Appendix 1

Publication of the directions and so on of elevators 1)

In accordance with section 2 (2), 2, section 4 (4). 3, section 6 (4). 3, section 7, paragraph. 2, section 8 (4). 3, section 9 (4). 3, section 11, section 13, section 17, paragraph 1. 4, section 20, section 21, paragraph. Paragraph 1, and section 27 (1). Amendment No 4. 155 of 20. February 2013 on the orientation of certain products, and under the authority of the Act of 22, the following shall be determined :

Scope of application

§ 1. This notice is implemented by Directive 95 /16/EC of the European Parliament and of the Council on the approximation of the laws of the Member States relating to lifts in future amendments The Directive is included in Annex 1 to this notice.

§ 2. The notice applies to elevators and safety components, as defined and delimited in Article 1 of Annex 1.

§ 3. The announcement shall apply to manufacturers of safety components, their representatives, the installer of the lift, notified bodies and others as provided for in Annex 1.

General provisions

§ 4. Lifts may only be made available to the user and in use if there is no risk of the safety and health of persons and, where appropriate, assets are placed at risk, provided that they are installed and maintained in an appropriate manner and shall be used in the use of : conformance with their purpose.

Paragraph 2. In addition, lifts shall comply with the provisions of Annex 1.

Paragraph 3. Safety components may only be put into circulation, made available on the market or in use if the lifts on which they are to be fitted do not entail the risk that the safety and health of persons and, where appropriate, assets are put at risk, shall be made ; so far as these components are fitted and maintained in a suitable manner and used in accordance with their purpose.

Paragraph 4. The safety components shall also comply with the provisions of Annex 1.

Paragraph 5. Manufacturers of safety components, their representatives, the installer of the lift, notified bodies and others in accordance with Annex 1 shall comply with the requirements laid down by this notice.

§ 5. The person responsible for the construction of a building or installation and the installer of the lift must both mutually exchange the necessary information and, on the other hand, take the necessary measures to ensure that the lift can function correctly and may be used ; Under comforting conditions.

§ 6. In exceptional cases, in existing properties where a free space or sanctuary cannot be established outside each of the outer positions of the lift, other measures may be taken to avoid the risk of hazard if the Health Safety Board has given one, advance approval for this purpose.

§ 7. In the lift shaft, no other pipe installations or installations may be found other than those necessary for the operation and safety of the lift.

§ 8. Lifts may only be put into circulation, made available on the market or in use, provided that the documentation in accordance with Annex I, section 6.2 of the Directive is made out in Danish.

§ 9. Safety components may only be placed in circulation, made available on the market or in use if the instructions provided for in Annex I, section 6.1 of the Directive are made out in Danish, so that the installation, connection, adjustment and maintenance of the Directive may occur ; in an efficient and perilable way. However, the use of the instructions for fitting and connecting must be made out in another EU language, if the company has this language as a working language, and the manufacturer / Montor is in charge of this language.

Notified bodies

§ 10. The Director of the Health Safety Board may appoint notified bodies, cf. Annex 1, Article 9.

Paragraph 2. In order to be designated as notified body, the applicant shall be a legal person established in Denmark.

Paragraph 3. In order to be designated as notified body, the applicant shall be accredited by the DANAK, cf. the notice of the appointment of the national accreditation body.

Paragraph 4. The accreditation under paragraph 1. 3 shall be carried out in relation to the assignment requested for the designation and ensure that the minimum requirements laid down in Annex VII of the Directive are met.

Paragraph 5. In order to be designated as notified body, the applicant must comply with the Annex VII Directive. The labor may be subject to conditions other than those laid down in the Annex.

Paragraph 6. The surveillance authorities may carry out checks and inspections that the notified bodies at any time meet the criteria laid down in Annex VII to this Directive. The notified body must, at its request, submit all relevant information.

Paragraph 7. The Director of the Health Safety Board may include the authorisation if it is established that the notified body no longer fulfils the criteria for the authorization, cf. paragraph 1-5.

§ 11. The work may be charged for the period during which the processing of applications to be appointed as notified body may be charged for the period during which the Work in the Employment is subject to the processing of applications. This applies, whether or not the request is withdrawn or withdrawn.

Paragraph 2. The processing of the procedures for the appointment of the appointment shall be fixed in such a way that the long-term average costs are covered. The labor fee shall amount to DKK DKK $6.00 a. Hour.

Paragraph 3. The fee shall be adjusted each year per year by the labor allowance. 1. April with the general price and wage index.

Paragraph 4. If the charges are not in a timely manner, the charges shall be forctually 1,5%. for each starting month from a due date.

Paragraph 5. If, despite repeated claims, an applicant has failed to pay the Labor of Work for this notice, the Health Safety Board will transfer the collection to the HIRP;

Crow

§ 12. Decisions pursuant to this notice shall not be subject to the second administrative authority, cf. However, section 13.

§ 13. Complaguing of decisions made by notified bodies may be brought before the WA within 4 weeks after the decision has been notified to the person concerned.

Punishment

§ 14. Unless higher penalties have been imposed on the introduction of certain products or other legislation, the penalty shall be penalised by the penalty which :

1) are breached sections 4, 5 and 7 to 9, or provisions in Annex 1, or

2) shall not be followed by decisions, including injunction or prohibitions issued in accordance with the provisions of the notice.

Paragraph 2. Companies can be imposed on companies, etc. (legal persons) punishable by the rules of the penal code 5. Chapter.

Entry into force and transitional provisions

§ 15. The announcement shall enter into force on 1. July, 2013.

Paragraph 2. The announcement shall apply to lifts and safety components that are put into circulation, be made available on the market or in use after the date of entry into force of the notice. In the case of the decor and safety components that have been put into circulation, made available on the market or in use before the entry into force of the notice, the applicable rules shall apply.

Paragraph 3. At the same time, notice No 678 of 27. June 2008 on the orientation of elevators.

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Appendix 1

In the Annex, the European Parliament and Council Directive 95 /16/EC of 29 are reproduced. June 1995 on the approximation of the laws of the Member States relating to

as modified by

Regulation No 2 of the European Parliament 1882/2003 of 29. September 2003, Directive 2006 /42/EC of the European Parliament and of the Council of 17. The Regulation No No no. 1025/2012 of 25. -October 2012.

The directive is reproduced in the consolidated version of 1. January 2013.

EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE 95 /16/EF

of 29. June 1995

on the approximation of the laws of the Member States relating

THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION HAVE-

Having regard to the Treaty establishing the European Community, and in particular Article 100a thereof,

Having regard to the proposal from the Commission, 2) ,

Having regard to the opinion of the Economic and Social Committee 3) ,

in accordance with the procedure laid down in Article 189b of the Treaty 4) , on the basis of the Conciliation Committee's joint text of 17. May 1995, and

in the following considerations :

Whereas it is up to the Member States in their territory to ensure the safety and health of our citizens ;

Whereas the White Paper on the completion of the internal market, approved by the European Council in June 1985, contains in paragraphs 65 and 68 provisions for the application of the new approach to the approximation of laws ;

Council Directive 84 /529/EEC of 17. September 1984 on the approximation of the laws of the Member States relating to electrical, hydraulic or electro-hydraulic-powered elevators, 5) , without allowing free circulation of all lifts, the essential provisions of the national legislation on the lifts which are not covered by Directive 84 /529/EEC, due to their differences, are obstacles to intra-Community trade in : whereas, therefore, the Community rules on lifts should be harmonized ;

