FujiFilm DryPix 7000 User manual

897N0324G (006-235-100)
This Operation Manual describes details on how to operate the
DRYPIX 7000 and cautions to be observed when operating it. Please
read the Operation Manual thoroughly before actually operating the
DRYPIX 7000 system. After reading this manual, store it nearby the
DRYPIX 7000 so that you can see it whenever necessary.
DRYPIX 7000
Operation Manual
11th Edition: July 2008

Introduction
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Thank you for purchasing the Fuji Medical Dry Laser Imager DRYPIX 7000.
This operation manual for the DRYPIX 7000 provides detailed explanations of operation
methods and cautions to promote proper understanding of functions and more effective usage.
We ask that first-time users read this manual thoroughly before actually using the DRYPIX 7000.
After reading this manual, please store it nearby the DRYPIX 7000 so that it may be used to
ensure that the machine is used under the best conditions.
Installation may only be conducted by authorized service personnel.
This Operation Manual is applicable to software versions V13.0/V7.0.
(V13.0 is for Windows XP and V7.0 is for Windows NT.)
1No part or all of this manual may be reproduced in any form without prior permission.
2The information contained in this manual may be subject to change without prior notice.
3FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from installation,
relocation, remodeling, maintenance, and repair performed by other than dealers specified by
FUJIFILM Corporation.
4FUJIFILM Corporation shall not be liable for malfunctions and damage of FUJIFILM Corporation
products due to products of other manufacturers not supplied by FUJIFILM Corporation.
5FUJIFILM Corporation shall not be liable for malfunctions and damage resulting from remodeling,
maintenance, and repair using repair parts other than those specified by FUJIFILM Corporation.
6FUJIFILM Corporation shall not be liable for malfunctions and damage resulting from negligence of
precautions and operating methods contained in this manual.
7FUJIFILM Corporation shall not be liable for malfunctions and damage resulting from use under
environment conditions outside the range for this product, such as power supply, installation
environment, etc., contained in this manual.
8FUJIFILM Corporation shall not be liable for malfunctions and damage resulting from natural
disasters such as fires, earthquakes, floods, lightning, etc.
Process waste correctly, as stipulated by local law or any regulations that apply.
When discarding the DRYPIX 7000 that incorporates the lithium battery, be sure to
contact service engineer because it cannot be disposed of as a general waste.
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.
The LCD display lamps in this product contain mercury, which must be recycled or
disposed of in accordance with local, state, or federal laws.
Caution: Rx Only in the United States (Federal law restricts this device to sale by or on the order of a
physician.)
The DRYPIX 7000 uses Vx Works.
Copyright of Vx Works belongs to Wind River Systems,Inc.
Trademark
FCR is a trademark or a registered trademark of FUJIFILM Corporation.
Copyright Reserved
Windows®NT is the registered trademark of US Microsoft Corporation in the U. S. A. and other countries.
Windows® XP is the registered trademark of US Microsoft Corporation in the U. S. A. and other countries.
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 © 2002-2008 FUJIFILM Corporation. All rights reserved.
CAUTIONS

Contents at a Glance
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Chapter 1 Introduction
1
Chapter 2 System Overview
2
Chapter 3 Basic Operation
3
Chapter 4 Utility Operation
4
Chapter 5 Troubleshooting
5
Chapter 6 Regular Care and Maintenance
6
Chapter 7 Specifications
7

