Kodak Dryview 8300 Manual de usuario

User Guide

Kodak DryView 8300 Laser Imager

1340744

41-1202-0185-4

3/02 Rev. E

Classification, Warnings, and Cautions

2002 March Rev. E 1340744

Classification, Warnings, and Cautions

for Kodak DryView 8300 Laser Imager

Read and understand all instructions before using.

Classifications

UL Classified

File Number E163816

Control Number 48VF

Medical Equipment

UL 2601-1 CAN/CSA No. 601.1

!Classified by Underwriters Laboratories Inc.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.

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.

!WARNING

Not protected against ingress of liquids, including bodily fluids.

User Guide

ii 1340744 2002 March Rev. E

!WARNING

For continued protection against fire, replace fuses only with fuses of the same type

and fuse rating.

8300-128A

Avoid touching the developer drum when removing film jams from the imager. The

developer drum may become hot during extended imager operation.

!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

U.S. Federal law restricts sale of this device to or on the order of a licensed health

care practitioner.

!CAUTION

Grounding reliability can only be achieved when this equipment is connected to an

equivalent receptacle marked “Hospital Only” or “Hospital Grade.”

!CAUTION

This equipment is intended to connect to other medical devices. Installation and

service maintenance are to be performed only by qualified service personnel. If a

Kodak PACS Link 9410 Acquisition System is used with the Kodak DryView 8300

Laser Imager, the Kodak PACS Link 9410 Acquisition System must be installed no

closer than 1.83 meters from a patient bed or chair.

Classification, Warnings, and Cautions

iii

2002 March Rev. E 1340744

!CAUTION

This equipment has been tested and found to comply with the limits for a Class A

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.

!CAUTION

Avoid Laser Beam

This equipment employs an invisible 25 milliwatt laser beam. 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.

There are no “user” serviceable parts in this machine other than the developer filter.

!CAUTION

Do not substitute or modify any part of this equipment without approval of Eastman

Kodak Company.

User Guide

iv 1340744 2002 March Rev. E

!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

Safety, EMC, and CE Marking Compliance

2002 March Rev. E 1340744

Safety, EMC, 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 for the following areas:

Australia/New Zealand:

AS/NZS 3548:1992

AS 2211-1991

AS3200.1-1990/NZS 6150:1990

Canada:

C108.8-M1983 Class A (Conducted and Emitted EMI/RFI Specs)

CAN/CSA-C22.2 No. 601.1

Europe:

EN50082-1 (EMC)

EN55011 Group 1 Class A (Medical Device Safety)

EN60601-1 (Safety Medical Equipment)

EN60825:1991 (Laser Safety)

EN61000-3-2: Harmonics

IEC61000-3-3:1995 Voltage Fluctuations/Flicker

IEC61000-4-2:1995 ESD

IEC61000-4-3:1996 Radiated Radio Frequency

IEC61000-4-4:1995 Fast Transient/Burst

IEC61000-4-5:1995 Surge

IEC61000-4-6: Conducted Radio Frequency

IEC61000-4-8: Power Frequency Magnetic Fields

IEC61000-4-11: Dips and Interrupts

User Guide

vi 1340744 2002 March Rev. E

Japan:

CISPR 11 Group 1 Class A

USA:

FCC (47CFR15B) Class A (Conducted and Emitted EMI/RFI Specs)

FDA: 21CFR CH-1. SCH-J. Part 1040 (Performance Standards for Light

Emitting Products)

UL 2601-1 (Medical and Dental Equipment)

IEC 601-1-2 (EMC for Medical Devices)

IEC 825-1 (Laser Safety)

ROW:

CISPR 11 Group 1 Class A (Conducted and Emitted EMI/RFI Specs)

IEC 1000-4-2, 3, 4, 5, 6, 8, and 11

CE Marking:

This equipment is part of a medical system and conforms to the medical safety and

EMC in EN60601-1, EN60601-1-2, and the 93/42/EEC, MDD (Medical Device

Directive).

A Technical File and Declaration of Conformity with the Essential Requirements of

the Medical Device Directive have been prepared and signed by the appropriate

personnel and are located at:

Kodak GmbH

Quality Services and Product Safety

70323 Stuttgart Germany

Telephone 49-0711-40-06-5291

Safety, EMC, and CE Marking Compliance

vii

2002 March Rev. E 1340744

FCC:

This device complies with the limits for a Class A digital device listed in Part 15 of

the FCC Rules. Operation is subject to the following two conditions:

(1) This device may not cause harmful interference, and

(2) This device must accept any interference received, including interference that

may cause undesired operation.

Industry Canada:

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.

EU:

This equipment complies with the January 1996 EU Community EMC Requirements,

per EN55011 Class A.

User Guide

viii 1340744 2002 March Rev. E

BLANK PAGE

Warnhinweise

2002 März Rev. E 1340744_DE i

Warnhinweise für das Kodak DryView 8300 Laser Imaging-System

:$5181*

Dieses Gerät wird mit Spannungen betrieben, die elektrische Schläge, Ver-

brennungen und tödliche Verletzungen verursachen können.

Vor der Wartung ist der Netzstecker zu ziehen. Niemals am Kabel ziehen, wenn Sie den

Stecker aus der Steckdose ziehen. Den Stecker fassen und herausziehen.

Das Gerät nicht mit einem beschädigten Netzkabel betreiben.

Beim Einsatz dieses Geräts kein Verlängerungskabel verwenden.

Das Netzkabel so verlegen, daß keine Stolpergefahr besteht und es nicht beschädigt wird.

Dieses Gerät darf nur an eine geerdete Steckdose angeschlossen werden.

Eine Steckdosenleiste nicht auf den Boden legen, sondern an einer Wand oder an der Un-

terseite eines Tisches befestigen.

:$5181*

Das Gerät vor dem Eindringen von Flüssigkeiten schützen.

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