Professional Documents
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The manufacturer OWANDY RADIOLOGY reserves the right to make modifications to its products or to their
specifications in order to improve the performance, quality, or ease of production. Specifications of products or
accessories may be modified without prior notice.
No part of this publication can be reproduced, transmitted, transcribed or translated without the approval of
OWANDY RADIOLOGY
This manual is the English translation of the original Italian manual version.
OWANDY RADIOLOGY
2 rue des Vieilles Vignes
77183 Croissy-Beaubourg, FRANCE
0051 Tel. (+33) 1 64 11 18 18
Year in which the CE marking was affixed: 2010 Fax (+33) 1 64 11 18 10
Contents
5.3 Loading curve tube and cooling curve anode .................................................................................. 47
5.4 Accessories...................................................................................................................................... 48
5.5 Measurement method technical factors........................................................................................... 49
5.5.1 Invasive method ....................................................................................................................... 49
5.5.2 Non-invasive method ............................................................................................................... 49
5.6 Technical service programs ............................................................................................................. 50
5.6.1 Accessing technical service menus ......................................................................................... 50
5.6.2 Control panel service mode ..................................................................................................... 51
5.6.3 CONFIGURATION menu (password 92) ................................................................................. 52
5.6.4 AXIS ALIGNMENT menu (password 118)............................................................................... 60
5.6.5 CEPH SETTINGS menu (password 124) ................................................................................ 63
5.6.6 TROUBLESHOOTING menu (password 112)......................................................................... 66
5.6.7 SYSTEM menu ........................................................................................................................ 70
5.6.8 BURN-IN menu ........................................................................................................................ 70
5.6.9 SHOW CONFIGURATION menu ............................................................................................ 71
5.6.10 Touch screen calibration.......................................................................................................... 71
6. PRE-INSTALLATION........................................................................................................................... 72
6.1 Electrical setup ................................................................................................................................ 72
6.2 Packaging ........................................................................................................................................ 74
6.3 Space requirements......................................................................................................................... 75
6.3.1 Standard version without Ceph option ..................................................................................... 75
6.3.2 Version with Ceph option ......................................................................................................... 76
6.4 Computer requirements ................................................................................................................... 77
6.4.1 I-Max Touch computer requirements ....................................................................................... 77
6.4.2 I-Max Touch 3D computer requirements ................................................................................. 77
7. INSTALLATION ................................................................................................................................... 79
7.1 Preparation wall ............................................................................................................................... 79
7.2 Column mounting ............................................................................................................................. 80
7.2.1 Unpacking column / ceph arm ................................................................................................. 80
7.2.2 Mounting the column ............................................................................................................... 84
7.3 Mounting of the head (rotating arm assembly) ................................................................................ 86
7.3.1 Unpacking the head ................................................................................................................. 86
7.3.2 Mounting the head ................................................................................................................... 88
7.4 Mounting of ceph arm (optional) ...................................................................................................... 91
7.5 How to mount the covers ................................................................................................................. 93
7.6 Inserting sensor in sensor holder .................................................................................................... 94
7.7 Computer installation ....................................................................................................................... 94
7.7.1 Installation I-Max Touch computer and network ...................................................................... 94
7.7.2 Installation I-Max Touch 3D computer and network ................................................................ 95
7.7.3 Installation O.S.P. (drivers) ...................................................................................................... 95
7.7.4 Installation 3D sensor calibration files ..................................................................................... 99
7.7.5 Installation pan and ceph sensor calibration files .................................................................. 100
7.7.6 Installation imaging software ................................................................................................. 100
7.8 Final installation checks ................................................................................................................. 100
7.8.1 Verification computer setup ................................................................................................... 100
7.8.2 Verification firmware versions ................................................................................................ 101
7.8.3 Verification panoramic function.............................................................................................. 101
7.8.4 Verification 3D function .......................................................................................................... 102
7.8.5 Verification ceph function....................................................................................................... 103
7.8.6 Verification exposure parameters - Invasive method ............................................................ 107
7.8.7 Verification exposure parameters - Non-invasive method ..................................................... 109
1. INTRODUCTION
NOTE: The present manual is updated for the product it is sold with in order to
guarantee an adequate reference to perform diagnostics and repairs normally carried out by
the service engineer. The manual may not reflect changes to the product not impacting
service operations.
This manual provides the instructions for proper and safe installation and maintenance of the appliance by
technical personnel.
This manual is limited to the description of the radiographic equipment; the instructions for the image
acquisition, manipulation and processing are given in the user manual supplied with the imaging software
used with the I-Max Touch or I-Max Touch 3D unit.
WARNING:
1. The I-Max Touch/I-Max Touch 3D is an electro-medical device and it can be used only
under the supervision of a physician or of highly qualified personnel, with the necessary
knowledge on X-ray protection.
2. The device must be used in compliance with the procedures described, and never be
used for purposes different from those herewith indicated.
3. The user is liable with regards to the legal fulfillment related to the installation and the
operation of the device.
For any technical queries please contact the technical service of your vendor.
The evolution of panoramic X-ray units now provides, in addition to traditional methods of examination
(Panoramic, TMJ, Sinus, etc.), the use of three-dimensional images of the patient's maxillofacial complex.
This allows the doctor to investigate a targeted selection of the patient's mouth and to use it both during the
planning phase of the treatment as well as a diagnostic aid. The I-Max Touch 3D produced by Owandy
Radiology is a complete panoramic system that allows for the acquisition of all X-ray examinations commonly
used in dentistry and orthodontics (excluding intraoral radiographs) and also allows the acquisition of
volumetric tomographic, or 3D, X-rays. In this type of device the linear digital sensor traditionally used in the
digital panoramic X-rays has been replaced by a wide range digital sensor also known as a flat panel. These
sensors allow for the capture of an area of the maxillofacial complex that includes the most important
anatomical details by acquiring a series of two-dimensional images (imaging) and reconstructing it with a
computer.
These options are available for the I-Max Touch and I-Max Touch 3D and must be ordered separately:
Digital ceph; allows the acquisition of the following exams, available in High Resolution mode or
Normal Resolution (high speed):
o Ceph exam in different formats.
o Carpus exam.
The I-Max Touch 3D uses the Varian PaxScan 1313DX wide range digital system, used for the acquisition of
3D and panoramic type images. The flat panel sensor functions as a normal digital sensor. Unlike traditional
sensors used for panoramic exams that normally return one image column at a time, the flat panel returns
the entire contents of the sensor. Special functions inside the sensor also allow the acquisition of a specific
part of the sensor, functioning as a normal digital sensor. The system must be connected to a dedicated
computer, on which is installed all the software needed for image acquisition, processing and display. The
resulting images are stored in the system's database in correspondence with the selected patient.
The cephalometric images on the I-Max Touch or I-Max Touch 3D are obtained using a cephalometric digital
system designed by Owandy, similar to that for the panoramic acquisitions on the I-Max Touch.
Indicates a NOTE; please read the items marked by this icon thoroughly.
This icon indicates a WARNING; the items marked by this icon refer to the safety aspects of the
patient and/or the operator.
2. USABILITY
The I-Max Touch or I-Max Touch 3D medical system is intended to be used in radiology or dental practices.
In the first case the user is either the radiologist or the technician specialized in radiology, in the latter case it
is the dentist. The radiologist or the dentist is responsible for the assessment of the risk/benefit ratio. In both
cases, these are people who already have basic knowledge about:
Emission of ionizing radiation.
Danger of physical harm related to the excessive use of ionizing radiation.
Methods to reduce the risk of excessive radiation to the patient (use of lead-lined protections, etc.).
The operator must be familiar in the use of a personal computer and related programs, in order to use the
functions on the computer easily.
2.1 Training
The operator training follows at the end of the system's installation and concerns both the use of the system
and the image acquisition and display programs. The training does not require the use of special tools. The
user manual describes the steps necessary to perform standard panoramic and cephalometric type X-rays
and volumetric X-rays (or 3D).
CAUTION: Federal law restricts this device to sale by or on the order of a dentist or
any other practitioner licensed by the law of the State in which he practices to use or order
the use of the device.
3. SAFETY INFORMATION
Owandy Radiology designs and builds its devices in compliance with the safety requirements; furthermore it
supplies all information necessary for the correct use and the warnings related to any danger associated with
X-ray generating units.
Installation and any technical interventions must only be performed by qualified technicians authorized by
Owandy Radiology. Only authorized personnel can remove the covers and/or have access to the
components under tension.
In compliance with the IEC 60601-1 standard, the modification of the equipment or its parts is strictly
prohibited.
3.1.1 Standards
The I-Max Touch complies with the following standards:
General safety:
o IEC 60601-1:1988+A1:1991+A2:1995
o IEC 60601-1-4:1996+A1:1999
o IEC 60601-2-7:1998
o IEC 60601-2-28:1993
o IEC 60601-2-32:1994
Electromagnetic compatibility:
o IEC 60601-1-2:2001
Protection against radiation:
o IEC 60601-1-3:1994
o IEC 60825-1:1993+A1:1997+A2:2001
0051 - Ensures the compliance of the I-Max Touch/I-Max Touch 3D to the Medical Device Directive
93/42/EEC and amendments issued by the European Community.
3.1.2 Classifications
The I-Max Touch is an electro-medical X-ray device belonging to Class 1 and Type B as per the IEC 60601-
1 classification; it foreseen for continuous working at intermittent load.
According to the CE 93/42 directive for medical devices the equipment belongs to class II B.
According to the Canadian MDR the equipment belongs to class II.
According to FDA 21 CFR the equipment belongs to class II (110-120V version only).
The I-Max Touch 3D is a class I electro-medical device and Type B as per the IEC 60601-1 classification.
The classification according to EC Directive 93/42 and subsequent amendments for medical devices is Class
II b.
3.2 Warnings
The I-Max Touch and I-Max Touch 3D units must be used in dental surgeries, radiology and hospital
surroundings.
The unit has been built to support a continuous operation at intermittent load; therefore please follow the use
cycles described in the manual to enable the device to cool down.
The unit must be switched off while using devices such as electrosurgical devices or similar apparatus.
This device has not been designed to be used in environments where vapors, anesthetic mixtures flammable
with air, or oxygen and nitrous oxide can be detected.
Do not let water or other liquids seep into the device as this could cause short-circuits and corrosion.
Wherever necessary use the appropriate accessories such as leaded aprons to protect the patient from
radiation.
While performing the image acquisition no-one apart from the operator and the patient must remain in the
room.
WARNING: Precautions to take when using the laser centring devices (Class I
according to EN60825-1):
It is necessary to have an adequate illumination in the room.
Do not look into the output windows of the laser centring units.
Do not stare at the reflections of the laser pointers.
Instruct the patient to keep his/her eyes closed as long as the laser pointers are
switched on.
Before starting an examination, the patient must remove earrings, glasses, necklaces
and anything else that could reflect the laser beam or affect the radiographic image.
Do not clean the openings of the laser centring devices with tools that could modify
the optics. Necessary cleaning must be performed only by authorised technicians.
Operations different than those indicated could cause dangerous non-ionising
radiations to be emitted.
WARNING: The USB port on the control panel MUST NOT be used with an external
harddisk; it must only be used only with USB memory sticks.
The centering bite or the protective bite sleeve, the head strip for 3D examinations and the ear
centering devices of the cephalostat must be replaced after each examination in which they were
used.
Clean and disinfect all parts that come into contact with the patient.
Before cleaning the device please disconnect it from the line voltage. Pushing the ON/OFF button at the
base of the equipment must not switch on the unit.
Although the dose supplied by dental X-ray units is quite low and distributed on a small surface, the operator
must adopt the precautions and/or suitable protection for the patient and himself during the image
acquisition. It is advisable to control the X-ray emission from a protected area by means of a remote control.
If it is necessary to operate the unit near the patient stay as far as the remote control cable allows or at least
1.5 m (4.9 ft) (I-Max Touch) or 2m (6.6 ft) (I-Max Touch 3D) both from the X-ray source and from the patient
as shown in the imagesfigures below.
Minimum distance from X-ray source 1.5 m (4.9 ft) or 2 m (6.6 ft) Protected area
Figure 1 - Panoramic version
Minimum distance from X-ray source 1.5 m (4.9 ft) or 2 m (6.6 ft) Protected area
Figure 2 - Cephalometric version
NOTE: Do not apply movements to the rotating arm or the tube-head when the
equipment is on. Never try to rotate the rotating arm manually when the unit is switched on,
to avoid permanent damage to the unit. The manual movement is only allowed in case of
error 206 (no power to motors) to allow the patient to exit the unit.
WARNING: The network connector on the base of the I-Max Touch 3D column must
be connected through a shielded Ethernet cable "Cat.5e" or greater to the dedicated
computer for image acquisition and 3D and panoramic reconstruction. Do not use this
connector to connect the I-Max Touch 3D to existing LAN networks. The Ethernet cable of an
I-Max Touch (2D) unit however can be connected to an existing network.
1 0.025 0.03 1
0 0.03 C 0.004 0
-1 0.03 0.02 -1
This figure illustrates the distribution of stray radiation in the horizontal plane at the centre of rotation of the
scanning unit in the area of a 3 x 3 m rectangle. The measurement was performed using a cylindrical
phantom with a diameter of 320 mm and a length of 140 mm placed in the centre of rotation of the scanning
unit, using the "3D Dentition" examination mode and these parameters: 86 kV - 10 mA - 8 s. The distribution
values in the table are expressed as air Kerma for mAs (µGy/mAs).