Contents
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Contents
Chapter 1 Introduction
1.1 What is the DRYPIX 7000? .................................................................................. 1-2
1.2 System Features .................................................................................................. 1-2
1.3 Safety ................................................................................................................... 1-3
1.4 Operational Precautions ....................................................................................... 1-4
1.4.1 Laser Handling Precautions ..................................................................... 1-4
1.4.2 Preventing Electric Shock ........................................................................ 1-4
1.4.3 Ventilation Precautions ............................................................................. 1-4
1.4.4 Handling Precautions ............................................................................... 1-4
1.4.5 Software Precautions ............................................................................... 1-4
1.5 Electromagnetic Compatibility (EMC) .................................................................. 1-5
1.5.1 Further information for IEC60601-1-2:2001 ............................................. 1-5
1.5.2 Classification ............................................................................................. 1-8
1.6 Precautions for Storing or Handling the DI-HL, DI-HLc, and DI-ML Films for
the Fuji Medical Dry Laser Imager ....................................................................... 1-9
1.6.1 Precautions for Storing or Handling Unused Films .................................. 1-9
1.6.2 Precautions for Storing or Handling Recorded Films ............................... 1-9
1.6.3 Other ......................................................................................................... 1-9
1.7 Other Precautions for Using the Equipment ......................................................... 1-10
1.7.1 Precautions for Inserting the Shutter......................................................... 1-10
1.8 Location of Each Label.......................................................................................... 1-11
Chapter 2 System Overview
2.1 System Configuration ........................................................................................... 2-2
2.2 Hardware Configuration ....................................................................................... 2-3
[1] DRYPIX 7000 Main Unit .................................................................................. 2-3
[2] Operation Panel .............................................................................................. 2-4
Chapter 3 Basic Operation
3.1 Routine Operations .............................................................................................. 3-2
Starting Up the System ......................................................................... 3-3
Reading (Storing) Images ..................................................................... 3-5
Printing Images (film output) ................................................................. 3-5
Shutting Down the System ................................................................... 3-6
3.2 Supplying Film (Replacing the Film Pack) ........................................................... 3-7
3.3 Urgent Print .......................................................................................................... 3-13
3.4 Deleting a Print Job .............................................................................................. 3-14
3.5 Print Job Details ................................................................................................... 3-16

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Chapter 4 Utility Operation
4.1 What is Utility? ..................................................................................................... 4-2
4.2 Starting Up and Quitting the Utility ....................................................................... 4-3
4.2.1 Starting Up the Utility ............................................................................... 4-3
4.2.2 Quitting the Utility ..................................................................................... 4-3
4.3 Auto F.D.C. .......................................................................................................... 4-4
4.4 Test Pattern ......................................................................................................... 4-8
4.5 Unlock Tray .......................................................................................................... 4-12
4.6 Print Queue .......................................................................................................... 4-15
4.7 Set Counters ........................................................................................................ 4-17
4.8 Economy Mode .................................................................................................... 4-20
4.8.1 Transition Time ........................................................................................ 4-21
4.8.2 Scheduler ................................................................................................. 4-24
4.8.3 Calendar ................................................................................................... 4-27
4.8.4 Save Power .............................................................................................. 4-33
4.9 Set Alarm ............................................................................................................. 4-35
4.10 Automated F.D.C. ................................................................................................ 4-37
4.11 Set Date/Time ...................................................................................................... 4-38
4.12 Software Version .................................................................................................. 4-40
4.13 Reprint ................................................................................................................. 4-41
4.14 Time Interval Determined for Animation Display ................................................. 4-45
Chapter 5 Troubleshooting
5.1 Items to be Confirmed First ................................................................................. 5-2
5.2 Error Window ....................................................................................................... 5-4
5.3 When the Film Jams ............................................................................................ 5-5
5.4 Failing in Reading a Barcode ............................................................................... 5-27
5.5 Failing in Loading Films ....................................................................................... 5-30
5.6 Failing in Auto F.D.C. (Automatic Density Calibration) ........................................ 5-34
5.7 Failing in Placing a Cleaning Roller ..................................................................... 5-35
5.8 Storing the Equipment Operation History ............................................................ 5-37
5.9
Failing in Turning the Power Switch OFF After Pressing the SHUTDOWN Button ... 5-38

