FujiFilm CR Console User manual

CR Console Operation Manual
897N0519M
FUJI COMPUTED RADIOGRAPHY
CR Console
OPERATION MANUAL
13th Edition
June 2011
This Operation Manual provides detailed information about how to use the Fuji
Computed Radiography CR Console as well as important points to note when using
the CR Console.
Before using this product, be sure to read this manual thoroughly. And keep it handy
for future references. In addition, please be sure to read the CR Console Operation
Guide for your understanding of product overview and its basic operation procedure.

.
END-USER SOFTWARE LICENSE AGREEMENT
FUJIFILM Corporation
The license of the Software (as defined below) granted hereunder is contingent upon the Licensee’s acceptance of
all the terms provided herein, and any use of the Software by the Licensee shall be deemed as such acceptance.
This Product contains software ("Software") and related written materials ("Documentation"). The term "Software"
shall include any updates, upgrades, modified versions, additions and copies of the Software licensed to you by
FUJIFILM Corporation ("FUJI").
1. License. Subject to the terms and conditions of this Agreement, you are granted a limited, non-exclusive, non-transferable and non-
sublicensable license to use the Software and the Documentation only on a single computer until such rights are terminated according to
Section 8 below.
2. Ownership. It is acknowledged and agreed that FUJI retains all title and rights to the Software the Documentation and all copies
thereof, and no title or rights to the Software or the Documentation is transferred or licensed to you except as expressly set forth herein.
3. Restriction on Use. You may: (i) make and retain one extra copy of the Software for backup purposes only; and (ii) copy the
Documentation only as reasonably necessary for user reference and backup purposes. Each copy of the Software and Documentation
made by you shall contain the same proprietary notices, labels, and marks as the original thereof without any alteration. You shall not: (i)
sell, sublicense, assign, lease, encumber or otherwise transfer the Software or the Documentation or the rights granted hereunder; (ii)
reverse engineer, decompile, disassemble or create derivative works of the Software; (iii) remove or alter any proprietary notices, labels or
marks on or contained in any part of the Software or the Documentation; (iv) make any copies of the Software or the Documentation
except as permitted above; or (v) install the Software on any computer other than as permitted by this Agreement. As a condition of the
use of the Software by you, you hereby represent and warrant that you shall not use the Software for any purpose that is unlawful or
prohibited by this Agreement. You agree to abide by all applicable laws and regulations in your use of the Software.
4. Export Control. You shall comply with all export and re-export restrictions and regulations imposed by the government of the United
States and other relevant countries or regions (“Export Restrictions”). You shall not knowingly transfer, directly or indirectly, any restricted
software or technical data received hereunder or the direct product of such data, to any country or region identified as an embargoed
destination or country in the Export Restrictions, unless prior written authorization is obtained from FUJI and each appropriate United
States or other government agencies. This Section shall survive the expiration or termination of this license agreement.
5. Update and Upgrade. FUJI may, at its sole discretion, make any update or upgrade of the Software available; however, FUJI shall
have no obligations to make any update or upgrade of the Software available.
6. Limited Warranty. FUJI hereby warrants that the Software shall operate in substantial conformity with the then current Documentation,
when used in strict compliance with such Documentation. This warranty shall be effective only for one year following your receipt of the
Software (hereinafter referred to as “Warranty Period”). This warranty is conditioned upon the installation and use of the latest version of
the Software released by FUJI in strict compliance with the then current Documentation. If the Software fails to perform as warranted in the
Warranty Period, FUJI shall use commercially reasonable efforts to correct such Software. THE FOREGOING STATES THE SOLE AND
EXCLUSIVE REMEDIES TO WHICH YOU ARE ENTITLED FOR FUJI'S BREACH OF WARRANTY. FUJI HEREBY DISCLAIMS ANY
OTHER WARRANTIES WITH RESPECT TO THE SOFTWARE AND DOCUMENTATION, EXPRESS OR IMPLIED, INCLUDING
WITHOUT LIMITATION ALL WARRANTIES REGARDING MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NON-
INFRINGEMENT.
7. Limitation of Liability. TO THE FULLEST EXTENT PERMITTED BY APPLICABLE LAW, FUJI SHALL NOT BE LIABLE FOR ANY
INDIRECT, SPECIAL, EXEMPLARY, PUNITIVE, INCIDENTAL, OR CONSEQUENTIAL DAMAGES OF ANY KIND (INCLUDING
WITHOUT LIMITATION, LOST PROFITS OR LOST DATA), WHETHER SUCH DAMAGES ARE BASED ON CONTRACT, TORT
(INCLUDING NEGLIGENCE), PRODUCT LIABILITY OR OTHERWISE (INCLUDING ANY DAMAGES WHICH ARE IN ANY WAY
CONNECTED WITH ANY USE OF THE SOFTWARE OR DOCUMENTATION), EVEN IF IT HAS BEEN ADVISED OF THE POSSIBILITY
OF SUCH DAMAGES.
8. General Provisions. This Agreement shall be governed by and construed according to the laws of Japan, excluding its conflict of laws
rules. You consent to the exclusive jurisdiction of Japanese courts and agree that the venue shall lie exclusively in Japan, in all disputes
arising out of or relating to this Agreement. The use of the Software or Documentation is not authorized in any jurisdiction that does not
give effect to all provisions of the terms and conditions of this Agreement, including without limitation this Section 8.
9. Termination. All the rights granted to you hereunder shall automatically terminate upon your breach of any provision herein, and you
must cease the use of the Software and Documentation and destruct all copies of the Software and Documentation in your possession,
including any of backup copy, upon such termination. Any provision herein that by its nature survives shall survive the termination of the
rights granted to you hereunder. _______________________________________________________________________________________________________________________________________

