DIGITAL RADIOGRAPHY

CXDI-40EG
User’s Manual

Before using the instrument, be sure to read this manual thoroughly.

Also, read the manuals of other instruments in the system.
Keep the manual where it is easily accessible.
PLEASE NOTE

1. The user is responsible for the use and maintenance of the product.
We suggest that a member of the user’s staff be designated as being in charge of mainte-
nance so as to ensure that the product is kept in a safe and good condition.
Also, medical products must be used only by a qualified person.

2. Roentgenography, image processing, reading of image, and storage of data must be per-
formed in accordance with the law of the country where the product is being used.
Also, the user is responsible for maintaining the privacy of image data.

3. In no event will Canon be liable for direct or indirect consequential damage arising out of
the use of this product. Canon will not be liable for loss of image data due to any reason.

4. This product may malfunction due to electromagnetic waves caused by portable personal
telephones, transceivers, radio-controlled toys, etc. Be sure to avoid having objects such
as these, which affect this product, brought near the product.

5. Canon reserves the right to change the specifications, configuration and appearance of
the product without prior notice.

System and product names in this manual are the trademarks of each manufacturer that
developed them.

© CANON INC. 2005

All rights reserved.

Under copyright laws, this manual may not be copied, in whole or in part, without the written
consent of Canon.
 Safety Information
Regulations

This instrument conforms to IEC 60601-1-2:2001.

For U.S.A.
This instrument is a CLASS I EQUIPMENT according to UL60601-1.

MEDICAL ELECTRICAL EQUIPMENT

WITH RESPECT TO ELECTRIC SHOCK,
FIRE AND MECHANICAL HAZARDS
ONLY IN ACCORDANCE WITH UL60601-1.
41C4

IN ACCORDANCE WITH CAN/CSA C22.2 NO. 601.1,

MEDICAL EQUIPMENT CERTIFIED FOR CANADA
CONTROL NUMBER 41C4

Grounding reliability can only be achieved when the equipment is connected to an equivalent
receptacle marked “Hospital Only” or “Hospital Grade”.

For EU Countries
The following mark shows compliance of the instrument with Directive 93/42/EEC.

This instrument has been classified into EN55011 Group 1/Class A.

This instrument is a CLASS I EQUIPMENT according to EN 60601-1.

(1)
Safety Information

Guidance and Manufacturer’s Declaration – Electromagnetic Emissions

The CXDI-40EG is intended for use in the electromagnetic environment specified below.
The user of the CXDI-40EG should assure that it is used in such an environment.

Emission Test Compliance Electromagnetic Environment – Guidance

RF emissions GROUP 1 The CXDI-40EG uses RF energy only for its internal func-
CISPR 11 tion. Therefore, its RF emissions are very low and are not
likely to cause any interference in nearby electromagnetic
equipment.

RF emissions Class A The CXDI-40EG is suitable for use in all establishments

CISPR 11 other than domestic and those directly connected to the
public low-voltage power supply network that supplies
Harmonic emissions Not Applica- buildings used for domestic purposes.
IEC 61000-3-2 ble

Voltage fluctuations/ Complies

flicker emissions
IEC 61000-3-3

IEC 60601 Compliance

Immunity Test Electromagnetic Environment – Guidance
Test Level Level

Electrostatic dis- ±(2, 4, 6) kV ±(2, 4, 6) kV Floors should be wood, concrete or

charge (ESD) contact contact ceramic tile. If floors are covered with syn-
IEC 61000-4-2 thetic material, the relative humidity
±(2, 4, 8) kV ±(2, 4, 8) kV should be at least 30%.
air air
Electrical fast tran- ±2 kV for ±2 kV for Mains power quality should be that of a
sient/burst power supply power supply typical commercial or hospital environ-
IEC 61000-4-4 lines lines ment.

