SN EN ISO 3826-3:2008
Current
The latest, up-to-date edition.
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 3: BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES
Hardcopy
01-03-2008
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Dimensions and designation
5 Design
6 Requirements
7 Packaging
8 Labelling
9 Anticoagulant and/or preservative solution
Annex ZA (informative) - Relationship between
this European Standard
and the Essential Requirements
of EU Directive 93/42/EEC
Medical Device
ISO 3826-3:2006 specifies requirements, including performance requirements, for integrated features on plastic, collapsible, non-vented, sterile containers (blood bag systems).
| Committee |
INB/NK 2205
|
| DocumentType |
Standard
|
| Pages |
0
|
| PublisherName |
Swiss Standards
|
| Status |
Current
|
| Standards | Relationship |
| DIN EN ISO 3826-3:2008-03 | Identical |
| NS EN ISO 3826-3 : 1ED 2007 | Identical |
| NEN EN ISO 3826-3 : 2008 | Identical |
| ISO 3826-3:2006 | Identical |
| NF EN ISO 3826-3 : 2008 | Identical |
| I.S. EN ISO 3826-3:2007 | Identical |
| EN ISO 3826-3:2007 | Identical |
| BS EN ISO 3826-3:2007 | Identical |
| NBN EN ISO 3826-3 : 2008 | Identical |
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