STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 1: REQUIREMENTS FOR TERMINALLY STERILIZED MEDICAL DEVICES

Available format(s)

Hardcopy , PDF

Published date

01-01-2002

Publisher

German Institute for Standardisation (Deutsches Institut für Normung)

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
Annex ZA (informative) Clauses of this European Standard
addressing essential requirements or other
provisions of EU Directives
Bibliography

This standard is included in DIN HDBK 263, 406, 268 and 267/2. Specifies the requirements for a terminally-sterilized medical device to be designated 'STERILE'.

DevelopmentNote	Supersedes DIN EN 556. (02/2002)
DocumentType	Standard
Pages	10
PublisherName	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Current

Standards	Relationship
NS EN 556-1 : 2002 AC 2006	Identical
UNE-EN 556-1:2002	Identical
BS EN 556-1:2001	Identical
SN EN 556-1 : 2001 CORR 2006	Identical
NF EN 556-1 : 2002	Identical
NBN EN 556-1 : 2001 COR 2006	Identical
I.S. EN 556-1:2002	Identical
NEN EN 556-1 : 2001 C1 2006	Identical
UNI EN 556-1 : 2002	Identical

DIN HDBK 267/2 : 2ED 2014
VDI 5700 Blatt 1:2015-04	Reprocessing hazards - Risk management in reprocessing of medical devices - Measures for risk control
DIN HDBK 406 : 2ED 2016
DIN HDBK 263 : 4ED 2014
DIN HDBK 268 : 3ED 2015	NICHT AKTIVE MEDIZINPRODUKTE - HORIZONTALE, HARMONISIERTE EUROPAEISCHE NORMEN GEMAESS EU-RICHTLINIEN AUF DEM GEBIET DER MEDIZIN

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DIN EN 556-1:2002-03

Current

Table of Contents

Abstract

General Product Information

International Equivalents

Standards Referenced By This Book

Category

Subcategory

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