Operation Manual
Operation Manual
Operation Manual
Console Advance
Precautions
Troubleshooting 5
Daily Inspection
and
Maintenance 6
Main
Specifications A
Optional Software B
Maintenance and
Inspection
897N101655E
END-USER SOFTWARE LICENSE AGREEMENT
FUJIFILM Corporation
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and you must cease the use of the Software and Documentation and destruct all copies of the Software and Documentation in
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the termination of the rights granted to you hereunder.
CAUTIONS
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.
Process waste correctly, as stipulated by local law or any regulations that apply.
When discarding the 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.)
For the Console Advance Lite, the following functions are optional.
• Detailed QA Software • X-ray Control Unit Online Software
• Image Magnification Software • DR Exposure Unit Connection Software
• Annotation Input Software
Trademark
FDR is a trademark or a registered trademark of FUJIFILM Corporation.
This Operation Manual describes the basic operations of the Console Advance.
Console Advance (DR-ID 300CL) Quality Control Test Software Reference Guide
The following is an outline of the Console Advance QC Test Software.
Chapter 1 Precautions
1.1 For Safe Operation.......................................................................................... 1-2
1.1.1 Warnings and Cautions Included in this Operation Manual.... 1-2
1.1.2 Precautions for Mammographic Exposure................................... 1-4
1.2 Electromagnetic Compatibility (EMC).................................................... 1-5
1.3 Safety Precautions.......................................................................................... 1-10
1.3.1 Wireless LAN. ......................................................................................... 1-10
1.3.2 Wireless Specifications........................................................................ 1-12
1.3.3 About USB Memory............................................................................. 1-14
1.3.4 Contraindications and Prohibitions.................................................. 1-14
1.4 Labels. .................................................................................................................. 1-15
1.5 System Configuration.................................................................................... 1-16
Chapter 5 Troubleshooting
5.1 Error Messages. ............................................................................................... 5-2
5.2 How to Cope with an Error......................................................................... 5-4
Precautions
Page
1.1 For Safe Operation················································································· 1-2
1.2 Electromagnetic Compatibility (EMC)····················································· 1-5
1.3 Safety Precautions················································································· 1-10
1.4 Labels···································································································· 1-15
1.5 System Configuration············································································· 1-16
This system supplies high voltage to the inside of unit, etc. The following
instructions must be carefully followed to prevent an electrical shock.
•N o one other than our official dealer 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.
• Do not use DR-ID 300CL in the patient environment. When you use commercially
available personal computers in the patient environment, use a notebook type with
a built-in battery with the power cable disconnected (use the built-in battery).
• Do not use a multiple tap connector.
•M ake sure that the devices to be connected to this system are authorized for connection.
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.
• While contacting the patient, do not operate the Console.
• 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.
• 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.
• Be careful to set each value not to excess the necessary X-ray exposure dose to patients.
• Prior to performing exposure, be sure to check exposure conditions on the X-ray control unit panel.
• Before operating the DR-ID 300CL, make sure that the monitor has appropriate brightness
(light intensity). If not, contact our official dealer. Regularly adjust the monitor settings to
keep optimum display images read by the DR-ID 300CL. Between the regular
adjustments, do not change the settings.
• If the monitor is used for an extended period of time, the brightness of its backlight
decreases (time degradation of the monitor).
As a result, the contrast of an image changes, which may lead to misdiagnosis. For this
reason, if this time degradation occurs, contact our official dealer.
Do not connect telephone lines to LAN connector. Only UTP-type straight LAN cables of
Category 5E or higher are appropriate for connection to this connector. 1
Read the Operation Manual thoroughly and specify the optimum exposure parameters.
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.
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
1 • Exposure menus for mammography and exposure menus for other than mammography cannot
be mixed together in the same study.
• Exposure menus for mammography and exposure menus for other than mammography cannot
be switched in the same study.
• For Anatomic Region Sequence, set the value specified in DICOM PS3-3 C.8.11.7.1.1. For
View Code Sequence, set the value specified in DICOM PS3-3 C.8.11.7.1.2. If you set values
other than those, images may not be read correctly.
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:
If the problem cannot be solved with the above measures, stop using this equipment and consult
the manufacturer or our official dealer for help.
This Operation Manual contains the names of standards applied in IEC 60601-1-2.
The names of standards applied in EN 60601-1-2 are replaced as follows.