CR Console Operation Manual
2011. 06 897N0519M iii
FOREWORD
Thank you for purchasing the CR Console.
This Operation Manual applies to the following software.
xCR-IR 348CL Application Software V8.3
1. Unauthorized transfer or duplication of all or any part of the content of this manual is strictly
prohibited.
2. The contents of this Operation Manual are subject to change without prior notice.
3. FUJIFILM Corporation accepts no liability whatsoever with regard to faults or damage arising
from installation, relocation, modifications, maintenance or repairs performed by anyone other
than FUJIFILM Corporation or a contractor approved by FUJIFILM Corporation.
4. FUJIFILM Corporation accepts no liability whatsoever with regard to faults of or damage to this
product caused by third-party products other than those supplied by FUJIFILM Corporation.
5. FUJIFILM Corporation accepts no liability whatsoever with regard to faults or damage arising
from modifications, maintenance or repairs in which replacement parts other than the genuine
parts approved by FUJIFILM Corporation were used.
6. FUJIFILM Corporation accepts no liability whatsoever with regard to faults or damage arising as
a result of a failure to observe the safety precautions and operational procedures provided in this
Operation Manual.
7. FUJIFILM Corporation accepts no liability whatsoever with regard to faults or damage caused by
ambient conditions that deviate from the operating conditions for this product, such as the power
supply and installation environment, that are specified in this Operation Manual.
8. FUJIFILM Corporation accepts no liability whatsoever with regard to faults or damage caused by
natural events such as fires, earthquakes, floods or lightning strikes.
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 not come into direct
contact with it or for operation by appropriately trained operator.
Process waste correctly, as stipulated by local law or any regulations that apply.
When discarding the CR Console that incorporates the lithium battery, be sure to contact a licensed
waste disposal contractor because it cannot be disposed of as a general waste.
Caution : Rx Only (Federal law restricts this device to sale by or on the order of a physician.)
Trademark
FCR is a trademark or a registered trademark of FUJIFILM Corporation.
Other holders’ trademarks
Windows is the registered trademark of US Microsoft Corporation in the U. S. A. and other countries.
All other company names and product names described in this manual are the trademarks or
registered trademarks of their respective holders.
Copyright © 2002-2011 FUJIFILM Corporation. All rights reserved.

