Fuji Profec One

(CR-IR 368)
Operation Manual
1st Edition: June 2012
Please read the Operation Manual thoroughly before

actually operating the FCR PROFECT ONE Plus (CR-IR
368) system.
After reading this manual, store it nearby the FCR
PROFECT ONE Plus (CR-IR 368) so that you can see it
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Introduction
The FUJI Computed Radiography FCR PROFECT ONE Plus performs Digital
Radiography by using an Imaging Plate (IP) as the X-ray detection device. It reads and
processes X-ray image information that is recorded on an exposed IP using a cassette-
type X-ray stand and can also display the image on the monitor or print out hard copies
on film.
This manual describes the operation procedures for the FCR PROFECT ONE Plus and
precautions for use.
CAUTION
1 No part or all of this manual may be reproduced in any form without prior permission.
2 The information contained in this manual may be subject to change without prior notice.
3 FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from installation,
relocation, remodeling, maintenance, and repair performed by other than dealers specified by
FUJIFILM Corporation.
4 FUJIFILM Corporation shall not be liable for malfunctions and damages of FUJIFILM Corporation
products due to products of other manufacturers not supplied by FUJIFILM Corporation.
5 FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from
remodeling, maintenance, and repair using repair parts other than those specified by FUJIFILM
Corporation.
6 FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from negligence
of precautions and operating methods contained in this manual.
7 FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from use under
environment conditions outside the range of using conditions for this product such as power
supply, installation environment, etc. contained in this manual.
8 FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from natural
disasters such as fires, earthquakes, floods, lightning, etc.
Process waste correctly, as stipulated by local law or any regulations that apply.
When discarding the FCR PROFECT that incorporates the battery, be sure to contact
a licensed waste disposal contractor because it cannot be disposed of as a general
waste.
Trademark
FCR is a trademark or a registered trademark of FUJIFILM Corporation.
Copyright © 2012 FUJIFILM Corporation. All rights reserved.
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Contents at a Glance
Chapter 1 Introduction
1
Chapter 2 Operations
2
Chapter 3 User Utility
3
Chapter 4 Troubleshooting
4
Appendix A Specifications
A
Appendix B IP Handling
B
Appendix Z Precautions for Exposure
Z
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Contents
Chapter 1 Introduction .......................................................................................................... 1-1
1.1 Features of the FCR PROFECT ONE Plus (CR-IR 368)....................................... 1-2
1.2 Operational Precautions........................................................................................ 1-3
1.2.1 Laser Handling Precautions....................................................................... 1-4
1.2.2 Authorized Safety Standards...................................................................... 1-4
1.2.3 Preventing Electric Shock.......................................................................... 1-4
1.2.4 Electromagnetic Compatibility (EMC) . ..................................................... 1-5
1.2.4.1 Further information for EN 60601-1-2 (Europe)....................................... 1-5
1.2.5 Classification............................................................................................... 1-9
1.2.6 Signal Input and Output Parts.................................................................... 1-9
1.2.7 Precautions to be Observed When Using the Electric Medical Equipment... 1-10
1.2.8 Usage Precautions...................................................................................... 1-11
1.2.9 Location of Each Label............................................................................... 1-12
1.3 Safety Precautions................................................................................................. 1-13
1.4 Component Names and Functions....................................................................... 1-14
1.4.1 FCR PROFECT ONE Plus (CR-IR 368) Main Unit...................................... 1-14
1.4.2 Operation Panel........................................................................................... 1-16
1.5 Routine Operation Diagram.................................................................................. 1-19
1.6 Operation Panel Screen Display for Each Scenario........................................... 1-20
1.6.1 Screens from Power ON to “Processing Status Display”....................... 1-20
1.6.2 Error Window............................................................................................... 1-21
1.7 System Conﬁguration............................................................................................ 1-22
Chapter 2 Operations ........................................................................................................... 2-1

2.1 Starting Up and Shutting Down the System ....................................................... 2-2
2.1.1 Starting Up the System .............................................................................. 2-2
2.1.2 Shutting Down the System......................................................................... 2-3
2.2 Routine Operations ................................................................................................ 2-6
Step 1 Registering Patient’s Information and Exposure Information
(at the CR Console) ............................................................................... 2-7
Step 2 Entering the IP No. (at the CR Console).............................................. 2-10
Step 3 X-ray Exposure....................................................................................... 2-11
Step 4 Inserting the Cassette (Starting Reading) ........................................... 2-12
Step 5 Removing the Cassette ......................................................................... 2-14
Step 6 Simplified QA Operation / Image Data Transfer .................................. 2-14
2.3 Conducting Image Erasure Only [PRIMARY ERASURE] ................................... 2-15
2.4 Conducting Exposure Using a Cassette (IP) Left Unused for 8 Hours or More
[SECONDARY ERASURE] .................................................................................... 2-16
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1
Chapter 3 User Utility ............................................................................................................ 3-1
3.1 What is the User Utility? ....................................................................................... 3-2 2
3
3.2 Starting Up and Shutting Down the User Utility . ............................................... 3-3
3.2.1 Starting Up the User Utility ........................................................................ 3-3
3.2.2 Shutting Down the User Utility ................................................................. 3-3
4
3.3 User Utility ............................................................................................................. 3-4
1 Equipment information ......................................................................................... 3-4
2 Set alarm ................................................................................................................ 3-5
A
3 Backlight OFF timer ............................................................................................. 3-6
4 Scanner cleaning ................................................................................................. 3-7
5 Set key touch tone ................................................................................................ 3-8
B
6 Set sleep timer . ..................................................................................................... 3-9
7 Select the Master CL ............................................................................................ 3-10
Chapter 4 Troubleshooting .................................................................................................. 4-1

4.1 Laser Power Insufficient . ..................................................................................... 4-2
4.2 CL Communication Error .................................................................................... 4-3
Z
4.3 ID Unregistered ..................................................................................................... 4-4
4.4 Cassette Loading Error ........................................................................................ 4-5
4.5 Cassette Release Error ......................................................................................... 4-6
4.6 IP Feed Error . ....................................................................................................... 4-7
4.7 Image Erasure Error . .......................................................................................... 4-8
4.8 Overexposed IP .................................................................................................. 4-9
4.9 Erasure Lamp Off ................................................................................................ 4-10
4.10 Image Retransmission Retry . ............................................................................ 4-11
4.11 Unread IP Ejected . .............................................................................................. 4-12
4.12 Barcode Reading Error ....................................................................................... 4-13
Appendix A Specifications . ................................................................................................. A-1

1. Processing Capacity................................................................................................... A-2
2. Image Reading............................................................................................................. A-3
3. Image Output............................................................................................................... A-5
4. Power Supply Conditions........................................................................................... A-7
5. Environmental Conditions......................................................................................... A-7
6. External Dimensions and Weight.............................................................................. A-7
7. Options......................................................................................................................... A-7
8. External View............................................................................................................... A-8
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Appendix B IP Handling ....................................................................................................... B-1
1. IP Erasure Processing................................................................................................ B-2

1.1 Secondary Erasure ............................................................................................ B-2
1.2 Primary Erasure.................................................................................................. B-2
2. Storage Conditions/Daily Maintenance..................................................................... B-2
2.1 Storage Conditions............................................................................................. B-2
2.2 Daily Maintenance............................................................................................... B-2
2.3 Cleaning............................................................................................................... B-3
3. IP Disposal................................................................................................................... B-4
Appendix Z Precautions for Exposure ............................................................................. Z-1

1 Precautions for Exposure in the AUTO MODE......................................................... Z-2
1.1 Radiation Field and IP Split Pattern Recognition............................................ Z-3
1.2 Depiction of the Cervical Region....................................................................... Z-4
1.3 Depiction of HIP JOINT AXL - 2......................................................................... Z-5
1.4 Precautions for “Panorama” X-ray Exposures Using a 10″x12″ Cassette.... Z-5
1.5 EDR Image Data Analysis................................................................................... Z-6
2 Precautions for Exposure in the SEMI-AUTO MODE............................................... Z-7
3 Precautions for Exposure in SEMI-X MODE............................................................. Z-8
4 Precautions for Exposure in FIX MODE.................................................................... Z-8
Maintenance and Inspection
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Chapter 1
Introduction
1
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Introduction
1.1 Features of the FCR PROFECT ONE Plus (CR-IR 368)
This system provides chest, abdomen, bone, spine, head and other plain X-ray imaging,
as well as spinal canal, bronchial tube, urinary organ, and other contrast medium X-ray
imaging and X-ray tomography.
Major features of this system are as follows.
1 Due to the effects of digital image processing, the system produces radiographs that
are easy to observe and have a high diagnostic value.
2 The system has a wide latitude for incident X-rays so that a large amount of X-ray di-
agnostic information is obtained.
3 The system has high sensitivity, resulting in a decrease in the X-ray radiation dose to
the patients.
4 As the system has a wide latitude and an automatic sensitivity adjustment function, its
radiographs are not affected by small changes in X-ray exposure conditions. Therefore,
consistent image density is obtained for all radiographs.
5 It is possible to input exposure information, such as patient information, regions targeted

for exposures, exposure menus, and other, from the CR Console connected to this
equipment.
6 The automatic feed/load mechanism results in more efficient operation.
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Introduction
1
1.2 Operational Precautions
Precautions Before Operating This Equipment
2
Before using this equipment, please read this page carefully so that you can operate it
correctly.
Whenever you operate this equipment, be sure to observe those precautions. Failure to do
3
so may cause you to subject to injuries or property damage to occur.
WARNING: Do not connect any unspecified device.
This system is classified as a medical device under EC Directive 93/42/EEC.

This equipment has been designed on the assumption that the patient would
4
A
not come into direct contact with it or for operation by appropriately trained
operator.
The operator of this equipment must comprehend the contents shown in the
B
labels or on the monitor.
To install or relocate the equipment, request it to a designated service supplier.