±1 kV for ±1 kV for
input/output input/output
lines lines

Surge ±1 kV differ- ±1 kV differ- Mains power quality should be that of a

IEC 61000-4-5 ential mode ential mode typical commercial or hospital environ-
ment.
±2 kV com- ±2 kV com-
mon mode mon mode

(2)
 Safety Information

IEC 60601 Compliance

Immunity Test Electromagnetic Environment – Guidance
Test Level Level

Voltage dips, short <5% UT <5% UT Mains power quality should be that of a
interruptions and volt- (>95% dip in (>95% dip in typical commercial or hospital environ-
age variations on UT) for 0.5 UT) for 0.5 ment. If the user of the CXDI-40EG
power supply input cycle. cycle. requires continued operation during power
lines mains interruptions, it is recommended
IEC 61000-4-11 40% UT 40% UT that the CXDI-40EG be powered from an
uninterruptible power supply.
(60% dip in (60% dip in
UT) for 5 UT) for 5
cycles cycles

70% UT 70% UT
(30% dip in (30% dip in
UT) for 25 UT) for 25
cycles cycles

<5% UT <5% UT
(>95% dip in (>95% dip in
UT) for 5 sec. UT) for 5 sec.

Power frequency 3 A/m 3 A/m Power frequency magnetic fields should

(50/60Hz) magnetic be at levels characteristic of a typical loca-
field tion in a typical commercial or hospital
IEC 61000-4-8 environment.

NOTE: UT is the a.c. mains voltage prior to application of the test level.

(3)
Safety Information

IEC 60601 Test Compliance

Immunity Test Electromagnetic Environment – Guidance
Level Level

Conducted RF 3 Vrms 3Vrms Portable and mobile RF communications

IEC 61000-4-6 150 kHz to 80 equipment should be used no closer to
MHz any part of the CXDI-40EG, including
cables, than the recommended separation
distance calculated from the equation
Radiated RF 3 V/m 3 V/m applicable to the frequency of the trans-
IEC 61000-4-3 80 MHz to 2.5 mitter.
GHz
Recommended separations distance
d = 1.2 P

d = 1.2 P 80 MHz to 800 MHz

d = 2.3 P 800MHz to 2.5 GHz

where P is the maximum output power rat-

ing of the transmitter in watts (W) accord-
ing to the transmitter manufacturer and d
is the recommended separation distance
in metres (m).

Field strengths from fixed RF transmitters,

as determined by an electromagnetic site
surveya, should be less than the compli-
ance level in each frequency rangeb.

Interference may occur in the vicinity of

equipment marked with the following sym-
bol:

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflections from structures, object and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) tele-
phones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast can-
not be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed
RF transmitters, an electromagnetic site survey should be considered. If the measured field strength
in the location where the CXDI-40EG is used exceeds the applicable RF compliance level above, the
CXDI-40EG should be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as reorienting or relocating the CXDI-40EG.

b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

(4)
 Safety Information

General Safety Information

Follow the safety instructions in this manual and all warnings and cautions printed on the warning
labels. Ignoring such cautions or warnings while handling the product may result in injury or accident.
Be sure to read and fully understand the manual before this product.
Keep this manual for future reference.

Meaning of Caution Signs

This indicates a potentially hazardous situation which, if not heeded, could
! WARNING result in death or serious injury to you or others.

This indicates hazardous situation which, if not heeded, may result in minor or
! CAUTION moderate injury to you or others, or may result in machine damage.

This is used to emphasize essential information.

NOTE Be sure to read this information to avoid incorrect operation.

Environment of Use and Storage

Do not use or store the instrument near any flammable chemicals such as
alcohol, thinner, benzine, etc. Also, this instrument is not a category AP or
APG equipment. If chemicals are spilled or evaporate, it may result in fire or
! WARNING electric shock through contact with electric parts inside the instruments. Also,
some disinfectants are flammable.
Be sure to take care when using them.

Do not install the instrument in a location with the conditions listed below.
Otherwise, it may result in failure or malfunction, fall or cause fire or injury.
• Close to facilities where water is used.
• Where it will be exposed to direct sunlight.
• Close to air-conditioner or ventilation equipment.
• Close to heat source such as a heater.
! CAUTION • Prone to vibration.
• Insecure place.
• Dusty environment.
• Saline or sulfurous environment.
• High temperature or humidity.
• Freezing or condensation.

Installation Operation
Do not connect the instrument with anything other than specified.
! WARNING Otherwise, it may result in fire or electric shock.

(5)
Safety Information

Power Supply
Be sure to turn OFF the power of each instrument before connecting or dis-
connecting the cables.
! WARNING Also, do not handle them with wet hands. Otherwise, you may get an electric
shock that may result in death or serious injury.

Be sure to hold the plug or connector to disconnect the cable.

