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The resulting standards shall be expressed as far as practicable in product performance terms, having regard to the interpretative documents. Whereas it is necessary to ensure the conformity of products with harmonized standards and with non-harmonized technical specifications recognized at European level by means of procedures of production control by rchtlinie and of supervision, testing assessment and certification by independent qualified third parties, or by the manufacturer himself.
filwtype The approval bodies designated by the Member States form an organization. Use the Advanced search. The committee referred to in Article 19 may, at the request of its chairman or a Member State, examine any question posed by the implementation and the practical application of this Dichtlinie. Artikel 24 Diese Richtlinie ist an die Mitgliedstaaten gerichtet. In the absence of technical specifications, as defined in Article 4, for any given product, the Member State of destination shall, on request in individual cases, consider the product to be in conformity with the national provisions in force if they have filetypr tests and inspections carried out by an approved body in the producing Member State according to the methods in force in the Member State of destination or recognized as equivalent by that Member State.
Member States shall presume that the products are fit for their intended use if they enable works in which they 89-106-wwg employed, provided the latter are properly designed and. At the request of an authorized approval body, a complete set of supporting documents for an approval which has been granted is to be forwarded to the latter for information. The manufacturer’s declaration of conformity or the certificate of conformity shall entitle the manufacturer, or his agent established in the Community, to affix the corresponding EC richtlijie on the product itself, on a label attached to it, on its packaging or on the accompanying commercial documents.
Dabei ist dem jeweils am wenigsten aufwendigen Verfahren, das mit den Sicherheitsanforderungen vereinbar ist, der Vorzug zu geben.
EUR-Lex Access to European Union law
This Directive shall not affect the right of Member States to specify – with due observance of the provisions of the Treaty – the requirements they deem necessary to ensure that workers are protected when using products, provided it does not mean the products are modified in a way unspecified in this Directive Article 3 1. Member States shall ensure that the EC mark is correctly used. Whereas paragraph 71 of the White Paper on completing the internal market, approved by the European Council in Junestates that, within the general policy, particular emphasis will be placed on certain sectors, including construction; whereas the removal of technical barriers in the construction field, to the extent that they cannot be removed by mutual recognition of equivalence among all the Member States, should follow the new approach set out in the Council resolution of 7 May 4 which calls for the definition of essential requirements on safety and other aspects which are important for the general well-being, without reducing the existing and justified levels of protection in the Member States.
Member States shall ensure that the use of such products, for the purpose for which they were intended, shall not be impeded by rules or conditions imposed by public bodies or. If the Commission or a Member State believes that a technical specification no longer fulfills the conditions necessary for presumption of conformity with the provisions of Articles 2 and 3, the Commission shall consult the committee referred to in Article Chapter 13 Volume P. Mechanical resistance and stability The construction works must be designed and built in such a way that the loadings that are liable to act on it during its constructions and use will not lead to any of the following: The representative of the Commission shall submit to the committee a draft of the measures to be taken.
Whereas performance levels and requirements to be fulfilled by products in future in the Member States shall be laid down in classes in the interpretative documents and in the harmonized technical specifications in order to take account of different levels of essential requirements for certain works and of different conditions prevailing in the Member States.
The EC mark shall indicate:. Hat ein Mitgliedstaat mehr als eine ZuIassungsstelle bestimmt, obliegt dem Mitgliedstaat die Koordinierung dieser Stellen; er bestimmt auch jeweils die Stelle, die im Gremium spricht.
The Member State of destination richtlibie the producing Member State shall provide each other with all necessary information. The European technical approval for a product shall be issued in a Member State in accordance with the procedure laid down in Annex II at the request of the manufacturer or his agent established in the Community. Dies gilt bis zum Inkrafttreten der harmonisierten Norm in den Mitgliedstaaten.
OJ L 40, Help Print this page. Where a Member State has designated more than one approval body, the Member State shall be responsible for coordinating such bodies; it shall also designate the body which shall be spokesman in the organization. The testing laboratories, the inspection bodies and the certification bodies designated by the Member States must filrtype the following minimum conditions:.
EUR-Lex – L – EN – EUR-Lex
C 95 vom The EC mark shall indicate: Would you like to keep them? If a Member State has misgivings, richtoinie shall substantiate its position and inform the Commission.
The approval bodies must satisfy the requirements of chis Directive and in particular must be able:. In the performance of its duties, this organization is obliged to work in close coordination with the Commission, which shall consult the committee referred to in Article 19 of the Directive on important matters. Whereas riichtlinie responsibility of Member States for safety, health and other matters covered by the essential requirements on their territory should be recognized in a safeguard clause providing for appropriate protective measures.
If the approval bodies cannot agree, the matter shall be referred to the committee referred to in Article The Commission shall publish the interpretative documents in the ‘G’ series of the Official Official Journal of the European Countries after Soliciting the opinion of the committee referred to in Article
