1. ISO 10993–1:2009 Biological evaluation of medical devices part 1: evaluation and testing in the risk management process.
2. ISO 10993–2:2006 Biological evaluation of medical devices part 2: animal welfare requirements.
3. ISO 10993–3:2003 Biological evaluation of medical devices part 3: tests for genotoxicity, carcinogenicity and reproductive toxicity.
4. ISO 10993–4:2002 Biological evaluation of medical devices part 4: selection of tests for interactions with blood.
5. ISO 10993–5:2009 Biological evaluation of medical devices part 5: tests for in vitro cytotoxicity.