! WARNING If you pull the cable, the core wire may be damaged, resulting in fire or electric
shock.

Do not cut or process the cables. Also, do not place anything heavy, including
the instrument on it, step on it, pull it, bend it, or bundle it.
! WARNING Otherwise, the cable may be damaged, which may result in fire or electric
shock.

Do not turn ON the system power when condensation is formed on the instru-
! WARNING ment. Otherwise, it may result in fire or electric shock.

Be sure to ground the instrument to an indoor grounded connector.

! CAUTION Otherwise, fire or electric shock may be caused due to leakage.

Handling
Always be sure to keep checking the condition of the system and the patient
to ensure they are normal during the use of the instrument.
! WARNING If any problem is found, take appropriate measures, such as stopping the
operation of the instrument, as required.

Never disassemble or modify the product as it may result in fire or electric

shock. Also, since the instrument incorporates high-voltage parts that may
! WARNING cause electric shocks and other hazardous parts, touching them may cause
death or serious injury.

Do not place anything on top of the instrument.

Otherwise, the object may fall and cause injury.
! WARNING Also, if metal objects such as needle or clip falls into the instrument, or if liquid
is spilled, it may result in fire or electric shock.

Have the patient take a fixed posture and do not let the patient touch parts
! WARNING unnecessarily. If the patient touches connectors or switches, it may result in
electric shock or malfunction of the instrument.

Do not hit or drop the instrument. The instrument may be damaged if it

! WARNING receives a strong jolt, which may result in fire or electric shock if the instru-
ment is used without it being repaired.

Wipe the CFRP plate and the chin rest of the sensor unit with ethanol or glut-
araldehyde solution to disinfect it each time a different patient uses the instru-
! CAUTION ment, in order to prevent infection.
Please consult a specialist for the procedure for disinfection.

(6)
 Safety Information

Handling
Do not apply weight of more than196 N (20 kgf) to the front cover of the sen-
sor unit. Also, do not apply weight when the grid unit is not fully inserted, or
! CAUTION when the cover of the slot for the grid unit is not completely closed.
Otherwise, the sensor will be damaged.
Sensor unit must be horizontal or vertical with the floor when mounting/remov-
! CAUTION ing the grid unit. Also, hold the grid unit firmly with both hands.
Otherwise, the grid unit may fall and cause injury.

Hold the grid unit firmly with both hands when mounting/removing or carrying
! CAUTION the grid unit. Otherwise, the grid unit may fall and cause injury.

Be sure to push the back of the grip with your palm when inserting the grid
! CAUTION unit fully into the slot. Do not grasp the grip. Otherwise, your hand may get
caught in the slot.

Do not put your fingers into the grid unit slot when the grid unit is not inserted.
! CAUTION Do not let the examinee put his/her fingers into it either.
Otherwise, the fingers may get injured.

Ensure that the grid unit is locked when moving or rotating the sensor unit
! CAUTION after grid unit is mounted. Otherwise, the grid unit may fall and cause injury.

Turn off the power of each instrument for safety when they are not going to be
! CAUTION used.

This instrument incorporates lead, which may pollute the environment if the
instrument is abandoned.
! CAUTION Please ask a professional waste disposal company to handle disposal, or con-
tact Canon representative or distributor before disposing of the instrument.

When Problem Occurs

Should any of the following occur, immediately turn OFF the power of each
instrument, unplug the power cable from the AC outlet, and contact Canon
representative or distributor.
! WARNING • When there is smoke, odd smell or abnormal sound.
• When liquid has been spilled into the instrument or a metal object has
entered through an opening.
• When the instrument has been dropped and it is damaged.

(7)
Safety Information

Maintenance and Inspection

For safety reasons, be sure to turn OFF the power of each instrument when
! WARNING the inspections indicated in this manual are going to be performed.
Otherwise, it may result in electric shock.

When the instrument is going to be cleaned, be sure to turn OFF the power of
each instrument, and unplug the power cable from the AC outlet.
! WARNING Never use benzine, thinner or any other flammable cleaning agents.
Otherwise, fire or electric shock may be caused.

The instrument must be repaired by a qualified engineer only.

! WARNING If it is not repaired properly, it may cause fire, electric shock, or accident.

! CAUTION For safety reasons, be sure to inspect the instrument before using it.

