Lijiang CE certification agency, high pole lamp CE certification is fast

CE certification, that is, it is only limited to the basic safety requirements of products that do not endanger the safety of human beings, animals and goods, rather than the general quality requirements. The coordination directive only stipulates the main requirements, and 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. It is the "main requirement" that constitutes the core of European directives.

The "CE" mark is a safety certification mark, which is regarded as a passport for manufacturers to open and enter the European market. CE stands for CONFORMITE EUROPEENNE.

The Declaration of Conformity/Declaration of Compliance issued by the enterprise itself is a self declaration and should not be issued by a third party agency (intermediary or testing certification agency). Therefore, it can be replaced by an enterprise's Declaration of Conformity in EU format.

EC Attestation of conformity, a certificate issued by the notified body of the European Union (NB for short). According to EU regulations, only NB is qualified to issue CE declaration of EC Type.

If exported to any of the 30 member countries of the EEA including the EU and EFTA, CE certification may be required.
Confirm the product category and relevant EU product directives If a product belongs to more than one category at the same time, it will meet the requirements listed in the product directives corresponding to all categories. Note: Some products excluded from the directive are sometimes listed in some product directives.

In order to ensure that the four requirements mentioned above during the implementation of CE Marking certification can be met, EU laws require manufacturers located outside the 30 EEA allies to have an authorized representative (EU authorized representative) in the EU to ensure that the products are "safe" during circulation and use after being put on the European market Consistency; Technical Files are stored in the EU for inspection by the supervision authority at any time; Remedial measures shall be taken for the products found by the market supervision authority that do not meet the CE requirements, or the products that have been affixed with CE labels due to accidents during use. (such as temporary removal from the shelf, or removal from the market); After the product model with CE label has been put on the European market, if there are changes or changes in the relevant EU laws, the subsequent products of the same model will also be changed or amended accordingly, so as to meet the new legal requirements of the EU.

The EU's product directive allows manufacturers of products with low risk levels in certain categories to choose the mode A: "internal production control (self declaration)" for CE certification. Products with high risk level are involved through the third-party certification agency NB (Notified Body). For products with high risk level, their manufacturers choose other modes other than mode A, or mode A plus other modes to achieve CE certification. In other words, the third-party certification agency NB (Notified Body) intervenes.

EU laws require that after the products with CE labels are put on the European market, their technical documents shall be stored in the EU for inspection by the supervision authorities at any time. In case of any change in the contents contained in the technical documents, the technical documents shall also be updated in a timely manner.
Technical documents shall generally include the following contents:
A. Name, trade name and address of the manufacturer (EU authorized representative (EU authorized agent) AR).
B. Model and number of the product.
C. Product instructions.
D. Safety design documents (key structure drawings, i.e. design drawings that can reflect the creepage distance, clearance, number of insulation layers and thickness).
E. Product technical conditions (or enterprise standards).
F. Electrical schematic diagram of the product.
G. Product circuit diagram.
H. List of key components or raw materials.
I. Testing Report.
J. Relevant certificates issued by the EU authorized certification authority NB (for other modes other than mode A).
K. Registration certificate of the product in the EU (for some products, such as Class I medical devices, ordinary IVD in vitro diagnostic medical devices).
L. CE declaration of conformity (DOC).

The testing time in China is relatively fast, while the real certification authority recognized by the EU takes a longer time. What kind of certification authority should be selected should also refer to the customer's requirements and their own needs. For example, if the other company wants to do TUV certification, it should do it according to the customer's requirements. It is a large multinational enterprise itself, and it should build a brand, Then TUV certification is completely in line with its own situation. At this stage, the certificates issued by domestic institutions can also be recognized by the EU, and there are also certification institutions that have acquired the EU.