Progress: Procedure completed
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | IMCO | ROITHOVÁ Zuzana ( PPE) | SCHALDEMOSE Christel ( S&D), MANDERS Antonius ( ALDE), RÜHLE Heide ( Verts/ALE), FOX Ashley ( ECR), SALVINI Matteo ( EFD) |
Committee Opinion | ITRE | ||
Committee Opinion | JURI |
Lead committee dossier:
Legal Basis:
TFEU 114-p1
Legal Basis:
TFEU 114-p1Subjects
Events
PURPOSE: to align Directive 2009/23/EC on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments with the new legislative framework, which established a common framework for the marketing of products (Goods Package).
LEGISLATIVE ACT: Directive 2014/31/EU of the European Parliament and of the Council on the harmonisation of the laws of the Member States relating to the making available on the market of non-automatic weighing instruments.
CONTENT: the Directive is part of a package aiming to recast eight directives in order to adapt them to the EU's new legislative framework on sectoral product harmonisation.
The recast seeks to further harmonise and simplify national laws applicable to:
· explosives for civil uses
· simple pressure vessels
· electromagnetic compatibility
· non-automatic weighing instruments
· measuring instruments
· lifts and safety components for lifts
· equipment for use in potentially explosive atmospheres
· electrical equipment designed for use within certain voltage limits .
The EU's "new legislative framework", which was adopted in 2008, is a general measure of the internal market with the objective of strengthening the effectiveness of the Union’s legislation on product safety and its implementation mechanisms. It aims to strengthen the safety of products available on the market, and ensures a better functioning internal market for instance through equal treatment of economic operators on the market.
It is made up of two complementary texts : regulation 765/2008 outlining the requirements concerning accreditation and surveillance for the marketing of products, and decision 768/2008/EC relating to a common framework for the marketing of products.
The main elements of the new Directive are as follows:
Scope and application : this Directive aims to ensure that non-automatic weighing instruments on the market fulfil the requirements providing for a high level of protection of public interests covered by this Directive while guaranteeing the functioning of the internal market.
This Directive covers non-automatic weighing instruments which are new to the Union market when they are placed on the market ; that is to say they are either new non-automatic weighing instruments made by a manufacturer established in the Union or non- automatic weighing instruments, whether new or second-hand, imported from a third country.
This Directive should apply to all forms of supply, including distance selling.
Obligations of economic operators and traceability requirements : the Directive clarifies the obligations of manufacturers and introduces obligations for importers and distributors:
· When placing their instruments on the market, manufacturers shall ensure that they have been designed and manufactured in accordance with the essential safety requirements set out in Annex I. Instruments which they have placed on the market must bear a type and serial or batch identification allowing their identification. Where the size or nature of the instrument does not allow it, the required information shall be placed on the packaging or in a document accompanying the instrument.
· Before placing instruments on the market, importers shall ensure that the appropriate conformity assessment procedure has been carried out by the manufacturer. They shall ensure that the manufacturer has drawn up the technical documentation, that the instrument bears the CE marking and that it is accompanied by the required documents and by instructions and safety information .
· Manufacturers and importers shall indicate on the instrument their name, registered trade name or registered trade mark and the postal address at which they can be contacted. The address shall indicate a single point at which the manufacturer can be contacted. The contact details shall be in a language easily understood by end-users and market surveillance authorities. The instructions and safety information should be in a language which can be easily understood by end-users , as determined by the Member State concerned.
Manufacturers who consider or have reason to believe that instruments which they have placed on the market is not in conformity with this Directive shall immediately take the corrective measures necessary to bring them into conformity, to withdraw or recall them, if appropriate.
EU declaration of conformity : the EU declaration of conformity shall have the model structure set out in Annex IV. In order to reduce the administrative burden on economic operators, that single EU declaration of conformity may be a dossier made up of relevant individual declarations of conformity.
CE marking : the Directive states that the CE marking and the inscriptions shall be affixed visibly, legibly and indelibly to the instrument or to its data plate. It shall be affixed before the instrument is placed on the market. As requested by the European Parliament, Member States shall build upon existing mechanisms to ensure correct application of the regime governing the CE marking and shall take appropriate action in the event of improper use of that marking.
