Conformite Europeene (French). Symbol used to indicated that a product conforms to the relevant European health, safety and environmental quality standards. Airfix and Humbrol products carry the CE mark on the product packaging.
a manufacturer's claim that its product meets specified essential safety requirements set out in relevant European directives
a marking which is placed on a product to indicate that the product underwent assessment procedures and was found to be in compliance with the European standards that apply to such product
mark applied to industrial products, including medical devices, representing the manufacturer’s declaration of conformity with relevant EU legal requirements for their sale
when displayed, this mark indicates a medical device fulfills requirements for sale in the 15-nation European Union.
The manufacturerâ€(tm)s declaration, following appropriate assessment by a CE Notified Body, that the product conforms to the essential requirements of the relevant European health, safety and environmental protection legislations. Once awarded, the CE Mark permits the marketing of the product throughout the European Union.
A marking on an instrument that indicates the instrument has been tested in accordance with the requirement for the European Union with regard to electromagnetic compatibility and electrical safety. This mark is required on products that are imported into any of the member states of the European Community.
A mark affixed to products marketed in the EU, showing that equipment complies with applicable EU Directives.
The European Mark of conformity Submitted by Piers from London, UK.
A mark, containing the letters 'CE' in a specific format, which may be affixed to a product, its packaging or instructions. The CE mark is a declaration by the manufacturer that the equipment complies with all applicable European Directives. In the context of this document, the Electromagnetic Compatibility Directive 89/336/EEC is of particular relevance.
CE marking is a declaration by the manufacturer that the product meets all the appropriate provisions of the relevant legislation implementing certain European Directives. CE marking gives companies easier access into the European market to sell their products without adaptation or rechecking. The initials "CE" do not stand for any specific words but are a declaration by the manufacturer that his product meets the requirements of the applicable European Directive(s).
a mark on contact lens and lens care product packaging showing that the products were designed, developed and manufactured using systems approved by the Regulatory Authorities of the European Union.
CE Marking on a product is a manufacturer's declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislations, in practice by many of the so-called product directives.
Indicating compliance with all relevant European Union directives.
CE Mark is a visible declaration by the manufacturer (or his representative, importer, etc.) that the equipment which is marked complies with all the requirements of all the applicable European Union (EU) directives.
European product compliance (conformity) mark.
A "passport" that allows manufacturers to trade industrial products freely within the internal EU market. The CE Mark is not a quality mark, but indicates conformity to the legal requirements of the EU Directives. It is mandatory for a wide range of products sold in the EU.
The CE mark (officially CE marking) is a mandatory safety mark on many products placed on the single market in the European Economic Area (EEA). The term initially used was "EC Mark" and it was officially replaced by "CE Marking" in the Directive 93/68/EEC in 1993. "CE Marking" is now used in all EU official documents.