Council Directive 84 /528/EEC of 17. September 1984 on the approximation of the laws of the Member States relating to common rules for the lifting of goods, lifting and transport equipment 6) the framework Directive for two separate Directives, specifically Directive 84 /529/EEC and Council Directive 86 /663/EEC of 22. December 1986 on the approximation of the laws of the Member States relating to self-driving 7) , repealed by Directive 91 /368/EEC of 20. June 1991 amending Directive 89 /392/EEC on the approximation of the laws of the Member States relating to machinery 8) ;

The Commission adopted the 8. June 1995 Recommendation 95 /216/EC 9) to Member States concerning the improvement of safety at existing lifts ;

Whereas the essential requirements of this Directive will only be able to ensure the level of safety required if, inter alia, the provisions of Council Decision 93 /465/EEC of 22. July 1993 on the modules for the various phases of conformity assessment procedures and the application of the CE conformity marking, in order to be applied to the technical harmonisation directives ; 10) , selected appropriate procedures for conformity assessment to ensure compliance with these requirements ;

lifts or some of their safety components which comply with the essential health and safety requirements of this Directive must be provided with visible CE marking in order to be marketed ;

Whereas this Directive lays down only the essential health and safety requirements which are of a general nature ; in order to make it easier for manufacturers to prove that the lifts are in accordance with these essential requirements, as well as to check that the lifts are carried out ; Whereas these requirements have been complied with, at European level, harmonised standards for the prevention of risks arising from the construction and installation of the lift ; these harmonised standards at European level are drawn up by private law bodies ; must retain the status of texts which are not legally binding ; in this context, the European Committee for Standardisation (CEN) and the European Committee for Electrotechnical Standardisation (CENELEC) as the bodies competent to adopt the harmonized standards in accordance with the general principles, guidelines for cooperation between the Commission and these bodies, which was signed on 13. In this Directive, a harmonized standard shall mean a technical specification adopted by one of these bodies or both by the mandate of the Commission in accordance with Council Directive 83 /189/EEC of 28. March 1983 laying down a procedure for the provision of information in the field of technical standards and regulations 11) , and in accordance with the abovementioned general guidelines ;

Whereas it is important to establish a transitional arrangement so that the installers can market elevators before the date of implementation of this Directive ;

this Directive is drawn up to cover all the risks associated with lifts, to which their users and the inhabitants of the building are exposed ; the Directive must therefore be considered as a Directive as referred to in Article 2 (1). 3, in Council Directive 89 /106/EEC of 21. December 1988 on the approximation of the laws, regulations and administrative provisions of the Member States concerning construction 12) ;

The European Parliament, the Council and the Commission reached 20. In December 1994, agreed on a modus vivendi concerning the implementing measures for acts adopted in accordance with the procedure laid down in Article 189b of the Treaty,

ISSUED THE FOLLOWING DIRECTIVE :

CHAPTER I

Scope, marketing and free circulation

ARTICLE 1

1. This Directive shall apply to lifts permanently serving buildings and facilities. It shall also apply to the safety components used in the elevators in question and listed in the list in Annex IV.

2. For the purposes of this Directive, ' lift ' shall mean the lifting and lifting material used by an elevator chair which is moving along the steady steering gear with a heel rate of more than 15 ° in relation to the horizontal plane and which is ; intended to transport :

-WHAT? people

-WHAT? persons and goods,

-WHAT? goods only if the lift chair is available, i.e. that a person can enter it without difficulty and is equipped with controls inside the lift or within reach of the person in the lift chair.

Lifting and lifting material if the lift chair is moving by a complete fixed course, even though it does not move along the steady steering gear, shall be regarded as lifts falling within the scope of this Directive.

' Elevator chair ` means any part of the lift that carries persons and / or goods to be hosed up or reduced.

3. This Directive shall not apply to :

-WHAT? lifting material at a speed of 0,15 m/s or less ;

-WHAT? build space elevator operators,

-WHAT? two-level installations, including levials,

-WHAT? lifts, specially designed and constructed for military or police purposes ;

-WHAT? lifting material from which work can be carried out,

-WHAT? miners in mine shafts,

-WHAT? material to move the performers during the stage of artistic conduct,

-WHAT? lifting equipment, installed in means of transport,

-WHAT? hey- and lifting material belonging to a machine and intended exclusively for access to the workplace, including maintenance and inspection of the machinery ;

-WHAT? orthodors

-WHAT? escalator and scrolling turbons.

4. For the purposes of this Directive :

-WHAT? lift installer : a natural or legal person who is responsible for the design, manufacture, installation and marketing of an elevators, and which puts the CE marking and issues the EC declaration of conformity

-WHAT? the placing on the market of the lift : the time when the installer first makes the elevator available to the user ;

-WHAT? safety component : a component listed in Annex IV ;

-WHAT? manufacturer of safety components : a natural or legal person who is responsible for the construction and manufacture of the safety components and affixing the CE marking and issuing the EC declaration of conformity ;

-WHAT? lifts model : a representative lift whose technical documentation shows how the essential safety requirements will be complied with in the lifts which are subsequently produced on the basis of the model of the lift, determined by objective parameters and uses similar safety components.

All permitted variations between the lift model and the elevators produced on the basis of this must be clearly indicated (with maximum and minimum values) in the technical documentation.

Calculations and / or on the basis of design drawings are permitted to demonstrate the uniformity of a series of devices and their installation in respect of compliance with the essential safety requirements.

When the risks referred to in the Directive are in full or in part covered by special directives, this Directive shall not apply, or shall cease to apply to such lifts and the risks, as soon as the separate directives have entered into force.

ARTICLE 2

1. Member States shall take the necessary measures to ensure that :

-WHAT? lifts covered by this Directive shall be possible only on the market and in use if there is no risk of the safety and health of persons and, where appropriate, goods, provided that the elevators are installed and maintained by appropriate means ; are used in accordance with their aims,

-WHAT? Whereas safety components covered by this Directive can only be placed on the market and in use if the lifts for which they are to be fitted do not pose a risk to the safety and health of persons and, where appropriate, goods at risk, provided that such lifts are put at risk ; components are fitted and maintained in an appropriate manner and shall be used in accordance with their objectives.

2. Member States shall take the necessary measures to ensure that the person responsible for the construction of a building or installation and the installer of the lift shall also share the necessary information, and on the other, they shall take the necessary information ; measures required to enable the lift to operate properly and may be used in order to be used in a safe and reassuring nature.

Member States shall take the necessary measures to ensure that there are no other plumbing installations or installations other than those necessary for the operation and safety of the lift.

4. Without prejudice to paragraph 1, In accordance with the Treaty, 1, 2 and 3, this Directive shall not affect the Member States ' ability to lay down the requirements which they consider necessary to ensure the protection of persons in the use and use of those concerned ; lifts, provided that this does not involve any changes to them in relation to this Directive.

Member States shall not oppose the presence of mass, exhibitions, exhibits or safety components which are not in accordance with the Community provisions in force ; in that case, it shall be visible ; signage clearly stipulates that they do not comply with the provisions and that the elevators or safety components concerned cannot be obtained before the installer of the lift or the manufacturer of the safety components or the latter are used in the Community ; established representative has brought them into line with that. In demonstrations, adequate safety measures must be taken to protect people.

ARTICLE 3

The lifts covered by this Directive shall comply with the essential health and safety requirements set out in Annex I ;

The safety components covered by this Directive must comply with the essential health and safety requirements set out in Annex I, or ensure that the lifts in which they are fitted meet the same essential requirements.

ARTICLE 4

Member States may not prohibit, restrict or impede the placing on the market and putting into service on their territory by lifts and / or safety components which comply with the provisions of this Directive.

Member States shall not prohibit, restrict or prevent the placing on the market of components which, according to the declaration by the manufacturer or his authorised representative established within the Community, are intended to be included in an elevator covered by this Directive.