For transmitters using frequencies below 800 MHz, the distance can be estimated using equation A: d = 4
P
For transmitters using frequencies between 800 MHz and 2.5 GHz, the distance can be estimated using
equation B: d = 2.3 P
where P is the rated power of the transmitter in watt (W) according to the transmitter manufacturer.
For transmitters rated at the maximum output power not listed above, the recommended separation distance
"d" in meters (m) can be estimated using the equation applicable to the frequency of the transmitter where
"P" is the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
NOTE: At 80 MHz and 800 MHz the separation distance for the higher frequency range
applies.
NOTE: These guidelines may not apply to all situations. Electromagnetic propagation
is affected by absorption and reflection of structures, objects and people.
The symbol with the waste bin crossed on the equipment or its packaging, indicates that the
product must be separately collected from other waste at the end of its life.
The separate collection of the present equipment that has reached the end of its life is
organized and managed by the manufacturer. The user who wishes to dispose of this
equipment must contact the manufacturer and follow their system to enable the separate
collection of the equipment at the end of its life.
Suitable separate waste collection for the subsequent start of the equipment discarded for
recycling, for treatment and for environmentally friendly disposal, contributes in preventing
possible adverse effects on the environment and health and promotes the reuse and/or
recycling of materials of which the equipment is comprised.
Illegal disposal of the product by the holder implies the application of administrative
sanctions provided by law
In some of its parts, the device contains materials and liquids that, at the end of the
lifespan of the unit, must be disposed of at the appropriate disposal centers
~
Alternating current
N Connection point to the neutral conductor
L Connection point to the line conductor
Protection earthing
Operation earthing
Laser
Dangerous voltage
Total filtration
Tube-head
X-ray tube
4. DESCRIPTION
6, 7
2 4
1, 8 (*)
8 - Warning label
7 - Laser symbol label (x2) (110-120V version only)
5, 6
1, 7
7 - Warning label
(110-120V version only)
The I-Max Touch 3D is a complete panoramic system that enables the user to perform all X-rays acquisitions
commonly required in the dental field (except for intra-oral X-rays) and volumetric three-dimensional images.
The standard version performs Panoramic, Emi-panoramic, Reduced dose panoramic, Frontal dentition,
Improved orthogonality Panoramic, Sinus, TMJ and volumetric (3D) examinations.
Optional functions enable the I-Max Touch or I-Max Touch 3D to perform these additional examinations:
Ceph; it allows you to carry out the following examinations:
o Ceph exam in different formats
o Carpus exam.
From the electrical point of view, the system can be divided into 4 main blocks:
Power supply assembly
Main CPU board (A5)
Generator board (A10), Generator CPU board (A9) and tubehead
Column CPU board (A1)
Control panel with its electronic board (A4)
All control boards above listed are equipped with a local microcontroller that shares information with the main
CPU (A5) using a CANBus transmission line and protocol.
Figure 4
Figure 4
The unit does not include a voltage selector circuit for the mains voltage. Therefore, the unit is manufactured
in different versions, depending on the line voltage of the installation place.
The power supply assembly module also includes the column CPU board (A1) that is dedicated to the
control of the vertical column motion during all phases (slow speed, ramp up to high speed, ramp down from
high to low speed, end run microswitches control, etc.).
The CPU board is based on a 32 bit Motorola microprocessor MCF5232 mounted on a piggy-back board
(A6), which also includes the Flash EPROM, the RAM and other logic and passive components. The CPU
board also includes a number of input/output channels necessary for the functioning of the system and 3
stepper motors. Each of these motors is associated to positioning sensors that monitor their functioning; the
signals of these sensors are fed back to the CPU board. The number and the type of sensors depend on the
function of each motor; in general optical switches are used.
Depending on the physical location of the motors in the machine, their signals and the ones of the relevant
positioning sensors are routed directly to the CPU through dedicated cables or through interconnection
boards located closeby. The transmission of the motion from the motor to the relevant movement assemblies
is achieved through toothed belts (rotation motor and Y axis motor) or through actuators (column motor,
primary collimator, Soft Tissue Filter, secondary collimator and ceph sensor). The functioning of the different
motors and relevant positioning sensors can be tested through the use of the service programs (passwords)
described further down in this manual.
The circuits of the CPU board are supplied starting from the +24Vdc (LED H12) provided by the power
supply assembly and generating the requested voltages (+5V, +3.3V and +1.5V). Three LED's on the board
indicate the presence of these 3 voltages (+5V=LED H2, +3.3V=LED H3, +1.5V=LED H5).
XJ6 XJ8
XJ13
XJ12
XJ11
The management of the generator board is done by the dedicated generator CPU board (A9) that is
interfaced with the main CPU board (A5) using a CANBus cable (X20-X20). This cable also has a dedicated
wire to bring the X-ray trigger signal to this board to handle the "dead man switch" directly from this board.
The high frequency (HF) circuit is based on an inverter circuit working at the frequency of about 100 kHz,
which drives the tubehead through an output stage based on IGBT components.
The generator board receives the signals about the X-ray dose it needs to provide (kV and mA) from the
CPU board through CANBus messages; it is the generator CPU that generates the commands used for the
X-ray emission. The generator board provides to the tubehead the voltages that drive the high voltage
transformers that then drive the anode and filament of the X-ray tube; it also provides the relevant timing.
The tubehead is composed of the X-ray tube (CEI OPX/105) inserted in a sealed container together with the
high voltage transformers and filled with dielectric oil.
Checking of the proper functioning of the X-ray emitting system is achieved through the analysis of feedback
signals generated inside the tubehead and transmitted to the generator board and relevant generator CPU.
Possible anomalous conditions are then communicated to the main CPU board (A5) which in turn generates
error codes to alert the operator.
The keyboard electronic board is directly connected to the main CPU board (A5) which controls it. The
language of the messages shown on the display can be selected among different options (English, French,
Spanish, Italian, Portuguese, German, Dutch and Turkish). The language selection is only available for the
user messages; the messages in the service programs are always in English.
9 11 Display
10
15
1 12
7
2
13
5
14
3 8
1
3
Acquired image
Legend: Buttons
1. “Main menu” button: returns to the main
Messages interface
Display: indicates operative messages, warnings 2. “USB” indicator: indicates the connection and
and exposure parameters status of a USB memory stick
3. “Zoom out” button
4. “Zoom in” button
WARNING: The USB port on the control panel MUST NOT be used with an external
harddisk; it must only be used only with USB memory sticks. The USB port is not active on
an I-Max Touch 3D unit.
Display
1 6
Legend: Buttons
1. Directional buttons to scroll through the menus
Messages and parameters
Display: indicates operative messages, warnings 2. “>O<” (patient centering) button: to accept a
and exposure parameters selection / modification
3. “T” (test) button: to cancel a selection /
modification
4. “P” button
5. “M” button
6. “Adult size” button
7. “Bone density” button
5. TECHNICAL CHARACTERISTICS
General features
Device type I-Max Touch / I-Max Touch 3D
Manufacturer OWANDY
Croissy-Beaubourg, France
Class I-Max Touch:
Class II B for European Directive for Medical Devices 93/42
Class II for Canadian MDR
Class I with type B applied parts according to IEC 60601-1
Class II according to 21CFR-subchapter J (for 110-120V version)
Exposure times
Panoramic (Pan) 13.8 s Adult/Child
R/L Emi-panoramic 7.4 s Adult / 7.3 s Child
Reduced dose Panoramic 11.4 s Adult/Child
Improved orthogonality dentition 11.9 s Adult/Child
Frontal dentition 4.4 s Adult/Child
Bitewing 3.2 s Right or Left
6.3 s Right and Left
TMJ mouth closed/open 2.44 s per image for left and right joint in open and closed
condition for a total of 9.7 s
Sinus 9.4 s
Implant I-Max Touch only:
9.2 s for incisives and canines
7.3 s for pre-molars and molars
Volumetric 3D exams I-Max Touch 3D only:
8 s for Dentition and Sinus (20 s rotation)
7.2 s for TMJ Left and TMJ Right (each) (18 s rotation)
Cephalometry (Ceph) Variable exposure time depending on the type of resolution and
size selected; minimum 4.5 s (18x22nR), maximum 15 s
(30x22hR)
Exposure time accuracy ± 10 %
Examination modes
Examination selection Automatic selection for Adult and Child and 3 bone density
types
Automatic selection for Adult and 3 bone density types (Implant
mode only)
Dentition type selection, 3 positions (Panoramic mode only)
Manual selection
Collimator with automatic positioning
Panoramic Standard Panoramic
Right and left Emi-panoramic
Reduced dose Panoramic
Improved orthogonality dentition
Frontal dentition
Right or left Bitewing
Right and left Bitewing
TMJ (Temporo-Mandibular Joint) TMJ mouth closed/open
Sinus Sinus P/A projection
Implant I-Max Touch only:
Automatic selection for Adult and Child, 3 bone density types
Manual selection of the quadrant and the toothnumber
Volumetric 3D exams I-Max Touch 3D only:
Automatic selection for Adult and Child, 3 bone density types
chosen between 4 types of exams: Dentition, TMJ Left, TMJ Right,
Sinus
Cephalometry and Carpus Normal resolution in Latero-Lateral or Antero-Posterior
projections (different sizes)
High resolution in Latero-Lateral or Postero-Anterior
projections (different sizes)
High resolution Carpus exams
Motorized Soft Tissue Filter
Image magnification
Standard Panoramic I-Max Touch: 1:1.23 Adult and Child
I-Max Touch 3D:1:1.28 Adult and Child
TMJ open/close mouth, 4 images I-Max Touch: 1:1.20 (nominal)
I-Max Touch 3D:1:1.25 (nominal)
Sinus I-Max Touch: 1:1.22 (nominal)
I-Max Touch 3D: 1:1.27 (nominal)
Implant I-Max Touch only: 1 : 1.32 (constant)
Ceph 1:1.10 on the sagittal medial plane in LL projection
Tube-head characteristics
Model MRE 05
Manufacturer Villa Sistemi Medicali S.p.A., 20090 Buccinasco (MI), Italia
Type High frequency 200 kHz
(constant potential, ripple 2x inverter frequency: 100kHz)
Maximum tube voltage 86 kVp
kVp accuracy ±8%
Maximum anodic current 12 mA
Anodic current accuracy ± 10 %
Output radiation linearity < 0.2 according to standard IEC 60601-2-7:1998 paragr. 50.102.2
Duty cycle Adaptive duty cycle depending on the exposure parameters: from
1:8 (at 60 kV, 6 mA) up to 1:20 (at 76 kV, 12 mA)
Further reduction for three exposures in close-up sequence: from
1:3.6 (at 60 kV, 6 mA) up to 1:9 (at 76 kV, 12 mA)
Nominal power 1.032 kW (86 kVp - 12 mA - 4 s)
Total filtration 2.5mm Al eq. at 70 kVp
HVL (Half value layer) > 2.0 mm Al eq. at 60 kVp
> 2.7 mm Al eq. at 74 kVp
> 3.1 mm Al eq. at 80 kVp
> 3.2 mm Al eq. at 86 kVp
Transformer insulation Oil bath
Cooling Convection
Leakage radiation at 1 m < 0.5 mGy/h at 86 kVp - 12 mA - 3 s duty cycle 1/16
Tube-head maximum thermal capacity 310 kJ
Pan sensor
Type CCD
Scintillator screen Cesium iodide (CsI)
Bit depth 14 bit
Resolution 10.4 lp/mm
5.2 lp/mm in binning 2x2
Sensor pixel size 48 µm
96 µm in binning 2x2
Sensitive area (H x L) 146 x 6 mm (8.7 x 0.2")
Number of pixels (H) 1536
PanCeph sensor
Type CCD
Scintillator screen Cesium iodide (CsI)
Bit depth 14 bit
Resolution 10.4 lp/mm
5.2 lp/mm in binning 2x2
Sensor pixel size 48 µm
96 µm in binning 2x2 (Pan and Ceph hR)
144 µm in binning 3x3 (Ceph nR)
Sensitive area (H x L) 220 x 6 mm (8.7 x 0.2")
Number of pixels (H) 1536 (Pan and Ceph nR)
2304 (Ceph hR)
NOTE: The I-Max Touch 3D version without the cephalometric arm uses only the flat
panel sensor for both the 3D volumes and for the panoramic images (narrow beam), while in
the version with the cephalometric arm a second (PanCeph) sensor is used for the Ceph
exams.