Notified bodies : the Directive reinforces the notification criteria for notified bodies. It clarifies that subsidiaries or subcontractors must also comply with the notification requirements. Specific requirements for notifying authorities are introduced, and the procedure for notification of notified bodies is revised. The competence of a notified body must be demonstrated by an accreditation certificate. A conformity assessment body shall be a third-party body independent of the organisation or the instrument it assesses. The impartiality of the conformity assessment bodies, their top level management and of the personnel responsible for carrying out the conformity assessment tasks shall be guaranteed.
Market surveillance and the safeguard clause procedure : the Directive revises the existing safeguard clause procedure. It introduces a phase of information exchange between Member States, and specifies the steps to be taken by the authorities concerned, when a non-compliant article is found. Member States should take all appropriate measures to ensure that instruments may be placed on the market only if, when properly stored and used for their intended purpose, or under conditions of use which can be reasonably foreseen, they do not endanger the health and safety of persons.
Restrictive measures in case of non-compliance : appropriate restrictive measures, such as withdrawal of the instrument concerned from the market should be taken in respect of the instrument concerned without delay.
Rules on penalties applicable to infringements by economic operators could include criminal penalties for serious infringements. The penalties provided for should be effective, proportionate and dissuasive.
Transitional provisions/products in stock : distributors should therefore be able to supply instruments that have been placed on the market, namely stock that is already in the distribution chain, before the 20 April 2016.
ENTRY INTO FORCE: 18/04/2014.
TRANSPOSITION: 19/04/2016. Measures shall apply from 20.04.2016.
The European Parliament adopted by 646 votes to 12, with 12 abstentions, a legislative resolution on the proposal for a directive of the European Parliament and of the Council on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments (recast).
Parliament adopted its position at first reading following the ordinary legislative procedure. The amendments adopted in plenary are the result of an agreement reached between the European Parliament and the Council. They amended the proposal as follows:
Further align the Directive to the “new legislative framework” and ensure legal certainty : the amendments made by the Parliament seek to ensure that the proposed Directive is more consistent with the terms used by Decision No 768/2008/EC and to eliminate any inconsistencies in the text which could otherwise create legal uncertainty.
Purpose and scope : it is stated that Directive covers non-automatic weighing instruments which are new to the Union market when they are placed on the market; that is to say they are either new non-automatic weighing instruments made by a manufacturer established in the Union or non-automatic weighing instruments, whether new or second-hand, imported from a third country.
This Directive should apply to all forms of supply, including distance selling .
Obligations of economic operators : manufacturers should draw up an EU declaration of conformity. Where compliance of an instrument has been demonstrated by the conformity assessment procedure, manufacturers shall draw up an EU declaration of conformity and affix the CE marking and the supplementary metrology marking.
Manufacturers and importers should indicate on the instrument their name, registered trade name or registered trade mark and the postal address at which they can be contacted. Where this would require the packaging to be opened, those indications may be given on the packaging and in a document accompanying the instrument.
In order to facilitate communication between economic operators, market surveillance authorities and end-users, Member States should encourage economic operators to include a website address in addition to the postal address.
Instructions and information, as well as any labelling, shall be clear, understandable and intelligible .
EU declaration of conformity : the EU declaration of conformity should contain the elements specified in the relevant modules set out in Annexes II and III and should be continuously updated.
EU declaration of conformity : in order to reduce the administrative burden on economic operators, that single EU declaration of conformity may be a dossier made up of relevant individual declarations of conformity.
CE marking : the conformity of an instrument should be indicated by the presence, on the instrument, of the CE marking and the supplementary metrology marking . The supplementary metrology marking shall consist of the capital letter ‘M’ and the last two digits of the year of its affixing, surrounded by a rectangle. The height of the rectangle shall be equal to the height of the CE marking.
Parliament called on the Member States to build upon existing mechanisms to ensure correct application of the regime governing the CE marking and shall take appropriate action in the event of improper use of that marking.
Notified bodies : a conformity assessment body shall have the means necessary to perform the technical and administrative tasks connected with the conformity assessment activities in an appropriate manner and shall have access to all necessary equipment or facilities. The impartiality of the conformity assessment bodies, their top level management and of the personnel responsible for carrying out the conformity assessment tasks shall be guaranteed.
Market surveillance : Member States should take all appropriate measures to ensure that non-automatic weighing instruments may be placed on the market only if, when properly stored and used for their intended purpose, they do not endanger the health and safety of persons.
Restrictive measures in case of non-compliance : Member States should ensure that appropriate restrictive measures, such as withdrawal of the instrument from the market, are taken in respect of the weighing instrument concerned without delay.