IEC 60601-1-2
Standards applied in EN 60601-1-2
(descriptions in this Operation Manual)
CISPR 11 EN 55011
IEC 61000-3-2 EN 61000-3-2
IEC 61000-3-3 EN 61000-3-3
IEC 61000-4-2 EN 61000-4-2
IEC 61000-4-3 EN 61000-4-3
IEC 61000-4-4 EN 61000-4-4
IEC 61000-4-5 EN 61000-4-5
IEC 61000-4-6 EN 61000-4-6
IEC 61000-4-8 EN 61000-4-8
IEC 61000-4-11 EN 61000-4-11
(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.
1 (2) Portable and mobile RF communications equipment can affect medical electrical equipment.
(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.
Table 1
Guidance and manufacturer’s declaration - electromagnetic emissions
The Console is intended for use in the electromagnetic environment specified below.
The customer or the user of the Console should assure that it is used in such an environment.
The Console is intended for use in the electromagnetic environment specified below.
The customer or the user of the Console should assure that it is used in such an environment.
Electromagnetic environment
Immunity test IEC 60601 test level Compliance level
- guidance 1
±6kV contact ±6kV contact
Floors should be wood, concrete or
Electrostatic discharge
ceramic tile. If floors are covered
(ESD)
with synthetic material, the relative
IEC 61000-4-2
humidity should be at least 30%.
±8kV air ±8kV air
Electrical fast transient/ ±2kV for power supply lines ±2kV for power supply lines Mains power quality should be that
burst of a typical commercial or hospital
IEC 61000-4-4 ±1kV for input/output lines ±1kV for input/output lines environment.
±1kV differential mode ±1kV differential mode Mains power quality should be that
Surge
of a typical commercial or hospital
IEC 61000-4-5
±2kV common mode ±2kV common mode environment.
<5% U T <5% U T
(>95% dip in U T ) (>95% dip in U T )
for 0.5 cycle for 0.5 cycle
Mains power quality should be that
40% U T 40% U T of a typical commercial or hospital
Voltage dips, short (60% dip in U T ) (60% dip in U T ) environment. If the user of the
interruptions and for 5 cycles for 5 cycles Console requires continued
voltage variations on operation during power mains
power supply input lines 70% U T 70% U T interruptions, it is recommended that
IEC 61000-4-11 (30% dip in U T ) (30% dip in U T ) the Console be powered from an
for 25 cycles for 25 cycles uninterruptible power supply or a
battery.
<5% U T <5% U T
(>95% dip in U T ) (>95% dip in U T )
for 5 s for 5 s
Power frequency Power frequency magnetic fields
(50/60Hz) magnetic should be at levels characteristic of
3 A/m 3 A/m
field a typical location in a typical
IEC 61000-4-8 commercial or hospital environment.
NOTE : U T is the a.c. mains voltage prior to application of the test level.
The Console is intended for use in the electromagnetic environment specified below.
The customer or the user of the Console should assure that it is used in such an environment.
Compliance
1 Immunity test IEC 60601 test level
level
Electromagnetic environment - guidance
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 Console is used exceeds the applicable RF
compliance, the Console should be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as reorienting or relocating the Console.
b Over the frequency range 150 kHz to 80 MHz, field strength should be less than 3 V/m.
The Console is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the Console can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the Console as recommended below,
according to the maximum output power of the communications equipment. 1
Rated maximum Separation distance according to frequency of transmitter
output power of m
transmitter 150 kHz~80 MHz 80 MHz~800 MHz 800 MHz~2.5 GHz
W d = 1.2 P d = 1.2 P d = 2.3 P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m)
can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power
rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 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.
• A channel to use for wireless units should be separated from channels being used by
otherequipment. If the same frequency is shared with such equipment, interference and/or the
degradation of communications quality may occur. For further information, please contact our
authorized distributor.
• Sharing study information under poor network connection conditions may increase processing
time.
• On a Console connected with the network via wireless LAN, do not read images directly from
the FCR image reader. Depending on the connection status of the network, images could be
lost. If you want to confirm an FCR image on a Console connected via wireless LAN, use the
study information sharing function or switch the network connection to wired LAN
connection before reading.
• If a Console connected with the network via wireless LAN fails to start up, the desktop screen
of the operating system is displayed. In this case, restart the mobile PC.
• Do not make an X-ray exposure when the network connection is poor.
Other cautions
Select wireless LAN devices to connect to the Console that meet the following conditions, and
have the customer arrange setup of the device.
