fujifilm DRYPIX 6000 User Manual

Fuji Medical Dry Laser Imager

For Safe Operation

(DRYPIX 6000)

Reference Guide

8th Edition : February 2017

Product Overview

Basic Operation

Utility

Troubleshooting

Care and Maintenance

Appendix

897N102437G

Maintenance and Inspection

This Manual describes details on how to operate the DRYPIX Smart and cautions to be observed when operating it. Please read this manual thoroughly before actually operating the DRYPIX Smart After reading this manual, store it nearby the DRYPIX Smart so that you can see it whenever necessary.

DRYPIX Smart Reference Guide 897N102437G

Introduction

CAUTIONS

This manual provides detailed explanations of operation methods and cautions to promote proper understanding of functions and more effective usage.

Accompanying documents were originally drafted in the English language.

Installation may only be conducted by authorized service personal.

This manual is applicable to the following software.

• DRYPIX Smart Main Software V. 1.0 or later

Indications for use (for U.S.)

Fuji Medical Dry Laser Imager, model DRYPIX Smart (DRYPIX 6000) is indicated for use in

providing diagnostic quality medical images on lm for aid in physician diagnosis, including the printing of images and associated identication 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.

Intended use (for European Union and other countries.)

Fuji Medical Dry Laser Imager DRYPIX Smart (DRYPIX 6000) is a device that prints digital image data transferred via the DICOM network from the FCR/FDR Image Reader or DR, CT, MRI and other imaging modalities onto the Fuji Medical Dry Laser Image Film.

Note : The above statements were determined by applicable medical device regulations which vary

throughout the world. These statements are subject to revision when additional clearance or approval is obtained.

1. No part or all of this manual may be reproduced in any form without prior permission.

2. The information contained in this manual may be subject to change without prior notice.

3. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from installation, relocation, remodeling, maintenance, and repair performed by other than

dealers specied by FUJIFILM Corporation.

4. FUJIFILM Corporation shall not be liable for malfunctions and damages of FUJIFILM Corporation products due to products of other manufacturers not supplied by FUJIFILM Corporation.

5. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from

remodeling, maintenance, and repair using repair parts other than those specied by

FUJIFILM Corporation.

6. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from negligence of precautions and operating methods contained in this manual.

7. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from use under environment conditions outside the range of using conditions for this product such as power supply, installation environment, etc. contained in this manual.

8. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from

natural disasters such as res, earthquakes, oods, lightning, etc.

Caution : Rx Only in the United States (Federal law restricts this device to sale by or on the

order of a physician.)

Open-Source Software Used in This Product

This product uses third party’s software that is made available as open source software or free software. SUCH SOFTWARE IS PROVIDED “AS IS” WITH NO WARRANTY OF ANY KIND AS TO ITS MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR PURPOSE. For information on open source software used in this product, please see the attached CD. Source codes for certain type of open source software used in this product are available at delivery cost. If you would like to receive such source codes, please contact FUJIFILM dealer or the service representatives at the agency from which you purchased this product. (Please be noted that any inquiries concerning the contents of source codes should be directed to original licensers of open source software.)

Trademark

FCR is a trademark or a registered trademark of FUJIFILM Corporation.

Other holder’s trademarks

All other company names and product names described in this manual are the trademarks or registered trademarks of their respective holders.

DRYPIX Smart Reference Guide 897N102437G

iii

DRYPIX Smart Manuals

DRYPIX Smart Reference Guide

DRYPIX Smart Quality Control Function Reference Guide

DRYPIX Smart Quality Control for Mammography Reference Guide

DRYPIX Smart Reference Guide 897N102437G

Contents at a Glance

For Safe Operation

Chapter

This chapter presents Warnings and Cautions we wish you to observe for the safe operation of this equipment.

Product Overview

This chapter presents overview and major features of this equipment.

Basic Operation

This chapter describes routine operation procedures, including how to start up/

shut down this equipment and also how to replace a lm pack.

Utility

This chapter describes the lm density calibration, date and time setting as well

as other functions.

Chapter

Appendix

Troubleshooting

This chapter explains how to troubleshoot an error.

Care and Maintenance

This chapter describes daily care and maintenance we wish you to perform so that you can use the equipment optimally.

Appendix A Specications

This chapter presents major specications of this equipment.

Maintenance and Inspection

DRYPIX Smart Reference Guide 897N102437G

How to Read This Manual

CAUTIONS

Basic page conguration

Please have a good grasp of the basic page conguration of this Manual, as illustrated below, for you to use it more efciently.

