NEN EN 556-2 : 2015
Current
The latest, up-to-date edition.
STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 2: REQUIREMENTS FOR ASEPTICALLY PROCESSED MEDICAL DEVICES
12-01-2013
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
Defines the requirements for an aseptically processed medical device to be designated 'STERILE'.
| DocumentType |
Standard
|
| PublisherName |
Netherlands Standards
|
| Status |
Current
|
| Standards | Relationship |
| DIN EN 556-2:2015-11 | Identical |
| BS EN 556-2:2015 | Identical |
| EN 556-2:2015 | Identical |
| I.S. EN 556-2:2015 | Identical |
| UNE-EN 556-2:2016 | Identical |
| UNI EN 556-2 : 2005 | Identical |
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