Safety Information; Regulations - Canon CXDI-50G User Manual

For U.S.A.
Do not make any changes or modifications to the equipment unless otherwise specified in the
manual. If such changes or modifications should be made, you could be required to stop oper-
ation of the equipment.
NOTE: This equipment has been tested and found to comply with the limits for a Class A dig-
ital device, pursuant to Part 15 of the FCC rules.
These limits are designed to provide reasonable protection against harmful interfer-
ence when the equipment is operated in a commercial environment.
This equipment generates, uses, and can radiate radio frequency energy and, if not
installed ad used in accordance with the instruction manual, may cause harmful inter-
ference to radio communications.
Operation of this equipment in a residential area is likely to cause harmful interfer-
ence in which case the user will be required to correct the interference at his own
expense.
Use of shielded cable is required to comply with class A limits in Subpart B of Part 15 of FCC
rules.
!
This instrument is a CLASS I EQUIPMENT according to UL2601-1.
MEDICAL ELECTRICAL EQUIPMENT
WITH RESPECT TO ELECTRIC SHOCK,
FIRE AND MECHANICAL HAZARDS
ONLY IN ACCORDANCE WITH UL2601-1.
41C4
WITH RESPECT TO ELECTRIC SHOCK,
FIRE , MECHANICAL AND OTHER SPECIFIED HAZARDS ONLY
IN ACCORDANCE WITH CAN/CSA C22.2 NO. 601.1,
MEDICAL EQUIPMENT CERTIFIED FOR CANADA
For EU Countries
The following mark shows compliance of the instrument with Directive 93/42/EEC.
This instrument complies with the standards EN60601-1, EN60601-1-1, EN601-1-2, EN601-1-
3 and EN60601-2-32.
This instrument conforms to IEC 60601-1-2:2001.
This instrument is a CLASS I EQUIPMENT according to EN 60601-1.

Safety Information

Regulations

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