BS 2463-2:1989
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by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 administration sets
Hardcopy , PDF
03-30-2007
BS ISO 3826-3 : 2006
BS EN ISO 3826-3:2007
BS EN ISO 1135-4:2015
BS EN ISO 3826-1:2013
BS EN ISO 1135-4:2004
BS EN ISO 3826-1:2003
English
04-28-1989
Foreword
Committees responsible
Specification
1. Scope
2. General
3. Closure-piercing and air-inlet devices
4. Filters
5. Drip chamber
6. Tubing
7. Flow regulator
8. Leakage
9. Performance
10. Particulate contamination
11. Burette for use in administration sets
12. Packaging
13. Labelling
Appendices
A. Method of test for haemolytic effects
B. Methods of test for chemical extracts
C. Preparation of test solutions for the pyrogenicity
test
D. Method of test for flow rate when using an air-
inlet device
E. Method of test for efficiency of the filter
F. Injection site resealing test
Table
1. Size and scale intervals for burettes
Figures
1. Diagram of typical blood administration set
2. Diagram of typical burette administration set
3. Diagram of typical air inlet assembly and
combined air inlet
4. Typical graduated scales for burettes for use in
burette administration sets
5. Reference filter assembly
Administration sets, including burette sets, for general use with blood, blood components and fluids other than blood.
Committee |
CH/212
|
DevelopmentNote |
Supersedes 85/55982 DC and BS 2463(1962) (06/2005)
|
DocumentType |
Standard
|
Pages |
18
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
ISO 1135:1977 | Similar to |
BS 2463-1:1990 | Transfusion equipment for medical use Specification for collapsible containers for blood and blood components |
BS 6314:1990 | Specification for sterile, single-use, naso-enteric feeding tubes and ancillary equipment |
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 2463-1:1990 | Transfusion equipment for medical use Specification for collapsible containers for blood and blood components |
BS 3930-1(1987) : AMD 8072 | CONICAL FITTINGS WITH A 6% (LUER) TAPER FOR SYRINGES, NEEDLES AND OTHER MEDICAL EQUIPMENT - SPECIFICATION FOR GENERAL REQUIREMENTS |
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