Article 5

1. Member States regard lifts and safety components bearing the CE marking and are accompanied by the EC declaration of conformity referred to in Annex II, in order to satisfy all the provisions of this Directive, including those laid down in Chapter II ; the conformity assessment procedures referred to.

Where harmonized standards are not available, Member States shall lay down the provisions they consider necessary for the parties concerned to be aware of the existing national standards and technical specifications, which are considered important or useful ; in the context of the correct application of the essential health and safety requirements laid down in Annex I.

2. When a national standard that carries out a harmonised standard if reference has been published in Official Journal of the European Communities includes one or more essential health and safety requirements ;

-WHAT? the lift prepared in accordance with this standard is assumed to be in accordance with the essential requirements concerned ;

-WHAT? the safety component produced in accordance with this standard shall be assumed to give the lift on which it is fitted properly, to meet the essential requirements concerned.

Member States shall publish the references of national standards implementing the harmonized standards.

Member States shall ensure that appropriate measures are taken to enable the social partners to have an influence on the preparation and follow-up of the harmonised standards at national level.

ARTICLE 6

-...

The Commission may in accordance with the procedure laid down in paragraph 1 3 adopt any appropriate measure to ensure that the practical application of this Directive is uniform.

3. The Commission shall be assisted by a Standing Committee, hereinafter referred to as ' the Committee `.

Where reference is made to this paragraph, Articles 3 and 7 of Decision 1999 /468/EC shall apply ; 13) , cf. its Article 8.

The Committee shall adopt its rules of procedure.

The Standing Committee may also examine any question relating to the application of this Directive, which the chairman shall submit, either on his own initiative or at the request of a Member State.

Article 7

1. If a Member State ascertains that an elevator or a safety component bearing the CE marking and used in accordance with its purpose will be capable of providing a risk to the safety and health of persons and, where appropriate, for goods, shall take all necessary measures to withdraw it from the market, prohibit its placing on the market and in use or limit its free circulation.

The Member State shall forthwith inform the Commission of this measure and shall state the reasons for its decision, in particular whether the failure to conform is due to :

a) the essential requirements referred to in Article 3 have not been met ;

b) incorrect application of the provisions of Article 5 (1). 2, standards referred to ;

c) a lack of the actual absence of the provisions of Article 5 (1). The standards referred to in paragraph 2

2. The Commission shall consult the parties concerned as soon as possible. If, after this consultation, the Commission finds :

-WHAT? the measures are justified, it shall immediately inform the Member State which has taken the initiative and the other Member States thereof. If the one in paragraph 1 The Commission shall, after consultation with the parties concerned, subject to the absence of the standards referred to in Article 6 (2), shall be submitted by the Commission, after consultation with the parties concerned. The Committee referred to in Article 6 (1) of the Member State referred to in Article 6 (1), as referred to in Article 6 (1), shall enter into the proceedings referred to in Article 6 (1). 1

-WHAT? the measures are unjustified, it shall immediately inform the Member State which has taken the initiative and the installer of the lift, the manufacturer of the safety components or the latter ' s representative established in the Community.

3. is an elevator or a safety component which does not comply with the conformity criteria, bearing the CE marking, the competent Member State shall take the necessary measures to the person who affixed the marking and shall inform the Member States thereof ; The Commission and the other Member States thereof.

4. The Commission shall ensure that the Member States are kept informed of the progress and results of the procedure.

CHAPTER II

Conformity assessment procedure

ARTICLE 8

1. before the placing on the market of the safety components referred to in Annex IV, the manufacturer of a safety component or its authorised representative established within the Community must :

2. before placing a lift on the market, an elevator must have undergone one of the following procedures :

i) either, if it is designed in accordance with an elevator which has undergone the EC type-examination referred to in Annex V, it shall be manufactured, installed and tested using :

-WHAT? the final inspection set out in Annex VI, or

-WHAT? the quality assurance system in Annex XII, or

-WHAT? the quality assurance system set out in Annex XIV.

Procedures concerning both the design and manufacturing stages of the installation and testing phases may be applied to the same lift ;

(ii) or, if it is designed in accordance with an elevator model that has undergone the EC type-examination referred to in Annex V, shall be produced, installed and tested using

-WHAT? the final inspection set out in Annex VI, or

-WHAT? the quality assurance system in Annex XII, or

-WHAT? the quality assurance system in Annex XIV ;

(iii) or, if it is designed in accordance with an elevator which has undergone the quality assurance referred to in Annex XIII, supplemented by a control of the design, provided that it is not fully in conformity with the harmonized ; standards, produced, installed and tested using :

-WHAT? the final inspection set out in Annex VI, or

-WHAT? the quality assurance system in Annex XII, or

-WHAT? the quality assurance system in Annex XIV ;

(iv) or it must have undergone a unit verification by a notified body as referred to in Annex X ;

(v) or it must have undergone the quality assurance referred to in Annex XIII, supplemented by a control of the design if this is not fully in conformity with the harmonized standards.

In the cases referred to in (i), (ii) and (iii), the person responsible for the design shall give the person responsible for the manufacture, installation and testing, all the information necessary for the latter to be able to take place ; Under comforting conditions.

Three, in all the pieces in the first paragraph. 2 mentioned cases

-WHAT? shall affix the CE marking to the lift and draw up a declaration of conformity with the particulars indicated in Annex II, taking into account the provisions of the Annexes used (respectively Annexes VI, X, XII, XIII or XIV),

-WHAT? retain the installer of the lift, a copy of the declaration of conformity for a period of 10 years from the date on which the lift was placed on the market for the first time ;

-WHAT? the Commission, the Member States and the other notified bodies, at the request of the installer, shall be able to obtain a copy of the declaration of conformity and of the test reports drawn up in connection with the final inspection.

5. The installer of the installer, the manufacturer of the safety components or his authorised representative established within the Community, has fulfilled the obligations laid down in the preceding paragraphs, the obligation on the part of any person who is placing the market on the market ; the lift or safety component of the Community. The same obligations shall be the responsibility of the one producing the lift or the safety component for its own use.

Article 9

Member States shall inform the Commission and the other Member States of the bodies they have designated to carry out the procedures referred to in Article 8 and the specific tasks and investigation procedures to which these bodies have been designated ; the undertaking and the identification numbers assigned to them by the Commission.

The Commission shall publish a list of the notified bodies and their identification numbers and the tasks for which they are appointed ; Official Journal of the European Communities. The Commission shall ensure that the list is kept up to date.

Member States shall apply the criteria set out in Annex VII in relation to the assessment of the notified bodies. Organs that meet the assessment criteria laid down in the relevant harmonized standards shall be presumed to meet these criteria.

3. A Member State which has notified a body must withdraw the authorization if it finds that this body no longer meets the criteria laid down in Annex VII. It shall forthwith inform the Commission and the other Member States thereof.

CHAPTER III

CE marking

Article 10

1. The CE conformity marking shall consist of the initials ' CE ` ; in Annex III, the model to be used is indicated.

2. The CE marking must be affixed in the single elevator chair in a clear and visible manner in accordance with section 5 of Annex I and must be affixed to the safety components listed in Annex IV, or, if this is not possible, on a sign that has been attached to the safety component.

3. It shall be prohibited to affix the affixing of the lifts or safety components which may deceive third parties as to the meaning and gravity of the CE marking. Any other marking may be affixed to the lifts or safety components provided that this does not make the CE marking less visible or easily legible.