○ Unauthorized access
Malicious third parties are able to obtain unauthorized access to personal and corporate
networks, retrieve personal and confidential information (information leakage),
impersonate certain individuals to communicate with others, send out unauthorized
information (by impersonating others), modified transferred information that has been
intercepted (modification), release computer viruses and other malicious software, and
destroy data or entire systems (destruction).
Wireless LAN cards and wireless access points come with security systems to prevent these
issues from arising, so using devices by adjusting wireless LAN device security settings can
largely prevent these issues. Customers are requested to fully understanding the issues that can
arise if security settings are not adjusted properly, and are recommended to adjust settings by
making their own decisions and taking responsibility for security settings before using devices.
* Attachment of the device to the unit may be difficult depending on the type of wireless LAN
device selected. Always inquire in advance before making a selection. Contact a designated
contractor for setting the Console and attaching the wireless LAN device.
1
2011-06
Identification label
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.
The Console is connected to the exposure unit and is equipped with the functions to acquire
1 digital images and to process, record, and output the acquired images.
■ Desktop type
DR-ID 300CL
DR exposure unit FCR Image Reader
Personal
computer
Monitor
Hub
NOTE
• For the Console Advance Lite, the function to connect the Console to a DR exposure unit is
optional.
• Keep the operation manual of each device comprising the system together with this manual.
• The system configuration varies depending on the environment.
• Up to two monitors can be connected.
• In addition to the mouse and keyboard, a barcode reader and a magnetic card reader can be
connected to the Console.
Mobile PC
1
wireless wireless
Wired or communication communication
wireless
communication
Utility Box
Hub
NOTE
• Keep the operation manual of each device comprising the system together with this manual.
• The system configuration varies depending on the environment.
• A barcode reader and magnetic card reader can be connected to the Console.
• On a Console connected with the network via wireless LAN, do not read images directly from
the FCR image reader. Depending on the connection status of the network, images could be
lost. If you want to confirm an FCR image on a Console connected via wireless LAN, use the
study information sharing function or switch the network connection to wired LAN
connection before reading.
• In the patient environment, use a notebook type with a built-in battery with the power cable
disconnected (use the built-in battery).
• For the utility box of the DR exposure device that can send images via wireless connection,
contact FUJIFILM or a designated distributor.
“Patient Information
Input screen” “Patient Information Selection box”
“Exposure Menu
“Patient Information Input box” Selection screen”
2
“Patient Information “Exposure Menu Addition box”
Input box”
To modify the patient To add exposure menus, select this.
information, select this.
“Exposure Parameter
Selection box”
“Study screen”
“Waiting QA list”
Tool button
* T he menu that appears by pressing the tool button varies, depending on the setting at the time of
installation and the display screen.
Deletes one character to the left of the caret (“|”) for character input.
Space Bar Inserts a space.
/ Moves the caret (“|”) for character input to the left/right by one character.
Reserves a study. The reserved study is added to the “Waiting Study list”.
Display group list Exposure menu list registered to the display group Selected exposure menu list (displaying exposure or
(displaying exposure or study menus registered to study menus selected in the exposure menu list
the selected display group) registered to the display group)
Allows you to modify the information input on the “Patient Information Input screen”.
Cancels setup data on the “Patient Information Input screen” and “Exposure Menu Selection screen”,
and displays the “Patient Information Input screen”.
Reserves a study. The reserved study is added to the “Waiting Study list”.
Allows you to modify the information input on the “Patient Information Input screen”.
Performs auto-repeat exposure. Exposures are automatically repeated with the selected exposure menu.
Allows you to make an additional exposure with the selected exposure menu.
Treats the image captured with the selected exposure menu as a mis-exposure image and makes an
exposure again.
Deletes the selected exposure menu. Note that only the exposure menus that have not yet undergone
image reading can be deleted.
Selects the combination of the tube, technique and flat panel sensor to be used.
Confirms or changes exposure parameters for the exposure menu before executing exposure (image
reading). The “Exposure Parameter Selection box” is displayed.
Allows you to edit the image. The read image cab be magnified and the exposure menu can be changed.
The six buttons on the left of this button are shortcut buttons for QA functions.
The type and number of the buttons to be displayed vary depending on the settings made at the time of
installation and the settings made in the User Utility.
For the Console Advance Lite, the image editing function is optional.
/
exposure unit display field.
and
indicates that the Console is being connected to the DR exposure unit,
that the Console is not connected to the DR exposure unit.
