Directive 2012/19/EU: Waste Electrical and Electronic Equipment
Disposal Notice:
Dispose of the instrument according to the Directive, “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.”
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 radioélectriques depassant les
limites applicables aux appareils numérique de la Class A prescrites dans le Réglement
sur le brouillage radioélectrique édicté par le ministère des Communications du Canada.
BioTek Instruments, Inc.
xx | Preface
Содержание Synergy H1
Страница 1: ...Hybrid Multi Mode Microplate Reader Synergy H1 TM Operator s Manual ...
Страница 2: ......
Страница 26: ...BioTek Instruments Inc xxiv Preface ...
Страница 52: ...Figure 2 9 Packing the dispense module accessories 26 Chapter 2 Installation BioTek Instruments Inc ...
Страница 53: ...Figure 2 10 Packing the dispense module Synergy H1 Operator s Manual Repackaging and Shipping Instructions 27 ...
Страница 54: ...BioTek Instruments Inc 28 Chapter 2 Installation ...
Страница 68: ...BioTek Instruments Inc 42 Chapter 3 Getting Started ...
Страница 132: ...BioTek Instruments Inc 106 Chapter 7 Instrument Qualification Process ...
Страница 180: ...Figure C 1 Top view 152 Appendix C Instrument Dimensions for Robotic Interface BioTek Instruments Inc ...