CR Console Operation Manual
iv 2011. 06 897N0519M
CONTENTS
Chapter 1. PRECAUTIONS ___________________________________1-1
1.1 For Safe Operation................................................................................................. 1-2
1.1.1 Warnings and Cautions Included in this Operation Manual....................... 1-2
1.1.2 Cautions in Using This Equipment Within the Patient Environment......... 1-3
1.1.3 Cautions in Using a USB Memory............................................................. 1-3
1.2 Electromagnetic Compatibility (EMC).................................................................. 1-4
Chapter 2. OPERATIONS BASICS ____________________________2-1
2.1 Starting Up and Shutting Down the CR Console .................................................. 2-2
2.1.1 Starting Up the CR Console ....................................................................... 2-2
(1) Login .......................................................................................................... 2-4
(2) Logoff......................................................................................................... 2-4
2.1.2 Shutting Down the CR Console ................................................................. 2-5
2.2 Operation Screen ................................................................................................... 2-6
2.2.1 Receiving Studies ....................................................................................... 2-6
(1) Inputting Patient Information ([3.1.1 Inputting Patient Information]) ....... 2-6
(2) Selecting Exposure Menu ([3.1.3 Selecting Exposure Menu]) .................. 2-6
2.2.2 Confirming Study Details........................................................................... 2-7
(1) Modifying Patient Information ([3.2.1 Modifying Patient Information]) .. 2-7
(2) Modifying Exposure Menu ([3.2.3 Modifying Exposure Menu]).............. 2-7
2.2.3 Issuing Examination Orders ....................................................................... 2-8
(1) Issuing Examination Orders ([3.3 Issuing Examination Orders])............... 2-8
2.2.4 Executing Studies ....................................................................................... 2-8
(1) Starting a Study ([3.4.1 Starting a Study]) ................................................. 2-8
(2) Preparation before Exposure (Study) ([3.2 Confirming Study Details]).... 2-9
(3) Reading Images ([3.4 Executing Studies]), (4) Performing
Re-exposure/Additional Exposure ([3.6 Performing Re-exposure and
Additional Exposure]) ................................................................................ 2-9
2.2.5 From “Editing Images”, “Distribution” to “Suspending Studies” and
“Completing Studies”................................................................................. 2-10
(1) Editing Images ([3.7 Editing Images]) ....................................................... 2-10
(2) Image Delivery ([3.8 Image Delivery])...................................................... 2-11
(3) Suspending Studies ([3.9 Suspending Studies]) and
Completing Studies ([3.10 Completing Studies]) ...................................... 2-11
2.2.6 Patient Information Input Screen................................................................ 2-12
(1) List tab ( ) .................................. 2-12
(2) Screen keyboard ......................................................................................... 2-13
(3) Patient information input field.................................................................... 2-13
(4) Scroll view display area (option) ............................................................ 2-15

CR Console Operation Manual
2011. 06 897N0519M v
(5) Image Reader status ....................................................................................2-15
(6) FCR button ( ) .............................................................................2-15
(7) If an Error Occurs on Destination Device...................................................2-17
(8) Display of the current time and date ...........................................................2-17
2.2.7 Exposure Menu Selection Screen ...............................................................2-18
2.2.8 Examination Order Issuance Screen ...........................................................2-20
2.2.9 Study Screen ...............................................................................................2-21
2.2.10 Image Edit Screen ......................................................................................2-25
2.3 Image Reader Status...............................................................................................2-27
2.4 Scroll View Display Area (option).........................................................................2-31
2.5 Study Information List ...........................................................................................2-32
(1) Display from the “Exposure Menu Selection Screen”,
“Study Execution Screen” and “Image Edit Screen” ..................................2-32
(2) Display from individual lists other than the “Queue” list ...........................2-32
2.6 Version Display......................................................................................................2-35
Chapter 3. OPERATIONS STUDY _____________________________ 3-1
3.1 Receiving Studies...................................................................................................3-2
3.1.1 Inputting Patient Information......................................................................3-2
(1) Inputting Patient Information in the “Patient Information Input Screen” ...3-2
(2) Ending Input of Patient Information to Display the “Exposure Menu
Selection Screen” ........................................................................................3-4
3.1.2 Patient Information Database function........................................................3-5
(1) Input by keyword retrieval..........................................................................3-5
(2) Input by list retrieval ...................................................................................3-7
(3) Deletion.......................................................................................................3-8
3.1.3 Selecting Exposure Menu ...........................................................................3-9
3.2 Confirming Study Details.......................................................................................3-10
3.2.1 Modifying Patient Information ...................................................................3-10
3.2.2 Resetting the patient ID issuance ................................................................3-12
3.2.3 Modifying Exposure Menu .........................................................................3-13
(1) Adding Exposure Menus.............................................................................3-13
(2) Changing Exposure Menus .........................................................................3-13
(3) Deleting Exposure Menus...........................................................................3-14
3.3 Issuing Examination Orders ...................................................................................3-15
3.3.1 Performance Setting....................................................................................3-18
(1) Property Setting...........................................................................................3-18
(2) Setting the Anatomical Region ...................................................................3-19
3.3.2 Setting for Issuing the Examination Order..................................................3-21
3.4 Executing Studies...................................................................................................3-22

