Read and understand all instructions before using.
For a translation of the following warnings, please refer to the applicable safety
addendum listed below:
DryView 8100 Imager User Guide Safety Addendum (Polish) 74-0500-5507-3
DryView 8100 Imager User Guide Safety Addendum (Hebrew) 74-0500-5508-1
DryView 8100 Imager User Guide Safety Addendum (Korean) 74-0500-5509-9
!
WARNING
This equipment is operated with hazardous voltage which can shock,
burn, or cause death.
Remove wall plug before servicing equipment. Never pull on cord to remove from
outlet. Grasp plug and pull to disconnect.
Do not operate equipment with a damaged power cord.
Do not use an extension cord to power this equipment.
Use only the power cord supplied with this equipment.
Position the power cord so it will not be tripped over or pulled.
Connect this equipment to a grounded outlet.
!
WARNING
This equipment contains moving parts that may be accessible to the user. Loose
clothing, jewelry, or long hair may cause minor personal injury or damage to the
equipment. Do not operate equipment with the covers open. Do not operate
equipment with any of the safety interlocks overridden.
!
WARNING
This equipment is not contained in a sealed cabinet. Therefore it must not be used in
locations where it can come in contact with liquids, including bodily fluids.
!
WARNING
For continued protection against fire, replace fuses only with fuses of the same type
and rating.
2000 March Rev. B 8754020
i
DryView 8100 Laser Imager User Guide
Read and understand all instructions before using.
!
CAUTION
Do not use in the presence of flammable anesthetics, oxygen or nitrous oxide. This
equipment does not have a gas sealed electronics enclosure and could ignite any
flammable or explosive gases present in its environment.
!
CAUTION
This equipment is intended to connect to other medical devices. Installation and
service maintenance are to be performed only by qualified service personnel. The
laser in the equipment is not a patient device. Therefore the equipment must be
installed no closer than 1.83 meters from a patient bed or chair.
!
CAUTION
Do not substitute or modify any part of this equipment without approval of Eastman
Kodak Company.
!
CAUTION
This equipment has been tested and found to comply with the limits for a Class B
digital device, pursuant to part 15 of the FCC rules. Those limits are designed to
provide reasonable protection against harmful interference in a residential
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 radio communications. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause
harmful interference to radio or television reception, which can be determined by
turning the equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving antenna.
Increase the separation between the equipment and the receiver.
Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected.
Consult the dealer or an experienced radio/TV technician for help.
ii
8754020 2000 March Rev.B
Safety, EMC, and CE Marking Compliance
Read and understand all instructions before using.
!
CAUTION
General External Cleaning: This equipment may be cleaned with a damp cloth
using water with mild detergent, or commercial electronic equipment cleaner.
2000 March Rev. B 8754020
8100–38L
iii
DryView 8100 Laser Imager User Guide
Read and understand all instructions before using.
!
DANGER
The equipment employs a 50 milliwatt laser. Laser radiation may be present when
the machine operates without the rear cover installed.
Use of controls or adjustments, or performance of procedures other than those
specified herein, may result in eye damage.
The rear cover shall be removed by authorized service personnel only.
DANGER
Bypassing interlocks (other than the Service Interlock above)
will allow the system to run with the laser energized.
Exposure to laser light may result in permanent eye damage.
Class 1 Laser
Laser de catégorie 1
Laser-Klasse 1
Laser di Classe 1
Klass 1 Laser
6E7000 Rev. A
iv
8754020 2000 March Rev.B
Safety, EMC, and CE Marking Compliance
Read and understand all instructions before using.
2000 March Rev. B 8754020
v
DryView 8100 Laser Imager User Guide
This equipment has been tested for and complies with the following Safety and
Emission Standards. Certificates of Compliance and Declarations of Conformity
have been issued as shown below.
