Over deze norm
|Commissie||Biocompatibiliteit en biologisch onderzoek|
This part of ISO 10993 specifies tests for the following biological aspects; - genotoxicity, - carcinogenicity, and - reproductive and development toxicity. These are relevant in the biological evaluation of some categories of medical devices. Guidance on selection of tests is provided in ISO 10993-1. Where the need for the evaluation of the potentioal for genotoxicity, carcinogenicity or reproductive toxicity has been identified, they should be evaluated in accordance with this part of ISO 10993. Most tests included in this part of the Standard refer to the OECD guidelines for testing of chemicals. Reference to these tests is made by the term "OECD guideline(s)" followed by the appropriate test number(s). At the time of testing, these tests are to be performed according to current OECD guidelines.
|Nederlandse titel||Biologische evaluatie van medische hulpmiddelen - Deel 3: Beproevingen op genotoxiciteit, carcinogeniteit en voortplantingstoxiciteit|
|Engelse titel||Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity|
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