Hivatkozási szám

MSZ EN ISO 22442-1:2016

Dokumentumazonosító

162488

Cím

Állati szöveteket és származékaikat felhasználó orvostechnikai eszközök. 1. rész: A kockázatirányítás alkalmazása (ISO 22442-1:2015)

Angol cím

Medical devices utilizing animal tissues and their derivatives. Part 1: Application of risk management (ISO 22442-1:2015)

Alkalmazási terület

This part of ISO 22442 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 nonviable. 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. This part of ISO 22442 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 a) contamination by bacteria, moulds or yeasts; b) contamination by viruses; c) contamination by agents causing Transmissible Spongiform Encephalopathies (TSE); d) material responsible for undesired pyrogenic, immunological or toxicological reactions. For parasites and other unclassified pathogenic entities, similar principles can apply. This part of ISO 22442 does not stipulate levels of acceptability which, because they are determined by a multiplicity of factors, cannot be set down in such an International Standard except for some particular derivatives mentioned in Annex C. Annex C stipulates levels of TSE risk acceptability for tallow derivatives, animal charcoal, milk and milk derivatives, wool derivatives and amino acids. This part of ISO 22442 does not specify a quality management system for the control of all stages of production of medical devices. This part of ISO 22442 does not cover the utilization of human tissues in medical devices. NOTE 1 It is not a requirement of this part of ISO 22442 to have a full quality management system during manufacture. However, attention is drawn to International Standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices. NOTE 2 For guidance on the application of this part of ISO 22442, see Annex A.

ICS

11.100.99 A kísérleti orvostudományhoz kapcsolódó egyéb szabványok

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2016-04-01

A visszavonás napja

2021-05-01

Forrás

idt ISO 22442-1:2015; idt EN ISO 22442-1:2015

Előd

MSZ EN ISO 22442-1:2008

Utód

MSZ EN ISO 22442-1:2021

Módosítás

Kiegészítő információk

SZK-közlemények

Kapcsolódó európai jogszabály

93/42/EGK A TANÁCS 93/42/EGK IRÁNYELVE (1993. június 14.) az orvostechnikai eszközökről (MDV93)

A szabvány

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