What is CE certification Europe?

CE certification Europe, that is, limited to the basic safety requirements of products that do not endanger the safety of humans, animals and goods, rather than the general quality requirements, the coordination directive only specifies the main requirements, the general directive requirements are standard tasks . Therefore, the accurate meaning is that the CE mark is a safety conformity mark rather than a quality conformity mark. Are the “main requirements” that form the core of the European directive.

The “CE” mark is a safety certification mark that is regarded as a passport for manufacturers to open and enter the European market. CE stands for CONFORMITE EUROPEENNE (European Unity).
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 Europe – Take the Right Steps to Verify Your Product

Selling your products in Europe can raise many questions throughout the entire process. Manufacturers, importers, and distributors constantly seek answers during the early stage of the certification process. The list of CE marking directives and regulations is massive. Stay calm. You are at the right place if you need expert advice on your product certification. Shenzhen HUAK does that well.

Before your product passes all the parameters and achieves the certified tag, it is essential to comprehend the full scope of the CE Certification Europe first. But do you know the steps in affixing the CE marking on your product? We’ll walk you through that as well!

How does the process of CE Certification begin?

To begin with, know the definition and prime areas of CE Certification Europe . The certification process allows attaching CE Marking on your respective product, which must ideally start when the product is in its development stage. It is due to product safety, user health, and environmental reliability.

Clarifying requirements from day 1 of the product development stage is recommended. It saves time, effort and allows more responsible operations. Moreover, it is also possible for ready-to-use products to obtain the CE Certificate. To trade freely in the European Economic Area (EEA), the economic operators must know that their products comply with European safety standards with the CE Certificate.

What is a CE MARKING?

The CE marking indicates the product absides by the relevant European product guidelines. It assures conformity with quality standards. Knowing that the marking is just an indication, not proof, is essential.

What does the CE marking aim at?

First and foremost, the CE marking permits trade in the European market regardless of its production in the EEA (the Member States of the European Union plus Norway, Iceland, and Liechtenstein), in Turkey, or elsewhere. It means that these Member States of the European Economic Area can only restrict the trade of CE-marked products if any authority finds them non-compliant with European legislation.

A CE mark does not mean that a product is made in the EU. This marking signifies that the product complies with EU regulations. Therefore, the CE marking can be regarded as a needful information to both the Member States authorities and other relevant parties. To be clear: a CE marking is not considered a marketing tool.

However, it is a legal mandate for the Manufacturers, importers, and distributors of non-food products to attach the CE Marking to their products. The products for which CE directives and/or regulations have been drafted need to follow this without fail. Any sale taking place without the CE marking is considered a violation of regulations and is declared an economic crime under the Commodities Act.

Moreover, the products for which no such regulations are drafted but they carry CE marking is also a violation. If you need clarification on your product requirement for CE marking, our experts at Shenzhen-HUAK can assist you with free product classification.

6 Steps For Successful Certification Of Your Product

1. Check which EU Directive(s) applies to your product
2. Search for requirements for your product
3. Verify if the product requires Notified Body approval.
4. Evaluate product conformity
5. Draft technical files
6. Generate the Declaration of Conformity and add the CE marking.

Your Product Certification Is In Trusted Hands

Our CNAS-accredited labs are well-equipped to test a broad product category list:

• Use of Certain Substances Restriction (RoHS)
• Machinery and Installations
• Pressure Equipment (PED)
• Toys
• Electronic Equipment (EMC)
• Electrical Equipment (LVD)
• Radio Equipment (RED)
• Others