Mechanical features
SID (Source to Image Distance) Pan, I-Max Touch: 50 cm (20”)
TMJ and Sinus I-Max Touch 3D: 52 cm (20.5")
SID (Source to Image Distance) Ceph 165 cm (65")
Telescopic motorized column run 85 cm (33.5")
Maximum total height 245 cm (96.5")
Weight 161 kg (355 lb) standard version
186 kg (410 lb) version with Ceph arm
Column weight 87 kg (192 lb)
Weight of head, rotating arm, tube- 74 kg (163 lb)
head and sensor holder
Ceph arm weight 25 kg (55 lb)
Weight optional free standing base 30 kg (66 lb)
Sensor holder weight (Pan and 2 kg (4.5 lb)
PanCeph sensors)
Working conditions
Minimum dimensions of the room 130 x 120 cm (52" x 47.2") without Ceph arm
(refer to the Service Manual) 145 x 200 cm (57" x 78.7") with Ceph arm
Recommended dimensions of the 130 x 140 cm (51.2" x 55.1") without Ceph arm
room (refer to the Service Manual) 160 x 220 cm (63" x 86.6") with Ceph arm
Maximum working temperature range +10°C to +40°C (+50°F to +104°F)
Relative working humidity (RH) range 30% to 75%
Temperature range for transport and -20°C to +70°C (-4°F to +158°F)
storing
Humidity range for transport and < 95% without condensation
storing
Minimum atmospheric pressure for 630 hPa
transport and storing
5.2 Dimensions
1020 (40,16")
Ø 1040 (40,95")
Ø 1140 (44,88")
with free standing base
Figure 7 – I-Max Touch dimensions, standard version
1020 (40,16")
Ø 1040 (40,95")
Ø 1140 (44,88")
with free standing base
1910 (75,20")
1970 (77,56") with free standing base
Figure 8 – I-Max Touch dimensions, version equipped with cephalometric option
1 6 0 0 (6 3 ,0 0 ") ÷ 24 5 0 (9 6 ,4 6 ")
9 0 5 (3 5 ,63 ") ÷ 17 5 5 (6 9 ,1 0 ")
1 2 71 (50,0 4")
Ø 1 0 4 0 (4 0 ,9 5 ")
Ø 1 1 4 0 (4 4 ,8 8 ")
w ith free standin g b ase
Figure 7 – I-Max Touch 3D dimensions, standard version
1 0 20 (40,16")
1 6 0 0 (6 3 ,0 0 ") ÷ 24 5 0 (9 6 ,4 6 ")
9 2 7 (3 6 ,50 ") ÷ 17 7 7 (6 9 ,9 6 ")
9 0 5 (3 5 ,63 ") ÷ 17 5 5 (6 9 ,1 0 ")
1 2 71 (50,0 4")
Ø 1 0 4 0 (4 0 ,9 5 ")
Ø 1 1 4 0 (4 4 ,8 8 ")
w ith free standin g b ase
1 9 1 0 (7 5 ,2 0 ")
197 0 (77 ,56 ") w ith free sta nding ba se
Figure 8 – I-Max Touch 3D dimensions, version equipped with cephalometric option
Load
400
350
300
250
E[kJ]
200
150
100
50
0
0 100 200 300 400 500 600
min
5.4 Accessories
The I-Max Touch/I-Max Touch 3D comes with the following removable accessories:
I-Max Touch 3D
Biteblocks, cephalometry ear centering pins,
Disposable and non-sterilized parts.
head strips for 3D exams, protective bite
Replace after every use.
sleeves
NOTE: These removable parts are considered "type B applied parts" in accordance
with IEC 60601-1 2nd edition. Some of these parts do not carry identification codes due to
their small size. The use of these parts on other devices is not possible as they are parts
designed specifically for the I-Max Touch 3D.
WARNING: These measurements require the removal of the HF group covers; this
means gaining access to internal parts where high voltage is normally present.
For the measurement of the exposure parameters with the invasive method, please follow the procedure
described further down in this manual.
WARNING: During the panoramic examination the KV and mA values vary according
to a predetermined curve to compensate for the different absorption of the X-rays due to
different anatomical structures. This makes it possible to obtain a good uniformity of the
image contrast. This is done by lowering the chosen value in the initial phase of the
panoramic exam and increased it in the inscissor/canine area to compensate for the denser
cervical spine. The value displayed during the panoramic examination corresponds to the
one selected by the user while the real value can differ; these effects must be considered
when measuring the exposure parameters using a standard diagnostic mode. As an example,
the variation follows this curve:
1 Selected value
2 Real mA value
3 Real KV value
Accuracy declared on the section "Technical data" is in reference of the actual values of kV
and/or mA. The manufacturer guarantees that the accuracy of the loading factors is always in
compliance with the international standard for safety of medical devices IEC 60601-1. In
accordance with IEC 60601-2-7, the maximum deviation (including the correction and
instrument’s accuracy) is less than or equal to ±10% for kV, while for the tube current (mA) it
is less than or equal to ± 15%.
WARNING: Changing the settings in the different service programs will affect the
system's functionality; only authorized field engineers should access and modify these
settings.
NOTE: The service menus can be accessed directly but some critical functions are
protected by further passwords.
2. Using the right and left arrow keys it is possible to scroll bidirectionally through the list of menus and
select a service program from the following list:
CONFIGURATION
AXIS ALIGNMENT
CEPH SETTINGS
TROUBLESHOOTING
SYSTEM
BURN-IN
SHOW CONFIG
CONFIGURATION
Select the desired service program and press the >O< key to confirm the selection; for each selection
different operations are possible.
NOTE: the SYSTEM and BURN-IN programs are only used during the setup at the
factory; they are protected with special passwords that are not accessible to service
engineers. For this reason, they are not explained in the manual.
The "Test" key (T) is used to quit a service program and return to a higher
level of menus. It can also be used to discard changes that were made on
specific parameters. This operation is indicated with a specific message
on the display.
The left and right arrow keys are used to scroll through the different
parameters or menus.
The up and down arrow keys are used to increment or decrease the value
of the selected parameter.
The "P", the "M", the "adult/child" and the "size" keys are special keys that
can be required for specific additional functions as referred to in the some
of the procedures in the following subchapters, such as for instance in the
CEPH SETTINGS menu (password 124).
5.6.3.1 Language
In this menu it is possible to change the language of the messages that are displayed on the control panel
(the language of the service menus is always English) to one of the following:
ENGLISH
ITALIANO
FRANCAIS
DEUTSCH
ESPANOL
PORTUGUES
NETHERLAND
TURKCE
ENGLISH
It is possible to change the set value using the up and down arrow keys.
NOTE: It will take into account standard timekeeping operations (hour and date
change, leap year calculation, etc.) but will not consider summer time changes (DST).
The RTC clock is set at the factory (Central Europe) date/time during the final test of the equipment; it is the
installer’s responsibility to set the local date/time. Once selected, this message is displayed:
SET DATE & TIME
DATE: DD/MM/YEAR
It is possible to scroll between the date and time set. After confirming the date change pressing the "Patient
centering" key >O<, the display changes as follows:
ADJUST DATE:
D>XX M XX Y XX
The ">" symbol is indicating which parameter is going to be modified; in this case the day, while the month
and year are to be modified if one of these messages is displayed respectively:
ADJUST DATE:
D XX M>XX Y XX
or
ADJUST DATE:
D XX M XX Y>XX
Use the right and left arrow keys to select the day, month or year value; use the up and down arrow keys to
change the value. Accept the modifications by pressing the "Patient centering" key >O<.
Use the right and left arrow keys to change to the time display; this message is displayed:
SET DATE & TIME
TIME: XX:XX:XX
Pressing the "Patient centering" key >O< to confirm the time change; the display changes as follows:
ADJUST TIME:
H>XX M XX S XX
To change the time setting, follow the same procedure as that to change the date setting.
NOTE: If the emission is set to OFF a warning message will be displayed just after the
initial message and before the TEST message at power on. The display is cleared by pressing
the "Patient centering" key >O< (5).
NOTE: The above options are not used on Owandy Radiology units.
WARNING: Changing this mode will affect the complete system functionality.
WARNING: A wrong setting will cause the "Close cassette to Panoramic" message
to be displayed when a pan only unit is started, or an Error 420 for pan with ceph units, when
the cephalometric exam is selected.
WARNING: This parameter should not be changed unless the collimator movement
mechanism has been changed from a screw-driven assembly to a belt-drive one; the
functionality of the unit can be severely impaired.
NOTE: This menu is disabled if the collimator setup type submenu has been set to
“PAN ONLY SYSTEM”. Trying to enter this submenu will generate an E420 error; press the
"Patient centering" key >O< (5) to reset.
In this submenu it is possible to set the Soft Tissue Filter type (STF). After selecting this submenu the
display will show one of these messages depending on the factory setting:
STF SETUP TYPE
3D SYSTEM
or
STF SETUP TYPE
WITHOUT SYSTEM
or
STF SETUP TYPE
PAN-CEPH SYSTEM
Use the up and down arrow keys to change the value and the “Patient centering” key >O< to accept the
modifications. Select “PAN-CEPH SYSTEM” for pan with ceph units. Select “3D SYSTEM” for 3D with ceph
units and “WITHOUT SYSTEM” for pan-only units.
WARNING: A wrong setting can severely impaire the functionality of the unit.
NOTE: For pan-only systems changes to this menu do not have any effect on the
system functionality.
This submenu allows for the configuration of the system for 1 mobile sensor or 2 fixed sensors. After the
selection the display will show one of these messages depending on the factory setting:
SENSOR HANDLING
SENSOR IS MOBILE
or
SENSOR HANDLING
SENSOR IS FIXED
Use the up and down arrow keys to change the value and the “Patient centering” key >O< to accept the
modifications. Select "SENSOR IS MOBILE" for a 1 sensor configuration and "SENSOR IS FIXED" for a 2
sensor fixed configuration.
WARNING: Wrong settings in this submenu will display messages during the
operation of the unit that are not consistent with the equipment configuration.
WARNING: This parameter should not be changed unless the column has been
changed from one version to another; the functionality of the unit can be severely impaired.
WARNING: This parameter should not be changed; the functionality of the unit and
the image quality can be severely impaired.
WARNING: This parameter should not be changed; the functionality of the unit and
the image quality can be severely impaired.
WARNING: This parameter should not be changed; the functionality of the unit is
compromised if set to “ON”.
NOTE: The centering operations must only be interrupted in case those functions are
used to check some hardware faults. If the system needs to be centered, the centering
operations must be fully completed before using the submenus.
Once the operation is finished (or interrupted) it is possible to access the following configuration submenus:
ROTATION ZERO
Y AXIS ZERO
Y AXIS ZERO EVO
Y AXIS ZERO BW
CASSETTE ZERO
PR. COLL. PAN
PR COLL. 3D
ROTATION ZERO
The selection is confirmed pressing the "Patient centering" key >O<. To exit from any menu use the "Test"
key (T); the values of a submenu will be updated or not by pressing the appropriate button in response to
this message:
UPDATE CHANGES?
>0< = Y, T = N
In both cases, the service menu returns to the higher level of menus.
WARNING: Changes to one or more offset values affect the system’s functionality;
take care not to alter those values if it is not needed. Normally only the replacement of faulty
parts (motors, belts, zero optical sensors, etc.) will require any change of these settings.
WARNING: This function is not active in the digital mode; if selected it will generate
an E420 error message.
WARNING: In this submenu the X-ray emission is enabled, it starts when the X-ray
trigger is pressed; care must be taken when performing this intervention.
This function allows centering the offsets of the linear slit collimator. Once the "Patient centering" key >O< is
pressed this message is displayed:
PCC ZERO [YY] a
ZERO OFS ±xxxxxx
Where:
"YY" is the stepper motor speed that can be changed using the up and down arrow keys.
"a" is the status of the zero optical barrier; 1 means engaged (barrier interrupted), 0 disengaged.
"xxxx" is the current value of the offset that can be changed with the left and right arrow keys, the
value can be negative or positive.
This function is used to check the beam alignment; the emission is started by pressing the X-ray trigger and
the exposure parameters can be set by pressing the "P" key; when it has been pressed use the right and left
arrow keys to change the value. Press the “T” key to accept or cancel the modifications.
NOTE: The position of the primary slit collimator is set to the correct value during the
testing procedure at manufacture; changes to the stored value must be done only in case of:
Replacement of one part of the linear slit collimator (motor, zero barrier sensor, etc.);
in this case the beam must be aligned to the sensor entrance acting on the offset
value.
Replacement of a defective tubehead; in this case the beam must be aligned by
moving the tubehead and leaving the offset value unchanged.
WARNING: This function is not active on an I-Max Touch; if selected it will generate
an E420 error message.
DIGITAL CEPH
CEPH IS DISABLED
It is possible to change the set value using the up and down arrow keys. Pressing the "T" key will quit the
menu and the disabled/enabled status is temporarily stored in the volatile memory.
5.6.5.6 Y Offset
This function allows the settting of the offset of the Y axis, the motion along the mid-sagittal plane of the
patient, to center the X-ray beam on the ceph sensor. Once the "Patient centering" key >O< is pressed this
message is displayed:
Y ZERO [YY] a
ZERO OFFS ±xxxxx
Where:
"YY" is the stepper motor speed that can be changed using the up and down arrow keys.
"a" is the status of the zero optical barrier; 1 means engaged (barrier interrupted), 0 disengaged.
"xxxx" is the current value of the offset that can be changed with the left and right arrow keys, the
value can be negative or positive.
Press the “T” key to accept or cancel the modifications.
NOTE: The acquisition start position offset is set to the correct value during the final
tests at the factory; changes to the stored value must be done only when ceph exams are to
be performed on adult patients.
NOTE: This table describes the correspondence between the figures that are
displayed and the corresponding input signal. The digits are numbered from "7" to "0". "7" is
the character furthest to the left on the display while "0" corresponds to the character
furthest to the right.
Microswitch/
Port Bit Association Logic status
Optical sensor
R4 7 Not used -
6 Not used -
0 for analog
5 DSPU board initialization
1 for digital
1
4 Motor +5V power supply
0=alarm status
3 Column CPU board A1 initialization 1
2 Generator board A10 initialization 1
1 Not used -
0 Not used -
R5 7 (*) Primary collimator position optical sensor B8 0
6 (**) Soft tissue filter 0 position B8 1
5 Not used -
4 Not used -
3 Not used -
2 (**) Digital sensor ready 0
1 Not used -
0 Not used -
R6 7 (*) Panoramic cassette start position B5 1
6 (*) Panoramic cassette end position B4 1
5 (*) Cephalometric cassette present S10 0
4 (*) Panoramic cassette present S9 0
3 Cassette / sensor holder in ceph position B7 1
2 Cassette / sensor holder in pan position B6 1
1 Remote control X-ray trigger X71-1 / X71-2 1
0 X-ray trigger on column S8 1
R7 7 Not used 1
6 (**) Ceph sensor holder start position B11 1
5 Not used 1
4 (**) Ceph secondary collimator start position B10 1
3 (**) Primary slit collimator 0 position B9 1
2 Y axis start position B1 1
1 Not used -
0 Rotation arm 0 position B3 1
(*) Functionality only available on analog version
(**) Functionality only available on digital version
NOTE: The logic status of these signals depends on the physical position of the
relevant optical sensor / microswitch with respect to the "0" position.