Z
Cautions on Network
After connecting this system to the network with other systems, confirm
that the other systems are not affected. If they are affected, take
countermeasures such as network separation.
Precautions on External Network Connection
When a setting of the network to which the equipment is connected has

been changed, check that the change does not affect the system operation
and take measures if necessary.
The setting change may include the following:
- Change of connection destination
- Addition of devices
- Removal of devices
- Update of devices
- Upgrade of devices
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Introduction
1.2.1 Laser Handling Precautions

IEC 60825-1:1993 +A1:1997 +A2:2001
This system consists of a Class 1 laser product.
FCR PROFECT ONE Plus (CR-IR 368) Laser Unit Specifications

Class 3B
Medium Semiconductor laser
Wavelength 660 nm
Maximum Output 50 mW (CW)
WARNING: The FCR PROFECT ONE Plus (CR-IR 368) incorporates a Class 3B laser with
maximum output of 50mW. To prevent exposure to its laser beams, the user should
observe the following precautions.
• Never open or remove the protective covers.
• Always contact our official dealer or local representative immediately if you
suspect there is a malfunction.
CAUTION: Use of controls or adjustments or performance of procedures other than those

specified herein may result in hazardous radiation exposure.
1.2.2 Authorized Safety Standards

EN 60601-1:2006
UL 60601-1:2003, CAN/CSA C22.2 NO.601.1:2005, IEC 60601-1-1:2000
ANSI/AAMI ES 60601-1:2005, CAN/CSA-C22.2 NO.60601-1-2008
Note, however, that UL certification does not take effect if this equipment is used mount-
ed on board a vehicle because it has not been applied for appropriate approval from UL.
1.2.3 Preventing Electric Shock
WARNING: High voltage is supplied to the photomultiplier incorporated in the FCR PROFECT
ONE Plus (CR-IR 368). To prevent electric shock to the user, please observe the
following precaution.
• Never open or remove the protective covers of the equipment. Don’t touch
high-voltage units of the equipment with your hand, otherwise you may receive
an electrical shock.
• Always contact our official dealer or local representative immediately if you
suspect there is a malfunction.
WARNING: The power supply to the unit is 100-240V ~. To prevent electric shock to the user,
please observe the following precautions.
• Avoid installation sites where the equipment will be exposed to water.
• Always ground the equipment to a protective earth line.
• Make sure that all connections are secure and connected correctly.
• When using the equipment within the environment where the patient may get
into touch with it, optionally connect additional protective earth conductor.
• When using the equipment within the environment where the patient may get
into touch with it, the user must not touch the equipment’s exterior, such as
covers and metal sections, and the patient at the same time. In addition, take
care that the patient does not touch the equipment.
• To avoid risk of electric shock, this equipment must only be connected to a
supply mains with protective earth.
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Introduction
1
1.2.4 Electromagnetic Compatibility (EMC)
The FCR PROFECT ONE Plus (CR-IR 368) system complies with the standards for EMC
that are applied in various countries as follows.
2
• IEC 60601-1-2 (USA)
• EN 60601-1-2 (Europe)
∗ Further information for Europe is described in section 1.2.4.1

WARNING: Electromagnetic wave-sensitive parts, such as the FDD, HDD, photo-
multiplier, etc., are used in this equipment.
Do not place any objects that emit strong electromagnetic waves near 3
4
the equipment.
This equipment generates, uses and can radiate radio frequency energy and, if not installed
A
and used in accordance with the instructions, may cause harmful interference to other
devices in the vicinity.
However, there is no guarantee that interference will not occur in a particular installation.
B
If this equipment does cause harmful interference to other devices, which can be determined
by tuning the equipment off and on, the user is encouraged to try to correct the interference
by one or more of the following measures:
Z
• Reorient or relocate the receiving device.
• Increase the separation between the equipment.
• Connect the equipment into an outlet on a circuit different from that to which the other
device(s) are connected.
Consult the manufacturer or field service technician for help.
1.2.4.1 Further information for EN 60601-1-2 (Europe)

Model name FCR PROFECT ONE Plus (CR-IR 368) is referred to as CR-IR 368 in this
section.
• Medical electrical equipment needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided in the accom-
panying documents.
• Portable and mobile RF communications equipment can affect medical electrical equip-
ment.
• The use of accessories, transducers and cables other than those specified, with the exception
of transducers and cables sold by FUJIFILM Corporation as replacement parts for internal
components, may result in increased emissions or decreased immunity of the CR-IR 368.
List of Cables
Name FUJIFILM parts code General specification
Power Cable 136N0376 (UK) –
136N0377 (Europe)
I/F Cable – Cat5E or more.
Straight cable of UTP type.
• The CR-IR 368 should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the CR-IR 368 should be observed to verify normal
operation in the configuration in which it will be used.
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Introduction
Guidance and manufacturer’s declaration - electromagnetic emissions

The CR-IR 368 is intended for use in the electromagnetic environment specified below.
The customer or the user of the CR-IR 368 should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance

RF emissions Group 1 The CR-IR 368 uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
CISPR 11
cause any interference in nearby electronic equipment.
RF emissions
Class A
CISPR 11
Harmonic emissions The CR-IR 368 is suitable for use in all establishments other than
Class A domestic and those directly connected to the public low-voltage
EN 61000-3-2 power supply network that supplies buildings used for domestic
Voltage fluctuations/ purposes.
flicker emissions Complies
EN 61000-3-3
Guidance and manufacturer’s declaration - electromagnetic immunity
Electromagnetic environment –
Immunity test EN 60601 test level Compliance level
guidance
Electrostatic 6kV contact 2kV contact Floors should be wood, concrete
discharge (ESD) 4kV contact or ceramic tile. If floors are
EN 61000-4-2 8kV air 6kV contact covered with synthetic material,
2kV air the relative humidity should be at
4kV air least 30%.
8kV air
Electrical fast 2kV for power supply lines 2kV for power supply lines Mains power quality should be
transient/burst 1kV for input/output lines 1kV for input/output lines that of a typical commercial or
EN 61000-4-4 hospital environment.
Surge 1kV differential mode 1kV differential mode Mains power quality should be that of a
EN 61000-4-5 2kV common mode 2kV common mode typical commercial or hospital environment.
Voltage dips, short <5% UT <5% UT Mains power quality should be

interruptions and voltage (>95% dip in UT) (>95% dip in UT) that of a typical commercial or
variations on power for 0.5 cycle for 0.5 cycle hospital environment. If the user
supply input lines 40% UT 40% UT of the CR-IR 368 requires
EN 61000-4-11 (60% dip in UT) (60% dip in UT) continued operation during power
for 5 cycles for 5 cycles mains interruptions, it is
recommended that
70% UT 70% UT the CR-IR 368 be powered from
(30% dip in UT) (30% dip in UT) an uninterruptible power supply or
for 25 cycles for 25 cycles a battery.
<5% UT <5% UT
(>95% dip in UT) (>95% dip in UT)
for 5 s for 5 s
Power frequency 3 A/m 3 A/m Power frequency magnetic fields
(50/60Hz) should be at levels characteristic of a
magnetic field typical location in a typical
commercial or hospital environment.
EN 61000-4-8
NOTE: UT is the a.c. mains voltage prior to application of the test level.
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Introduction
1
Guidance and manufacturer’s declaration - electromagnetic immunity
2
Immunity test EN 60601 test level Compliance level Electromagnetic environment – guidance
Conducted RF 3 Vrms 3 Vrms Portable and mobile RF communications equipment should be
3
used no closer to any part of the CR-IR 368, including cables,
EN 61000-4-6 150 kHz to 80 MHz
than the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
4
Recommended separation distance
d = 1.2 P
A
Radiated RF 3 V/m 3 V/m d = 1.2 P 80 MHz to 800 MHz
EN 61000-4-3 80 MHz to 2.5 GHz d = 2.3 P 800 MHz to 2.5 GHz
where P is the maximum output power rating of the transmitter in
B
watts (W) according to the transmitter manufacturer and d is the
recommended separation distance in metres (m).
Field strengths from fixed RF transmitters, as determined
Z
by an electromagnetic site survey, a should be less than
the compliance level in each frequency range.b
Interference may occur in the vicinity of equipment
marked with the following symbol:
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 reflection
from structures, objects and people.
a Field strength from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot 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 CR-IR 368 is used exceeds the applicable RF compliance, the CR-IR
368 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the CR-IR 368.
b Over the frequency range 150 kHz to 80 MHz, field strength should be less than 3 V/m.
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Introduction
Recommended separation distances between

Portable and mobile RF communications equipment and the CR-IR 368
The CR-IR 368 is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the CR-IR 368 can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the CR-IR 368 as recommended
below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter

Rated maximum output
m
power of transmitter
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
W
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.
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Introduction
1
1.2.5 Classification
1) According to the type of protection against electrical shock
CLASS 1 EQUIPMENT
2) According to the degree of protection against electric shock
2
NO APPLIED PART
3) Protection against harmful ingress of water or particulate matter
IP00
3
4) According to the degree of safety of application in the presence of a flammable anes-
thetics mixture with air or with oxygen or nitrous oxide.
Equipment not suitable for use in the presence of a flammable anesthetics mixture
with air or with oxygen or nitrous oxide.
4
5) According to the mode of operation
CONTINUOUS OPERATION
1.2.6 Signal Input and Output Parts
IMG17B-REMOTE
(Used only when
Rear of machine
A
B
an optional product
is connected)
Z
CPU91A-LAN
CPU91A - LAN : Connected to the image network devices.

10base-T/100base-TX interface
* Service engineers take responsibility for connections of these devices.
CAUTION Equipment connected to this interface must be certified according to the respective
IEC standards (i.e. IEC 60950 for data processing equipment and IEC 60601-
1 for medical equipment). Furthermore, all configurations shall comply with
the system standard IEC 60601-1-1:2000 and IEC 60601-1:2005 Chapter 16.
Everybody who connects additional equipment to the signal input part or signal
output part configures a medical system, and is therefore responsible that the
system complies with the requirements of IEC 60601-1-1:2000 and IEC 60601-
1:2005 Chapter 16. If in doubt, consult the technical services department or your
local representative.
Do not connect a non-Ethernet cable, such as telephone line, to LAN. Only UTP-
type straight LAN cables of Category 5E or higher are appropriate for connection
to this connector.
REMOTE: Connected to the Console. Optional interface for controlling on/off of the
remote power supply
CAUTION Only the remote power supply option manufactured by FUJIFILM Corporation can
be connected to this interface. Contact our official dealer or local representative for
details on the remote power supply option. Our service engineer is responsible for
connecting the device; you are not allowed to connect this optional product.
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Introduction
1.2.7 Precautions to be Observed When Using the Electric Medical Equipment

