DIN EN 556-1:2002-03
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Sterilization of medical devices - Requirements for medical devices to be designated \"STERILE\" - Part 1: Requirements for terminally sterilized medical devices; English version of DIN EN 556-1
Hardcopy , PDF
09-01-2024
03-01-2002
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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 |
Superseded
|
| SupersededBy | |
| Supersedes |
| 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 |
| ONORM EN 556-1 : 2006 | Identical |
| EN 556-1:2001/AC:2006 | 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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