(8)
 Safety Information

Labels and Markings on the Instrument

The CXDI-40EG has a few labels and markings on it.

Contents of labels and markings and positions where they are attached are indicated below.
The illustrations below are examples of sensor units with the grid unit slot on the left hand side.

Upright Stand Type Sensor Unit

This mark indicates that this is a Type B

Applied Part according to EN60601-1.
This unit can be installed in the patient
environment.

Name Label

Universal Stand Type Sensor Unit

This mark indicates that this is a Type B
Applied Part according to EN60601-1.
This unit can be installed in the patient
environment.

Name Label

(9)
Safety Information

Table Type Sensor Unit

This mark indicates that this is a Type B

Applied Part according to EN60601-1.
This unit can be installed in the patient
environment.

Name Label

(10)
 Contents

Safety Information .................................................................................................... (1)

Regulations ................................................................................................................................(1)
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions .................................(2)
General Safety Information ........................................................................................................(5)
Labels and Markings on the Instrument .....................................................................................(9)

1. Overview .................................................................................................................1

2. Notes for Using the Instrument ...............................................................................2

3. Description ..............................................................................................................3
3.1 Sensor Unit .......................................................................................................................... 3
3.2 Grid Frame Unit ................................................................................................................... 5

4. Operation ................................................................................................................6
4.1 Turning ON/OFF the Power of the System ......................................................................... 6
4.2 Calibration ........................................................................................................................... 6
4.3 Mounting/Removing the Grid Unit ........................................................................................ 7
4.4 Special Notes on Handling the Ready Lamp ..................................................................... 11
4.5 Aligning the Table Type Sensor Unit with X-ray Field ....................................................... 12

5. Inspection and Maintenance .................................................................................13

5.1 Inspection .......................................................................................................................... 13
5.2 Cleaning ............................................................................................................................. 16
5.3 Storage of Grid Unit ........................................................................................................... 17

6. Service Information ...............................................................................................18

7. Specifications ........................................................................................................19
7.1 Main Specifications ............................................................................................................ 19
7.2 Characteristics ................................................................................................................... 20

8. Components ..........................................................................................................22

9. Dimensions ...........................................................................................................23
9.1 Sensor Unit ........................................................................................................................ 23
9.2 Grid Frame Unit ................................................................................................................. 24
9.3 Ready Lamp ...................................................................................................................... 25
1. Overview

The Digital Radiography CXDI-40EG directly converts the X-ray images captured by
the LANMIT (Large Area New MIS Sensor and TFT) sensor into a high-resolution digital
images.
There are three types of CXDI-40EG. They can be installed on an upright stand, universal
stand or a table.

–1–
2. Notes for Using the Instrument

Before Exposure
Sudden heating of the room in cold areas will cause condensation to form on the instru-
ment. In this case, wait until condensation disappears before performing exposure.
If the instrument is used with condensation formed on it, problems may occur in the qual-
ity of the instrument.
When an air-conditioner is going to be used, be sure to raise/lower the temperature gradu-
ally so that a difference in temperature in the room and in the instrument does not occur, to
prevent forming of condensation.

During Cleaning
Do not use anything other than neutral detergent for cleaning the cover of the instrument.
Otherwise, the coating will be corroded.

During Installation
Handle the instrument carefully, as preadjustment may be altered if the instrument receives
a strong jolt.

Others
Be sure to reconnect the cables to the proper connectors. Otherwise, the instrument may
malfunction or may be damaged.

–2–
3. Description

3.1 Sensor Unit

This unit is installed in the patient environment.
The illustrations below are examples of sensor units with the grid unit slot on the left hand
side.

Upright Stand Type

Eject button Chin rest

Press this button to release the primary The patient’s chin is placed on
lock when removing the grid unit. this rest.

Grid unit slot

Insert the grid unit into this slot.

–3–
3.1 Sensor Unit

Universal Stand Type

Eject button Chin rest
Press this button to release the primary The patient’s chin is placed on this rest.
lock when removing the grid unit.

Grid unit slot

Insert the grid unit into this slot.

Table Type
Eject button
Press this button to release the primary lock when removing
the grid unit.

Grid unit slot

Insert the grid unit into this slot.

–4–
 3.2 Grid Frame Unit

3.2 Grid Frame Unit

This unit is for holding the optional grid.

