Примери за използване на Authorised representative must 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
The authorised representative must be based within the EU.
(b) In selecting the most appropriate methods, the manufacturer or his authorised representative must apply the following principles, in the order given.
The authorised representative must be based within the EU.
If the claimant is represented by an authorised representative for the proceedings, the name and address of the authorised representative must be stated in the summons.
The authorised representative must also give the business.
For the purposesof Union harmonisation legislation, to be able to act on behalf of the manufacturer, the authorised representative must be established inside the Union.
The manufacturer or the authorised representative must keep the technical documentation and a copy of the EU declaration of conformity.
To initiate enforcement of a ruling,the enforcement order granted to the enforcement officer or their authorised representative must be submitted to a court bailiff together with a letter of application.
The manufacturer or his authorised representative must keep a copy of the declaration of conformity with the technical documentation.
In order to verify that the structure complies with the requirement laid down in the second paragraph,the manufacturer or his authorised representative must, for each type of structure concerned, perform appropriate tests or have such tests performed.
The manufacturer of machinery or his authorised representative must ensure that a risk assessment is carried out in order to determine the health and safety requirements which apply to the machinery.
(c) When designing and constructing machinery andwhen drafting the instructions, the manufacturer or his authorised representative must envisage not only the intended use of the machinery but also any reasonably foreseeable misuse thereof.
M5 The manufacturer or his authorised representative must, for a period ending at least five years, and in the case of implantable devices at least 15 years, after the last product has been manufactured, make available to the national authorities:◄.
To that end, the manufacturer or his authorised representative must use the appropriate verification methods.
The manufacturer or his authorised representative must, for a period ending at least five years, and in the case of implantable devices at least 15 years, after the last product has been manufactured, keep at the disposal of the national authorities:';
When lifting machinery or lifting accessories are placed on the market orare first put into service, the manufacturer or his authorised representative must ensure, by taking appropriate measures or having them taken, that the machinery or the lifting accessories which are ready for use- whether manually or power-operated- can fulfil their specified functions safely.
The manufacturer or his authorised representative must keep a copy of the EC declaration of conformity with the technical documentation for a period of 10 years after the last interoperability constituent has been manufactured.
The delegation of tasks from the manufacturer to the authorised representative must be explicit and set out in writing, in particular to define the contents and limits of the representative's tasks.
The manufacturer or his authorised representative must make this documentation, including the declaration of conformity, available to the national authorities for inspection purposes for a period ending at least five years after the last product has been manufactured.
The manufacturer of machinery for pesticide application or his authorised representative must ensure that an assessment is carried out of the risks of unintended exposure of the environment to pesticides, in accordance with the process of risk assessment and risk reduction referred to in the General Principles, point 1.
The manufacturer or his authorised representative must make this documentation, including the declaration of conformity, available to the national authorities for inspection purposes for a period ending at least five years after the last product has been manufactured.
The manufacturer must establish the technical documentation described in point 3 and he or his authorised representative established within the Community must keep it on Community territory at the disposal of the relevant national authorities for inspection purposes for a period ending at least 10 years after the last product has been manufactured.
The manufacturer must draw up the technical documentation described in point 3 and either the manufacturer or his authorised representative established within the Community must keep it at the disposal of the relevant national authorities for inspection purposes for a period of 10 years after the last of the transportable pressure equipment has been manufactured.
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 CE marking to each component and must draw up a written declaration of conformity.
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.
You will then be asked to complete andsubmit a confidentiality declaration, which must be signed by an authorised representative of your company.
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.
This notification must be signed by an authorised representative of the tenderer and specify the name of the person who will attend the opening of the tenders on the tenderer's behalf.
The manufacturer(or the authorised representative established within the EU) must draw up and sign an EC declaration of conformity(DoC) as part of the conformity assessment procedure provided for in the applicable legislation.