xii | Preface
Directive 73/23/EEC Low Voltage (Safety)
The system has been type-tested by an independent testing laboratory and was
found to meet the requirements of EC Directive 73/23/EEC for Low Voltage.
Verification of compliance was conducted to the limits and methods of the
following:
EN 61010-1 (2001) 2
nd
Edition. “Safety requirement for electrical equipment for
measurement, control and laboratory use. Part 1, General requirements.”
Directive 2002/96/EC: Waste Electrical and Electronic Equipment
Disposal Notice: This instrument contains printed circuit boards and wiring
with lead solder. Dispose of the instrument according to Directive
2002/96/EC, “on waste electrical and electronic equipment (WEEE)” or local
ordinances.
Directive 98/79/EC: In Vitro Diagnostics (if labeled for this use)
Product registration with competent authorities.
Traceability to the U.S. National Institute of Standards and Technology
(NIST):
Optical density measurements are traceable to NIST.
Electromagnetic Interference and Susceptibility
USA FCC CLASS A
Changes or modifications to this unit not expressly approved by the
manufacturer could void the user's authority to operate the
equipment.
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. Like
all similar equipment, 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 interference, in which case
the user will be required to correct the interference at his own expense.
BioTek
®
Instruments, Inc.
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