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Directive 2014/33/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to lifts and safety components for lifts (recast) (Text with EEA relevance)

EU Directive 2014/33 · Adopted 26 February 2014 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Directive 2014/33/EU of the European Parliament and of the Council

of 26 February 2014

on the harmonisation of the laws of the Member States relating to lifts and safety components for lifts

(recast)

(Text with EEA relevance)

THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION,

Having regard to the Treaty on the Functioning of the European Union, and in particular Article 114 thereof,

Having regard to the proposal from the European Commission,

After transmission of the draft legislative act to the national parliaments,

Having regard to the opinion of the European Economic and Social Committeef1,

Acting in accordance with the ordinary legislative proceduref2,

Whereas:

(1)

Directive 95/16/EC of the European Parliament and of the Council of 29 June 1995 on the approximation of the laws of the Member States relating to liftsf3 has been substantially amendedf4. Since further amendments are to be made, that Directive should be recast in the interests of clarity.

(2)

Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of productsf5 lays down rules on the accreditation of conformity assessment bodies, provides a framework for the market surveillance of products and for controls on products from third countries, and lays down the general principles of the CE marking.

(3)

Decision No 768/2008/EC of the European Parliament and of the Council of 9 July 2008 on a common framework for the marketing of productsf6 lays down common principles and reference provisions intended to apply across sectoral legislation in order to provide a coherent basis for revision or recasts of that legislation. Directive 95/16/EC should be adapted to that Decision.

(4)

The lifts covered by this Directive only come into existence as finished products once they have been permanently installed in buildings or constructions. Consequently, lifts cannot be imported into the Union and are only placed on the market and not subsequently made available: there are no ‘importers’ or ‘distributors’ of lifts.

(5)

This Directive covers safety components for lifts which are new to the Union market when they are placed on the market; that is to say they are either new safety components made by a manufacturer in the Union or new or second-hand safety components imported from a third country.

(6)

On 8 June 1995 the Commission adopted Recommendation 95/216/EC of 8 June 1995 concerning improvement of safety of existing liftsf7 to the Member States concerning improvement of safety of existing lifts.

(7)

This Directive should apply to all forms of supply, including distance selling.

(8)

Economic operators should be responsible for the compliance of lifts and safety components for lifts with this Directive, in relation to their respective roles in the supply chain, so as to ensure a high level of protection of health and safety of persons and, where appropriate, the safety of property, and to guarantee fair competition on the Union market.

(9)

All economic operators intervening in the supply and distribution chain should take appropriate measures to ensure that they only place on the market lifts and make available on the market safety components for lifts which are in conformity with this Directive. It is necessary to provide for a clear and proportionate distribution of obligations which correspond to the role of each economic operator in the supply and distribution chain.

(10)

In order to facilitate communication between economic operators, market surveillance authorities and consumers, Member States should encourage economic operators to include a website address in addition to the postal address.

(11)

The manufacturer and the installer, having detailed knowledge of the design and production process, are best placed to carry out the conformity assessment procedure. Conformity assessment should therefore remain solely the obligation of the manufacturer or of the installer.

(12)

It is necessary to ensure that safety components for lifts from third countries entering the Union market comply with this Directive, and in particular that the appropriate conformity assessment procedures have been carried out by the manufacturer with regard to those safety components for lifts. Provision should therefore be made for importers to make sure that the safety components for lifts they place on the market comply with the requirements of this Directive and that they do not place on the market safety components for lifts which do not comply with such requirements or present a risk. Provision should also be made for importers to make sure that conformity assessment procedures have been carried out and that marking of safety components for lifts and documentation drawn up by manufacturers are available for inspection by the competent national authorities.

(13)

When placing a safety component for lifts on the market, every importer should indicate on the safety component for lifts his name, registered trade name or registered trade mark and the postal address at which he can be contacted. Exceptions should be provided for in cases where the size or nature of the safety component for lifts does not allow it.

(14)

The distributor makes a safety component for lifts available on the market after it has been placed on the market by the manufacturer or the importer and should act with due care to ensure that its handling of the safety component for lifts does not adversely affect the compliance of the safety component for lifts.

