Biotek MicroFlo select, Operator'S Manual

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xiv | MicroFlo Select™
BioTek Instruments, Inc.
Directive 2002/95/EC: Reduction of Hazardous Substances (RoHS)
This instrument is exempt from RoHS requirement per Article 2, Category 9.
Directive 98/79/EC: In Vitro Diagnostics

Product registration with competent authorities

Traceability to the U.S. National Institute of Standards and Technology (NIST)
Electromagnetic Interference and Susceptibility
USA FCC CLASS A
Warning: 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 their own expense.
Canadian Department of Communications Class A
This digital apparatus does not exceed Class A limits for radio emissions from
digital apparatus set out in the Radio Interference Regulations of the Canadian
Department of Communications.
Le present appareil numerique n'met pas du bruits radioelectriques depassant les
limites applicables aux appareils numerique de la Class A prescrites dans le
Reglement sur le brouillage radioelectrique edicte par le ministere des
Communications du Canada.
User Safety
This device has been type tested by an independent laboratory and found to meet the
requirements of the following:
 Underwriters Laboratories UL 61010-1: 2004