Rules on penalties applicable to infringements by economic operators may include criminal penalties for serious infringements. These penalties should be effective, proportionate and dissuasive.
Stock : distributors should therefore be able to supply non-automatic weighing instruments that have been placed on the market, namely stock that is already in the distribution chain, before the date of application of national measures transposing this Directive.
Implementing measures : in order to ensure uniform conditions for the implementation of this Directive, implementing powers should be conferred on the Commission.
The amended text stated that the examination procedure should be used for the adoption of implementing acts with respect to compliant non-automatic weighing instruments which present a risk to the health or safety of persons or to other aspects of public interest protection.
When matters relating to this Directive, other than its implementation or infringements, are being examined, i.e. in a Commission expert group, the European Parliament should receive full information and documentation and, where appropriate, an invitation to attend such meetings.
The Committee on the Internal Market and Consumer Protection adopted the report by Zuzana ROITHOVÁ (EPP, CZ) on the proposal for a directive of the European Parliament and of the Council on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments (recast).
The committee recommends that the European Parliament’s position adopted at first reading, under the ordinary legislative procedure, should amend the Commission proposal as follows:
Further align the Directive with the new legislative framework and ensure legal certainty : Members consider it important to bring a number of changes to the proposed Directive in order to reach a higher level of consistency with the terms used by the Decision No 768/2008/EC and eliminate the possible inconsistencies in the text which could otherwise create legal uncertainty.
They also consider it important to clarify the legal situation for products which have been legally placed on the market in compliance with the current Directive before the new Directive applies, but which are still in stock. They propose that economic operators should be able to sell stocks of non-automatic weighing instruments that are already in the distribution chain on the date of application of national measures transposing this Directive.
Obligations imposed on economic operators : an amendment stipulates that manufacturers shall indicate, on the instrument (or on the label if this is not possible), their name, registered trade name or registered trade mark the postal, or, if available, the website address at which they can be contacted. The contact details shall be in a language easily understood by end-users and market surveillance authorities. With a view to consumer protection , Members state that such instructions and safety information as well as any labelling shall be clear, understandable and intelligible. Moreover, they consider that all obligations imposed on economic operators by this Directive should also apply in the case of distance selling .
EU declaration of conformity : upon request of the market surveillance authority, the economic operator shall provide a copy of the EU declaration of conformity in paper form or by electronic means and shall ensure that it is translated into the language or languages required by the Member State in which market the non-automatic weighing instruments is placed or made available.
To cut red tape , Members state that when issuing a single EU declaration of conformity could cause specific problems due to the complexity or scope of that single EU declaration, it should be possible to replace that single EU declaration by individual EU declarations of conformity.
Restrictive measures in the case of non-compliance : appropriate restrictive measures should be taken, such as withdrawal of the instrument from their market , without delay.
Improve market surveillance : Members propose that the Member States: (i) provide, on an annual basis, the Commission with details of the activities of their market surveillance authorities; (ii) provide adequate funding to their market surveillance authorities in order to ensure that their activities are coherent and effective across the Union.
Improper marking and penalties : Members call on the Member States to build upon existing mechanisms to ensure correct application of the regime governing the CE marking and to take appropriate action in the event of improper use of the marking. Rules on penalties applicable to infringements by economic operators may include criminal penalties for serious infringements. The penalties shall be effective, proportionate to the seriousness of the offence.
Transparency : the Commission should have the obligation to publish on the Internet the national provisions of transposed Directive and relevant sanctions.
PURPOSE: to align Directive 2009/23/EC on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments with the new legislative framework, in particular to Decision No 768/2008/EC establishing a common framework for the marketing of products (Goods Package).
PROPOSED ACT: Directive of the European Parliament and of the Council.
BACKGROUND: experience with the implementation of Union harmonisation legislation has shown – on a cross-sector scale – certain weaknesses and inconsistencies in the implementation and enforcement of this legislation , leading to:
the presence of non-compliant or dangerous products on the market and consequently a certain lack of trust in CE marking; competitive disadvantages for economic operators complying with the legislation as opposed to those circumventing the rules; unequal treatment in the case of non-compliant products and distortion of competition amongst economic operators due to different enforcement practices; differing practices in the designation of conformity assessment bodies by national authorities; problems with the quality of certain notified bodies.