Without prejudice to Article 7 :

a) the installer of the lift, the manufacturer of a safety component or the latter ' s representative established within the Community, shall be established by a Member State, if a Member State ascertains that the CE marking has been affixed unjustifiable-obliged to ensure that the product is re-established ; the provisions relating to the CE marking must be brought to an end and that the infringement is terminated in accordance with the conditions laid down by the Member State ;

b) the Member State must, if the product continues to fail to meet the requirements, take all necessary measures to restrict or prohibit the placing on the market of the safety component concerned or to ensure that it is withdrawn from the market and prohibit ; use of the lift and inform the other Member States in accordance with the procedure laid down in Article 7 (3). 4.

CHAPTER IV

Final provisions

Article 11

Any decision taken pursuant to this Directive and which restrides

-WHAT? placing on the market and / or putting into service and / or use of an elevator ;

-WHAT? the placing on the market and / or putting into service of a safety component ;

the reasons must be carefully justified. The decision shall be communicated as soon as possible to the party concerned, specifying the existing redress inequalities and the time limits for the application of these measures.

Article 12

The Commission shall take the necessary measures to make the records available to all relevant decisions concerning the application of this Directive be made available.

ARTICLE 13

Directive 84 /528/EEC and 84 /529/EEC are hereby repealed with effect from 1. July, 1999.

ARTICLE 14

The directive before us is a directive in accordance with Article 2 (2). 3, in Directive 89 /106/EEC, with regard to the aspects related to the installation of an installer.

Article 15

1. Member States shall adopt and publish before 1. In January 1997, the laws, regulations and administrative provisions necessary to comply with this Directive shall forthwith inform the Commission thereof.

When Member States adopt these provisions, they shall contain a reference to this Directive or shall be accompanied by such reference on the occasion of their official publication. The methods of making such reference shall be laid down by the Member States.

Member States shall apply these provisions from 1. July 1997.

Two, until the 30. June 1999 permits Member States

-WHAT? placing on the market and putting in service of lifts,

-WHAT? the placing on the market and putting into service of safety components ;

which are in accordance with the provisions in force in their territory at the time of the issue of this Directive.

Member States shall communicate to the Commission the texts of the provisions of national law which they adopt in the field covered by this Directive.

Article 16

By the 30. In June 2002 the Commission shall, in consultation with the provisions referred to in Article 6 (2), The Committee shall, on the basis of reports from the Member States, examine how the procedures provided for in this Directive are to operate and propose appropriate amendments.

Article 17

This Directive is addressed to the Member States.

ANNEX I

ESSENTIAL SAFETY AND HEALTH REQUIREMENTS IN CONNECTION WITH

WITH THE DESIGN AND MANUFACTURE OF LIFTS AND

SECURITY COMPONENTS

PRELIMINARY REMARKS

1. The obligations laid down by the essential health and safety requirements shall apply only when the relevant risk is present for the lift or safety component associated with the use of this under the conditions of use, the installer of the lift, or the manufacturer of the safety component, fixed conditions.

The essential health and safety requirements laid down in the directive are essential. However, in the light of the technical stage, it is possible that the objectives set are not achievable. If this is the case, the lift or safety component shall be construed and produced in order to enable these objectives to be pursued as far as possible.

3. The manufacturer of the safety component and the installer of the lift must carry out a risk analysis with a view to identifying all of the risks associated with their product ; the product must then be constructed and produced in the interests of this ; analysis.

In accordance with Article 14, the essential requirements of Directive 89 /106/EEC, which have not been included in this Directive, shall apply to lifts.

1. GENERAL REMARKS

1.1. Application of Directive 89 /392/EEC as amended by Directives 91 /36 8 / EEC, 93 /44/EEC and 93 /68/EEC

Where the relevant risk is available but not dealt with in this Annex, the essential health and safety requirements set out in Annex I to Directive 89 /392/EEC shall apply. In any event, the essential requirements of section 1.1.2 of Annex I to Directive 89 /392/EEC shall apply.

1.2. Elevator Chair

The elevator chair in each lift must be a cabinine. This cab must be designed and constructed in such a way that the area and carrier capacity corresponds to the maximum number of people and the nominal nominal of the lift, as determined by the manufacturer.

If the lift is intended for the carriage of persons and its dimensions, the cabin must be prepared and constructed in such a way that it does not impede or prevent the access of disabled persons as a result of the construction of the person concerned or preventing the access of disabled persons ; or use it, and so it may be equipped with any suitable equipment which makes it easier for these people to use it.

1.3. Repeating and carrying means

All the suspension components and / or lifts of the lift must be chosen and constructed in such a way as to ensure a sufficient overall level of safety, and so that the risk of reducing the lift is reduced to a minimum in the light of the conditions of use, the materials used and the conditions of manufacture.

Where the traction or chains are used as a carrier for the lift, there must be at least two independent two-way or chains, and each rope or chain must be fitted with its own fastening system. Tova and chains shall not be either spliced or collected except where this is necessary in order to be able to be attached or retainted.

1.4. Control of movement (including speed limitation)

1.4.1. The lifts must be so designed and constructed and installed in such a way that the initiation is not possible for so long as the load exceeds the nominal highest rated.

1.4.2. The elevators must be equipped with speed limits.

However, this does not apply to lifts which, because of the construction of the drift system, will not be able to achieve too much speed.

1.4.3. Rapid lifts must be fitted with a device enabling the speed to be controlled and controlled.

1.4.4. Lifts in the use of the friction rods shall be so constructed as to ensure that the stability of the two-valve stability on the friction board is ensured.

1.5. Elevator Plays

1.5.1. Each person lift must have its own elevator game. This requirement does not apply to lifts where, instead of the counterweight, there is yet another lift chair.

1.5.2. The installer of the lift shall ensure that an elevator's game and its associated devices are not available, except in the case of maintenance and in case of emergency.

1.6. Control devices

1.6.1. The service devices in lifts intended to be used by disabled persons without a whitelighter must be designed and fitted in an appropriate manner.

1.6.2. The function of processing anordings must be clearly specified.

1.6.3. An elevator group's call systems can be common or interconnected.

1.6.4. The electrical equipment must be installed and connected in such a way as to :

-WHAT? any confusion with circuits not belonging to the lift is excluded ;

-WHAT? the energy supply can be switched off to under load,

-WHAT? the movements of the lift are dependent on the electrical safety devices placed in an independent security circuits ;

-WHAT? an electrical installation error does not create a dangerous situation.

2. THE RISKS TO PERSONS OUTSIDE THE LIFT

2.1. The lift must be designed and constructed in such a way that access to the lift shaft is impossible, except in the case of maintenance or in case of emergency. Before a person can enter the lift shaft, the normal use of the lift must be made impossible.

2.2. The lift must be designed and constructed in a manner which preclates danger of being squeezing when the lift chair is located in one of its external positions.

This purpose shall be fulfilled by a free space or a safe house outside of each of the extrematic positions.

In specific cases, particularly in existing properties, any other measure may be taken to avoid such danger. The Member States must be given the opportunity to give prior authorisation.

2.3. The opening doors of the lift chair must be fitted with floor doors having a sufficiently large mechanical resistance to the conditions of use of the manufacturer.

A contraption device shall prevent :

-WHAT? that the lift chair may be initiated intentionally or unintentionally if not all floor doors are closed and locked ;

-WHAT? the opening of a floor door, while the car is in motion, and if it is not on a floor.

However, the progress of an open establishment door with a view to bringing the car seat to a level with an establishment threshold, however, is permitted in defined zones if this is carried out at a controlled rate.

3. THE RISKS OF PERSONS IN THE LIFT CHAIR

3.1. The lift must be completely closed with whole walls, ceilings and floors, except for ventilation, and equipped with whole doors. The lift doors must be designed and fitted in such a way that the lift chair cannot be moved, except for the transference referred to in the third subparagraph of point 2.3, unless the doors are closed and that it stops if the doors are opened.

