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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.
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.
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 ...
The MarED Product Database contains information about approved equipment to be installed on EU flagged merchant vessels according to the European Marine Equipment Directive. Access to the MarED Database and to the MarED website is available for the public, but limited to registered users only. The registration is free of charge.
The database serves as a quick reference for checking the good manufacturing practice (GMP) of a potential contract manufacturer. One can search by the “company name, location, or certificate number and find details on the types of products or activities that the company conducts and the date of the most recent GMP inspection.” [ 3 ]
The article GE Healthcare Announces CE Marking for Its Breast Tomosynthesis Solution, SenoClaire originally appeared on Fool.com. Try any of our Foolish newsletter services free for 30 days .
An example of such local implementation of the Directive is now present in Italy. Italy requires, in addition to the CE marking (as opposed to the essence of the CE marking which is “Free Circulation of Goods”), that ALL Medical Devices to be placed in the Italian market will go through a Device registration process.
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.