 3 % for times ≥ 0.33s
Reference current time product (CEPH) 3 mAs @ 70% of the max power
Exposure interval (CEPH) 60s
Film size (CEPH) 18x24 cm (8"x10") std.,
24x30 cm (10"x12") optional
Focus-Patient distance (CEPH) 150cm (59")
Focus-Film distance (CEPH) 165cm (65")
Image mean enlargement (CEPH) 1.1 : 1
NOTE 1:
* These examination are not available on the "ST" version; this feature
cannot be field upgraded.
Tubehead features
Type MR05
Manufacturer VILLA SISTEMI MEDICALI
Buccinasco (MI) Italy
Max peak tube potential 85 kV
Nominal power 0.630 kW (85kVp, 10mA)
Total filtration 2.5mm Al eq. at 85 kV
Insulation Oil bath
Cooling Ambient
Leakage radiation at 1 m < 0.25 mGy/h
(85 kV, 10mA, 1:16 duty cycle)
Maximum power 85 kVp, 10mA
Type of circuit Single-phase, self-rectifying

USER'S MANUAL
Technical features
X-ray tube features
Manufacturer CEI – Bologna Italy

Type CEI OPX/105
Focus 0.5 IEC 336
Inherent filtration 0.5 mm Al eq.
Anode tilt 5°
Anode material Tungsten
Nominal voltage 105 kVp
Filament maximum current 4A
Filament maximum voltage 8V
Anode thermal capacity 30 kJ
Weight of apparatus and parts
Slider net weight 56 kg (123.5 pounds)

Column net weight 48 kg (106 pounds)
Tubehead net weight 24 kg (53 pounds)
CEPH device net weight 12 kg (26.5 pounds)
Control unit net weight 28 kg (62 pounds)
Slider counterweights net weight 92 kg (203 pounds)
Environmental conditions
Maximum operating temperature range +10° ÷ +40° (+50°F ÷ +104°F)

Operating relative humidity range 30% ÷ 75%
Transportation and storage temperature -20° ÷ +70° (-4°F ÷ +158°F)
range
Maximum transportation and storage < 90% non condensing
relative humidity
Minimum atmospheric pressure for 630 hPa
transportation and storage

USER'S MANUAL
Technical features
5.1 Standards and regulation
The ROTOGRAPH PLUS equipment is manufactured according to the

following standards:
• General safety:
IEC 601-1
IEC 601-1-1
IEC 601-2-7
IEC 601-2-28
IEC 601-2-32
• Electromagnetic compatibility
IEC 601-1-2
• Protection from radiation

IEC 601-1-3
The symbol CE grants that ROTOGRAPH PLUS complies with

directives 93/42 for medical devices issued by the European
Community.
Classifications
ROTOGRAPH PLUS is an electro-medical X-ray device belonging to
Class I type B as per classifications IEC 601-1, foreseen for a continuous
working at intermittent load.

USER'S MANUAL
Technical features
5.2 X-ray tubehead curves
Tube "CEI - OPX/105" (0.5x0.5)
Loading chard
Anode cooling chard

USER'S MANUAL
Technical features
5.3 Technical factors measuring method
kVp The peak tube potential is directly measured with a non invasive
kVp-meter, accuracy ±3kVp. When performing the measurement, make
sure that measuring probe is completely covered by the X-ray beam.
A direct measurement of the high voltage can only be carried out by
specialized technicians in a suitable testing laboratory as it requires
disassembling of the tubehead.
mA The output current is determined by measuring with a digital

multimeter, accuracy 0.5%, by connecting the probes to the connectors
of A1 PCB as indicated in the Service Manual (digital multimeter set to
VDC 20V, 1V=1mA).
t The exposure times are determined by using a timer/counter, having an

accuracy of 0.1%, measuring the duration of part of the voltage applied
to the primary side of the tubehead, during the exposure phase.

USER'S MANUAL
Technical features
5.4 Overall dimension
Figure 1: ROTOGRAPH PLUS overall dimension

USER'S MANUAL
Operating instructions
6. OPERATING INSTRUCTIONS
NOTE:
* The procedures explained in the next pages make often reference to
Figure 8, Figure 9 and Figure 10 located at the end of this chapter. To
easily consult this Figures, unfold pages in order to make it visible while
reading other pages of the manual.
6.1 Switching on the equipment
1. Push the button on the control panel to turn the equipment ON. The
"CHECK" function is so activated, verified by the lighting up of the
LED'S on the remote-control and the display pixels. The software
checks the enabled operating function with the corresponding LED
signal.
In the event that the equipment is not set for a proper function, the
display will show the message "Equipment not set" and the
panoramic function LED will blink. Select the chosen function and
push for the second time the same button (with blinking LED): the
display will now indicated the step which needs to be performed.
Should there be more steps to be enabled, they will be displayed one
at a time and automatically excluded after the corresponding action
has been performed.
2. With the proper steps performed for the selected function (see
chapters regarding the single tests), the LED stops blinking (27, 28,
29 or 30 Figure 9) and the procedure will remain lit with the
equipment sets as default in the following configurations:
• ADULT with push button 33 LED lighted up
• MEDIUM SIZE with push button 36 LED lighted up
• Display 44 shows the kV alternatively to the exposure times.
THE UNIT IS READY

USER'S MANUAL
6.2 Panoramic X-ray examination
6.2.1 Preparing the equipment (refer to Figure 8 and Figure 9))
For NON "ST" version, the equipment has to be prepared for PANORAMIC
examination by inserting the appropriate beam limiter, unlocking the
rotating arm and inserting the film holder.
If pressing the button 27 the message "Equipment not set" is displayed

and the relevant function LED blinks, push the button a second time in
order to display the message concerning the interlock to be enabled.
The messages that can be read during the Panoramic function setting
and the relevant actions to perform are the following:
1. PAN/TMJ film holder not present: insert the X-ray cassette in the
appropriate support
2. Please rotate X-ray generator on PAN/TMJ position: push the
lever 4 and rotate the tubehead anti-clockwise until insertion of the
mechanical lock is noted
3. Rotating arm unlocked: rotate the upper knob 5 anti-clockwise
4. Please insert the PAN/TMJ beam limiter: install the PAN/TMJ
collimator in place of the CEPH collimator.
5. Press again the button 27.
After completing the system SET UP, adjust the chin support as follows :
Chin support Chin support