2
Displays the status of the Console.
/ / indicates that the Console is operating normally, that a warning-level event is occurring, and
that an error-level event is occurring.
Displays the status of the connected device (DR exposure unit or FCR Image Reader). indicates
/ / that the unit is operating normally, that the Image Reader is being prepared or an error is occurring,
and that the unit is operating in emergency mode.
Displays the online status of the optional software, when the DICOM Modality Worklist Management
Software, DICOM Modality Performed Procedure Step Software, or FUJIFILM standard ordering
/
optional software is installed. indicates that software is online, and that the software is
offline.
Displays the output status.
/ / indicates that the Console is waiting for image output, that the Console is processing image
output, and that an output error is occurring.
NOTE
For the Console Advance Lite, the image editing function is optional.
QA function buttons
Displays the current image number and the number of images in the study. Selecting returns to the
previous image, and selecting proceeds to the next image.
TIP
The GA/GS values can be adjusted on the “QA Main screen”. For details, see “6.3 Changing GA/GS”
of “Console Advance Reference Guide”.
Each time this button is selected, the image is zoomed in with the center of the image display field
determined to be its center.
Each time this button is selected, the image is zoomed out with the center of the image display field
determined to be its center.
The image is displayed in the condition that one pixel of the original image equals one pixel on the
display.
The image is displayed in proper size for the image display field.
By selecting any position on the image and then moving the position from side to side and up and down,
the image can be moved freely.
/ Outputs the currently displayed image to the print device or delivers it to the storage device.
Outputs the files (PDI output) of the studies selected in the study list.
Displays the “Study List Settings dialog box”. Use this dialog box to rename the list, or configure the
information items to display.
Clears the search conditions entered in the information item entry fields.
Proceeds to the next processing stage for the study selected on the study list. The “Study screen” or “Image
Edit screen” appears, depending on the current status of the study.
Displays the order of the selected study as well as the total number of studies.
2
1
Turn on the exposure unit and the NOTE
Be sure to turn on the monitor first, and then turn on the
monitor connected to the Console. Console main unit. Otherwise, the touch panel may not
For startup procedures of the connected devices, respond to operations. It is recommended to always
see their operation manuals. keep the monitor turned on.
3
2
Turn on the Console main unit. Opening screen
3
Turn on the Image Reader. NOTE
Exposure in the emergency mode is possible until
Make sure that the display of the connected calibration of the exposure unit is completed. However,
device status is normal. calibration for acquiring an image properly is not
n For details, see “Chapter 7 Connected performed in the emergency mode. For this reason, the
Devices Status” in “Console Advance quality of the image exposed in this mode cannot be
Reference Guide”. guaranteed. Thoroughly check the condition of the
image when using it.
4
Input the patient information and TIP
The user logged in the system will be logged off
select . automatically unless any manipulation is performed
The “Patient Information Input screen” is within a certain period of time. To resume operation, log
displayed. in again in the “Login box”.
TIP
If the time displayed on the personal computer is earlier
than that of the last time when it was turned on, the
following message appears.
NOTE
Depending on the setting in the User Utility, the “Study
List screen” is displayed.
3
333333 Shutting Down the Console
Shut down the Console and turn off the personal computer. To temporarily stop operation
without turning off the power, log out the Console.
1
Patient Information Input screen
Select on the “Patient Input
(1) Select
Information screen” or “Study List
screen” (1) and then in
the menu (2).
The “Shutdown confirmation box” appears.
(2) Select
TIP
The Console can also be shut down by selecting
displayed in the “Login box”.
(3) Select
NOTE
The Console is not designed to operate continuously all
day long. Turn off the main unit at least once a day.
If the Console has been operating continuously for 24
hours, a message will be displayed recommending the
system to be restarted, so select [OK].
3
Do not turn off the Image Reader singly which is being
powered in conjunction with the Console.
NOTE
Depending on your system configuration, the Console
may take time to shut down since calibration is
performed.
TIP
To temporarily stop operation without turning off the
power, make sure to log out the Console.
To log out, select [Logout] in the menu of the
“Patient Information Input screen” and then [OK] in the
“Confirmation box” that appears.
1
Select one of the input fields such Patient Information Input screen
2
Input necessary information in the
3
Input all information in the same
manner.
(2) Enter
4
After inputting the patient
information, select (3). (3) Select
The “Exposure Menu Selection screen” appears.