(15)

Any economic operator that either places a safety component for lifts on the market under his own name or trade mark or modifies a safety component for lifts in such a way that compliance with this Directive may be affected should be considered to be the manufacturer and should assume the obligations of the manufacturer.

(16)

Distributors and importers, being close to the market place, should be involved in market surveillance tasks carried out by the competent national authorities, and should be prepared to participate actively, providing those authorities with all necessary information relating to the safety components for lifts concerned.

(17)

Ensuring traceability of a safety component for lifts throughout the whole supply chain helps to make market surveillance simpler and more efficient. An efficient traceability system facilitates market surveillance authorities’ task of tracing economic operators who made non-compliant safety components for lifts available on the market. When keeping the information required under this Directive for the identification of other economic operators, economic operators should not be required to update such information in respect of other economic operators who have either supplied them with a safety component for lifts or to whom they have supplied a safety component for lifts.

(18)

This Directive should be limited to the expression of the essential health and safety requirements. In order to facilitate conformity assessment for lifts and safety components for lifts with those requirements it is necessary to provide for a presumption of conformity for lifts and safety components for lifts which are in conformity with harmonised standards that are adopted in accordance with Regulation (EU) No 1025/2012 of the European Parliament and of the Council of 25 October 2012 on European Standardisationf8 for the purpose of expressing detailed technical specifications of those requirements. The essential health and safety requirements of this Directive will guarantee the intended level of safety only if appropriate conformity assessment procedures ensure compliance therewith.

(19)

Regulation (EU) No 1025/2012 provides for a procedure for objections to harmonised standards where those standards do not entirely satisfy the requirements of this Directive.

(20)

The harmonised standards relevant to this Directive should also take into account the United Nations Convention on the Rights of Persons with Disabilitiesf9.

(21)

In order to enable economic operators to demonstrate and the competent authorities to ensure that lifts placed on the market and safety components for lifts made available on the market conform to the essential health and safety requirements, it is necessary to provide for conformity assessment procedures. Decision No 768/2008/EC establishes modules for conformity assessment procedures, which include procedures from the least to the most stringent, in proportion to the level of risk involved and the level of safety required. In order to ensure inter-sectoral coherence and to avoid ad-hoc variants, conformity assessment procedures should be chosen from among those modules.

(22)

The installer or the manufacturer should draw up an EU declaration of conformity to provide information required under this Directive on the conformity of a lift or safety component for lifts with this Directive and with other relevant Union harmonisation legislation.

(23)

To ensure effective access to information for market surveillance purposes, the information required to identify all applicable Union acts should be available in a single 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.

(24)

The CE marking, indicating the conformity of a lift or safety component for lifts, is the visible consequence of a whole process comprising conformity assessment in a broad sense. General principles governing the CE marking are set out in Regulation (EC) No 765/2008. Rules governing the affixing of the CE marking should be laid down in this Directive.

(25)

The conformity assessment procedures set out in this Directive require the intervention of conformity assessment bodies, which are notified by the Member States to the Commission.

(26)

Experience has shown that the criteria set out in Directive 95/16/EC that conformity assessment bodies have to fulfil to be notified to the Commission are not sufficient to ensure a uniformly high level of performance of notified bodies throughout the Union. It is, however, essential that all notified bodies perform their functions to the same level and under conditions of fair competition. That requires the setting of obligatory requirements for conformity assessment bodies wishing to be notified in order to provide conformity assessment services.

(27)

If a conformity assessment body demonstrates conformity with the criteria laid down in harmonised standards, it should be presumed to comply with the corresponding requirements set out in this Directive.

(28)

In order to ensure a consistent level of conformity assessment quality it is also necessary to set requirements for notifying authorities and other bodies involved in the assessment, notification and monitoring of notified bodies.

(29)

The system set out in this Directive should be complemented by the accreditation system provided for in Regulation (EC) No 765/2008. Since accreditation is an essential means of verifying the competence of conformity assessment bodies, it should also be used for the purposes of notification.

