Carestream Health 5700 DRYVIEW 5700 Laser Imager User Manual 9G3888 en A

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Document ID	1462985
Application ID	v2KEe78k6za9rysHmcLNJw==
Document Description	User Manual 2
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Document Type	User Manual
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Filesize	44.72kB (558952 bits)
Date Submitted	2011-05-11 00:00:00
Date Available	2011-05-12 00:00:00
Creation Date	2011-03-23 10:06:24
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Document Title	9G3888_en_A.book
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Document Author:	l486095

Safety Manual
Carestream Health, Inc.
150 Verona Street
Rochester, New York 14608
© Carestream Health, Inc., 2011
Pub No. 9G3888_en
Rev. A
Table of Contents
Safety and Related Information
Safety, Warnings, and Cautions ................................................................................................. 1-1
Safety Labels ......................................................................................................................... 1-4
Safety and Health Compliance ................................................................................................... 1-8
Safety..................................................................................................................................... 1-8
EMC ...................................................................................................................................... 1-9
EU Directives ...................................................................................................................... 1-14
CE Marking ......................................................................................................................... 1-14
Please Note.......................................................................................................................... 1-15
Imager Specifications ............................................................................................................... 1-15
Publication History................................................................................................................... 1-15
Safety and Related Information
Safety, Warnings, and Cautions
Please read and understand all instructions before using this product.
RISK OF ELECTRIC SHOCK:
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
attempt to service or repair the laser imager yourself to avoid
exposure to dangerous voltage, laser beam, or other danger. Always
call an authorized service provider for any service or repair.
• Do not operate equipment with a damaged power cord.
• Do not use an extension cord to power this equipment.
• Do not operate equipment with any of the safety interlocks
overridden.
• Position the power cord so it will not be tripped over or pulled.
• Connect this equipment to a grounded wall outlet.
• A power cord is provided with this equipment. All countries must
use an Agency-approved power cord with plug type suitable for the
country of use. Contact a qualified dealer for help.
DANGER: THIS EQUIPMENT CONTAINS MOVING PARTS
THAT MAY BE ACCESSIBLE TO THE USER. LOOSE
CLOTHING, JEWELRY OR LONG HAIR MAY
CAUSE PERSONAL INJURY OR DAMAGE TO THE
EQUIPMENT.
• Do not operate equipment with the covers open.
DANGER: THIS EQUIPMENT IS NOT CONTAINED IN A
SEALED CABINET. DO NOT USE THIS EQUIPMENT
IN LOCATIONS WHERE IT CAN COME IN
CONTACT WITH LIQUIDS, INCLUDING BODY
FLUIDS.
CAUTION:
Do not use a cell phone within 2 m of a laser imager. This
proximity includes any imager behind a wall adjacent to your
location.
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Safety and Related Information
CAUTION:
Do not use a microwave oven within 4 m of a laser imager.
Electromagnetic radiation from a microwave oven is only an
issue if after the oven door is closed and latched, the seal does
not maintain an electromagnetic tight fit between the oven
door and oven main housing. Determining if the seal has an
electromagnetic tight fit requires special detection equipment.
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 uses a DICOM network port, and is intended
to connect to other medical devices. It is not intended to be
connected directly outside the building. Only qualified
personnel may provide installation and service.
CAUTION:
This device should not be used in close contact with MRI
devices, due to possible very high magnetic fields near an MRI
unit. The magnetic field in the area where this equipment is
installed must be less than 50 G.
CAUTION:
Do not substitute or modify any part of this equipment.
CAUTION:
Federal law prohibits dispensing without a prescription.
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. These limits are designed to provide reasonable
protection against harmful interference when the equipment is
operated in a commercial environment. This equipment
generates, uses, and can radiate radio frequency energy and, if
not installed and used in accordance with the User Guide and
other User Documentation, may cause harmful interference to
radio communications. Operation of this equipment in a
residential area is likely to cause harmful interference in which
case the user will be required to correct the interference at his
own expense.
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Safety and Related Information
CAUTION:
Changes or modifications not expressly approved by the party
responsible for compliance could void the user’s authority to
operate the equipment.
CAUTION:
Do not use isopropyl alcohol to clean the exterior surfaces of
the laser imager.
CAUTION:
In the U.S., exhausted filters are considered to be
non-hazardous waste according to the US Environmental
Protection Agency Resource Conservation Recovery Act
(RCRA). Municipality owned and licensed solid waste
management facilities are an appropriate disposal option.
