NF EN IEC 61010-2-101

NF EN IEC 61010-2-101

November 2022
Standard Current

Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101 : safety requirements for in vitro diagnostic (IVD) medical equipment

Le présent document s'applique aux appareils destinés aux applications médicales de diagnostic in vitro (DIV) , y compris aux appareils médicaux d'autotest DIV. Le présent document doit être lu conjointement avec la norme homologuée NF EN 61010-1, de janvier 2011.

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Main informations

Collections

National standards and national normative documents

Publication date

November 2022

Number of pages

22 p.

Reference

NF EN IEC 61010-2-101

ICS Codes

11.100.10   In vitro diagnostic test systems
11.040.55   Diagnostic equipment
19.080   Electrical and electronic testing

Classification index

C42-020-2-101

Print number

1

International kinship

IEC 61010-2-101:2018

European kinship

EN IEC 61010-2-101:2022
Sumary
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101 : safety requirements for in vitro diagnostic (IVD) medical equipment

Le présent document s'applique aux appareils destinés aux applications médicales de diagnostic in vitro (DIV) , y compris aux appareils médicaux d'autotest DIV. Le présent document doit être lu conjointement avec la norme homologuée NF EN 61010-1, de janvier 2011.
Replaced standards (1)
NF EN 61010-2-101
April 2017
Standard Cancelled
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101 : particular requirements for in vitro diagnostic (IVD) medical equipment

Le présent document s'applique aux appareils destinés aux applications médicales de diagnostic in vitro (DIV) , y compris aux appareils médicaux d'autodiagnostic DIV. Le présent document doit être utilisé conjointement avec la norme homologuée NF EN 61010-1, de janvier 2011. Le présent document entre dans le champ d'application de la Directive 98/79/CE du Parlement européen et du Conseil du 27 octobre 1998 relative aux dispositifs médicaux de diagnostic in vitro.

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