enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    There are mechanisms in place to ensure that the CE marking is put on products correctly. Controlling products bearing CE marking is the responsibility of public authorities in member states, in cooperation with the European Commission. Citizens may contact national market surveillance authorities if the misuse of the CE marking is suspected or ...

  3. European Organisation for Technical Approvals - Wikipedia

    en.wikipedia.org/wiki/European_Organisation_for...

    Once a building product has an ETA certificate, it can display the CE mark [2] and can be sold Europe wide. ETAs are a European alternative to national agrément certificates (for example, the British Board of Agrément). The first ETA was issued in 1998 by the DIBt in the Liechtenstein.

  4. 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.

  5. European Union Intellectual Property Office - Wikipedia

    en.wikipedia.org/wiki/European_Union...

    The Office is in charge of managing the registration of the EU trade mark and the registered Community design and offers businesses and citizens exclusive rights for trade mark and design protection throughout the European Union (EU), with a single application. Every year, it registers an average of 135,000 EU trade marks and close to 100,000 ...

  6. 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 ...

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

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

    PAUL, Minn.--(BUSINESS WIRE)-- St. Jude Medical, Inc. (NYS: STJ) , a global medical device company, today announced European CE Mark approval of its ViewFlex ™ Xtra Intracardiac Echocardiography ...

  8. 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.

  9. 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