DIGITAL RADIOGRAPHY

CXDI-50G
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.

European Union (and EEA*) only.

This symbol indicates that this product is not to be disposed of with your
household waste, according to the WEEE Directive (2002/96/EC) and your
national law. This product should be handed over to a designated collection
point, e.g., on an authorized one-for-one basis when you buy a new similar
product or to an authorized collection site for recycling waste electrical and
electronic equipment (EEE). Improper handling of this type of waste could
have a possible negative impact on the environment and human health due
to potentially hazardous substances that are generally associated with EEE.
At the same time, your cooperation in the correct disposal of this product will
contribute to the effective usage of natural resources. For more information
about where you can drop off your waste equipment for recycling, please
contact your local city office, waste authority, approved WEEE scheme or
your household waste disposal service.
For more information regarding return and recycling of WEEE products,
please visit www.canon-europe.com.
* EEA : Norway, Iceland and Liechtenstein

• System and product names in this manual are the trademarks of each manufacturer that devel-
oped them.

© CANON INC. 2008

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. and Canada

This instrument is a CLASS I EQUIPMENT according to UL60601-1.

WITH RESPECT TO ELETRIC SHOCK, FIRE MECHANICAL MEDICAL EQUIPMENT WITH RESPECT
AND OTHER SPECIFIED HAZARDS ONLY IN TO ELETRICAL SHOCK, FIRE AND
ACCORDANCE WITH CAN/CSA C22.2 NO. 601.1, MECHANICAL HAZARDS ONLY IN
MEDICAL EQUIPMENT CERTIFIED FOR CANADA ACCORDANCE WITH UL60601-1
<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 for EMC Directive

Electromagnetic Emissions
The CXDI-50G is intended for use in the electromagnetic environment specified below.
The user of the CXDI-50G should assure that it is used in such an environment.

Emission Test Compliance Electromagnetic Environment – Guidance

RF emissions GROUP 1 The CXDI-50G 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-50G 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 Applicable
buildings used for domestic purposes.
IEC 61000-3-2

Voltage fluctuations/ 100-120VAC:

flicker emissions Not Applicable
IEC 61000-3-3
200-240VAC:
Complies

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 Safety Information

Electromagnetic Immunity
The CXDI-50G is intended for use in the electromagnetic environment specified below.
The user of the CXDI-50G should assure that it is used in such an environment.

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

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-50G requires
power supply input cycle. cycle. continued operation during power mains
lines interruptions, it is recommended that the
IEC 61000-4-11 40% UT 40% UT CXDI-50G be powered from an uninter-
ruptible power supply or a battery.
(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-50G, 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 in which the CXDI-50G is used exceeds the applicable RF compliance level
above, the CXDI-50G should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as reorienting or relocating the CXDI-50G.

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

(4)
 Safety Information

Recommended Separation Distances

The CXDI-50G is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The user of the CXDI-50G can help prevent electromagnetic
interference by maintaining a minimum distance between portable and mobile RF communica-
tions equipment (transmitters) and the CXDI-50G as recommended below, according to the
maximum output power of the communications equipment.

Rated maximum Separation distance according to frequency of transmitter

output power of m
transmitter
150 kHz ~ 80 MHz 80 MHz ~ 800 MHz 800 MHz ~ 2.5 GHz
W d = 1 .2 P d = 1 .2 P d = 2 .3 P

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23

For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in metres (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 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected
by absorption and reflection from structures, objects and people.

(5)
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 use.
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.

Installation and Environment of Use

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.

(6)
 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.

Because the instrument’s cable is long, take care so cables do not get tangled
! CAUTION during use. Also, be careful not to get your feet caught in the cable.

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 parts that may cause electric
! WARNING shocks and other hazardous parts, touching them may cause death or serious
injury.

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.

Do not spill liquid or chemicals onto the instrument or, in cases where the
patient is injured, allow it to become wet with blood or other body fluids, as
! CAUTION doing so may result in fire or electric shock. In such situation, protect the
instrument with disposable covering as necessary.

Wipe the CFRP plate of the sensor unit with ethanol or glutaraldehyde solu-
tion to disinfect it each time a different patient uses the instrument, in order to
! CAUTION prevent infection.
If the optional grid unit is being used, disinfect its surface.
Please consult a specialist for the procedure for disinfection.

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

(7)
Safety Information

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.

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 alcohol, benzine, thinner or any other flammable cleaning agents.
Otherwise, fire or electric shock may result.

