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DKE German Commission for Electrical, Electronic & Information Technologies of DIN and VDE
DIN EN IEC 80601-2-77 ; VDE 0750-2-77:2022-10 [Withdrawn] references following documents:
Document number | Edition | Title |
---|---|---|
IEC 60601-1 | 2005-12 | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance More |
IEC 60601-1-2 | 2014-02 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests More |
IEC 60601-1-6 | 2010-01 | Medical electrical equipment - General requirements for basic safety and essential performance - Collateral Standard: Usability More |
IEC 62366-1 | 2015-02 | Medical devices - Part 1: Application of usability engineering to medical devices More |
DIN EN IEC 60601-2-2 ; VDE 0750-2-2:2018-12 | 2018-12 | Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2017); German version EN IEC 60601-2-2:2018 More |
DIN EN IEC 60601-2-46 ; VDE 0750-2-46:2020-04 | 2020-04 | Medical electrical equipment - Part 2-46: Particular requirements for the basic safety and essential performance of operating tables (IEC 60601-2-46:2016); German version EN IEC 60601-2-6:2019 More |
DIN EN ISO 10218-1 | 2012-01 | Robots and robotic devices - Safety requirements for industrial robots - Part 1: Robots (ISO 10218-1:2011); German version EN ISO 10218-1:2011 More |
DIN EN ISO 13482 | 2014-11 | Robots and robotic devices - Safety requirements for personal care robots (ISO 13482:2014); German version EN ISO 13482:2014 More |
DIN EN ISO 13855 | 2010-10 | Safety of machinery - Positioning of safeguards with respect to the approach speeds of parts of the human body (ISO 13855:2010); German version EN ISO 13855:2010 More |
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 |