Directive 2011/65/EU of the European Parliament and of the Council of 8 June 2011... (32011L0065)
Directive 2011/65/EU of the European Parliament and of the Council of 8 June 2011 on the restriction of the use of certain hazardous substances in electrical and electronic equipment (recast) Text with EEA relevance
- DIRECTIVE 2011/65/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
- of 8 June 2011
- on the restriction of the use of certain hazardous substances in electrical and electronic equipment
- (recast)
- (Text with EEA relevance)
- Article 1
- Subject matter
- Article 2
- Scope
- Article 3
- Definitions
- Article 4
- Prevention
- Article 5
- Adaptation of the Annexes to scientific and technical progress
- Article 6
- Review and amendment of list of restricted substances in Annex II
- Article 7
- Obligations of manufacturers
- Article 8
- Obligations of authorised representatives
- Article 9
- Obligations of importers
- Article 10
- Obligations of distributors
- Article 11
- Cases in which obligations of manufacturers apply to importers and distributors
- Article 12
- Identification of economic operators
- Article 13
- EU declaration of conformity
- Article 14
- General principles of the CE marking
- Article 15
- Rules and conditions for affixing the CE marking
- Article 16
- Presumption of conformity
- Article 17
- Formal objection to a harmonised standard
- Article 18
- Market surveillance and controls of EEE entering the Union market
- Article 19
- Committee procedure
- Article 20
- Exercise of the delegation
- Article 21
- Revocation of the delegation
- Article 22
- Objections to delegated acts
- Article 23
- Penalties
- Article 24
- Review
- Article 25
- Transposition
- Article 26
- Repeal
- Article 27
- Entry into force
- Article 28
- Addressees
- ANNEX I
- Categories of EEE covered by this Directive
- ANNEX II
- Restricted substances referred to in Article 4(1) and maximum concentration values tolerated by weight in homogeneous materials
- ANNEX III
- ANNEX IV
- Applications exempted from the restriction in Article 4(1) specific to medical devices and monitoring and control instruments
- Equipment utilising or detecting ionising radiation
- Sensors, detectors and electrodes
- Others
- ANNEX V
- Applications for granting, renewing and revoking exemptions as referred to in Article 5
- ANNEX VI
- EU DECLARATION OF CONFORMITY
- ANNEX VII
- PART A
- PART B
- ANNEX VIII
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