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

(8)
 Safety Information

Labels and Markings on the Instrument

The CXDI-50G has a few labels and markings on it.

Contents of those and positions where they are attached are indicated below.

Sensor Unit

Front
This mark indicates that this is a Type B
Applied Part according to UL60601-1 and
EN60601-1.
This unit can be installed in the patient
environment.

These marks indicate that the instrument

100kg must be handled with care.
Do not jolt or apply excessive load to the
instrument.

Rear

Name Label

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 Contents

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

Regulations ................................................................................................................................(1)
Guidance and Manufacturer’s Declaration for EMC Directive ................................................... (2)
General Safety Information ........................................................................................................ (6)
Labels and Markings on the Instrument .....................................................................................(9)

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

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

3. Description ..............................................................................................................5

4. Operation ................................................................................................................6
4.1 Turning ON/OFF the Power of the System ........................................................................... 6
4.2 Calibration ............................................................................................................................. 6

5. Inspection and Maintenance ...................................................................................7

5.1 Inspection .............................................................................................................................. 7
5.2 Cleaning ............................................................................................................................... 10

6. Service Information ...............................................................................................11

7. Specifications .......................................................................................................12
7.1 Main Specifications ............................................................................................................. 12
7.2 Characteristics .................................................................................................................... 13

8. Components .........................................................................................................15

9. Dimensions ...........................................................................................................16

Appendix: Attaching the Optional Grid Unit ...............................................................17

1. Overview

The Canon Digital Radiography CXDI-50G is a portable X-ray digital camera that can
take images of any part of the body.
It directly converts the X-ray images captured by the LANMIT (Large Area New MIS
Sensor and TFT) sensor into a high-resolution digital images.
The instrument is suited for use inside a patient environment.

–1–
2. Notes for Using the Instrument

(1) Handling
Handle the instrument carefully, as
it may be damaged if something is
hit against it, dropped, or receives a
strong jolt.
Also, handle the optional grid unit
with care too.

Do not pull the cable. Also, do not

pull the sensor unit when the cable
is tangled with something. Other-
wise, the cable may be damaged,
which may result in fire or electric
shock.

(2) Before Exposure

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

–2–
 2. Notes for Using the Instrument

(3) During Exposure

Do not apply excessive weight to the sensor unit. Otherwise, the sensor may be
damaged.

Limit of Load
Uniform load: 150 kg over the
whole area of sensor unit surface.

Local load: 100 kg on an area

40 mm in diameter.

Be sure to use the sensor unit on a

flat place so it will not bend. Other-
wise, the sensor may be damaged.

Perform exposure after checking that the exposure conditions are optimally suited to
this product. The sensitivity of this product's sensor differs from that of the series
product CXDI-50C.

–3–
2. Notes for Using the Instrument

(4) During Cleaning

Do not use anything other than neutral detergent for cleaning the cover of the instru-
ment. Otherwise, the coating will be corroded.

(5) Storage
Be sure to store the sensor unit and the optional grid unit in a safe place where it will
not fall or drop.

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

For U.S.A.
Rx only-Caution:
Federal law restricts this device to sale by or on the order of a licensed practitioner.
Intended Use:
Canon digital radiography CXDI-50G provides digital image capture for conven-
tional film/screen radiographic examinations.
The device is intended to replace radiographic film/screen systems in all general
purpose diagnostic procedures.
This device is not intended for mammography applications.

For European Union

Intended Use:
This device provides digital X-Ray image for diagnosis of disease, injury, or any
applicable health problem. The image is obtained as the result of imaging X-ray
passed through human body with the X-ray flat panel detector and importing digital
signals output from the detector into the image processor.

–4–
3. Description

Sensor Unit

This unit converts the X-rays into digital signals.

a d
b
c e

Name Description

a Grip Hold this grip when carrying the sensor unit.

b CFRP (Carbon Fiber The part of the patient’s body to which an image is to be
Reinforced Plastic) plate taken should be placed against this plate.
This plate should be disinfected each time a different
patient uses the instrument in order to prevent infection.

c Sensor cable Connect this cable to the power box.

d BUSY lamp Blinks when the sensor unit is busy communicating.

e SENSOR lamp Blinks when the sensor unit is ready for exposure or when
error has occurred.

f POWER lamp Turns ON when the power of sensor unit is ON.

–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-50G 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–
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.

–7–
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.