We ask that you heed these usage precautions and use the equipment correctly.
1. This equipment should be used only by people who have the proper skills.
2. Heed the following precautions when installing the equipment.
2-1. Install the equipment where water will not splash it.
2-2. Install the equipment where it will not be adversely affected by air pressure,
temperature, humidity, ventilation, sunlight, dust or the presence of salt, sulfur
or like substances in the atmosphere.
2-3. Make sure the equipment will remain in stable condition, kept level and not
subjected to vibration or shock.
2-4. Do not install the equipment in places where chemicals are stored or gases emitted.
2-5. Make sure that the power frequency, voltage and power consumption are appropriate.
2-6. Connect the ground wire correctly.
2-7. In an emergency, disconnect the power plug or the inlet.
Ensure sufficient space around the power plug or the inlet.
2-8. An additional MULTIPLE SOCKET-OUTLET or extension cord shall not be con-
nected to the ME SYSTEM.
3. Observe the following precautions before beginning to use the device.
3-1. Inspect the switch contacts, polarities, dial settings and meters and confirm that
the equipment is functioning properly.
3-2. Confirm that the ground wire has been completely connected.
3-3. Make sure that all cords have been connected properly and safely.
3-4. Be aware that correct diagnosis can be hindered and danger can result from
using different pieces of equipment together .
4. Heed the following precautions after using the equipment.
4-1. Using the established procedure, restore the operation switches, dials, etc., to
what they were prior to use and then turn the power off.
4-2. When unplugging cords, do not pull on the body of the cord itself or apply un-
necessary force.
4-3. After using the accessories, recollect them and put them back in order.
5. If there is trouble with the equipment, do not attempt to fix it randomly. Instead, do
what is indicated and entrust repairs to a professional.
6. Do not remodel the equipment.
7. Maintenance and Inspection
7-1. Make inspect the equipment and parts periodically.
7-2. If the equipment has not been used for a long time, make sure that it operates
normally and safely prior to using it again.
8. Other Items
8-1. When subjecting patients (particularly infants and pregnant women) to radia-
tion, make sure not to exceed the necessary time and dose. Also, ensure that
radiation is contained within the region for exposure.
8-2. For cleaning and disinfecting the parts that patients come in contact with in
a normal usage environment, slightly moisten a soft cloth (non-woven cloth:
Kimwipe®) in neutral detergent or ethanol anhydride and wipe away any dirt. Do
not use any other cleansers or disinfectants. Also, do not scrub the equipment’s
surface vigorously. Ensure cloth is free of residual water and water does not
enter the device.
8-3. Follow the Operation Manual and operate the equipment correctly.
9. If the network is shut down due to a network device failure or any other cause, this
device is no longer able to transfer image data.
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Introduction
1
1.2.8 Usage Precautions
1. After checking information attached to radiographic images for correctness, use such
2
information for image interpretation work.
2. Before inserting a cassette into this equipment, verify patient identification without
fail by means of the patient’s full name, birthdate and the like.
3. Before inserting a cassette into this equipment, be sure to read the exposure
3
menu.
4. Before inserting a cassette into this equipment, make sure that this equipment is in
image-reading mode. This is because cassette erasure will take place if this equip-
4
ment is in erase mode.
5. When you install this equipment close to a wall, use caution not to block its air outlet
openings.
A
If the temperature inside this equipment rises abnormally high, the image on the IP
may be imperfectly erased, possibly causing an output image that does not allow
accurate image interpretation.
B
6. Clean the air outlet openings periodically to keep them clear of dust or the like which
can cause blocking. If they are blocked, the temperature inside this equipment rises
abnormally high and the image on the IP may be imperfectly erased, possibly caus-
ing an output image that does not allow accurate image interpretation.
Z
7. Do not place an unspecified IP into the cassette, otherwise an image that may affect
image reading can be output.
8. Replace the erasure lamp when the message prompting for replacement is dis-
played.
For the replacement of the lamp, please contact your local authorized distributor.
When the lamp fails, image erasure becomes impossible.
9. Do not remove a cassette already subjected to exposure before image reading. It is
possible that a read image is lost.
10. For precautions to observe when reading images from an IP, make sure to see
[Appendix Z Precautions for Exposure] so that IPs are handled correctly.
11. Stand in front of the equipment to operate it.
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Introduction
1.2.9 Location of Each Label

<Right Side> <Left Side> <Back>
Caution Label 2
(Used only when
an optional product
is connected)
Caution Label 2
Year of Manufacture and

EFUP (Environmentally
Friendly Use Period) Label Rating Label
IEC 60825-1
HHS Certification and Class 3B Panel Label
IEC 60825-1 Identification Label
Class 3B Panel Label
Mercury-containing
Products Label
IEC 60825-1
Class 3B Panel Label Caution Label 1
Cassette Insertion
Operation Label 2
Cassette Insertion
Operation Label 1
IEC 60825-1
Class 3B Panel Label
IEC 60825-1
Class 3B Panel Label Mercury-containing Products Label
Be sure to use the power Do not connect telephone lines

Sample year of manufacture cord our official dealer or local to LAN connector. Only UTP-type
presentative provided. If an straight LAN cables of Category
inappropriate cord is used, it may 5E or higher are appropriate for
Year of Manufacture and generate heat or fire. connection to this connector.
EFUP (Environmentally Caution Label 1 Caution Label 2
Friendly Use Period) Label
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Introduction
Cassette Insertion
Operation Label 2
1
2
Rating Label HHS Certification and 3
4
Identification Label
A
Cassette Insertion Operation Label 1
The following symbols are used on this equipment.
B
Their meanings are described below.
This symbol indicates compliance of the equipment with Directive 93/42/EEC.
Z
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.
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 waste, please contact FUJIFILM dealers.
1.3 Safety Precautions

This section contains safety precautions required for the safe operation of this equipment.
Carefully read and follow these precautions before using the equipment.
If these precautions are not followed, injury or damage to the equipment may occur. Safety
precautions are marked as WARNING or CAUTION and additional information as “ ”.
The meanings of these precautions are as follows:
WARNING: Indicates hazardous situations that may lead to serious injuries

or even death if the precaution is not or cannot be followed.
CAUTION: Indicates hazardous situations that may lead to mild or moderate inju-
ries if the precaution is not or cannot be followed. Precautions against
accidents causing only physical damage.
Indicates procedures requiring special attention, instructions that must be followed,

supplementary explanations, etc.
The institution where the equipment is installed is responsible for its use and maintenance.
In addition, this equipment should not be used by persons other than doctors or suitably trained staff.
The official dealer should make a necessary connection to the equipment’s power cable.
At equipment installation, the official dealer makes the connection to the equipment’s power
cable using a dedicated cable.
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Introduction
1.4 Component Names and Functions

1.4.1 FCR PROFECT ONE Plus (CR-IR 368) Main Unit
The external view of the FCR PROFECT ONE Plus (CR-IR 368) and the names of each
component are shown below.
[Fig. 1.1] FCR PROFECT ONE Plus (CR-IR 368) <External View and Component Names>
Operation Panel
POWER Lamp
Cassette Setting Unit System Power Switch
Cassette Removal Lamp
Cassette Processing Lamp
Cassette Ready Lamp
<Front>
Dust-proof Filter
Circuit Breaker
“|” : ON
“O” : OFF
<Left Side>
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Introduction
1
[ Table 1-1 ] FCR PROFECT ONE Plus (CR-IR 368) Component Names and Functions
Name Description
Operation Panel Operation panel for the FCR PROFECT ONE Plus (CR-IR 368).
2
See next page for details.
POWER Lamp Lights (green) when circuit breaker is set to the “|” side and the
power is turned ON. As the circuit breaker is normally left ON,
3
the POWER Lamp will also normally be lit.
System Power Switch Power switch for the equipment. This equipment has been provided
(Stand-by Switch) with the system power switch and when the switch is pressed
4
while the circuit breaker is ON (“|”) status, power turns ON.
Cassette Setting Unit For setting the cassette containing an exposed IP. Cassette can
be inserted in the rack.
A
Cassette Ready Lamp Lights (green) when the equipment has started up normally,
indicating that the cassette can be inserted. Cassette cannot
be inserted when the lamp is off.
B
Cassette Processing Lamp Displays cassette processing status.
(See page 1-17 “5 Processing Status Bar”.)
Cassette Removal Lamp Blinks (blue) when the processed cassette can be removed.
Dust-proof Filter
Circuit Breaker
Installed at the inlet of the ventilation fan.
Leave it turned ON (“|”).
To turn the power OFF, set it to the “O” side.
Z
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Introduction
1.4.2 Operation Panel

Basically, the operation panel is configured as follows.
[Fig. 1.2] Operation Panel Configuration <Processing Status Display Window>
3 Master

CR Console
Connection Status Monitor
1 Warning Display
2 Processing
Indicator
Mode
4 Processing Mode
Switchover Button
5 Processing
Status Bar
6 Processing Status Bar

Switchover Button
7 Shutdown Button
8 User Utility Button
[ Table 1-2] FCR PROFECT ONE Plus (CR-IR 368) Operation Panel Component and Functions (1/3)
Name Description
1 Warning Display If any abnormal condition such as an error occurs, the back-
ground color will change to yellow reporting the content of
the error.
2 Processing Mode Indicator Displays the specified processing mode for the cassette to
be inserted next. Any one of the modes of Image Reading
, Secondary Erasure or Primary Erasure will be
displayed as selected.
3 Master CR Console Displays the connection status with the Master CR Console.
Connection Status Monitor When the connection is established (connected) correctly,
will be displayed. Otherwise, will be displayed.
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Introduction
1
Name Description
4 Processing Mode When you press the button, the following “processing mode selection screen”
2
Switchover Button will be displayed.
3
Currently selected processing mode
Primary Erasure Mode (See page 2-15.)
4
Secondary Erasure Mode (See page 2-16.)
Reading Mode
A
B
Then, select the processing mode for the next cassette to be inserted.
Here, if any one of the buttons is touched, the screen will return to the former one, and
the selected processing mode will be displayed in the 2 Processing Mode Indicator.
However, if either Primary Erasure button or Secondary Erasure button is selected and left
Z
for a while without inserting cassette, the processing mode will be changed automatically
to Image Reading Mode.
Ainserted
cassette can be inserted when the processing mode selection screen is displayed. The
cassette will be processed as the currently selected processing mode.
When either Primary Erasure mode or Secondary Erasure mode is selected and the cassette
is inserted, the setting will be returned to the default Image Reading Mode. Thus, the
selection for Primary Erasure and Secondary Erasure is valid one time only.
5 Processing Status Bar Displays processing status.
Processing Status Bar displays IP processing status from cassette inserting
to its removal. Bar is divided into 4 blocks to signify processing status.
In IP reading process, the division will be displayed green, and in primary
and secondary erasure process, the division will be displayed orange.
Refer to the following illustration for supplementary explanation.
Lamp display
Cassette
Processing Lamp
Cassette Cassette
Ready Lamp Removal Lamp
LEVEL 0
Cassette not inserted (after cassette has been removed)
Lights
LEVEL 1
Cassette received; reading to begin

Lights
LEVEL 2
Reading begins – Erasure begins

Lights
LEVEL 3
Erasure in process – Erasure completed

Lights
LEVEL 4
Erasure completed – IP processing completed

Blinks
LEVEL5
IP processing completed (cassette removal awaited)
Blinks
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Introduction
Name Description
6 Processing Status Bar If image delivery destination has been set at the time of installation
Switchover Button of the device, the following screen (image delivery destination
display) will be shown when the button is touched. The
height of the division bar becomes lower and the image
delivery destination name is displayed above the bar.
If processing status is switched over, this status is saved.