(30)

Transparent accreditation as provided for in Regulation (EC) No 765/2008, ensuring the necessary level of confidence in certificates of conformity, should be considered by the national public authorities throughout the Union as the preferred means of demonstrating the technical competence of conformity assessment bodies. However, national authorities may consider that they possess the appropriate means of carrying out that evaluation themselves. In such cases, in order to ensure the appropriate level of credibility of evaluations carried out by other national authorities, they should provide the Commission and the other Member States with the necessary documentary evidence demonstrating the compliance of the conformity assessment bodies evaluated with the relevant regulatory requirements.

(31)

Conformity assessment bodies frequently subcontract parts of their activities linked to the assessment of conformity or have recourse to a subsidiary. In order to safeguard the level of protection required for the lifts and safety components for lifts to be placed on the Union market, it is essential that conformity assessment subcontractors and subsidiaries fulfil the same requirements as notified bodies in relation to the performance of conformity assessment tasks. Therefore, it is important that the assessment of the competence and the performance of bodies to be notified and the monitoring of bodies already notified cover also activities carried out by subcontractors and subsidiaries.

(32)

It is necessary to increase the efficiency and transparency of the notification procedure and, in particular, to adapt it to new technologies so as to enable online notification.

(33)

Since notified bodies may offer their services throughout the Union, it is appropriate to give the other Member States and the Commission the opportunity to raise objections concerning a notified body. It is therefore important to provide for a period during which any doubts or concerns as to the competence of conformity assessment bodies can be clarified before they start operating as notified bodies.

(34)

In the interests of competitiveness, it is crucial that notified bodies apply the conformity assessment procedures without creating unnecessary burdens for economic operators. For the same reason, and to ensure equal treatment of economic operators, consistency in the technical application of the conformity assessment procedures needs to be ensured. That can best be achieved through appropriate coordination and cooperation between notified bodies.

(35)

Member States should take all appropriate measures to ensure that safety components for lifts 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. Safety components for lifts should be considered as non-compliant with the essential health and safety requirements laid down in this Directive only under conditions of use which can be reasonably foreseen, that is when such use could result from lawful and readily predictable human behaviour.

(36)

In order to ensure legal certainty, it is necessary to clarify that rules on Union market surveillance and control of products entering the Union market provided for in Regulation (EC) No 765/2008 apply to lifts and safety components for lifts covered by this Directive. This Directive should not prevent Member States from choosing the competent authorities to carry out those tasks.

(37)

In order to increase transparency and to reduce processing time, it is necessary to improve the existing safeguard procedure, with a view to making it more efficient and drawing on the expertise available in Member States.

(38)

The existing system should be supplemented by a procedure under which interested parties are informed of measures intended to be taken with regard to lifts or safety components for lifts presenting a risk to the health or safety of persons or where appropriate, to the safety of property. It should also allow market surveillance authorities, in cooperation with the relevant economic operators, to act at an earlier stage in respect of such lifts and safety components for lifts.

(39)

Where the Member States and the Commission agree as to the justification of a measure taken by a Member State, no further involvement of the Commission should be required, except where non-compliance can be attributed to shortcomings of a harmonised standard.

(40)

In order to ensure uniform conditions for the implementation of this Directive, implementing powers should be conferred on the Commission. Those powers should be exercised in accordance with Regulation (EU) No 182/2011 of the European Parliament and of the Council of 16 February 2011 laying down the rules and general principles concerning mechanisms for control by Member States of the Commission’s exercise of implementing powersf10.

(41)

The advisory procedure should be used for the adoption of implementing acts requesting the notifying Member State to take the necessary corrective measures in respect of notified bodies that do not meet or no longer meet the requirements for their notification.

(42)

The examination procedure should be used for the adoption of implementing acts with respect to compliant lifts or safety components for lifts which present a risk to the health or safety of persons or to other aspects of public interest protection.

(43)

The Commission should adopt immediately applicable implementing acts where, in duly justified cases relating to compliant lifts or safety components for lifts which present a risk to the health or safety of persons, imperative grounds of urgency so require.

(44)

In line with established practice, the committee set up by this Directive can play a useful role in examining matters concerning the application of this Directive raised either by its chair or by a representative of a Member State in accordance with its rules of procedure.

(45)

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 in line with existing practice receive full information and documentation and, where appropriate, an invitation to attend such meetings.

