Definition of CE mark in English:

CE mark

noun

A symbol applied to products to indicate that they conform with relevant EU directives regarding health and safety or environmental protection.
CE标志（表明产品符合欧盟有关卫生、安全和环境保护等相关标准的一种标志）
Example sentencesExamples
- All too often, fraudulent CE marks are slapped on products indiscriminately, reducing the system to a charade.
- If you do not see the CE mark or an EN standard mark, do not buy the toy.
- Products marketed in France need not only a CE mark but also demonstrable proof "that the product provides value and does something unique from products already on the market."
- Europe requires the CE mark, which is not too difficult to obtain, especially once you've received FDA clearance.
- Particularly look out for a CE mark.
- How do I put the CE mark on a product?
- Special care needs to be taken when buying bicycles, skateboards and scooters, again checking the CE marks.
- Meeting the essential requirements is a major step toward receiving a CE mark for a device.
- Globally speaking, the typical event progression for manufacturers wishing to sell a medical device is to first conduct clinical studies in Europe to obtain a CE mark.
- The CE mark is applied to the packaging, the product or the user documentation.
- Instead, the data and final report are made available to the notified body as part of the technical file to support the CE mark.
- They carry the CE mark, which means they comply with the essential requirements of the relevant European health, safety end environmental protection legislation.
- Consumers should check labels or packaging for the name, trade mark and address of the manufacturer, the agent or importer within the EC and CE mark.
- The European approval with the CE mark is for a relatively narrow peripheral vascular application.
- This is usually satisfied by the use of a CE mark.
- Note that manufacturers must have a risk management system in place even if they do not need a notified body to help them apply the CE mark.
- Since its entry into the EU, all medical devices sold in Poland need to bear the CE mark.
- Do they still require a CE mark?
- A CE mark is not a guarantee of quality or safety but it is a legal requirement for all toys sold in the European Union.
- There are approximately 60 such organizations that conduct audits in accordance with the three medical device directives and authorize manufacturers to affix the CE mark to their devices.

Origin

1980s: CE from the initial letters of French Conformité Européenne 'European Conformity' or Communauté Européenne 'European Community'.

单词	CE mark
释义	Definition of CE mark in English: CE mark noun A symbol applied to products to indicate that they conform with relevant EU directives regarding health and safety or environmental protection. CE标志（表明产品符合欧盟有关卫生、安全和环境保护等相关标准的一种标志） Example sentencesExamples All too often, fraudulent CE marks are slapped on products indiscriminately, reducing the system to a charade. If you do not see the CE mark or an EN standard mark, do not buy the toy. Products marketed in France need not only a CE mark but also demonstrable proof "that the product provides value and does something unique from products already on the market." Europe requires the CE mark, which is not too difficult to obtain, especially once you've received FDA clearance. Particularly look out for a CE mark. How do I put the CE mark on a product? Special care needs to be taken when buying bicycles, skateboards and scooters, again checking the CE marks. Meeting the essential requirements is a major step toward receiving a CE mark for a device. Globally speaking, the typical event progression for manufacturers wishing to sell a medical device is to first conduct clinical studies in Europe to obtain a CE mark. The CE mark is applied to the packaging, the product or the user documentation. Instead, the data and final report are made available to the notified body as part of the technical file to support the CE mark. They carry the CE mark, which means they comply with the essential requirements of the relevant European health, safety end environmental protection legislation. Consumers should check labels or packaging for the name, trade mark and address of the manufacturer, the agent or importer within the EC and CE mark. The European approval with the CE mark is for a relatively narrow peripheral vascular application. This is usually satisfied by the use of a CE mark. Note that manufacturers must have a risk management system in place even if they do not need a notified body to help them apply the CE mark. Since its entry into the EU, all medical devices sold in Poland need to bear the CE mark. Do they still require a CE mark? A CE mark is not a guarantee of quality or safety but it is a legal requirement for all toys sold in the European Union. There are approximately 60 such organizations that conduct audits in accordance with the three medical device directives and authorize manufacturers to affix the CE mark to their devices. Origin 1980s: CE from the initial letters of French Conformité Européenne 'European Conformity' or Communauté Européenne 'European Community'.
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