TIP
For details of how to input patient information, see “2.1
Study Reception” of “Chapter 2 Study Reception” in
“Console Advance Reference Guide”.
TIP
Pressing the Tab key on the keyboard of the personal
computer after Step 2, the caret (“|”) for character input
moves to the next field.
TIP
If is selected instead of in Step 4, the study
will be reserved. The reserved study is added to the
“Waiting Study list”.
n For details, see “4.5 Using a Study List”.
Go to “4.2 Starting a Study”.
NOTE
If is selected, the input information will be deleted.
1
Input a patient ID on the “Patient Patient Information Input screen
(2) Select
2
Select (2).
If two or more items meet the condition, the
“Patient Information Selection box” appears.
If only 1 item meets the search condition, the
box does not appear and the information is
reflected on the “Patient Information Input
screen”.
3
Select the tab for the initial of the Example of display in “Patient Information Selection box”
(3) Select
desired patient name (3), select the
patient (4) and then (5).
The selected patient information is input on the
(4) Select
4
“Patient Information Input screen”.
Make sure that the displayed patient information
is correct.
(6) Select
TIP
If no search condition is entered, all registered items are
displayed.
TIP
Go to “4.2 Starting a Study”. If only 1 item meets the search condition, the information
is reflected on the “Patient Information Input screen”.
1
Select a display group(s) (1). Exposure Menu Selection screen
Display group list
Exposure menus registered in the selected
display group will be shown in the “Exposure
menu list registered to the display group”.
(1) Select
2
Select an exposure menu(s) (2).
The selected exposure menu(s) will be listed in
the “Selected exposure menu list” on the right
side of the screen.
(2) Select
If an exposure menu is selected two or more
4 times, the selected exposure menus are
displayed in the “Selected exposure menu list”
(3) Select
3
After selecting all necessary TIP
Selection of exposure (menu)s is necessary to make an
exposure menus, select (3). exposure by using a cassette or film. On the “Exposure
The “Study screen” appears. Menu Selection screen” or “Study screen”, add an
exposure menu(s) as necessary.
TIP
Two or more exposure menus that differ in anatomical
region, positioning, exposure method may be registered
for a display group.
TIP
If is selected in Step 3, information input on the
“Patient Information Input screen” and the “Exposure
Menu Selection screen” is canceled and the “Patient
Information Input screen” reappears.
TIP
If is selected in Step 3, the study will be reserved.
The reserved study is added to the “Waiting Study list”.
n For details, see “4.5 Using a Study List”.
1
With the exposure menu being Exposure Menu Selection screen
1
Select the exposure menu to be Exposure Menu Selection screen
2
Select a display group(s) and
exposure menu(s) anew (2 and 3).
The exposure menu(s) has been changed.
(3) Select
4
1
Select the exposure menu to be Exposure Menu Selection screen
2
Select (2).
The exposure menu has been deleted. (2) Select
TIP
To delete all exposure menus, select .
NOTE
For the Console Advance Lite, the function to connect the Console to a DR exposure unit is optional.
1
On the “Study screen”, select the Study screen
4
needed.
NOTE
Before making an exposure, make sure that
the selected exposure menu(s) has not yet
been used for an exposure. If an exposure
is made with an exposure menu already
used for an exposure (image reading)
selected, a system error will occur in the
Console.
2
Confirm that the exposure unit (3) Confirm
status icon is lit in green (3).
3
Make an X-ray exposure with the
DR exposure unit (4). (4) Make an
exposure.
The captured image is displayed on the “Study
screen ”.
(4) Make an
exposure.
NOTE
Be sure to perform calibration before starting an X-ray
exposure.
“Study screen”.
Make an X-ray exposure and check the image
for each selected exposure menu(s) by using this
procedure.
To display an image in a different exposure
menu, select the thumbnail of the desired
exposure menu at the right side of the “Selected
exposure menu list”.
When a thumbnail and then is selected, the
“Image Edit screen” is displayed. On the “Image
Edit screen”, the image editing (QA) by using
various utility functions can be performed.
n For details of image editing, see “4.4 Editing
an Image”.
NOTE
For the Console Advance Lite, the image editing
Go to “4.6 Completing a Study”. function is optional.
TIP
By using the User Utility, it is possible to set the
processing (automatic study completion/action after
study completion) to the study for which image reading
4
has been completed.
For details, see “A.4 Property Setting” of “Appendix A
User Utility Operations” in “Console Advance Reference
Guide”.