CR Console Operation Manual
vi 2011. 06 897N0519M
3.4.1 Starting a Study .......................................................................................... 3-22
(1) Starting Studies from the Exposure Menu Selection Screen ...................... 3-22
(2) Starting Studies from the “Local WL” List ................................................ 3-24
(3) Starting Studies from the “Delivered” List (additional exposures) ............ 3-26
(4) Starting Studies from the “Examination Order Issuance Screen” .............. 3-27
(5) Starting Studies from the Scroll View (option) .......................................... 3-29
(6) Settings to Get the Next Study Started ....................................................... 3-31
3.4.2 Preparation before Exposure (Image Reading):
Confirmation and Modification of Exposure Parameters........................... 3-32
(1) Setting image flip ....................................................................................... 3-35
(2) Film output format...................................................................................... 3-36
(3) EDR mode .................................................................................................. 3-36
(4) Filing mode................................................................................................. 3-37
(5) Function ..................................................................................................... 3-38
(6) Film mark ................................................................................................... 3-39
(7) Number of film output ............................................................................... 3-40
(8) Distribution code ....................................................................................... 3-40
(9) Reading size ............................................................................................... 3-41
(10) SS/CS ......................................................................................................... 3-42
(11) Pixel density ............................................................................................... 3-42
(12) Trimming.................................................................................................... 3-43
3.4.3 Preparation before Exposure (Image Reading):
Adding Exposure Menus ............................................................................ 3-45
3.4.4 Preparation before Exposure (Image Reading):
Changing Exposure Menus......................................................................... 3-47
3.4.5 Preparation before Exposure (Image Reading):
Deleting Exposure Menus .......................................................................... 3-49
3.4.6 Preparation before Exposure (Image Reading):
Setting the Auto-repeat Exposure............................................................... 3-50
3.4.7 Preparation before Exposure (Image Reading):
Setting the Multi-frame Format.................................................................. 3-51
3.5 Reading Images ..................................................................................................... 3-53
3.5.1 Differences in the Operation of Connected Image Readers ....................... 3-55
(1) FCR Cassette Type Equipment .................................................................. 3-55
(2) FCR 5000 series Built-in type .................................................................... 3-59
(3) FCR VELOCITY series Built-in type ........................................................ 3-61
3.5.2 Changing the Order of Exposure Menus .................................................... 3-62
3.5.3 Switching Images ...................................................................................... 3-62
3.5.4 Scrolling the Exposure Menu List.............................................................. 3-63
3.5.5 Changing Display Image ............................................................................ 3-63
3.5.6 Changing the Monitor Mode ...................................................................... 3-63