To remedy these horizontal shortcomings in Union harmonisation legislation observed across several industrial sectors, the “ New Legislative Framework ” was adopted in 2008 as part of the goods package. Its objective is to strengthen and complete the existing rules and to improve practical aspects of their application and enforcement. The New Legislative Framework (NLF) consists of two complementary instruments, Regulation (EC) No 765/2008 on accreditation and market surveillance and Decision No 768/2008/EC establishing a common framework for the marketing of products .
This proposal on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments is presented in the framework of the implementation of the “goods package” adopted in 2008. It is part of a package of proposals aligning ten product directives to Decision No 768/2008/EC establishing a common framework for the marketing of products.
IMPACT ASSESSMENT: based on the information collected, the Commission carried out an impact assessment which examined and compared three options:
Option 1 – No changes to the current situation; Option 2 – Alignment to the NLF Decision by non-legislative measures; Option 3 – Alignment to NLF Decision by legislative measures: this option consists in integrating the provisions of the NLF Decision into the existing directives.
Option 3 was found to be the preferred option for the following reasons: (i) it will improve the competitiveness of companies and notified bodies taking their obligations seriously, as opposed to those cheating on the system; (ii) it will improve the functioning of the internal market by ensuring equal treatment of all economic operators, notably importers and distributors, as well as notified bodies; (iii) it does not entail significant costs for economic operators and notified bodies; (iv) it is considered more effective than option 2: due to the lack of enforceability of option 2 it is questionable that the positive impacts would materialise under that option.
LEGAL BASIS: Article 114 of the Treaty on the Functioning of the European Union (TFEU).
CONTENT: the alignment to the NLF Decision requires a number of substantive amendments to the provisions of Directive 2009/23/EC. To ensure the readability of the amended text, the technique of recasting has been chosen. The proposal does not change the scope of Directive 2009/23/EC and the essential requirements.
The main elements of the proposal are as follows:
Horizontal definitions : the proposal introduces harmonised definitions of terms which are commonly used throughout Union harmonisation legislation and should therefore be given a consistent meaning throughout that legislation. Obligations of economic operators and traceability requirements : the proposal clarifies the obligations of manufacturers and introduces obligations for importers and distributors. Importers must verify that the manufacturer has carried out the applicable conformity assessment procedure and has drawn up a technical documentation. They must also make sure with the manufacturer that this technical documentation can be made available to authorities upon request. Furthermore importers must verify that the instruments are correctly marked and accompanied by instructions and safety information. They must keep a copy of the Declaration of conformity and indicate their name and address on the product, or where this is not possible on the packaging or the accompanying documentation. Distributors must verify that the article bears the CE marking, the name of the manufacturer and of the importer, if relevant, and that it is accompanied by the required documentation and instructions. Harmonised standards : compliance with harmonised standards provides a presumption of conformity with the essential requirements. On 1 June 2011 the Commission adopted a proposal for a Regulation on European Standardisation that sets out a horizontal legal framework for European standardisation. The proposal for the Regulation contains inter alia provisions on standardisation requests from the Commission to the European Standardisation Organisations, on the procedure for objections to harmonised standards and on stakeholder participation in the standardisation process. Consequently, the provisions of Directive 2009/23/EC which cover the same aspects have been deleted in this proposal for reasons of legal certainty. The provision conferring presumption of conformity to harmonised standards has been modified to clarify the extent of the presumption of conformity when standards only partially cover the essential requirements. Conformity assessment and CE marking : Directive 2009/23/EC on the placing on the market of pyrotechnic articles has selected the appropriate conformity assessment procedures which manufacturers have to apply in order to demonstrate that their pyrotechnic articles comply with the essential safety requirements. The proposal aligns these procedures to their updated versions set out in the NLF Decision. Notified Bodies : the proposal reinforces the notification criteria for notified bodies. It clarifies that subsidiaries or subcontractors must also comply with the notification requirements. Specific requirements for notifying authorities are introduced, and the procedure for notification of notified bodies is revised. The competence of a notified body must be demonstrated by an accreditation certificate. Market surveillance and the safeguard clause procedure : the proposal revises the existing safeguard clause procedure. It introduces a phase of information exchange between Member States, and specifies the steps to be taken by the authorities concerned, when a non-compliant instrument is found.
BUDGETARY IMPLICATIONS: this proposal does not have any implications for the EU budget.
