BS 2463-1:1990
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Transfusion equipment for medical use Specification for collapsible containers for blood and blood components
Hardcopy , PDF
03-30-2007
BS EN ISO 3826-1:2013
BS ISO 3826-3 : 2006
BS EN ISO 1135-4:2015
BS EN ISO 3826-3:2007
BS EN ISO 1135-4:2004
BS EN ISO 3826-1:2003
English
12-31-1990
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Committees responsible
Foreword
Specification
1 Scope
2 Definitions
3 General
4 Design
5 Anticoagulants
6 Packaging
7 Labelling and marking
Appendices
A Method of test for water vapour transmission
B Method of test for haemolytic effects
C Methods of test for chemical extracts
D Preparation of test solutions for the pyrogenicity
test
E Method of test for rate of collection
F Recommendations for packaging
Figure
1 Example of apparatus for applying the pressure
Requirements for collapsible non-vented containers for blood components. Also covers transfer packs for processing or administration of blood or its components.
| Committee |
CH/212
|
| DevelopmentNote |
Supersedes 86/51017 DC and BS 2463(1962) (04/2002)
|
| DocumentType |
Standard
|
| Pages |
14
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| BS 2463-2:1989 | Transfusion equipment for medical use Specification for administration sets |
| BS 5736-6:1983 | Evaluation of medical devices for biological hazards Methods of test for sensitization; assessment of the potential of medical devices to produce delayed contact dermatitis |
| BS 5736-4:1981 | Evaluation of medical devices for biological hazards Method of test for intracutaneous reactivity of extracts from medical devices |
| BS 5736-5:1982 | Evaluation of medical devices for biological hazards Method of test for systemic toxicity; assessment of pyrogenicity in rabbits of extracts from medical devices |
| BS 5736-3:1981 | Evaluation of medical devices for biological hazards Method of test for systemic toxicity; assessment of acute toxicity of extracts from medical devices |
| BS 2463-2:1989 | Transfusion equipment for medical use Specification for administration sets |
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