(46)

The Commission should, by means of implementing acts and, given their special nature, acting without the application of Regulation (EU) No 182/2011, determine whether measures taken by Member States in respect of non-compliant lifts or safety components for lifts are justified or not.

(47)

The Member States should lay down rules on penalties applicable to infringements of the provisions of national law adopted pursuant to this Directive and ensure that those rules are enforced. The penalties provided for should be effective, proportionate and dissuasive.

(48)

Since the objective of this Directive, namely to ensure that lifts and safety components for lifts on the market fulfil the requirements providing for a high level of protection of health and safety while guaranteeing the functioning of the internal market, cannot be sufficiently achieved by the Member States but can rather, by reason of its scale and effects, be better achieved at Union level, the Union may adopt measures, in accordance with the principle of subsidiarity as set out in Article 5 of the Treaty on European Union. In accordance with the principle of proportionality, as set out in that Article, this Directive does not go beyond what is necessary in order to achieve that objective.

(49)

It is necessary to provide for reasonable transitional arrangements that allow the making available on the market, without the need to comply with further product requirements, of safety components for lifts that have already been placed on the market in accordance with Directive 95/16/EC before the date of application of national measures transposing this Directive. Distributors should therefore be able to supply safety components for lifts 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.

(50)

In order to monitor and ensure the correct implementation and functioning of this Directive, the Commission is invited to submit a report to the European Parliament and to the Council, exploring also the need for a new legislative proposal in this sector.

(51)

The obligation to transpose this Directive into national law should be confined to those provisions which represent a substantive amendment as compared to the earlier Directive. The obligation to transpose the provisions which are unchanged arises under the earlier Directive.

(52)

This Directive should be without prejudice to the obligations of the Member States relating to the time limits for transposition into national law and the dates of application of the Directives set out in Annex XIII, Part B,

HAVE ADOPTED THIS DIRECTIVE:

Annotations to the whole text

Footnotes

f1

OJ C 181, 21.6.2012, p. 105.

f2

Position of the European Parliament of 5 February 2014 (not yet published in the Official Journal) and decision of the Council of 20 February 2014.

f3

OJ L 213, 7.9.1995, p. 1.

f4

See Annex XIII, Part A.

f5

OJ L 218, 13.8.2008, p. 30.

f6

OJ L 218, 13.8.2008, p. 82.

f7

OJ L 134, 20.6.1995, p. 37.

f8

OJ L 316, 14.11.2012, p. 12.

f9

Approved by Council Decision 2010/48/EC of 26 November 2009 concerning the conclusion, by the European Community, of the United Nations Convention on the Rights of Persons with Disabilities (OJ L 23, 27.1.2010, p. 35).

f10

OJ L 55, 28.2.2011, p. 13.

