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SFS-EN IEC 60601-2-83:2020/A1:2025:en

Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment

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Scope


The standards writing body responsible for this document in Finland is Electrotechnical Standardization in Finland.
Product group(s)
11.040.60 Therapy equipment »
Relationships
Normative references
EN 60601-1-11:2015 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
EN 60601-1-11:2015/A1:2021 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
EN 60601-1-2:2015 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
Show normative references associated with publication
Technical committee
CLC/TC 62 Electrical equipment in medical practice »
Directive
93/42/EEC Medical devices
2017/745 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

http://ec.europa.eu »
Date of implementation
19.06.2025
Published
24.06.2025
Edition
1
Pages
20
Language(s)
English

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