BS 5736-6:1983
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Evaluation of medical devices for biological hazards Methods of test for sensitization; assessment of the potential of medical devices to produce delayed contact dermatitis
Hardcopy , PDF
15-05-1996
English
31-10-1983
Foreword
Committees responsible
Methods
1 Scope
2 Definitions
3 Animals and husbandry
4 Preparation of extracts
5 Preparation of ingredients
6 Test procedures
7 Presentation of results
8 Assessment of results
Table
1 Classification system for skin reactions
Figure
1 Locations of intradermal injection sites for method 1
Gives scope, definitions, animals and husbandry, preparation of extracts of final products, preparation of ingredients, test procedures, presentation of results and assessment of result.
Committee |
CH/194
|
DocumentType |
Standard
|
Pages |
10
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
UNE-EN 4692:2017 | Identical |
BS 6788-1:1986 | Neurosurgical implants Specification for sterile, single-use hydrocephalus shunts and components |
BS 5736-1:1979 | Evaluation of medical devices for biological hazards Guide for the selection of biological methods of test |
BS 2463-1:1990 | Transfusion equipment for medical use Specification for collapsible containers for blood and blood components |
BS 5736-7:1983 | Evaluation of medical devices for biological hazards Method of test for skin irritation of extracts from medical devices |
BS 2574-1:1991 | Lower limb orthoses Guide to the design and manufacture of lower limb orthoses, excluding foot orthoses |
BS 1695-1:1990 | Urological catheters Specification for sterile, single-use urethral catheters of the Nélaton and Foley types |
BS 5736-2:1990 | Evaluation of medical devices for biological hazards Methods of testing by tissue implantation |
BS 4843:1987 | Specification for sterile intravascular cannula units for single use |
BS 2463-2:1989 | Transfusion equipment for medical use Specification for administration sets |
BS 7253-3:1990 | Non-metallic materials for surgical implants Specification for surgical implants made of heat-vulcanized silicone elastomer |
BS 3531-16:1985 | Surgical implants Specification for surgical implants made of heat-vulcanized silicone elastomer |
BS 1695-2:1990 | Urological catheters Specification for sterile, single-use urethral catheters of the Tiemann, whistle tip, 3-way and haematuria types |
BS 5736-1:1989 | Evaluation of medical devices for biological hazards Guide for the selection of biological methods of test |
BS 5736-4:1981 | Evaluation of medical devices for biological hazards Method of test for intracutaneous reactivity of extracts from medical devices |
BS 5736-1:1979 | Evaluation of medical devices for biological hazards Guide for the selection of biological methods of test |
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 5736-8:1984 | Evaluation of medical devices for biological hazards Method of test for skin irritation of solid medical devices |
BS 5736-7:1983 | Evaluation of medical devices for biological hazards Method of test for skin irritation of extracts from medical devices |
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