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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.

  3. Type approval - Wikipedia

    en.wikipedia.org/wiki/Type_approval

    Type approval or certificate of conformity is granted to a product that meets a minimum set of regulatory, technical and safety requirements. Generally, type approval is required before a product is allowed to be sold in a particular country, so the requirements for a given product will vary around the world.

  4. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    The manufacturer draws up an EU declaration of conformity or a declaration of performance (for Construction Products) and affixes the CE marking on the product. If stipulated in the directive(s) or regulation(s), an authorized third party ( Notified Body ) must be involved in the conformity assessment procedure or in setting up a production ...

  5. Notified body - Wikipedia

    en.wikipedia.org/wiki/Notified_Body

    A notified body, in the European Union, is an organisation that has been designated by a member state to assess the conformity of certain products, before being placed on the EU market, with the applicable essential technical requirements. These essential requirements are publicised in European directives or regulations.

  6. RoHS - Wikipedia

    en.wikipedia.org/wiki/RoHS

    The CE logo now indicates compliance and RoHS 2 declaration of conformity is now detailed (see below). [ citation needed ] In 2012, a final report from the European Commission revealed that some EU Member States considered all toys under the scope of the primary RoHS 1 Directive 2002/95/EC, irrespective of whether their primary or secondary ...

  7. Regulation (EU) No. 305/2011 - Wikipedia

    en.wikipedia.org/wiki/Regulation_(EU)_No._305/2011

    Regulation No. 305/2011 [1] (Construction Products Regulation, or CPR) of the European Parliament and of the Council of the European Union is a regulation of 9 March 2011 which lays down harmonised conditions for the marketing of construction products and replaces Construction Products Directive (89/106/EEC).

  8. Demonic dad allegedly beheads 1-year-old son with knife after ...

    www.aol.com/demonic-dad-allegedly-beheads-1...

    A demonic California dad has been arrested for allegedly beheading his 1-year-old son Friday in an early-morning frenzy of violence that also injured his wife and her mother, according to police.

  9. Product certification - Wikipedia

    en.wikipedia.org/wiki/Product_certification

    product certifications (many nations) Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).