Operation procedure

Describes an operation procedure according to sequential numbers.

Section title

Shows the title of an operation procedure described in the section.

Lead

Describes information we wish you to know in advance of your operating the system or information that may help you to operate it.

3.2 Replacing the Film Pack

When it is printed with the lm in the lm tray set to “0”, “EP1” (Film Tray 1) or “EP2” (Film Tray 2) is displayed in the Display panel. Prepare Fuji Medical Dry Laser Image Film “DI -HL” or “DI-ML”, pull out the lm tray, and replace the lm pack.

1 When the lm in the  lm tray runs out

during the lm feedin g, the lm being fed is automatically out put and “EP1” or “EP2” is displayed in the Display pane l.

2 Press the Enter bu tton and unlock the lm

tray lock.

“oPn” appears on the Display panel.

Be sure to pull the lm tray out o nly after it has bee n unlocked. Other wise, a system malfunction wi ll result.

3 When an error occ urs during lm feeding ,

rst the lm being fed i s automatically output, and the n the error code appe ars on the Display panel.

When the stand-by Switc h, Enter Button or Utility Button is pressed to stop the al arm and clear the error, “EP1” or “EP2” appears on t he Display panel.

4 Pull the lm tray out ca refully (1.), and

remove the protective mat erial together with the lm cushioning c ardboard (2.).

Discard the removed protect ive material and lm cushioning cardboard.

Film cushioning cardboard

Protective material

5 Make sure that the ar row mark on the new

lm pack points to the ba ck side of the lm tra y.

Film pack side

Check the arrow mark direction.

6 Raise one end of the l m pack to tear off

the label (1.), and open both ends of the lm pack (2.), as illustrated.

1. Tear off the label.

2. Open both ends.

Index

A caption that facilitates you to open a desired [Chapter] quickly.

Basic Operation

Illustrated operation procedure

Operation steps are presented in the illustration following specified order. Multiple sub-steps that consist of an operation step

is numbered, 1., 2. .....

DRYPIX Smart Reference Guide 897N102437G

1. Pull out.

2. Remove.

DRYPIX Smart Reference Guide 897N102437G

Page number

Displayed in conjunction with the chapter number.

3-3

Marks

WARNING

CAUTIONS

HINT

Information items to be observed when you are operating this system and the supplementary remarks are described in this manual with the respective marks. For the safe system operation, be sure to observe Warning/Caution.

Indicates hazardous situations that may lead to serious injury or even death if the precaution is not or could not be followed.

Indicates hazardous situations that may lead to mild or moderate injury or physical damages if the caution is not or cannot be followed.

Indicates information that should be noted.

Indicates information that may be helpful.

Shows a more detailed operation method or an item that describes additional information.

Expressions

Messages appear on the display panel as shown below.

● A message displayed on the display panel (sample)

-----------------------------

“U-1”

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vii

Contents

Introduction .......................................................................................................................... iii

DRYPIX Smart Manuals ...................................................................................................... iv

Contents at a Glance ............................................................................................................ v

How to Read This Manual ................................................................................................... vi

Chapter 1 For Safe Operation

1.1 Precautions Before Operating This Equipment ......................................................... 1-1

1.1.1 Precautions to be Observed When Using the Electric Medical Equipment................ 1-2

1.2 Safety ........................................................................................................................ 1-3

1.3 Electromagnetic Compatibility (EMC) ........................................................................1-5

1.4 Handling and Storing Cautions for lms for the Fuji Dry Imager ............................... 1-9

1.5 Locations of labels and signs .................................................................................. 1-10

1.5.1 Locations .................................................................................................................. 1-10

1.5.2 Safety and Other Signs ............................................................................................ 1-13

1.6 Equipment Installation Space .................................................................................. 1-14

1.6.1 Installation Space ..................................................................................................... 1-14

1.6.2 Space Required for Maintenance Work .................................................................... 1-14

1.7 Precautions on DRYPIX Smart Operations ............................................................. 1-15

1.7.1 Precautions for Use .................................................................................................. 1-15

1.7.2 Precautions When Outputting Film Prints ................................................................ 1-16

Chapter 2 Product Overview

2.1 Overview of the DRYPIX Smart ................................................................................ 2-1

2.2 Features of the DRYPIX Smart ................................................................................. 2-3

2.3 Units Names and the Functions ................................................................................2-4

2.3.1 DRYPIX Smart Main Unit ...........................................................................................2- 4