This submenu allows for the activation and deactivation of the sensor clock using the left and right arrow
keys. Press the “T” key to exit this submenu.
In this submenu it is possible to set the tubehead pre-heating time. Once the "Patient centering" key >O< is
pressed this message is displayed:
PRE-HEATING TIME
VALUE = 2000
It is possible to change the set value using the up and down arrow keys. Press the “T” key to exit this
submenu.
In this submenu it is possible to set the tubehead pre-heating values. The value must be set according to the
data reported on the "Equipment parameters table" in this manual. Once the "Patient centering" key >O< is
pressed this message is displayed:
IDLE FIL LEVEL
LEVEL = 30
Pressing the right arrow key displays the next message:
FIL LEVEL @ XXmA
LEVEL = YYY
Where:
"XX" is the tubehead filament current value that can be changed using the left and right arrow keys.
"YYY" is the tubehead pre-heating value that can be changed with the up and down arrow keys.
Press the “T” key to exit this submenu.
WARNING: In this submenu the X-ray emission is enabled, it starts when the X-ray
trigger is pressed; care must be taken when performing this intervention.
Pressing the "P" key it is possible to choose a different combination of parameters. Once pressed, the
display will show:
>72kV 06mA 1.00s
Where the symbol ">" is showing the parameter to be changed; in this case the kV. To move to the "mA" and
exposure time parameters, press the "P" key once or twice again. The up and down arrow keys will change
the selected parameter. Pressing the X-ray trigger will start the X-ray emission. Press the “T” key to exit this
submenu.
5.6.6.8 Auto-calibration
In this submenu it is possible to set different calibration parameters. Press the “T” key to exit this submenu.
In this submenu it is possible to set test the I2C bus. Press the “T” key to exit this submenu.
NOTE: The last value that is displayed value is the "Hardware Protection Key code";
this is an alternate method to view it.
6. PRE-INSTALLATION
The instructions of this and the following chapter guarantee a correct installation and will ensure that the I-
Max Touch/I-Max Touch 3D will function correctly. The supplier can provide the assistance and the
necessary technical advice for pre-installation, while all masonry work and the pre-installation phase are at
the customer’s charge and must be performed complying with the indications given below. The requirements
for a correct installation of the unit are:
Minimum height of the room: 2.5 m (8.20 ft) and a surface area that varies according to the
configuration of the unit to be installed (see diagram further down).
A certain distance from heating devices.
The entries to the room must have a minimum width of 80 cm (31.50") to be able to enter the unit in
the room.
WARNING: In its standard version the unit must be attached to the wall with the two
brackets supplied with the unit. Each dowel must support a maximum extraction force of 120
kg (264 lbs). Depending on the type of wall use these fixing dowels:
Full or concrete bricks: screw anchors (provided with the installation kit) in cast iron
M6 or WURTH chemical screws (not provided).
Wood mountings: self-threading screws (not provided).
Hollow bricks: chemical dowels (not provided).
A special floor mount (feet) option is available; in this case the equipment MUST be attached
to the floor. The manufacturer is not responsible for any installations that do not comply with
the specifications stated above.
The unit must be connected to a differential magneto-thermal switch to separate the unit from the electrical
supply. This switch must comply with the electrical regulations in force in the country of installation. The
supply conductors must have a section of 1.5mm2 (16 AWG). The general grounding must comply with the
rules in force; if the grounding is of bad quality it could be dangerous for the operator’s safety and could
cause a malfunction of the electrical devices.
NOTE: The electrical connection must be done on the terminal board X0 (see
operation circuit diagram at the end of the manual).
NOTE: The unit provides connectors for the control and warning devices to be
mounted at the entrance of the X-ray room:
Remote X-rays button: "Dead man switch" type remote control that allows launching
the exam at a distance; the operator can stand outside the X-ray emission area. This
button must be suitable to prevent unwanted emission. The standard X-ray trigger
supplied with the unit matches the above characteristics.
READY light: Green light (24V 40W max.); it signals that the unit is ready to perform
an exam (contact N.O.).
X-RAYS light: Yellow light (24V 40 W max.); it signals that entry in the X-ray room is
forbidden because an exposure is underway (contact N.O.).
NOTE: The unit only provides closing contacts for the functions mentioned above.
Power voltages for the relevant devices have to be provided from outside, making sure not to
exceed the indicated ratings.
To connect all control and warning devices it is advisable to use 6 wires with a 0.5 mm² section as a
minimum.
6.2 Packaging
The I-Max Touch/I-Max Touch 3D with or without cephalometric option is shipped in two cardboard boxes.
Weight
Contents Dimensions
Net Gross
- Unit head with rotation arm including the
80 kg 90 kg
tubehead and sensor connector 120 x 80 x 67 cm
(176 lbs) (198 lbs)
- Covers
- Column including the touch screen
- Covers
145 x 67 x 87 cm 85 kg 95 kg
- Digital sensor holder
(187 lbs) (209 lbs)
- Accessories
NOTE: All boxes are equipped with shock detectors; at reception and before opening
the boxes verify that those sensors have not been activated.
WARNING: Owandy will not bear any responsibility for damages and costs caused
to the equipment due to an improper unpacking procedure.
Figure 10
(*) A = minimum 600 mm (23.6"), recommended 800 mm (31.5") for service purpose
Figure 11
(*) A = 600 mm (23.6") minimum, 800 mm (31.5") recommended for service purpose
(**) B = 1460 mm (57.52") minimum front space, 1610 mm (63.39") recommended frontal space for service
purpose
The acquisition computer(s) (not provided with the unit) must match the following minimal configuration:
Minimum configuration Recommended configuration
Operating system: Windows XP SP2 or 7 Windows 7
32 or 64 bits 64 bits
Processor: Pentium4 2 GHz Core 2 Duo 3 GHz or higher
Memory: 2 GB 4 GB
Speed network connection: 100 Mbit 100 Mbit
NOTE: On windows 7 and 8 the UAC (User Account Control) should be deactivated.
It is strongly recommended to install the QuickVision patient and image database on a workstation that is
different from the workstation connected to the 3D unit (e.g. on the server for the practice management
software data) and to use a 1Gbit network (switch/hub and cables) to optimize the transfer times of the files
and to facilitate the backup of the data.
NOTE: On windows 7 and 8 the UAC (User Account Control) should be deactivated.
7. INSTALLATION
NOTE: The unit has been designed for wall attachment with two brackets, each of
which requires to be fixed by dowels. In order to mark the right position of the brackets, it is
necessary to use the dimenions indicated in the figure below. The vertical alignment of the
central holes and the perpendicularity with the floor is very important; it is necessary to use a
plumb.
1. Mark the wall with a centre punch at the level of the fixing holes; drill holes in the wall according to the
type of dowels to be used (see previous chapter).
70.5 70.5
(2.76") (2.76")
1040 (40.95")
99 99
(3,9") (3,9")
(4.5")
114
Figure 12
2. Open the upper side of the box. If the unit is equipped with a ceph arm remove the carpus plate placed
at the side of the ceph head.
3. Remove the wooden transversal support frame at the bottom end of the column.
4. Lift and remove the cardboard box to expose the column and ceph arm.
5. Remove the other wooden frames and the box containing the accessories and covers.
6. If the unit is equipped with a ceph arm remove the ceph arm using the special grip.
Position the ceph arm on one of the wooden with the ceph head resting on one of the polyethylene foam
blocks.
7. Remove the polyethylene foam blocks from the top of the column and the ceph covers located at the
bottom of the column.
8. Remove the column following the sequence shown in the images below. Move the bottom of the column
about 30 cm over the side of the wooden pallet.
About 30 cm
Lift the column’s top part until the column stands vertically on the floor next to the wooden pallet.
If the unit is freestanding and is equipped with feet, remove the 2 feet from the pallet.
NOTE: This procedure is only valid for the wall-mounted standard version.
1. Mount lower fixing plate "D" on the column base and mount upper fixing plate "E" on the column.
2. Insert the external back cover on upper fixing plates "E" without fixing it; you will fix it at the end of the
mechanical and electrical installation.
3. Mount upper wall bracket "C" on fixing plates "E" without tightening the screws.
4. Position the column close to the wall.
5. Fix upper wall bracket "C" to the wall, then tighten the screws between upper fixing plates "E" and wall
bracket "C".
6. Fix lower fixing plate "D" to the wall, without tightening the screws.
7. Verify the parallelism between the column and the wall by positioning a spirit level on the chin rest
support. In order to correct the position it is possible to insert some spacers (provided with the column)
between the lower bracket and the wall. Once the right position is reached, tighten the screws.
8. Acting on the feet grub screws, adjust them in order to level the feet on the floor. When finished, cover
the grub screws with the provided plastic cups.
Retaining bracket
"B"
Screws "F"
Spacers
Figure 14
To easily reach the back side of the column whilst keeping it attached to the wall, remove the fixing screws
located on the back side of the column base and remove the two "F" screws from upper bracket "C", then
rotate the column.
NOTE: The unit is equipped with a switch (S2) which allows the user to lower or raise
column for servicing; it is located on the lower back side of the column and is protected by a
small metallic cover.
NOTE: The unit is shipped with the column pre-set at the minimum height. If the room
height allows for a higher position it is possible to increase the stroke of the column by
adjusting the reference cams located inside the column, close to the end-run microswitch
plate. Remove the microswitch plate and lift the column in order to access the reference cam
holes.
NOTE: It is very important to position the foam blocks as described below, to prevent
the head from falling on the ground.
2. Place the polyethylene and polystyrene foam blocks as pictured below to support the head when the box
is tilted over. Empty the corner below the back of the head and position a polyethylene foam block at the
bottom of the box. Place the polystyrene foam block on top.
Lock both foam blocks in place by inserting another polyethylene foam block in the corner.
3. Close the box and slide it off the pallet. Tilt it over so it rests on its side.
4. Cut the box along the edges and open it. Remove the polyethylene foam blocks protecting the head.
The head should be supported by the handles mounted on the generator and by the foam blocks under the
rear of the head.
2. Position the rotating arm on the column inserting it in retaining bracket "B" at the back of the column.
While one person keeps it in position the other attaches the two backside "A" screws to the column
without tightening them.
Retaining bracket
Figure 16
3. Remove the two posterior screws fixing the CPU board support plate to the head of the unit and lift it up
at about 75° then tighten screws "A" to firmly lock the head of the unit to the top of the column.
B C A
Retaining bracket
Figure 17
4. Insert reference pins "B" in the rotating arm and column using a hammer then insert the remaining two
"C" screws and tighten all the fixing screws.
5. Remove all the handling brackets on the head and rotate the rotating arm about 90° in clockwise
direction in order to easily reach the screws of the tubehead covers.
6. Remove the tubehead cover then remove the two "D" spacers and fixing bracket "E".
Spacers "D"
Lower fixing
bracket "E"
Figure 18
7. Open the sensor holder and mount the lower cover of the rotating arm.
Figure 19
8. Mount the temple support group by positioning the notch on the group to the front of the unit, sliding it on
the shaft attachment and rotating it clockwise until it is locked. This operation is identical for the temple
support group of the I-Max Touch and the I-Max Touch 3D.
Figure 20
9. Insert the cables coming from the column through the holes left and right in the back of the column and
the head of the unit. Lower the CPU board support plate and screw it back in place. Connect the column
cables to the corresponding connectors on the different boards checking the labels on the cable
extremities and next to the connectors.
NOTE: To access the CPU board connectors on the 110-120V version, it is necessary
to remove the metallic cover. After making the connections, position the cables in the
relevant location and remount the cover.
10. Remove the transportation strap that locks the primary collimator and make sure the collimator is
positioned in front of the X-ray output window of the tube assembly before mounting the tube cover.
The ceph device upgrade is shipped with the column and is already pre-assembled in a single piece
composed of these parts:
Ceph arm including the handle for installation
Skull clamp and ear centering device
Arm covers
Sensor holder
If the ceph arm still needs to be unpacked, please refer to the subchapter about the unpacking of the column
and the ceph arm above.
Handling zone
Red handle
Figure 21
NOTE: Do not remove the handle before the complete installation of the ceph arm on
the column.
1. Remove the column rotation fixing screw located on the back side of the column base of the unit and
remove the two "F" screws (see previous subchapter) from upper bracket "C".
2. Rotate the column in a clockwise direction to be able to reach the back side of the column.
3. Detach the attachment box from the end of the ceph arm (separate the base plate from the cover plate)
and attach the ceph base plate to the back of the column using the reference pins and screws.
Reference pin
Reference pin
Figure 22
4. Screw the cover plate on the ceph base plate on the back of the column without tightening the screws;
the cover plate should be able to move freely over the screws.