Contact your local or state solid waste authorities to determine
if additional disposal requirements apply. In other regions,
contact local or regional solid waste authorities for proper
disposal guidance.
CAUTION:
Lithium batteries should only be replaced by an authorized
service provider. The laser imager uses a lithium battery to
power the clock and calendar circuitry. THERE IS A
DANGER OF EXPLOSION IF THE BATTERY IS
REPLACED INCORRECTLY. The battery must be replaced
only with the same or equivalent type. The U.S. EPA’s RCRA
does not regulate disposal of this lithium battery. Users should
discard spent batteries in municipal trash unless their
community offers a battery collection program. In other
regions, contact local or regional solid waste authorities for
proper disposal guidance.
LASER WARNING:
The equipment uses an invisible laser beam with a maximum
power of 120 milliwatts. Laser radiation may be present when the
machine operates without the rear cover installed. Covers with
this label may only be removed by an Authorized Service
Provider. USE OF CONTROLS OR ADJUSTMENTS, OR
PERFORMANCE OF PROCEDURES OTHER THAN THOSE
SPECIFIED HEREIN, MAY RESULT IN EYE DAMAGE.
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Safety and Related Information
Safety Labels
Safety labels are attached to the laser imager in compliance with
international standards.
English Text on Labels
Some names on the labels are shortened and left in English. Below is a
key to understand the meanings of the shortened words on the labels:
Symbol on label
Definition
Model Number
Serial Number
CAT Number
Manufactured Date
Manufactured By
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Safety and Related Information
Labels
DryView Laser Imager
DryView 6800
68000501
7F2301
6551576
August 2007, 2007 08
100/120/200/220/240V
12/12/7/7/7A
50/60Hz
311346
3JZT
Carestream Health, Inc.
Rochester, NY 14608
TM: DryView
7F3118.E
This label shows the serial number and model number of the laser imager
along with other important data items. (The label shown above is an
example serial plate label.)
Laser Radiation Warning Labels
Class 3B invisible laser radiation. This label states: “When
open and interlocks defeated, avoid exposure to the beam.”
Hazard symbol
Laser Specifications
Type
Scanning (moving) laser beam emitting from a
diode
Wavelength
810 +/- 10 nanometers
Maximum power
120 milliwatts
Beam divergence
from Laser Diode
Minimum: 5 degrees, maximum: 32 degrees
High Voltage Warning Label
This warning label indicates that high voltage is present under panels or
enclosures where labels are attached. These panels may only be removed
by an Authorized Service Provider.
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Safety and Related Information
Laser Imager Back Panel
Agency Statements
Product Label. This label states that the imager is a Laser Imaging Printer.
Agency Symbols and Class 1 Laser Safety.
High voltage. Indicates that high voltage is present under panels where the label
is attached. Only an Authorized Service Provider should attempt access.
Static Sensitive Equipment. Identifies static-sensitive components. Connect a
personal grounding strap to the appropriate ground before servicing this laser
imager. These panels may only be removed by an Authorized Service Provider.
Radio Frequency Energy. Indicates that the laser imager can radiate radio
frequency energy. If not installed and used in accordance with the instructions,
the laser imager may cause harmful interference to radio communications.
Class 1 Laser. Indicates that the laser imager complies with IEC requirements
for Class 1 Laser systems.
Grounding Reliability. This label states that grounding reliability can only be
achieved when the equipment is connected to an equivalent receptacle marked
“Hospital Only” or “Hospital Grade.”
Japanese Import License
FCC Compliance. Provides FCC ID and Industry Canada; describes
compliance.
NOTE: This label is not applicable for the 5700C Laser Imager.
Power Cord Inlet. Covers the power cord inlet when shipped from
manufacturing. Shows the voltage at which the laser imager must be operated.
The label is removed or moved during installation.
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Safety and Related Information
Hot Surface Labels
This label indicates that you must use care where the label is installed to
avoid possible burns.
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Safety and Related Information
Safety and Health Compliance
This equipment has been tested for and complies with the following
Safety and Emissions Standards. Certificates of Compliance and
Declarations of Conformity have been issued as shown below.
Safety
United States
FDA 21CFR 807 Subpart E - Premarket Notification
Procedures.
