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  2. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    CE marking example on a mobile phone charger. The presence of the logo (from French, "conformité européenne" meaning "European conformity") [2] on commercial products indicates that the manufacturer or importer affirms the goods' conformity with European health, safety, and environmental protection 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. European Committee for Standardization - Wikipedia

    en.wikipedia.org/wiki/European_Committee_for...

    The CE mark is a declaration by the manufacturer that a product complies with all relevant EU directives. CEN (together with CENELEC) provide a CEN/CENELEC platform [4] for the development of European Standards and other technical specifications across a wide range of sectors, also ensuring that standards correspond with any relevant EU ...

  5. St. Jude Medical Announces CE Mark Approval of ViewFlex ... - AOL

    www.aol.com/news/2013-01-17-st-jude-medical...

    St. Jude Medical Announces CE Mark Approval of ViewFlex Xtra ICE Catheter New catheter provides real-time, high-resolution ultrasound images of blood flow and cardiac anatomy when paired with the ...

  6. CE - Wikipedia

    en.wikipedia.org/wiki/CE

    CE marking (stylized ), a mandatory administrative marking asserting conformity with relevant standards, applied certain products offered for sale within the European Economic Area; Customer equity, the total combined customer lifetime values of all of the company's customers; Combustion Engineering, a former American manufacturer of power systems

  7. 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.

  8. Type approval - Wikipedia

    en.wikipedia.org/wiki/Type_approval

    The CE mark found on the back of many electronic devices does not mean that the product has obtained type approval in the European Union. The CE mark is the manufacturer's declaration that the system/assembly meets the minimum safety requirements of all the directives (laws) applicable to it, and of itself, does not signify any third party ...

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