NF EN 12442-1

NF EN 12442-1

December 2000
Standard Cancelled

Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 1 : analysis and management of risk

Le présent document complète la norme NF EN 1441 (Dispositifs médicaux Analyse des risques) en décrivant des exigences et des conseils supplémentaires pour des dispositifs médicaux utilisant des tissus d'origine animale non viables ou rendus non viables. Les principes généraux décrits sont réputés s'appliquer à tous les virus et agents transmissibles. Ce document s'inscrit dans une norme en trois parties. La partie 2 décrit les prescriptions relatives aux contrôles de l'origine, de la collecte et du traitement des tissus animaux. La partie 3 spécifie les exigences relatives à la validation de l'élimination et/ou de l'inactivation des virus et autres agents transmissibles lors de la fabrication des dispositifs médicaux.

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Main informations

Collections

National standards and national normative documents

Publication date

December 2000

Number of pages

20 p.

Reference

NF EN 12442-1

ICS Codes

11.040.01   Medical equipment in general

Classification index

S97-601-1

Print number

1 - 28/04/2004

European kinship

EN 12442-1:2000
Sumary
Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 1 : analysis and management of risk

Le présent document complète la norme NF EN 1441 (Dispositifs médicaux Analyse des risques) en décrivant des exigences et des conseils supplémentaires pour des dispositifs médicaux utilisant des tissus d'origine animale non viables ou rendus non viables. Les principes généraux décrits sont réputés s'appliquer à tous les virus et agents transmissibles. Ce document s'inscrit dans une norme en trois parties. La partie 2 décrit les prescriptions relatives aux contrôles de l'origine, de la collecte et du traitement des tissus animaux. La partie 3 spécifie les exigences relatives à la validation de l'élimination et/ou de l'inactivation des virus et autres agents transmissibles lors de la fabrication des dispositifs médicaux.
Standard replaced by (1)
NF EN ISO 22442-1
March 2008
Standard Cancelled
Medical devices utilizing animal tissues and their derivatives - Part 1 : application of risk management

ISO 22442-1:2007 applies to medical devices other than in vitro diagnostic medical devices manufactured utilizing materials of animal origin, which are non-viable or have been rendered non-viable. It specifies, in conjunction with ISO 14971, a procedure to identify the hazards and hazardous situations associated with such devices, to estimate and evaluate the resulting risks, to control these risks, and to monitor the effectiveness of that control. Furthermore, it outlines the decision process for the residual risk acceptability, taking into account the balance of residual risk, as defined in ISO 14971, and expected medical benefit as compared to available alternatives. ISO 22442-1:2007 is intended to provide requirements and guidance on risk management related to the hazards typical of medical devices manufactured utilizing animal tissues or derivatives such as: contamination by bacteria, moulds or yeasts; contamination by viruses; contamination by agents causing Transmissible Spongiform Encephalopathies (TSE); material responsible for undesired pyrogenic, immunological or toxicological reactions.

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