PANORAMIC (1) SINUS (21)
ADULT YES NO
PANORAMIC
CHILD YES YES

USER'S MANUAL
6.2.2 Programmed/Manual exposure
After setting the unit as previously described previous point, it is now

possible to choose whether to operate an exposure in a preset mode,
meanings with the kV values preset by the manufacturer or to operate
an examination in the manual function, with possibility to change the
preset kV values.
6.2.2.1 Programmed exposure (refer to Figure 9)
Push button 33 for adult program or 34 for child's.
To check the new configuration depress push buttons Adult 33 and

Child 34, there will only be a variation on kV and time; pressing buttons
Large Size 35, Medium Size 36 and Small Size 37, there will be a
variation on kV.
The following table shows the programmed values according to the

selection made:
Large Size Medium Size Small Size

(35) (36) (37)
Adult (33) 85kV - 17sec 75kV - 17sec 70kV - 17sec
Child (34) 70kV - 14sec 65kV - 14sec 60kV - 14sec
Child (34)
(with deceleration 70kV - 15sec 65kV - 15sec 60kV - 15sec
ramp)
These values have been set bearing in mind the screen-film combination
and consequent mA calibration, as described at chapter 4.

USER'S MANUAL
6.2.2.2 Manual exposure (refer to Figure 9)
To select the manually technical factors follow the next procedure:

1. Depress button 38 (kV), the button function will blink.
2. Depress buttons 41 (increase) or 40 (decrease) on the hand control
selecting the desired kV value to be used. After 2 seconds, the
function button LED stops blinking. The unit is now ready for the
next step.
NOTE:
* The kV can vary from a minimum of 60kV to a maximum of 85kV with
steps of 5kV.
If, after having reached the minimum or maximum values of the kV
range additional decrease or increase is requested, the following
messages will be displayed: Minimum or Maximum; the minimum or
maximum set kV values will subsequently be displayed.

USER'S MANUAL
6.2.3 Preparing the patient (refer to Figure 2 and Figure 3)
1. Ask the patient to remove all metal objects located in the zone
involved in radiography (necklaces, earrings, spectacles, hair-clips,
movable dental plates etc.).
Make sure that there are no heavy articles of clothing (such as
overcoats, jackets, ties, polo-neck sweaters, etc.) in the radiography
zone.
2. Have the patient put on the protecting apron or similar protective
devices in accordance with the regulations in force in the various
countries, making sure that it does not interfere with the trajectory
of the X-rays beam.
3. Bring the patient in standing position up to the chin support and,
using the handle 22, release the brake button 24 in order to position
the slider so that the chin support resting plane is aligned with the
patient's chin.
4. Position the patient in the skull clamp with the chin resting on the
appropriate support and rest the hands on the side handles 22; have
the patient bite with the incisors in the groove of the bite block
mounted on the appropriate rod 2, making sure both upper and
lower anteriors are set in the groove of the bite piece.
5. Press the centring device activation button 20. When this is done,
two crossed beams of light illuminate both the sagittal median line
45 and the horizontal line for the Frankfurt plane reference 46.
The centring device stays illuminated for about 40 seconds; if this
time is insufficient to carry out the centring operations, the
activation button 20 may be pressed again.
6. Bring the height of the skull-clamp a little above the patient's orbital
bone and centre the patient until the position of perfect alignment
with the Frankfurt and sagittal median lines is obtained.
The Frankfurt plane light beam must be adjusted for height in
relation to the patient's size; the adjustment is made by acting on
the appropriate knob 18.
In order to check the patient's centring, the operator can tilt the
mirror 6 towards himself, thus obtaining a front view of the patient.
Lastly bring the patient's head into contact with the two temples
clamp rods 7 by acting on the appropriate knob 9.
7. After the head has been positioned, the patient has to make a
movement with his feet towards the stand. This will give better
distension of the spinal column in the cervical region, eliminating
white ghosting of the spine on the radiograph in the zone of the
lower incisors.
8. Check centring again, advise the patient to close mouth and eyes,
ask then to swallow and bring the tongue against the palate and
remain motionless for the exposure.

USER'S MANUAL
16 18
17
24
1
20
22
Figure 2: Panoramic position
Figure 3
45 - Sagittal median line
46 - Frankfurt plane line

USER'S MANUAL
6.2.4 Making the exposure (refer to Figure 9)
NOTE:
* During the emission of X-rays protection of the operator and
surrounding personnel must be in accordance with the rules in force in
the respective countries.
The X-ray activation always be commanded from an X-ray protected area
via remote control. If it is necessary the operator must stand at a
distance of at least 2 meters (6.6 feet) away from the X-ray source and, if
possible, on the opposite direction. No other persons other than the
operator and the patient, are allowed to stay in the examination room
during the examination.
1. Check if the exposure data are correct (paragraph 6.2.2), then press
the X-ray button 42 during the whole time of the exposure as the
control is a dead man type, checking the simultaneous operation of
the rays signaling light 43 and the acoustic ray signal.
NOTE:
* The start of arm rotation and the emission of rays take place with a delay
of four seconds after the activation of button 42 allowing preheating of
the tube filament and check all the set value.
2. After exposure, the message "Push RESET" will be displayed: the

patient may then be released from the positioning device, the film
cassette removed by pulling upwards, the return button 32 pressed
to move the machine back to the starting position. After full return,
the message "OK" will be displayed, which will disappear when the
button 32 is released.
3. With Reset operation performed, and with button 32 released the
following message is displayed "Wait, please ......." indicating a
waiting time of 4 minutes to allow cooling of the tubehead anode.
4. It will now be possible to open the film cassette in the dark room and
develop the film.
NOTE:
* After each examination, clean carefully both chin support and temples-
clamp and replace the bite.