21 CFR 1040.10 Class I
Code of Federal Regulations Title 21 Food and Drugs
Chapter I Food and Drug Administration, Department of Health
and Human Services
Volume 8 - Parts 800 to 1299
Subchapter J - Radiology Health
Part 1040 - Performance Standards for Light Emitting Products
Section 10 - Laser Products
UL 60601-1: Medical electrical equipment - Part 1: General
requirements for safety.
IEC 60825-1 Ed. 2 (2007): Safety of laser products - Part 1:
Equipment classification, requirements and user’s guide.
Canada
CAN/CSA - C22.2 NO 60601-1 Ed. 2 - Medical electrical
equipment - Part 1: General requirements for safety.
IEC 60825-1 Ed. 2 (2007): Safety of laser products - Part 1:
Equipment classification, requirements and user’s guide.
Europe
EN60601-1 Ed. 2 - Medical electrical equipment - Part 1:
General requirements for safety.
EN60825-1 Ed. 2 (2007): Safety of laser products - Part 1:
Equipment classification, requirements and user's guide.
Rest of World
IEC 60601-1 Ed. 2 - Medical electrical equipment - Part 1:
General requirements for safety.
IEC 60825-1 Ed. 2 (2007): Safety of laser products - Part 1:
Equipment classification, requirements and user's guide.
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Safety and Related Information
EMC
United States
FCC Rules and Regulations, Title 47, Part 15, Subpart B, Class
A: Radio Frequency Devices: Unintentional Radiators.
This equipment has been tested and been 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.
FCC Rules and Regulations, Title 47, Part 15, Subpart C, Radio
Frequency Devices: Intentional Radiators. “FCC ID: U725700”
Canada
CAN/CSA-C22.2 NO. 60601-1-2-08 Medical Electric
Equipment - Part 1-2: General requirements for safety Collateral standard: Electromagnetic compatibility Requirements and Tests.
Intentional Radiation “IC: 7027A-5700”
This Class A digital apparatus complies with Canadian
ICES-003.
CET APPAREIL NUM ENRIQUE DE CLASSE A EST
CONFORME A LA NORME NMB-003 DU CANADA.
This Class A digital apparatus meets all requirements of the
Canadian Interference-Causing Equipment Regulations.
Europe
EN60601-1-2: Medical Electrical Equipment - Part 1-2:
General requirements for safety - Collateral standard:
Electromagnetic compatibility - Requirements and Tests.
Rest of World
IEC 60601-1-2: Medical Electrical Equipment - Part 1-2:
General requirements for safety - Collateral standard:
Electromagnetic compatibility - Requirements and Tests.
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Safety and Related Information
Europe and the Rest of World
Guidance and Manufacturer’s Declaration for Electromagnetic Emissions
The Laser Imaging System is intended for use in the electromagnetic environment specified below. The
customer or user of the Laser Imager should ensure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment - Guidance
RF emissions:
Group 1
The Laser Imager uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
Class A
The Laser Imager 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.
Class A
The Laser Imager is suitable for use everywhere, including those
establishments directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
Complies
The Laser Imager is suitable for use everywhere, including those
establishments directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
• EN55011
• CISPR 11
RF emissions:
• EN55011
• CISPR 11
Harmonics emissions:
• EN61000-3-2
• IEC 61000-3-2
Voltage fluctuations
and flicker emissions:
• EN61000-3-3
• IEC 61000-3-3
10
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Safety and Related Information
Guidance and Manufacturer’s Declaration for Electromagnetic Immunity
The Laser Imager is intended for use in the electromagnetic environment specified below. The
customer or user of the Laser Imager should ensure that it is used in such an environment.
Immunity Test
IEC 60601 Test
Level
Electrostatic
discharge (ESD):
6 kV contact
8 kV air
• EN61000-4-2
• IEC
61000-4-2
Electrical fast
transient/burst:
Compliance Level
6 kV contact
8 kV air
Electromagnetic Environment Guidance
Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
2 kV for power
supply lines
1 kV for
• EN61000-4-4
input/output lines
2 kV for power
Mains power quality should be that of a
supply lines
typical commercial or hospital
1 kV for input/output environment.
lines
Surge:
1 kV differential
mode
• EN61000-4-5
2 kV common
• IEC
mode
1 kV differential
Mains power quality should be that of a
mode
typical commercial or hospital
2 kV common mode environment.
Voltage dips,
short
interruptions and
voltage variations
on power supply
lines:
<5% U * (>95% dip in
U *) for 0.5 cycle
40% U * (60% dip in
U *) for 5 cycles
70% U * (30% dip in
U *) for 25 cycles
<5% U * (>95% dip in
U *) for 5 sec.