Contents

  1. Chapter I: GENERAL PROVISIONS
  2. 1Scope
  3. 2Definitions
  4. 3Free movement
  5. 4Placing on the market, making available on the market and putting into service
  6. 5Essential health and safety requirements
  7. 6Buildings or constructions in which lifts are installed
  8. Chapter II: OBLIGATIONS OF ECONOMIC OPERATORS
  9. 7Obligations of installers
  10. 8Obligations of manufacturers
  11. 9Authorised representatives
  12. 10Obligations of importers
  13. 11Obligations of distributors
  14. 12Cases in which the obligations of manufacturers apply to importers or distributors
  15. 13Identification of economic operators
  16. Chapter III: CONFORMITY OF LIFTS AND SAFETY COMPONENTS FOR LIFTS
  17. 14Presumption of conformity of lifts and safety components for lifts
  18. 15Conformity assessment procedures for safety components for lifts
  19. 16Conformity assessment procedures for lifts
  20. 17EU declaration of conformity
  21. 18General principles of the CE marking
  22. 19Rules and conditions for affixing the CE marking and other markings
  23. Chapter IV: NOTIFICATION OF CONFORMITY ASSESSMENT BODIES
  24. 20Notification
  25. 21Notifying authorities
  26. 22Requirements relating to notifying authorities
  27. 23Information obligation on notifying authorities
  28. 24Requirements relating to notified bodies
  29. 25Presumption of conformity of notified bodies
  30. 26Subsidiaries of and subcontracting by notified bodies
  31. 27Application for notification
  32. 28Notification procedure
  33. 29Identification numbers and lists of notified bodies
  34. 30Changes to notifications
  35. 31Challenge to the competence of notified bodies
  36. 32Operational obligations of notified bodies
  37. 33Appeal against decisions of notified bodies
  38. 34Information obligation on notified bodies
  39. 35Exchange of experience
  40. 36Coordination of notified bodies
  41. Chapter V: UNION MARKET SURVEILLANCE CONTROL OF LIFTS OR SAFETY COMPONENTS FOR LIFTS ENTERING THE UNION MARKET AND UNION SAFEGUARD PROCEDURE
  42. 37Union market surveillance and control of lifts or safety components for lifts entering the Union market
  43. 38Procedure for dealing with lifts or safety components for lifts presenting a risk at national level
  44. 39Union safeguard procedure
  45. 40Compliant lifts or safety components for lifts which present a risk
  46. 41Formal non-compliance
  47. Chapter VI: COMMITTEE PROCEDURE, TRANSITIONAL AND FINAL PROVISIONS
  48. 42Committee procedure
  49. 43Penalties
  50. 44Transitional provisions
  51. 45Transposition
  52. 46Review
  53. 47Repeal
  54. 48Entry into force and application
  55. 49Addressees
  56. Signature
  57. Annex I: ESSENTIAL HEALTH AND SAFETY REQUIREMENTS
  58. PRELIMINARY REMARKS
  59. 1Division 1
  60. 2Division 2
  61. 3Division 3
  62. General
  63. 1.1Application of Directive 2006/42/EC
  64. 1.2Carrier
  65. 1.3Means of suspension and means of support
  66. Control of loading (including overspeed)
  67. 1.4.1Division 1.4.1
  68. 1.4.2Lifts must be equipped with an overspeed governor.
  69. 1.4.3Division 1.4.3
  70. 1.4.4Division 1.4.4
  71. Machinery
  72. 1.5.1Division 1.5.1
  73. 1.5.2Division 1.5.2
  74. Controls
  75. 1.6.1Division 1.6.1
  76. 1.6.2Division 1.6.2
  77. 1.6.3Division 1.6.3
  78. 1.6.4Electrical equipment must be so installed and connected that:
  79. Risks for persons outside the car
  80. 2.1Division 2.1
  81. 2.2The lift must be designed and constructed to prevent the risk of crushing when the car is in one of its extreme positions.
  82. 2.3The landings at the entrance and exit of the car must be equipped with landing doors of adequate mechanical resistance for the conditions of use envisaged.
  83. Risks for persons in the car
  84. 3.1Lift cars must be completely enclosed by full-length walls, fitted floors and ceilings included, with the exception of ventilation apertures, and with full-length doors. These doors must be so designed and installed that the car cannot move, except for the landing movements referred to in the third subparagraph of point 2.3, unless the doors are closed, and comes to a halt if the doors are opened.
  85. 3.2In the event of a power cut or failure of components the lift must have devices to prevent free fall or uncontrolled movements of the car.
  86. 3.3Buffers must be installed between the bottom of the shaft and the floor of the car.
  87. 3.4Division 3.4
  88. Other risks
  89. 4.1Division 4.1
  90. 4.2Division 4.2
  91. 4.3Division 4.3
  92. 4.4Division 4.4
  93. 4.5Division 4.5
  94. 4.6Division 4.6
  95. 4.7Division 4.7
  96. 4.8Division 4.8
  97. 4.9Division 4.9
  98. 4.10Division 4.10
  99. Marking
  100. 5.1Division 5.1
  101. 5.2Division 5.2
  102. Instructions
  103. 6.1The safety components for lifts referred to in Annex III must be accompanied by instructions, so the following can be carried out effectively and without danger:
