欧洲议会和理事会指令94/27/EC,对各成员国有关限制销售和使用某些危险材料及制品的法律、法规和管理条例的协调与统一的理事会指令76/769/EEC进行第12次修改

技术法规类型:欧盟Eurlex法规 来源:tbtmap

EURLEX ID:31994L0027

OJ编号:OJ L 188, 22.7.1994, p. 1-2

中文标题:欧洲议会和理事会指令94/27/EC,对各成员国有关限制销售和使用某些危险材料及制品的法律、法规和管理条例的协调与统一的理事会指令76/769/EEC进行第12次修改

原文标题:European Parliament and Council Directive 94/27/EC of 30 June 1994 amending for the 12th time Directive 76/769/EEC on the approximation of the laws, regulations and administrative provisions of the Member States relating to restrictions on the marketing and use of certain dangerous substances and preparations

分类:13.30.18_危险物质;15.10.20.50_化学品、工业风险与生物技术;15.20.30_健康与安全保护

文件类型:二级立法 Directive|指令

生效日期:1994-08-11

废止日期:2009-05-31

法规全文:查看欧盟官方文件

EUR-Lex - 31994L0027 - EN
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31994L0027


Title and reference

European Parliament and Council Directive 94/27/EC of 30 June 1994 amending for the 12th time Directive 76/769/EEC on the approximation of the laws, regulations and administrative provisions of the Member States relating to restrictions on the marketing and use of certain dangerous substances and preparations

?OJ L 188, 22.7.1994, p. 1–2 (ES, DA, DE, EL, EN, FR, IT, NL, PT)
?Finnish special edition: Chapter 13 Volume 26 P. 0128
?Swedish special edition: Chapter 13 Volume 26 P. 0128
?Special edition in Czech Chapter 13 Volume 013 P. 224 - 225
?Special edition in Estonian Chapter 13 Volume 013 P. 224 - 225
?Special edition in Hungarian Chapter 13 Volume 013 P. 224 - 225
?Special edition in Lithuanian Chapter 13 Volume 013 P. 224 - 225
?Special edition in Latvian Chapter 13 Volume 013 P. 224 - 225
?Special edition in Maltese Chapter 13 Volume 013 P. 224 - 225
?Special edition in Polish Chapter 13 Volume 013 P. 224 - 225
?Special edition in Slovakian Chapter 13 Volume 013 P. 224 - 225
?Special edition in Slovenian Chapter 13 Volume 013 P. 224 - 225

?DA?DE?EL?EN?ES?FR?IT?NL?PT

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Authentic language

  • The official languages, Icelandic, Norwegian

Dates

    of document: 30/06/1994
    of effect: 11/08/1994; Entry into force Date pub. + 20 See 192E191-P 1
    end of validity: 31/05/2009; See 376L0769
    of transposition: 20/01/2000; See Art 2

Classifications

Miscellaneous information

  • Author:
    European Parliament, Council
  • Form:
    Directive
  • Addressee:
    The Member States
  • Internal reference:
    COM/93/633COM/93/633
  • Additional information:
    Extended to the EEA by 21995D0302(07) Directive amending COD 456

Relationship between documents

Text

Bilingual display: BG CS DA DE EL EN ES ET FI FR HU IT LT LV MT NL PL PT RO SK SL SV

EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE 94/27/EC

of 30 June 1994

amending for the 12th time (*) Directive 76/769/EEC on the approximation of the laws, regulations and administrative provisions of the Member States relating to restrictions on the marketing and use of certain dangerous substances and preparations

THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION,

Having regard to the Treaty establishing the European Community, and in particular Article 100a thereof,

Having regard to the proposal from the Commission (1),

Having regard to the opinion of the Economic and Social Committee (2),

Acting in accordance with the procedure referred to in Article 189b of the Treaty (3),

Whereas Article 8a of the Treaty establishes an area without internal frontiers in which the free movement of goods, persons, services and capital is ensured;

Whereas work on the internal market should gradually improve the quality of life, health protection and consumer safety; whereas the measures proposed by this Directive are in line with the Council resolution of 9 November 1989 on future priorities for relaunching consumer protection policy;

