The WEEE Directive correctly applied to CE marking.

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CE AS PRODUCER

The 7m high "WEEE Man" sculpture in London is made from 3.3tons of electronic waste. The average amount of electronic waste a person leaves during their lifetime.

WEEE stands for Waste Electrical and Electronic Equipment. WEEE Directive 2012/19/EU is the European Community Directive on Waste Electrical and Electronic Equipment (WEEE), which, together with RoHS Directive 2002/95/EC, became European law in February 2003. It is a major step towards implementing the zero-waste concept by setting collection, recycling and recovery targets for all types of e-waste. The WEEE Directive covers 14 different categories of electrical and electronic equipment.

Certain types of electrical and electronic equipment are excluded from the requirements of the WEEE-RL. WEEE compliant products currently do not require CE marking unless otherwise required to have a CE marking For example, products that are classified as medical devices, products that contain hazardous substances according to RoHS, or products that fall under the Low Voltage Directive. Learn more about the application of the WEEE directive, the connection with other directives and the CE marking

The experts at easyCE will be happy to help you place your products on the market and assess special cases. We are happy to support you with CE, UKCA and other labelling.

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FAQ

What is the WEEE Directive?

WEEE steht für Elektro- und Elektronikaltgeräte. The WEEE-Directive 2012/19/EU is the European Community Directive on Waste Electrical and Electronic Equipment (WEEE), which together with the RoHS-Directive 2002/95/EG became European

Which products are covered by the WEEE Directive?

The WEEE Directive covers 14 different categories of electrical and electronic equipment. Based on various provisions of the WEEE Directive, electrical and electronic equipment can be divided into 14 categories for practical reasons:

What are the requirements for classifying products for the WEEE Directive?

Due to the heterogeneity of e-waste, there is no uniform classification rule for regulators. However, the WEEE Directive includes a number of product classifications relevant to the variety of functions involved. All applicants for compliance with the WEEE Directive must choose a product category within the four levels, taking into account their national legal and business considerations.

What types of products are NOT affected by the WEEE Directive?

WEEE does not apply to certain types of electrical and electronic equipment, in particular

How does the WEEE Directive relate to the CE marking?

WEEE compliant products currently do not require CE marking unless otherwise required to have a CE marking. For example medical devices or devices covered by the Low Voltage Directive.

What is the link between the Low Voltage Directive (2006/95/EC) and the WEEE Directive?

The relationship between The Low Voltage Directive and WEEE-Directive is that the product class overlaps which are regulated by the guidelines.

How are RoHS and WEEE related?

The relationship between RoHS- und WEEE-Directive is dangerous electronic waste. The WEEE Directive and the RoHS Directive (Restrictions on Hazardous Substances) have been harmonised

What measures does the WEEE Directive require?

A main focus of the WEEE Directive is the principle of extended producer responsibility (EPR). EPR ensures an effective implementation of WEEE because product manufacturers know best about the design and manufacture of a product. Therefore, they have the most direct impact on how their products can be recycled. The transfer of responsibility also includes financial responsibility and thus enables reinvestment in recycling systems.

What does EPR or extended producer responsibility (Extended Producer Responsibility) mean?

The principle of Extended Producer Responsibility (EPR) states that "companies bringing products to market should be responsible for the entire life cycle of these products and packaging. By making them responsible, they have more incentives to produce less waste and recycle more.

What is the Manufacturer Compliance Scheme (PCS) of the WEEE Directive?

A Producer Compliance Scheme (PCS) is an organization whose members are involved in the production and sale of electrical and electronic equipment (EEE). National governments support EEE manufacturers in establishing PCS among themselves.

What do I have to implement to be compliant with the WEEE Directive and to comply with all requirements?

The implementation of the WEEE Directive generally entails that manufacturers or. Distributor who must meet extended manufacturer responsibility (EPR principle). However, the implementation requires a certain infrastructure for the collection and recycling of waste.

What is a withdrawal management infrastructure under the WEEE Directive and what does it consist of (HWRC, DCF, AATF)?

The withdrawal management infrastructure is designed to comply with the EPR principle and consists of several components. Infrastructure for delivery of waste to domestic waste recycling centres (HWRC)

What is a WEEE certified recycler?

Certified recyclers play a central role in the recycling process. The Environmental Protection Agency (EPA) promotes the role of certified recyclers to ensure a responsible recycling process. All electronic recyclers are certified by demonstrating to an accredited and independent auditor that they meet certain standards for safe recycling.

How can I register as an EPR?

Officially, the WEEE Directive is not a CE marking directive. However, it applies to products that must meet CE requirements.There are many overlaps with RoHS RL and low voltage RL

What do I need to prove to register and receive an ERP certificate?

In order to comply with the directive, a manufacturer must register for the EPR certificate by fulfilling the following points.

How does the regular declaration of the material placed on the market work?

Manufacturers must declare their actual quantities and weights placed on the EU market to the regulatory authority. This data is carefully stored and analyzed to calculate the collection and recycling targets to be achieved globally for the member states and individually per manufacturer.

What are the labelling requirements of the WEEE Directive?

