Warnings and Cautions for
Kodak DryView 8700/8500 Laser Imager
Safety Instructions
Read and understand all instructions before using.
!
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.
Position the power cord so it will not be tripped over or pulled.
Connect this equipment to a grounded outlet.
Use only the power cord supplied with this equipment.
!
WARNING
For Continued Protection against Fire, Replace Fuses with only the Same Type and
Fuse Rating.
!
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.
2001 March Rev. B 8599110
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User Guide
!
CAUTION
Avoid Laser Beam
This equipment employs a 150 milliwatt laser. Laser radiation may be
present when the machine operates without panels or covers installed.
Use of controls or adjustments, or performance of procedures other than those
specified herein, may result in eye damage.
Covers shall be removed by authorized service personnel only.
!
CAUTION
Do not substitute or modify any part of this equipment without approval of Eastman
Kodak Company.
!
CAUTION
General External Cleaning: This equipment may be cleaned with a damp cloth
using water with mild detergent, or commercial electronic equipment cleaner.
Do not touch, Hot Surface!
!
CAUTION
ATTENTION:
Surface Chaude. Ne pas toucher!
ACHTUNG:
Nicht anfassen. Heisse Oberflache!
ATTENZIONE:
Non toccare. Superficie Calda!
CAUTION:
Do not touch. Hot surface!
ADVERTENCIA:
No tocar. Superficia Caliente!
OPGEPAST:
Niet aanraken. Heet Oppervlak!
U.S. Federal law restricts this device to the sale by, or on the order of, a licensed
health care practitioner.
ii
8599110 2001 March Rev. B
Warnings and Cautions
!
CAUTION
This equipment is intended to connect to other medical devices. Only qualified
service personnel may perform installation and service maintenance. 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 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 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.
FCC ID: PA4870085007E2620
2001 March Rev. B 8599110
iii
User Guide
Class 1 Laser
Laser de catégorie 1
Laser-Klasse 1
Laser di Classe 1
Klass 1 Laser
Front
Left
DANGER-Invisible Laser Radiation When Open.
Avoid Direct Exposure to Beam.
ATTENTION -Rayonnement Laser Invisible En Cas
D’Ouverture. Exposition Dangereuse
Au Faisceau.
VORSICHT -Unsichtbare Laserstrahlung Wenn Abdeckung
Geöffnet. Nicht Dem Strahl Aussetzen.
VARNING-Osynlig Laserstrålning. Laserstråining När
Denna Del Ä Öppnad. Strålen Är Farlig.
Rear
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8599110 2001 March Rev. B
Warnings and Cautions
WarningsandCautions
for External Interface Box Accessories
Read and understand all instructions before using.
Classifications
UL Classified
File Number E183646
Control Number 9R46
Medical Equipment
UL 2601-1CAN/CSA No. 601.1
!
Classified by Underwriters Laboratories Inc.Ò With Respect to Electric Shock,
Fire, Casualty and Medical Hazards only in Accordance with UL 2601-1, CAN/CSA
C22.2 No. 601.1 and IEC 601.1.
!
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.
¯Do not place a portable multiple--socket outlet (power strip) on the floor. Mount
the power strip on a wall or on the underside of a table.
2001 March Rev.B 8599110
v
User Guide
!
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 with only the Same Type and
Fuse Rating.
!
CAUTION
Do not substitute or modify any part of this equipment without approval of Eastman
Kodak Company.
!
CAUTION
General External Cleaning: This equipment may be cleaned with a damp cloth
using water with mild detergent, or commercial electronic equipment cleaner.
Type B Applied Part
!
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. Only qualified
service personnel may perform installation and service maintenance.
!
CAUTION
U.S. Federal law restricts this device to the sale by, or on the order of, a licensed
health care practitioner.
vi
8599110 2001 March Rev. B
Read and understand all instructions before using.
Warnings and Cautions
Label located on back of machine.
2001 March Rev.B 8599110
vii
User Guide
BLANK PAGE
viii
8599110 2001 March Rev. B
Agency, Regulatory and CE Marking Compliance
Agency, Regulatory and CE Marking Compliance
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
CSA–CS–03: Rules for Telecommunication Equipment
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
47 CFR Part 68: FCC Rules for Telecommunication Equipment
2001 March Rev. B 8599110
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User Guide
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
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
EN300330: 1999 European Telecommunication Standard, Sections 7.2 and 7.4
Emission Requirements
EN300683: 1997 European Telecommunication Standard, Section 8 Emission
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
x
8599110 2001 March Rev. B
Agency, Regulatory and CE Marking Compliance
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
EN61000–4–8 (IEC1000–4–8): Electromagnetic Compatibility (EMC) – Part 4:
Testing and Measurement Techniques – Section 8: Power Frequency Magnetic
Field
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; Part 15, Subpart C, Section 15.209
Radiated Emission Requirements
Rest of World:
CISPR 22 Class B Group 1: Limits and Methods of Measurement of Radio
Interference Characteristics of Information Technology Equipment
Directives:
EU:
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
99/5/EEC Council Directive on Radio Equipment and Telecommunications
Terminal Equipment
2001 March Rev. B 8599110
0123
xi
User Guide
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:
Canada 1016104159A
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.
xii
8599110 2001 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.
IMPORTANT NOTICE TO PURCHASER6-6. . . . . . . . . . . .