CR Console Operation Manual
2011. 06 897N0519M vii
3.5.7 Alternately Changing Image Display Mode ...............................................3-64
3.6 Performing Re-exposure and Additional Exposure................................................3-65
3.6.1 Re-exposure ................................................................................................3-65
3.6.2 Additional Exposure ...................................................................................3-69
3.7 Editing Images........................................................................................................3-70
3.8 Image Delivery.......................................................................................................3-73
(1) Auto-delivery after QA completion ............................................................3-73
(2) Distributes images automatically to all attributes
whenever an image is read ..........................................................................3-73
(3) Distributes images automatically only to Print attribute
whenever an image is read ..........................................................................3-73
(4) Distributes images to all attributes individually..........................................3-74
(5) Distributes images to the Print attribute only individually .........................3-74
(6) Distributes only Print attribute automatically when a certain period
of time has passed after image reading .......................................................3-75
3.9 Suspending Studies ................................................................................................3-81
(1) In the case that the image reading has been done for all exposure menus
in the study ...................................................................................................... 3-81
(2) In the case that exposure menus of unregistered IP remain in the study.....3-81
3.10Completing Studies ................................................................................................3-84
(1) In the case that the image reading has been done for all exposure menus
in the study ...................................................................................................... 3-84
(2) In the case that the exposure menus of unregistered IP remain
in the study..................................................................................................3-86
Chapter 4. OPERATIONS IMAGE EDIT ________________________ 4-1
4.1 Operation Outline...................................................................................................4-2
(1) Displaying Screen .......................................................................................4-2
(2) Editing Images ............................................................................................4-2
(3) Using Utility................................................................................................4-3
(4) Outputting Images.......................................................................................4-3
(5) Completing Image Edit ...............................................................................4-3
(6) Image Edit Function Authentication button................................................4-3
4.2 Displaying Screen ..................................................................................................4-4
4.3 Editing Images........................................................................................................4-6
4.3.1 Palette..........................................................................................................4-6
(1) Changing exposure menus ..........................................................................4-7
(2) Editing patient information .........................................................................4-8
(3) Editing image information ..........................................................................4-9
(4) Editing technologist information ...............................................................4-10
(5) Film marker.................................................................................................4-11
(6) Comments on image/study..........................................................................4-12

CR Console Operation Manual
viii 2009. 09 897N0519H
(7) Changing GA/GS ....................................................................................... 4-12
(8) Flip/Rotation............................................................................................... 4-13
(9) Trimming Adjustment ............................................................................... 4-15
(10) Inputting markers ....................................................................................... 4-17
(11) Inputting annotation characters ................................................................. 4-20
(12) Changing S/L.............................................................................................. 4-24
(13) Changing SS/CS ......................................................................................... 4-25
(14) FNC ............................................................................................................ 4-26
(15) Detailed Image Processing Parameters Change Box.................................. 4-27
4.3.2 Delivery ...................................................................................................... 4-28
(1) Print setting................................................................................................. 4-29
(2) Filing device/soft copy device setting ........................................................ 4-32
(3) Changing a filing device ............................................................................ 4-33
(4) Changing filing mode................................................................................. 4-34
(5) Registering additional soft copy devices .................................................... 4-35
(6) Deleting a soft copy devices....................................................................... 4-36
(7) Setting density of soft copy image ............................................................. 4-36
4.3.3 List.............................................................................................................. 4-37
(1) Changing order .......................................................................................... 4-37
(2) Alternately switching images .................................................................... 4-37
(3) Changing display images ........................................................................... 4-37
4.4 Using Utility (QA Image Controller Buttons) ....................................................... 4-38
4.4.1 Magnifying Display Image......................................................................... 4-39
4.4.2 Changing Parameters.................................................................................. 4-41
4.4.3 Reprinting Display Image ......................................................................... 4-41
4.4.4 Setting the rejection................................................................................... 4-42
4.4.5 Locking Studies.......................................................................................... 4-44
4.4.6 Saving Image.............................................................................................. 4-45
4.4.7 Outputting DICOM Files............................................................................ 4-48
4.4.8 Special Image Print .................................................................................... 4-50
(1) Example of a specified special print........................................................... 4-51
(2) Trimming and release of the range to be magnified/reduced .................... 4-51
(3) Assigning a trimmed image into a film format and its release .................. 4-51
(4) Specifying a magnification/reduction ratio to assign it into
an image format (edit mode) ..................................................................... 4-52
(5) Moving the trimming image frame ............................................................ 4-52
(6) Changing the number of printouts.............................................................. 4-52
(7) Displaying a printer list ............................................................................. 4-53
(8) Changing format......................................................................................... 4-53
(9) Displaying the previous/next image .......................................................... 4-55
(10) Image magnification/reduction .................................................................. 4-55
(11) Printing image ............................................................................................ 4-55