  104. 6.2Each lift must be accompanied by instructions. The instructions shall contain at least the following documents:
  105. Annex II
  106. ACONTENT OF THE EU DECLARATION OF CONFORMITY FOR SAFETY COMPONENTS FOR LIFTS
  107. BCONTENT OF THE EU DECLARATION OF CONFORMITY FOR LIFTS
  108. Annex III: LIST OF SAFETY COMPONENTS FOR LIFTS
  109. 1Division 1
  110. 2Division 2
  111. 3Division 3
  112. 4Division 4
  113. 5Division 5
  114. 6Division 6
  115. Annex IV
  116. (module B)
  117. EU-type examination of safety components for lifts
  118. 1Division 1
  119. 2The application for EU-type examination shall be lodged by the manufacturer, or his authorised representative, with a single notified body of his choice.
  120. 3The technical documentation shall make it possible to assess whether the safety component for lifts meets the conditions referred to in point 1 and shall include an adequate analysis and assessment of the risk(s). The technical documentation shall specify the applicable requirements and cover, as far as relevant for the assessment, the design, manufacture and operation of the safety component for lifts.
  121. 4The notified body shall:
  122. 5Where the type of the safety component for lifts meets the conditions referred to in point 1, the notified body shall issue an EU-type examination certificate to the manufacturer. That certificate shall contain the name and address of the manufacturer the conclusions of the EU-type examination, any conditions of validity of the certificate and the particulars necessary to identify the approved type.
  123. 6Division 6
  124. 7The manufacturer shall inform the notified body that holds the technical documentation relating to the EU-type examination certificate of any modification to the approved type that may affect the conformity of the safety component for lifts with the conditions referred to in point 1 or the conditions of validity of the EU-type examination certificate.
  125. 8Each notified body shall inform its notifying authority concerning the EU-type examination certificates and any additions thereto which it has issued or withdrawn, and shall, periodically or upon request, make available to its notifying authority the list of such certificates and any additions thereto refused, suspended or otherwise restricted.
  126. 9Division 9
  127. 10Division 10
  128. 11Authorised representative
  129. EU-type examination of lifts
  130. 1EU-type examination of lifts is the part of a conformity assessment procedure in which a notified body examines the technical design of a model lift, or a lift for which there is no provision for an extension or variant, and verifies and attests that the technical design of the model lift or the lift meets the applicable essential health and safety requirements set out in Annex I.
  131. 2The application for EU-type examination shall be lodged by the installer or his authorised representative with a single notified body of his choice.
  132. 3The technical documentation shall make it possible to assess the conformity of the lift with the applicable essential health and safety requirements set out in Annex I.
  133. 4The notified body shall:
  134. 5Division 5
  135. 6Where the type meets the essential health and safety requirements set out in Annex I applicable to the lift concerned, the notified body shall issue an EU-type examination certificate to the installer. That certificate shall contain the name and address of the installer, the conclusions of the EU-type examination, any conditions of validity of the certificate and the particulars necessary to identify the approved type.
  136. 7Division 7
  137. 8The installer shall inform the notified body of any modifications to the approved type, including variations not specified in the original technical documentation, that may affect the conformity of the lift with the essential health and safety requirements set out in Annex I or the conditions of validity of the EU-type examination certificate.
  138. 9Each notified body shall inform its notifying authority concerning the EU-type examination certificates and any additions thereto which it has issued or withdrawn, and shall, periodically or upon request, make available to its notifying authority the list of such certificates and any additions thereto refused, suspended or otherwise restricted.
  139. 10Division 10
  140. 11Division 11
  141. 12Authorised representative
  142. Annex V: FINAL INSPECTION FOR LIFTS
  143. 1Division 1
  144. 2Obligations of the installer
  145. 3Final inspection
  146. 3.1The installer shall lodge an application for final inspection with a single notified body of his choice and shall provide to the notified body the following documents:
  147. 3.2The examinations shall include at least one of the following:
