NA 022
DKE German Commission for Electrical, Electronic & Information Technologies of DIN and VDE
DIN EN IEC 80601-2-78 ; VDE 0750-2-78:2021-05 [CURRENT] references following documents:
Document number | Edition | Title |
---|---|---|
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 15223-1 | 2022-02 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021); German version EN ISO 15223-1:2021, with CD-ROM More |
DIN EN ISO 22523 | 2007-04 | External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006); German version EN ISO 22523:2006 More |
DIN EN 60601-2-33 ; VDE 0750-2-33:2017-11 | 2017-11 | Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis(IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 60601-2-33:2010 + Cor.:2010 + A11:2011 + A1:2015 + A2:2015 + AC:2016 + A12:2016 More |
IEC Guide 109 | 2012-06 | Environmental aspects - Inclusion in electrotechnical product standards More |
IEC 60601-1 | 2005-12 | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance More |
IEC 60601-1-9 | 2007-07 | Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design More |
IEC 80601-2-78 | 2019-07 | Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation More |
IEC/TR 60601-4-1 | 2017-05 | Medical electrical equipment - Part 4-1: Guidance and interpretation - Medical electrical equipment and medical electrical systems employing a degree of autonomy More |
IEC/TR 62366-2 | 2016-04 | Medical devices - Part 2: Guidance on the application of usability engineering to medical devices More |