PURPOSE: to align Directive 2009/23/EC on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments with the new legislative framework, in particular to Decision No 768/2008/EC establishing a common framework for the marketing of products (Goods Package).
PROPOSED ACT: Directive of the European Parliament and of the Council.
BACKGROUND: experience with the implementation of Union harmonisation legislation has shown – on a cross-sector scale – certain weaknesses and inconsistencies in the implementation and enforcement of this legislation , leading to:
the presence of non-compliant or dangerous products on the market and consequently a certain lack of trust in CE marking; competitive disadvantages for economic operators complying with the legislation as opposed to those circumventing the rules; unequal treatment in the case of non-compliant products and distortion of competition amongst economic operators due to different enforcement practices; differing practices in the designation of conformity assessment bodies by national authorities; problems with the quality of certain notified bodies.
To remedy these horizontal shortcomings in Union harmonisation legislation observed across several industrial sectors, the “ New Legislative Framework ” was adopted in 2008 as part of the goods package. Its objective is to strengthen and complete the existing rules and to improve practical aspects of their application and enforcement. The New Legislative Framework (NLF) consists of two complementary instruments, Regulation (EC) No 765/2008 on accreditation and market surveillance and Decision No 768/2008/EC establishing a common framework for the marketing of products .
This proposal on the harmonisation of the laws of the Member States relating to making available on the market of non-automatic weighing instruments is presented in the framework of the implementation of the “goods package” adopted in 2008. It is part of a package of proposals aligning ten product directives to Decision No 768/2008/EC establishing a common framework for the marketing of products.
IMPACT ASSESSMENT: based on the information collected, the Commission carried out an impact assessment which examined and compared three options:
Option 1 – No changes to the current situation; Option 2 – Alignment to the NLF Decision by non-legislative measures; Option 3 – Alignment to NLF Decision by legislative measures: this option consists in integrating the provisions of the NLF Decision into the existing directives.
Option 3 was found to be the preferred option for the following reasons: (i) it will improve the competitiveness of companies and notified bodies taking their obligations seriously, as opposed to those cheating on the system; (ii) it will improve the functioning of the internal market by ensuring equal treatment of all economic operators, notably importers and distributors, as well as notified bodies; (iii) it does not entail significant costs for economic operators and notified bodies; (iv) it is considered more effective than option 2: due to the lack of enforceability of option 2 it is questionable that the positive impacts would materialise under that option.
LEGAL BASIS: Article 114 of the Treaty on the Functioning of the European Union (TFEU).
CONTENT: the alignment to the NLF Decision requires a number of substantive amendments to the provisions of Directive 2009/23/EC. To ensure the readability of the amended text, the technique of recasting has been chosen. The proposal does not change the scope of Directive 2009/23/EC and the essential requirements.
The main elements of the proposal are as follows:
Horizontal definitions : the proposal introduces harmonised definitions of terms which are commonly used throughout Union harmonisation legislation and should therefore be given a consistent meaning throughout that legislation. Obligations of economic operators and traceability requirements : the proposal clarifies the obligations of manufacturers and introduces obligations for importers and distributors. Importers must verify that the manufacturer has carried out the applicable conformity assessment procedure and has drawn up a technical documentation. They must also make sure with the manufacturer that this technical documentation can be made available to authorities upon request. Furthermore importers must verify that the instruments are correctly marked and accompanied by instructions and safety information. They must keep a copy of the Declaration of conformity and indicate their name and address on the product, or where this is not possible on the packaging or the accompanying documentation. Distributors must verify that the article bears the CE marking, the name of the manufacturer and of the importer, if relevant, and that it is accompanied by the required documentation and instructions. Harmonised standards : compliance with harmonised standards provides a presumption of conformity with the essential requirements. On 1 June 2011 the Commission adopted a proposal for a Regulation on European Standardisation that sets out a horizontal legal framework for European standardisation. The proposal for the Regulation contains inter alia provisions on standardisation requests from the Commission to the European Standardisation Organisations, on the procedure for objections to harmonised standards and on stakeholder participation in the standardisation process. Consequently, the provisions of Directive 2009/23/EC which cover the same aspects have been deleted in this proposal for reasons of legal certainty. The provision conferring presumption of conformity to harmonised standards has been modified to clarify the extent of the presumption of conformity when standards only partially cover the essential requirements. Conformity assessment and CE marking : Directive 2009/23/EC on the placing on the market of pyrotechnic articles has selected the appropriate conformity assessment procedures which manufacturers have to apply in order to demonstrate that their pyrotechnic articles comply with the essential safety requirements. The proposal aligns these procedures to their updated versions set out in the NLF Decision. Notified Bodies : the proposal reinforces the notification criteria for notified bodies. It clarifies that subsidiaries or subcontractors must also comply with the notification requirements. Specific requirements for notifying authorities are introduced, and the procedure for notification of notified bodies is revised. The competence of a notified body must be demonstrated by an accreditation certificate. Market surveillance and the safeguard clause procedure : the proposal revises the existing safeguard clause procedure. It introduces a phase of information exchange between Member States, and specifies the steps to be taken by the authorities concerned, when a non-compliant instrument is found.