USER'S MANUAL
WARNING:
, If the patient should move during the exposure, stop the exposure
immediately by releasing the rays control button 42 interrupting the
rays emission and the arm movement.
The message "Change film please" will appear for a few seconds on the
display and successively the message "Push RESET". The cassette is
then to be removed and, in the dark room , a new film inserted; the
return button 32 is, then, to be pressed to bring the machine in the
starting position. The return end is evidenced by the message "OK"
which will disappear when the button 32 is released.
NOTE:
* If the event the film in the cassette has not been replaced, and a further
exposure made, no impediment message will appear, but, due to the
double exposure, the film will give no diagnostic results.
If, for external reasons or incorrect operation the X-ray emission times
should exceed 17 seconds, a backup security timer will come into
operation cutting out the emission after 20 seconds, the arm rotation
will continue until the natural stop point.

USER'S MANUAL
6.3 TMJ examination (not available on "ST" version)
NOTE:
* When performing TMJ examinations the rays emissions is discontinuous
as it is interrupted during the transition phases between the different
projections.
NOTE:
* For “ST” version , pressing the TMJ1 or TMJ2 button will appear the
message “TMJ modality not enabled”.
The TMJ functions allow to obtain 4 different images on the same film by
means of two different programs. The 4 images represent the right and
left condyle of the temperomandibular joint (TMJ) both with closed
(TMJ1) or open (TMJ2) mouth.
With TMJ1 projection there is exposure of the film lateral portions, while
the centre part will be exposed with the TMJ2 projection.
We suggest to follow the sequence TMJ1 and TMJ2.

USER'S MANUAL
6.3.1 Performing the TMJ1 examination
6.3.1.1 Preparing the equipment
1. The modality is selected by pressing one of the keys 29 or 30

(Figure 9); if the message “Equipment not ready” and the
corresponding LED is blinking, press once again the key to visualize
the message explaining which action has to be performed to finish
the equipment’s preparation.
2. Messages that can be displayed for TMJ1 preparation are the same
as for the panoramic modality, so please refer to this section of the
manual for the explanation and actions (reference to paragraph
6.2.1).
3. The equipment preparation has to be completed removing the chin’s
support for standard panoramic 1 (Figure 8) and replacing it with the
one for sinuses’ examination 21 (Figure 8).

ADULT NO YES
TMJ
CHILD NO YES
6.3.1.2 Programmed/Manual exposure
To change from the programmed to the manual function and viceversa,

proceed as described at paragraph 6.2.2 bearing in mind that the kV and
time parameters in the programmed exposure are indicatively the
following (numbers refer to Figure 9):

(35) (36) (37)
TMJ 1 and 2
85kV - 5,20sec 75kV - 5,20sec 70kV - 5,20sec
Adult (33)
TMJ 1 and 2
70kV - 4,70sec 65kV - 4,70sec 60kV - 4,70sec
Child (34)
Such values have been set considering the screens-films combinations

and consequent mA calibration, as mentioned in chapter 4.
The times reported in the previous table are the sum of the exposure
time for the right condyle with the one of the left condyle, while the arm
rotation time remains the same as the one reported for the panoramic
examination.

USER'S MANUAL
6.3.1.3 Preparing the patient (refer to Figure 4))
1. Ask the patient to remove all metal objects located in the zone
involved in radiography (necklaces, earrings, spectacles, hair-clips,
movable dental plates etc.).
Make sure that there are no heavy articles of clothing (such as
overcoats, jackets, ties, polo-neck sweaters, etc.) in the radiography
zone.
2. Have the patient put on the protecting apron or similar protective

devices in accordance with the regulations in force in the various
countries, making sure that it does not interfere with the trajectory
of the X-rays beam.
3. Bring the patient in standing position up to the chin support and,

using the handle 22, release the brake button 24 in order to position
the slider so that the chin support resting plane is aligned with the
patient's chin.
4. Position the patient in the skull-clamp with the chin resting on the
appropriate support and against the vertical reference rod of the
same. Furthermore, position the hands on the lateral knobs 22.
5. Press the push button 20 to light on the beam centering lights. In

this way both reference lights, mid sagittal (45) and Frankfurt’
planes (46), are lighted on; adjust the patient’s head in such a way
that mid sagittal light is on the respective anatomical plane while the
Frankfut’s one is parallel to the corresponding plane. Horizontal
beam (Frankfurt plane 46), if needed, can be height adjusted in
relation to the patient’s dimensions; the adjustment is made by
acting on the appropriate knob 18. In order to check the patient’s
centring, operator can tilt the mirror 6 towards himself, thus
obtaining the a front view of the patient.
6. After the end of the patient’s centring, bring the height of the skull-
clamp a little above the patient’s orbital bone and close the skull-
clamp leaving the two temple clamp roads 7, by acting on the
appropriate knob 9. This will help the patient to hold the correct
position during the examination.

USER'S MANUAL
13
18
7 24
46
20
45
22
Figure 4: TMJ1 position

USER'S MANUAL
6.3.1.4 Performing the exposure (refer to Figure 9)
1. With the LED of push button 29 lit up, check if the exposure data
are correct (paragraph 6.2.2), then press the X-ray button 42 during
the whole time of the exposure as the control is a dead man type,
checking the simultaneous operation of the rays signaling light 43
and the acoustic ray signal.
NOTE:
* • X-ray emission starts with a delay of four seconds after the operation
of the exposure push button, in order to allow the preheating time of
the tube filament and check all the set values.
Arm’s rotation will start a little in advance regarding the emission.
• On TMJ examination, the X-ray emission does not last for all the
rotation, but it is interrupted corresponding with the central middle
part of the mouth. As a consequence, both acoustic and visual
emission signals are interrupted in accordance with the emission.
• X-ray push button is a “dead man type”; this means that the
emission and arm’s rotation are interrupted if the push button is
released. The push-button must be held pressed also during the
above emission interruption.
• In case of patient’s moving during arm’s rotation, the exam has
to be interrupted releasing the emission push-button; in this way
both emission and rotation will be interrupted. On the display will
appear the message “Change film” and, after about two seconds,
“Press reset” alternating. The cassette has to be removed and loaded
with a new film on the dark room. The return button 32 is, then, to
be pressed to bring the machine in the starting position. The return
end is evidenced by the message “OK” which will disappear when the
NOTE:
* In the event that the film in the cassette not being substituted, and
a further examination made, no error message will appear, but, due
to a double exposure, the film will give no diagnostic result.
2. At the end of second emission step, on the display of the hand held
control the message “Press Reset” will appear. The return button 32
is, then, to be pressed to bring the machine in the starting position.
The return end is evidenced by the message “OK” which will
disappear when the button 32 is released.