2.3.2 Operation Panel ..........................................................................................................2-6

Chapter 3 Basic Operation

3.1 Starting / Shutting Down the Equipment ................................................................... 3-1

3.1.1 Starting the Equipment ...............................................................................................3-1

3.1.2 Shutting Down the Equipment ....................................................................................3-2

3.2 Replacing the Film Pack ............................................................................................3-3

3.3 Replacing Film Tray ...................................................................................................3-6

Chapter 4 Utility

4.1 Utility List ................................................................................................................... 4-1

4.2 Starting Up the Utility ................................................................................................ 4-2

4.3 Quitting the Utility ...................................................................................................... 4-3

4.4 Automatically Calibrating the Film Density ................................................................4-4

4.5 Outputting a QC Test Pattern ....................................................................................4-5

4.6 Resetting the Remaining Film Counter .....................................................................4-6

4.7 Setting the Sensitive Material Correction Parameter ................................................4-7

4.8 Setting the Date and Time ........................................................................................4-9

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viii

4.9 Outputting the SMPTE pattern ................................................................................ 4-10

4.10 Outputting the Mammography QC Pattern .............................................................. 4-12

Chapter 5 Troubleshooting

5.1 In Case a Problem May Arise ...................................................................................5-1

5.2 The Equipment Cannot be Powered ON ................................................................... 5-2

5.2.1 The Equipment Does Not Start Up Normally ..............................................................5-2

5.3 The Power to the Equipment Does Not Turn OFF .....................................................5-3

5.4 Error Code List ..........................................................................................................5-4

5.5 When a Film Jam Occurred ......................................................................................5-5

5.5.1 Film jamming when the error code “221” or “223” is displayed ................................. 5-6

5.5.2 Film jamming when the error code “226” or “227” is displayed ................................ 5-10

5.5.3 Film jamming when the error code “228” is displayed .............................................. 5 -11

5.5.4 Film jamming when the error code “230” is displayed .............................................. 5 -12

5.5.5 Film jamming when the error code “232” is displayed .............................................. 5-13

Chapter 6 Care and Maintenance

6.1 Cleaning the Inside and Surroundings of the Equipment .......................................... 6-1

6.1.1 Cleaning a lm tray .....................................................................................................6-2

6.1.2 Cleaning the Air Filter .................................................................................................6-3

6.1.3 Washing the Cleaning Roller (Optional) with Water .................................................. 6-4

6.1.4 Image Verication ...................................................................................................... 6-6

6.2 Users Checksheet (Care and Maintenance).............................................................. 6-7

6.3 About Preventive Maintenance..................................................................................6-8

Appendix A Specications

A.1 Specications ............................................................................................................A-1

A.2 External View and Weight ........................................................................................ A-2

Maintenance and Inspection

DRYPIX Smart Reference Guide 897N102437G

Chapter 1

WARNING

For Safe Operation

1.1 Precautions Before Operating This

Equipment

Before using this equipment, please read “Precautions Before Operating This Equipment” carefully so that you can operate it correctly. Whenever you operate this equipment, be sure to observe those precautions. Failure to do so may cause you to subject to injuries or property damage to occur.

Do not connect any unspecied device.

This system is classied 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 operator of this equipment must comprehend the contents shown in the labels or on the monitor.

Process waste correctly, as stipulated by local law or any regulations that apply. When discarding the DRYPIX Smart that incorporates the lithium battery, be sure to contact a licensed waste disposal contractor because it cannot be disposed of as a general waste. Not doing so may cause environmental pollution.

For Safe Operation

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

Cautions on Network

After connecting this system to the network with other systems, conrm that the

other systems are not affected. If they are affected, take countermeasures such as network separation.

Precautions on External Network Connection

When a setting of the network to which the equipment is connected has been changed, check that the change does not affect the system operation and take measures if necessary. The setting change may include the following:

- Change of connection destination

- Addition of devices

- Removal of devices

- Update of devices

- Upgrade of devices

DRYPIX Smart Reference Guide 897N102437G

1-1

1.1.1 Precautions to be Observed When Using the Electric

For Safe Operation

Medical Equipment

• Do not remodel the equipment.

• In an emergency, disconnect the power plug or the inlet.

Ensure sufcient space around the power plug or the inlet.

