CE Certification Canada

JJR Laboratory provides CE certification services for a variety of products for Canadian manufacturers, including electronic products, wireless devices, medical devices, footwear, and more, helping businesses export smoothly to the European Union. We can also help you save up to 40% on certification testing fees. Feel free to send us your product specifications to get detailed information on ce certification costs.

What is CE Certification?

CE certification is a mandatory product safety certification system implemented by the European Union to protect the safety of people and property in EU countries. The CE mark is considered the "passport" for manufacturers to enter the European market. It applies to 80% of industrial and consumer products, as well as 70% of EU-imported products. According to EU law, CE certification is mandatory, and if a product is exported to the EU without CE certification, it is considered illegal.

What are the specific requirements for the CE mark?

• The height of the CE letters must be at least 5mm, with a total length not exceeding 12mm, and the width should be no less than 1/5 of the height.

• The thickness should be at least 1/5 of the height, and the radius of the internal crossbar should be at least 80% of the external radius.

• In addition to the CE mark, the product label should also include:

  o Warnings and precautions printed in the local market language;

  o The name, trademark, and address of the manufacturer, authorized representative, or importer;

  o For electronic products sold to Germany, the product must also include the electronic waste recycling symbol, etc.

Cross-border e-commerce operators should note that these marks cannot be added arbitrarily to comply. They must entrust an agent to handle the related registration and sign a recycling contract.

Which countries require CE certification?

• The CE mark applies to all 27 EU member countries.

• In addition to EU members, the European Free Trade Association (EFTA) countries, such as Iceland, Liechtenstein, and Norway, also require the CE mark.

• Semi-EU countries like Turkey also require CE certification as a mandatory entry requirement.

Which products need CE certification?

Almost all products exported to the EU require CE certification, especially the following categories:

• Power supplies: communication power supplies, chargers, display power supplies, etc.;

• Lighting: chandeliers, garden lights, table lamps, etc.;

• Home appliances: fans, electric kettles, audio equipment, etc.;

• Electronics: earplugs, routers, mobile phone batteries, etc.;

• Wireless products: Bluetooth devices, wireless mice, remote controls, etc.;

• Machinery: welding machines, CNC drills, excavators, etc.

Consequences of not having CE certification or non-compliant products

Products that do not pass CE certification or do not comply with EU standards will face the following consequences:

• Cannot pass customs;

• May be detained or confiscated;

• Face high fines;

• Product withdrawal from the market and recall;

• May face criminal liability;

• Notification across the entire EU.

Legal Basis for CE Certification

The basis for CE certification is several technical directives issued by the EU, covering a wide range of product categories from toys, electrical appliances to machinery. Each directive stipulates basic safety requirements for products and how to meet these requirements.

How to obtain CE certification?

The methods of obtaining CE certification are divided into three categories based on product risk levels:

• The company self-issues a Declaration of Conformity;

• A third-party organization issues a conformity certificate;

• An EU notified body issues a standard conformity certificate.

Required documents for CE certification

• Product Declaration of Conformity

• Technical documentation

• User manual

• Testing reports

Contents of the Declaration of Conformity (DoC)

The DoC is issued by the manufacturer or importer to prove the product's compliance with EU regulations. It includes:

• Product name, model, and manufacturer/importer information;

• Applicable EN standards or directives;

• Signature of the responsible person, etc.

Responsible party for the Declaration of Conformity

• Importer: If the manufacturer is located outside the EU, the importer is responsible for product safety and ensuring the accuracy of the Declaration of Conformity.

Who can request the Declaration of Conformity?

• Importer: The importer has the right to request the Declaration of Conformity from the manufacturer.

• Market surveillance authorities: They have the right to assess whether the product meets relevant standards.

• Consumers: According to regulations, consumers also have the right to request the Declaration of Conformity from the manufacturer.

• Retailers: To avoid product recalls or consumer complaints, retailers usually require the Declaration of Conformity.

Obligations of the manufacturer

The manufacturer should ensure that the product complies with relevant regulations and:

• Provide the Declaration of Conformity and/or a certificate of conformity;

• Ensure compliance with the production process;

• Provide clear product identification, name, and contact information;

• If the product is non-compliant, take corrective actions.

What should technical documentation include?

• Product description, design drawings;

• List of applicable standards;

• Testing reports and quality control records;

• User manual, risk assessment reports, etc.

What should the user manual include?

• Installation instructions;

• Parts names and overview;

• Safety instructions;

• Usage and environmental handling instructions.

The necessity of testing reports

Although not all products require a testing report, a testing report is usually necessary to ensure compliance. Customs and market surveillance authorities have the right to request and verify whether a product meets the standards based on the testing report.

Why is an EU Authorized Representative needed?

To ensure product safety, EU law requires manufacturers outside the EU to designate an EU Authorized Representative to ensure that the product complies with all safety requirements during its market circulation within the EU.

For more information or assistance, please feel free to contact us. JJR Laboratory is dedicated to providing professional CE certification services to help your products enter the European market smoothly.