Примери за използване на His authorised representative established на Английски и техните преводи на Български
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Name and address of the manufacturer or his authorised representative established in the Community.
The manufacturer, or his authorised representative established within the Community, must affix the II marking to each item of transportable pressure equipment and draw up a written declaration of conformity.
Name and address of the manufacturer or his authorised representative established in the Community(2).
The manufacturer, or his authorised representative established within the Community, must keep a copy of the declaration of conformity for a period of 10 years after the last of the transportable pressure equipment has been manufactured.
The CE marking is affixed by the manufacturer(established inside or outside the Union), or by his authorised representative established within the Union.
The manufacturer, or his authorised representative established within the Community, must keep a copy of the declaration of conformity with the technical documentation.
Before a safety component isplaced on the market, the manufacturer or his authorised representative established in the Community must.
The manufacturer, or his authorised representative established within the Community, must affix the Π marking to each product and draw up a written declaration of conformity.
The CE marking must be affixed by the manufacturer(established inside or outside the Union), or by his authorised representative established within the Union'European Commission.
The manufacturer or his authorised representative established within the Community must affix the CE marking to each product and draw up a written declaration of conformity.
(9) In the module,‘the contracting entity' means‘the subsystem contracting entity,as defined in the directive, or his authorised representative established within the Community'.
The disposal of products from the manufacturer to his authorised representative established in the EU who is responsible on behalf of the manufacturer for ensuring compliance with the Directive;
In general the CE marking must be affixed during the production control phase by the manufacturer or his authorised representative established within the European Union.
The manufacturer or his authorised representative established within the Community must affix the CE marking to each component and must draw up a written declaration of conformity.
For the conformity assessment procedure of an interoperability constituent of the Energy subsystem,the manufacturer or his authorised representative established within the Community may choose either.
If the manufacturer or his authorised representative established within the Community is denied an EC type-examination certificate, the notified body must provide detailed reasons for such denial.
Assessment of the conformity orsuitability for use of an interoperability constituent shall be carried out by the notified body with which the manufacturer or his authorised representative established in the Community has lodged the application.
The manufacturer or his authorised representative established within the Union must draw up and sign an EU Declaration of Conformity as part of the conformity assessment procedure provided for in the Union harmonisation legislation.
Article 8 of the directive describes the procedures whereby the manufacturer or his authorised representative established within the EU ensures and declares that the product complies with directive 94/9/EC.
The manufacturer or his authorised representative established within the Community shall keep the notified body that has approved the quality assurance system informed of any intended updating of the quality assurance system.
To establish the declaration«CE»conformity or suitability for use of an interoperability constituent, the manufacturer or his authorised representative established in the European Union shall apply the provisions laid down in the TSIs relating.
Where neither the manufacturer nor his authorised representative established in the Community has met the obligations of paragraphs 1 and 3, those obligations shall be incumbent on any person who places interoperability constituents on the market.
In order to establish the‘EC' declaration of conformity or suitability for use of an interoperability constituent, the manufacturer or his authorised representative established in the Community shall apply the provisions laid down by the relevant TSIs.
The name and address of the manufacturer or his authorised representative established within the Community(give trade name and full address and in the case of an authorised representative also give the trade name of the manufacturer or constructor).
As far as required by the modules specified in Annex A to this TSI, the assessment of conformity of an interoperability constituent shall be conducted by the Notified Body,appointed by the manufacturer or his authorised representative established within the Community.
The name and address of the manufacturer or his authorised representative established within the Community(give trade name and full address and in the case of an authorised representative also give the trade name of the manufacturer or constructor).
When required by the corresponding TSI, the assessment of the conformity orthe suitability for use of an interoperability constituent is performed by the notified body with which the manufacturer or his authorised representative established in the European Union has made the request.
The manufacturer, or his authorised representative established within the Community, must keep with the technical documentation copies of EC type-examination certificates and their additions for a period of 10 years after the last of the transportable pressure equipment has been manufactured.
Where the corresponding STI so requires, assessment of the conformity orsuitability for use of an interoperability constituent shall be carried out by the notified body with which the manufacturer or his authorised representative established in the Community has lodged the application.
The manufacturer, his authorised representative established within the Community or the person responsible for placing the apparatus on the market, must present the file to one or more notified bodies, each of the notified bodies must be informed of others who have received the file.