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  2. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    CE marking is mandatory for certain product groups intended for sale within the European Union, the European Free Trade Association (EFTA), and Turkey. The manufacturers of products made within these countries, and the importers of goods made in other countries, affirm that CE-marked goods conform to EU standards.

  3. Notified body - Wikipedia

    en.wikipedia.org/wiki/Notified_Body

    CE Mark. 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.

  4. Geprüfte Sicherheit - Wikipedia

    en.wikipedia.org/wiki/Geprüfte_Sicherheit

    The main difference between GS and CE mark is that the compliance with the European safety requirements has been tested and certified by a state-approved independent body. [1] [2] [3] CE marking, in contrast, is issued for the signing of a declaration that the product is in compliance with European legislation. The GS mark is based on the ...

  5. 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.

  6. European Authorized Representative - Wikipedia

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

    As clarified in the Medical Devices Directive — Directive 93/42/EEC [4] — it is required that alongside the CE mark all products must also have an Authorised Representative. As stated in this amendment, an Authorised Representative should serve as a contact point with the EU member states competent authorities.

  7. 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).

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  9. Certification mark - Wikipedia

    en.wikipedia.org/wiki/Certification_mark

    Canadian certification label on a bag of rockwool Counterfeit electrical cords with false UL certification marks. A certification mark on a commercial product or service is a registered mark that enables its owner ("certification body") to certify that the goods or services of a particular provider (who is not the owner of the certification mark) have particular properties, e.g., regional or ...