BUDGETARY IMPLICATIONS: this proposal does not have any implications for the EU budget.
Documents
- Commission response to text adopted in plenary: SP(2014)446
- Final act published in Official Journal: Directive 2014/31
- Final act published in Official Journal: OJ L 096 29.03.2014, p. 0107
- Draft final act: 00050/2013/LEX
- Results of vote in Parliament: Results of vote in Parliament
- Decision by Parliament, 1st reading: T7-0086/2014
- Debate in Parliament: Debate in Parliament
- Committee report tabled for plenary, 1st reading: A7-0257/2012
- Amendments tabled in committee: PE491.168
- Committee draft report: PE488.061
- Contribution: COM(2011)0766
- Contribution: COM(2011)0766
- Legislative proposal: COM(2011)0766
- Legislative proposal: EUR-Lex
- Legislative proposal published: COM(2011)0766
- Legislative proposal published: EUR-Lex
- Legislative proposal: COM(2011)0766 EUR-Lex
- Committee draft report: PE488.061
- Amendments tabled in committee: PE491.168
- Draft final act: 00050/2013/LEX
- Commission response to text adopted in plenary: SP(2014)446
- Contribution: COM(2011)0766
- Contribution: COM(2011)0766
Votes
A7-0257/2012 - Zuzana Roithová - Résolution législative #
Amendments | Dossier |
45 |
2011/0352(COD)
2012/06/07
IMCO
45 amendments...
Amendment 29 #
Proposal for a directive Recital 10 (10) When placing a non-automatic weighing instrument on the market, every importer should indicate on the non- automatic weighing instrument his name and the address at which he can be contacted.
Amendment 30 #
Proposal for a directive Recital 35 (35) Manufacturers and importers need to be given reasonable, but limited, time to exercise any rights under national rules in force before the date of application of national rules transposing this Directive in order, for example, to sell their stocks of manufactured products. It is necessary to provide for transitional arrangements that allow making available on the market and putting into service non-automatic weighing instruments that have already been placed
Amendment 31 #
Proposal for a directive Article 2 – paragraph 1 – point 1 (1) ‘weighing instrument’ means a measuring instrument serving to determine the mass of a body by using the action of gravity on that body
Amendment 32 #
Proposal for a directive Article 2 – paragraph 1 – point 1 1) ‘weighing instrument’ means a measuring instrument serving to determine the mass of a body by using the action of gravity on that body
Amendment 33 #
Proposal for a directive Article 3 – paragraph 1 1. Member States shall take all steps to ensure that only instruments that meet the applicable requirements of this Directive may be made available on the market.
Amendment 34 #
Proposal for a directive Article 3 – paragraph 3 3. Member States shall take all steps to ensure that instruments continue to conform to the applicable requirements of this Directive
Amendment 35 #
Proposal for a directive Article 3 – paragraph 3 3. Member States shall take all steps to ensure that instruments
Amendment 36 #
Proposal for a directive Article 4 – paragraph 1 Instruments used or intended to be used for the applications listed in points (a) to (f) of Article 1(2) must satisfy the essential requirements set out in Annex I and bear the CE marking and the inscriptions provided for in point 1 of Annex III .
Amendment 37 #
Proposal for a directive Article 6 – paragraph 1 – subparagraph 1 1. When placing on the market their instruments intended to be used for the applications listed
Amendment 38 #
Proposal for a directive Article 6 – paragraph 1 – subparagraph 2 When placing on the market their instruments not intended to be used for the applications listed in points (a) to (f) of Article 1(2), manufacturers shall ensure that they bear the inscriptions provided for in point 2 of Annex III.
