NF EN 60601-1/A2
NF EN 60601-1/A2

NF EN 60601-1/A2

December 1999
Standard Cancelled

Medical electrical equipment - Part 1 : general requirements for safety

Le présent amendement modifie et complète certaines définitions et articles de la norme NF EN 60601-1 (février 1991)

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Main informations

Collections

National standards and national normative documents

Publication date

December 1999

Number of pages

52 p.

Reference

NF EN 60601-1/A2

ICS Codes

11.040.01   Medical equipment in general

Classification index

C74-011/A2

Print number

1 - février 2000

International kinship

IEC 60601-1/A2:1995

European kinship

EN 60601-1/A2:1995
Sumary
Medical electrical equipment - Part 1 : general requirements for safety

Le présent amendement modifie et complète certaines définitions et articles de la norme NF EN 60601-1 (février 1991)
Replaced standards (3)
NF EN 60601-1/A11
NF EN 60601-1/A11
November 1993
Standard Cancelled
Medical electrical equipment - Part 1 : general requirements for safety

Le présent amendement modifie l'annexe ZA (normative) de la norme NF EN 60601-1 (février 1991).

NF EN 60601-1/A12
NF EN 60601-1/A12
November 1993
Standard Cancelled
Medical electrical equipment - Part 1 : general requirements for safety

Le présent amendement modifie deux valeurs du Tableau XVI de la norme NF EN 60601-1.

NF EN 60601-1/A12/AC
NF EN 60601-1/A12/AC
November 1999
Standard Cancelled
Rectificatif à la norme NF EN 60601-1/A12 de novembre 1993 (indice de classement : C74-011/A12)

Standard replaced by (1)
NF EN 60601-1
NF EN 60601-1
January 2007
Standard Current
Medical electrical equipment - Part 1 : general requirements for basic safety and essential performance

La présente Norme internationale s'applique à la SECURITE DE BASE et aux PERFORMANCES ESSENTIELLES des APPAREILS ELECTROMEDICAUX et des SYSTEMES ELECTROMEDICAUX, désignés ci-après sous le terme APPAREILS EM et SYSTEMES EM. Ce document entre dans le champ d'application de la Directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux et de la Directive n° 90/385/CEE relatives aux dispositifs médicaux implantables actifs.

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