UNE-EN 556-2:2016
Superseded
View Superseded by
Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE" - Part 2: Requirements for aseptically processed medical devices
Hardcopy , PDF
Spanish, Castilian, English
20-01-2016
18-06-2025
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
Describes the requirements for an aseptically processed medical device to be designated 'STERILE'.
| Committee |
CTN 111
|
| DocumentType |
Standard
|
| Pages |
16
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| EN 556-2:2015 | Identical |
| NEN EN 556-2 : 2015 | Identical |
| BS EN 556-2:2015 | Identical |
| NBN EN 556-2 : 2015 | Identical |
| DIN EN 556-2:2015-11 | Identical |
| I.S. EN 556-2:2015 | Identical |
| NS EN 556-2 : 2003 | Identical |
| NF EN 556-2 : 2015 | Identical |
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