USER'S MANUAL
6.3.2 Performing the TMJ2 examination
6.3.2.1 Preparing the equipment
1. Select TMJ2 modality by pressing the push-button 30 (Figure 9).

2. Leaving the film used on the previous examination on the cassette,
rotate the film holder from PAN/TMJ position to the TMJ2, rotating
anticlockwise the knurled knob 13 (Figure 5).
NOTE:
* Operator has to evaluate the needs to increase the kV selection of
one step; from some clinical results; this will increase image’s
quality. Eventually, use a manual programming mode.

USER'S MANUAL
6.3.2.2 Preparing the patient (refer to Figure 5)
1. Open the skull-clamp support 7 by acting on the appropriate knob 9.
2. If not already use for TMJ1, place a standard bite on the chin
support.
3. Instruct the patient to open the mouth up to the maximum,

maintaining the mandible fixed and lining on the chin support;
patient’s chin has to stay against the vertical plane of the chin
support. As a consequence, patient’s head will be slightly rotated
backward.
4. Instruct the patient to place the inferior scissors teeth against the
lower part of the bite used for the panoramic examination; this
procedure will help the patient to stay in a correct position during
the exposure.
5. Press push-button 20 to light on the centring device. In this way,

both mid sagittal (45) and Frankfurt plane (46) will light on. Adjust
the patient’s head in order to have the vertical light beam 45 to lean
on the corresponding anatomical reference. In order to check the
patient’s centring, operator can tilt the mirror 6 towards himself,
thus obtaining the a front view of the patient.
WARNING:
, Do not align the patient to the Frankfurt plan; in the case the patient
will be re-positioned again with the Frankfurt’ plane horizontal, it is
possible that the condiles will fall out from the exposed area of the film.
6. After the end of the patient’s centring, bring the height of the skull-
clamp a little above the patient’s orbital bone and close the skull-
clamp leaving the two temple clamp roads 7, by acting on the
appropriate knob 9. This will help the patient to hold the correct
position during the examination.

USER'S MANUAL
13
46
20
45
Figure 5: TMJ2 position

USER'S MANUAL
6.3.2.3 Performing the exposure (refer to Figure 9)
1. After having the modality selected and with LED 30 on signalling the
correct machine set, press X-ray push-button 42 on the hand held
control.
NOTE:
* • In the event of the x-ray control button being activated before the
correct placement of the cassette, the message “Please rotate film
holder to TMJ2 position” will be displayed.
• X-ray emission starts with a delay of four seconds after the operation
of the exposure push-button, in order to allow the preheating time of
the tube filament and check all the set values. Arm’s rotation will
start a little in advance regarding the emission.
• On TMJ examination, the X-ray emission does not last for all the
rotation, but it is interrupted corresponding with the central middle
part of the mouth. As a consequence, both acoustic and visual
emission signals are interrupted in accordance with the emission.
• X-ray push button is a “dead man type”; this means that the
emission and arm’s rotation are interrupted if the push button is
released. The push-button must be held pressed also during the
above emission interruption.
• In case of patient’s moving during arm’s rotation, the exam has
to be interrupted releasing the emission push-button; in this way
both emission and rotation will be interrupted. On the display will
appear the message “Change film” and, after about two seconds,
“Press reset” alternating. The cassette has to be removed and loaded
with a new film on the dark room. The return button 32 is, then, to
be pressed to bring the machine in the starting position. The return
end is evidenced by the message “OK” that will disappear when the
• In the event that the patient will move during TMJ2 exposure and
after TMJ1 mode already executed, it is not mandatory to repeat also
TMJ1 exposures. This modality has to be repeated if, for
diagnostic reasons, both open and closed moth results has to be
on the same film.
2. At the end of the TMJ2 examination, on the display of the hand held
control the message “Press Reset” will appear. The return button 32
is, then, to be pressed to bring the machine in the starting position.
The return end is evidenced by the message “OK” that will disappear
when the button 32 is released. At this point the message “Wait
please....” will appear, indicating that the automatic pause to allow
anode cooling down procedure is acting. At the end of this
procedure, the LED of the last examination performed will light on.
The cassette holder has automatically placed itself to the TMJ1
position.

USER'S MANUAL
3. It will be now possible to remove the film cassette and, in the dark
room, open it and develop the film.
NOTE:
* If for external reasons or incorrect operation the emission times should
exceed 5 seconds, a safety backup timer intervention will come into
operation, interrupting emission but the arm rotation will continue until
the end.

USER'S MANUAL
6.4 Sinus examination
The SINUS examination aim is to show the structure located in the

sinomaxillary area.
6.4.1 Preparing the equipment
The equipment setting is like the one described at point 6.2.1 as the only
difference between the Panoramic Exposure and the Sinus one is due to
the different chin support used: the chin support to be used in the Sinus
examination is as follows (numbers refer to Figure 8 at the end of this
manual):

ADULT NO YES
SINUS
CHILD NO YES
To change from the programmed function to the manual one and

viceversa, proceed as described at point 6.2.2 bearing in mind that the
kV and Time (seconds) parameters in Sinus exposure are like the
Panoramic ones.
6.4.3 Preparing the patient
1. Proceed operating as for points 6.2.3. steps 1, 2 and 3.