5.1.1.2 After Turning ON the Power

Result
Inspection Remedy
Date Date Date
/ / /

Connect the power cable and

Check that power lamp is lit. Good/Bad Good/Bad Good/Bad
sensor cable properly.

Take measures if error mes-

General

sage is displayed by refer-

ring to the CXDI Series
Perform test exposure. Good/Bad Good/Bad Good/Bad
Operation Manual. Contact
Canon or distributor if the
problem cannot be solved.

–8–
 5.1 Inspection

5.1.2 Monthly Inspection

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

Result
Inspection Remedy
Date Date Date
/ / /

Check the performance of Refer to the CXDI Series

the instrument by perform- Operation Manual for the
General

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 there is any problem or 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 exposures using a phan- if there is any problem.
tom or a 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.

–9–
5.2 Cleaning

5.2 Cleaning

5.2.1 CFRP (Carbon Fiber Reinforced Plastic) Plate of the Sensor Unit

Wipe the CFRP plate of the sensor unit with ethanol or glutaralde-
hyde solution to disinfect it each time a different patient uses the
instrument, in order to prevent infection.
If the optional grid unit is being used, disinfect its surface.
! 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 and grid
unit.

Disinfect the CFRP plate of the sensor unit each time a different patient uses the instru-
ment. If the optional grid unit is being used, disinfect its surface.

5.2.2 Cover

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, fire or electric shock may result.

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

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

Shut down the 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.

– 10 –
6. Service Information

(1) Repair
If problem 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.

(2) Limit for Supplying Performance Parts for Repair

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

* Parts required to maintain the functioning of the product

– 11 –
7. Specifications

7.1 Main Specifications

Sensor Unit

Purpose General radiography

Pixel size 160 × 160 µm

Image matrix size 2208 × 2688 pixels

Number of pixels Approx. 5.9 million pixels

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 +50 °C
Humidity: 10 to 60 %RH (no condensation)
Atmospheric pressure: 700 to 1060 hPa

Power Supplied from the power box.

Dimensions and mass 491 (W) × 477 (H) × 23 (D) mm,

4.8 kg (without sensor cable)

– 12 –
 7.2 Characteristics

7.2 Characteristics

(1) Required patient doses

Equivalent to exposure dose of 200 or 400 speed film/screen system.

(2) Sensitometric characteristics and dynamic range

Dynamic range is determined by the levels of system noise and saturation.

The level of uncertainty is estimated to be less than ±10%.

– 13 –
7.2 Characteristics

(3) Presampling MTF

The level of uncertainty is estimated to be less than ±2% or ±0.015, whichever is

greater.

(4) DQE

The level of uncertainty is estimated to be less than ±10% or 0.02, whichever is

greater.

– 14 –
8. Components

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

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

Options

Digital Radiography CXDI-50 Power Box (with Remote switch)

Grid unit for CXDI-50

Grid: 40 line/cm 110 cm (4:1)
40 line/cm 110 cm (8:1)
40 line/cm 150 cm (6:1)
40 line/cm 180 cm (10:1)

– 15 –
9. Dimensions

Sensor Unit

477

491 23

Unit: mm

– 16 –
Appendix: Attaching the Optional Grid Unit

Attach the optional grid unit to the sensor unit by the procedure indicated below.

NOTE: Structure of grid unit is delicate. Do not drop, knock over, bend, or apply force or
jolt to it. Otherwise, the unit may be damaged.
When the grid unit is not in use, remove it from the sensor unit and store it in a
safe place where it will not fall.
Even if it is not extremely damaged, its characteristics may be changed, which
may cause a problem in image quality.

(1) Blow off the dust on the front and back of the grid unit.

(2) Place the sensor unit horizontally on a table.

(3) Hold the grid unit with both hands and

engage the hooks on the bottom of the
grid unit to the holes on the bottom of
the sensor unit.

Hook

– 17 –
Appendix: Attaching the Optional Grid Unit

(4) Gently set the grid unit over the sensor unit. A click sound is heard when the grid unit
is locked properly.

NOTE: Ensure that the grid unit is locked before lifting the sensor unit. Otherwise, the
grid unit will fall and be damaged.

To remove the grid unit

While sliding the locks on top of the Lock
grid unit outward, lift and remove the
grid unit.

– 18 –
 CANON INC. Medical Equipment Group
30-2, Shimomaruko 3-chome, Ohta-ku, Tokyo, Japan
Telephone: (81)-3-3758-2111

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-4134E 0808P0.001 Printed in Japan