The lift doors shall remain closed and locked in the event of a stop between two floors if there is otherwise a risk of falling between the car chair and the shaft or if there is no harm.

3.2. In the event of an energy failure or a component, the lift must be equipped with devices intended to prevent free fall or uncontrolled upward movements of the lift chair.

The mechanism for preventing the free fall of the lift shall be independent of the suspension devices of the lift chair.

This device shall be able to stop the chair at the nominal highest mark and the maximum speed for which the installer of the lift has been determined. The standpoint of this device must not, under any conditions, convene a deceleration that is dangerous to those who are in the chair.

3.3. Buffer devices must be installed between the floor of the lift shaft and the floor of the lift shaft.

In this case, the free space referred to in point 2.2 shall be measured with the buffer devices in total summary.

This requirement does not apply to lifts in which the lift chair, due to the design of the driving system, cannot enter the free space referred to in paragraph 2.2.

3.4. The lifts must be designed and manufactured so that they cannot be started unless the device referred to in 3.2 is in a position where it can operate.

4. OTHER HAZARDS

4.1. If the doors and doors or both of these doors are being moved by mechanical means, they must be equipped with a device which excludes the risk of clamps when they are moved.

4.2. The doors of the doors, including the parts supplied with glass, shall, when they are intended to contribute to the fire of fire, have an appropriate heat-resistant, denoted by the fact that they are all intact and undamaged, as well as in their isolating (fire must not spread) ; thermal transmissible properties (heat radiation).

4.3. Any counterweights must be fitted in such a way as to exclude the possibility of colliding with the lift or downgrading on this one.

4.4. The lifts must be fitted with devices which allow free and assisting persons to be released into the lift chair.

4.5. The lift must be fitted with a two-way means of communication, which will allow for all time to be connected with a particular alarm centre.

4.6. The lifts must be designed and manufactured so that, by exceeding the highest temperature of the lift installer, they may terminate the movements in progress but not perform any new operations ; control orders.

4.7. The lift chairs must be designed and constructed so as to provide adequate ventilation to passengers, even in the case of long-term standings.

4.8. The lift must be provided with sufficient illumination when used, or when a door is opened ; it must also be equipped with emergency lighting.

4.9. The means of communication referred to in point 4.5 and the emergency lighting referred to in point 4.8 must be designed and constructed in such a way as to operate at a power outage. They must be able to function during the period that normally takes before help reaches its way.

4.10. The operating system in elevators which can be used in the event of fire must be so designed and constructed that it can be fought from certain floors and provide the right of the rescue card to the service.

5. TAGGING

5.1. In addition to the minimum declarations made by any machine in accordance with section 1.7.3 of Annex I to Directive 89 /392/EEC, the lift must be provided with a clear sign on which the label of the label in kilograms and the maximum number of passengers is clearly marked ; specified.

5.2. If the apparatus is designed so that persons who are stuck in the lift chair can enter without outside help, the lift must be clearly and visibly specified in the lift and visible.

6. USAGE VIEW

6.1. The safety components referred to in Annex IV must be accompanied by an instruction manual in an official language of the installer of the lift, or a different Community language approved by this person, so that :

-WHAT? mounting

-WHAT? connection

-WHAT? adjustment

-WHAT? maintenance

can be done in an efficient and dangerous manner.

6.2. Each lift shall be provided with documentation drawn up in one or more Community languages which may be established in accordance with the Treaty of the Member State in which the lift is installed. This dossier shall include at least :

-WHAT? an instruction manual with the plans and diagrams necessary for normal use as well as for maintenance, inspection, repair, periodic verification and the rescue efforts referred to in Section 4.4 ;

-WHAT? a service book, in which repairs and, where appropriate, periodic verifications may be indicated.

ANNEX II

A. Contents of the EC declaration of conformity for safety components 14)

The EC declaration of conformity must include the following information :

-WHAT? name and address of the manufacturer of safety components, 15)

-WHAT? the name and address of his authorised representative established within the Community ; 15)

-WHAT? description of the safety component, type and serial number and, where appropriate, serial number,

-WHAT? the safety feature of the safety component, if this is not clear from the description,

-WHAT? the manufacturing year of the safety component ;

-WHAT? all relevant provisions satisfying the safety component,

-WHAT? any reference to the harmonized standards used,

-WHAT? where appropriate, the name, address and identification number of the notified body which has carried out the EC type-examination in accordance with Article 8 (2) ; paragraph 1 (a) (a), i) and (ii),

-WHAT? where appropriate, a reference to the EC type-examination certificate issued by the notified body,

-WHAT? where appropriate, the name, address and identification number of the notified body which carried out the production control in accordance with Article 8 (3) ; paragraph 1 (a) (a), (ii)

-WHAT? where appropriate, the name, address and identification number of the notified body which has checked the quality assurance system used by the manufacturer in accordance with Article 8 (2) ; paragraph 1 (a) (a), (iii)

-WHAT? identification of the signatory authorised to oblige the manufacturer of safety components, or his authorised representative established within the Community.

B. Contents of the EC declaration of conformity for installed lifts 16)

The EC declaration of conformity must include the following information :

-WHAT? name and address of the installer installer, 17)

-WHAT? description of the lift, the type and serial number, serial number and address of the place where the lift is installed ;

-WHAT? the installer of the lift,

-WHAT? all relevant provisions which the lift satisfies ;

-WHAT? any reference to the harmonized standards used,

-WHAT? where appropriate, the name, address and identification number of the notified body which has carried out the EC type-examination of the lift model in accordance with Article 8 (1). 2, no. i) and (ii),

-WHAT? any reference to the EC type-examination certificate,

-WHAT? where appropriate, the name, address and identification number of the notified body which has carried out the EC verification of the lift in accordance with Article 8 (3) ; 2, no. (iv)

-WHAT? where appropriate, the name, address and identification number of the notified body which has carried out the final checks on the lift in accordance with Article 8 (1). 2, no. i), (ii), (iii), first indent,

-WHAT? where appropriate, the name, address and identification number of the notified body responsible for checking the quality system, the installer of the lift, has been applied in accordance with Article 8 (1). 2, second and third indenus in paragraph 1. (i), (ii) and (iii) and Article 8 (1). 2, no. (v)

-WHAT? identification of the signatory to which the lift installer is required.

ANNEX III

CE-CONFORMITY MARKING

The CE conformity marking shall consist of the initials ' CE ` in accordance with the following model :

If the CE marking is reduced or enlarged, the size of the model as indicated above must be complied with.

The various components of the CE marking must, as far as possible, be of the same height, and this must be at least 5 mm above. This minimum size may be exempted from small safety components.

The CE marking shall be followed by the identification number of the notified body in connection with :

-WHAT? the procedures referred to in Article 8 (1) paragraph 1 (a) (a), (ii) or (iii)

-WHAT? the procedures referred to in Article 8 (1) 2.

ANNEX IV

LIST OF SAFETY COMPONENTS REFERRED TO IN ARTICLE 1 (1) AND ARTICLE 8 (1)

1. Facilitation of Floor-Exit devices.

2. Facility (see, cf. section 3.2 of Annex I) for the hurdle of the free fall of the lift or uncontrolled upward movements.

3. Speed limiters.

5. Safety devices on hydraulic cylinders in hydraulic systems when used as devices for preventing fall.

6. Electrical safety devices in the form of safety-breakers in the form of electronic components.

ANNEX V

EF TYPE-EXAMINATION

(module B)

A. EC type-examination of safety components

1. EC type-examination is the procedure whereby a notified body ascertains and certifies that a representative copy of a safety component will give the lift on which it is properly installed, the possibility of complying with the relevant provisions ; in this Directive.

