Is it necessary to European representative detail in DOC when the manufacture from out side the EU region. The product here I mentioned in not in the category of MD or IVD. Just use for food and water testing laboratory. Please clarify?
Europe.eu is a great place for the DOC process, how and what to submit to ensure that your product complies with the requirements, for example, by “applying harmonised standards.“
Technical documentation and EU declaration of conformity (DOC) info and steps in order to get the CE marking is here:https://europa.eu/youreurope/business/product-requirements/compliance/technical-documentation-conformity/index_en.htm
for more specific info and examples to submit in your situation, use the examples available for businesses via “Your Europe” at Europe.eu