Slide levers (on the Slide levers (on the

front and back sides) front and back sides)
Slide the levers to release Slide the levers to release
the secondary lock for the secondary lock for
removing the grid frame removing the grid frame
unit. unit.

Grip
Hold this grip when
mounting/removing/
carrying the grid frame
unit.

–5–
4. Operation

4.1 Turning ON/OFF the Power of the System

When turning ON/OFF the power of the sensor unit, refer to the Power Box (option) Oper-
ation Manual.

4.2 Calibration
Calibration is important to ensure that a good image is achieved with the CXDI-40EG by
obtaining the calibration data of the sensor unit. Perform calibration when exposure condi-
tions have changed significantly.

NOTE: For procedure for calibrating, refer to “Calibrating the Instrument” in the CXDI
Series Operation Manual.

–6–
 4.3 Mounting/Removing the Grid Unit

4.3 Mounting/Removing the Grid Unit

Sensor unit must be horizontal (A) or vertical (B) with the floor as illustrated
below when mounting/removing the grid unit.
If the grid unit slot is faced upward or downward when mounting/removing the
grid unit, the grid unit may move in the slot, or may fall and cause injury.

! CAUTION

Hold the two parts of the grid unit (the grip and the side for upright stand/uni-
versal stand type, or the two sides for table type sensor unit) indicated below
firmly with both hands when mounting/removing the grid unit. Be sure to hold
the grip and a side when carrying it too.
Otherwise, the grid unit may fall and cause injury.

! CAUTION
When the grid unit For the table type
slot is on the right sensor unit or
side of the upright when the grid unit
stand/universal slot is on the left
stand type sensor side of the upright
unit. stand/universal
stand type sensor
unit.

Be sure to push the back of the grip with your palm when inserting the grid unit
! CAUTION fully in the slot. Do not grasp the grip. Otherwise, your hand may get caught
into the slot.

Ensure that the grid unit is locked when moving or rotating the sensor unit after
! CAUTION grid unit is mounted. Otherwise, the grid unit may fall and cause injury.

Do not put your fingers into the grid unit slot when the grid unit is not inserted.
! CAUTION Do not let the examinee put his/her fingers in it either.
Otherwise, the fingers may get injured.

–7–
4.3 Mounting/Removing the Grid Unit

NOTES: 1. Do not hit or drop the grid unit. The unit is delicate and may be damaged if it
receives a strong jolt. Also, do not apply excessive force to the sensor unit
while mounting/removing the grid unit.

2. When the grid unit is not in use, ensure it is protected from dust and
scratches. Blow off any dust from the grid unit before mounting it.

3. Do not leave the grid unit halfway out from the sensor unit. Also, do not apply
excessive force to it when it is in that position. Otherwise, it may fall and be
damaged.

Special Notes on Handling the Grid (Option)

NOTE: Structure of grid is delicate. Do not drop, knock over, bend, or apply force or jolt
to it. Even if it is not externally damaged, its characteristics may be changed,
which may cause a problem in image quality.

–8–
 4.3 Mounting/Removing the Grid Unit

4.3.1 Mounting the Grid unit

NOTES: 1. The procedures indicated below may slightly differ when the sensor unit is
horizontal.

2. Be sure to insert the grid unit slowly into the slot. Otherwise, the unit may be
damaged.

(1) Clean the grid unit.

Blow off the dust on the surface of the grid and the grid unit before mounting them.

(2) Hold the grid unit.

Firmly hold the grip and one side of the grid unit with both hands.

(3) Slowly insert the grid unit into the slot.

Insert the grid unit slowly into the
slot of the sensor unit with the cau-
tion labels on the grid unit facing the
X-ray tube.
If the grid unit is inserted inside out,
Caution labels
an error message will be displayed
on the operation unit, and exposure
will not be able to be performed.

(4) Lock the grid unit.

When the grid unit is inserted half-
way in (about 25 cm), take your hand
off from the grip and fully insert the
grid unit into the slot by pushing the
back of the grip with the palm of the
hand.
At this time, do not grasp the grip.
Otherwise, your hand may get caught
in the slot.

(5) Take your hand off.

When the grid unit is fully inserted, it will be locked. Make certain that the grid unit
is locked and take your hand off.
If the grid unit is not properly inserted and locked, the grid unit will automatically
be ejected. Repeat the procedure from step (3) again.