CR Console Operation Manual
2010. 10 897N0519K ix
4.5 Outputting Images ..................................................................................................4-56
4.6 Completing Image Edit ..........................................................................................4-57
(1) When is displayed...........................................................................4-57
(2) / is displayed .......................................................................4-57
Chapter 5. OPERATIONS LIST _______________________________ 5-1
5.1 List..........................................................................................................................5-2
(1) Study-information sharing function ............................................................5-3
5.1.1 Local WL ....................................................................................................5-4
5.1.2 QA...............................................................................................................5-5
5.1.3 Queue ..........................................................................................................5-6
5.1.4 Delivered.....................................................................................................5-7
5.1.5 All ...............................................................................................................5-8
5.1.6 Today ..........................................................................................................5-9
5.2 List Operation.........................................................................................................5-10
(1) Filtering.......................................................................................................5-10
(2) Search..........................................................................................................5-11
(3) Setting the Sorting Order ............................................................................5-11
(4) Updating the List.........................................................................................5-12
(5) Terminating Studies ....................................................................................5-12
(6) Deletion.......................................................................................................5-13
(7) Select All.....................................................................................................5-14
(8) Urgent Output .............................................................................................5-14
(9) Switching Display Information Alternately................................................5-15
(10) Moving Images ...........................................................................................5-15
(11) Filtering/update of the study list .................................................................5-19
(12) Execution of Next Processing .....................................................................5-20
(13) Study Information List ................................................................................5-22
(14) Scroll ...........................................................................................................5-22
(15) Printing 12 Frames of Multiple Study Images on One Film.......................5-23
(16) Setting Study List........................................................................................5-24
(17) Redelivery ...................................................................................................5-29
Chapter 6. TROUBLESHOOTING _____________________________ 6-1
6.1 Error Messages.......................................................................................................6-2
(1) If an Error Occurs on This Equipment........................................................6-2
(2) If an Error Occurs on Destination Device...................................................6-2
6.2 How to Cope with an Error ....................................................................................6-3
(1) When the System Hangs Up .......................................................................6-3
(2) When the Dose Area Product Measuring System is used ...........................6-5
(3) If a hard disk is damaged ............................................................................6-7

CR Console Operation Manual
x2010. 03 897N0519J
Chapter 7. DAILY INSPECTION AND MAINTENANCE _____________7-1
7.1 Performing Daily Inspection and Maintenance ..................................................... 7-2
(1) PC Main Unit.............................................................................................. 7-2
MAINTENANCE AND INSPECTION______________________________ 1
Maintenance and Inspection Items Assigned to Specified Dealer .....................................2

CR Console Operation Manual
2006. 10 897N0519C 1 - 1
FUJI COMPUTED RADIOGRAPHY
Chapter
1
PRECAUTIONS

CR Console Operation Manual
1 - 2 2010. 10 897N0519K
1.1 For Safe Operation
This chapter lists the precautions required to use the CR Console safely. Before starting use, read this
chapter very carefully and understand its operations thoroughly first.
1.1.1 Warnings and Cautions Included in this Operation Manual
Safety precautions described in this manual include “WARNING ( WARNING)” and
“CAUTION ( CAUTION)”, which are explained as follows.
WARNING
Indicates hazardous situations which may lead to serious injuries or even death if the precaution is
not or could not be followed.
CAUTION
Indicates hazardous situations which may lead to mild or medium injuries if the precaution is not or
could not be followed. Precautions against accidents causing only physical damages.
NOTE
Gives procedures requiring special attention, instructions which must be followed, supplementary
explanations, etc.
WARNING
This system supplies high voltage to the inside of unit, etc. The following instructions must be
carefully followed to prevent an electrical shock.
• No one other than service engineers should open the unit cover. Do not touch the high voltage
portion of the above-mentioned parts with your hand, or you may get an electric shock.
WARNING
The supply voltage of the units comprising this system is AC100V to 120V or AC200V to 240V.
The instructions below must be followed to prevent an electrical shock.
• Install the unit where no water may subject the units.
• Check that the ground of each unit has been perfectly connected.
• Check that all the cables have been properly and perfectly connected.
CAUTION
In extended uses of the unit, set aside 10 to 15 minutes after every hour to rest your eyes and hands.
• For image reading purposes, use an image display monitor suited for X-ray imaging diagnosis.
The image display monitor making part of this system is not suited for X-ray imaging diagnosis.
CAUTION
As the CR Console is not supposed to be operated continuously all day long, turn off the personal
computer once a day by performing the shutdown operation.
NOTE
The contents (objects) of the operation screens described in this manual may be changed/added/deleted
without any prior notice because of the software version upgrade.

