Kodak DryView 8100 User manual

7 X 9 inside cover
User Guide
Kodak DryView 8100 Laser Imager
8754020
96-0000-0197-2
3/00 Rev. B

Safety, EMC, and CE Marking Compliance
i
2000 March Rev. B 8754020
Safety, EMC, and CE Marking Compliance
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.

DryView 8100 Laser Imager User Guide
ii 8754020 2000 March Rev.B
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.

Safety, EMC, and CE Marking Compliance
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2000 March Rev. B 8754020
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.
8100–38L

DryView 8100 Laser Imager User Guide
iv 8754020 2000 March Rev.B
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.
6E7000 Rev. A
Class 1 Laser
Laser de catégorie 1
Laser-Klasse 1
Laser di Classe 1
Klass 1 Laser
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.
DANGER

Safety, EMC, and CE Marking Compliance
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2000 March Rev. B 8754020
Read and understand all instructions before using.

DryView 8100 Laser Imager User Guide
vi 8754020 2000 March Rev.B
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

Safety, EMC, and CE Marking Compliance
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2000 March Rev. B 8754020
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:
Testing and measurement techniques –Section 2: Electrostatic discharge
immunity test. Basic EMC Publication
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

DryView 8100 Laser Imager User Guide
viii 8754020 2000 March Rev.B
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:
Kodak AG
Quality Services
Product Safety
70323 Stuttgart
Germany
Phone: ++49 711 406 2993
Fax: ++49 711 406 3513
DOC:
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.

Table of Contents
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2000 March Rev. B 8754020
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
Description Page
Safety, EMC, and CE Marking Compliance i. . . . . . . . . . . .
Introduction 1-1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introducing the Kodak DryView 8100 Laser Imager 1-1. . .
System Configurations 1-2. . . . . . . . . . . . . . . . . . . . . . . . . . . .
DryView 8100 Laser Imager 1-2. . . . . . . . . . . . . . . . . . . .
Dryview 8100 PACS Link Laser Imager 1-2. . . . . . . . . .
Keypad Features 1-3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
How the DryView 8100 Laser Imager Works 1-4. . . . . . . . .
Automatic Image Quality Control 1-4. . . . . . . . . . . . . . . . . . .
Manual Mode of Operation 1-4. . . . . . . . . . . . . . . . . . . . . . . . .
How This Manual is Organized 1-6. . . . . . . . . . . . . . . . . . . . .
Controls and Indicators 2-1. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Main Cabinet Controls and Indicators 2-1. . . . . . . . . . . . . . .
Local Panel Functions 2-2. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Operation and Maintenance 3-1. . . . . . . . . . . . . . . . . . . . . . . . .
System Power Up 3-1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Methods for Acquiring and Printing Images 3-2. . . . . . . . . .
Methods for Adjusting Image Density and Contrast 3-2. . .
Adjusting Density from the Local Panel 3-3. . . . . . . . . . . . . .
Adjusting Contrast from the Local Panel 3-4. . . . . . . . . . . . .