NOTE: Be sure to confirm that the grid unit is locked after mounting it.
Otherwise, it may fall and be damaged.

–9–
4.3 Mounting/Removing the Grid Unit

4.3.2 Removing the Grid Unit

NOTES: 1. The procedures indicated below may slightly differ when the sensor unit is
horizontal.

2. Be sure to remove the grid unit slowly from the slot. Also, do not forcibly pull
out the grid unit any further after it is locked part of the way in. Otherwise, the
unit may be damaged.

(1) Press EJECT button on the sensor unit.

The grid unit will be ejected about
4.5 cm. Be careful as the grid unit
may pop out if it is light.

(2) Pull the grid unit.

Hold the grip of the grid unit and slowly pull the unit halfway out (about 40 cm)
until the grid unit stops at the mid-lock position. Do not pull the grid unit any fur-
ther.

(3) Slide the slide lever.

Hold the side of the grid unit, near
the slide lever on the opposite side of
the chin rest.
Slide the slide lever on the opposite
side of the chin rest to release the
lock. Do not pull the grid unit while
sliding the lever, as it will become
difficult to slide one.

(4) Remove the grid unit.

While holding the slide lever,
remove the grid unit slowly from the
sensor unit with both hands.

(5) Check the sensor unit.

Confirm that the cover of the slot is
closed.

– 10 –
 4.4 Special Notes on Handling the Ready Lamp

4.4 Special Notes on Handling the Ready Lamp

Do not remove the cap of the ready lamp.

Cap

Ready Lamp

– 11 –
4.5 Aligning the Table Type Sensor Unit with X-ray Field

4.5 Aligning the Table Type Sensor Unit with X-ray Field
Perform the following alignment when the top of the table in which the grid unit is
installed is not transparent.

NOTE: Grid unit is used in place of cassette and tray, for aligning the sensor unit with the
X-ray field.

(1) Position the X-ray tube.

Position the X-ray tube in the transverse center of the sensor unit, i.e. lateral center
of the table. Positioning can be done manually, by using either a mechanical or elec-
trical indicator. For details, see the tube conveyor installation manual.

(2) Place the X-ray tube.

Place the X-ray tube over the area that is going to be exposed. Use the collimator
light field for proper positioning.

(3) Pull the grid unit.

Pull the grid unit approximately 25 cm out from the sensor unit.

(4) Align the sensor unit.

Move the sensor unit until the slit on the grip of the grid unit is aligned with the cen-
ter alignment light from the collimator, i.e. the center of the table in longitudinal
direction.

(5) Push in the grid unit.

Fully insert the grid unit into the slot by pushing the back of the grip with the palm
of the hand. Then, perform exposure.

– 12 –
5. Inspection and Maintenance

The instrument must be repaired by a qualified engineer only.

! WARNING If it is not repaired properly, it may cause fire, electric shock, or
accident.

For safety reasons, be sure to inspect the instrument before using

! CAUTION it. In addition, carry out a regular inspection at least once a year.

5.1 Inspection
In order to ensure that the instrument is used safely and normally, please be sure to inspect
the instrument before use.
If any problem is found during the inspection, please take measures indicated in this chap-
ter.
If problem still cannot be corrected, please contact Canon representative or distributor.

It is recommended that a record of the inspection be kept by making copies of the check
lists in this section, or making a separate check list.

– 13 –
5.1 Inspection

5.1.1 Daily Inspection

5.1.1.1 Before Turning ON the Power

For safety reasons, be sure to turn OFF the power of each instru-
! WARNING ment when the following inspections are going to be performed.
Otherwise, it may result in electric shock.

Result
Inspection Remedy
Date Date Date
/ / /

Check that cables are not

Contact Canon or distribu-
damaged or cover of cables Good/Bad Good/Bad Good/Bad
tor if there is any problem.
is not torn.
Cable

Check that the plugs and

Fully insert the cables and
locks of connectors are not Good/Bad Good/Bad Good/Bad
lock them.
loose.
Sensor unit

Check that the cover or parts

Contact Canon or distribu-
are not damaged and not Good/Bad Good/Bad Good/Bad
tor if there is any problem.
loose.