2. The request for EC type-examination shall be lodged by the manufacturer or his authorized representative established within the Community to a notified body of his choice.

The request shall contain :

-WHAT? the name and address of the manufacturer of the safety component and the name and address of the manufacturer ' s representative, where the device is lodged by it and the location of the safety components ;

-WHAT? a written declaration that the same request has not been lodged with other notified bodies ;

-WHAT? technical documentation,

-WHAT? a representative sample of the safety component or an indication of the place where it can be investigated. The notified body may, with justification, request other copies.

The technical documentation must enable the conformity of the safety component and its ability to give the lift on which it is properly installed, the possibility of complying with the provisions of the directive.

The technical documentation must, to the extent necessary for the assessment of the conformity, contain the following information :

-WHAT? a general description of the safety component, including the scope (in particular any restrictions on speed, load, energy), and conditions (in particular explosive atmospherance, adverse weather conditions),

-WHAT? design drawings or diagrams and manufacturing drawings or diagrams ;

-WHAT? relevant essential requirements and the ways in which these requirements have been met (e.g. harmonised standards),

-WHAT? where appropriate, the results of the tests or calculations carried out by the manufacturer or by the manufacturer ;

-WHAT? a copy of the installation instructions for the safety components,

-WHAT? the measures which will be taken at the manufacturing stage to ensure that the series of safety components is in accordance with the safety component tested.

4. The notified body :

-WHAT? examine the technical documentation, in order to assess whether it is capable of meeting the objectives pursued ;

-WHAT? examine the safety component to check whether it corresponds to the technical documentation ;

-WHAT? carry out or carry out the appropriate checks and tests to verify whether the solutions of the safety component manufacturer are in accordance with the requirements of the Directive and make it possible for the safety component to be able to comply with the requirements of the Directive ; its function when it is fitted correctly on an elevator.

If the representative copy of the safety component of the directive is to be representative, the notified body must issue a EC type-examination certificate to the applicant. The certificate must include the name and address of the manufacturer of the safety component, the results of the checks, the conditions of validity of the certificate and the necessary data for identification of the approved type.

The Commission, the Member States and the other notified bodies may have a copy of the certificate and, on a reasoned request, a copy of the technical documentation and the reports for the studies carried out, calculations or tests. If the notified body must issue a EC type-examination certificate to the manufacturer, it shall provide a detailed account of the reasons for this. A procedure shall be established.

6. The manufacturer of the safety component or its authorised representative established within the Community must notify the notified body of all, including minor, changes which he has made or intends to make of the approved security component, including new ; editions which are not specified in the initial technical documentation (cf. point 3, first indent). The notified body must examine these modifications and inform the manufacturer or his representative whether the EC type-examination certificate is still valid. 18)

7. Each notified body must communicate to the Member States the relevant information concerning :

-WHAT? EC type-examination certificates issued by the EC type-examination,

-WHAT? the withdrawn EC type-examination certificates.

In addition, all notified bodies must communicate to the other notified bodies the relevant information relating to the EC type-examination certificates of the EC type-examination.

8. The EC type-examination certificate, case files and correspondence relating to EC type-examination procedures shall be drawn up in an official language of the Member State in which the notified body is established or in a language approved by that body.

9. The manufacturer of the safety component or its authorised representative established within the Community must also keep, in addition to the technical documentation, a copy of the EC type-examination certificates and any addendum to these for a period of 10 years from the safety component Date of manufacture.

Where neither the manufacturer of a safety component nor his representative is established in the Community, the obligation to present the technical documentation shall be the responsibility of the person responsible for the placing on the market of the safety component in the Community.

B. EC type-examination of the lift

1. EC type-examination is the procedure whereby a notified body ascertains and certifies that an elevator model or an elevator, for which no other versions are foreseen, comply with the provisions of this Directive.

2. The request for EC type-examination of the lift shall be submitted by the installer of the lift to a notified body of his choice.

The request must contain

-WHAT? the name and address of the lift installer,

-WHAT? a written declaration that the same request has not been lodged with other notified bodies ;

-WHAT? technical documentation,

-WHAT? Indication of the place where the lift model can be examined. This shall include the connectivity and the equipment for at least three levels (the upper, the bottom and the intermediate).

The technical documentation must enable the assessment of the lift to be assessed in accordance with the provisions of the Directive and to understand its design and its function.

The technical documentation must, to the extent necessary for the assessment of the conformity, contain the following information :

-WHAT? a general description of the lift model. The technical documentation must clearly specify all of the change options that are in connection with the model of the lift submitted for testing (see. Article 1 (1). 4)

-WHAT? design drawings or diagrams and manufacturing drawings or diagrams ;

-WHAT? relevant essential requirements and the ways in which these requirements have been met (e.g. harmonised standards),

-WHAT? a copy of the EC declaration of conformity for the safety components used in the manufacture of the lift ;

-WHAT? where appropriate, the results of the tests or calculations carried out by the manufacturer or by the manufacturer ;

-WHAT? a copy of the lift instruction for the lift,

-WHAT? the measures which will be taken at the installation to ensure that the serial-producing lift is in accordance with the provisions of the Directive.

4. The notified body :

-WHAT? examine the technical documentation, in order to assess whether it is capable of meeting the objectives pursued ;

-WHAT? examine the model of the lift in order to check whether it corresponds to the technical documentation,

-WHAT? carry out or carry out the appropriate checks and tests to verify whether the installer of the installer is in accordance with the requirements of the Directive and allows the lift to be able to meet them.

5. The elevator model of the Directive is to be filled with the relevant provisions of the Directive, issuing the notified body a EC type-examination certificate to the applicant. The certificate must include the name and address of the lift installer, the results of the checks, the conditions of validity of the certificate and the necessary data for identification of the approved type.

The Commission, the Member States and the other notified bodies may have a copy of the certificate and, on a reasoned request, a copy of the technical documentation and the reports for the studies carried out, calculations or tests.

If the notified body must issue a EC type-examination certificate to the manufacturer, it shall provide a detailed account of the reasons for this. A procedure shall be established.

6. The installer of the installer shall inform the notified body of all, even less, amendments that he has made or intend to make of the approved lift, including new editions which are not specified in the initial technical documentation (see. point 3, first indent). The notified body must examine these modifications and notify the installer whether the EC type-examination certificate is still valid ; (19) .

7. Each notified body must communicate to the Member States the relevant information concerning :

-WHAT? EC type-examination certificates issued by the EC type-examination,

-WHAT? the withdrawn EC type-examination certificates.

In addition, all notified bodies must communicate to the other notified bodies the relevant information relating to the EC type-examination certificates of the EC type-examination.

8. The EC type-examination certificate, dossiers and correspondence relating to EC type-examination procedures shall be drawn up in an official language of the Member State in which the notified body is established or in a language approved by that body.

9. The installer of the installer must also keep, in addition to the technical documentation, a copy of the EC type-examination certificates and any addendum to these for a period of 10 years from the date of manufacture of the lift conforming to it ; the lift model.

ANNEX WE

FINAL CHECKS

1. The final inspection is the procedure whereby the installer of the lift, satisfying the conditions laid down in point 2, ensures and declares that the lift that is placed on the market meets the requirements of the Directive ; the installer of the lift must affix the CE marking to each of them ; the lift chair and draw up a declaration of conformity of the EC.

2. The installer of the installer shall take all necessary measures to ensure that the lift placed on the market is in accordance with the model of the lift described in the EC type-examination certificate and with the essential health and safety requirements, which : apply to it.

3. The installer of the installer shall keep a copy of the EC declaration of conformity and of the final inspection certificate referred to in paragraph 6 for 10 years from the date on which the lift was first placed on the market.

