NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 20417 [CURRENT] references following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN ISO 17664-1 | 2021-11 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021); German version EN ISO 17664-1:2021 More |
| DIN EN ISO 18113-1 | 2013-01 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011 More |
| DIN EN ISO 3166-1 | 2020-12 | Codes for the representation of names of countries and their subdivisions - Part 1: Country code (ISO 3166-1:2020); English version EN ISO 3166-1:2020 More |
| DIN EN ISO 7010 | 2020-07 | Graphical symbols - Safety colours and safety signs - Registered safety signs (ISO 7010:2019); German version EN ISO 7010:2020 More |
| DIN EN ISO 780 | 2016-05 | Packaging - Distribution packaging - Graphical symbols for handling and storage of packages (ISO 780:2015); German version EN ISO 780:2015 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 ISO 3864-1 | 2012-06 | Graphical symbols - Safety colours and safety signs - Part 1: Design principles for safety signs and safety markings (ISO 3864-1:2011) More |
| DIN ISO 8601-1 | 2020-12 | Date and time - Representations for information interchange - Part 1: Basic rules (ISO 8601-1:2019) 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 |
| EUV 2017/746 | 2017-04-05 | Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU More |
