Примери за използване на His authorised representative на Английски и техните преводи на Български
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
Manufacturer or his authorised representative.
The CE marking shall be affixed only by the manufacturer or his authorised representative.
For this purpose, the exporter or his authorised representative shall fill out both the movement certificate EUR.
The name and address of the manufacturer and, where appropriate, his authorised representative.
To that end, the manufacturer or his authorised representative must use the appropriate verification methods.
Хората също превеждат
The decision shall be notified to the manufacturer and,where appropriate, to his authorised representative.
Name and address of the manufacturer or his authorised representative established within the Community,-.
Before placing machinery on the market and/or putting it into service,the manufacturer or his authorised representative shall.
Name and address of the manufacturer or his authorised representative established in the Community.
The exporter or his authorised representative shall enter the name of the exporting or importing Contracting Party and'Ceuta and Melilla' in Box 2 of movement certificates EUR.
Name and address of the manufacturer or his authorised representative established in the Community(2).
Where a Member State establishes that the"CE" marking and supplementary metrology marking have been affixed unduly,the manufacturer or his authorised representative shall be obliged.
The manufacturer or his authorised representative shall be notified of the decision.
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.
The manufacturer or his authorised representative is requested to keep copies of the technical documentation as well.
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 must keep a copy of the declaration of conformity with the technical documentation.
For at least 15 years from the last date of manufacture of the product, the manufacturer or his authorised representative shall keep available for the national authorities.
The exporter or his authorised representative shall enter"Israel" and"Ceuta and Melilla" in box 2 of movement certificates EUR.1.
Alternatively, the producer may mandate his authorised representative to draw up the declaration on his behalf.
The exporter or his authorised representative shall enter‘Lebanon' and‘Ceuta and Melilla' in Box 2 of movement certificates EUR.1 or on origin declarations.
Yes, the CE marking is always affixed by the manufacturer himself or his authorised representative after the necessary conformity assessment procedure has been performed.
The producer may mandate his authorised representative to draw up the declaration on his behalf provided that the mandate explicitly mentions it.
Where the device presents a risk,the importer shall inform the manufacturer, his authorised representative and the competent authority of the Member State in which he is established.
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.
However, at the discretion of the manufacturer or of his authorised representative in the Community, the procedure described in Annex III may also be followed.
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.
Where an innovative solution is proposed,the manufacturer or his authorised representative should state in what way it deviates from or how it complements the relevant provision of the TSI.
The manufacturer or his authorised representative in the Community shall specify to the notified body which aspects of the essential requirements must be assessed by the notified body.
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.