4. A notified body, selected by the installer of the lift, carries out or shall allow the final check of the lift to be placed on the market. Check and appropriate tests, as referred to in the relevant standards referred to in it or in accordance with, shall be carried out. the provisions of Article 5 of the Directive or equivalent tests to check whether the lift meets the relevant requirements of the Directive.

These checks and tests shall include, inter alia :

The marker layer shall be the load listed in Annex I (5).

Following these tests, the notified body must ensure that no deformation or deterioration has not been carried out, which would prevent the use of the lift.

5. The notified body must receive a technical documentation consisting of :

-WHAT? a general plan above the lift,

-WHAT? the necessary plans and diagrams to ensure that the final checks may be carried out, e.g. control circuits over the control circuits ;

-WHAT? a copy of the instructions for use referred to in Annex I, Section 6.2.

The notified body may not require detailed plans or precise information which is not necessary to verify that the lift to be placed on the market is in accordance with the model of the lift, as described in : EC type-examination declaration.

6. Recover the provisions of the lift directive, the notified body shall affix its identification number or place it next to the CE marking, cf. Annex III and draw up a final inspection certificate in which the checks carried out and the tests carried out.

The notified body must fill in the appropriate pages of the service book referred to in Annex I, Section 6.2.

If the notified body must issue the final certificate of inspection, it shall provide a detailed justification for this dissenting and the manner in which approval can be achieved. When the installer of the lift is rerequesting final inspection, he must turn to the same notified body.

7. The final inspection certificate, files and correspondence relating to the authorisation procedures shall be made out in an official language of the Member State in which the competent body is established or in a language approved by it.

ANNEX VII

MINIMUM CRITERIA TO BE OBSERVED BY THE MEMBER STATES BY THE AUTHORISATION OF BODIES

1. The body, its leader and its staff, who shall carry out the inspection work, must not be constructor, supplier or manufacturer of the safety components or installer of the lifts which they control, or be any of those persons ; representative. In the same way, the body, its leader and its staff must carry out checks on the quality assurance systems referred to in Article 8 of the Directive neither be a constructor, supplier nor manufacturer of the safety components or installer of the installation ; the lifts which they control, or be any of the representative of these parties. They shall not, either directly or as a representative, participate in the design, manufacture, marketing or maintenance of these safety components or in the installation of these lifts. This does not preclude the possibility of exchanges of technical information between the manufacturer of the safety components or the installer of the lift and the body.

2. The inspection body and personnel must carry out the control of the highest technical integrity and technical competence and be independent of any pressure and incentive, in particular of financial nature, which may affect their assessment or the results of : their checks, in particular by persons or groups of persons who are interested in the results of the checks.

3. The body must have the necessary staff and possess the necessary resources to carry out the technical and administrative tasks in carrying out the checks ; it must also have access to the equipment that : are necessary to carry out specific verifications.

4. The staff to carry out the checks shall have :

-WHAT? a sound technical and vocational training ;

-WHAT? sufficient knowledge of the requirements concerning the control it carries out and adequate practical experience of such controls ;

-WHAT? the ability to draw up attestations, records and reports, which render the results of the checks carried out.

The staff who are to carry out checks must be guaranteed full independence. The remuneration of each employee must not be dependent on the number of control operations carried out by the person concerned, or the results of the check.

6. The body shall draw up liability insurance unless the liability of civil liability is covered by the State on the basis of national law, or unless the checks are carried out directly by the Member State.

7. The staff of the Body shall be subject to professional secrecy in the course of the execution of the work (except with the competent administrative authorities of the State in which it performs its work) under the Directive or any national ; the rule of law issued in accordance with this.

ANNEX VIII

QUALITY ASSURANCE OF PRODUCTS

(module E)

1. Quality assurance of the products is the procedure whereby a manufacturer of safety components satisfying the provisions of point 2 ensures and declares that the safety components are in accordance with the type as described in : The EC type-examination certificate and fulfils the relevant requirements of the Directive and that the safety component will give the lift on which it is properly installed, the possibility of complying with the provisions of the directive.

The manufacturer of the safety component or its authorised representative established within the Community shall affix the CE marking to each safety component and draw up a EC declaration of conformity. The CE marking must be accompanied by the identification number used by the notified body responsible for the checks referred to in paragraph 4.

2. The manufacturer must operate an approved quality system for final checks on the safety component and testing as described in point 3 and shall be subject to the checks referred to in Section 4.

3. Quality management system

3.1. The manufacturer of the safety component shall submit an application for assessment of the quality assurance system for the relevant safety components to a notified body of his choice.

The application shall include :

-WHAT? all relevant information on the safety components envisaged,

-WHAT? the documentation concerning the quality system,

-WHAT? the technical documentation relating to the approved safety components and a copy of the EC type-examination certificate.

3.2. The quality assurance system shall examine each component safety component and the tests referred to in the relevant standards shall be carried out in accordance with the quality system. Article 5 or equivalent tests to ensure that the product meets the relevant requirements of the Directive.

All the conditions, requirements and provisions laid down by the manufacturer of safety components shall be documented in a systematic and orderless manner in a written review of the measures, procedures and instructions. This quality assurance system documentation must ensure that quality programmes, plans, manuals and records are interpreted in a similar way.

In particular, the statement shall contain an adequate description of :

a) quality objectives,

b) the organizational structure and responsibilities and powers of the management with regard to the quality of the safety components ;

c) the examinations and tests that will be carried out after manufacture ;

d) the means of verification of the effective operation of the quality system,

(e) the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

3.3. The notified body must assess the quality assurance system to determine whether it satisfies the requirements of point 3.2. The organism must assume that these requirements are met if the quality assurance systems are applying the relevant harmonized standard ; 20) .

The assessment team shall include at least one member with experience of assessing the level of the lift in question. The assessment procedure shall include a visit to the premises of the safety component manufacturer.

The decision must be notified to the manufacturer of the safety components. The communication shall contain the results of the checks and the reasoned assessment decision.

3.4. The manufacturer of the safety component undertakes to fulfil its obligations under the quality assurance system as approved and to ensure that it remains appropriate and effective.

The manufacturer of the safety components or its authorised representative established within the Community must inform the notified body which has approved the quality assurance system informed of any intended change.

The notified body must assess the proposed changes and decide whether the modified quality system still complies with the requirements referred to in 3.2 or whether a re-evaluation is necessary.

It shall notify its decision to the manufacturer. The communication shall contain the results of the checks and the reasoned assessment decision.

4. Monitoring under the responsibility of the notified body

4.1. The purpose of the verification is to ensure that the manufacturer of the safety component duly fulfils its obligations under the approved quality assurance system.

4.2. The manufacturer must allow the notified body access to verify the inspection, testing and storage facilities and provide it with all necessary information, including :

-WHAT? the documentation concerning quality assurance systems,

-WHAT? technical documentation,

-WHAT? the quality records, such as inspection reports, test and calibration data, reports on the qualifications of the personnel concerned, etc.

4.3. The notified body must carry out periodic inspection visits to ensure that the manufacturer of the safety components maintains and applies the quality assurance system and must provide a control report to the manufacturer of safety components.

4.4. In addition, the notified body may pay unreported visits to the manufacturer of safety components.

During such visits, the notified body may, if necessary, carry out tests to verify the functioning of the quality assurance system ; it shall issue a visit report and, where appropriate, a test report to the manufacturer, of safety components.

5. The manufacturer must, for a period of 10 years, from the date of manufacture of the safety component, be able to submit to the national authorities :

-WHAT? the documentation referred to in the third indent of the second subparagraph of 3.1,

-WHAT? the updating referred to in the second paragraph of point 3.4,

-WHAT? the decisions and reports from the notified body referred to in points 3.4, last paragraph, and points 4.3 and 4.4.

