The CE marking (an acronym for the French "Conformite Europeenne") certifies that a product has met EU health, safety, and environmental requirements, which ensure consumer safety. Manufacturers in the European Union (EU) and abroad must meet CE marking requirements where applicable in order to market their products in Europe.
Last Published: 10/18/2016

Manufacturers in the European Union (EU) and abroad must meet CE marking requirements where applicable in order to market their products in Europe. For a list of countries that require the CE marking, see: CE Marking Countries.

Countries That Require CE Marking
Greece
Norway
Germany
United Kingdom
Netherlands
France
Turkey
Malta
Finland
Switzerland
Luxembourg
Estonia
Sweden
Lithuania
Denmark
Spain
Liechtenstein
Czech Republic
Slovenia
Latvia
Cyprus
Slovakia
Italy
Croatia
Romania
Ireland
Bulgaria
Portugal
Iceland
Belgium
Poland
Hungary
Austria

A manufacturer who has gone through the conformity assessment process, may affix the CE marking to the product. With the CE marking, the product may be marketed throughout the EU. CE marking now provides product access to 32 countries with a population of nearly 500 million.

Unfortunately, there is no comprehensive list of the products that require a CE marking. Therefore, it is the manufacturer's responsibility to determine if a product requires a CE marking. The "New Approach Directives" are documents that contain the legislation issued by the European Commission on the requirements that need to be met and procedures that must be followed in order for a particular product to be CE marked for sales in the EU.

In order to determine if your product needs a CE marking, you should look in each directive that you judge as related to your product. Our Guide to navigating the CE marking process is organized by directives: CE Marking Guide. Under each directive, we explain the route to CE marking certification step-by-step and in one place.

Some products require conformance to more than one directive. For example, the Safety of Machinery directive, the Electromagnetic Compatibility (EMC) directive, and the Low Voltage Equipment directive may all apply to one product.

Many of the CE marking directives allow manufacturers to self-certify their products.

Some examples for which manufacturers can self-certify include:
· Safety of Machinery Directive
· Electromagnetic Compatibility (EMC) Directive
· Low Voltage Directive
· Class I products of the Medical Device Directive
· Most products covered by the Radio and Telecommunications Terminal Equipment (R&TTE) Directive

Some examples of the directives that do not allow manufacturers to self-certify include:
· Simple Pressure Vessels Directive
· Appliances Burning Gaseous Fuels Directive
· Most products covered by the Pressure Equipment Directive
· Most products covered by the Equipment and Protective Systems in Potentially Explosive Atmospheres Directive

If you are not permitted to self-certify your product, you will need to employ the services of a testing laboratory that is affiliated with a "European Notified Body" to test and certify your product for the CE marking. There are labs in the U.S. that subcontract for European notified bodies and are qualified to do the testing and certifying. We have provided a list of labs, including labs affiliated with notified bodies as well as labs that are not authorized with a notified body, but which are independent labs and can test that a product covered by a non-regulated directive (such as the EMC or Low Voltage Directives), has met a European standard: Testing/Certifying Labs.

If you are permitted to self-certify your product, you may need to order the standards that apply to your product, particularly in the case of the Low Voltage and EMC Directives. We have provided sources for ordering standards and for locating CE Marking consultancy services: Consultants/Ordering Standards.

Once the manufacturer has conformed to the requirements laid out in the applicable directive(s), whether through self-certification or approval by a notified body, and has obtained a certificate/report from a lab to prove conformance, the manufacturer needs to affix the CE marking to its product. The manufacturer must also include a "declaration of conformity" with each shipment stating which CE marking directive(s) has been met and include a signature of a company official indicating the company's responsibility for its CE marking compliance claim. We have provided an example of a declaration of conformity: Declaration of Conformity.

The exporter must maintain a file called a "technical file" containing the paperwork that proves conformity to the CE marking directive(s) covering its product. The exporter or authorized representative must be able to provide the supporting paperwork to prove CE marking conformity at any time, if requested by the appropriate member state authorities. See: Technical File Procedures for a framework for compiling a technical file.

Finally, it is the manufacturer/exporter's responsibility to regularly check for and comply with any standards changes that might affect its product. Therefore, it is important to periodically visit the EU website http://www.newapproach.org that lists the CE marking directives and their standards.

For additional information on the CE marking process, see the National Institute of Standards and Technology (NIST) publication "TO U.S. MANUFACTURERS: ALERT PRODUCT "MARK" REQUIRED FOR U.S. EXPORTS TO EUROPE!"

WHAT IS THE EU's NEW APPROACH TO PRODUCT CERTIFICATION?

The European Union (EU) developed "New Approach" Directives to streamline product approvals for a broad range of goods in order to facilitate trade within the EU single internal market. The "Old Approach" Directives contained a high degree of technical detail. EU member states introduced national standards or regulations at a faster pace than the European Commission could finalize these "Old Approach" Directives. These national specifications often proved to be trade barriers.

New Approach Directives are limited to essential health and safety requirements for sectors such as machinery, electrical products, or medical devices. They do not cover specific products such as motor vehicles, cosmetics, or chemicals, which are still covered under the Old Approach Directives. The main difference between the New and Old Approach Directives is that under the New Approach, the technical details outlining the minimum requirements a product must meet are usually not found in the directive itself. The New Approach Directives are more general.

Technical details on how to meet these minimum health and safety requirements are left to the following three groups: 1) Manufacturers who self-certify products by meeting the requirements of the applicable directives, in some cases by using appropriate European standards; 2) the three regional European standards organizations (CEN, CENELEC and ETSI), which now develop Europe-wide standards covering product sectors falling under the New Approach Directives; and, 3) government-appointed product certification bodies (called notified bodies), which provide testing and product approvals.

Under the New Approach, the European Commission gives mandates to the European standards organizations to develop technical standards that meet the essential health and safety requirements of CE Marking directives. The New Approach Directives are designed to facilitate product certification, to maintain a high level of consumer and workplace safety, and to expand intra-European trade.

Prepared by the International Trade Administration. With its network of 108 offices across the United States and in more than 75 countries, the International Trade Administration of the U.S. Department of Commerce utilizes its global presence and international marketing expertise to help U.S. companies sell their products and services worldwide. Locate the trade specialist in the U.S. nearest you by visiting http://export.gov/usoffices.



Foreign Trade Regulations Quality Assurance CE Marking