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Illumipro-10 Compliance Testing Summary - Meridian Bioscience illumipro-10 Manual Del Operador

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Manuel de l'opérateur 
 
 
Annexe V

illumipro-10 Compliance Testing Summary

 
The illumipro-10 has been tested and found to be in compliance with the following requirements and
Standards:
Standard
IEC 61010-1
IEC 61010-2-010
IEC 61010-2-081
IEC 61010-2-101
UL 61010-1
CSA C22.2# 61010-1
CSA C22.2#61010-2-010
CSA C22.2#61010-2-081
CSA C22.2#61010-2-101
illumipro-10 Manuel de l'opérateur: FRANÇAIS
Copyright© Meridian Bioscience, Inc.
SN11007, REV. 07/2010
All manuals and user guides at all-guides.com
Safety requirements for electrical equipment for measurement, control, and
laboratory use - Part 1: General requirements
Safety requirements for electrical equipment for measurement, control, and
laboratory use - Part 2-010: Particular requirements for laboratory equipment
for the heating of materials
Safety requirements for electrical equipment for measurement, control, and
laboratory use - Part 2-081: Particular requirements for automatic and semi-
automatic laboratory equipment for analysis and other purposes
Safety requirements for electrical equipment for measurement, control and
laboratory use - Part 2-101: Particular requirements for in vitro diagnostic
(IVD) medical equipment
UL standard for Safety Electrical Equipment for Measurement, Control, and
Laboratory Use - Part 1: General Requirements
UL standard for Safety Electrical Equipment for Measurement, Control, and
Laboratory Use - Part 1: General Requirements
Safety requirements for electrical equipment for measurement, control, and
laboratory use - Part 2-010: Particular requirements for laboratory equipment
for the heating of materials
Safety Requirements for Electrical Equipment for Measurement, Control and
Laboratory Use - Part 2-081: Particular Requirements for Automatic and
Semi-Automatic Laboratory Equipment for Analysis and Other Purposes
Safety Requirements for Electrical Equipment for Measurement, Control, and
Laboratory use - Part 2-101: Particular Requirements for In Vitro Diagnostic
(IVD) Medical Equipment
Description
Page 67

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