2001 March Rev. B 8599110
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User Guide
BLANK PAGE
xvi
8599110 2001 March Rev. B
Introduction
Introduction
Introducing the Kodak DryView 8700 and 8500 Laser Imagers
The Kodak DryView 8700 Laser Imager (8700 Laser Imager) and the Kodak
DryView 8500 Laser Imager (8500 Laser Imager) are continuous–tone laser
imagers with an integrated photothermographic film developer.
The two imagers are nearly identical except for film size. The 8700 Laser Imager
uses only 14” x 17” (35 x 43 cm) Kodak DryView Laser Imaging Film (DryView film).
The 8500 Laser Imager also uses DryView film but accepts only 11 in. x 14 in.
(28 x 35 cm) film sheets.
Both film sizes are available in clear or blue base, packaged in 125-sheet Kodak
Instant Daylight Load Film Cartridges.
The 8700/8500 Laser Imagers are both available in three different configurations,
with two different remote keypads, described later in this manual.
Figure 1-1. Kodak DryView 8700/8500 Laser Imager
2001 March Rev. B 8599110
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User Guide
System Configurations
The 8700/8500 Laser Imagers are both available in three different configurations.
Key features of each configuration are:
8700/8500 Laser Imager Standard System
Supports up to two inputs (can be upgraded to support multiple inputs).
Provides up to 64 megabytes of image memory, in 16 megabyte increments.
Uses copper cable for external connections.
Image acquisition and printing are accomplished via host control, Kodak
DryView 8700/8500 Keypad, or Kodak Keypad.
8700/8500 Laser Imager Plus System
Supports up to two inputs (can be upgraded to support multiple inputs).
Provides up to 128 megabytes of image memory, in 32 megabyte increments.
Uses fiber optic cable for external connections.
Image acquisition and printing are accomplished via host control or Kodak
Keypad.
Multi-Input/Dual Printer System
Consists of an 8700 or 8500 Dual Printer connected to a Kodak DryView 8800
Multi-Input Manager (8800 Multi–Input Manager) or 969 HQ Laser Imager.
Supports up to eight inputs.
Provides 32 or 64 megabytes of image memory per input.
Uses fiber optic cable for external connections.
Image acquisition and printing are accomplished via host control or Kodak
Keypad.
The 8800 Multi–Input Manager can provide output connects for one or two laser
printers. Connects to any of the following printers:
If dual printers are connected, the two printers can be the same or mixed.
1-2
8599110 2001 March Rev. B
Introduction
Keypad Feature Comparison
This table compares the features provided by the DryView 8700/8500 Keypad and
the Kodak Keypad. Note that the Kodak Keypad is available with all DryView
8700/8500 Laser Imager systems, but the DryView 8700/8500 Keypad is available
only with the DryView 8700/8500 Laser Imager Standard system.
Feature
DryView 8700/8500 KeypadKodak Keypad
Format SelectYesYes
Custom FormatsNoYes
Multiple Copies SettingYesYes
Sequential Image AcquireYesYes
Random Image AcquireNoYes
Sequential Image EraseYesYes
Random Image EraseNoYes
Move Acquired ImageNoYes
PrintYesYes
Stop PrintYesYes
Density or Dmax SettingNo *Yes
Contrast SettingNo *Yes
Print Density TestNo *Yes
Print Contrast TestNo *Yes
Smooth/Sharp SelectNoYes
Image Polarity SelectNoYes
Image Framing SelectNoYes
Auto-Print SelectNo **Yes
Auto-Format SelectNo **Yes
Alarm Volume SettingNoYes
*Can be set at the imager’s local panel.
** Can be set by service personnel during installation.
2001 March Rev. B 8599110
1-3
User Guide
How the 8700/8500 Laser Imager Works
The following sequence occurs each time the 8700/8500 Laser Imager receives a
print command. The circled numbers in Figure 1-2 correspond to the numbered
steps below. Dashed lines indicate the film path.
1. Suction cups in the pickup area lift a single sheet of film out of the supply
cartridge and feed it into the film transport rollers.
2. The film transport drives the film down into the exposure module.
3. The film is exposed by a laser beam and then fed back into the film transport.
4. The film transport drives the film up into the film developer.
5. As the film passes over the film developer drum, the heat generated by the drum
develops the film.
6. The film transport drives the film out of the film developer, through the
densitometer, and out to the receive tray. The densitometer is a key element in
the Kodak Automatic Image Quality Control (AIQC) process, which allows the
imager to automatically adjust image processing parameters to ensure optimum
image quality.
1-4
8599110 2001 March Rev. B
Introduction
Film Developer
Receive Tray
Densitometer
5
6
1
2
4
Supply
Cartridge
Film
Transport
2001 March Rev. B 8599110
3
Figure 1-2. Print Sequence
Exposure
Module
1-5
User Guide
BLANK PAGE
1-6
8599110 2001 March Rev. B
Controls and Indicators
Controls and Indicators
Kodak DryView 8700/8500 Laser Imager
The controls and indicators for the Kodak DryView 8700/8500 Laser Imager
(8700/8500 Laser Imager) are identified in the figure. The numbered descriptions
correspond to the numbered callouts in Figure 2-1.
1. Local Panel – Includes a message display, status indicator lights, and push
button controls. For more detailed description, refer to Local Panel in this
section.
2. Power Switch – Controls power to the imager.
3. Supply Door – Enables access to the film cartridge.
4. Receive Tray – Collects developed film.
4
3
Figure 2-1. 8700/8500 Laser Imager – Controls and Indicators
2001 March Rev. B 8599110
1
2
2-1
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