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WARNING:
In the USA or Canada, use the AC power cord according to the recommendation as below, in
order to comply with UL60601-1 and CAN/CSA C22.2 No. 601.1.
Case 1. Connect to the 120V receptacle of the room or the host equipment.
Use the attached AC power cord.
The AC power cord should be UL or CSA approved and consist of type SJT, size
16AWG, length 2.5m or shorter cord with IEC60320-1/C13 type, 125V 13A or higher
rating connector and NEMA 5-15 type, 125V 13A or higher rating, Hospital Grade plug.
Case 2. Connect to the 230V receptacle of the room or the host equipment.
The AC power cord should be UL or CSA approved and consist of type SJT, size
16AWG, length 2.5m or shorter cord with IEC60320-1/C13 type, 250V 13A or higher
rating connector and NEMA 5-15 type, 250V 13A or higher rating, Hospital Grade plug.
CAUTION:
Changes or modifications not expressly approved by the party responsible for compliance
could void the user's authority to operate the equipment.
NOTE:
This equipment has been tested and found to comply with the limits for a Class A digital de-
vice, 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
instruction manual, 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 or her own expense.
Information:
This class A digital apparatus complies with Canadian ICES-003.
"CLASSIFIED BY UNDERWRITERS LABORATORIES INC.®
WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN AC-
CORDANCE WITH UL60601-1 AND CAN/CSA C22.2 No. 601.1."
Indications according to IEC60601-1
1. Functions and intended usage of this product
This product receives signals from diagnostic imaging equipment or various signal equip-
ment, and automatically prints and ejects the received image data on the paper.
2. Classifi cation of this product
•
According to the type of protection against electric shock: Equipment energized from an
external electrical power source, Class I equipment
•
According to the degree of protection of the applied part against electric shock: - (No ap-
plied part)
•
According to the degree of protection against harmful ingress of water: Ordinary equip-
ment (Enclosed equipment without protection against ingress of water)
•
According to the degree of safety of application in the presence of a fl ammable anesthetic
mixture with air or with oxygen or nitrous oxide: Equipment not suitable for use in the pres-
ence of a fl ammable anesthetic mixture with air or with oxygen or nitrous oxide
•
According to the mode of operation: Continuous operation with intermittent loading
3.
CAUTION:
slot or ribbon cartridge loading slot. This product has mechanical parts (switches and roll-
ers) and parts that are heated to a very high temperature or sensitive to static electricity.
4.
CAUTION:
under any circumstances.
CAUTION:
5.
6. Follow the applicable laws and regulations in your country or region or the hospital rules
when disposing of this product or the accessories or consumables thereof.
Do not put your hand inside the product from the paper cassette loading
There are no user or fi eld serviceable components. Do not open covers
Use screws 5-mm long for main body installation.
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