CR Console Operation Manual
2011. 06 897N0519M 1 - 3
1.1.2 Cautions in Using This Equipment Within the Patient Environment
When connecting to other equipment such as an Image Reader, ensure that the equipment to be
connected is installed properly so that it can be used safely.
For details of installation of equipment to be connected, see the documents provided with it, and
contact our service engineer as necessary.
While this equipment is in operation, pay due attention not to have the patient come into direct
contact with it.
1.1.3 Cautions in Using a USB Memory
• When purchasing a USB memory, note the following points:
• Purchase a product that complies with the FCC/VCCI/CE standards or equivalent.
• Select a product that supports USB2.0 specification.
• Select a product that does not require you to install an exclusive driver or software.
• Select a product with a capacity of 2GB or more.
• Make sure that the product operates normally by performing “Write/Read & Compare” in
Windows Explorer.
If you have any enquiries, contact our authorized distributor.
• When using a USB memory, be careful not to lose it by mistake.
• Connect only one USB memory.
If more than two USB memories are connected simultaneously, they may not operate normally.
• When removing a USB memory from the personal computer, select “Safely Remove Hardware”,
and make sure that the USB memory access lamp is not flashing.

CR Console Operation Manual
1 - 4 2009. 09 897N0519H
1.2 Electromagnetic Compatibility (EMC)
■Electromagnetic Compatibility (EMC) Related Standard
This equipment complies with the following standard regarding Electromagnetic Compatibility
(EMC).
EMC standard : IEC 60601-1-2:2001+A1:2004
This does not guarantee that there is no harmful electromagnetic interference under any
installation environment.
This equipment can generate, use and radiate radio frequency energy. If the equipment is not
installed and used in accordance with the instructions, or if peripheral devices that are not
complied with the EMC standard, harmful interference may be generated under a particular
environment causing malfunction of the equipment and other devices.
If this equipment causes harmful interference to other devices, or if this equipment is affected by
interference from other devices, the user is encouraged to try to correct the interference by one or
more of the following measures:
• Reorient or relocate the 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.
If the problem cannot be solved with the above measures, stop using this equipment and consult
the manufacturer or our official dealer for help.
WARNING
Do not place devices generating electromagnetic wave near this equipment.

CR Console Operation Manual
2010. 03 897N0519J 1 - 5
■Further information for IEC
60601-1-2
(1) Medical electrical equipment is subject to special precautions regarding EMC. The equipment must be
installed and put into service according to the EMC information provided in Tables 1 to 4.
(2) Portable and mobile RF communications equipment can affect medical electrical equipment.
(3) Information regarding the cable affecting EMC is as follows.
Name General
Specification
Network Cable Cat5e or more,
UTP
type and
straight cable
(4) 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 equipment.
(5) The equipment should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the equipment should be observed to verify normal operation
in the configuration in which it will be used.
(6) Test items (Tables 1 to 4)
Table 1
Guidance and manufacturer’s declaration -
electromagnetic emissions
The CR-IR 348CL is intended for use in the electromagnetic environment specified below.
The customer or the user of the CR-IR 348CL should assure that it is used in such an environment.
Emissions
test
Compliance
Electromagnetic environment -
guidance
RF emissions
CISPR 11 Group 1
The CR-IR 348CL uses RF energy only for its internal
function. Therefore, its RF emissions are very low and are
not likely to cause any interference in nearby electronic
equipment.
RF emissions
CISPR 11 Class A
Harmonic emissions
IEC 61000-3-2
Class D
Voltage fluctuations / flicker
emissions
IEC 61000-3-3
Does not
comply
The CR-IR 348CL is suitable for use in all establishments
other than domestic and those directly connected to the
public low-voltage power supply network that supplies
buildings used for domestic purposes.