Safety:
Canada:
C22.2 NO 950-95–CAN/CSA Safety for Information Technology Equipment,
Including Electrical Business Equipment
C22.2 NO 601.1–M90–CAN/CSA Medical Electrical Equipment – Part 1:
General Requirements for Safety
Europe:
EN60950: Safety of Information Technology Equipment, Including Electrical
Business Equipment (IEC 60950 : 1991, Modified) (Includes Amendment A1 and
A2: 1993)
EN60601–1–1: Medical electrical equipment – Part 1: General requirements for
safety – Section 1: Collateral standard: Safety requirements for medical electrical
systems
EN60825–1: Safety of laser products – Part 1: Equipment classification,
requirements and user’s guide
U.S.A.:
UL 1950: Safety of Information Technology Equipment, Including Electrical
Business Equipment DOD (Bi–National Standard) with UL 2601–1 Medical
Electrical Equipment, Part 1: General Requirements for Safety
21CFR1040.10 Class I: FDA CDRH Code of Federal Regulations Title 21,
Volume 8, Food and Drugs, Part 1040 Performance Standards For
Light–Emitting Products, Section 10 Laser Products
FDA Premarket Notification 510(K): Regulatory Requirements For Medical
Devices
Rest of World:
IEC 950: Safety of information technology equipment
IEC 60601–1–1: Medical electrical equipment – Part 1: General requirements for
safety – Section 1: Collateral standard: Safety requirements for medical electrical
systems
IEC 60825–1: Safety of laser products – Part 1: Equipment classification,
requirements and user’s guide
vi
8754020 2000 March Rev.B
Safety, EMC, and CE Marking Compliance
EMC:
Canada:
CAN/CSA–C108.6–M91 Class A: Limits and Methods of Measurement of
Electromagnetic Disturbance Characteristics of Industrial, Scientific and Medical
(ISM) Radio–Frequency Equipment
Europe:
EN55022 (CISPR 22) Class B Group 1: Limits and Methods of Measurement of
Radio Interference Characteristics of Information Technology Equipment
EN61000–3–2 (IEC 1000–3–2): Electromagnetic compatibility (EMC) – Part 3:
Limits – Section 2: Limits for harmonic current emissions (equipment input
current <= 16 per phase)
EN 61000–4–2 (IEC 1000–4–2): Electromagnetic compatibility (EMC) – Part 4:
EN 61000–4–3 (IEC 1000–4–3): Electromagnetic compatibility (EMC) – Part 4:
Testing and measurement techniques – Section 3: Radiated, radio–frequency,
electromagnetic field immunity test
EN 61000–4–4 (IEC 1000–4–4): Electromagnetic compatibility (EMC) – Part 4:
Testing and measurement techniques – Section 4: Electrical fast transient/burst
immunity test. Basic EMC Publication
EN 61000–4–5 (IEC 1000–4–5): Electromagnetic compatibility (EMC) – Part 4:
Testing and measurement techniques – Section 5: Surge immunity test
EN 61000–4–6 (IEC 1000–4–6): Electromagnetic compatibility (EMC) – Part 4:
Testing and measurement techniques – Section 6: Immunity to conducted
disturbances, induced by radio–frequency fields
EN 61000–4–11 (IEC 1000–4–11): Electromagnetic compatibility (EMC) – Part 4:
Testing and measuring techniques – Section 11: Voltage dips, short interruptions
and voltage variations immunity tests
U.S.A.:
FCC Rules and Regulations, Title 47, Part 15, Subpart B, Class B: Radio
frequency devices: Unintentional Radiators
Rest of World:
CISPR 22 Class B Group 1: Limits and Methods of Measurement of Radio
Interference Characteristics of Information Technology Equipment
2000 March Rev. B 8754020
vii
DryView 8100 Laser Imager User Guide
EU Directives:
73/23/EEC Council Directive on the Harmonization of the Laws of Member
States Relating to Electrical Equipment Designed for Use within Certain Voltage
Limits
89/336/EEC Council Directive on the Approximation of the Laws of the Member
States Relating to Electromagnetic Compatibility
93/42/EEC Council Directive Concerning Medical Devices
CE Marking:
Documents concerning the conformance of this product to Council Directive
93/42/EEC of 14 June 1993 concerning Medical Devices can be obtained from the
Eastman Kodak Health Imaging Systems European Representative at:
This Class A digital apparatus meets all requirements of the Canadian
Interference-Causing Equipment Regulations.
Cet appareil numérique de la Classe A respecte toutes les exigences du Règlement
sur le matérial brouilleur du Canada.
viii
8754020 2000 March Rev.B
T able of Contents
PLEASE NOTE
The information contained herein is based on the experience
and knowledge relating to the subject matter gained by Eastman
Kodak Company prior to publication.
No patent license is granted by this information.
Eastman Kodak Company reserves the right to change this
information without notice and makes no warranty, express or
implied, with respect to this information. Kodak shall not be liable
for any loss or damage, including consequential or special
damages, resulting from the use of this information, even if loss
or damage is caused by Kodak’s negligence or other fault.
Table of Contents
DescriptionPage
Safety, EMC, and CE Marking Compliancei. . . . . . . . . . . .
IMPORTANT NOTICE TO PURCHASER7-6. . . . . . . . . . . .
2000 March Rev. B 8754020
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DryView 8100 Laser Imager User Guide
BLANK PAGE
xii
8754020 2000 March Rev. B
Introduction
Introduction
Introducing the Kodak DryView 8100 Laser Imager
The DryView 8100 Laser Imager is a continuous tone laser imager with an internal
photothermographic film developer. Heat, rather than photo chemicals, is used to
develop the film. The imager can be connected to and print images from a variety of
medical image source devices such as CT scanners or Ultrasound. It can also be
connected to a DICOM medical image network via the PACS Link 9410 Acquisition
System.
