Directive 2012/19/Eu: Waste Electrical And Electronic Equipment; Directive 98/79/Ec: In Vitro Diagnostics (If Labeled For This Use); Electromagnetic Interference And Susceptibility; Usa Fcc Class A - Biotek BioStack 4 Operator's Manual

Directive 2012/19/EU: Waste Electrical and Electronic Equipment

Disposal Notice: Dispose of the instrument according to Directive 2012/19/EU,
"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
n
Traceability to the U.S. National Institute of Standards and Technology (NIST).
n
EN 61010-2-101 Particular requirements for in vitro diagnostic (IVD) medical
equipment.

Electromagnetic Interference and Susceptibility

USA FCC CLASS A

RADIO AND TELEVISION INTERFERENCE
NOTE: 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. 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 their own expense.
In order to maintain compliance with FCC regulations shielded cables must be
used with this equipment. Operation with non-approved equipment or
unshielded cables is likely to result in interference to radio and television
reception.
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'émet pas de 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.
Electromagnetic Interference and Susceptibility| xvii
BioTek Instruments, Inc.