NA 176
DIN Standards Committee Health Technologies
DIN EN 13060 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| EN 868-10 | 2018-12 | Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods More |
| EN 868-5 | 2018-12 | Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods More |
| EN 868-8 | 2018-12 | Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods More |
| EN 868-9 | 2018-12 | Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods 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 10993-4 | 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 |
