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What is CE Certification - CE Certification Application Process in the EU
Publish Time:2023-02-14        View Count:22        Return to List

  What does CE product certification mean?


Products not only need to comply with the CE certification, but certified products must also display the "CE" certification logo on the product label or packaging box. The CE certification is a right to affix the CE mark to a product, and products with the CE mark are deemed to comply with European product safety regulations, allowing free circulation within the European Economic Area (EEA).


 What is the CE Mark Certification?


CE certification is the right to affix the CE mark to a product, and it should begin at the product development stage, as there are some CE requirements related to product safety, user health, and the environment that are ideal during the development process; however, CE certificates can be issued for ready-to-use products. Products with a CE certificate must comply with European safety regulations and can only operate freely within the European Economic Area (EEA) after that.


To understand the scope of CE certification, it's first necessary to grasp the specific directives that CE certification encompasses. This involves an important concept: "Directive." A "Directive" refers to a technical regulation that specifies the fundamental safety requirements and procedures for products. Each directive is tailored to a specific product category, so understanding the meaning of directives will clarify the exact scope of products covered by CE certification.


Generally, the CE certification is a mandatory certification in the European Union. There are specific regulations in the EU market. All products exported to the EU must obtain CE certification. The CE certification is a pass for products to enter the EU market and is a must-have. Without it, the products will not be able to clear customs and sold in the EU market.


The CE mark is a safety symbol, not a quality symbol. It is a primary requirement at the core of European directives.


In the EU market, the CE mark is a mandatory certification symbol. Whether the product is produced by a domestic company within the EU or by a company in another country, you must affix the CE mark to freely circulate your product in the EU market, indicating that it meets the basic requirements of the EU. This is a mandatory requirement for products under EU law, concerning new technical harmonization and standardization methods.



  Section 3: CE Certification Requirements


Our products must not pose any harm to health, the environment, or consumers before entering the market.


Products legally sold in EU countries can also be sold in other member states.


Manufacturers may affix the EU CE marking on their products to indicate that they fully comply with the relevant EU directives. If permitted by laws and regulations, the CE mark can also be indicated on the packaging or accessories.


The EU CE mark is not a test mark; it merely indicates that the manufacturer declares their product complies with all relevant regulations. Currently, there are many qualified assessment models to determine if they meet basic requirements, which may involve manufacturers, importers, distributors, and other entities. If you wish to apply for CE certification to demonstrate product compliance with standards, you still need to find a third-party testing agency for certification.


  Section 4: Purpose of CE Certification:


The EU not only has a vast array of laws, regulations, and unified standards but also a complex content. Therefore, it is wise to save time, effort, and risk with the assistance of EU institutions.


Obtaining the CE certification from EU institutions can, to some extent, gain the trust of consumers and market regulatory authorities.


Effectively prevent the emergence of irresponsible accusations.


In the face of litigation, the CE certification certificates from EU institutions will serve as legally binding technical evidence.


Once penalized by the EU, certification bodies will share the risk with enterprises, thereby reducing the risk for businesses.


1. CE certification enhances product competitiveness.


2. Risk of seizure upon customs clearance is eliminated.


Reduce the risk of being investigated during inspections.


4. Upon product inspection, a third-party testing agency assumes partial responsibility to mitigate risks.


Consumers are more likely to trust products with the CE certification mark when making purchases.


6. Products bearing the CE mark signify the manufacturer's responsibility to comply with standards and are a guarantee of safety.


  Five: Products requiring CE certification:


1. Machinery and Equipment (MD)


2. Explosion Protection Directive (ATEX)


Electrical Equipment (LVD)


4. Electromagnetic Compatibility Directive (EMC)


5. Building Products (CPR)


6. Medical Device and Diagnostic (MDD)


7. Personal Protective Equipment (PPE)


8. Pressure Equipment (PED)


Radio Equipment (RED)


Toy CE Certification


Ceramic CE Certification


Measurement Instruments


13. Elevator Commands (LIFTS)


  Section VI: CE Certification Process


Client provides product information and related requirements to GTT for assessment and quotation.


2. Client confirms return signed quotation, fills out application form, provides samples and materials (see notes), arranges payment (initial deposit), and GTT opens the case.


3. GTT schedules product testing and reviews documentation.


4. In case of issues with testing or documentation, arrange for corrections and retesting until they meet the required standards.


Upon passing the test and approval of the documents, GTT will issue the CE certificate report.


6. For obtaining the CE certificate issued by the EU Notified Body (NB), GTT submits test reports and relevant documents to the NB for review and certification.


7. For international certification reports, such as CE certificates from institutions like TUV, GTT arranges for witnessing tests with the issuing authorities.


After the witnessing test is completed, the certification body issues a CE test report and grants the CE certificate.


9. Client pays the final payment, receives the certificate and report, and the case is closed.


  Section 7: CE Certification Documentation Requirements


1. Circuit schematics & PCB layout diagrams


2. Product manuals and product labels


3. Product working principle diagrams and block diagrams.


4. Key Component List (wires, plugs, threads, pressure-sensitive resistors, optocouplers, X/Y capacitors, transformers, casings, etc.)


5. Product BOM Sheet


6. Product specifications.


Note:


CE-EMC Certification for Low-Voltage Cabled Products Requires the Following Documentation: Product Manual/Specification Sheet.


Required Documentation for CE-EMC+LVD Certification of Wires and Cables Products: Product manual/specification, circuit diagram, PCB layout, certification certificates/specifications of critical components, nameplates, etc.


Wireless Product CE-EMC+LVD+RED Certification Requirements: Product manual/sheet, circuit diagram, PCB layout, certification certificates/sheets for critical components, label, block diagram, circuit description, fixed-frequency software, antenna specifications, etc.


Key components include: plugs, power cables, rubber enclosures, PCB boards, transformers and materials, switches, X capacitors, Y capacitors, optocouplers, inductors, temperature control, fuses, rechargeable batteries, external adapters/supplies/chargers, etc.


  What is the CE certification cycle?


Our standard cycle is approximately 1-2 weeks, with a customer-centric approach at our core. We prioritize our clients' urgency, and your time requirements are our collective pursuit at Yibo.


  What's the difference between a certificate issued by an announcement authority and a self-issued certificate?


The EU's Official Announcement Agency, known as the NB Agency, is an official EU institution and each has a corresponding announcement number.


The number of independent EU notification bodies conducting business in the Chinese market is limited; many are handled through domestic third-party certification and testing agencies.


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