When the suspension processing can be applied to the
study for which image reading is completed, it will remain
in the “Waiting Study”. So that users can re-display it on
the “Study screen” and continue operations to complete
exposures.
1
On the “Study screen”, select the Study screen
4 (2) Select
2
Make an exposure.
3
Read the IP No. of the exposed (3) Scan the barcode
cassette using the Barcode Reader
(3).
TIP
When a user repeats the selection of exposure menus
and barcode reading above mentioned, multiple IPs can
be registered at once. Therefore, if studies are
suspended after the IP registration, the image reading
for multiple studies can be performed at once.
TIP
If the Barcode Reader fails to read the IP No., you can
select and then manually enter it via the keyboard.
Select at the lower left of the exposure menu list. The
IP number input box will be displayed.
NOTE
This operation is not necessary when the FCR PRIMA is
connected to the Console.
4
4
Make certain that the IP No. shown Study screen
NOTE
If you change the technique for the exposure menu by
which an image has not yet been read on the exposure
unit after registering the IP, the IP number registration is
cancelled and the warning message below appears on
the Console.
NOTE
This operation is not necessary when the FCR PRIMA is
connected to the Console.
NOTE
The same IP cannot be registered continuously to
prevent the mis-registration of IPs. If the IP just
registered needs to be registered again to the next
exposure menu, delete the exposure menu just
registered, or register a different IP once and re-register
the desired exposure menu by overwriting it. (The same
IP can be registered continuously according to the
setting performed at installation. If necessary, contact
our official dealer.)
4 TIP
The image reading is a background operation. Thus,
when it takes a long time to complete image
reading because of continuous multiple-IP insertion,
users can go to next study operation before the
completion of image reading. In this case, select
, and perform next study operations. The study whose
image reading is to be performed is stacked in the
“Waiting Study”, and mark will be displayed on the
list when one or more images are read for it.
TIP
By using the User Utility, it is possible to set the
processing (automatic study completion/action after
study completion) to the study for which image reading
has been completed.
For details, see “A.4 Property Setting” of “Appendix A
User Utility Operations” in “Console Advance Reference
Guide”.
When the suspension processing can be applied to the
study for which image reading is completed, it will
remain in the “Waiting Study”. So that users can
re-display it on the “Study screen” and continue
operations to complete exposures.
1
On the “Study screen”, select the Study screen
NOTE
Before making an exposure, make sure that
the selected exposure menu(s) has not yet (2) Select
been used for an exposure. If an exposure
is made with an exposure menu already
used for an exposure (image reading)
selected, a system error will occur in the
Console.
2
Confirm that the exposure unit (3) Confirm
status icon is lit in green (3).
3
Make an X-ray exposure with the 4
built-in FCR equipment (4). (4) Make an
exposure.
The captured image is displayed on the “Study
screen”.
(4) Make an
exposure.
“Study screen”.
Make an X-ray exposure and check the image
for each selected exposure menu(s) by using this
procedure.
To display an image in a different exposure
menu, select the thumbnail of the desired
exposure menu at the right side of the “Selected
exposure menu list”.
When a thumbnail and then is selected, the
“Image Edit screen” is displayed. On the “Image
Edit screen”, the image editing (QA) by using
various utility functions can be performed.
n For details of image editing, see “4.4 Editing
an Image”.
NOTE
For the Console Advance Lite, the image editing
Go to “4.6 Completing a Study”. function is optional.
TIP
NOTE
For the Console Advance Lite, the image editing function and the image magnification function are optional.
1
On the “Study screen”, select the Study screen
then (2).
The “Image Edit screen” is displayed.
(2) Select
4
TIP
The buttons at the left of the are shortcuts to image
editing operations. For example, the image can be
magnified by selecting .
2
Edit the image. Image Edit screen
(4) Select
3
When the image editing is finished, TIP
The buttons (Use Utility functions) at the bottom of the
select or (to end QA screen enable operations such as image magnification
function) (4). and output.
The edited image is saved and the display
returns to the “Study screen”.
Waiting QA list Lists up studies for which exposures have been performed but
image editing (QA) has not yet.
If a study in the “Waiting QA list” is not selected within
the period specified in the User Utility, QA of the study is
determined automatically.
Finish QA list Lists up studies for which both exposures and image editing (QA)
have been performed.
4 All list Lists up all studies stored in the hard disk of the Console main
unit.