5. Lift the ceph arm with the red handle and the handling zone and remove it from the package.
6. Position the ceph arm near the column and slide the end of the arm between the ceph base plate and
the cover plate; the arm should be pushed in until it touches the lateral side of the base plate. Attach the
ceph arm firmly to the column by thightening the screws of the cover plate. Make sure not to damage the
cables of the ceph arm when inserting the arm in the ceph base.
7. Insert the cables through the hole between the column and the head of the unit then connect the ceph
cables to the corresponding connectors on the different boards checking the labels on the cable
extremities and next to the connectors.
8. Remove the red handle from the ceph arm.
NOTE: If necessary and to easily access the screws on the back side of the covers,
remove the column rotation fixing screw located on the back side of the column base and
remove the two "F" screws (see previous subchapter) from upper bracket "C". Rotate the
column in clockwise direction to reach the back side of the column.
Figure 23
NOTE: Not applicable to the Pan-only and 3D-only versions; those versions have a
fixed sensor.
In order to insert the sensor in the desired docking station on the unit or the ceph arm, carry out these
operations:
1. Grip the sensor by the handgrip and close your fingers around the grip and the lever; squeeze the lever
until it disappears inside the handgrip and the whole mobile connector system on the side retracts.
2. Keep the sensor vertical with the handgrip so that the upper plane is parallel to the horizontal top part of
the sensor holder, then move the sensor close to the docking station, align the holes on the side of the
sensor with the protruding rails/hooks of the docking station and slide the sensor on the hooks.
3. Push the sensor cassette until it touches the back side of the sensor holder then lower the cassette until
it hooks completely to the attachment.
4. Only at this point release the lever while checking that the sensor is correctly attached to the docking
station before completely releasing the handgrip.
WARNING: Hold the sensor firmly to prevent it from falling when releasing the lever
during the insertion phase.
NOTE: The different types of sensors are equipped with a shock detection indicator;
this indicator is visible on the side of the sensorcasing. Possible shocks are displayed by a
change in color (from transparent/white to red) of this indicator. The digital sensor can still
function correctly even when the color has changed, indicating a fall that might not have
damaged the sensor.
NOTE: The color change of the shock detection indicator voids the warranty on that
sensor.
The Ethernet cable from the back of the base of the column can be connected directly to the network
connector of a dedicated computer or can be connected to a network switch/hub so it can be controlled by
multiple computers on the network of the dental practice. It will be necessary to add a network board to the
dedicated computer if that computer needs to be connected to the network. The network speed of the
Ethernet connection must be at least 100 Mbps; a 1 Gbps network is recommended.
If the computers will be used in an existing computer network it is recommended to install an antivirus
program prior to the connection.
The Intel Pro 1000 Gigabit network board provided with the I-Max Touch 3D unit must be installed in the
dedicated computer using a free PCI-express slot; it must be connected using the network cables provided
with the unit or Ethernet cables with similar specifications (Cat 5e, 5+ or 6).
If the computer will be connected to an existing computer network it is recommended to install an antivirus
program on it prior to the connection.
Use the Intel Pro 1000 board with 2 network ports that was provided with the unit and that has been installed
in the computer to connect the 3D unit to the computer.
NOTE: The 3D unit must be connected to the Intel Pro 1000 PT PCI-express board that
was provided with the unit only.
Connect a network cable from the “SENSOR” port at the back of the base of the column of the unit to port B
of the Intel Pro 1000 network board; connect the second network cable from the “ETHERNET” port at the
back of the column to port A of the Intel Pro 1000 board.
WARNING: The O.S.P. is currently compatible with all Owandy equipment in 32 and
64 bits, Windows XPSP2, Vista, 7 and 8; the I-Max Touch 3D however cannot be installed on
Windows XPSP2 or SP3 and Windows 7.
NOTE: Uninstall any old version of the O.S.P. (LAN drivers) and then uninstall any old
version of the 3D SDK (Evo3D) and of the Varian ViVa software before installing a new
version of the O.S.P.. Please verify and uninstall manually using the programs list as some of
these drivers need to be uninstalled manually.
Port A of the Intel Pro 1000 board will appear as “Intel(R) 82579LM Gigabit Network
Connection” in the network boards section of the device list; port B will appear as “Intel
PRO/1000 Grabber Adapter” in the PRO/1000 Grabber Devices section.
NOTE: When installing an I-Max Touch 3D with 1 network cable leave the dropdown
list for the Intel Pro 1000 board on “Do nothing” and click on”Close” to proceed.
NOTE: Do not change the IP settings of the PRO/1000 Grabber Device in the Windows
device manager.
f. Click “OK” in the pop-up window, then “Close” in the VirtualCP window to finalize the installation
of the 3D drivers.
The O.S.P. drivers will install a folder called “OWANDY SOFTWARE PACKAGE” on the Windows desktop
containing a "LAN PANORAMIC" folder with these utilities:
Hardware settings: allows to manually change the type of I-Max Touch unit (between 2D and 3D).
LAN PANORAMIC: launches the Panolan utility used for testing the unit and its sensor(s); this
software performs 2D and 3D acquisitions without having to use imaging software.
10. Open folder "LAN PANORAMIC" in the "OWANDY SOFTWARE PACKAGE" folder on your Windows
desktop and double click the "LAN PANORAMIC" shortcut to start the Panolan utility.
11. Select “English” and click on “OK”.
12. Select the "Settings" menu, then "Network" and finally "Network settings". In the window that appears,
set the IP addresses according to those of the 3D unit. Accept with the "OK" button.
Figure 25
NOTE: The IP addresses are stored in the "PANO_LAN_DLL.ini" file in this folder:
Windows XP: "C:\Documents and Settings\ All Users\Application Data\OWANDY\OSP -
LAN PANORAMIC\"
Windows 7: "C:\Program Data\ OWANDY\OSP - LAN PANORAMIC\"
The IP addresses should not be changed directly in this file but through the Panolan utility or
the I-Max control panel accessible through the preferences of your imaging software.
13. The IP address of the network board (I-Max Touch) or the Intel Pro 1000 board (I-Max Touch 3D) in the
computer must be set according to the IP addresses stored in the I-Max Touch 3D unit:
a. From the Windows control panel display the list of network boards and select the network board
you wish to configure (network board of the computer for the 2D unit or Intel Pro 1000 for the 3D
unit); double-click the board to open its network window then open its properties window.
b. Double-click the TCP/IP connection (TCP/IPv4 in Windows 7) to open the window allowing you
to set the network port's IP address which has to be in the same range as the addresses of the
unit. For example:
For the I-Max Touch 2D the IP address is set to the default value 192.168.002.215
(subnet mask 255.255.255.0); in that case you have to set the address of the network
board to 192.168.002.xx so that it is in the same IP address range and use the same
subnet mask 255.255.255.0 (xx=any address other than the addresses set in the unit, in
this example .215, or used on the other computers).
For the I-Max Touch 3D the IP addresses are set to the default values 192.168.002.215
and 192.168.002.045 (subnet mask 255.255.255.0); in that case you have to set the
address of the network board to 192.168.002.xx so that it is in the same IP address
range and use the same subnet mask 255.255.255.0 (xx=any address other than the
addresses set in the unit, in this example .215 and .45, or any addresses used on the
other computers).
c. Verify the connectivity between the computer and the unit by opening a command line window
(key "Windows" + "R" on the computer keyboard, then enter "CMD" in the field and click on
"OK"). In the command line window ping the unit to verify the connection:
"Ping 192.168.2.215" + "Enter" of the keyboard.
Also "Ping 192.168.2.45" + "Enter" of the keyboard in case of a 3D unit.
If the two ping commands display 4 latency times the connection with the unit is configured
correctly and is working; if the ping commands fail to display a latency time:
Verify the network cable between the computer and the unit.
Check the IP addresses configured in the service menu of the unit (see service menu
chapter).
Check the IP addresses configured in the O.S.P. (see above); they must match those
of the unit.
Check the proper installation and configuration of the network board in Windows.
Try to connect with the unit after deactivating any firewall used in Windows.
NOTE: The 1313DX flat panel sensor of the 3D unit is configured by default to IP
192.168.003.034. This configuration is stored in the “HcpConfig.ini” file in this section:
[HcpFgPleora]
PleoraIpAddress=192.168.3.34
The 1313 flat panel sensor remains on 192.168.002.034.
NOTE: If the "Calibration" folder has been created manually, make sure to write its
filename with an uppercase "C".
NOTE: "Application Data" is a hidden folder; to be able to visualize hidden folders the
option "Display Hidden Files and Folders" of your File Explorer needs to be actived.
Calibration files, dedicated to the sensor mounted in the 3D unit, must be copied to the computer using this
procedure:
1. Insert the Receptor installation disc in the CD-ROM-drive. The interface will launch automatically and will
guide you through the different installation steps. Refer to the Windows help if the CD-Rom does not
automatically launch or launch the "Setup.exe" file manually from the CD-Rom.
2. Use default folder "C:\IMAGERs" and follow the steps of the installer. Inside the "C:\IMAGERs" folder the
setup program will have created a folder named with the serial number of the sensor of the 3D unit; e.g.
"C324-04E".
3. Copy the content of folder "C:\IMAGERs\XXXX-XXX" to "C:\Documents and Settings\All
Users\Application Data\OWANDY\OSP - LAN PANORAMIC\Calibration"; do not copy "the XXXX-XXX"
folder but only its content. Use folder "C:\Program Data\ OWANDY\OSP - LAN
PANORAMIC\Calibration" on Windows 7.
4. Open file "HcpConfig.ini" from folder "C:\Documents and Settings\All Users\Application
Data\OWANDY\OSP - LAN PANORAMIC\Calibration" (folder "C:\Program Data\ OWANDY\OSP - LAN
PANORAMIC\Calibration" on Windows 7) in notepad by double-clicking it.
5. Modify the "PleoraMacAddress=00-11-1C-00-86-9C" line by replacing the Mac address by that
mentioned on the form provided with the 3D unit. The Mac address is required to communication with the
Pleora board responsible for the network communication with the sensor.
6. Save the file.
NOTE: Do not delete the "C:\IMAGERs" folder; it will be used by the ViVA (sensor
software) program.
NOTE: Should the Receptor installation disc not contain a setup program, manually
copy the content of the folder on the CD-Rom to folder "C:\Documents and Settings\All
Users\Application Data\OWANDY\OSP - LAN PANORAMIC\Calibration" (folder "C:\Program
Data\ OWANDY\OSP - LAN PANORAMIC\Calibration" on Windows 7); only copy the files in th
folder, do not copy the root folder of the CD-Rom.
NOTE: If the form is not provided with the unit the Mac address can be found on the
sensor. To access the sensor switch off the unit, remove the front and back covers of the
sensor and check the Mac address mentioned on the sticker on the back of the sensor.
Remount the covers.
NOTE: "Application Data" is a hidden folder; to be able to visualize hidden folders the
option "Display Hidden File and Folders" of your File Explorer needs to be actived.
1. Start the imaging software and select/create a patient file for the test images.
2. Open the virtual keyboard of the unit and select the Pan program.
3. Place the centering phantom tool on the chin rest and the sensor calibration tool in front of the sensor
(refer to the accessories and tools in the schematics chapter for details) attaching it with tape.
5. Set contrast and brightness levels to have a good visibility of all the centering balls of the centering tool.
Select the measurement tool in the imaging software and measure on the image the distance between
the two external balls; this distance for a Pan exam with the standard curve has to be:
188 mm +/- 2 mm for the standard curve on a 2D unit
191 mm +/- 2 mm for the standard curve on a 3D unit
For a Pan exam with the alternative curve the distance between the two external balls; this distance has
to be:
172 mm +/- 2 mm for the alternative curve on a 2D unit
174 mm +/- 2 mm for the alternative curve on a 3D unit
If the distance is not correct it is necessary to adjust the Y axis using the procedure for the Panoramic X-
ray beam centering verification (for the I-Max Touch or the I-Max Touch 3D) in the maintenance chapter .
4. The arch of the centering tool in the axial view should be continuous and without any breaks
Figure 29
5. In case the arch is displaying a break, it will be necessary to modify the lateral offset as described in the
3D image adjustement procedure in the maintenance chapter.
NOTE: The CEPH arm has been adjusted on the unit during the testing procedure at
manufacture and adjustments are not usually necessary in the field. Before proceeding, verify
if the arm has been properly mounted during field installation.
If a ceph arm is present it is necessary to verify the alignment of the X-ray beam with the rings in the ear
plugs and the digital sensor.
1. It is possible to make an exposure without the presence of the secondary collimator and without
movement of the digital sensor by entering the technical menu, using the CEPH SETTINGS menu
(password 124) and selecting "Rotation offset" (for more information refer to the Technical service
programs chapter).
NOTE: When verifying the ceph function on an I-Max Touch 3D, select the I-Max
Touch (not the I-Max Touch 3D) unit in the panoramic control panel of the O.S.P. (drivers)
before working on the Ceph arm. Switch back to the I-Max Touch 3D unit once Ceph
maintenance has been finalized.
2. Press the "Exam mode selection" key (9); the digital sensor will be aligned with the X-ray beam.
3. Position the ear plugs in Latero-Lateral (LL) position and make an exposure using 60kV - 6mA - 0,5 s in
order to see the image of the primary collimator on the digital sensor.
4. Verify that the rings in the ear plugs are centered in the exposed area:
Figure 30
a. If the beam is centered but the rings are not centered, it is necessary to adjust the mechanical
position of the rings (see the ear rings alignement procedure in the maintenance chapter.
Figure 31
b. If the beam is not centered in the window it is necessary to adjust the rotation offset using the
CEPH SETTINGS menu (password 124) in the technical menu.