When the system is started the next time, it starts operating
with this status.
Re-touch the button to return to the former display.
7 Shutdown Button Press the button to exit the operation. When you press the
Shutdown button, the “exit confirmation window” opens.
8 User Utility Button The User Utility will be started. As for User Utility, see
“Chapter 3 User Utility.”
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Introduction
1
1.5 Routine Operation Diagram
The routine operation diagram for the FCR PROFECT ONE Plus (CR-IR 368) system
is as follows.
[Fig. 1.3] Routine Operation Diagram

2
3
CR Console
FCR PROFECT
ONE Plus (CR-IR 368) Erased IP
4
X-ray exposure
Exposed IP
A
B
Image data
Image data
Image Recorder
Z
Online digital signal
Data Management System
Offline operation
Image Display/ Image
Filing Unit Console
Image storing
Image displaying
Image re-outputting
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Introduction
1.6 Operation Panel Screen Display for Each Scenario

1.6.1 Screens from Power ON to “Processing Status Display”
When the system power switch is turned ON, system startup processing begins. The software
version indication will be displayed for a few seconds (Fig. 1.4).
System startup status will then be shown on the “Initialization Processing Screen” one line by
one line. When the “Processing Status Display Screen” (Fig. 1.6) opens after the completion
of initialization processing, you can operate the FCR PROFECT ONE Plus (CR-IR 368)
system.
[Fig. 1.4] Software Version Indication Screen
[Fig. 1.5] Initialization Processing Screen
[Fig. 1.6] Processing Status Display Screen
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Introduction
1
1.6.2 Error Window
If some trouble occurs within the equipment, the “Error Window” as shown below will open
and the content of the trouble reported. Read the message and instruction in the window
2
and then press the appropriate selection key.
The following example is one that informs that the barcode of the IP has not been read
resulting then in processing suspended. Take appropriate measures as instructed by the
3
message.
[Fig. 1.7] Error Window (Ex.: Barcode Reading Error)
4
A
B
Z
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Introduction
1.7 System Conﬁguration

The machine (CR-IR368) may be connected to a network to achieve various system
configurations.
Basic system configuration examples are described here.
Accessory equipment connected to the analog and digital interfaces must be certified
according to the respective IEC standards (i.e. IEC 60950 for data processing equipment
and IEC 60601-1 for medical equipment).
Furthermore all configurations shall comply with the system standard IEC 60601-1-1:2000
and IEC 60601-1:2005 Chapter 16. Everybody who connects additional equipment to
the signal input part or signal output part configures a medical system, and is therefore,
responsible that the system complies with the requirements of IEC 60601-1-1:2000 and
IEC 60601-1:2005 Chapter 16. If in doubt, consult the technical services department or
your local representative.
Use an IEEE 802.3 conformant HUB.
The machine may be connected to a plurality of CLs, including a single master CL.
The master CL contains the RU’s configuration data and other information.
RU A RU B RU A RU B Printer
Network
CL CL
CL CL
RU A RU B
Master CL of Master CL of CL of RU A CL of RU B
RU A RU B
: Configuration data
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Chapter 2
Operations
2
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Operations
2.1 Starting Up and Shutting Down the System

2.1.1 Starting Up the System
1 Press the CR Console power button to start it up.
[ Fig. 2.1] Turning the CR Console Power ON
2 Confirm that the POWER lamp on the operation panel lights green. (If it is not
lit, the circuit breaker has been turned OFF. Turn the circuit breaker back ON by
turning it to the “|” side.)
[ Fig. 2.2] Confirming that POWER Lamp has lit
3 Press the System Power Switch on the operation panel.

All the lamps turn ON and Now Loading is displayed on the window.
[ Fig. 2.3] Turning the System Power Switch ON
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Operations
1
4 The window displays the software version and then the startup status. The window will
then be changed to the Processing Status Display Screen, as presented below, to show
that the equipment has started up normally.
[ Fig. 2.4] Processing Status Display Screen (immediately after startup)

2
3
4
A
B
Z
For the screen displays from when the power is turned ON until the “Pro-
cessing Status Display Screen” appears, see p. 1-20, 1.6.1 Screens from
Power ON to “Processing Status Display”.
2.1.2 Shutting Down the System

1 Confirm that processing of the inserted cassette has been completed and then remove it.
2 Select the Shutdown button.
[ Fig. 2.5] Shutting Down the System Power Switch
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Operations
3 The “Confirm shutdown” window opens. Select .
[ Fig. 2.6] Confirm Shutdown Window
4 Shutdown processing will then start.
5 After a while, the power for the entire system, including the equipment, will be turned
OFF. Leave the circuit breaker ON (“|”).
The shutdown of the equipment can be remote-controlled by the registered Master

CR Console (As for the shutdown method through the CR Console, refer to the
CR Console Operation Manual.)
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Operations
2
To move the system to the power-saving mode with the power left ON

3
If is selected, the system goes to the sleep mode for power saving pur-
poses.
4
A
B
Z
Ifthetheroutine
operation panel is touched or the cassette is inserted, the system restores
mode in about 30 seconds from the sleep mode condition.
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Operations
2.2 Routine Operations

FCR PROFECT ONE Plus routine operations can be broadly divided into the follow-
ing six steps.
Step 1 Registering Patient’s Information and Exposure Information (See p. 2-7.)
Step 2 Entering the IP No. (See p. 2-10.)
Step 3 X-ray Exposure (See p. 2-11.)
Step 4 Inserting the Cassette (Starting Reading) (See p. 2-12.)
Step 5 Removing the Cassette (See p. 2-14.)
Step 6 Simplified QA Operation / Image Data Transfer (See p. 2-14.)
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Operations
Step 1 Registering Patient’s Information and Exposure Information

(at the CR Console)
1 The “Study Reception window” like that shown below is displayed on the CR 1
2
Console display immediately after the CR Console has been activated.
Enter the following patient information items appropriately, and then select .
3
Not all the items of patient information, however, need to be input.
Input any one of the items in order to proceed to the next operation.
When the optional card reader is provided, input patient information can be read using
a magnetic card.
Patient information input field
4
Turns one page backward.
Shows page number of the
patient information input field. A
B
Turns one page forward.
Clears patient information

(except for technologist).
Z
Operates the Patient
Information Database
function to input patient
information.
Touch panel soft keyboad
Patient information includes the following items.

Accession No. / Reception No. / Patient ID / Patient’s Name / Sex / Date of birth /
Requesting department code / Requesting department name / Technologist /
Patient comment / Physical disorder information / Infection information /
Contraindication information / Pregnancy / Height (cm) / Weight (kg) / Telephone no. /
Outpatient/Inpatient / Blood type (ABO) / Blood type (Rh) / Comments on study
You can change patient information input items and order of its display according to
User Utility settings.
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Operations
2 The “Exposure Menu Selection window” is displayed.

Select an anatomical region to display the desired exposure menu, and then
select an exposure menu (more than one menu can be selected). The selected
exposure menu(s) is displayed in the selected exposure menu list on the right
side of the screen.
3 Select after selection of exposure menu(s).

Exposure region list Selected exposure menu list
Exposure menu list by region 3

4 The “Study Start (Study Reserve) window” is then displayed.
Select , and proceed to the next step.
Selected exposure menu
When “Study Reserve” is selected, the menu thus registered will be stored in the
“Local WL” list. For how to operate “Study Reserve” and “Local WL” list, refer to the [CR Console
Operation Manual] for details.
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Operations
1
5 The “Study Execution window” is displayed, which makes it possible to start the
study (IP reading).
Operate appropriately according to mode (one-image display/six-image display) dis-
2
played on the Study Execution window.
The mode can be switched alternately by selecting .
To add exposure menus, select (selection of exposure menus). The “Exposure
3
Menu Selection window” is then displayed.
One-image display mode
4
A
B
Z
Six-image display mode
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Operations
Step 2 Entering the IP No. (at the CR Console)

Using the CR Console barcode reader, read the IP barcode (IP number) contained
in the cassette that has been subjected to exposure.
[ Fig. 2.7] Entering the IP No.
When the IP registration is completed, the equipment displays the registered IP number
at the exposure menu field. Carefully check it for preventing mis-registration.
Registered IP number
The patient ID and exposure information entered in Step 1 and the cassette (IP) will
be verified with each other.
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Operations
1
Step 3 X-ray Exposure
Using a cassette that contains an erased IP, conduct X-ray exposure using the same
technique as for the conventional film/screen method.
2
For precautions particular to exposure using the FCR system, see Appendix Z, Pre-
cautions for Exposure. Read it well first and then conduct exposure while observing
the related caution.
For the IP erasure method, refer to “2.3 Conducting Image Erasure Only (PRIMARY
ERASURE)” and “2.4 Conducting Exposure Using a Cassette (IP) Left Unused 3
4
for 8 Hours or More (SECONDARY ERASURE).”
A
B
Z
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Operations
Step 4 Inserting the Cassette (Starting Reading)
Insert the cassette (IP) that has been registered at the CR Console into the setting unit.
1 Confirm that the Cassette Ready Lamp lights (green).
2 With the cassette’s barcode window facing up and in front, insert the cassette straight
along the guide on the right of the cassette setting unit.
3 When the cassette is inserted, the Cassette Ready Lamp turns OFF and the Cassette
Processing Lamp turns ON. Moreover, the processing status bar display starts changing.
(For the processing status bar display, refer to “5 Processing Status Bar” on page
1-17.)
1 Be sure to insert the cassette straight along the guide on the right of the cassette setting unit, as
illustrated.
A cassette that was set upside-down, in the wrong direction or at a slant will not only result in
abnormalities but may also damage the machine.
2 Make sure to remove all exposure markers used at the time of exposure before inserting the
cassette.
[ Fig. 2.8] Inserting the Cassette
Cassette Ready Lamp lights.
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Operations
1
■ Precautions when inserting the cassette
Make sure to insert the cassette Slowly so that it is straight along the guide on the right.
2
3
4
Cassette guide
A
Slowly insert straight.
B
CAUTION: Never insert a cassette as illustrated below or damage to the device could result.
Z
Incorrect: Cassette is not straight along the guide. There is a gap.
Incorrect: Cassette is inserted at a slant.
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Operations
Step 5 Removing the Cassette