NOTE
The study lists above are set by default.
1
Select on the “Patient Patient Information Input screen
NOTE
Depending on the setting in the User Utility, the “Study
List screen” is displayed when the Console starts up.
2
Check the displayed study Waiting Study list
1
After checking the image, select Study screen
(2) If a communication error occurs between the Console and the connected
exposure unit
The error message box “MD11001” is displayed not only when the Console starts up but also when a
communication error occurs.
When the problem is not solved within a short time after the message box is displayed, perform the following
procedure.
1. Select [OK] on the message box.
2. Check if the equipment connected with the Console is turned on.
If any equipment is turned off, turn it on and wait for a while.
3. If the problem is not solved, restart the Console.
When the Console is restarted and the same error message box is displayed, contact our official dealer.
Similarly, if an error level and error ID such as shown below are displayed in the error message box, contact
our official dealer.
NOTE
If the screen freezes and a hangup occurs, remove the keyboard and mouse and reconnect
them. If this operation does not solve the problem, restart the Console.
NOTE
• Make sure to perform the shutdown operation following the above procedures in the case of
a hangup of the Console.
If the personal computer is turned off without performing the shutdown operation, an error
may occur on the computer.
• Note that forcible shutdown processing of the equipment is an emergency action. Do not
use this action under normal situations.
When restarting the Console, follow the procedure for the system startup.
If the precautions are not followed, inconsistencies may arise in the setup data used for each exposure,
possibly causing the data to be lost or to fall outside of the guaranteed range.
Precautions regarding the line connection to the Dose Area Product Measuring System
• When the is displayed on the Console monitor, select the and check to see if any
error message regarding the dose area product measuring system or its connection status 5
appears or not. If an error message appears, check the connection between the Console and the
dose area product measuring system. If the connection is fine but the error message remains,
contact our authorized distributor.
• If a problem with the line condition occurs at the start of a study, the following error message
box will appear.
If you see this message, select . If the error message box remains even after selecting
several times, contact our authorized distributor.
If you select , exposure will be started without the receipt of X-ray exposure parameters.
Precautions
• After performing one exposure, it is important that you follow the procedure to perform a single
IP registration. When you have performed the IP registration, the X-ray exposure parameters are
received and the parameters are reset. For this reason, when you do multiple IP registrations
after one batch of multiple exposures, the actual setup data for the batch exposures are counted
as a single set of X-ray exposure parameters when the first IP registration is performed.
• If a problem occurs in the line condition during step 4, the following error message box will
5 appear.
Select . If this error message box appears, the X-ray exposure parameters cannot be
received.
NOTE
• If you use the X-ray Control Unit Online Software in a hardware configuration for receiving
X-ray exposure parameters (actual setup data), make sure the dose area product measuring
system is turned on before you start up the Console.
If the dose area product measuring system is not turned on, the Console will not be able to
receive any X-ray exposure parameters.
• The unit may be different between exposure results on the display unit of an area dosimeter
and those the Console has received.
Check the unit on both to make sure that exposure results are the same.
■ Desktop type
PC Power Supply Conditions
(HP Compaq 6200 Pro SF) Input voltage : 90V to 264V
Input current : 4.0A / 2.0A
Frequency : 47 to 63 Hz
Environmental Conditions
(1) Operating
Temperature : 10°C to 35°C
Humidity : 10%RH to 90%RH (No dew condensation)
(2) Not operating
Temperature : -30°C to 60°C
Humidity : 10%RH to 90%RH (No dew condensation)
Spec
Processor : Intel(R) Core(TM) i3-2120/3.3GHz, 3M
Chipset : Intel(R) Q65 Express Chipset
Memory : 4GB (2GBx2) DDR3 SDRAM
System Board Connectors : PCI Slots x1, PCIe x16x1 Slot, PCIe x2
Operating System : Windows 7(R) Professional SP1 (32 bit)
Video Controller : Integrated Intel
External Ports : USB 2.0 x10