Figure 32
c. If the image is not symmetric in the window it is necessary to adjust the ceph sensor position
using the CEPH SETTINGS menu (password 124) in the technical menu.
5. Select the "Ceph sensor zero" menu using the CEPH SETTINGS menu (password 124) in the technical
menu to check the secondary ceph collimator position.
6. Open folder "LAN PANORAMIC" in the "OWANDY SOFTWARE PACKAGE" folder on your Windows
desktop and double click the "LAN PANORAMIC" shortcut to start the Panolan utility. Wait until the
message "Board is connected" is displayed at the bottom left. Check that in the "Image processing"
menu all the items are deselected (no "V" sign).
Figure 33
7. Press the "Patient entry" key >O< (5); the primary and secondary collimators and the ceph sensor move
to the central ceph position.
8. Place the ceph centering tool (refer to the accessories and tools in the schematics chapter for details) on
the secondary ceph collimator.
9. Use the arrow keys to set the values for the exposure (suggested values: 60kV, 6mA and 0.5s).
10. Acquire an X-ray image by pressing the X-ray trigger and check if in the obtained narrow image the
projection of the slit of the ceph centering tool is vertical and positioned in the middle of the area which is
defined by the arc marked in the figure below.
Figure 34
Figure 35
12. Enter in "STF zero" (using the CEPH SETTINGS menu (password 124) in the technical menu) to verify
the functionality of the Soft Tissue Filter.
13. Press the "Exam selection" key (9) to also insert the secondary collimator in the field.
14. In the imaging software acquire an exposure with the same parameters (60kV – 6mA – 0.5s).
Figure 36
13. Measure the distance between the center of the ear rings and the edge of the soft tissue filter; the value
has to be about 50mm.
NOTE: If these actions are performed during maintenance some covers have to be
removed:
a. Remove the outer cover of the H.F. generator on the rotating arm.
b. Remove the protection grid of the generator board.
The exposure parameters can be checked using the TROUBLESHOOTING menu (password 112) in the
technical menu (for more information refer to the Technical service programs chapter). In that menu use the
right and left arrow keys to reach the "RX EMISSION" submenu and confirm with the "Patient Entrance" key
>O< (5). At the selection of the X-ray emission test, the display will show this message:
X-RAY EMISSION
72kV 06mA 14.0S
WARNING: From this point onward X-ray emission is enabled; it will start when
pressing the X-ray trigger.
Pressing the "P" key it is possible to choose a different combination of parameters. Once pressed, the
display will show:
>72kV 06mA 14.0S
The symbol ">" is showing the parameter to be changed; in this case the kV. To move to the "mA" and
exposure time parameters, press the "P" key once or twice again. The up and down arrow keys will
change the selected parameter. Pressing the X-ray trigger will start the X-ray emission. The allocatable
values for the exposure parameters are listed in the table below:
Parameter Minimum value Maximum value
kV 6 86
s 0,2 15
mA 6 12
NOTE: This action allows you to carry out the measurement of the exposure
parameters with the rotating arm in a fixed (non-rotating) position.
If all the measures are within the specified range and there is an evidence of performance loss, measure the
high voltage supplied by the tubehead and the exposure time using a non-invasive kilovoltmeter with ≤±3kVp
tolerance. The high voltage value must be within 8% of the set value while the time value must be within
10% of the set value. If the voltage is not within the expected range replace the tubehead otherwise replace
the generator CPU board.
7.8.6.2 mA check
Use a multimeter (R input >= 10MΩ) in working conditions VDC and end of scale 5/10 V (maximum value
4VDC), position the cold pole on TP40 (GND) and the hot pole on TP29 (mA). Set these parameters on the
unit: 60kV - 6mA - 3s. Acquire an exposure and, considering that a ratio 1V DC ≈ 3 mA, verify that the value
indicated by the multimeter ranges from 1,86V to 2,138V (6mA±8%). Set 80kV - 12mA - 3s on the unit and
acquire a new exposure. After acquisition the value read must range from 3,643V to 4,276 V (12mA±8%).
Measured values for the different set values are listed in the table below:
mA Nominal value Minimum value Maximum value
6 1.98 1.822 2.138
7 2.31 2.125 2.495
8 2.64 2.429 2.851
9 2.97 2.732 3.208
10 3.30 3.036 3.564
11 3.63 3.340 3.920
12 3.96 3.643 4.277
In case the detected values are outside these ranges, check that the voltage between TP40 (GND) and
TP34 (mA) is contained on the above ranges. If not, replace the generator CPU board (A9).
7.8.6.3 Time
Verify the accuracy of the exposure time using an oscilloscope connected at the same test points used to
measure mA (TP40 for GND and TP29 for mA) of the generator board (A10). The exposure time calculated
at about 75% of the maximum kV value must correspond to the set one ±10%. In case the time is outside the
prescribed values replace the CPU board.
The exposure parameters can be checked with a non-invasive instrument by performing this procedure:
1. With the unit switched on select the panoramic examination mode by pressing the "Exam selection" key
(9).
2. Press the "Anatomic/Manual" mode indicator (13) until it turns green and displays "S", then press the
"Test" key (4); the display will show:
xxkV xxmA xx.xs
EMISSION PROGRAM
NOTE: This program allows for the measurement of the exposure parameters with the
rotating arm in a fixed (non-rotating) position without variations due to spine compensation.
5. Acquire an exposure; the emitted parameters (kV and Time) can be read on the measuring instrument.
NOTE: The performances are guaranteed only if the measurement of kV and time is
done with the invasive method because the non-invasive method may introduce errors due to
instrument tolerance or wrong measurement conditions.
6. To end the control program, press the "Test" key (4); the unit will return to standard mode and the
display will indicate:
xxkV xxmA xx.xs
PANORAMIC-STD
UPDATE CHANGES?
>0< = Y, T = N
Press the "Patient entry" key >O< (5) to confirm or the "Test" key (4) to cancel the setting.
Alternatively make an acquisition using the imaging software installed on the dedicated computer.
NOTE: When using an I-Max Touch 3D it is possible to recuperate the .RAW and .INI
files in the "AcquisitionSave" folder for a later manual reconstruction (refer to the chapter
about manual reconstruction).
Alternatively make an acquisition using the imaging software installed on the dedicated computer.
NOTE: When using an I-Max Touch 3D it is possible to recuperate the .RAW and .INI
files in the "AcquisitionSave" folder for a later manual reconstruction (refer to the chapter
about manual reconstruction).
8. TROUBLESHOOTING
8.1 LEDs
NOTE: If all the LEDs are OFF verify column fuse F3; if it is OK verify cable X11
between column CPU board A1 and CPU board A5 on both sides. Verify the column CPU
board A1.
The error messages are divided into different areas that can be distinguished by the error number; the table
below contains the different errors with their meanings. More detailed information on each error can be found
in the following subchapters.
The last 3 error messages are displayed during the power on phase when the system is controlling the
functionality of the whole system. Errors E281 and E282 mean that the zero position sensor is never
activated due to a motor that is not running or to a fault of the optical barrier (the sensor or its harness); error
E283 means that this sensor is always activated, in this case the problem can also be the motor or the
optical barrier.
Check that during the power on phase there are movements on these axes; the normal motion is
going to engage the sensor and a reverse motion disengage it. If no motion is observed the problem
can be the stepper motor or the cable connecting it to the main CPU. Check that the cables between
motor M9 and X6 of board A12 is well inserted and check the cable X1-X2 of A12 to X23, X24 and
X34 of the main CPU A5.
Check the continuity of the above cables from M9 to board A12 and from X1-2 of board A12 to X23,
X24 and X34 of the main CPU (A5).
Repeat the power on sequence while checking the motion.
If still there is no motion replace the stepper motor and if not repaired replace the CPU.
If a motion has been observed but messages are displayed the problem can be the sensor or its wiring:
Power off the system and try to manually disengage the sensor with a smooth movement.
Power on the system and check the functioning of the sensor, measuring the DC voltage on the
terminal of sensor B10 with and without an obstacle manually inserted. A variation of about 3.5 V
minimum should be observed; if not replace the sensor.
If the variation is observed and the message is still displayed check the correct insertion of cable X5
on board A12 and from X1-2 of the board to X23, X24 and X34 of the main CPU; check the
continuity of the wires and replace the faulty ones (if any).
If all cables are OK the fault is on the main CPU and it needs to be replaced.
8.2.3.3 E302: Zero position sensor for secondary ceph collimator never active
8.2.3.4 E303: Zero position sensor for secondary ceph collimator always active
The X-ray beam coming out of the tubehead assembly is collimated to the area required for the exam by a
secondary collimator that is moving synchronously with the ceph sensor holder; this collimator is moved by
stepper motor M7. All these messages refer to this mechanism; all the procedures described above for errors
E280 to E283 for patient collision are applicable. In case of absence of collision between the secondary
collimator and the patient the cause can be a fault on motor M8 and/or optical sensor barrier B11.
Check that during the power on phase there are movements on these axes; the normal motion is
going to engage the sensor and a reverse motion disengage it. If no motion is observed the fault can
be the stepper motor or the cable connecting it to the main CPU (A5). Check that the cables
between motor M7 and X4 of board A12 is well inserted as for cable X1-X2 of A12 to X23, X24 and
X34 of the main CPU.
Check the continuity of the cables mentioned above from M7 to X4 of board A12 and from X1-2 of
A12 up to X23, X24 and X34 of the main CPU.
Repeat the power on sequence while checking the motion.
If there is still no motion replace the stepper motor and if not fixed replace the CPU.
If a motion has been observed but messages are displayed this can be due to the sensor or its wiring.
Power off the system and try to manually disengage the sensor with a smooth motion.
Power on the system and check the functioning of the sensor, measuring the DC voltage on the
terminal of sensor B11 with and without an obstacle manually inserted. A variation of about 3.5 V
minimum should be observed; if not replace the sensor.
If the variation is observed and the message is still displayed check the correct insertion of cable X3
on board A12 and from X1-2 of the board up to X23, X24 and X34 of the main CPU; check the
continuity of these wires and replace the faulty ones (if any).
If all cables are OK the fault is on the main CPU and it needs replacing.
8.2.3.7 E322: Zero position sensor for primary collimator Ceph never active
8.2.3.8 E323: Zero position sensor for primary collimator Ceph always active
All the messages refer to the optical barrier that is sensing the zero position of the primary beam collimator
that is moved by a stepper motor. This mechanism is located in front of the tubehead assembly. The slit
collimator does not move during the pan examination while it has a scanning motion during ceph exams that
is synchronous with the secondary collimator and the ceph sensor holder. The first error message E320 may
also occur at the end of an examination while the system is checking if the motion is correct, meaning that
the senor activation has occurred before the expected time. This can be caused by the loss of motion of the
stepper motor. The last 3 error messages are displayed during the power on phase when the system is
controlling the functionality of the whole system. Errors E321 and E322 mean that the zero sensor position is
never activated due to a motor not running or to a fault of the optical barrier (the sensor or its harness); error
E323 means that this sensor position is always activated, in this case the fault can also be the motor or the
optical barrier.
Power off the system and remove the front cover of the tubehead assembly.
Check that during the power on phase there are movements on the primary slit collimator; the
normal motion is going to engage the sensor and a reverse motion disengage it. If no motion is
observed the fault can be stepper motor M5 or the cable connecting it to the main CPU. Check that
the cables between motor M5 and X64 is well inserted as for the cable X64 to X29 and X30 of the
main CPU A5.
Check the continuity of the above cables from M5 to X64 and from X64 to X29 and X30 of the main
CPU A5.
Repeat the power on sequence checking the motion.
If there is still no motion replace the stepper motor and if not fixed replace the CPU.
If a motion has been observed but messages are displayed this can be due to the sensor or its wiring.
Power off the system and try to manually disengage the sensor with a smooth motion.
Power on the system and check the functioning of the sensor, measuring the DC voltage on the
terminal of sensor B8 with and without an obstacle manually inserted. A variation of about 3.5 V
minimum should be observed. If not replace the sensor.
If the variation is observed and the message is still displayed check the correct insertion of the cable
from sensor B8 to X58 and from that connector to X31 of the main CPU A5; check the continuity of
these wires and replace the faulty ones (if any).
If all cables are OK the fault is on the CPU and it needs replacing.
WARNING: On generator board (A10) there are dangerous high voltages, 230 VAC
and 400 VDC. Before accessing the generator CPU and power board (A9 and A10) it is
mandatory to switch off the mains and wait up to 2 minutes in order to allow the discharge of
the capacitors.
8.2.3.13 E380: Invalid CANBus message (from generator CPU board A9)
This error is displayed when the main CPU board (A5) receives an invalid message from the generator board
(A10); this is a message whose contents are not listed on the valid data dictionary of the unit. This can be
generated by a bad connection or by a fault of the local generator CPU board (A9). Check CANBus cable
X20-X20 and replace it if faulty, otherwise replace the generator CPU board and then the generator board.
8.2.4.2 E401: Zero position sensor for Soft Tissue Filter always active
The Soft Tissue Filter for cephalometric exams is controlled by a stepper motor. During power on the system
checks if the motion is correct, checking the activation and deactivation of optical sensor B9. If it is not
sensed activated timeout message E400 is displayed; while if it is always active, error E401 is displayed. In
both cases the error can be generated by the loss of movement of the stepper motor or by a fault of sensor
B9.
Power off the system and remove the front cover of the tubehead assembly.