When the Cassette Removal Lamp blinks (blue), the cassette that has been processed
can be removed. Remove the cassette slowly and straight and it can be used directly for
the next exposure.
[ Fig. 2.9] Removing the Cassette
Cassette Removal Lamp

blinks.
Step 6 Simplified QA Operation / Image Data Transfer

A read image will be transferred to the CR Console and then displayed on the monitor.
Simplified QA operations, such as rotation, reversal, gradation adjustment, etc., can be
performed on the image.
In addition, the image can also be transferred to the Image Recorder and other devices.
For detailed operation procedures, see the [CR Console Operation Manual].
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Operations
1
2.3 Conducting Image Erasure Only [PRIMARY ERASURE]
To erase an image on IP – owing to exposure errors, etc. – without reading it, use the fol-
lowing procedure to conduct primary erasure processing.
1 Select
screen”.
Processing Mode Switchover to display the “Processing Mode Selection
2
1 3
4
A
B
2 Select Primary Erasure. The “Primary Erasure” window opens. Z
3 Primary erasure processing has been specified for the cassette to be inserted.
Insert an appropriate cassette in the cassette setting unit. The IP inside the cassette
will be subjected to primary erasure processing.
As the IP returned to the cassette has undergone primary erasure, it can be used
as is for exposure.
When PRIMARY ERASURE has been specified, at the stage when the cassette is inserted, the
settings for that IP will be considered completed, and the setting (display) will return to the default
(Reading). Thus, the setting is valid one time only.
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Operations
2.4 Conducting Exposure Using a Cassette (IP) Left Unused for 8

Hours or More [SECONDARY ERASURE]
When conducting exposure with an IP that has not been used for 8 hours or more, the
cassette (IP) should first be subjected to secondary erasure processing because natural
radioactive rays will have accumulated on the IP, making it necessary to eliminate the excess
energy. Operation method follows.
1 Select Processing Mode Switchover to display the “Processing Mode Selection

screen.”
2 Select Secondary Erasure. (The “Secondary Erasure” window opens.)
3 SECONDARY ERASURE processing has been selected for the cassette to be inserted.
Insert an appropriate cassette in the cassette setting unit. The IP inside the cassette will
be subjected to SECONDARY ERASURE processing.
As the IP returned to the cassette will have undergone secondary erasure, it can
be used as is for exposure.
When SECONDARY ERASURE has been specified, at the stage the cassette is inserted , the set-
ting for that IP will be considered completed, and the setting (display) will be returned to the default
(reading). Thus, the setting is valid one time only.
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Chapter 3
User Utility
3
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User Utility
3.1 What is the User Utility?

The User Utility provides users with the following functions that are different from routine
operating functions.
Note that you are not allowed to insert a cassette in the equipment while in the User Utility mode.
[Fig. 3.1] User Utility Initial Screen
1 4 7
2 5
3 6
1 Equipment information
Displays information covering operating conditions of the equipment..... Page 3-4
2 Set alarm
Sets up alarm tone that sounds when an error occurs............................. Page 3-5
3 Backlight OFF timer

Sets up the time when the LCD screen turns OFF................................... Page 3-6
4 Scanner cleaning
Cleans the scanner................................................................................... Page 3-7
5 Set key touch tone

Sets up the key touch tone....................................................................... Page 3-8
6 Set sleep timer

Sets up the time after which the equipment goes into
the sleep mode......................................................................................... Page 3-9
7 Select the Master CL

Selects and sets up (changes) a master CR Console when
two or more CR Consoles are connected and registered
to the equipment. . ................................................................................... Page 3-10
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User Utility
1
3.2 Starting Up and Shutting Down the User Utility
3.2.1 Starting Up the User Utility
Select [Utility] on the “Processing Status Display screen.”
2
In a few seconds, the User Utility mode starts up.
[ Fig. 3.2] User Utility Screen (1/2)
3
4
A
B
Select this button.
Z
3.2.2 Shutting Down the User Utility
Return to the “User Utility Initial screen” and select at the lower left corner of
the screen.
The User Utility mode shuts down returning then to the “Processing Status Display
screen”.
[ Fig. 3.3]
Select this button.
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User Utility
3.3 User Utility

1 Equipment information
Displays information covering operating conditions of the equipment.
1 Select .
The “Equipment Information Display” screen then opens as follows.
[ Fig. 3.4] Equipment Information Display Screen
The number of IP readings by

the equipment.
The number of IP conveyances
for other than image readings.
(The number of IP conveyances for
Primary or Secondary Erasure purposes.)
2 After you have confirmed necessary information items, select .

The system returns then to the “User Utility Initial screen”.
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User Utility
1
2 Set alarm
Sets up the alarm tone that sounds when an error occurs.
2
1 Select on the “User Utility initial screen.”
The Set Alarm screen like that shown below opens.
3
[ Fig. 3.5] Set Alarm Screen
4
A
Disables the alarm to sound
even if an error occurs.
B
Sets the alarm to sound for Sounds the alarm at
a certain period and then the maximum volume.
stops it automatically.
Enables the alarm to stop Sounds the alarm at
manually.
Z
the medium volume.
Sounds the alarm at

the minimum volume.
2 Touch a button to select a desired setup and then select at the lower right corner
of the screen.
3 The system returns to the “User Utility initial screen.”

An error will be indicated hereafter as set up at these steps.
Note that the alarm will not sound when the alarm tone has been set to OFF.
897N102379A 3-5
897N102379A_Z72N2680A.indb 5 2013/01/31 14:30:52

User Utility
3 Backlight OFF timer

Sets up the time when the LCD backlight turns OFF.
1 Select on the “User Utility Initial screen”.

The “LCD Backlight OFF Setup screen” will then opens, as shown below.
[ Fig. 3.6] LCD Backlight OFF Setup Screen
Disables LCD backlight OFF

to be set up automatically.
Displays the currently set up

Enables LCD backlight OFF backlight OFF time.
to be set up automatically.
Increases the value of lower Increases the value of lower one

two digits (minutes) one by one digit (minutes) one by one (in the
(in the increment of ten minutes). increment of one minute).
Decreases the value of lower two Decreases the value of lower one
digits (minutes) one by one (in digit (minutes) one by one (in the
the increment of ten minutes). increment of one minute).
2 Touch a button to select a desired setup and then select at the lower right corner
of the screen.
3 The system returns to the “User Utility Initial screen”.

The LCD backlight will be turned OFF hereafter as set up at these steps.
Note that the LCD backlight will not turn OFF when it has been set to OFF.
3-6 897N102379A
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User Utility
1
4 Scanner cleaning
This function cleans the scanner.
2
1 Select .
The “Scanner Cleaning Confirmation screen” opens as follows.
3
[ Fig. 3.7] Scanner Cleaning Confirmation Screen
4
A
B
Z
2 Select at the lower right corner of the screen.
A screen like that shown below opens to indicate that the scanner is being cleaned.
At the completion of scanner cleaning, the system then returns to the “User Utility Initial
screen.”
897N102379A 3-7
897N102379A_Z72N2680A.indb 7 2013/01/31 14:30:52

User Utility
5 Set key touch tone

This function sets up the key touch tone.
1 Select .
The “Key Touch Tone Setup screen” opens, as shown below.
[ Fig. 3.8] Key Touch Tone Setup Screen
Silences the key

touch tone.
Does not silence Sounds the key touch tone

the key touch at the maximum volume.
tone.
Sounds the key touch tone
at the medium volume.
Sounds the key touch tone

at a minimum volume.
2 Touch a button to select a desired setup and then select .

The key touch tone will be generated hereafter as set up at these steps.
Note that no key touch tone will be generated when OFF has been selected.
3-8 897N102379A
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User Utility
1
6 Set sleep timer
For the power saving purposes, the equipment can be set to sleep mode when it has
not been running or the operation panel not touched for a certain period of time.
2
This function sets up the non-operating time of the equipment after which it goes into the
sleep mode.
3
1 Select .
A screen opens where the time after which the equipment goes into the sleep mode is
to be set up.
[ Fig. 3.9] A Screen for Setting Up the Time the Equipment Enters the Sleep Mode
4
A
Does not put the equip-
ment in the sleep mode. B
Z
Displays the time set up cur-
Puts the equipment in the rently.
sleep mode.
Increases the value of lower Increases the value of lower

two digits (minutes) one by one one digit (minutes) one by one (in
(in the increment of ten minutes). the increment of one minute).
Decreases the value of lower two Decreases the value of lower
digits (minutes) one by one (in one digit (minutes) one by
the increment of ten minutes). one (in the increment of one
minute).
2 Touch a button to select a desired setup and then select .

The equipment will go into the sleep mode hereafter when the time set up at these steps
has elapsed.
Note that the equipment will not go into the sleep mode when OFF was selected.
Touching the operation panel or inserting the cassette will bring the equipment from
the sleep mode back to the routine mode in about 30 seconds.
897N102379A 3-9
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User Utility
7 Select the Master CL

Network-connected to the FCR PROFECT ONE Plus, the Master CL serves as a CR Con-
sole that monitors or controls the FCR PROFECT ONE Plus status.
Be sure to connect one Master CL to each equipment unit. When the Master CL is shut
down, the power to the FCR PROFECT ONE Plus will go off automatically.
The FCR PROFECT ONE Plus becomes ready for reading images only after it has
been connected to the Master CL.
If an error occurs on the Master CL side, follow the “Set up the Master CL” described
herein to determine a normal CR Console as a Master CL.
According to settings to be performed at installation, a maximum of 4 CR Consoles can

be registered to the FCR PROFECT ONE Plus to become the Master CLs.
With the use of an optional cable, it is also possible to turn the power to the equipment
ON remotely from the Master CL.
When two or more CR Consoles are connected and registered to the equipment, this function
selects and sets up (changes) a CR Console that will be the master from among those
CR Consoles.
Note that restarting the equipment will activate this function.

1 Touch the [2/2] tab on the “User Utility Initial screen” to display the 2nd page.
2 Select .
The “Master CL Console Selection screen” will be displayed, as shown below. On the
screen that opens, the background of the CR Console set up currently as the master
will be displayed blue.
[ Fig. 3.10] Master CR Console Selection Screen
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User Utility
1
3 Touch the icon of the CR Console you want to set up as the master to turn the
background blue. The CR Console whose background has been turned blue will thus
be selected as the master.
[ Fig. 3.11] CR Console Selected as the Master

2
3
4
Press any of the but-
tons to select a master.
A
B
Z
A screen like that shown below opens confirming that the CR Console set up (changed) to be
the master will be activated when the equipment is started up next time and thereafter.
[ Fig. 3.12] Confirmation Screen

The system then returns to the “User Utility Initial screen”.
897N102379A 3-11
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3-12 897N102379A
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Chapter 4
Troubleshooting
4
897N102379A 4-1
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Troubleshooting
4.1 Laser Power Insufficient
[Fig. 4.1]
Cause The laser is damaged.
Countermeasure 1 Select to stop the alarm.