  148. 3.3The tests of the lift shall include at least the following:
  149. 4Division 4
  150. CE marking and EU declaration of conformity
  151. 5.1Division 5.1
  152. 5.2Division 5.2
  153. 6Division 6
  154. 7Authorised representative
  155. Annex VI
  156. (module E)
  157. 1Division 1
  158. 2Obligations of the manufacturer
  159. Quality system
  160. 3.1The manufacturer shall lodge an application for assessment of his quality system for the safety components for lifts concerned with a single notified body of his choice.
  161. 3.2Under the quality system, each safety component for lifts shall be inspected and appropriate tests as set out in the relevant harmonised standards or equivalent tests shall be carried out in order to ensure that it meets the conditions referred to in point 1. All the elements, requirements and provisions adopted by the manufacturer shall be documented in a systematic and orderly manner in the form of written policies, procedures and instructions. This quality system documentation shall permit a consistent interpretation of the quality programmes, plans, manuals and records.
  162. 3.3The notified body shall assess the quality system to determine whether it satisfies the requirements referred to in point 3.2. It shall presume conformity with those requirements in respect of the elements of the quality systems that comply with the corresponding specifications of the relevant harmonised standard.
  163. 3.4Division 3.4
  164. 3.5The manufacturer or his authorised representative shall keep the notified body which has approved the quality system informed of any intended changes of the quality system.
  165. Surveillance under the responsibility of the notified body
  166. 4.1Division 4.1
  167. 4.2The manufacturer shall for assessment purposes allow the notified body access to the premises where final inspection, testing and storage are carried out and provide it with all necessary information, in particular:
  168. 4.3Division 4.3
  169. 4.4Additionally, the notified body may pay unexpected visits to the manufacturer’s premises where final inspection and testing of safety components for lifts are carried out.
  170. CE marking and EU declaration of conformity
  171. 5.1Division 5.1
  172. 5.2Division 5.2
  173. 6Division 6
  174. 7Division 7
  175. 8Authorised representative
  176. Annex VII
  177. (module H)
  178. 1Division 1
  179. 2Obligations of the manufacturer
  180. Quality system
  181. 3.1The manufacturer shall lodge an application for assessment of his quality system with a single notified body of his choice. The application shall include:
  182. 3.2The quality system shall ensure compliance of the safety components for lifts with the conditions referred to in point 1. All the elements, requirements and provisions adopted by the manufacturer shall be documented in a systematic and orderly manner in the form of written policies, procedures and instructions. This quality system documentation shall permit a consistent interpretation of the quality programmes, plans, manuals and records.
  183. 3.3The notified body shall assess the quality system to determine whether it satisfies the requirements referred to in point 3.2. It shall presume conformity with those requirements in respect of the elements of the quality systems that comply with the corresponding specifications of the relevant harmonised standard.
  184. 3.4Division 3.4
  185. 3.5The manufacturer shall keep the notified body which has approved the quality system informed of any intended change to the quality system.
  186. Surveillance under the responsibility of the notified body
  187. 4.1Division 4.1
  188. 4.2The manufacturer shall for assessment purposes allow the notified body access to the design, manufacture, inspection and testing, and storage locations, and shall provide it with all necessary information, in particular:
  189. 4.3Division 4.3
  190. 4.4Division 4.4
  191. CE marking and EU declaration of conformity
  192. 5.1Division 5.1
  193. 5.2Division 5.2
  194. 6Division 6
  195. 7Division 7
  196. 8Authorised representative
  197. Annex VIII
  198. (module G)
  199. 1Division 1
  200. Obligations of the installer
  201. 2.1Division 2.1
  202. 2.2The installer shall apply to a single notified body of his choice for unit verification.
  203. 3Division 3
  204. 4Verification
  205. CE marking and EU declaration of conformity
  206. 5.1Division 5.1
  207. 5.2Division 5.2
  208. 6Division 6
  209. 7Authorised representative
  210. Annex IX
  211. (module C 2)
  212. 1Division 1
  213. 2Manufacturing
  214. 3Division 3
  215. 4Division 4
  216. CE marking and EU declaration of conformity
  217. 5.1Division 5.1
  218. 5.2Division 5.2
  219. 6Authorised representative
  220. Annex X
  221. (module E)
  222. 1Division 1
