Back to all regulations
EN ISO 10993-3in-force

EN ISO 10993-3:2014 — Biological evaluation of medical devices - Part 3: Genotoxicity, carcinogenicity and reproductive toxicity

EN ISO 10993-3:2014

Applies from 2011-01-01

Summary

EU MDR harmonised standard EN ISO 10993-3:2014: Biological evaluation of medical devices - Part 3: Genotoxicity, carcinogenicity and reproductive toxicity.

Scope

MDR (Regulation (EU) 2017/745) harmonised standard — Biological evaluation of medical devices - Part 3: Genotoxicity, carcinogenicity and reproductive toxicity.

Expert analysis

Save

Our compliance experts are preparing a detailed analysis for this regulation. Check back soon.

Want this analysis for your product?

Enter your product features once — ComplyMatrix maps all applicable EU regulations, obligations and testing requirements in minutes.