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Chapter 6 Regular Care and Maintenance
6.1 Cleaning the Cleaning Roller with Water ............................................................. 6-2
6.2 Cleaning the Suction Filter ................................................................................... 6-5
Chapter 7 Specifications
1 System Components ............................................................................................... 7-2
1.1 Standard Components .................................................................................... 7-2
1.2 Options ........................................................................................................... 7-2
1.3 Supplies .......................................................................................................... 7-2
2 Processing Capacity ................................................................................................ 7-2
3 Applicable Film ......................................................................................................... 7-2
4 Recording Pixel Size ................................................................................................ 7-2
5 CR Image Size Reduction ....................................................................................... 7-2
6 Gray Scale ............................................................................................................... 7-2
7 Maximum Density .................................................................................................... 7-3
8 Power Supply Conditions ......................................................................................... 7-3
9 Environmental Conditions ........................................................................................ 7-3
10 External View and Weight ........................................................................................ 7-4
10.1 External Dimensions and Weight ................................................................... 7-4
10.2 Internal Construction ...................................................................................... 7-5
Maintenance and Inspection
1 User’s Maintenance and Inspection Items
1.1 Daily Inspection
1.2 Periodical Inspection
2 Maintenance and Inspection Items Assigned to Specified Dealer

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Chapter 1
Introduction

Introduction
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1.1 What is the DRYPIX 7000?
The Fuji Medical Dry Laser Imager DRYPIX 7000 is a device that prints digital image data
transferred via the DICOM network from the FCR Image Reader or CT, MRI and other
imaging modalities onto dedicated film in the selected format.
1.2 System Features
The main features of the Fuji Medical Dry Laser Imager DRYPIX 7000 are as follows.
1Water, developer, fixer and other chemicals are completely unnecessary, doing away
with the need for drainage and exhaust facilities and related construction. There is also
no need for space to store chemicals.
2Chemical handling, replenishment, disposal processing and the related time and effort
are not necessary. Moreover, environmental pollution is prevented.
3Film can be handled under daylight room conditions, doing away with the need for
darkrooms.
4You can select blue-base film (DI-HL), clear-base film (DI-HLc), or blue-base film for
mammography use (DI-ML) depending on the intended use. It is possible to determine
type of film that is to be used for each tray.
5Compact size does not limit installation site selection.
Fuji Medical Dry Laser Imager, model DRYPIX 7000 is indicated for use in providing
diagnostic quality medical images on film for aid in physician diagnosis, including the printing
of images and associated identification information from various digital imaging source
modalities, including but not limited to, Computed Tomography (CT), Magnetic Resonance
Imaging (MRI), Ultrasound, Computed Radiography, Digital Radiography, Digital
Mammography and Nuclear Medicine.
Note: For digital Mammography images, the high resolution mode (50 micron recording pixel
size) is used.

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1.3 Safety
This section contains safety precautions required for the safe operation of this equipment.
Carefully read and follow these precautions before using the equipment.
If these precautions are not followed, injuries or damage to the equipment may occur.
The safety precautions are marked as WARNING or CAUTION, and additional information
“ ”. The meanings of these precautions are as follows:
Indicates hazardous situations that may lead to serious injury or even death if
the
p
recaution is not or could not be followed.
Indicates hazardous situations that may lead to mild or moderate injury if the
precaution is not or cannot be followed. Precautions against accidents
causing only physical damage.
Indicates procedures requiring special attention, instructions that must be
followed, supplementary explanations, etc.

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1.4 Operational Precautions
1.4.1 Laser Handling Precautions
DRYPIX 7000 Laser Unit Specifications
Class 3B
Medium Semiconductor laser
Wavelength 660 nm
Maximum Output 50 mW (CW)
The DRYPIX 7000 incorporates a Class 3B laser with a maximum output of 50mW.
To prevent exposure to its laser beams, observe the following precautions.
yNever remove the protective covers.
yWhen opening the outer covers for coping with film jams, be sure to observe procedures
set forth in the Operation Manual.
yAlways contact a qualified service engineer immediately if you suspect there is a
malfunction.
Use of controls or adjustments or performance of procedures other than those
specified herein may result in hazardous radiation exposure.
1.4.2 Preventing Electric Shock
The power supply to the DRYPIX 7000 is AC200-240V.
To avoid possible electrical shock, users should observe the following
precautions.
yAvoid installation sites where water may splash on the equipment.
yMake sure that the equipment is properly grounded to a protective earth lead
for indoor wiring.
yMake sure that all cable connections have been properly connected.
Inside the DRYPIX 7000 are parts through which a high voltage is conducted,
putting the user at risk for electric shock. Never remove any covers other than
the eject and front covers.
1.4.3 Ventilation Precautions
Be sure to install this equipment in a well-ventilated environment.
Good ventilation must attend its use (at least 54m3/hour for one unit).
1.4.4 Handling Precautions
If the room temperature increases abruptly when the equipment is cold, dew
condensation may occur. Exercise care so that dew condensation does not
occur because it may cause the equipment to be damaged.