• An additional MULTIPLE SOCKET-OUTLET or extension cord shall not be connected to this device.

• If the network is shut down due to a network device failure or any other cause, image data is no longer transferred to this device.

DRYPIX Smart Reference Guide 897N102437G

1-2

1.2 Safety

WARNING

CAUTIONS

WARNING

Before using the DRYPIX Smart, read this section thoroughly to ensure that you use the product properly.

Laser Handling Precautions

This equipment is a Class 1 Laser Product (IEC 60825-1/EN 60825-1).

This device contains an embedded laser with the following specication:

Class : 3B Medium : Semiconductor laser Wavelength : 659nm (TYP)

Maximum output - Specication of Laser Diode : 130mW (CW)

Maximum output - Fault Condition : 400mW (CW) Beam emittance : 20°

To prevent the user from being exposed to laser beams, always observe the following precautions.

● Never remove any covers other than the front cover, right-side cover and bottom right-side cover of the equipment.

● When opening covers for coping with lm jams, strictly observe procedures set forth in this

manual. Never perform any other procedures.

● Always contact Fujilm service personnel immediately if a malfunction is suspected in the equipment.

For Safe Operation

Use of controls or adjustment or performance of procedures other than those specied herein

may result in hazardous radiation exposure.

Electric Shock Warnings

The power supply to the DRYPIX Smart is AC 100/110/120V in North America and AC 200/220/230/240V in other countries.

To avoid electric shocks, users should always take the following precautions:

● Only allow a trained operator to use the printer.

● Install the printer in a location where it will not be exposed to water.

● Check that the printer is securely earthed.

● Check that all of the cords and cables are completely and securely connected.

● When using the equipment within the environment where the patient may get into touch

with it, optionally connect additional protective earth conductor.

● When using the equipment within the environment where the patient may get into touch with it, the user must not touch the equipment’s exterior, such as covers and metal sections, and the patient at the same time. In addition, take care that the patient does not touch the equipment.

● To avoid risk of electric shock, this equipment must only be connected to a supply mains

with protective earth.

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1-3

WARNING

CAUTIONS

Never remove the printer cover.

The printer contains high-voltage components that could cause an electric shock.

Ventilation precautions

For Safe Operation

Be sure to install this equipment in a well-ventilated environment.

Good ventilation must be ensured (at least 54m3/hour for one unit).

Precaution about High Temperature

Be careful with units where High-temperature Caution Labels are afxed as those units may

be hot during operation.

Declaration of Conformity

This equipment is in conformance with the following standards: North America

● UL 60601-1

Other countries

● IEC 60601-1/EN60601-1

● IEC 60601-1-2/IEC 60601-1-2

Classication

1) According to the type of protection against electric shock CLASS 1 EQUIPMENT

2) According to the degree of protection against electric shock NO APPLIED PART

3) Protection against harmful ingress of water or particulate matter IP00

4) According to the degree of safety of application in the presence of a ammable anesthetics

mixture with air or with oxygen or nitrous oxide.

Equipment not suitable for use in the presence of a ammable anesthetics mixture with air or

with oxygen or nitrous oxide.

5) According to the mode of operation CONTINUOUS OPERATION

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1-4

1.3 Electromagnetic Compatibility (EMC)

This equipment has been tested and found to comply with the limits for medical devices to the IEC60601-1-2+A1 (North America), IEC60601-1-2+A1 (EN60601-1-2+A1), IEC60601-1-2, Medical Device Directive 93/42/EEC (other than North America). 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 followingmeasures:

• Reorient or relocate the receiving device.

• Increase the separation between the equipment.

• Connect the equipment into an outlet on a circuit different from that to which the other device(s) are connected.

Consult the manufacturer or eld service technician for help.

Further information for IEC 60601-1-2 (EN60601-1-2)

For Safe Operation

• 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 should not be used near this medical electrical equipment, as such communications equipment can affect this equipment and the images.

• Information regarding the cable affecting EMC is as follows.

Name General Specication

Network Cable Cat5e or more,

UTP type and straight cable

• The use of accessories, transducers and cables other than those specied, 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 Smart.

• The DRYPIX Smart should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the DRYPIX Smart should be observed to verify normal

operation in the conguration in which it will be used.

Guidance and manufacturer’s declaration - electromagnetic emissions

The DRYPIX Smart is intended for use in the electromagnetic environment specied below.

The customer or the user of the DRYPIX Smart should assure that it is used in such an environment.