2. Position the patient in the skull clamp with the chin resting on the
appropriate support and against the vertical reference rod of the
same and rest the hand on the side handles but, instead of biting
with the incisors the centring bit, as in the Panoramic exposure, the
examination has to be carried out with a closed mouth.
3. Proceed operating as for points 6.2.3. steps 5, 6, 7 and 8.
6.4.4 Performing the exposure
Proceed as for point 6.2.4, following the relevant notes.

USER'S MANUAL
6.5 Ceph examination (not available on "ST" version)
6.5.1 Preparing the equipment
If depressing button 28 (Figure 9)the message "Equipment not set" is

displayed and the function LED blinks, press a second time the button,
so as to obtain reading of the message regarding the interlock to be
enabled.
The following are the messages that can be read during preparation of
the Cephalometric function and the concerned operations to follow:
1. Rotating arm unlocked: rotate anticlockwise the upper knob 5
(Figure 8).
2. Please rotate X-ray generator on CEPH position: release lever 4
and rotate anticlockwise the tubehead until insertion of the
mechanical locks is noted.
3. Please insert the CEPH beam limiter: remove the PAN/TMJ
collimator if present and insert the appropriate CEPH collimator.
NOTE:
* In CEPH examination different types of collimators are used according to
the X-ray cassette size; the available collimators are:
• Standard size in inch: 10"x8" asymmetrical (L.L.)
Optional: 8"x10" symmetrical (P.A.-A.P.), 8"x10" asymmetrical (L.L.),
12"x10" symmetrical (P.A.A.P.)
• Standard size in cm: 18x24 asymmetrical (L.L.)
Optional: 18x24 symmetrical (P.A.-A.P.), 24x18 asymmetrical (L.L.),
30x24 symmetrical (P.A.-A.P.)
The first value of the above mentioned collimator sizes refers to the
horizontal dimension of the film.
4. Loosen knob 50 (Figure 10), raise pin 51 (Figure 10) so that the
skull-clamp unit can be adjusted according to the examination to be
made, i.e. latero-lateral, postero-anterior, antero-posterior, put back
the pin and lock knob 50.
5. Load in the dark room the film holder cassette, the size of which is
indicated on the collimator. Insert it in the cassette holder unit 53
(Figure 10), in the correct position according to the installed
collimator, following the position indicated on the cassette holder
panel; lock it lowering the upper guide by mean of the special knob.
NOTE:
* During a CEPH exposure, no chin support of any kind is needed.

USER'S MANUAL
After having set the equipment as described in the previous point, it is

now possible to chose whether to operate an exposure in the pre-
programmed mode, i.e. with the kV and time values set by the
manufacturer according to the size or to operate a manual function, i.e.
with the possibility to change the set values.
6.5.2.1 Programmed exposure (Latero-Lateral) (refer to Figure 9)
Change the previous examination be made in manual exposure, to pass

to the pre-programmed exposure press on of the program button: Adult
33 or Child 34.
To program the new configuration operate on push button Adult 33 and

Child 34, and on push buttons Large Size 35, Medium Size 36 and
Small Size 37; in the different programmed configurations there are only
variations in the exposure time but not in the kV values. The following
shows the pre-programmed values according to the combination made
for a Latero Lateral exposure:

(35) (36) (37)
Adult (33) 80kV - 1sec 80kV - 0,8sec 80kV - 0,7sec
Child (34) 80kV - 0,7sec 80kV - 0,5sec 80kV - 0,4sec
Such values have been set bearing in mind the screens-film combination
and subsequent mA calibration as reported in chapter 4.
NOTE:
* The kV and time values for Postero-Anterior or Anterior-Posterior
examination must be manually set as indicated on the table of next
paragraph.

USER'S MANUAL
6.5.2.2 Manual exposure (refer to Figure 9)
Should a manual exposure be chosen, there will be the possibility to

change both the kV and time values operating as hereunder described:
1. Press the button kV 38 or time 39 the enabling button will light up.
2. Depress buttons 41 (increase) or 40 (decrease) on the hand control
selecting the desired kV value to be used. After 2 seconds, the
function button LED stops blinking. The unit is now ready for the
next step.
NOTE:
* The kV can vary from a minimum of 60kV to a maximum of 85kV by
steps of 5kV.
The time (second) can have one of the following values:
0.20 - 0.23 - 0.26 - 0.30 - 0.33 - 0.36 - 0.40 - 0.45 - 0.50 - 0.60
0.70 - 0.80 - 0.90 - 1.00 - 1.30 - 1.60 - 2.00 - 2.50 - 3.00
If, after having selected the maximum or minimum value of kV or

seconds, a further increase or decrease is erroneously asked, the
following messages Minimum o Maximum; will be displayed. Afterwards
the set minimum or maximum value of kV or seconds will appear on
display.
To take a Postero-Anterior (PA) or Anterior-Postero (AP) projection you

must set kV and Times as specified in the following table taking into
consideration the screens-films combinations and consequent mA
calibration as reported at chapter 4.

(35) (36) (37)
Adult (33) 80kV - 2sec 80kV - 1,6sec 80kV - 1,3sec
Child (34) 80kV - 1,3sec 80kV - 1sec 80kV - 0,8sec

USER'S MANUAL
6.5.3 Preparing the patient (refer to Figure 10)
1. The patient must be prepared as per point 6.2.3. steps 1and 2.

2. Open the skull-clamp rods 60, to maximum aperture by means of
knob 61.
3. Move the nose-rest unit 54 outwards as far as possible after
releasing it by means of knob 59.
4. Raise the nose-rest rod 57 as much as possible and rotate the
Frankfurt plane alignment rod 55 outwards.
5. Bring the patient to the skull-clamp unit in erect position and
position the centre of the skull-clamp rods (previously disinfected) in
the auricular opening. To do this turn the slider by means of handle
62 and the brake release button 63.
6. Fastern the patient's head between the rods so that the points enter
the auricular opening (Figure 6).
7. Bring up the nose-rest 54 and adjust the patient's Frankfurt plane
(plane passing through the auricular openings and the lower part of
the orbital cavity) according to the plane defined by the centre points
58 and the alignment rod 55 when the latter is fully downward
(Figure 6).
8. Exclude alignment rod 55 by rotating it outwards and bring up the
nose rest unit 53, at the same time adjusting rod 57 until contact
with the front-to-nasal (Figure 7).