CR Console Operation Manual
1 - 6 2009. 09 897N0519H
Table 2
Guidance and manufacturer’s declaration -
electromagnetic immunity
The CR-IR 348CL is intended for use in the electromagnetic environment specified below.
The customer or the user of the CR-IR 348CL should assure that it is used in such an environment.
Immunity
test
IEC 60601 test
level
Compliance
level
Electromagnetic
environment - guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6kV contact
±8kV air
±2kV, ±4kV, ±6kV
contact
±2kV, ±4kV, ±8kV air
Floors should be wood, concrete
or ceramic tile . If floors are
covered with synthetic material,
the relative humidity should be
at least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
±2kV for power supply
lines
± 1kV for input / output
lines
±2kV for power supply
lines
± 1kV for input / output
lines
Mains power quality should be
that of a typical commercial or
hospital environment.
Surge
IEC 61000-4-5
±1kV differential mode
±2kV common mode
±0.5kV, ±1kV
differential mode
±0.5kV, ±1kV, ±2kV
common mode
Mains power quality should be
that of a typical commercial or
hospital environment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 s
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 s
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the CR-IR 348CL requires
continued operation during
power mains interruptions, it is
recommended that the CR-IR
348 C L be powered from an
uninterruptible power supply or
a battery.
Power frequency
(50/60Hz) magnetic
field
IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital
environment.
NOTE : UTis the a.c. mains voltage prior to application of the test level.

CR Console Operation Manual
2009. 09 897N0519H 1 - 7
Table 3
Guidance and manufacturer’s declaration - electromagnetic immunity
The CR-IR 348CL is intended for use in the electromagnetic environment specified below.
The customer or the user of the CR-IR 348CL should assure that it is used in such an environment.
Immunity test
IEC 60601 test level Compliance
level
Electromagnetic environment - guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m
80 MHz to 2.5 GHz
3 Vrms
3 V/m
Portable and mobile RF communications
equipment should be used no closer to any part
of the CR-IR 348CL, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency of
the transmitter.
Recommended separation distance
d = 1.2 P
d = 1.2 P80 MHz to 800 MHz
d = 2.3 P800 MHz to 2.5 GHz
where Pis the maximum output power rating of
the transmitter in watts (W) according to the
transmitter manufacturer and dis the
recommended separation distance in meters
(m). Field strengths from fixed RF transmitters,
as determined 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.
aField 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 348CL is used
exceeds the applicable RF compliance, the CR-IR 348CL 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 348CL.
bOver the frequency range 150 kHz to 80 MHz, field strength should be less than 3 V/m.

CR Console Operation Manual
1 - 8 2009. 09 897N0519H
Table 4
Recommended separation distances between Portable and mobile RF communications
equipment and the CR-IR 348CL
The CR-IR 348CL is intended for use in the electromagnetic environment in which radiated RF disturbances
are controlled.
The customer or the user of the CR-IR 348CL can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the CR-IR
348CL as recommended below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
m
Rated maximum
output power of
transmitter
W
150 kHz~80 MHz
d= 1.2 P
80 MHz~800 MHz
d= 1.2 P
800 MHz~2.5 GHz
d= 2.3 P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
11.2 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 din
meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where Pis 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.

CR Console Operation Manual
2006. 10 897N0519C 2 - 1
FUJI COMPUTED RADIOGRAPHY
Chapter
2
OPERATIONS
BASICS

CR Console Operation Manual
2 - 2 2009. 09 897N0519H
2.1 Starting Up and Shutting Down the CR Console
This section explains how to start up and shut down the CR Console. Be sure to start up peripheral
devices which are required for the work as well as the Image Reader and display.
2.1.1 Starting Up the CR Console
Turn on the display, then turn on the personal computer.
The application software of the CR Console automatically starts. When the Patient Information Input
Screen is displayed, startup is completed. Depending on the setting of the User Utility, the
“Examination Order Issuance Screen” is displayed.
NOTES
• Do not start up the CR Console before turning on the CR exposure unit. Otherwise, a message
indicating a communication error may appear on the CR Console.
• Be sure to turn on the display first, then turn on the personal computer.
Note that the touch panel may not respond accordingly.
We recommend that you use the equipment with the display turned on.
• User authentication may be required to log into the system, depending on the setting performed at
installation.
Other manuals for CR Console
1
Table of contents
Other FujiFilm Music Mixer manuals