Emissions test Compliance Electromagnetic environment - guidance

The DRYPIX Smart uses RF energy only for its internal RF emissions CISPR 11

RF emissions CISPR 11

Harmonic emissions IEC61000-3-2

Voltage uctuations/ icker emissions

IEC61000-3-3

Group 1

Class A

Complies

function.

Therefore, its RF emissions are very low and are not likely

to cause any interference in nearby electronic equipment.

The DRYPIX Smart 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.

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Guidance and manufacturer’s declaration - electromagnetic immunity

The DRYPIX Smart is intended for use in the electromagnetic environment specied below.

The customer or the user of the DRYPIX Smart should assure that it is used in such an environment.

Immunity test IEC 60601 test level Compliance level

Electrostatic

discharge (ESD) IEC61000-4-2

For Safe Operation

Electrical fast transient/burst IEC61000-4-4

Surge IEC61000-4-5

Voltage dips, short interruptions and voltage variations on power supply input lines IEC61000-4-11

Power frequency (50/60Hz) magnetic

eldIEC61000-4-8

NOTE: U

±2kV contact

±4kV contact ±6kV contact ±8kV air

±6kV contact

±2kV air

±4kV air

±8kV air

±2kV for power supply lines ±1kV for input/output lines

±1kV differential mode ±2kV common mode

<5% U

(>95% dip in UT) for 0.5 cycle 40% U

(60% dip in UT) for 5 cycles 70% U

(30% dip in UT) for 25 cycles <5% U

(>95% dip in UT) for 5 s

±2kV for power supply

lines

±1kV for input/output

lines

±1kV differential mode

±2kV common mode

<5% U

(>95% dip in UT)

for 0.5 cycle

40% U

(60% dip in UT)

for 5 cycles

70% U

(30% dip in UT)

for 25 cycles

<5% U

(>95% dip in UT)

for 5 s

3 A/m 3 A/m

is the a.c. mains voltage prior to application of the test level.

Electromagnetic environment -

guidance

Floors should be wood, concrete or

ceramic tile. If oors are covered with

synthetic material, the relative humidity should be at least 30%.

Mains power quality should be that of a typical commercial or hospital environment.

Mains power quality should be that of a typical commercial or hospital environment. If the user of the DRYPIX Smart requires continued operation during power mains interruptions, it is recommended that the DRYPIX Smart be powered from an uninterruptible power supply or a battery.

Power frequency magnetic elds should

be at levels characteristic of a typical location in a typical commercial or hospital environment.

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1-6

Guidance and manufacturer’s declaration - electromagnetic immunity

The DRYPIX Smart is intended for use in the electromagnetic environment specied below.

The customer or the user of the DRYPIX Smart 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 Smart, 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

where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).

Field strengths from xed RF transmitters, as

determined by an electromagnetic site survey, should be less than the compliance level in each frequency range. vicinity of equipment marked with the following

800 MHz to 2.5 GHz

Interference may occur in the

For Safe Operation

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

reection from structures, objects and people.

a Field strength from xed 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 xed RF transmitters, an electromagnetic site survey should be considered. If the measured eld strength in the location in which the DRYPIX Smart is used exceeds

the applicable RF compliance, the DRYPIX Smart should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the DRYPIX Smart.

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

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1-7

Recommended separation distances between

Portable and mobile RF communications equipment and the DRYPIX Smart

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

For Safe Operation

Rated maximum output

power of transmitter

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

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 reection from structures, objects and people.

Separation distance according to frequency of transmitter

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

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1-8

1.4 Handling and Storing Cautions for films for the Fuji Dry Imager

Please be aware of the following cautions for handling and storing of the lm.

Precautions for storing or handling unused lms

1 Use only the “Fuji Medical Dry Laser Image Film DI-HL” or “Fuji Medical Dry Laser Image Film

DI-ML” that is compatible with this equipment. If a lm other than DI-HL or DI-HM is used, a

malfunction may be caused to the equipment.

2 Be sure to store unused lms contained in the lm pack in a cool, dry and dark place of low

temperature and low humidity (temperature: 25°C or lower), avoiding radioactivity and reactive

gases, same as for the conventional wet-type lm.

3 The DI-HL lms are light-sensitive. Do not open a lm pack before it is loaded properly in the

equipment.

4 Do not touch unused lms with bare hands, otherwise adverse effects can appear on recorded

images.

