Examples of using Eu-type in English and their translations into Polish
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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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Financial
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Official/political
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Programming
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Computer
EU-type examination may be carried out in any of the following manners.
The European versions are easier to re-register in the UK as they have EU-type approval.
EU-type examination(Module B- production type) set out in Annex IV combined with either of the following.
The technical documentation of the approved type and a copy of the EU-type examination certificate(s);
Applicability of EU-type examination(Module B) and conformity to type based on internal production control Module C.
Conformity assessment procedures for subsystems and safety components:module b: eu-type examination- production type.
Reference to the EU-type examination certificate with details, including its date, and where appropriate, information on the duration and conditions of its validity;
Where the type meets the requirements of this Directive, the notified body shall issue an EU-type examination certificate to the manufacturer.
The application for EU-type examination shall be lodged by the manufacturer or by his authorised representative with a single notified body in respect of a prototype vessel or of a prototype representing a family of vessels.
Where the appliance orthe fitting type meets the requirements of this Regulation, the notified body shall issue an EU-type examination certificate to the manufacturer.
The manufacturer shall keep a copy of the EU-type examination certificate, its annexes and additions together with the technical documentation at the disposal of the national authorities for 10 years after the apparatus has been placed on the market.
Where the type meets the requirements of this Directive that applyto the product concerned, the notified body shall issue an EU-type examination certificate to the manufacturer.
EU-type examination shall be carried out by assessment of the adequacy of the technical design of the apparatus through examination of the technical documentation and supporting evidence referred to in point 3, without examination of a specimen design type.
Each notified body shall inform its notifying authorities and the other notified bodies concerning the EU-type examination certificates and/or any additions thereto which it has issued.
The manufacturer shall inform the notified body that holds the technical documentation relating to the EU-type examination certificate of all modifications to the approved type that may affect the conformity of the appliance or the fitting with the essential requirements of this Regulation or the conditions for validity of the certificate.
The manufacturer shall affix the CE marking to each individual fertilising product that is in conformity with the type described in the EU-type examination certificate and satisfies the requirements of this Regulation.
The manufacturer shall inform the notified body that holds the technical documentation relating to the EU-type examination certificate of all modifications to the approved type that may affect the conformity of the CE marked fertilising product with the requirements of this Regulation or the conditions for validity of the certificate.
The manufacturer shall affix the CE marking set out in this Directive to each individual vessel that is in conformity with the type described in the EU-type examination certificate and satisfies the applicable requirements of this Directive.
The manufacturer shall inform the notified body that holds the technical documentation relating to the EU-type examination certificate of any modifications to the approved type that may affect the conformity of the subsystem or the safety component with the essential requirements of this Regulation or the conditions for validity of the certificate.
The manufacturer shall affix the inscriptions provided for in point 3 of Annex IV to each individual fitting that is in conformity with the type described in the EU-type examination certificate and satisfies the applicable requirements of this Regulation.
The notified body which refuses to issue or withdraws, suspends or otherwise restricts an EU-type examination certificate must inform its notifying authorities and the other notified bodies accordingly, giving the reasons for its decision.
A notified body chosen by the manufacturer shall carryout appropriate examinations and tests in order to check the conformity of the instruments with the approved type described in the EU-type examination certificate and with the appropriate requirements of this Directive.
The quality system shall ensure complianceof the appliances or the fittings with the type described in the EU-type examination certificate and with the applicable requirements of this Regulation.
Conformity to type based on quality assurance of the production process is the part of a conformity assessment procedure whereby a the manufacturer fulfils the obligations laid down in points 2.2 and 2.5, and ensures and declares on his sole responsibilitythat the subsystems or safety components concerned are in conformity with the type described in the EU-type examination certificate and satisfy the requirements of this Regulation that apply to them.
The quality system shall ensure that the appliances orfittings are in conformity with the type described in the EU-type examination certificate and comply with the requirements of this Regulation that apply to them.
The manufacturer shall take all measures necessary so that the manufacturing process and its monitoring ensure conformity ofthe manufactured subsystems or safety components with the approved type described in the EU-type examination certificate and with the requirements of this Regulation.
This was caused by the need to use mostly external translators- many of whom had little experience of EU-type translation- and by a lack of internal capacity to revise freelance translations sufficiently.
A notified body chosen by the manufacturer shall carry out appropriate examinations and tests, or have them carried out, in order tocheck the conformity of the appliances or fittings with the approved type described in the EU-type examination certificate and with the appropriate requirements of this Regulation.
The quality system shall ensure that the subsystems orsafety components are in conformity with the type(s) described in the EU-type examination certificate(s) and comply with the requirements of this Regulation that apply to them.
The manufacturer shall affix the CE marking andthe inscriptions provided for in Annex IV to each individual appliance that is in conformity with the type described in the EU-type examination certificate and satisfies the applicable requirements of this Regulation.