Directive 2011/65/EU of the European Parliament and of the CouncilShow full title
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)
Introductory Text
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
Signature
ANNEX I
Categories of EEE covered by this Directive
1. Large household appliances.
2. Small household appliances.
3. IT and telecommunications equipment.
4. Consumer equipment.
5. Lighting equipment.
6. Electrical and electronic tools.
7. Toys, leisure and sports equipment.
8. Medical devices.
9. Monitoring and control instruments including industrial monitoring and control instruments....
10. Automatic dispensers.
11. Other EEE not covered by any of the categories above....
ANNEX II
Restricted substances referred to in Article 4(1) and maximum concentration values tolerated by weight in homogeneous materials
Lead (0,1 %) Mercury (0,1 %) Cadmium (0,01 %) Hexavalent chromium (0,1 %) Polybrominated...
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
1. Lead, cadmium and mercury in detectors for ionising radiation.
2. Lead bearings in X-ray tubes.
3. Lead in electromagnetic radiation amplification devices: micro-channel plate and capillary...
4. Lead in glass frit of X-ray tubes and image intensifiers...
5. Lead in shielding for ionising radiation.
6. Lead in X-ray test objects.
7. Lead stearate X-ray diffraction crystals.
8. Radioactive cadmium isotope source for portable X-ray fluorescence spectrometers.
Sensors, detectors and electrodes
1a. Lead and cadmium in ion selective electrodes including glass of...
1b. Lead anodes in electrochemical oxygen sensors.
1c. Lead, cadmium and mercury in infra-red light detectors.
1d. Mercury in reference electrodes: low chloride mercury chloride, mercury sulphate...
Others
9. Cadmium in helium-cadmium lasers.
10. Lead and cadmium in atomic absorption spectroscopy lamps.
11. Lead in alloys as a superconductor and thermal conductor in...
12. Lead and cadmium in metallic bonds to superconducting materials in...
13. Lead in counterweights.
14. Lead in single crystal piezoelectric materials for ultrasonic transducers.
15. Lead in solders for bonding to ultrasonic transducers.
16. Mercury in very high accuracy capacitance and loss measurement bridges...
17. Lead in solders in portable emergency defibrillators.
18. Lead in solders of high performance infrared imaging modules to...
19. Lead in Liquid crystal on silicon (LCoS) displays.
20. Cadmium in X-ray measurement filters.
ANNEX V
Applications for granting, renewing and revoking exemptions as referred to in Article 5
Applications for exemptions, renewal of exemptions or, mutatis mutandis, for...
the name, address and contact details of the applicant; information...
ANNEX VI
EU DECLARATION OF CONFORMITY
1. No … (unique identification of the EEE):
2. Name and address of the manufacturer or his authorised representative:...
3. This declaration of conformity is issued under the sole responsibility...
4. Object of the declaration (identification of EEE allowing traceability. It...
5. The object of the declaration described above is in conformity...
6. Where applicable, references to the relevant harmonised standards used or...
7. Additional information:
Signed for and on behalf of: …
(place and date of issue):
(name, function) (signature):
ANNEX VII
PART A
PART B
ANNEX VIII