USER'S MANUAL
Figure 6
Figure 7

USER'S MANUAL
6.5.4 Performing the exposure (refer to Figure 9)
NOTE:
* During the emission of X-rays protection of the operator and
surrounding personnel must be in accordance with the rules in force in
the respective countries.
The X-ray activation always be commanded from an X-ray protected area
via remote control. If it is necessary the operator must stand at a
distance of at least 2 meters (78 ¾ inches) away from the X-ray source
and, if possible, on the opposite direction. No other persons other than
the operator and the patient, are allowed to stay in the examination
room during the examination.
1. Check if the exposure data are correct (paragraph 6.2.2), press the
rays button 42 during the whole time of the exposure as the control
is a dead man type, checking the simultaneous operations of the
X-ray signalling light 43 and the acoustic ray signal.
Should the X-ray Cassette not be inserted, the message "CEPH FILM
HOLDER NOT PRESENT" will be displayed.
NOTE:
* The start of arm rotation and the emission of rays take place with a delay
of four seconds after pressing button 42 allowing preheating of the tube
filament and check all the set value.
2. After exposure, release the patient from the positioning device,

remove the film cassette and proceed to open the cassette and
develop the film in the dark room. The following message will be
displayed "Wait, please ......." which identify an automatic
countdown of 1 minute allowing the cooling of the tubehead anode.
NOTE:
* After each examination, replace the ear centering pins.
WARNING:
, Should the patient move during the exposure, stop the exposure
immediately by releasing the rays control button 42 thus stopping the
rays emission.
The message "Change film please" will be displayed for a few seconds, it
will then be opportune to remove the cassette and insert a new film in
the dark room.

USER'S MANUAL
NOTE:
* Should the film in the cassette not be replaced and a subsequent
exposure carried out, no impediment message will be displayed, but due
to the double exposure the film will give non diagnostic results.
If for external reasons or incorrect operation the rays emission times

should exceed 3 seconds, a backup security timer will come into
operation cutting out the emission after 5 seconds.

USER'S MANUAL
6.6 Messages on display (refer to Figure 8 and Figure 9)
As described in chapter 4, ROTOGRAPH PLUS is entirely controlled by a

microprocessor that, besides controlling the emission parameters and
the line voltage fluctuation, indicates the different equipment's operating
modes by means of appropriated messages on display 44, the eventual
anomalies and mistakes. The following table shows the different
messages that could be displayed, their cause and relevant actions.
Message displayed Reference Cause What to do
Minimum 6.2.2.2 and With control button 40 Select a correct value

6.5.2.2 it has been required a
value lower than the
allowed one
Maximum 6.2.2.2 and With control button 41 Select a correct value
6.5.2.2 it has been required a
value higher than the
allowed one
Wait, please..... 6.2.4, X-ray exposure has Waiting time (4min) for
6.3.1.4, been performed PAN or TMJ exposures,
6.3.2.3 and 1min CEPH exposures
6.5.4
Equipment not set 6.2.1, Not all interlocks are Press a second time the
6.3.1.1 and enabled function button to
6.5.1 display the interlock to
be enabled
PAN/TMJ film holder 6.2.1. step 1 Missing of the PAN film Insert the cassette in
not present holder cassette 17 in the relevant support 16
the relevant support
Please rotate film NO reference The film holder cassette Rotate the knurled knob
holder to PAN/TMJ1 support 16 is not in the 13 clockwise to position
position correct position the cassette
Rotating arm unlocked 6.5.1. step 1 The arm is in PAN/TMJ Rotate clockwise the
condition arm upper knob 5
CEPH film holder not 6.5.4 CEPH X-ray has been Set the cassette in the
present requested without the special support
cassette being inserted
Please rotate X-ray 6.2.1 The X-ray generator is Operating on the lever 4
generator on PAN/TMJ in CEPH position rotate the X-ray
position generator clockwise
Please rotate X-ray 6.5.1. step 2 The X-ray generator is Operating on the lever 4
generator on CEPH in PAN/TMJ position rotate the X-ray
position generator anti-clockwise
Please insert the 6.2.1 The CEPH collimator is Insert the PAN/TMJ
PAN/TMJ beam limiter in or there is no collimator
collimator inserted

USER'S MANUAL
Message displayed Reference Cause What to do
Please insert the CEPH 6.5.1. step 3 The PAN/TMJ Insert the CEPH
beam limiter collimator is in or there collimator
is no collimator
inserted
CEPH modality not NO reference CEPH control button Press the button of
enabled 28 pressed and unit another examination
not equipped with this (NOT CEPH)
device
Please unlock rotating 6.2.1 The arm is in CEPH Rotate the upper knob 5
arm position anti-clockwise
Please rotate film 6.3.2.3 After having requested Rotate the film holder
holder to TMJ2 a TMJ2 exposure, the anti-clockwise operating
position film holder is not in the on the knurled knob 13
correct position
Line voltage too low NO reference Line voltage outside the (1) Make sure the line
-10% of the nominal voltage is within the
value ±10% of the nominal
value.
Line voltage too high NO reference Line voltage outside the (1) Make sure the line
+10% of the nominal voltage is within the
value ±10% of the nominal
value.
Impossible to regulate NO reference There is a continuous Call Technical
the line voltage voltage fluctuation Assistance
during the cathode
pre-ignition phase
Push "RESET" 6.2.4, A PAN or TMJ cycle has Press the RESET button
6.3.1.4 and been interrupted while 32
6.3.2.3 in progress
OK 6.2.4, The arm return run is Release button RESET
6.3.1.4 and completed 32
6.3.2.3
TMJ modality not NO reference TMJ examination has Press the button of
enabled been requested on a another examination
unit not equipped with (NOT TMJ)
this feature
Memory data NO reference Call Technical
corrupted! Call Assistance
Technical Assistance
NO ANSWR NO reference Call Technical
Assistance
Out of Order N° 1 ! Call NO reference Call Technical
Technical Assistance Assistance
(1) If line voltage is outside the specified range (± 10%), contact the local
power company in order to take the necessary corrective actions.
Villa Sistemi Medicali S.p.a. will not bear any cost for proper line
set-up.