Remove dust and dirt by

Grid unit

Check that the grid and grid

gently wiping the grid/grid
unit are not free of dust and Good/Bad Good/Bad Good/Bad
unit with a dry cloth so as
dirt.
not to scratch them.

5.1.1.2 After Turning ON the Power

Result
Inspection Remedy
Date Date Date
/ / /

Take measures if error mes-

sage is displayed by refer-
ring to the CXDI Series
General

Operation Manual attached

Perform test exposure. Good/Bad Good/Bad Good/Bad
to the Control Station. Con-
tact Canon or distributor if
the problem cannot be
solved.

– 14 –
 5.1 Inspection

5.1.2 Monthly Inspection

Perform the following inspection periodically more than once a month. Contact Canon
representative or distributor if you cannot do it.

Result
Inspection Remedy
Date Date Date
/ / /

Check the performance of Refer to the CXDI Series

General

the instrument by perform- Operation Manual for the

ing exposures using a phan- Good/Bad Good/Bad Good/Bad procedure for self-test. Con-
tom or a resolution chart, or tact Canon or distributor if
perform self-test. there is any problem.

5.1.3 Yearly Inspection

Perform the following inspection periodically more than once a year. Contact Canon repre-
sentative or distributor if you cannot do it.

Result
Inspection Remedy
Date Date Date
/ / /

Check the performance of

General

the instrument by perform- Contact Canon or distributor

Good/Bad Good/Bad Good/Bad
ing an exposure using a if there is any problem.
phantom or resolution chart.

5.1.4 Calibration
Perform calibration when exposure conditions have changed significantly.
See the CXDI Series Operation Manual for the procedure for calibration.

– 15 –
5.2 Cleaning

5.2 Cleaning

5.2.1 Cover
Clean the cover by the following procedure if it is dirty.

When the instrument is going to be cleaned, be sure to turn OFF

the power of each instrument, and unplug the power cable from
! WARNING the AC outlet.
Never use alcohol, benzine, thinner or any other flammable clean-
ing agents. Otherwise, it may result in fire or electric shock.

(1) Turn OFF the power of the power box.

Shut down the control station or control computer, and press side “0” of the power
switch.

(2) Turn OFF the power of each instrument.

Turn OFF the power of each instrument if connected.

(3) Unplug the power cables.

Unplug the power cables of each instrument from the AC outlet.

(4) Wipe the cover using neutral detergent.

Wipe the cover with a piece of cloth soaked in neutral detergent diluted in water and
wrung dry.

(5) Wipe out neutral detergent.

Wipe the cover with a piece of cloth soaked in water and wrung dry whenever neur-
tral detergent has been used.

– 16 –
 5.3 Storage of Grid Unit

5.2.2 CFRP (Carbon Fiber Reinforced Plastic) Plate and Chin Rest

Wipe the CFRP (carbon fiber reinforced plastic) plate and chin
rest of the sensor unit with ethanol or glutaraldehyde solution to
disinfect them each time a different patient uses the instrument, in
order to prevent infection.
! WARNING Please consult a specialist for the procedure for disinfection.
If you are using disinfectant other than those specified above, or
you are mixing another disinfectant with ethanol, please also con-
sult a specialist, because they may harm the CFRP plate.

The illustration below is an example of the upright stand type sensor unit.
Chin rest is only fitted on the upright stand or universal stand type sensor unit.

Chin rest

CFRP plate

5.3 Storage of Grid Unit

It is recommended that the grid unit is kept when not in use so as to keep dust off and pre-
vent it from getting scratched.

– 17 –
6. Service Information

Repair
If problems cannot be solved even after taking the measures indicated in chapter 5, contact
Canon representative or distributor for repair.
Please refer to the name label and let us have the following information:

Name of the unit: It is indicated on the name label.

Serial number: 6-digit number indicated on the name label.
Phenomenon: In detail.

Limit for Supplying Performance Parts for Repair

Performance parts* of this product will be stocked for eight years after discontinuance of
production, to allow for repair.

* Parts required to maintain the functioning of the product

Expendable Parts Replaced by Service Personnel

Following parts are apt to become worn out or to deteriorate due to the characteristics of
the material or structure.
These parts cannot be replaced by the user.
If these parts are found to be worn out or to have deteriorated during daily inspection or
use, contact Canon representative or distributor for repair.
• Tungsten lamp (ready lamp of optional CXDI-40EG setting unit)

Disposal of the Instrument

This instrument incorporates lead, which may pollute the environ-

ment if the instrument is abandoned.
! CAUTION Please ask professional waste disposal company to handle dis-
posal, or contact Canon representative or distributor before dis-
posing of the instrument.