2 If you select (illust), the output image quality will be that of the same
exposure achieved with X-ray dose smaller by about 20%.
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Troubleshooting
1
4.2 CL Communication Error
[Fig. 4.2]
2
3
4
A
B
Z
Cause Connection to the master CR Console is cut off.
Countermeasures 1 Make sure that the master CR Console application is up and running
properly.
2 Check the network cable for connection status.
3 If the master CR Console cannot be started due, for example, to an
operation error, use User Utility mode to select another equipment unit
to be the master CL.
This alternative is available only when multiple CLs are connected to the
equipment, with necessary settings performed appropriately.
See [3.3 (7) Select the Master CL under Chapter 3].
897N102379A 4-3
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Troubleshooting
4.3 ID Unregistered
[Fig. 4.3]
Cause No IP barcode numbers (patient information) are registered.
Countermeasures 1 Select to unload the cassette.

2 Reregister the IP barcode number (patient information) on the CR Con-
sole and then reload the cassette.
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Troubleshooting
1
4.4 Cassette Loading Error
[Fig. 4.4]
2
3
4
A
B
Z
Cause The cassette is not positioned correctly.

2 Reinsert the cassette.
Insert the cassette securely as far as it will go along the right side of the
equipment.
897N102379A 4-5
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Troubleshooting
4.5 Cassette Release Error
[Fig. 4.5]
Cause The cassette can not be released as it is not at the right position.
Countermeasures Select while pressing the cassette against the back on the
right side to unload the cassette.
4-6 897N102379A
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Troubleshooting
1
4.6 IP Feed Error
[Fig. 4.6]
2
3
4
A
B
Z
Cause The cassette may have been loaded improperly.
It wasn’t possible to take IPs out the cassette.

The IP unload mechanism assumes responsibility for try-
ing to take IPs out the cassette at a maximum of three times.
When doing so, a strange noise may be generated, which, though, does
not imply an error.
2 Load the cassette securely as far as it will go along the right side of the
equipment.
897N102379A 4-7
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Troubleshooting
4.7 Image Erasure Error
[Fig. 4.7]
Cause IP images are not erased properly.

2 Subject the IP to Primary Erasure processing.
Be sure to subject IPs to Primary Erasure processing unfailingly.
Make sure to erase IP images completely, otherwise, double exposure
may occur.
4-8 897N102379A
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Troubleshooting
1
4.8 Overexposed IP
[Fig. 4.8]
2
3
4
A
B
Z
Cause An overexposed IP was loaded into the cassette, with IP images not erased
completely.
Countermeasures 1 To erase IP images completely, let the IP stand for at least 16 hours.
2 Subject then the IP to Primary Erasure processing again.
897N102379A 4-9
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Troubleshooting
4.9 Erasure Lamp Off
[Fig. 4.9]
Cause The IP erasure lamp is not on.
Countermeasures The IP erasure lamp needs to be checked.

Contact our official dealer or local representative if the IP erasure lamp still
does not go on even after the equipment has been rebooted.
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Troubleshooting
1
4.10 Image Retransmission Retry
[Fig. 4.10]
2
3
4
A
B
Z
Cause Connection to the CR Console is cut off.
Countermeasures 1 Check to see that the cable connection is established properly and also
that the HUB is working correctly.
2 Make sure that the CR Console is operating properly.
Image data will be lost if the equipment is rebooted while image
retransmission is being retried.
∗ When connection is reestablished, processing resumes and images are

displayed.
The “Retry transmission” message appears on the window.
897N102379A 4-11
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Troubleshooting
4.11 Unread IP Ejected
[Fig. 4.11]
Cause There is an IP that is halfway through image reading, while the equipment
is at startup process.

2 Load the cassette when the equipment becomes available again.
(You need not to register barcode.)
Images may not be output correctly when there was an IP halfway through
image reading in the equipment.
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Troubleshooting
1
4.12 Barcode Reading Error
[Fig. 4.12]
2
3
4
A
B
Z
Cause IP barcode cannot be read.

2 Enter an eight-digit barcode number on the operation panel keyboard.
3 Select to unload the cassette.
When you are prompted for loading a cassette, load it in the rack.
Check to see that the IP barcode is not stained being clearly visible.
897N102379A 4-13
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Troubleshooting
4-14 897N102379A
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Appendix A
Specifications
A
897N102379A A-1
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Specifications
1 Processing Capacity
(1) Processing Capacity
With DRYPIX 7000

24 × 30cm (HR-BD) Approx. 38 IPs / hr.
18 × 24cm (HR-BD) Approx. 43 IPs / hr.
24 × 30cm (ST-BD) Approx. 42 IPs / hr.
18 × 24cm (ST-BD) Approx. 48 IPs / hr.
14” × 17” (35 × 43cm) (ST-VI) Approx. 67 IPs / hr.
14” × 14” (35 × 35cm) (ST-VI) Approx. 72 IPs / hr.
10” × 12” (ST-VI) Approx. 77 IPs / hr.
8” × 10” (ST-VI) Approx. 90 IPs / hr.
24 × 30cm (ST-VI) Approx. 77 IPs / hr.
18 × 24cm (ST-VI) Approx. 90 IPs / hr.
15 × 30cm (ST-VI) Approx. 67 IPs / hr.*
24 × 30cm (HR-VI) Approx. 58 IPs / hr.
18 × 24cm (HR-VI) Approx. 67 IPs / hr.
* To use the 15×30cm (ST-VI) IP, the IP adapter (optional) and 14”×17” cassette are
required.
The data were acquired under the following conditions;

1) the time required for exchanging the cassette is assumed to be zero.
2) X-ray dose exposed on IP;
6,450 nC/kg (25mR) for ST,
154,800 nC/kg (600mR) for HR.
The performance described above shows typical value.
It varies depending on the exposure level outside of the breast.
(2) Total Processing Time

For the DRYPIX 7000: Approx. 140 sec. (with 18×24cm size HR-BD IP,
from cassette insertion to 26×36cm size film output),
MFP processed, but PEM not processed.
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Specifications
1
2 Image Reading
(1) Available IP types and sizes
1. Inch settings ST-VI / ST-VN (standard type): 14”×17", 14"×14", 10"×12", 8"×10"
2
ST-BD (standard type): 24×30cm, 18×24cm
HR-V (high resolution type): 24×30cm, 18×24cm
3
HR-BD (high resolution type): 24×30cm, 18×24cm
2. Metric settings ST-VI / ST-VN (standard type): 35×43cm, 35×35cm,

24×30cm, 18×24cm, 15×30cm*
4
ST-BD (standard type): 24×30cm, 18×24cm
HR-V (high resolution type): 24×30cm, 18×24cm
A
HR-BD (high resolution type): 24×30cm, 18×24cm
(2) IP auto feed/load mechanism cycle time
B
IP auto feed/load mechanism cycle time
14” × 17” (35 × 43cm) (ST-VI) Approx. 54 sec.
14” × 14” (35 × 35cm) (ST-VI) Approx. 50 sec.
Z
10” × 12” (ST-VI) Approx. 47 sec.
8” × 10” (ST-VI) Approx. 40 sec.
24 × 30cm (ST) Approx. 47 sec.
18 × 24cm (ST) Approx. 40 sec.
15 × 30cm (ST-VI) Approx. 54 sec.*
24 × 30cm (ST-BD) Approx. 85 sec.
18 × 24cm (ST-BD) Approx. 75 sec.
24 × 30cm (HR-BD) Approx. 95 sec.
18 × 24cm (HR-BD) Approx. 82 sec.
24 × 30cm (HR-V) Approx. 60 sec.
18 × 24cm (HR-V) Approx. 53 sec.
* To use the 15×30cm (ST-VI) IP, the IP adapter (optional) and 14”×17” cassette are
required.
The data were acquired under the following condition;

X-ray dose exposed on IP;
6,450 nC/kg (25mR) for ST
154,800 nC/kg (600mR) for HR
The performance described above shows typical value.
It varies depending on the exposure level outside of the breast.
(3) Gray scale

• Reading gray scale: 12 bits/pixel
• Output gray scale (Output from the Console): 10 bits/pixel
897N102379A A-3
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Specifications
(4) Reading Specification
Standard Pixel-density High Pixel-density

Reading Size Sampling Rate Number of Sampling Rate Number of
(pixels/mm) Pixels (pixels/mm) Pixels
24×30cm HR-BD 10 2364 × 2964 20 4728 × 5928
18×24cm HR-BD 10 1770 × 2370 20 3540 × 4740
24×30cm ST-BD 10 2364 × 2964 20 4728 × 5928
18×24cm ST-BD 10 1770 × 2370 20 3540 × 4740
24×30cm HR 10 2364 × 2964 10 2364 × 2964
18×24cm HR 10 1770 × 2370 10 1770 × 2370
14"×17" 5 1760 × 2140 10 3520 × 4280
14"×14" 5 1760 × 1760 10 3520 × 3520
10"×12" 6.7 1670 × 2010 10 2505 × 3015
8"×10" 10 2000 × 2510 10 2000 × 2510
24×30cm 6.7 1576 × 1976 10 2364 × 2964
18×24cm 10 1770 × 2370 10 1770 × 2370
For 15×30cm (ST-VI) IP

• The 15×30cm (ST-VI) IP is read using the IP adapter (optional) and 14”×17”
cassette.
• The sampling rate and number of pixels are the same as those of the 14”×17”
IP.
• The 15×30cm (ST-VI) IP can be output in 10”×12” size by the Console’s menu
settings.
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Specifications
1
3 Image Output
(1) Film output at the Image Recorder
Connection to the Image Recorder will make it possible to obtain hard copy in
2
the following image reduction ratios and formats.
● For standard pixel-density images
3
Reading size Reduction ratio
Two-image output One-image output
24 × 30cmHR 67% 100%
18 × 24cmHR 100% / 86%* 100%
4
14” × 17” (35 × 43cm) 50% 67%
14” × 14” (35 × 35cm) 50% 67%
10” × 12” 67% 100%
8” × 10” 86% 100%
A
24 × 30cm 67% 100%
18 × 24cm 86% 100%

* 18×24cmHR output format is depending on the service settings.
[Fig. A.1] (a) One-Image Output (b) Two-Image Output B

Image
Z
Image
ID
information
ID (26 x 36cm film)
information
(26 x 36cm film)
● For high pixel-density images