Network Adapter : I ntel(R) 82579LM Gigabit1 Ethernet LAN
10/100/1000
HDD : 250GB SATA 7200 RPM HDD
Optical Drive : DVD Super Multi Drive
Keyboard USB keyboard
Mouse USB mouse
■ Monitor
17” (1280 x 1024) Electrical
Color LCD monitor Power supply : 35W or less, 100 to 120 V / 200 to 240 V ±10%
A (FlexScan L560T-C) Frequency : 50/60Hz
Environmental Conditions
(1) Operating
Temperature : 0°C to 35°C
Humidity : 30%RH to 80%RH (No dew condensation)
(2) Not operating
Temperature : -20°C to 60°C
Humidity : 30%RH to 80%RH (No dew condensation)
21.3” (1600 x 1200) Electrical
Color LCD monitor Power supply : 105W or less, 100 to 120 V / 200 to 240 V ±10%
(RadiForce RX240) Frequency : 50/60Hz
Environmental Conditions
(1) Operating
Temperature : 0°C to 35°C
Humidity : 20%RH to 80%RH (No dew condensation)
(2) Not operating
Temperature : -20°C to 60°C
Humidity : 10%RH to 90%RH (No dew condensation)
Environmental Conditions
(1) Operating
Temperature : 0°C to 35°C
Humidity : 20%RH to 80%RH (No dew condensation)
(2) Not operating
Temperature : -20°C to 60°C
Humidity : 10%RH to 90%RH (No dew condensation)
■ Mobile type
Mobile PC Power Supply Conditions AC Adapter
TOUGHBOOK CF-19RW1ADS Input voltage : AC 100V to 240V
Frequency : 50Hz to 60Hz
Output voltage : 16.0V DC
Output current : 3.75A
Environmental Conditions
(1) Operating A
Temperature : 5 °C to 35 °C
Humidity : 30% RH to 80% RH (No dew condensation)
(2) Not operating
Temperature : -20 °C to 60 °C
Humidity : 30% RH to 90% RH (No dew condensation)
Complied standards
IEC 60950-1
■ Wireless Specifications
The specifications in the table below are used in wireless communication.
Between Console Advance and Between Console Advance and
Utility Box Hospital Network
Technical Specification 11n 11n/g
Transmission frequency 5.2GHz 2.4GHz
Modulation OFDM OFDM
Frequency Tolerance ±20pps ±20pps
Data transfer rate 35Mbps(max) 32.2Mbps(ave)
Transfer Power 37bBm(max) 26bBm(max)
■ Desktop type
Width (mm (in.)) Depth (mm (in.)) Height (mm (in.)) Weight (kg (lb))
■ Mobile type
Width (mm (in.)) Depth (mm (in.)) Height (mm (in.)) Weight (kg (lb))
Mobile PC TOUGHBOOK 49 (1.9)
A CF-19RW1ADS (NOTE) 271 (10.7) 216 (8.5) (excludes
protrusions)
2.3 (5.1)
(excludes stopper)
NOTE
• On a Console connected with the network via wireless LAN, do not read images directly from
the FCR image reader. Depending on the connection status of the network, images could be
lost. If you want to confirm an FCR image on a Console connected via wireless LAN, use the
study information sharing function or switch the network connection to wired LAN connection
before reading.
• When carrying the mobile PC outside, take care not to drop it or subject it to shocks.
• When using the mobile PC, take sufficient care such as applying a password lock and other
security measures to prevent information leakage.
• When using the mobile PC, set the security of the wireless LAN in accordance to hospital
security policies.
• If you are leaving your notebook computer, always log out so that a username and
password is required when you return. This prevents malicious third parties from using
your notebook computer without permission or acquiring personal information (leakage
of information).
• The monitor brightness of the mobile PC is set as follows by default.
If the default setting is changed by mistake, it is recommended to restore the setting.
(To adjust the monitor brightness, press the [Fn] and [F2] keys on the keyboard
simultaneously.)
When the power cable is connected: 100%
When the built-in battery is used: 100%
DICOM Modality Worklist Management Software (Specifications for the Network WL)
The DICOM Modality Worklist Management Software permits query/retrieve of the study information with the Console
that is connected online (DICOM specification interface) to the host units (DICOM server, RIS terminal unit, and others).
NOTE
Study information that does not comply with the specification of the Console cannot be retrieved.
X-ray Control Unit Online Software (for the Console Advance Lite)
B The X-ray Control Unit Online Software is designed to set the X-ray control parameters in the User Utility.
NOTE
Prior to performing exposure, be sure to check exposure conditions on the X-ray control unit
panel.
Periodical Maintenance
Make sure that the periodical maintenance and inspection assigned to our official dealer are performed as
specified.
Checking of the operation record by referring to the error log Every year
The cycles of periodical maintenance and inspection differ depending on the usage and the daily operation
time.
For details, contact us directly or our official dealer.