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I.S. EN ISO 22442-1:2020

Current

Current

The latest, up-to-date edition.

Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

28-12-2020

Preview

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Risk management process
Annex A (informative) Guidance on the application of this document
Annex B (informative) Graphical representation of part of the risk management process for medical devices utilizing animal material
Annex C (normative) Special requirements for some animal materials considering the risk management for TSE agents
Annex D (informative) Information relevant to the management of TSE risk
Bibliography

This document 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.

Committee
TC 194
DocumentType
Standard
Pages
46
ProductNote
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
PublisherName
National Standards Authority of Ireland
Status
Current
Supersedes

Standards Relationship
ISO 22442-1:2020 Identical
EN ISO 22442-1:2020 Identical

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