The DryView 8100 Laser Imager uses 14 inch x 17 inch (35 cm x 43 cm) DryView
Laser Imaging Film, which is packaged in 125-sheet Kodak Instant Daylight Load
Film Cartridges.
A DryView V2 Keypad can be used to control the imager, or the system can be
controlled from the host modality. A footswitch is also available, providing an optional
method of acquiring images for printing.
2000 March Rev. B 8754020
Figure 1-1. DryView 8100 Laser Imager
1-1
DryView 8100 Laser Imager User Guide
System Configurations
The DryView 8100 Laser Imager can be used in two system configurations. The key
features of these are described below.
DryView 8100 Laser Imager
The imager connects directly to up to three image source devices. (The standard
unit has one input, but it can be upgraded for additional inputs.)
Copper cables are used for connections to the source imaging device and
keypad.
The operator controls image acquisition and printing from either a keypad or a
console on the host source imaging device.
Dryview 8100 PACS Link Laser Imager
The imager connects to a DICOM medical image network via a PACS Link
Interface.
The imager prints images sent from image source devices or archiving stations
connected to the DICOM network.
1-2
8754020 2000 March Rev. B
Keypad Features
The table below lists the features provided by the DryView V2 Keypad.
DryView
Feature
Format SelectYes*
Multiple Copies SettingYes
Sequential Image AcquireYes
Random Image AcquireYes
Sequential Image EraseNo
Random Image EraseYes
Move Acquired ImageNo
PrintYes
Stop PrintNo
Density or Dmax SettingYes**
Contrast SettingYes**
From DryView V2 Keypad: 1:1, 2:1, 4:1, 6:1, 9:1, 12:1, 15:1, 16:1, and 20:1.
From host console: Same as for the DryView V2 Keypad, plus 24:1.
** Can also be set at the imager’s Local Panel.
2000 March Rev. B 8754020
1-3
DryView 8100 Laser Imager User Guide
How the DryView 8100 Laser Imager Works
Using the keypad or host console, the operator acquires an image from the
image source device. The image is stored on a hard disk in the imager.
Using the keypad or host console, the operator prints the image.
The following sequence occurs each time the operator issues a print command. The
step numbers refer to the circled numbers in Figure 1-2. The dashed lines in the
illustration indicate the film path.
1. Suction cups lift a single sheet of film out of the supply cartridge and route it into
the film feed rollers.
2. The film feed rollers move the film down to the platen rollers.
3. The platen rollers drive the film into the exposure module platen.
4. A moving laser beam writes the image onto film, which is held stationary in the
platen.
5. The platen rollers reverse direction and move the exposed film up through the
vertical transport area.
6. Transport rollers drive the film onto the processor drum.
7. The heated processor drum develops the film as it passes over the drum.
8. Rollers move the developed film from the processor drum, through the
densitometer (see the next paragraph), and onto the receive tray.
Automatic Image Quality Control
The built-in densitometer is a key element in the Automatic Image Quality Control
(AIQC) process. AIQC allows the imager to automatically adjust processing
parameters to ensure optimum image quality. The imager adjusts these parameters
each time it prints a calibration film. A calibration film is printed whenever:
The DryView 8100 Laser imager is powered on.
A calibration film is requested from the Local Panel.
The imager has not been used for 7 days, and a print is requested.
Manual Mode of Operation
The imager can be operated in a “manual” mode, without AIQC. Use of this mode is
explained in Section 3 of this manual.
1-4
8754020 2000 March Rev. B
Film
Processor
Drum
Introduction
Receive Tray
7
Transport
Rollers
Vertical
Transport
Area
Platen
Rollers
Laser
Beam
6
5
1
2
3
4
8
Densitometer
Film
Supply
Cartridge
Suction
Cups
Film Feed
Rollers
Exposure
Module
2000 March Rev. B 8754020
8100–49C
Figure 1-2. Print Sequence
1-5
DryView 8100 Laser Imager User Guide
How This Manual is Organized
The remainder of this manual is organized as follows:
Section 2 describes operator controls and indicators on the main cabinet,
including the Local Panel.
Section 3 provides general procedures for operating and maintaining the system.
(It does not include instructions for using the keypad. These are provided in
Section 4.)
Section 4 provides instructions for using the DryView V2 Keypad, including:
descriptions of keypad controls, procedures for operating the imager from the
keypad, and keypad error messages.
Section 5 includes system troubleshooting procedures.
Section 6 provides system specifications.
