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NF EN ISO 7376 : NOV 2009

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by

ANAESTHETIC AND RESPIRATORY EQUIPMENT - LARYNGOSCOPES FOR TRACHEAL INTUBATION

Withdrawn date

09-29-2021

Superseded by

NF EN ISO 7376:2020

Published date

01-12-2013

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Avant-propos
Introduction
1 Domaine d'application
2 Références normatives
3 Termes et définitions
4 Exigences générales
5 Exigences de performance
6 Lampe pour lame traditionnelle
7 Lampes pour laryngoscopes à éclairage par fibres optiques
8 Douilles pour lames traditionnelles
9 Nettoyage, désinfection et stérilisation
10 Marquage et étiquetage
11 Documents d'accompagnement
Annexe A (normative) - Méthode d'essai relative à la sécurité
         du contact de la lampe
Annexe B (normative) - Méthode d'essai relative à la
         résistance, à la rigidité et à l'éclairage
Annexe C (informative) - Marquages des dimensions de
         lames
Annexe D (informative) - Conceptions des lames de
         laryngoscope
Annexe E (informative) - Justification de l'inclusion de
         certaines exigences
Bibliographie

Gives general requirements for laryngoscopes and critical dimensions for the handle and lamp of hook-on type laryngoscopes. Applicable only to instruments with an electrical power source for illuminating the larynx, since electrical safety requirements may be more stringent for instruments connected to mains or external power packs.

DevelopmentNote
Indice de classement: S95-122. PR NF EN ISO 7376 November 2002. (12/2002) Supersedes NF EN 1819. (10/2004) PR NF EN ISO 7376 January 2008. (01/2008) PR NF EN ISO 7376 February 2009. (02/2009)
DocumentType
Standard
PublisherName
Association Francaise de Normalisation
Status
Withdrawn
SupersededBy

IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
ISO 5864:1993 ISO inch screw threads Allowances and tolerances
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process

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