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1.5 Electromagnetic Compatibility (EMC)
This equipment has been tested and found to comply with the limits for medical devices to
the IEC60601-1-2:2001, Medical Device Directive 93/42/EEC.
These limits are designed to provide reasonable protection against harmful interference in a
typical medical installation.
This equipment generates, uses and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to other
devices in the vicinity.
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to other devices, which can be determined
by tuning the equipment off and on, the user is encouraged to try to correct the interference
by one or more of the following measures:
yReorient or relocate the receiving device.
yIncrease the separation between the equipment.
yConnect the equipment into an outlet on a circuit different from that to which the other
device(s) are connected.
Consult the manufacturer or field service technician for help.
1.5.1 Further information for IEC60601-1-2:2001
•Medical electrical equipment needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided in the
accompanying documents.
•Portable and mobile RF communications equipment can affect medical electrical
equipment.
•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
DRYPIX 7000.
List of Cables
Name FUJIFILM Parts code
General Specification
I/F Cable
−TIA/EI
A
-568 Cat5 or more.
Straight cable of UTP type.
•The DRYPIX 7000 should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the DRYPIX 7000 should be observed to verify
normal operation in the configuration in which it will be used.

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Guidance and manufacturer’sdeclaration -
electroma
g
netic emissions
The DRYPIX 7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DRYPIX
7000 should assure that it is used in such an environment.
Emissions test Compliance
Electromagnetic environment -
guidance
RF emissions
CISPR 11 Group 1 The DRYPIX 7000
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
The DRYPIX 7000 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.
Harmonic emissions
IEC61000-3-2 Class A
Voltage fluctuations/
flicker emissions
IEC61000-3-3 Complies
Guidance and manufacturer’sdeclaration -
electroma
g
netic immunit
y
The DRYPIX 7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DRYPIX 7000 should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment
–
guidance
Electrostatic discharge
(ESD)
IEC61000-4-2
±6kV contact
±8kV air
±2kV contact
±4kV contact
±6kV contact
±2kV air
±4kV air
±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
IEC61000-4-4
±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
IEC61000-4-5 ±1kV differential mode ±2kV common mode ±1kV differential mode
±2kV common mode Mains power quality should be that of a
typical commercial or hospital
environment.
Voltage dips, short
interruptions and voltage
variations of power supply
input lines
IEC61000-4-11
<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 DRYPIX
7000 requires continued operation
during power mains interruptions, it is
recommended that the DRYPIX 7000
be powered from an uninterruptible
power supply or a battery.
Power frequency
(50/60Hz) magnetic field
IEC61000-4-8
3 A/m 3 A/m
Power frequency magnetic fields
should be at levels characteristic of a
typical locationin a typical commercial
or hospital environment.
NOTE: UTis the a.c. mains voltage prior to application of the test level.

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Guidance and manufacturer’sdeclaration -
electroma
g
netic immunit
y
The DRYPIX 7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DRYPIX 7000 should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level
Electromagnetic environment
–
guidance
Conducted RF
IEC61000-4-6
Radiated RF
IEC61000-4-3
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 DRYPIX
7000, including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance
d= 1.2
d= 1.2 80 MHz to 800 MHz
d= 2.3 800 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 metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,ashould
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 :
A
t 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 DRYPIX 7000 is used exceeds the applicable RF compliance, the
DRYPIX 7000 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the DRYPIX 7000.
b Over the frequency range 150 kHz to 80 MHz, field strength should be less than 3 V/m.