Products must have a special symbol for the marking of electrical and electronic equipment: the crossed-out garbage can. A WEEE symbol on a product informs customers that the product with this label must not be disposed of in a landfill or with household waste. Instead, customers can claim the return by refunding the manufacturer.

What information must be provided to the recycling company?

Manufacturers of electrical and electronic equipment must provide disassembly instructions and recommendations for easy disassembly, removal of pollutants and recycling of electrical and electronic waste.

How must return and recycling be organized?

Manufacturers must be able to offer end users return logistics. They must therefore implement a withdrawal management infrastructure.

What does the WEEE symbol look like and what does it mean?

The WEEE symbol is a crossed-out garbage can. The black line below indicates that the goods were placed on the market after 2005, when the directive entered into force. Goods without the black line were produced between 2002 and 2005.

What is the purpose of the WEEE Directive?

The WEEE Directive pursues the goal of a zero-waste system. At present, our production system is on a linear path from extracting raw materials from the earth to careless production and irresponsible disposal.

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Reference Projects

CE marking of laboratory machines developed in-house

CE marking of laboratory machines developed in-house

In the course of an upcoming ISO 45001 occupational health and safety audit, easyCE supported a laboratory technology manufacturer in ensuring CE conformity for its internally used validation machines for medical equipment. Our specialists conducted a comprehensive assessment of occupational health and safety aspects and integrated these into the CE documentation. Particular attention was paid to safe operation by laboratory staff and the documentation of risk assessments that meet both CE and ISO 45001 requirements.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU EN ISO 12100, EN 60204-1

CE marking for a laboratory robot

CE marking for a laboratory robot

In the course of an upcoming ISO 45001 occupational health and safety audit, easyCE supported a medical technology manufacturer in achieving CE conformity for its coagulation robot—a specialized laboratory machine for the automated performance of coagulation cycles for testing purposes. Our specialists conducted a comprehensive assessment of occupational health and safety aspects and integrated these into the CE documentation. Particular attention was paid to the safe handling of electrosurgical components and the documentation of risk assessments that meet both CE and ISO 45001 requirements.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU, EN ISO 12100, EN 60204-1, etc.

CE marking and consulting for laboratory equipment

CE marking and consulting for laboratory equipment

In the context of an upcoming ISO 45001 certification, easyCE supported a medical technology manufacturer with the CE documentation for a specialized testing and calibration machine for insufflators in the laboratory sector. Our specialists developed integrated documentation that covers both the CE requirements and the occupational health and safety aspects according to ISO 45001. Particular attention was paid to the safety requirements for handling various hose systems and connections, which can vary depending on the insufflator model.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU, EN ISO 12100, EN 60204-1 etc.

CE marking for electrical equipment in medical laboratories

CE marking for electrical equipment in medical laboratories

As part of the ISO 45001 certification preparation process, easyCE supported a manufacturer of electrical laboratory equipment in the correct classification and CE conformity of its products. Our experts carried out a precise analysis to distinguish between medical devices and electrical equipment in order to ensure correct classification in terms of occupational health and safety. This clarity was crucial for the ISO 45001 requirements regarding hazard identification and risk assessment in the workplace. Successful documentation and conformity assessment enabled the customer to operate its laboratory equipment in full compliance with occupational health and safety guidelines and to pass the ISO audit without any objections.

Takes into account, among others: EN 55032, EN 55035, EN 60335-1 etc.

CE marking for test station for low-pressure units

CE marking for test station for low-pressure units

In the run-up to an ISO 45001 occupational health and safety audit, easyCE supported an industrial company in compiling CE documentation for an internal test bench for low-pressure units in accordance with occupational health and safety regulations. Our experts first analyzed the regulatory classification of the test bench and were able to prove through precise measurements that the Pressure Equipment Directive was not applicable. This clarification was crucial for the correct risk assessment within the framework of the ISO 45001 management system. The CE documentation subsequently created took particular account of occupational health and safety aspects such as operational safety and emergency procedures. This enabled the customer not only to demonstrate CE conformity, but also to pass its ISO 45001 certification without any deviations in the area of work equipment.

Takes into account, among others: 2006/42/EG, EN ISO 12100, EN 60204-1, EN ISO 4414, EN ISO 13849-1 etc.

Learn more about our project references and success stories

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Willy Lebherz - Founder and Managing Director of easyCE

  • Expert in product safety and conformity since 1995
  • Recipient of the "Medal of the Order of Merit of the Federal Republic of Germany", awarded in 1983 by the then Federal President Carl Carstens
  • Master of measurement and control technology
  • Captain (ret.), Project Officer for Technical Logistics in the Army Material Office and Chief of the Telecommunications Repair Company

easyCE is a digital, dynamic engineering office with a focus on product safety and product conformity - especially CE-marking. We support manufacturers, operators and dealers in designing products safely and offering them on the market in compliance. We are a "full-service provider" and can take over the entire conformity assessment process for you if you wish. To do this, we support you in carrying out risk assessments, researching standards, product analyses, developing suitable safety precautions, preparing user-friendly technical documentation, coordinating tests and all other accompanying measures. easyCE was founded in southern Germany, but is now active globally.

We know what you need to do to get CE-marking done, worry-free.