Section 7 includes technical information about DryView 8100 Laser Imaging
Film.
1-6
8754020 2000 March Rev. B
Controls and Indicators
Controls and Indicators
Main Cabinet Controls and Indicators
This section describes the operator controls on the DryView 8100 Laser Imager
cabinet, focusing on the Local Panel. For keypad functions, refer to Section 4.
The numbered descriptions below correspond to the circled numbers in Figure 2-1.
1. Local Panel – Includes a message display, status indicator lights, and
pushbutton controls. The Local Panel is described in greater detail on the
following pages.
2. Power Switch – Controls power to the imager. (On rear of cabinet.)
3. Front Door – Accesses the film cartridge.
4. Upper Hood - Accesses upper assemblies.
5. Receive Tray – Collects developed film.
6. Floppy Disk Drive – Used to update the imager internal software.
4
3
2
1
6
5
Figure 2-1. DRYVIEW 8100 Laser Imager – Controls and Indicators
8100–27C
2000 March Rev. B 8754020
2-1
DryView 8100 Laser Imager User
Local Panel Functions
This paragraph describes the controls and indicators on the Local Panel. Use of
these controls is covered in Section 3. Display window messages are explained in
Section 6.
1. Power Light – Indicates that the imager is powered up.
2. Ready Light – ON: Indicates that the imager is available for printing.
– Blinking:Indicates that the imager is printing.
– OFF: Indicates that the imager is not available for printing.
3. Attention Light – Indicates an error condition that may affect imager operation
(e.g., imager warming or film low). Check the display window for a related
message.
4. Alarm Light – Indicates that an error condition exists (e.g., a film jam or open
door), and imager operation cannot continue until the error has been cleared.
Check the display window for a related message.
5. Display Window – Provides information about the status and function of the
imager and the prints in progress. Refer to Section 5 for descriptions of the
messages displayed in this window.
6. (Enter) Key – Press to enter a selected value or to return to the status and
error screen.
After you have changed the contrast or density setting, press to lock in the
new setting.
After viewing maintenance information or IP addresses on the message
display, press to return to the status and error message screen.
7. Maintenance Information Key – Press to display a scrollable list that includes:Maintenance information such as total lifetime print count and number of
prints remaining until preventive maintenance is required.
IP address of the imager.
Reserved service IP address.
8. Calibrate Key – Press to print a calibration test (step wedge pattern) as the next
film. (The test film will interrupt a multiple-sheet print job.)
2-2
8754020 2000 March Rev. B
Controls and Indicators
Figure 2-2. Local Panel Controls
9. Backlight Key – When system power is applied, the message display backlightturns on and the Ready, Attention, and Alarm lights are enabled for use.
Press the Backlight key once
Press the Backlight key a second time
to turn off the backlight.
to disable the Ready, Attention, and
Alarm lights. The backlight remains off. (This is darkroom mode.)
Press the Backlight key a third time to return the backlight and the three
indicator lights to their original state (enabled for use).
2000 March Rev. B 8754020
2-3
DryView 8100 Laser Imager User
10. Open Door Key – Press momentarily to open the front door. The film cartridge
first closes to prevent exposing the film. Then the front door is unlatched.
If a film jam at the cartridge prevents the cartridge from closing, error message
P138 (Press Open 5S) will display. This indicates that you must hold down the
OpenDoor key for 5 seconds to unlatch the door. Since the film cartridge is
open, when you open the door the top sheets of film will be exposed. To
minimize exposure, you should make the room as dark as possible before
opening the door.
!
Caution
Do not leave the imager unattended after pressing the Open Door Key.
11. Test Print Key – Press this key after you press the Contrast or Density key, to
initiate a test print for examination of contrast or density.
12. Density Key – Press this key to display and change the density setting. Use the
and keys to adjust the setting up or down (The density range for blue film is
from 1.7 to 3.1. For clear film it is from 1.7 to 3.0.) Then press the Test Print or
Enter key to apply the new setting. (Do not use this key to change density if your
system includes a DryView V2 keypad.)
Note
If your system includes the DryView V2 keypad, density must be set via the
keypad rather than the Local Panel. The values set at the keypad will override
values entered at the Local Panel.
13. Contrast Key – Press this key to display and change the contrast setting. Use
the and keys to adjust the setting up or down ( range: -15 to -1 and 1 to 15).
Then press the Test Print or Enter key to apply the new setting.
Note
If your system includes the DryView V2 keypad, contrast must be set via the
keypad rather than the Local Panel. The values set at the keypad will override
values entered at the Local Panel.
14. Key– Press to move up through item lists or increase a parameter value.
15. Key – Press to move down through item lists or decrease a parameter value.
2-4
8754020 2000 March Rev. B
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