Mains power quality should be that of a
typical commercial or hospital
environment. If the user of the Laser
Imager requires continued operation
during power mains interruptions, it is
recommended that the Laser Imager be
powered from an uninterruptible power
supply or a battery.
3 A/m
Mains power quality should be that of a
typical commercial or hospital
environment.
• IEC
61000-4-4
61000-4-5
<5% U * (>95% dip
in Ut*) for 0.5 cycle
40% U * (60% dip
in U *) for 5 cycles
70% U * (30% dip
in U *) for 25 cycles
• EN61000-4-11
<5% U * (>95% dip
• IEC
in U *) for 5 sec.
61000-4-11
Power frequency
(50/60 Hz)
magnetic field:
3 A/m
• EN61000-4-8
• IEC
61000-4-8
* U is the a.c. mains voltage prior to application of the test level.
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11
Safety and Related Information
Guidance and Manufacturer’s Declaration for Electromagnetic Immunity
The Laser Imager is intended for use in the electromagnetic environment specified below. The
customer or user of the Laser Imager should ensure that it is used in such an environment.
Immunity Test
IEC 60601 Test
Level
Compliance Level
Electromagnetic Environment Guidance
Portable and mobile RF communications
equipment should be used no closer to any
part of the Laser Imager, including cables,
than the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz–80 MHz
3 Vrms
d = 1.17 P
Radiated RF
IEC 61000-4-3
3 v/m
80 MHz–2.5 GHz
3 v/m
d = 1.17 P
80 MHz–800 MHz
d = 2.33 P 800 MHz–2.5 GHz
d is the recommended separation distance
in meters (m).
P is the maximum output rating of the
transmitter in watts (W) according to the
transmitter manufacturer.
Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
surveya, should be less than the
compliance level in each frequency
rangeb.
Interference may occur in the vicinity of
equipment marked with the following
symbol:
NOTE:
• At 80 MHz and 800 MHz, the higher frequency range applies.
• These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects, and people.
aSee NOTE 1 on the top of the next page.
bSee NOTE 2 on the top of the next page.
12
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Safety and Related Information
Guidance and Manufacturer’s Declaration for Electromagnetic Immunity
Note 1
Field strengths from fixed transmitters, such as base station 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 fixed RF transmitters, an
electromagnetic site survey should be considered. If the measured field strength in
the location in which the Laser Imager is used exceeds the applicable RF
compliance level above, the Laser Imager should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the Laser Imager.
Note 2
Over the frequency range 150 kHz–80 MHz, field strengths should be less than 3 v/m.
Recommended separation distance between portable and mobile RF communications equipment and
the Laser Imager
The Laser Imager is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the Laser Imager can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communication equipment (transmitters) and the Laser Imager as recommended below, according
to the maximum output of the communications equipment.
Rated maximum output Separation distance (d) according to frequency of transmitter
power of transmitter (P) in meters (m)
in Watts (W)
150 kHz–80 MHz
80 MHz–800 MHz
800 MHz–2.5 GHz
d = 1.17 P
d = 1.17 P
d = 2.33 P
0.01
0.1
10
100
For transmitters rated at a maximum output power not listed above, the recommended separation distance d
in meters (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 reflection from structures, objects, and people.
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9G3888_en
13
Safety and Related Information
EU Directives
93/42/EEC Title: Council Directive Concerning Medical Devices.
1999/5/CE Title: Council Directive Concerning Radio Equipment and
Telecommunications Terminal Equipment.
Recycling Label
In the European Union, this symbol indicates that when the last user
wishes to discard this product, it must be sent to the appropriate facilities
for recovery and recycling. Contact your local authorized representative
for additional information.
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 Carestream Health, Inc. European Representative
at:
Carestream Health France
1, rue Galilée
93192 NOISY-LE-GRAND CEDEX
France
14
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Safety and Related Information
Please Note
The information contained herein is based on the experience and
knowledge relating to the subject matter gained by the manufacturer
prior to publication. No patent license is granted by this information. The
manufacturer reserves the right to change this information without notice
and makes no warranty, express or implied, with respect to this
information. The manufacturer 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 the manufacturer’s
negligence or other fault.
Specifications
See the User’s Guide.
Publication History
Revision
2011-03-17
Date
2011-03-17
9G3888_en
Reason for Change
First release
15


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