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Recommended separation distances between
Portable and mobile RF communications equipment and the DRYPIX 7000
The DRYPIX 7000 is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the DRYPIX 7000 can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the DRYPIX 7000 as recommended below,
according to the maximum output power of the communications equipment.
Rated maximum output
power of transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d=1.2 80 MHz to 800 MHz
d=1.2 800 MHz to 2.5 GHz d=2.3
0.01 0.12 0.12
0.23
0.1 0.38 0.38
0.73
1 1.2 1.2
2.3
10 3.8 3.8
7.3
100 12 12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d
in metres (m) can be
estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 : At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 : These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
1.5.2 Classification
1) According to the type of protection against electrical shock
CLASS 1 EQUIPMENT
2) According to the degree of protection against electric shock
NO APPLIED PART
3) Protection against harmful ingress of water
IPXO
4) According to the degree of safety of application in the presence of a flammable anesthetics
mixture with air or with oxygen or nitrous oxide.
Equipment not suitable for use in the presence of a flammable anesthetics mixture with air or
with oxygen or nitrous oxide.
5) According to the mode of operation
CONTINUOUS OPERATION

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1.6 Precautions for Storing or Handling the DI-HL, DI-HLc, and
DI-ML Films for the Fuji Medical Dry Laser Imager
1.6.1 Precautions for Storing or Handling Unused Films
1Use only the “Fuji Medical Dry Laser Imager Film DI-HL, DI-HLc, or DI-ML” that is
compatible with this equipment. If a film other than DI-HL, DI-HLc, or DI-ML is used, a
malfunction may be caused to the equipment.
2Be sure to store unused films contained in the film pack in a cool, dry and dark place of
low temperature and low humidity (temperature: 10 to 23°C, relative humidity:
45±15%), avoiding radioactivity and reactive gases, same as for the conventional wet-
type film.
3The DI-HL, DI-HLc, or DI-ML films are light-sensitive. Do not open a film pack before it is
loaded properly in the equipment.
4Do not touch unused films with bare hands, otherwise adverse effects can appear on
recorded images.
5 Do not take unused films out of the film pack that has once been loaded into the
equipment and opened or add films to the film pack loaded, which will result in
misoperation or failure of the equipment.
6The film pack contains a protective sheet that is a film, in addition to specified number of
recording films. This protective sheet will remain in the film pack even after those
recording films have been printed and it cannot be used for image recording. Discard it
together with unused films.
7Because this system allows film loading in illuminated room, the film pack can be loaded
under the illuminated environment. For how to load the film pack in the machine, see
page 3-7 in this manual, or refer to the operation panel display.
1.6.2 Precautions for Storing or Handling Recorded Films
1Store recorded films in a cool, dry and dark place of low temperature and low humidity.
The higher the temperature and humidity, the more the density of recorded images will
increase. Long-term storage at high temperature, high humidity and/or daylight
conditions, such as in car or in room during summer, may cause discoloration. Using
films in the slide projector or in the overhead projector will also cause discoloration.
2For the long-term storage performance of recorded films, we assume based on the result
of the acceleration test that it will be over 30 years at the storage temperature of 25°C
and over 25 years at 30°C, until the portion on an image of density (D) = 1.2 at time of
output to change 10% (∆D=0.12).
1.6.3 Other
1After an image has been recorded, the film immediately after it was ejected from the
machine is still in the process of image development and the room illumination or light
emanating from the viewing box will cause slight changes in the optical density. Due to
such optical effect, traces of overlapped films or transferred images can be visually
recognized temporarily, which will disappear when those films are left under the normal
light condition.
2Note that lucid surfaces of recorded films can be lost or traces of contact with any
chemicals that contain water, alcohol, developer, etc., and with other objects that contain
a large amount of salt may appear on images, if they are handled under high-humidity
environment or due to such undesirable contacts.
3Do not store films with its image recording faces attached with each other.

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1.7 Other Precautions for Using the Equipment
1.7.1 Precautions for Inserting the Shutter
Be sure to turn the power OFF first and then insert the shutter, because a system error may
result.
Note, however, that you do not have to turn the power OFF if an instruction is indicated on
the operation panel to insert the shutter.

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1.8 Location of Each Label

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JAM Handling Label 1
JAM Handling Label 2 Caution Label

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