Reading size Reduction ratio
Two-image output One-image output
24 × 30cmHR 67% 100%
18 × 24cmHR 100% / 86%* 100%
14” × 17” (35 × 43cm) 50% 100%
14” × 14” (35 × 35cm) 50% 100%
10” × 12” 67% 100%
8” × 10” 86% 100%
24 × 30cm 67% 100%
18 × 24cm 86% 100%
* 18×24cmHR output format is depending on the service settings.
For one-image output using 14”×17” or 14”×14” IPs, images are output on
14”×17” size film. In other cases, images are output on 26×36cm size film.
Depending on the printer connected or CR Console software version used, image
outputs in the following formats are available.
• 14” × 14” image 100%-size output on 14” × 14” film
• 100%-size image output of 8” × 10” or 18 × 24cm image on 8” × 10” film,
as well as reduced image output on films of other sizes
• 100%-size image output of 10” × 12” or 24 × 34cm image on 10” × 12” film
897N102379A A-5
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Specifications
[Fig. A.2]
(a) 14”x17” One-Image Output (b) 14”x14” One-Image Output
ID information
Image
Image
ID
information
(14"x17" film) (14"x17" film)
(c) One-Image Outputusing IPs of other sizes (d) Two-Image Output
Image
Image
ID ID
information information
(26x36cm film) (26x36cm film)
(e) One-image output for Mammography (f) One-image output for Mammography
(Right-sided) (Left-sided)
Right Left
image image
ID ID
information information
(26x36cm film) (26x36cm film)
(g) Set menu for Mammography (2 in 1) (h) Set menu for Mammography (2 in 1)
Two-image Output (reduction) Two-image Output (Actual size output) (18×24cm)
ID information ID information
Right Left Right Left

breast breast breast breast
ID information ID information
(26×36cm film) (26x36cm film)
(i) Set Menu for Mammography (4 in 1)
Four Image Output
Image
Standard pixel-density images

ID ID Reading Size Reduction Ratio (4 in 1 Image)
information Image information
24 × 30cmHR 67%
18 × 24cmHR 86%
(14"×17" film)
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Specifications
1
4 Power Supply Conditions
Image reader (CR-IR368)
Single phase 50– 60Hz: 100 – 240V ~ (AC) ±10%
2
7-2.9A
5 Environmental Conditions
3
(1) Operating Conditions
Temperature: 15 – 30°C
Humidity: 40 – 80%RH (No dew condensation)
4
Atmospheric pressure: 750 – 1060 hPa
Heating value: 300Wh
A
(2) Non-Operating Conditions
Temperature: 0 – 45°C
Humidity: 10 – 90%RH (No dew condensation)
B
Atmospheric pressure: 750 – 1060 hPa
Z
6 External Dimensions and Weight
Width (mm (in.)) 655 (25.8)
Depth (mm (in.)) 740 (29.1)
Height (mm (in.)) 1330 (52.4)
Weight (kg (lb)) 240 (529.2)
Dimensions and weight are approximate and are subject to change without prior notice.
7 Options
・Fall prevention kit
・IP adapter
897N102379A A-7
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Specifications
8 External View
[Fig. A.3] Image Reader main unit

(Unit: mm (in.))
740 (29.1) 655 (25.8)
1330 (52.4)
<Left-side> <Front>
<Right-side> <Rear>
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Appendix B
IP Handling
B
897N102379A B-1
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IP Handling
1 IP Erasure Processing
1.1 Secondary Erasure
Even when stored in a room, an IP is very sensitive and absorbs and accumulates natu-
ral radioactivity such as cosmic rays or radiation energy emanating from radioisotopes
contained in construction materials such as those used for floors and walls. Perform
secondary erasure for IPs which have not been used that day.
For the detailed operation procedure, refer to Chapter 2, section 2.4, Conducting
Exposure Using a Cassette (IP) Left Unused for 8 Hours or More [SECONDARY
ERASURE].
1.2 Primary Erasure

The following IPs must always be submitted to primary erasure prior to use for expo-
sure.
(1) Over-exposed IP
(2) Incorrectly exposed IP
(3) IP that is to be used for high-sensitivity exposure
For the detailed operation procedure, refer to Chapter 2, section 2.3, Conducting Image
Erasure Only [PRIMARY ERASURE].
2 Storage Conditions/Daily Maintenance

2.1 Storage Conditions
(1) Store IPs under the following environmental conditions.
No dew condensation
Packed : Under 35˚C
Unpacked : Under 33˚C and 80%RH
(2) Store IPs in a place where they are not exposed to direct sunlight or excessive ul-
traviolet rays or various radioactive rays.
(3) Do not bend IPs or impose strong force on them.
2.2 Daily Maintenance

(1) Do not use damaged IPs because image diagnosis can be affected.
(2) Handle IPs as carefully as possible. Do not damage or stain IPs.
(3) Do not bend IPs, hit them against some other objects or drop on the floor or table.
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IP Handling
1
2.3 Cleaning
(1) Materials required
Lint free non-woven cotton
2
Gauze (100% cotton),
Lens cleaner
3
(2) Method
For cleaning of a dual-side reading IP, always use the sponge sheet supplied with the IP.
4
IP
A
Sponge sheet
Clean one side of the IP, then turn it over on

the sponge sheet for cleaning the other side. B
1 Using any of the above dry cloths, wipe the IP surface in the following patterns,
A and B, in order: Z
A B
2 For stains which fail to come off by cleaning with dry cleaning cloths, dampen the
above cloth with ethanol anhydride (ethanol purity ≥ 99.5%) before cleaning.
(Do not use another cleaning agent.)
When the IP surface has been cleaned using ethanol anhydride-dampened cloths,
slightly wipe it off with dry cloths listed above. Make sure the surface of the IP is
completely dry before use.
Frequent cleaning with ethanol anhydride can cause yellowing of the IP edges.
(3) Precautions
1 Be sure not to damage the IP.
2 Never use eraser or any other solvents.
3 Do not scratch the IP with your nails.
4 Replace the sponge sheet used for cleaning back to the cover for storage.
5 Never moisten the IP with water to wipe off stains.
Do not apply light to the IP exposed but not yet processed.
897N102379A B-3
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IP Handling
3 IP Disposal
When disposing of the IP, follow instructions stipulated by local law or any regulations
that apply.
We provide product safety information upon request.
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Appendix Z
Precautions for Exposure
Z
897N102379A Z-1
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It is recommended to use Bucky’s device to remove scatter lines and obtain a high quality im-
age. When carrying out exposure using a stationary grid, it is recommended to use a 60 grids/
cm grid with fewer artifacts. However, it is also possible to use 80 grids/cm for 8 x 10” IP.
Green mark
Top
A
Bottom
Cassette
Precautions to Observe Before Using an IP

(1) IP erasure processing
Before using an IP, ensure that the IP has been subjected to image erasure pro-
cessing. Particularly when performing a low-dose exposure (high-sensitivity expo-
sure), be sure to use an IP that has been subjected to erasure processing.
Though in rare cases, remaining images may appear on an IP from which images
have already been read out, if such IP is used for re-reading with no due image
erasure processing. Subject IPs to proper image erasure processing and avoid the
use of insufficiently erased IPs.
(2) “Over-exposed IP. Poor erasure.”

If the “Over-exposed IP. Poor erasure.” error code is displayed for an IP exposed
to a large X-ray dose shown below, which is then read on the Image Reader, you
press Eraser button.
If the IP removed from the Image Reader is to be subjected to erasure processing
later, wait at least for 16 hours and then perform erasure processing.
<Exposure at large X-ray dose>

ST-VI : Tungsten (or W) target, about 400 mR or more
Subjecting an IP to exposure continuously at large X-ray dose may cause damage

due to X-rays (sensitivity deterioration) to occur on the IP. For this reason, avoid
using the same IP for exposure at large X-ray dose repeatedly.
1 Precautions for Exposure in the AUTO MODE

In the AUTO MODE, stable image output can be obtained by means of the following.
(1) Radiation field and IP split pattern recognition (PRIEF)
(2) Detailed depiction of the cervical region
(3) EDR image data analysis
However, problems may arise due to differences in multiple diaphragm or scattered rays
of the X-ray equipment. For such problems, contact our service engineer and use such
other recording modes as the SEMI-AUTO MODE or FIX MODE.
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1
1.1 Radiation Field and IP Split Pattern Recognition
1 Be sure that the center (25 × 25mm (1.0 × 1.0 in.)) of the IP is in the radiation field. If the
IP is split for multiple exposures, each center of the split portions must be covered by the
2
radiation field.
( ) ( ) ( ) ( ) ( )
3
IP center: 25mm×25mm (1.0 in.×1.0 in.)
area (black rectangles in examples above)
located in the center of the IP
Center of the split portion: 25mm×25mm (1.0 in.×1.0 in.)
area (black rectangles in examples above) located in the
center of each split portion 4
A
2 Do not set the radiation field extremely small. Be sure to expose X-rays on one thirds
or more of the length of each side of the IP.
3 Be sure that each side of the radiation field does not overlap with the contrast medium.
B
Error will occur if they overlap each other.
4 The IP split pattern recognition is as follows. “S” in PRIEF4S or 1S is a mark showing
that the IP split recognition is possible.
Z
Full-IP exposure Half-split IP (vertical) Half-split IP (horizontal) Quarter-split IP
* For multiple exposures with a split IP, split portion(s) can be left unexposed.
(Only when using PRIEF 4S or 1S.)
[Table. Z-1] Available for Each Anatomical Region/Method
Plain Contrast Medium Tomography

Head 4S 4S 4S (1 for pantomography)
Neck 4S 4S 1S
Chest 4S 4S (1 for esophagus) 1
Breast 2 2 –
Abdomen 4S 4S (1S for stomach and intestines) 1
Pelvis 4S 4S 1
Upper extremity 4S 4S 1
Lower extremity 4S 4S 1
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5 Notes on PRIEF
[PRIEF 4S] Used, with some exceptions, for both plain and contrast medium exposure
menus, from head to lower extremities.
(1) The diaphragm shape will be any convex polygons including rectangle, circle,
ellipse, track, etc.
[PRIEF 2] Used to the mammography menu.