5 Do not take unused lms out of the lm pack that has once been loaded into the equipment and

opened or add lms to the lm pack loaded, which will result in misoperation or failure of the

equipment.

6 The lm pack contains a protective sheet, in addition to the specied number of recording

lms. This protective sheet will remain in the lm pack even after those recording lms have been printed and it cannot be used for image recording. Because the protective sheet is a lm, discard it appropriately together with other used lms.

Precautions for storing or handling recorded lms

For Safe Operation

1 Store recorded lms 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 change sharply. Longterm storage at high temperature, high humidity and/or daylight conditions, such

as in a car or room during summer, may cause discoloration. Using lms in the slide projector

or overhead projector will also cause discoloration.

2 For the long-term storage performance of recorded lms, we assume based on the result of the

acceleration test that it will be over 30 years at the storage temperature of 25ºC and over 25 years at 30ºC, until the portion on an image of density (D) = 1.2 at time of output to change 10%

(ΔD =0.12) .

3 After an image has been recorded, the lm 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 boxwill cause slight changes in the optical density. Due to such optical effect, traces

of overlapped lms or transferred images can be visually recognized temporarily, which will disappear when those lms are left under the normal light condition.

4 Note that lucid surfaces of recorded lms 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.

5 Do not store lms with its image recording faces attached directly for preventing them from

sticking to each other.

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1.5 Locations of labels and signs

Locations of labels and signs afxed to the DRYPIX Smart, and the relevant safety signs are shown

below.

1.5.1 Locations

For Safe Operation

Class 3B Panel Label #1

Rating Label

HHS Certification and Identification Label

Caution Label

Caution Label (other than North America）

High-temperature Caution Label

Additional protective earth mark

Caution Label Caution Label

Class 3B Panel Label #2

Power

(other than North America）

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DRYPIX Smart Reference Guide 897N102437G

North America

Class 3B Panel Label #1

For Safe Operation

Rating Label

HHS Certification and Identification Label

Class 3B Panel Labels #2

Be aware that the temperature may be high in the area where the following label is affixed.

High-temperature Caution Label

Be sure to use the power cord our official dealer or local presentative provided. If an inappropriate cord is used, it may generate heat or fire.

Caution Label (Inlet)

Do not connect a telephone wire to the LAN connector. Only UTP-type straight LAN cables of Category 5e or higher are appropriate for connection to this connector.

Caution Label (LAN connector)

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Other countries

For Safe Operation

Class 3B Panel Label #1

Rating Label

HHS Certification and Identification Label

Class 3B Panel Labels #2

Be aware that the temperature may be high in the area where the following label is affixed.

High-temperature Caution Label

Be sure to use the power cord our official dealer or local presentative provided. If an inappropriate cord is used, it may generate heat or fire.

Caution Label (Inlet)

Do not connect a telephone wire to the LAN connector. Only UTP-type straight LAN cables of Category 5e or higher are appropriate for connection to this connector.

Caution Label (LAN connector)

Additional Option Tray

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DRYPIX Smart Reference Guide 897N102437G

Identication Label

1.5.2 Safety and Other Signs

The following safety signs are used in the DRYPIX Smart labels or on its body.

Sign Description

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

Refer to operation manual

Attention, consult ACCOMPANYING DOCUMENTS.

High-temperature caution

Power-OFF

Power-ON

Protective grounding (to the earth)

For Safe Operation

Alternating current

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.

Year of manufacture

Environmentally Friendly Use Period (EFUP)

Stand-by switch

Enter button

Utility button

Serial number

Manufacture

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1.6 Equipment Installation Space

1.6.1 Installation Space

When Not Fixed with Fixtures

For Safe Operation

1.6.2 Space Required for Maintenance Work

Front : More than 800 mm (31.5 in.) Rear : More than 100 mm (3.9 in.) Left : More than 50 mm (1.9 in.) Right : More than 200 mm (7.87 in.)

When Fixed with Fixtures

Front : More than 800 mm (31.5 in.) Rear : More than 100 mm (3.9 in.) Left : More than 250 mm (9.8 in.) Right : More than 250 mm (9.8 in.)

Rear : More than 600 mm (23.6 in.)

Left : More

than 800 mm

(31.5 in.)

Right : More than 800 mm (31.5 in.)

Left : More

than 800 mm

(31.5 in.)

Top : More than 400 mm (15.7 in.)

Right : More than 800 mm (31.5 in.)

Front : More than 1000 mm (39.3 in.)

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