NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 80601-2-79 [Pre-order] references following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN 60601-1-6 ; VDE 0750-1-6:2021-11 | 2021-11 | Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability (IEC 60601-1-6:2010 + A1:2013 + A2:2020); German version EN 60601-1-6:2010 + A1:2015 + A2:2021 More |
| DIN EN 60601-1-8 ; VDE 0750-1-8:2021-12 | 2021-12 | Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (IEC 60601-1-8:2006 + A1:2012 + A2:2020); German Version EN 60601-1-8:2007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 More |
| DIN EN 61672-1 | 2014-07 | Electroacoustics - Sound level meters - Part 1: Specifications (IEC 61672-1:2013); German version EN 61672-1:2013 More |
| DIN EN 62304 ; VDE 0750-101:2016-10 | 2016-10 | Medical device software - Software life-cycle processes (IEC 62304:2006 + A1:2015); German version EN 62304:2006 + Cor.:2008 + A1:2015 More |
| DIN EN 62366-1 ; VDE 0750-241-1:2021-08 | 2021-08 | Medical devices - Part 1: Application of usability engineering to medical devices (IEC 62366-1:2015 + COR1:2016 + A1:2020); German version EN 62366-1:2015 + AC:2015 + A1:2020 More |
| DIN EN 62570 | 2016-09 | Standard practice for marking medical devices and other items for safety in the magnetic resonance environment (IEC 62570:2014); German version EN 62570:2015 More |
| EUV 2017/745 | 2017-04-05 | Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC More |
| IEC 60601-1-10 | 2007-11 | Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral standard: Requirements for the development of physiologic closed-loop controllers More |
| IEC 60601-1-10 AMD 1 | 2013-11 | Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral standard: Requirements for the development of physiologic closed-loop controllers More |
| IEC 60601-1-10 AMD 2 | 2020-07 | Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral standard: Requirements for the development of physiologic closed-loop controllers; Amendment 2 More |