USER'S MANUAL
6.7 Identification and correction of defects in dental

radiographs exposure
6.7.1 Defects due to wrong patient positioning
• Incisor too wide and indistinct

The patient does not grip the bite block with the incisors or bends
the rod towards the outside of the equipment.
Corrective action:
Reposition the patient, also checking alignment of the Frankfurt
plane through the centring device. Please refer to the note on the
centring (see paragraph 6.2.3. steps 3, 4 and 5)
• Incisor too small and indistinct

The patient is positioned with an error opposite to point "a" above.
Corrective action:
Refer to point "a" above
• Radiograph with white central zone

The patient's spinal column prevents the rays from passing because
it is too compressed.
Corrective action:
Recheck alignment of Frankfurt plane, and try to stretch the cervical
tract of the column as much as possible by correcting slider height
and shifting the patient's feet towards the stand; (see paragraph
6.2.3. steps 3, 4, 5 and 6)
• Dental arch not symmetrical

The sagittal median line does not correspond to the reference
centring light.
Corrective action:
Reposition the patient (see paragraph 6.2.3. step 6)
• Upper apical zone too dense

The patient is not keeping his lips tightly together and is not holding
the tongue against the palate.
Corrective action:
See point 6.2.3. step 8.

USER'S MANUAL
6.7.2 Defects due to wrong setting of radiological data and dark

room
• Under-exposed or over-exposed film

The number of kV set are not adequate for the patient's build, more
likely an error in development.
Remedy: repeat the examination with a different value: see
paragraph 6.2.4. If the error happens again, call the
Technical Assistance
• Film completely black

The film has been exposed to light or undergone radiation.
Remedy: check efficiency of the dark-room and do not keep new
film near the source of X-rays
• Veiled film
The edges of the film not involved in the dental arch are not fully
transparent, with absence of definition on whole film.
Remedy: do not use expired films, check the efficiency of the safe
light in the dark-room and do not keep films near to
sources of radiation
• Film with branched striations

The film has accumulated electrostatic charges owing to rapid
rubbing against its casing, or the intensifying screens have not been
treated with antistatic liquid.
Remedy: clean the screens with the appropriate liquid
• Film with indistinct detail but good contrast

The film is not well pressed between the intensifying screens.
Remedy: change the cassette and the plate felt
• Completely white film

It has not been exposed to X-rays or wrong development.
Remedy: verify the X-rays emission by checking light and acoustic
signal (light 43 Figure 9), If the defect persist, check the
development process. If still not corrected, call for
Technical Assistance.

USER'S MANUAL
6.7.3 Defects in the film due to equipment
• If the film exhibits zones not fully radiated or even completely white,
it almost certainly means a defect of alignment between beam of
X-rays and film or partial or total absence of radiation: in this cases
call the Technical Assistance
• In case of Ceph examinations with absence of evidencing of patients

profile in a latero-lateral sense, have the filter setting checked by the
Technical Assistance.

USER'S MANUAL
11
5
9
ROTOGRAPH PLUS
12 14
7 10 15
13
4 25
16
3
17
26
18
24
2
22 23 20
1
21
Figure 8: Stand
1. "PANORAMIC" chin support 14. Slit assembly

2. Bite Block 15. Rotating arm
3. Tubehead 16. Film cassette support
4. Tube rotation release-lever for 17. Film cassette
panoramic-ceph position
5. Arm locking pin 18. Horizontal light beam height control
knob
6. Centering mirror 20. Light cross beam button
7. Skull / Temple clamp support 21. Chin support TMJ, SINUS. Also used
as an accessory to raise children's
chin by sandwiching it with the
standard Panoramic chin support
9. Skull / Temple clamp control knob 22. Patient positioning handle and slider
10. Motor group unit 23. Support unit of the motor group
11. Column 24. Brake release button
12. Slider 25. Collimator for PAN/TMJ/CEPH
13. Release handle for positioning 26. Focus position point
cassette in PAN/TMJ modes

USER'S MANUAL
Figure 9: Remote control
27 Panoramic mode Selection 36 Medium Size Selection

28 CEPH mode Selection 37 Small Size Selection
29 TMJ1 mode Selection 38 kV Selection
30 TMJ2 mode Selection 39 Push-button Multifunctional
31 Test mode ("dead man" button) 40 Decrease kVangles or
times(CEPH)
32 RESET ("dead man" button) 41 Increase kV angles or
times(CEPH)
33 Adult Selection 42 X-rays push-button ("dead man"
button)
34 Child Selection 43 X-rays emission pilot LED
35 Large Size Selection 44 Alphanumeric display

USER'S MANUAL
Figure 10: Skull-clamp unit for cephalometry
50. Skull-clamp unit release knob 58. Centring ring

51. Reference pin for skull-clamp 59. Nose-rest block knob
53. Cassette support unit 60. Skull-clamp unit rod
54. Nose-rest unit 61. Distance regulating knobs for
skull-clamp unit rods
55. Frankfurt plane reference rod 62 Handle for arm positioning
according to the patient tallness
56. Scale referred to nose, for 63 Break button
repetition of exposure
57. Nose-rest rod

USER'S MANUAL
Maintenance
7. MAINTENANCE
As for all the electrical devices, in addition to proper use this unit also
requires periodical checks and maintenance. This precautions will
insure a safe and efficient performance of the device.
The preventive maintenance consists of checks that can be carried out

directly by the operator or by the authorized service personnel.
The checks that can be carried out directly by the operator are the
following:
Interval Type of check

Daily - check that the tubehead does not have oil
leakage
- check that the cable of the remote control is not
damaged
- check that the unit does not show damages that
may affect the protection against radiation
- check that no metallic noise are generated by the
column or the rotating assembly.
Once a week - check that the metal ropes of the column are not
damaged or broken (the ropes can be seen on the
side of the column)
- while performing exposure, release the X-ray
push button and check that the beeper stops
beeping immediately.
Every 6 months - check that the label are not damaged and well
attached.
WARNING:
, If any of the above checks give negative results, the operator must
contact the authorized service personnel.

