![Biotek 50 TS Скачать руководство пользователя страница 9](http://html.mh-extra.com/html/biotek/50-ts/50-ts_instructions-for-use-manual_2756089009.webp)
| ix
BioTek Instruments, Inc.
EN 61000-4-6, Conducted Disturbances from RFI
EN 61000-4-11, Voltage Dips, Short Interruptions and Variations
Directive 2014/35/EU Low Voltage (Safety)
The system has been type-tested by an independent testing laboratory and was
found to meet the requirements of this Directive. Verification of compliance was
conducted to the limits and methods of the following:
EN 61010-1, “Safety requirement for electrical equipment for measurement,
control and laboratory use. Part 1, General requirements.”
EN 61010-2-081, “Particular requirements for automatic and semi-automatic
laboratory equipment for analysis and other purposes.”
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.
•
Traceability to the U.S. National Institute of Standards and Technology (NIST).
•
EN 61010-2-101 Particular requirements for in vitro diagnostic (IVD) medical
equipment.