Check that during the power on phase there are movements on the primary slit collimator; the
normal motion is going to engage the sensor and a reverse motion disengage it. If no motion is
observed the problem can be stepper motor M6 or the cable connecting it to the main CPU. Check
that the cables between motor M6 and X65 are well inserted as for cable X65 to X29 and X30 of
main CPU board A5.
Check the continuity of these cables from M6 to X65 and from X65 to X29 and X30 of main CPU
board A5.
Repeat the power on sequence checking the motion.
If there is still no motion replace the stepper motor and if not fixed replace the CPU.
If a motion has been observed but messages are displayed this can be due to the sensor or its wiring.
Power off the system and try to manually disengage the sensor wuth a smooth motion.
Power on the system and check the functioning of the sensor, measuring the DC voltage on the
terminal of sensor B9 with and without an obstacle manually inserted. A variation of about 3.5 V
minimum should be observed; if not replace the sensor.
If the variation is observed and the message is still displayed check the correct insertion of the cable
from B9 to X33 of the main CPU board and the continuity of the connection.
If all cables are OK the fault is on the CPU and it needs replacing.
WARNING: These errors are related to the X-ray generator, so they can be safety
related. In case of error messages E759 and E755 the system must be immediately powered
off because there is an unexpected X-ray emission (error E759) or the emission has not been
terminated in the expected time.
WARNING: On the generator board (A10) there are dangerous high voltage, 230 V
AC and 400 VDC. Before accessing the generator CPU and power board (A9 and A10) it is
mandatory to switch off the mains and wait up to 2 minutes in order to allow the discharge of
the capacitors.
The CPU command for the emission, the X-ray on signal, is set to the on condition when it reaches 75% of
its set value at the beginning and is higher than 25% at the end of emission.
If the first condition is not met the exam is halted and the system has to be reset; message E758 "No X-ray"
is displayed. In this case check the correct insertions of cables X56 and X57 between the generator board
and the tubehead and X53-X53 (flat ribbon cable) between the generator board (A10) and the generator
CPU board (A9). Check the CANBus connection between the generator CPU board (A9) and main CPU A5
(cable X20-X20). If all the connections are OK and the fault is repetitive apply the procedure for LED H1 (see
LED subchapter).
If the second condition is not met and the X-ray emission does not drop below the value in a pre-set time,
message E759 "Unexpected emission" is displayed. This message can be also displayed if the X-ray on
signal is sensed during the idle state. In this case check the main CPU board (A5) and the generator CPU
board (A9) and cable X20-X20. If all are OK replace the generator board.
The emission is also controlled through a safety backup timer that interrupts the power to the tubehead in
case of a hardware or software fault in the generator CPU board. The intervention of the backup timer,
message E755, is signalled by red LED H4 lighting up. This alarm can be reset only by powering off the unit
and waiting for at least 1 minute before powering it on again. If LED H4 remains lit (on) replace the generator
board. If the LED does not remain lit (off) after powering on the unit make a new acquisition and replace the
generator board if the message appears again.
8.2.6.2 E801: On/off command for vertical motor not changed at planned time
This message is displayed when there is a fault on the column movement. Check that column movement
power supply fuse F4 is not blown. Check that the column movement safety microswitches work correctly
otherwise replace the microswitch assembly (microswitch and cable). Check CANBus cable X11-X11 and
replace it if faulty otherwise replace the column CPU board.
Release the corresponding key if pressed and repeat the power on procedure otherwise replace the
keyboard membrane and if necessary control board.
9. MAINTENANCE
As with all electrical appliances, this unit must be used correctly and maintenance and inspections must be
made at regular intervals. Such precautions shall guarantee the safe and efficient function of the unit.
Periodic maintenance consists in inspections made directly by the operator and/or technical service
department. The inspections made directly by the operator are these:
Ensure that the rating labels are intact and correctly fastened.
Check whether there are any traces of oil on the tubehead.
Check to ensure that the cable from the X-rays push-button is not split or damaged.
Check to ensure that there is no external damage to the appliance which could jeopardise protection
from radiation.
The unit's performance is checked and, where necessary corrected, during the maintenance activities
performed by the technical service department, in accordance with the indications provided in the following
chapters. Such interventions are recorded in the maintenance log in the User Manual. The periodic
maintenance performed by the technical service department comprises these additional inspection points to
be made yearly:
General visual inspection.
Grounding of all the accessible conductive parts.
Condition of the internal and external cables: wear and tear and fastenings.
Tightening of the primary bolts and screws such as the wall attachment, the moving mechanisms
and the chin rest arm.
Status of cleanliness of the console.
Correct functioning of the light indicators of the console.
Verification of the exposure parameters: kV, mA, time.
Verification of the correct function and status of cleanliness of the laser centering devices.
Verification of the correct centering of the secondary collimator and of the Ceph sensor.
3D digital sensor calibration every 6 months (see following paragraph).
NOTE: The service engineer has to take special care with regards to all the points that
concern electrical safety of the device and must make sure to restor all provisions for
electrical safety which may be affected during a service intervention; he/she should solicit
the customer to have the electrical safety tests repeated every time an intervention has
caused the replacement of important parts or the intervention has significantly affected the
safety provisions of the device.
Refer to the accessories and tools in the schematics chapter for visuals of the tools.
Figure 38
6. Click on the "Acquisition" menu and select the "System settings" options; disable the options "Offset
Calibration", "Gain calibration", "Pixel defect map" and "T Pixel Correction" - uncheck all the checkboxes.
7. In the "Acquisition" menu, select the option "Mode settings". Check the "User Sync" checkbox in order to
manually manage the exposure.
Figure 39
8. Open the "Acquisition" menu and perform an "Offset Calibration"; this calibration does not require X-ray
emission. At the end of the procedure select "Gain Calibration" in the "Acquisition" menu.
9. Make sure the unit is set to "3D dentition" mode and set these parameters: 76kV - 10mA. Position the
copper (Cu) filter of 1.5mm thickness. Start the X-ray emission; as soon as the emission starts press on
the "Continue" button to start the data acquisition for the gain calibration.
Figure 40
10. When the progress bar reaches the end press on the "Continue" button again.
Figure 41
11. At the end it will be possible to check the median gain value which should be between 2000 and 3000. In
case the value is not within this range it will be necessary to repeat the calibration and select the
exposure parameters (kV and if necessary mA) that provide the correct median value.
Figure 42
12. Repeat the calibration (steps 6 to 13) by selecting the other 3D modalities which are "2x2 4pF G4 30fps"
and "1x1 0,5pF G4 10fps" in the dropdown menu at the top left.
13. In order to calibrate the panoramic modality, select the "1x1 0,5pF G4 64 zoom" option in the dropdown
menu at the top left.
14. In the "Acquisition" menu, select the option "Mode settings" and disable the "User Sync" parameter.
Figure 43
15. Open the "Acquisition" menu and perform an "Offset Calibration"; this calibration does not require X-ray
emission. At the end of the procedure select "Gain Calibration" in the "Acquisition" menu, this screen is
displayed.
Figure 44
16. Set the I-Max Touch to "Panoramic" mode and set these parameters: 60kV - 6mA. Remove the copper
(Cu) filter of 1.5mm thickness used for the 3D calibration. Start the X-ray emission; as soon as the
emission starts press on the "Continue" button to start the acquisition for the gain calibration.
17. At the end it will be possible to check the median gain value which should be between 2000 and 3000. In
case the value is not within this range it will be necessary to repeat the calibration and select the
exposure parameters (kV and if necessary mA) that provide the correct median value.
18. At the end of calibration verify that the calibration files present in the directory "C:\IMAGERs\sensor
S/N/working modality" have been updated. In folder "C:\Documents and Settings\All Users\Application
Data\OWANDY\OSP - LAN PANORAMIC\" rename subfolder "Calibration" to "CalibrationOld". Create a
new folder "Calibration" and copy the content of folder "C:\IMAGERs\sensor S/N\" to the new
"Calibration" folder.
NOTE: After the calibration, enter the service menu, go to the CONFIGURATION menu
(password 92) and set the parameter "Skip Sensor" to OFF.
NOTE: In case of the replacement of a ceph sensor the alignment of the ceph axes
should also be verified using the ceph arm alignment procedure further down in this chapter.
In case of a 3D digital sensor replacement it will be necessary to follow the procedure described in the
subchapter about the 3D calibration files installation, in the Installation chapter, in order to:
1. Install the calibration files using the Receptor installation disc provided with the new sensor. Make sure
the calibration files have been correctly copied to the "C:\Documents and Settings\All Users\Application
Data\OWANDY\OSP - LAN PANORAMIC\Calibration" folder (or "C:\Program Data\ OWANDY\OSP -
LAN PANORAMIC\Calibration" on Windows 7).and make a copy in “C:\IMAGERs\”.
2. Configure the Mac address of the new sensor in the "Hcpconfig.ini" file of the new calibrations files, in
section “[HcpFgPleora]” under the heading “PleoraMacAddress=”.
NOTE: This subchapter is applicable for both a sensor and a tubehead replacement.
Figure 27
5. Set contrast and brightness levels to have a good visibility of all the centering balls of the centering tool.
Select the measurement tool in the imaging software and measure on the image the distance between
the two external balls; this distance has to be:
188 mm +/- 2 mm for the standard curve on a 2D unit
191 mm +/- 2 mm for the standard curve on a 3D unit
If the distance is not correct it is necessary to adjust the Y axis using the AXIS ALIGNMENT menu
(password 118) in the technical menu and make a new exposure (for more information refer to the
Technical service programs chapter).
Figure 28
6. Measure the two halves of the image (from each outer ball to the center ball) in order to check the
symmetry; the difference must be max. 1 mm. If there is a problem with the symmetry it is necessary to
adjust the rotation offset using the AXIS ALIGNMENT menu (password 118) in the technical menu and
make a new exposure.
7. In the technical menu, program the unit to use the alternative curve (please refer to the “Pan order”
option in the CONFIGURATION menu of the technical menu).
8. Open the virtual keyboard of the unit and select the Pan program - make sure the alternative curve has
been selected and not the standard curve. The name of the alternative Pan program is displayed with an
accent (‘).
9. Check that the centering phantom tool on the chin rest and the sensor calibration tool in front of the
sensor are positioned correctly.
10. Acquire in the imaging software an exposure in Adult mode:
At 72 kV - 6 mA for the I-Max Touch
At 68kV - 6mA for the I-Max Touch 3D using the copper filter or 60kV - 6mA without the copper
filter
Figure 27
11. Set contrast and brightness levels to have a good visibility of all the centering balls of the centering tool.
Select the measurement tool in the imaging software and measure on the image the distance between
the two external balls; this distance has to be:
172 mm +/- 2 mm for the alternative curve on a 2D unit
174 mm +/- 2 mm for the alternative curve on a 3D unit
If the distance is not correct it is necessary to adjust the Yevo axis using the AXIS ALIGNMENT menu
(password 118) in the technical menu and make a new exposure.
Figure 28
12. Measure the two halves of the image (from each outer ball to the center ball) in order to check the
symmetry; the difference must be max. 1 mm. If there is a problem with the symmetry it is necessary to
adjust the rotation offset using the AXIS ALIGNMENT menu (password 118) in the technical menu and
make a new exposure.
13. If needed, in the technical menu reprogram the unit with the curve required by the user (please refer to
the “Pan order” option in the CONFIGURATION menu of the technical menu)
NOTE: This subchapter is applicable for both a sensor and a tubehead replacement.
Figure 45
In case of digital sensor replacement select "No" in the message that is displayed and set the correct
sensor serial number by selecting the "Receptor setup" option in the "Acquisition" menu. It is possible to
select the serial number of the detector in the "Receptor Serial #" window that appears if it has been
previously installed in the directory "C:\IMAGERs".
Figure 46
4. Click on "OK" to verify the communication. When communication is established the "Mode" window lists
the available calibration files of the different modalities for the digital sensor; select "1x1 0.5pF G4 64
zoom" in the drop-down menu at the top left. In the window that appears set the number of frames
(acquired images) to “1000” and confirm with the "OK" button.
Figure 47
5. Move the small black square present in the upper window of the screen to the lower window and stop the
acquisition by clicking on the "Red square" button at the top right of the screen. Close the message by
clicking on the "Yes" button.
Figure 48
6. In order to center (align) the tubehead, the primary collimator, the chin support and the digital sensor it is
necessary to make exposures without any rotation of the unit. Position the centering phantom tool (refer
to the accessories and tools in the schematics chapter for details) on the chin rest and set the unit to
66kV - 6mA - 0,5sec.
7. Click on the "Acquire image" button at the top to start the acquisition and then press the X-ray trigger.
When a white image appears in the green rectangle on the screen, stop the acquisition with the "Red
square" button at the top right. Finally release the X-ray trigger. The green rectangle is the area of the
detector that is used and allows checking the centering of the image.
8. The acquisition sequence can be reviewed by pressing the "Play" key ("Green triangle" button at the top
right) and freeze the image when the white frames appear. Optimize the image selecting "Awl" on the left
side of the screen and adjust brightness and contrast with the cursors. It is also possible to select the
zoom to enlarge the image and read the position more easily. The center of the image is 32 pixels from
both sides of the window.
NOTE: When you replace the digital sensor, ONLY move the sensor in order to center
the X-ray beam. In case you replace the tubehead, move ONLY the tubehead. It is very
important to have a fixed reference point for the beam centering.
a
b d c
Figure 49
9. Depending on the result on-screen, corrections have to be made to the alignment of the parts. Points “a”,
“b”, “c” and “d” in the image above are handled in this way:
a. In case the three reference pins in the grey area of the image are aligned and centered but the X-ray
beam is not centered in the green frame, it is necessary to move the tubehead by acting on screws
number "4" (see below).
b. In case the reference pins and the X-ray beam are centered but there is a horizontal misalignment of
the image (to the left or right) in the green frame, which correspond to a vertical misalignment on the
sensor, it is necessary to move the primary collimator by acting on screws "1", "2" and "3" (see
below).