Amendment 39 #
Proposal for a directive Article 6 – paragraph 2 – subparagraph 1 2. For the instruments intended to be used for the applications listed in points (a) to (f) of Article 1(2), manufacturers shall draw up the required technical documentation and carry out the relevant conformity assessment procedure referred to in Article 14 or have it carried out.
Amendment 40 #
Proposal for a directive Article 6 – paragraph 2 – subparagraph 3 For the instruments not intended to be used for the applications listed in points (a) to (f) of Article 1(2), manufacturers shall affix the inscriptions provided for in point 2 of Annex III.
Amendment 41 #
Proposal for a directive Article 6 – paragraph 3 3. For the instruments intended to be used for the applications listed in points (a) to (f) of Article 1(2), manufacturers shall keep the technical documentation and the EU declaration of conformity for 10 years after the instrument has been placed on the market.
Amendment 42 #
Proposal for a directive Article 6 – paragraph 6 6. Manufacturers shall indicate their name, registered trade name or registered trade
Amendment 43 #
Proposal for a directive Article 6 – paragraph 6 6. Manufacturers shall indicate their name, registered trade name or registered trade mark and the address at which they can be contacted on the
Amendment 44 #
Proposal for a directive Article 6 – paragraph 7 7. Manufacturers shall ensure that the instrument is accompanied by a copy of the EU declaration of conformity and instructions and information in a language which can be easily understood by consumers and other end-users, as determined by the
Amendment 45 #
Proposal for a directive Article 8 – paragraph 2 – subparagraph 1 2. Before placing on the market an instrument intended to be used for the applications listed in points (a) to (f) of Article 1(2), importers shall ensure that the appropriate conformity assessment procedure has been carried out by the manufacturer. They shall ensure that the manufacturer has drawn up the technical documentation, that the instrument bears the CE marking, the inscriptions provided for in point 1 of Annex III and is accompanied by the required documents, and that the manufacturer has complied with the requirements set out in Article 6(5) and (6).
Amendment 46 #
Proposal for a directive Article 8 – paragraph 2 – subparagraph 2 Where an importer considers or has reason to believe that an instrument intended to be used for the applications listed in points (a) to (f) of Article 1(2) is not in conformity with the
Amendment 47 #
Proposal for a directive Article 8 – paragraph 2 – subparagraph 3 Before placing on the market an instrument not intended to be used for the applications listed in points (a) to (f) of Article 1(2) importers shall ensure that the instrument bears the inscriptions provided for in point 2 of Annex III and that the manufacturer has complied with the requirements set out in Article 6(5) and (6).
Amendment 48 #
Proposal for a directive Article 8 – paragraph 3 3. Importers shall indicate their name, registered trade name or registered trade mark, their web address in a language easily understood by end-users and market surveillance authorities, and the address at which they can be contacted on the instrument or, where that is not possible, on its packaging or in a document accompanying the instrument.
Amendment 49 #
Proposal for a directive Article 8 – paragraph 4 4. Importers shall ensure that the instrument is accompanied by a copy of the EU declaration of conformity and instructions and information in a language which can be easily understood by consumers and other end-users, as determined by the Member State concerned.
Amendment 50 #
Proposal for a directive Article 8 – paragraph 5 5. Importers shall ensure that, while an instrument intended to be used for the applications listed in points (a) to (f) of Article 1(2) is under their responsibility, storage or transport conditions do not jeopardise its compliance with the essential requirements set out in Annex I.
Amendment 51 #
Proposal for a directive Article 8 – paragraph 8 8. For the instruments intended to be used for the applications listed in points (a) to (f) of Article 1(2), importers shall, for 10 years after the instrument has been placed on the market keep a copy of the EU declaration of conformity at the disposal of the market surveillance authorities and ensure that the technical documentation can be made available to those authorities, upon request.
Amendment 52 #
Proposal for a directive Article 9 – paragraph 2 – subparagraph 1 2. Before making an instrument intended to be used for the applications listed in points (a) to (f) of Article 1(2) available on the market, distributors shall verify that the instrument bears the CE marking, the inscriptions provided for in point 1 of Annex III, that it is accompanied by the required documents and by instructions and information in a language which can be easily understood by consumers and other end-users in the Member State in which the instrument is to be made available on the market, and that the manufacturer and the importer have complied with the requirements set out in Article 6(5) and (6) and Article 8(3).