Whereas the presence of nickel in certain objects coming into direct and prolonged contact with the skin may cause sensitization of humans to nickel and may lead to allergic reactions; whereas for these reasons the use of nickel in such objects should be limited;

Whereas one Member State has already introduced a set of control measures on its territory to counteract nickel sensitization and nickel allergy and a second Member State plans to introduce on its territory a different set of control measures; whereas there is therefore a risk of barriers to trade;

Whereas the test methods to be used in demonstrating conformity with this Directive should be defined and published before the Directive is implemented; whereas these test methods should be the subject of a European standard;

Whereas limitations already adopted or planned by certain Member States on the use of nickel directly affect the completion and functioning of the internal market; whereas it is therefore necessary to approximate the laws of the Member States in this field and consequently to amend Annex I to Directive 76/769/EEC (4),

HAVE ADOPTED THIS DIRECTIVE:

Article 1

Annex I to Directive 76/769/EEC is hereby supplemented

Article 2

1. Member States shall adopt the laws, regulations and administrative provisions necessary to comply with this Directive not later than six months after publication by the Commission in the Official Journal of the European Communities, of the standards adopted by the European Committee for Standardization (CEN) on all the test methods used in demonstrating the conformity of the products with this Directive, or six months after the adoption of this Directive if that date is later than the former, so that:

- six months after the expiry of one or other of those periods, whichever is applicable, no manufacturer or importer may place on the market products which fail to comply with this Directive,

- 18 months after the expiry of one or other of those periods, whichever is applicable, products which fail to comply with this Directive cannot be sold or made available to the final consumer, unless they have been placed on the market before the expiry of the period in question.

They shall forthwith inform the Commission thereof.

2. When Member States adopt the measures referred to in paragraph 1, they shall contain a reference to this Directive or shall be accompanied by such reference on the occasion of their official publication. The methods of making such reference shall be laid down by the Member States.

Article 3

This Directive is addressed to the Member States.

Done at Brussels, 30 June 1994.

For the European Parliament

E. KLEPSCH

The President

For the Council

A. BALTAS

The President

(*) The Commission proposal was presented at the 14th amendment of Directive 76/769/EEC (OJ No C 116, 27. 4. 1993, p. 18).

(1) OJ No C 116, 27. 4. 1993, p. 18.

(2) OJ No C 304, 10. 11. 1993, p. 2.

(3) Opinion of the European Parliament of 2 December 1993 (OJ No C 342, 20. 12. 1993, p. 15), Council common position of 4 March 1994 (OJ No C 137, 19. 5. 1994, p. 60) and Decision of the European Parliament of 5 May 1994 (not yet published).

(4) OJ No L 262, 27. 9. 1976, p. 201. Directive as last amended by Directive 91/339/EEC (OJ No L 186, 12. 7. 1991, p. 64).

ANNEX

'28. Nickel CAS No 7440-0-20 EINECS No 2311114 and its compounds

May not be used:

1. in post assemblies which are inserted into pierced ears and other pierced parts of the human body during epithelization of the wound caused by piercing, whether subsequently removed or not, unless such post assemblies are homogeneous and the concentration of nickel - expressed as mass of nickel to total mass - is less than 0,05 %;

2. in products intended to come into direct and prolonged contact with the skin such as:

- earrings,

- necklaces, bracelets and chains, anklets, finger rings,

- wrist-watch cases, watch straps and tighteners,

- rivet buttons, tighteners, rivets, zippers and metal marks, when these are used in garments

if the rate of nickel release from the parts of these products coming into direct and prolonged contact with the skin is greater than 0,5 ìg/cm?/week;

3. in products such as those listed in point 2 where these have a non-nickel coating unless such coating is sufficient to ensure that the rate of nickel release from those parts of such products coming into direct and prolonged contact with the skin will not exceed 0,5 ìg/cm?/week for a period of at least two years of normal use of the product.

Furthermore, products which are the subject of points 1, 2 and 3, may not be placed on the market unless they conform to the requirements set out in those points'.

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