It applies the harmonised standard EN ISO 12100 to assess the product for the compliance of MD. In the conformity report, it validates each clause using a few standards such as EN 60335-1, EN 527, EN 55014-1:2017+A11:2020, EN 61000-3-2:2019, EN 62233 : 2008 etc. Is it necessary to quote all the standards or just EN ISO 12100 only in the DoC inside the instructions manual?
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