Product Certification
Summary:
【CE Certification Introduction 】 The word "CE" is shortened from the French "Conformite Europeene", which means the European Community. The "CE" mark is a safety certification mark that is regarded as a passport for manufacturers to open and enter the European market. In the EU market, the "CE" mark is a mandatory certification mark, whether it is a product produced by an enterprise within the EU, or a product produced in other countries, in order to circulate freely in the EU market, it must be affixed with the "CE" mark to show that the product meets the basic requirements of the EU's "New Method of Technical coordination and standardization" directive. This is a mandatory requirement for products under EU law.
【CE Certification Introduction 】
The word "CE" is shortened from the French "Conformite Europeene", which means the European Community. The "CE" mark is a safety certification mark that is regarded as a passport for manufacturers to open and enter the European market.
In the EU market, the "CE" mark is a mandatory certification mark, whether it is a product produced by an enterprise within the EU, or a product produced in other countries, in order to circulate freely in the EU market, it must be affixed with the "CE" mark to show that the product meets the basic requirements of the EU's "New Method of Technical coordination and standardization" directive. This is a mandatory requirement for products under EU law.
【CE Certification Process 】
This process applies to all products covered by CE:
The first step: Determine the directives and harmonized standards to which the product conforms
Different directives cover different ranges of products, and the basic requirements of the covered products are listed in the directives. Eu harmonised standards are detailed technical documents used to guide products to meet the basic requirements of the Directive.
Step 2: Determine the detailed requirements that the product should meet
You must ensure that your products meet the basic requirements of the relevant EU law. A product is considered to meet the relevant essential requirements only if it meets the requirements of all harmonized standards to which it applies. The application of harmonized standards is entirely voluntary, and you can also choose other ways to meet the corresponding basic requirements.
Step 3: Determine whether the product requires notified body participation in the inspection
Your products need to be notified by a third party to participate in the CE audit there are detailed regulations. Notified body certification is not mandatory for all products, so it is important to determine if notified body involvement is really required. These notified bodies are authorised by the European Commission and are listed in detail in the NANDO(New Methods Directive Notified Bodies and Designated Bodies) file.
Step 4: Test the product and verify its compliance
Manufacturers are responsible for testing products and checking whether they comply with EU regulations (conformity assessment process). Risk assessment is the basic rule in the assessment process, and only after meeting the requirements of relevant EU harmonized standards can you meet the basic requirements of official EU regulations.
Step 5: Draft and save the technical documents required by the directive
The manufacturer must establish a technical document (TCF) for the product in accordance with the requirements of the Directive and the need for risk assessment. If required by the relevant authorizing authority, the manufacturer shall submit the technical documentation together with the EC declaration of conformity for inspection.
Step 6: Put CE mark on your products and make EC Declaration of Conformity
The CE marking must be affixed to the product by the manufacturer or its authorized representative. The CE mark must be clearly and permanently affixed to the product or its nameplate in accordance with its standard drawing. If the notified body is involved in the certification of the product, the CE mark must bear the notice number of the notified body. Manufacturers are obliged to draft an EC declaration of conformity and sign it to certify that the product meets the CE requirements.
After the above six steps, your products with the CE mark can be smoothly circulated in the European market.
CE Directives
|
Name |
Directive Number |
|
Pressure vessel |
2014/68/EU |
|
Plaything |
2009/48/EC |
|
Building supplies |
No 305/2011-CPR |
|
Electromagnetic vessel |
2014/30/EU |
|
Machine |
2006/42/EC |
|
Personal Protective Equipment (PPE) |
EU2016/425 |
|
Gas appliance |
|
|
Explosion-proof instruction ATEX |
2014/34/EU |
|
General medical device |
93/42/EEC |
|
Radio equipment |
2014/53/EU (RED) |
|
Measuring Instruments Directive MID |
2014/32/EU |
|
Instruction number |
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