(1)
Safety Information
Regulations
For U.S.A.
Federal law restricts this device to sale by or on the order of an ophthalmologist or optometrist.
This instrument is a CLASS I EQUIPMENT and TYPE B APPLIED PARTS according to
UL2601-1.
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 operation 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 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 interfer-
ence in with 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. The following mark shows compliance of the instrument with Directive 93/42/EEC.
For Canada
This equipment complies with the Canadian ICES-003 class A specifications.
Summary of Contents for TX-F
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