Figure 50
c. In case the image is not parallel to the window, it is possible to move the digital sensor by acting on
screws "2" (see below).
d. In case the reference pins are not positioned in the center, it is necessary to move the digital sensor
by acting on screws "1" (see below).
Figure 51
10. At the end of the adjustment, the image must be completely visible and well aligned and centered in the
green window.
Figure 52
Figure 53
4. Press the exposure button and wait for the end of the acquisition. The 3D volume will be automatically
processed.
5. Open folder C:\Program Files\Owandy\OSP_LAN_PANORAMIC\Centring. This folder contains a series
of images; each image corresponds to the same slice in the 3D volume but rebuilt with a different
horitzontal offset value. The file name of the each image contains the offset value in pixels, either
negative or positive.
6. Double-click an image in the series to open it in the Windows photo viewer or use another graphics
program to open the .bmp files. Fracture artefacts will be visible on the rounded edge of the centering
phantom tool; depending on the offset value the fracture will be offset to the left or to the right.
7. Select the image where the fracture on the rounded edge of the centering phantom tool disappears or is
minimal and note the 4-digit value mentioned in that image's filename; e.g. the value is "-1524" for file
"004 - OFFSET_HORIZONTAL_UM=-1524 (-6 pixels).bmp".
8. Open the "PANO_LAN_DLL.ini" file in this folder:
Windows XP : C:\Documents and Settings\ All Users\Application Data\OWANDY\OSP - LAN
PANORAMIC\
Windows Vista, 7 and 8: C:\Program Data\ OWANDY\OSP - LAN PANORAMIC\
9. Modify line "OFFSET_HORIZONTAL_UM=xxx" and replace the value by the 4-digit value from the
centring file that was selected above; e.g. OFFSET_HORIZONTAL_UM=-1524. Save the file.
10. In the Panolan utility, select the "3D centring" option in the "Image processing" menu again to disable it;
verify in the "Image processing" menu that the "3D centring" option is unchecked.
11. Reset the unit and make a standard 3D acquisition. The 3D volume will be automatically reconstructed
and displayed in the Panolan utility.
12. Verify that the 3D volume does not show any alignment or fracture artefacts.
WARNING: On the board shipped as a replacement the hardware key and the
EEPROM are not configured.
Hardware key A13 (code V5807302700) must be retrieved from the failed board and mounted on the new
board to activate the new CPU board in the system. This component includes the U.I.C. (Unique
Identification Code) that determines the enabling codes for the radiological exams.
D19
A13
Figure 54
The hardware key is positioned on connector XJ26 of microprocessor board A6 (code V5807302300) as
indicated in the figure below; to reach the board remove the metallic cover. The EEPROM, identified as D19
on microprocessor board A6, stores the system configuration data; remove the EEPROM from the new
board and replace it with the one present on the failed board. In case the old EEPROM is not functioning it
will be necessary to mount the EEPROM that does not contain the configuration data and manually restore
the configuration data present in the equipment parameters table by following the procedure in the technical
menu subchapter. Check that the jumpers are in the following position: X11 (closed with Pan-only) - X12
always OPEN - X13 always CLOSED.
NOTE: At the end of the board replacement reposition the metallic cover and the
ground connection. Both parts have to be recuperated from the failed board.
NOTE: This adjustment requires that a computer is directly connected to the unit and
it must be installed with the O.S.P. (drivers) and imaging software.
NOTE: When aligning the ceph on an I-Max Touch 3D unit select the I-Max Touch (not
the I-Max Touch 3D) unit in the panoramic control panel of the O.S.P. (drivers) before working
on the Ceph arm. Switch back to the I-Max Touch 3D unit once Ceph maintenance has been
finalized.
2. Press the >O< key (5). The unit will move and this message will be displayed:
WAIT FOR
MACHINE SETTING
followed by:
CEPH POSITIONING
PLEASE WAIT
When the machine stops moving, this message will be displayed:
DIGITAL CEPH
ENABLE SENSOR
These are the different steps of the digital ceph centering procedure; they must be performed in the
correct order:
1. Verification of the alignement of the ear rods
2. Ceph sensor centering
3. Secondary collimator centering
4. Soft Tissue Filter afjustment
Each step is described in detail in the following subchapters.
WARNING: X-rays will be emitted during the performance of these operations. The
authorised technicians are therefore recommended to use the greatest caution and to comply
with the safety regulations and laws of their country.
NOTE: If this message is displayed check the connection with the computer. Press
the Patient entrance" key >O< (5) to reset the message.
DIGITAL SENSOR
IS NOT READY
7. Press the X-ray trigger and keep it pressed until the end of the exposure.
Figure 55
8. At the end of the ear centering calibration evaluate on the acquired image if the X-ray beam is vertically
displaced (if more than 10 mm of upper or lower white border is present); if it is necessary to change the
height of the ceph arm loosen the two "A" screws and adjust the height of the ceph arm acting on screw
"B". Repeat the exposure until the vertical alignment is reached then tighten the "A" screws.
Figure 56
9. Evaluate on the acquired image if the ear rings are concentric (the small circle falls within the larger
circle) To adjust the vertical alignment between the two rings, loosen the two "F" screws (see image
above) and adjust the position of the arm acting on screw "G" (see image below). Check the alignment
with a new exposure and repeat until the alignment is done, then tighten bolt "H" and screws "F".
G
H
Figure 57
10. If in the image the big circle it is not positioned horizontally in the middle of the X-ray beam, it is
necessary to turn the rotation arm. With the up and down arrow keys set the speed value (suggested
value: 2) and with the right and left arrow keys turn the rotation arm:
a. Increasing the offset value if the distance on the left of the big circle is smaller than the distance
on the right.
b. Decreasing the offset value it if the distance on the left of the big circle is larger than the distance
on the right.
When the correct setting is reached press Test key “T”to display this message:
UPDATE CHANGES?
>0< = Y, T = N
Press the "Patient centering" key >O< to store the changes and the Test key “T” to exit the technical
menu. Access the CEPH SETTING menu (password 124) in the technical menu again (for more
information refer to the Technical service programs chapter) and enter the “Rotation Offset” submenu
again as described at the beginning of this procedure. Make another exposure and repeat until the big
circle is centered in the X-ray beam.
NOTE: Write down the new value in the relevant box in the appendix of this manual.
11. To adjust the horizontally alignment between the two rings, loosen the two "C" screws and rotate the ear
rod assembly support acting on screw "D". Once the alignment is done tighten screws "C".
Figure 58
Figure 59
2. Should the central vertical strip not be centered, use the "Size Selection" key to select "CEPH SENSOR
ZERO" menu; this message will be displayed:
S ZERO [ff] a
ZERO OFFS ±eeeee
With the up and down arrow keys set the speed value (suggested value 2) and with the left and right
arrow keys move the ceph sensor:
a. Increasing the offset value if the distance on the left of the stripe is larger than the distance on
the right.
b. Decreasing the offset value it if the distance on the left of the stripe is smaller than the distance
on the right.
3. Close the sensor holder, if open and press key "Adult/Child Selection" key, this message will be
displayed:
UPDATE CHANGES?
>0< = Y, T = N
Press the "Patient centering" key >O< to store the changes and reset the axis position.
4. Press the "Exam Mode Selection" key to move the ceph sensor in the acquisition start position.
5. Press the X-ray trigger to make a new image acquisition.
6. Repeat the procedure from the beginning until the stripe is centered correctly.
7. When the correct setting is reached press Test key “T” to exit the Rotation offset menu and return to the
main technical menu:
NOTE: Write down the new value in the appendix of this manual.
8. Acquire an X-ray image by pressing the X-ray trigger and check if in the obtained narrow image the
projection of the slit of the ceph sensor centering tool is vertical and positioned in the middle of the area
which is defined by the arc (see figures below).
Figure 60
Figure 61
10. If it is not the case use the up and down arrow keys to set a speed value (suggested value 3) and with
the left and right arrow keys move the secondary collimator:
a. Increasing the offset value if the distance on the left is smaller than the distance on the right.
b. Decreasing the offset value it if the distance on the left is larger than the distance on the right.
NOTE: This is a fine setting; if the zero offset (±eeeee) is lower than –1000 steps or
greater than 1000 steps repeat the first step of the ceph arm centering described in the ear
rings alignment procedure above.
11. When the correct setting is reached press Test key “T”to display this message:
UPDATE CHANGES?
>0< = Y, T = N
Press the "Patient centering" key >O< to store the changes and the Test key “T” to exit the technical
menu.
NOTE: Write down the new value in the appendix of this manual.
6. Press the "P" key then use the up and down arrow keys to set the exposure parameters (suggested
values: 60kV, 6mA and 0.2s).
WARNING: X-rays will be emitted during the performance of these operations. The
authorised technicians are therefore recommended to use the greatest caution and to comply
with the safety regulations and laws of their country.
7. Press the X-ray trigger and keep it pressed until the end of the exposure; this message will be displayed:
ENTER IMG OFFSET
OFFSET (mm) 50
8. On the acquired image measure (in mm) distance "A" between the Soft Tissue Filter edge and the center
of the ear rings.
Figure 62
9. If distance "A" is different from 50±2mm, press the up and down arrow keys to reach the measured
value; press the >O< key to store the change; the system will calculate automatically the new Soft
Tissue Filter offset. If distance "A" is 50±2mm no correction is needed; press "Test" key (T) to exit. In
either case this message will be displayed:
STF ZERO OFFS a
OFFSET ±xxx
10. Check the correct alignment of the Soft Tissue Filter by performing a new exposure (repeat the actions
above until the alignment is correct). Store the new setting by pressing the "Test" key (T). The display
will show:
UPDATE CHANGES?
>0< = Y, T = N
Press the >O< key to permanently store the changes.
11. Press the "Test" key (T) to exit the CEPH SETTINGS menu (password 124), this message will be
displayed
CONFIRM EXIT?
>0< = Y, T = N
Press the "Test" key (T) again to exit the menu and store the changes.
NOTE: Write down the new value in the appendix of this manual.
Refer to the computer installation instructions for the different installation procedures.
Layout & circuit diagram rotation arm board A7 - Code 58073025 Rev. P - Page 1 of 1
10.14 Layout and circuit diagram ceph arm connection board A12
1 2 3 4
1
X5 1 1 X2
X4 X3 1
1
X6 X1
1
B
C
1 1
2 3
3 2
4 4
5 X4
6 1
7 4
8 2
X1 3
X6
D 3 1 + FOTOCEL. (+PHOTOCELL)
4 2 - FOTOCEL. (-PHOTOCELL)
2 3 B2
1 4
X2 X3
1 + FOTOCEL. (+PHOTOCELL)
2 - FOTOCEL. (-PHOTOCELL)
3 B1
4
X5
Layout & circuit diagram board A12 - Code 58098150 Rev. 0 - Page 1 of 1
Layout & circuit diagram rotation arm board A7 - Code 58073025 Rev. P - Page 1 of 1
11.14 Layout and circuit diagram ceph arm connection board A12
1 2 3 4
1
X5 1 1 X2
X4 X3 1
1
X6 X1
1
B
C
1 1
2 3
3 2
4 4
5 X4
6 1
7 4
8 2
X1 3
X6
D 3 1 + FOTOCEL. (+PHOTOCELL)
4 2 - FOTOCEL. (-PHOTOCELL)
2 3 B2
1 4
X2 X3
1 + FOTOCEL. (+PHOTOCELL)
2 - FOTOCEL. (-PHOTOCELL)
3 B1
4
X5
Layout & circuit diagram board A12 - Code 58098150 Rev. 0 - Page 1 of 1
Circuit diagram power hub board A21 - Code 39079038 Rev. P - Page 1 of 1
COMPONENTS SIDE
58073031/
SOLDER SIDE
12.1 Column
12.1.2 Cables
7
2
4
13
3
8
16
12
14
10
11
15
12.2.1 Cables
2
6 (B3)
3
6 (B1)
6 (B2)
11
1
10
5 (B 6 / B 7 )
8
7
5 (B 8 / B 9 )
6 12 13
5
1 (B11)
1 (B10)
1 (B11) 4
3 6
5
2 1 (B10)
6 4
10
12.5 Covers
1
4
2
7
14
10
13 11
6
12
Symmetry check tool (P/N 5207900200) Copper filter for digital sensor (P/N 5607900800)
13.1 Column
13.1.2 Cables
7
2
4
13
3
8
16
12
14
10
11
15
13.2.1 Cables
1
6 (*)
8 (B3)
7
3
2
8 (B1)
8 (B2)
11
14
1
13
12
5 (B8 / B9)
6
1 (B11) 4
3 6
5
2 1 (B10)
6 4
10
13.2.1 Covers
1
4
2
7
14
10
13 11
12 15
Symmetry check tool (P/N 5207900200) Copper filter for digital sensor (P/N 5607900800)
14. APPENDICES
Panoramic Bitewing
NOTE: The data listed in the table are the technical parameters set during factory
testing. Preferences set by the user (e.g. exposure parameters different than the default ones)
are not listed.
The table also contains columns with blank cells; those cells must be filled in when during installation or
during the life on the unit any of the listed parameters are modified (e.g. after replacing a motor or a
positioning sensor).