(1) Use “Breast-Chest Wall” in mammography for very small breast such as male
breast.
[PRIEF 1] Used to tomography menus for chest, abdomen, pelvis, upper and lower
extremities.
(1) When the IP is not split and the diaphragm is closed, adjust the shape so that it
is parallel to the IP side.
(2) When conducting multiple exposures with a split IP using the PRIEF 1 menu,
1) do not close the diaphragm.
2) expose all the split portions of the IP.
[PRIEF 1S] Used to neck tomography and stomach contrast medium menus.
(1) When the IP is not split and the diaphragm is closed, adjust the shape so that it
is parallel to the IP side.
1.2 Depiction of the Cervical Region

1 The radiation field must not include the whole head. Be sure to secure transparent
portions on both sides of the neck.
( ) ( )
Use the “Head” menu to include the whole head in the radiation field.
2 For exposure of the pharynx or larynx, be sure that the neck comes to the center of the radiation
field so that the frontal and lateral orientations can be recognized appropriately.
Image area
Radiation field
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1
3 In pharynx and/or larynx exposure, do not use lead characters in the oblique line
section.
2
3
1.3 Depiction of HIP JOINT AXL - 2
1 Make sure to position the region of interest to the slanted-line area shown below. Do 4
A
not collimate further inside.
2 Positioning should be done so that the condyle and the femur run along the longer
B
edge. (Do not have them positioned against the shorter edge.)
Z
Condyle side 7/12
Femur side
1/12
1/4 1/4
1.4 Precautions for “Panorama” X-ray Exposures Using a 10″×12″ Cassette

1 To obtain properly displayed images, set the 10″x12″ cassette in the dedicated cas-
sette holder of the exposure unit so that the green mark on top of the cassette is
positioned on the right-hand side when viewed from the X-ray tube, as illustrated
below.
Right side
Green mark
10″×12″ cassette
2 For image output, the “Panorama” X-ray exposure menu (M2004) takes only an area
of 15×30cm from the 10″×12″ exposure area.
If you wish an image be output using the entire 10″×12″ area, use the “Panorama-2”
(7004) exposure menu.
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1.5 EDR Image Data Analysis

1 Image unevenness appearing when the grid used for exposure is not correctly posi-
tioned in terms of the bulb, clothes shadow or unevenly radiated X-ray to the X-ray
exposure area can be referred to as the problems occurring during the EDR image
data analysis, which cause unstable density on the image. Avoid such unevenness
in the X-ray exposure area as far as possible.
2 If the target includes such materials as gypsum, denture, etc., stable density may
not be obtained because such materials make it difficult to analyze EDR image data.
In such a case, use the S-Shift/C-Shift or FIX MODE.
3 For multiple exposures with a split IP, make exposure doses on each portion of the
IP as equal as possible (maximum 1.6 times). In other words, for multiple exposures,
submit each portion of the IP to the appropriate exposure dose according to the
intended anatomical region as usual.
4 Precautions when using the AUTO MODE.
Auto mode Precautions

I As this mode is available on the assumption that it extracts
information concerning the skin, secure the positioning so
that there is an area other than the target where the direct
X-rays are incident.
II No special precautions
III Be sure to use the Ba contrast medium.
IV 1 Be sure to secure the positioning so that the X‑rays are
incident directly in the area outside the target.
2 As the reading latitude is fixed, it is necessary to control
the tube voltage as usual according to the thickness of the
target.
V As the reading latitude is fixed, it is necessary to control
the tube voltage as usual according to the thickness of the
target.
VI No special precautions
VII No special precautions
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1
2 Precautions for Exposure in the SEMI‑AUTO MODE
The precautions are common to Semi I, II, III or III(**).
1 Center area of the IP
2
10 × 10cm (3.9×3.9 in.) (Semi I)
7 × 7 cm (2.8×2.8 in.) (Semi II)
5 × 5 cm (2.0×2.0 in.) (Semi III)
3
Position the portion you need to display often in each of the 5 × 5cm (2.0×2.0 in.)
center areas of the half-split IPs (both upper and lower halves and right and left
halves) and the quarter-split IP.
4
2 Never position anything other than the subject in the above mentioned areas. If
anything other than the subject is positioned in such areas, the image density will
become thinner.
A
In addition, do not position any metals or artificial bones in such areas. The image
density will become higher if such an object is positioned in such areas.
B
( )
3 It is necessary to control the tube voltage as usual according to the subject thickness.
Z
The following precautions should be observed for Semi IV.
y
Area Center Coordinate (x:y) cm (in.) Size (cm (in.))

b c a (0(0), 0(0)) 10×10 (3.9×3.9)
b (-5(-2.0), 7(2.8)) 6×6 (2.4×2.4)
a
x c (5(2.0), 7(2.8)) 6×6 (2.4×2.4)
d (-5(-2.0), -7(-2.8)) 6×6 (2.4×2.4)
d e
e (5(2.0), -7(-2.8)) 6×6 (2.4×2.4)
(1) Do not position transparent portions (area other than the subject) in the above-
mentioned five areas.
(2) It is necessary to control the tube voltage as usual according to the subject thick-
ness.
The SEMI-AUTO MODE has been preset around the magnification menu.
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3 Precautions for Exposure in SEMI-X MODE

The user will select the nine areas accordingly, on which SEMI-AUTO MODE applies.
(See the illustration below.)
The same precautions as for SEMI-AUTO MODE apply.
L C R
5cm × 5cm (2.0 in.×2.0 in.) T

M
4 Precautions for Exposure in FIX MODE

As reading conditions are fixed, exposure conditions must be controlled in the same way
as for conventional X-ray exposure.
The reading conditions (sensitivity and latitude) have been preset according to the relevant
menu in FIX MODE. Thus, select the exposure conditions that correspond to that
menu.
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During maintenance and inspection, strictly observe precautions contained in “1.2 Operational Precautions”
(page 1-3) and “1.3 Safety Precautions” (page 1-13) in this manual for you to use the FCR PROFECT
ONE Plus (CR-IR 368) system under best conditions.
1 User’s Maintenance and Inspection Items

1.1 Daily Inspection
(1) Inspection Before Use
• Make sure that the equipment starts up normally.
• Make sure that the equipment communicates with connected devices normally.
➡ Figures 2.1 to 2.4 in “2.1.1 Starting Up the System” (page 2-2)
(2) Inspection During Use

• Make sure that the equipment handles cassettes normally.
➡ “2.2 Routine Operations” (page 2-6)
• Make sure that the cassette opens / closes and locks normally.
• Make sure that images are output normally.
If any failures, such as transparent images etc., result, clean the equipment.
➡ “2.3 Cleaning” (page B-3)
(3) Inspection After Use

• Make sure that the power turns OFF normally after the equipment has been shut down.
➡ Figures 2.5 and 2.6 in “2.1.2 Shutting Down the System” (page 2-3)
1.2 Periodical Inspection

Using a vacuum cleaner, remove any dirt or dust accumulated in each unit of the equipment once every
three months. Clean then with a slightly moistened soft cloth and wipe off any moisture with a dry cloth.
CAUTION: Ensure cloth is free of residual water and water does not enter the
device.
➡ Figure 1.1 in “1.4 Component Names and Functions” (page 1-14)
No. Unit for Cleaning No. Unit for Cleaning

1 Main unit cover 4 Air filter
2 Operation panel 5 Periphery of devices
3 Cassette setting unit
The air filter on the side of the equipment can be removed as an assembly,
together with the filter cover. Remove first the cover and then the air filter
fit in the cover. Clean them using a vacuum cleaner.
Be sure to turn the equipment power OFF (“O”) before
cleaning the air filter.
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2 Maintenance and Inspection Items Assigned to Specified Dealer

For periodical inspection of the equipment and necessary arrangements, consult our official dealer or local
representative.
CAUTION: The life of this equipment is six years.

To use the equipment after this period, contact a designated service
supplier to perform an overhaul.
For maintenance and inspection after that, consult with a designated
service supplier.
Periodical Maintenance
Make sure that the periodical maintenance and inspection assigned to our official dealer are performed as specified.
Maintenance and Inspection Items Assigned to Specified Dealer
Periodical Maintenance and Inspection Items Period
Cleaning of the cleaning guide plate and the internal cleaning roller Every year
Checking of the internal units Every year
Checking of the movability Every year
Checking of the image output Every year
Cleaning of the internal units Every 2 years
Main Periodical Replacement Parts

Periodical Replacement Parts Period
Cleaning roller Every 2 years
Air filter Every 2 years
Erasure lamp Every 2 or 3 years
Erasure unit filter Every 3 years
Cleaning guide plate Every 3 years
The cycles of periodical maintenance and inspection and of parts replacement differ depending on the
usage and the daily operation time.
The replacement cycle of erasure lamp differs depending on the production lot.
For details, contact us directly or our official dealer.
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897N102379A
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Fuji Profec One

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Fuji Profec One

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(CR-IR 368)

Please read the Operation Manual thoroughly before

897N102379A_Z72N2680A.indb 1 2013/01/31 14:30:43

Copyright © 2012 FUJIFILM Corporation. All rights reserved.

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Chapter 2 Operations ........................................................................................................... 2-1

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Chapter 4 Troubleshooting .................................................................................................. 4-1

Appendix A Specifications . ................................................................................................. A-1

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1. IP Erasure Processing................................................................................................ B-2

Appendix Z Precautions for Exposure ............................................................................. Z-1

Maintenance and Inspection

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1.1 Features of the FCR PROFECT ONE Plus (CR-IR 368)

Major features of this system are as follows.

5 It is possible to input exposure information, such as patient information, regions targeted

6 The automatic feed/load mechanism results in more efficient operation.

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Precautions Before Operating This Equipment

WARNING: Do not connect any unspecified device.

This system is classified as a medical device under EC Directive 93/42/EEC.

To install or relocate the equipment, request it to a designated service supplier.

Precautions on External Network Connection

When a setting of the network to which the equipment is connected has

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1.2.1 Laser Handling Precautions

FCR PROFECT ONE Plus (CR-IR 368) Laser Unit Specifications

CAUTION: Use of controls or adjustments or performance of procedures other than those

1.2.2 Authorized Safety Standards

1.2.3 Preventing Electric Shock

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1.2.4.1 Further information for EN 60601-1-2 (Europe)

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Guidance and manufacturer’s declaration - electromagnetic emissions

Emissions test Compliance Electromagnetic environment - guidance

Guidance and manufacturer’s declaration - electromagnetic immunity

Voltage dips, short <5% UT <5% UT Mains power quality should be

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Conducted RF 3 Vrms 3 Vrms Portable and mobile RF communications equipment should be

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Recommended separation distances between

Separation distance according to frequency of transmitter

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

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CPU91A - LAN : Connected to the image network devices.

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1.2.7 Precautions to be Observed When Using the Electric Medical Equipment

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1.2.9 Location of Each Label

Year of Manufacture and

Be sure to use the power Do not connect telephone lines

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The following symbols are used on this equipment.

This symbol indicates compliance of the equipment with Directive 93/42/EEC.

1.3 Safety Precautions

WARNING: Indicates hazardous situations that may lead to serious injuries