What is CE Certification for Electrical Equipment?

CE certification is a mandatory conformity assessment mark established by the European Union (EU) for products entering its market, signifying that the products meet the essential safety requirements of relevant EU regULations. For electrical equipment, obtaining CE certification allows free circulation within EU member states and European EconoMIC Area (EEA) countries, eliminating the need to comply with separate technical regulations of individual countries.

Core Directives for CE Certification of Electrical Equipment

CE certification for electrical equipment does not follow a single standard, but must comply with corresponding EU-specific directives. Among them, the two most core and widely applied directives are the low voltage directive (LVD) and the Electromagnetic Compatibility Directive (EMC). Most electrical equipment must meet the requirements of both directives before the CE mark can be affixed.

1. Low Voltage Directive (LVD, 2014/35/EU)

This is the fundamental directive for CE certification of electrical equipment, applicable to all types of electrical devices with a rated voltage range of 50–1000V AC or 75–1500V DC. It covers the vast majority of common electrical products, such as household appliances, industrial motors, power adapters, and lighting equipment.

Core Requirements: Ensure that products do not pose hazards to human health or property safety under normal use and reasonably foreseeable misuse. Specific safety criteria include electrical insulation, temperature rise limits, mechanical strength, and short-circuit protection.

2. Electromagnetic Compatibility Directive (EMC, 2014/30/EU)

Applicable to all electrical equipment that may generate electromagnetic interference or be affected by it, its core purpose is to control the electromagnetic emissions of products, prevent interference with the normal operation of surrounding devices, and ensure that the products themselves can resist certain electromagnetic environmental impacts.

Core Requirements: Products must meet two key indicators: Electromagnetic Emission (EMI) and Electromagnetic Susceptibility (EMS).

3. Other Specialized Directives (Applied as RequiRED)

In addition to the two basic directives above, some special electrical equipment must also comply with corresponding specialized directives:

①　Medical electrical devices: Must comply with the Medical Device Regulation (MDR 2017/745). For example, domestically produced ECMO systems exported to the EU need to obtain MDR certification.

②　Electrical equipment for explosive atmospheres: Must comply with the ATEX Directive (2014/34/EU).

③　Radio equipment (e.g., Bluetooth speakers, routers): Must comply with the Radio Equipment Directive (RED 2014/53/EU).

Scope of Application for CE Certification of Electrical Equipment

The EU clearly defines the scope of CE certification for electrical equipment, which primarily covers "devices with electrical functions intended to be placed on the EU market", including but not limited to:

①　Household electrical appliances: Refrigerators, washing machines, air conditioners, rice cookers, electric fans, lighting fixtures, etc.

②　Industrial electrical equipment: Motors, welding machines, frequency converters, control cabinets, sensors, solenoid valves, etc.

③　Electronic devices: Power adapters, power banks, printers, monitors, audio equipment, etc.

④　Medical electrical equipment: Electrocardiographs, ultrasonic diagnostic instruments, medical monitors, etc. (additional compliance with MDR is required).

⑤　Important Note: Not all electrical-related products require the CE mark. For example, household plugs and sockets are not within the scope of ce marking application. EU member states still implement separate certification controls (e.g., VDE in Germany, BS in the UK). Enterprises should avoid the compliance risks caused by misusing the CE mark.

Required Documentation and Certification Process

3. Clarify Requirements and Prepare Basic Documentation

Confirm the directives applicable to the product (e.g., LVD + EMC) and corresponding standards.

Required Documentation: Product technical parameters, design drawings, production process specifications.

4. Entrust Testing and Obtain Test Reports

Commission a compliant laboratory to conduct a full scope of tests (e.g., LVD insulation/temperature rise tests, EMC emission/susceptibility tests).

Required Documentation: Test samples, basic technical data.

Output: Formal test reports.

1. Compile Technical Documentation to Ensure Traceability

Required Documentation/Output: Product instruction manuals, component lists, test reports, risk assessment reports, Declaration of Conformity (DoC).

4. Conformity Assessment and Complete Declaration/Certification

①　Low-risk products: Manufacturers sign the DoC to complete self-declaration.

②　High-risk products: Entrust a notified body for audit, then sign the DoC after obtaining the certification certificate.

Required Documentation: Full set of technical documentation, test reports.

5. Affix CE Mark and Legally Launch on the Market

Required Documentation: Certification-related supporting documents.

Operation: Affix the clear and permanent CE mark on the product/package, indicating the manufacturer’s/authorized representative’s information and product model. After completion, the product can be launched on the EU market.

If you need assistance with other aspects of CE certification, please feel free to contact JJR LAB at any time!