  223. 2Obligations of the installer
  224. Quality system
  225. 3.1The installer shall lodge an application for assessment of his quality system for the lifts concerned with a single notified body of his choice.
  226. 3.2Under the quality system, each lift shall be examined and appropriate tests as set out in the relevant harmonised standards or equivalent tests shall be carried out in order to ensure its conformity with the applicable essential health and safety requirements set out in Annex I.
  227. 3.3The notified body shall assess the quality system to determine whether it satisfies the requirements referred to in point 3.2. It shall presume conformity with those requirements in respect of the elements of the quality systems that comply with the corresponding specifications of the relevant harmonised standard.
  228. 3.4Division 3.4
  229. 3.4.1Division 3.4.1
  230. 3.4.2The notified body shall assess the modifications proposed and decide whether the modified quality system will continue to satisfy the requirements referred to in point 3.2 or whether a reassessment is necessary.
  231. Surveillance under the responsibility of the notified body
  232. 4.1Division 4.1
  233. 4.2The installer shall, for assessment purposes, allow the notified body access to the installation, inspection and testing locations, and shall provide it with all necessary information, in particular:
  234. 4.3Division 4.3
  235. 4.4Additionally, the notified body may pay unexpected visits to the lift installation sites.
  236. 5Division 5
  237. 6Division 6
  238. CE marking and EU declaration of conformity
  239. 7.1Division 7.1
  240. 7.2Division 7.2
  241. 8Authorised representative
  242. Annex XI
  243. (module H1)
  244. 1Division 1
  245. 2Obligations of the installer
  246. Quality system
  247. 3.1Division 3.1
  248. 3.2Division 3.2
  249. Design examination
  250. 3.3.1Division 3.3.1
  251. 3.3.2Where the design does not satisfy the applicable essential health and safety requirements set out in Annex I, the notified body shall refuse to issue an EU design examination certificate and shall inform the installer accordingly, giving detailed reasons for its refusal.
  252. 3.3.3Division 3.3.3
  253. 3.3.4Each notified body shall inform its notifying authority of the EU design examination certificates and/or any additions thereto which it has issued or withdrawn, and shall, periodically or upon request, make available to its notifying authority the list of EU design examination certificates and/or any additions thereto refused, suspended or otherwise restricted.
  254. 3.3.5Division 3.3.5
  255. 3.4Assessment of the quality system
  256. 3.5Division 3.5
  257. Surveillance under the responsibility of the notified body
  258. 4.1Division 4.1
  259. 4.2The installer shall, for assessment purposes, allow the notified body access to the design, manufacture, assembly, installation, inspection, testing and storage locations, and shall provide it with all necessary information, in particular:
  260. 4.3Division 4.3
  261. 4.4Division 4.4
  262. 5Division 5
  263. 6Division 6
  264. CE marking and EU declaration of conformity
  265. 7.1Division 7.1
  266. 7.2Division 7.2
  267. 8Authorised representative
  268. Annex XII
  269. (module D)
  270. 1Division 1
  271. 2Obligations of the installer
  272. Quality system
  273. 3.1The installer shall lodge an application for assessment of his quality system with a single notified body of his choice.
  274. 3.2The quality system shall ensure compliance of the lifts with the applicable essential health and safety requirements set out in Annex I.
  275. 3.3The notified body shall assess the quality system to determine whether it satisfies the requirements referred to in point 3.2. It shall presume conformity with those requirements in respect of the elements of the quality system that comply with the corresponding specifications of the relevant harmonised standard.
  276. 3.4Division 3.4
  277. 3.4.1Division 3.4.1
  278. 3.4.2The notified body shall assess the modifications proposed and decide whether the modified quality system will continue to satisfy the requirements referred to in point 3.2 or whether a reassessment is necessary.
  279. Surveillance under the responsibility of the notified body
  280. 4.1Division 4.1
  281. 4.2The installer shall, for assessment purposes, allow the notified body access to the manufacture, assembly, installation, inspection, testing and storage locations, and shall provide it with all necessary information, in particular:
  282. 4.3Division 4.3
  283. 4.4Division 4.4
  284. 5Division 5
  285. 6Division 6
  286. CE marking and EU declaration of conformity
  287. 7.1Division 7.1
  288. 7.2Division 7.2
  289. 8Authorised representative
  290. Annex XIII
  291. APart A
  292. BPart B
  293. Annex XIVAnnex XIV
  294. Attachment