How much is the international mainstream product certification system---CE certification

CE is the abbreviation of French, meaning "European Conformity" is the European Community. In fact, CE is the abbreviation of the phrase "European Community" in many national languages â€‹â€‹of the European Community. The original English phrase EUROPEAN COMMUNITY is abbreviated as EC. After the European Community is COMMUNATE EUROPEIA in French, COMUNITA EUROPEA in Italian, COMUNIDADE EUROPEIA in Portuguese , COMUNIDADE EUROPE in Spanish, etc., so change EC to CE. Of course, you can also consider CE as CONFORMITY WITH EUROPEAN (DEMAND) (in line with Europe (requirements)), constitutes the "main requirement" of the core of the European Directive.

The basic safety requirements for centrifuge CE certification means that the product is not limited to the safety aspects of humans, animals and goods, rather than the general quality requirements. The coordination directive only specifies the main requirements, and the general directive requirements are standard tasks. Therefore, the exact meaning is that the CE mark is a safety pass mark and not a quality pass mark.

Apply for CE certification

CE certification provides a unified technical specification for trade of products in the European market and simplifies trade procedures. To enter the EU and the European Free Trade Area, any country's products must be CE-certified and affixed with the CE mark on the product. This is a mandatory requirement of the EU law for products to indicate that the product complies with the EU's technical coordination and standardization. The basic requirements of the new method instructions. Therefore, CE certification is a passport for products entering the EU and European Free Trade Zone countries. CE certification indicates that the product has met the safety requirements stipulated by the EU Directive; it is a commitment of the company to consumers, increasing the level of consumer trust in the product.

Centrifuge ce

Advantages of applying for CE certification

â—The EU's laws, regulations and harmonized standards are not only numerous, but the content is very complicated. Therefore, it is a wise move to save time and effort and reduce risks.

â— Obtain CE certification from the designated agency of the European Union to maximize the trust of consumers and market surveillance agencies;

â— Effectively prevent the occurrence of irresponsible allegations;

â— In the case of litigation, the CE certification of the designated body of the European Union will become technical evidence with legal effect;

â— Once the EU country is punished, the certification body will share the risk with the company, thus reducing the risk of the company.

ã€€ã€€ Process for applying for CE certification

This process applies to all products covered by CE:

Step 1: Determine the instructions and harmonized standards for product compliance

Products covered by more than 20 instructions require a CE mark. These instructions cover a wide range of products, and the instructions list the basic requirements of the products covered. EU harmonized 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 relevant EU laws. A product that meets all of the harmonized standards it applies is considered to meet the relevant basic requirements. Whether or not the harmonized standards are applicable is entirely voluntary, and you can choose other ways to meet the basic requirements.

Step 3: Determine if the product needs to be notified by the notified body

Each instruction involved in your product has detailed requirements for whether or not a third-party notified body is required to participate in the CE review. Not all products are mandatory to pass the notified body certification, so it is very important to determine whether it is really necessary to participate in the notified body. These notified bodies are authorized by the European Commission and have a detailed list in the files of NANDO (New Method Directives and Designated Agencies).

Step 4: Test the product and verify its compliance

It is the responsibility of the manufacturer to test the product and check that it complies with the EU regulations (conformity assessment process). The risk assessment is the basic rule in the evaluation process. After meeting the requirements of the relevant EU harmonized standards, you are likely to meet the EU official regulations. Basic requirements.

Step 5: Draft and save the technical documents required by the directive

The manufacturer must establish a technical documentation (TCF) of the product based on the requirements of the product and the requirements of the risk assessment. If requested by the relevant authority, the manufacturer must submit the technical documentation and the EC Declaration of Conformity together for inspection.

Step 6: affix the CE mark on your product and make an EC Declaration of Conformity

The CE mark must be affixed to the product by the manufacturer or its authorized representative. The CE mark must be clearly and permanently attached to the product or its nameplate in accordance with its standard drawings. If the notified body participates in the certification of the product, the CE mark must carry the announcement number of the notified body. The manufacturer is obliged to draft an EC Declaration of Conformity and sign it to prove that the product meets the CE requirements.