Amendment 53 #
Proposal for a directive Article 9 – paragraph 2 – subparagraph 3 Before making an instrument not intended to be used for the applications listed in points (a) to (f) of Article 1(2) available on the market, distributors shall verify that the instrument bears the inscriptions provided for in point 2 of Annex III and that the manufacturer and the importer have complied with the requirements set out in Article 6(5) and (6) and Article 8(3).
Amendment 54 #
Proposal for a directive Article 9 – paragraph 3 3. Distributors shall ensure that, while an instrument intended to be used for the applications listed in points (a) to (f) of Article 1(2) is under their responsibility, storage or transport conditions do not jeopardise its compliance with the essential requirements set out in Annex I.
Amendment 55 #
Proposal for a directive Article 13 – paragraph 1 – introductory part 1. The conformity of instruments to the essential requirements set out in Annex I may be certified by either of the following procedures as selected by the
Amendment 56 #
Proposal for a directive Article 14 – paragraph 2 2. The EU declaration of conformity shall have the model structure set out in Annex III of Decision No 768/2008/EC, shall contain the elements specified in the relevant modules set out in Annex II to this Directive and shall be continuously updated. It
Amendment 57 #
Proposal for a directive Article 19 – paragraph 2 2.
Amendment 58 #
Proposal for a directive Article 22 – paragraph 3 – subparagraph 2 Amendment 59 #
Proposal for a directive Article 22 – paragraph 4 – subparagraph 1 4. A conformity assessment body, its top level management and the personnel responsible for carrying out the conformity assessment tasks shall not be the designer, manufacturer, supplier, installer, purchaser, owner, user or maintainer of
Amendment 60 #
Proposal for a directive Article 22 – paragraph 4 – subparagraph 2 A conformity assessment body, its top level management and the personnel responsible for carrying out the conformity assessment tasks shall not be directly involved in the design, manufacture or construction, the marketing, installation, use or maintenance of
Amendment 61 #
Proposal for a directive Article 25 – paragraph 2 2. That application shall be accompanied by a description of the conformity assessment activities, the conformity assessment module or modules and the instrument or instruments for which that body claims to be competent, as well as by an accreditation certificate
Amendment 62 #
Proposal for a directive Article 25 – paragraph 3 Amendment 63 #
Proposal for a directive Article 26 – paragraph 4 Amendment 64 #
Proposal for a directive Article 26 – paragraph 5 – subparagraph 1 5. The body concerned may perform the activities of a notified body only where no objections are raised by the Commission or the other Member States within two weeks of a notification
Amendment 65 #
Proposal for a directive Article 36 – paragraph 7 7. Where, within t
Amendment 66 #
Proposal for a directive Article 42 – paragraph 1 – subparagraph 1 Member States shall adopt and publish by [insert date -
Amendment 67 #
Proposal for a directive Annex II – part 2 – point 2.5 – point 2.5.2 – paragraph 2 A copy of the declaration of conformity shall be
Amendment 68 #
Proposal for a directive Annex II – part 3 – point 3.7 – point 3.7.2 – paragraph 2 A copy of the declaration of conformity shall be
Amendment 69 #
Proposal for a directive Annex II – part 4 – point 4.3 – paragraph 1 An accredited in-house body or a notified body chosen by the manufacturer shall carry out appropriate examinations and tests in order to check the conformity of the instruments with the
Amendment 70 #
Proposal for a directive Annex II – part 4 – point 4.5 – point 4.5.2 – paragraph 2 A copy of the declaration of conformity shall be
Amendment 71 #
Proposal for a directive Annex II – part 5 – point 5.4 – paragraph 1 An accredited in-house body or a notified body chosen by the manufacturer shall carry out appropriate examinations and tests to check the conformity of the instruments with the applicable requirements of this Directive.
Amendment 72 #
Proposal for a directive Annex II – part 5 – point 5.6 – point 5.6.2 – paragraph 2 A copy of the declaration of conformity shall be
Amendment 73 #
Proposal for a directive Annex II – part 6 – point 6.4 – paragraph 1 An accredited in-house body or a notified body chosen by the manufacturer shall carry out appropriate examinations and tests, set out in the relevant harmonised standards and/or technical specifications, or equivalent tests, to check the conformity of the instrument with the applicable requirements of this Directive, or have them carried out. In the absence of such a harmonised standard and/or technical specification the notified body concerned shall decide on the appropriate tests to be carried out.
source: PE-491.168
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