Examples of using Representative established in English and their translations into Polish
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Colloquial
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Medicine
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
It shall forthwith so inform the manufacturer or its authorised representative established in the Community.
The manufacturer or his authorized representative established within the Community shall keep the following information available for inspection.
The application for EC type-examination shall be lodged with an approved body by the manufacturer or by his authorized representative established within the Community.
The manufacturer may instruct his authorized representative established in the Community to initiate the procedures provided for in Annexes III, IV, VII and VIII.
Identification of the signatory who has been empowered to enter into commitments on behalf of the manufacturer or his authorized representative established within the Community.
People also translate
The manufacturer or his authorized representative established in the Community shall affix the CE marking to each piece of equipment and shall draw up a declaration of conformity.
The application for type-examination shall be lodged by the manufacturer or his authorised representative established within the Community with a single notified body.
The manufacturer or his authorized representative established in the Community shall keep the report referred to in point 2.3.7 of Annex X at the disposal of the competent authorities.
The application for the EC-type examination shall be lodged by the manufacturer or his authorized representative established within the Community with a notified body of his choice.
The manufacturer or his authorised representative established within the Community shall affix the CE marking to each instrument and the inscriptions provided for in Annex IV and shall draw up a written declaration of conformity.
Equipment referred to in Article 2(1) shall not be placed on the market or put into service until the manufacturer,or his authorised representative established in the Community, ensures that.
However, Member States shall allow the manufacturer, or his authorised representative established in the Community, to avail himself of the provisions of this Directive as from 3 July 2001.
The measures are unjustified, it shall immediately so inform the Member State which took the initiative, the other Member States andthe manufacturer or his authorised representative established in the Community.
The manufacturer or his authorised representative established in the Community should be responsible for ensuring that the equipment is in conformity with the provisions of this Directive and of any other directives that apply to it.
Where a manufacturer who places devices on the market under his own name does not have a registered place of business in a Member State,he shall designate a single authorized representative established in the Community.
Prior to the series production of PPE other than those referred to in paragraph 3,the manufacturer or his authorized representative established in the Community shall submit a model for EC type-examination as referred to in Article 10.
The third country issuer shall designate a representative established in its home Member State, among the entities which are subject to and supervised under EU financial services regulation, on the basis of an authorisation.
Pressure equipment and/or assemblies must be accompanied by adequate instructions for use andmust bear markings to permit identification of the manufacturer or of his authorized representative established within the Community.
The notified body and the manufacturer,or his authorized representative established in the Community, shall lay down, by common accord, the time limits for completion of the assessment and verification operations referred to in Annexes II to VI.
In order to draw up the EC declaration of conformity or suitability for use of an interoperability constituent,its manufacturer or his authorized representative established within the Community must apply the provisions laid down in the TSIs referring to it.
Where neither the manufacturer nor his authorized representative established within the Community has met the obligations of the paragraphs 1, 2 and 3, those obligations shall be incumbent on any person who places that interoperability constituent on the market.
Where, following that consultation, the Commission establishes that the measure is unjustified, it shall forthwith so inform the Member State that has taken the initiative andthe manufacturer or his authorized representative established within the Community.
Equipment-group II, equipment-category 3 The manufacturer or his authorized representative established in the Community must, in order to affix the CE marking, follow the procedure relating to internal control of production referred to n Annex VIII;
Where the Commission considers, after this consultation, that the measure is unjustified, it shall immediately so inform the Member State which took the initiative and the manufacturer,or his authorized representative established within the Community.
Before placing a PPE model on the market, the manufacturer or his authorized representative established in the Community shall assemble the technical documentation referred to in Annex III so that this can, if necessary, be submitted to the competent authorities.
Where so required by the TSIs, the assessment of conformity orsuitability for use of an interoperability constituent shall be appraised by the notified body with which the manufacturer or his authorized representative established within the Community has lodged the application.
Equipment-group I and II, equipment-category M 1 and1 The manufacturer or his authorized representative established in the Community must, in order to affix the CE marking, follow the CE type-examination procedure(referred to in Annex III), in conjunction with.
The manufacturer or his authorized representative established in the Community shall keep with the technical documentation copies of EC-type-examination certificates and their additions for a period ending at least 10 years after the last equipment or protective system was manufactured.
Before placing on the market or putting into service any equipmentreferred to in Article 12 the manufacturer, or his authorised representative established in the Community, shall subject each type of equipment to one of the following conformity assessment procedures.
The manufacturer, or its authorised representative established in the Community, shall ensure and declare, by means of the EC declaration of conformity or suitability for use, that he has applied the provisions laid down in the essential requirements and in the relevant implementing rules for interoperability.