– 18 –
7. Specifications

7.1 Main Specifications

Purpose General radiography

Scintillator GOS

Dynamic range Approx. 80 dB

Resolution 3.1 lp/mm

Gray scale 12-bit, 4,096 gray scale

Environmental requirements Operation:

Temperature: +5 to +35°C
Humidity: 30 to 75%RH (no condensation)
Storage and transportation:
Temperature: -30 to +60°C
Humidity: 10 to 60%RH
Atmospheric pressure: 700 to 1060hPa

Power Supplied from the Power Box

Sensor Unit
Number of pixels Approx. 7,200,000 pixels

Pixel size 160µm × 160 µm

Image matrix size 2688 × 2688 pixels

Dimensions and mass Upright stand type

550 (W) × 553.5 (H) × 118.7 (D) mm,
25 kg (without grid frame unit and cables)
Universal stand type
550 (W) × 553.5 (H) × 101 (D) mm,
19 kg (without grid frame unit and cables)
Table type
580.3 (W) × 550 (H) × 67.5 (D) mm,
19 kg (without grid frame unit and cables)

Grid Frame Unit

Dimensions and mass 481 (W) × 17.8 (H) × 523.2 (D) mm,
1.2 kg (without grid)

– 19 –
7.2 Characteristics

7.2 Characteristics

7.2.1 Clinical Considerations

Required patient doses: Equivalent to exposure dose of 200 or 400 speed film/screen
system.

7.2.2 Nonclinical considerations

(1) Sensitometric characteristics and dynamic range

The output is normalized to 1000 [LSB/mR] at the beam quality of 80 kVp+26mmAl

when the sensor is operated in linear acquisition mode.
Dynamic range is determined by the levels of system noise and saturation.
The level of uncertainty is estimated to be less than ±10%.

– 20 –
 7.2 Characteristics

(2) Presampling MTF

Where horizontal direction is coincident with the direction in which the grid slides, fast
scan means scan in horizontal direction, and slow scan means scan in vertical direction.
The level of uncertainty is estimated to be less than ±3% or ±0.02, whichever is greater.

(3) DQE

The fast scan direction and the slow scan direction are identical.
The level of uncertainty is estimated to be less than ±15% or 0.03, whichever is greater.

– 21 –
8. Components

Sensor unit ................................................................1

Grid frame unit .........................................................1

Cables .......................................................................1 set

Installation parts .......................................................1 set

NOTE: Grid is not included in the grid frame unit. It is available as an option.

System Requirements

Power box

Control Station CXDI-C3S

Operation Unit 15

Upright stand, universal stand or table

Options

Digital Radiography CXDI-40EG Power Box

Digital Radiography CXDI-40EG Power Box/Auto-Collimation

Grid
40 line/cm 110 cm (8:1)
40 line/cm 110 cm (10:1)
40 line/cm 150 cm (10:1)
40 line/cm 180 cm (10:1)
40 line/cm 180 cm (12:1)

Grid Frame Unit

– 22 –
9. Dimensions

9.1 Sensor Unit

Upright Stand Type

553.5

Unit: mm

Universal Stand Type

553.5

Unit: mm

– 23 –
9.2 Grid Frame Unit

Table Type

30.3

Unit: mm

9.2 Grid Frame Unit

481
523.2
17.8

Unit: mm

– 24 –
 9.3 Ready Lamp

9.3 Ready Lamp

Unit: mm

– 25 –
CANON INC. Medical Equipment Group
20-2 Kiyohara-Kogyodanchi, Utsunomiyashi, Tochigiken, Japan
Telephone: (81)-28-667-5711

CANON U.S.A., INC.

CANON MEDICAL SYSTEMS
15955 Alton Parkway, Irvine, CA 92618-3616, U. S. A.
Telephone: (1)-949-753-4160

CANON EUROPA N.V. Medical Products Division

Bovenkerkerweg 59-61, 1185 XB Amstelveen, The Netherlands
Telephone: (31)-20-545-8926

PUB. L-IE-4116 0505C0.004 Printed in Japan