DIN EN 14683 [CURRENT] references following documents:
| Document number | Edition | Title |
|---|---|---|
| EN ISO 11737-1 | 2018-01 | Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018) More |
| ISO 22609 | 2004-12 | Clothing for protection against infectious agents - Medical face masks - Test method for resistance against penetration by synthetic blood (fixed volume, horizontally projected) More |
| EN ISO 10993-11 | 2018-05 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017) More |
| EN ISO 10993-13 | 2010-06 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010) More |
| EN ISO 10993-14 | 2009-04 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) More |
| EN ISO 10993-16 | 2017-12 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017) More |
| EN ISO 10993-3 | 2014-10 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014) More |
| EN ISO 10993-4 | 2017-10 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) More |
| EN ISO 10993-5 | 2009-06 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) More |
| EN ISO 10993-6 | 2016-12 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016) More |
