Iso 10993-3

Publication date : This standard contributes to the following Sustainable Development Goal :. CHF Buy. Life cycle Previously Withdrawn. Full report circulated: decision for new DIS ballot. Final text received or FDIS registered for formal approval. Proof sent to secretariat or FDIS ballot initiated: 8 weeks. Close of voting. Proof returned by secretariat. International Standard under systematic review. Under development. ISO specifies strategies for hazard identification and tests on medical devices for the following biological aspects: genotoxicity, carcinogenicity, and reproductive and developmental toxicity.

ISO is applicable for evaluation of a medical device whose potential for genotoxicity, carcinogenicity or reproductive toxicity has been identified. Check out our FAQs. This standard has been revised by ISO Abstract ISO specifies strategies for hazard identification and tests on medical devices for the following biological aspects: genotoxicity, carcinogenicity, and reproductive and developmental toxicity.

Guidance on selection of tests is provided in ISO Status : Withdrawn. Publication date :