USER'S MANUAL
MAINTENANCE LOG-BOOK
This log-book has to be filled in by the authorized VILLA SISTEMI MEDICALI

engineer after installation and after performing the preventive or corrective
maintenance visits.
Installation: Date ........... Technician ...................
Maintenance: Date ............. Technician ...................
Cause .............................................
Cause .............................................
Cause .............................................
Cause .............................................
Cause .............................................
Cause .............................................

USER'S MANUAL
Final test table

This table is reserved to Qualified and Trained Service Technician
Data setted on Hand Control for Rotograph PLUS S.N. ................................

Voltage supply for rotation motor A1 V1 ........ R39 A1 V1 ........ R40
Decelerating ramp for Central OPG R41 ........ sec
S0 = On Off S3 = On Off
SA= On Off
S1 = ITA ENG FRA ESP DEU
S7 = 0 1 2 3 4 5 6 7
Angular Control Settings

S5 Machine Control Functions
Adult OPG Values Adult TMJ1 Adult TMJ 2

T1= 2.00 sec T1= 2.00 sec T1= 2.00 sec
A2= . . . . . . . . . . .Degrees A1= . . . . . . . . . . .Degrees A1= . . . . . . . . . . .Degrees
T2= 18 sec ± 10% T2= 16 sec ± 10% T2= 16 sec ± 10%
T3= 17 sec ± 10% T3= 5,20 sec ± 10% T3= 5,20 sec ± 10%
Child OPG Child TMJ 1 Child TMJ 2
T1= 2.00 sec T1= 2.00 sec T1= 2.00 sec
T2= 16 sec ± 10% T2= 16 sec ± 10% T2= 16 sec ± 10%
T3= 14 sec ± 10% T3= 4,70 sec ± 10% T3= 4,70 sec ± 10%
T2= 16 sec ±10% with decel.
T3= 14 sec ±10% with decel.
Diaphragm Diaphragm Diaphragm
(PAN) (18x24 asym.) (10x8” asym.)
S/N ............. ............. ............
(18x24 sym.) (8x10” sym.) (24x18 asym.)
S/N ............. ............. ............
(8x10” asym.) (30x24 sym.) (12x10” sym.)
S/N ............. ............. ............
Control
Villa Sistemi Medicali S.p.a.
...................... Date . . . . . . . . . . . . .

USER'S MANUAL
THIS PAGE IS INTENTIONALLY LEFT BLANK

Cod. 6908914203_Rev.2 0434
VILLA SISTEMI MEDICALI S.p.a.

Via Delle Azalee, 3
20090 Buccinasco (MI) - ITALY
Tel. (+39) 02 48859.1
Fax (+39) 02 4881844

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ROTOGRAPH PLUS 0434

Rev. Date Page/s Modification description

0 21.07.98 - First release

2 22.11.02 10, 45 New intensifying screens.

(Rev. 2) RTG PLUS - CE

THIS PAGE IS INTENTIONALLY LEFT BLANK

RTG PLUS - CE (Rev. 2)

3. CLEANING AND DISINFECTING PROCEDURES 6

(Rev. 1) i RTG PLUS - CE

6.4 Sinus examination ................................................................................ 36

This publication can only be reproduced, transmitted, transcribed, or translated

RTG PLUS - CE ii (Rev. 1)

ROTOGRAPH PLUS, manufactured by Villa Sistemi Medicali, is a

ROTOGRAPH PLUS is available in the following version:

1.1 Icons appearing in the manual

Indicates a “NOTE”; the utmost attention shall be devoted to the

Indicates a “WARNING”; paragraphs marked with this icon cover

(Rev. 1) 1 RTG PLUS - CE

VILLA SISTEMI MEDICALI designs and manufactures equipment in

Villa Sistemi Medicali shall not be responsible for:

Only qualified service personnel, authorized by VILLA SISTEMI

Only authorized personnel is allowed to remove the tubehead from

RTG PLUS - CE 2 (Rev. 1)

The system has not been designed to be used in presence of vapours,

Always disconnect from mains before cleaning the machine.

Where necessary, accessories such as lead-sealed aprons must be used

ROTOGRAPH PLUS has been developed for continuous use with

Although the appliance has been designed to have a reasonable degree of

Clean or eventually disinfect the chin support, positioning handles,

(Rev. 1) 3 RTG PLUS - CE

Although the X-ray dosage supplied by dental radiology appliances is on

2.2 Environmental risk and disposal

A number of machine parts contain materials and liquids that upon

The machine contains the following materials and/or components:

RTG PLUS - CE 4 (Rev. 1)

2.3 Symbols used

Equipment with Type B applied parts (according to

N Connection to neutral conductor

L Connection to line conductor

OFF ; equipment not connected to power line

 ON ; equipment connected to power line

Warning: read the documentation provided with the

Conformity to the CE 93/42 Directive

(Rev. 1) 5 RTG PLUS - CE

3. CLEANING AND DISINFECTING

• Clean the painted surfaces, the accessories and the connection

RTG PLUS - CE 6 (Rev. 1)

4.1 Identification labels

ROTOGRAPH PLUS is labeled with a set of labels identifying different

The following picture shows the position of the different labels:

(Rev. 1) 7 RTG PLUS - CE

RTG PLUS - CE 8 (Rev. 1)

ROTOGRAPH PLUS has been designed to perform the following

• Panoramic examination (all versions)

All the allowed examination may be made with different parameters

ROTOGRAPH PLUS is controlled by a soft touch console and equipped

The excellent quality radiographs thus obtained is the result of a clever

ROTOGRAPH PLUS, besides operating in the programmed mode, can

In the Panoramic and TMJ modes, with all interlock enabled, it is