NF EN 60601-2-18/A1

NF EN 60601-2-18/A1

February 2006
Standard Cancelled

Medical electrical equipment - Part 2-18 : particular requirements for the safety of endoscopic equipment

Le présent amendement ajoute une exclusion du paragraphe 56.3 c) de l'Amendement 2 de la Norme Générale. Il modifie le sommaire, l'introduction, les articles 1, 2, 6, 20, 42, 56, la figure 101 et les annexes L et AA de la NF EN 60601-2-18.Ce document entre dans le champ d'application de la Directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux.

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Main informations

Collections

National standards and national normative documents

Thematics

Sécurité, Gestion des risques et SST, QSE

Publication date

February 2006

Number of pages

13 p.

Reference

NF EN 60601-2-18/A1

ICS Codes

11.040.55   Diagnostic equipment
13.280   Radiation protection

Classification index

C74-318/A1

Print number

1 - 28/02/2006

International kinship

IEC 60601-2-18/A1:2000

European kinship

EN 60601-2-18/A1:2000
Sumary
Medical electrical equipment - Part 2-18 : particular requirements for the safety of endoscopic equipment

Le présent amendement ajoute une exclusion du paragraphe 56.3 c) de l'Amendement 2 de la Norme Générale. Il modifie le sommaire, l'introduction, les articles 1, 2, 6, 20, 42, 56, la figure 101 et les annexes L et AA de la NF EN 60601-2-18. Ce document entre dans le champ d'application de la Directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux.
Standard replaced by (1)
NF EN 60601-2-18
January 2016
Standard Current
Medical electrical equipment - Part 2-18 : particular requirements for basic safety and essential performance of endoscopic equipment

Le présent document s'applique à la SECURITE DE BASE et aux performances ESSENTIELLES des APPAREILS D'ENDOSCOPIE, ainsi qu'à leurs CONDITIONS DE RACCORDEMENT et D'INTERFACE. Le présent document doit être lu conjointement avec la NF EN 60601-1, de janvier 2007 et son amendement A1, de mars 2014. Le présent document entre dans le champ d'application de la directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux

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