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  2. European Authorized Representative - Wikipedia

    en.wikipedia.org/wiki/European_Authorized...

    An authorised representative may also carry out a conformity assessment of a medical device on behalf of the manufacturer. [7] European ‘Blue Guide" [8] describes that delegation of an authorised representative should be set out in writing (as an agreement, mandate, or power of attorney) to define contents and limits of tasks. The copy of the ...

  3. Advance healthcare directive - Wikipedia

    en.wikipedia.org/wiki/Advance_healthcare_directive

    An advance healthcare directive, also known as living will, personal directive, advance directive, medical directive or advance decision, is a legal document in which a person specifies what actions should be taken for their health if they are no longer able to make decisions for themselves because of illness or incapacity. In the U.S. it has a ...

  4. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    Not all products are required to bear CE marking, only the products that fall within the scope of at least one of the sectoral norms (directives and regulations) requiring CE marking. There are more than 20 sectoral product norms requiring CE marking covering, but not limited to, products such as electrical equipment, machines, medical devices ...

  5. What is a Power of Attorney? A comprehensive guide - AOL

    www.aol.com/power-attorney-comprehensive-guide...

    A medical power of attorney costs between $200 and $500, though this can vary from state to state. Additionally, principals with complex wishes regarding treatment and end-of-life care may need to ...

  6. List of European Union directives - Wikipedia

    en.wikipedia.org/wiki/List_of_European_Union...

    Commission Directive 66/683/EEC of 7 November 1966 eliminating all differences between the treatment of national products and that of products which, under Articles 9 and 10 of the Treaty, must be admitted for free movement, as regards laws, regulations or administrative provisions prohibiting the use of the said products and prescribing the use of national products or making such use subject ...

  7. Medical Devices Directive - Wikipedia

    en.wikipedia.org/wiki/Medical_Devices_Directive

    The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the ...

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