6. Each notified body must communicate to the other notified bodies the relevant information concerning the quality assurance system approvals issued or withdrawn.

APPENDIX IX

FULL QUALITY ASSURANCE

(module H)

1. Full quality assurance is the procedure whereby a manufacturer of safety components satisfying the provisions of point 2 ensures and declares that safety components comply with the relevant requirements of the Directive and that the safety component will be give the lift on which it is properly installed, the possibility of complying with the provisions of the Directive.

The manufacturer or his authorized representative established within the Community must affix the CE marking to each of the security component and draw up a declaration of EC declaration of conformity. The CE marking must be accompanied by the identification number used by the notified body responsible for the checks referred to in paragraph 4.

2. The manufacturer must operate an approved quality assurance system for design, production, final checking of the safety components and testing as described in point 3, and shall be subject to the checks referred to in Section 4.

3. Quality management system

3.1. The manufacturer must submit an application for assessment of the quality assurance system to a notified body of his choice.

The application shall include :

-WHAT? all relevant information on the safety components,

-WHAT? the documentation concerning the quality assurance system.

3.2. The quality assurance system must ensure that safety components comply with the relevant requirements of the Directive and give the lifts to which they are properly installed, the possibility of complying with those provisions.

All the conditions, requirements and provisions for which the manufacturer has taken into account shall be documented in a systematic and manageable manner in a written review of precautions, procedures and instructions. This quality assurance system documentation must ensure that quality policy and procedures such as quality programmes, plans, manuals and records are interpreted in the same way.

In particular, the statement shall contain an adequate description of :

-WHAT? the quality objectives and the organizational structure, responsibilities and powers of the management with regard to the quality of design and safety components ;

-WHAT? the technical design specifications, including standards that will be used and, where the standards referred to in Article 5 are not fully applied, how to ensure that the essential requirements of the directive which apply to safety components, will be met

-WHAT? the design control and verification techniques and processes and systematic actions that will be used in the design of the safety components ;

-WHAT? the relevant production, quality control and quality assurance techniques, and the systematic practices and measures which will be used ;

-WHAT? the examinations and tests to be carried out before, during and after production, and the frequency with which it is carried out ;

-WHAT? the quality records, such as inspection reports and test data, calibration data, qualification reports and so on.

-WHAT? the means of verification of the achievement of the required design and product quality and the effective operation of the quality assurance system.

3.3. The notified body must assess the quality assurance system to determine whether it satisfies the requirements of point 3.2. The organism must assume that these requirements are met if the quality assurance systems are applying the relevant harmonized standard ; 21) .

The assessment team shall include at least one member with experience of assessing the level of the lift in question. The assessment procedure shall include a visit to the manufacturer ' s premises.

The decision must be notified to the manufacturer of safety components. The communication shall contain the results of the checks and the reasoned assessment decision.

3.4. The manufacturer of safety components undertakes to fulfil its obligations under the quality assurance system as approved and to ensure that it remains appropriate and effective.

The manufacturer or his authorised representative established within the Community must inform the notified body which has approved the quality assurance system informed of any intended change.

The notified body must assess the proposed changes and decide whether the modified quality system still complies with the requirements referred to in 3.2 or whether a re-evaluation is necessary.

It shall notify its decision to the manufacturer. The communication shall contain the results of the checks and the reasoned assessment decision.

4. Monitoring under the responsibility of the notified body

4.1. The purpose of the verification is to ensure that the manufacturer of safety components correctly fulfils its obligations under the approved quality assurance system.

4.2. The manufacturer of the safety components must allow the notified body access to control of the design, production, control and testing and storage facilities and must provide it with all necessary information, including :

-WHAT? the documentation concerning the quality system,

-WHAT? the quality records as provided for in the design part of the quality system, such as results of analyses, calculations, tests, etc. ;

-WHAT? the quality records in accordance with the production part of the quality system, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

4.3. The notified body shall make periodic inspection visits to ensure that the manufacturer of the safety components maintains and applies the quality assurance system and must provide a control report to the manufacturer.

4.4. In addition, the notified body may pay unannounced visits to the manufacturer of safety components. During such visits, the notified body may, if necessary, carry out or perform tests to check whether the quality system functions satisfactorily. It shall issue a visit report and, where appropriate, a test report to the manufacturer of safety components.

5. The manufacturer of the safety components or its authorized representative must, for a period of 10 years, from the last manufacturing date of the safety component, submit to the national authorities :

-WHAT? the documentation referred to in the second indent of the second subparagraph of 3.1,

-WHAT? the updating referred to in the second paragraph of point 3.4,

-WHAT? the decisions and reports from the notified body referred to in points 3.4, last paragraph, and points 4.3 and 4.4.

Where neither the manufacturer of safety components nor his authorised representative is established in the Community, the obligation to present the technical documentation shall be the responsibility of the person responsible for placing the safety components in the Community.

6. Each notified body must communicate to the other notified bodies the relevant information concerning the quality assurance system approvals issued or withdrawn.

7. Case files and correspondence relating to the procedures for full quality assurance shall be made out in an official language of the Member State in which the notified body is established or in a language approved by it.

APPENDIX X

DEVICE VERIFICATION

(module G)

1. The unit verification is the procedure whereby an installer of the lift ensures and declares that the lift which is placed on the market and for which the certificate of conformity has been issued is in accordance with the requirements of the Directive. The installer of the lift shall affix the CE marking to the lift chair and draw up a declaration of EC declaration of conformity.

2. The installer of the installer shall submit a request for the unit verification to be notified to a notified body of his choice.

The request shall contain :

-WHAT? the name and address of the lift installer, and the place where the lift is installed ;

-WHAT? a written declaration that the same request has not been lodged with other notified bodies ;

-WHAT? technical documentation.

3. The technical documentation must permit the assessment of the conformity of the lift with the requirements of the Directive and to understand the design, installation and operation of the lift.

To the extent necessary for the assessment of conformity, the technical documentation must contain the following elements :

-WHAT? a general description of the lift,

-WHAT? design drawings or diagrams and manufacturing drawings or diagrams ;

-WHAT? relevant essential requirements and the ways in which these requirements have been met (e.g. harmonised standards),

-WHAT? where appropriate, the results of the tests or calculations carried out by the installer or of the installer ;

-WHAT? a copy of the instructions for the lift,

-WHAT? a copy of the EC type-examination certificates for the safety components used.

4. The notified body must examine the technical documentation and the lift and carry out the tests as provided for in the relevant standard (s), cf. Article 5 of the Directive or equivalent tests to verify that the lift is in accordance with the relevant requirements of this Directive.

If the lift is to be provided to the lift, the notified body shall affix its identification number or place it on the side of the CE marking, cf. Annex III, and draw up a certificate of conformity relating to the tests carried out.

The notified body must fill in the appropriate pages of the service book referred to in Annex I, Section 6.2.

If the notified body must issue the certificate of conformity, it shall provide a detailed justification for this disceration and shall provide the means by which approval is to be achieved. When the installer of the lift reasks for verification, he must turn to the same notified body.

5. The certificate of conformity, dossiers and correspondence relating to the unit verification procedures shall be drawn up in an official language of the Member State in which the notified body is established or in a language approved by this.

6. The installer of the installer must keep together with the technical documentation a copy of the certificate of conformity for a period of 10 years from the date on which the lift was placed on the market for the first time.

APPENDIX XI

CONFORMITY WITH SPOT CHECKS

(module C)

1. The conformity procedure is the procedure whereby the manufacturer of the safety components or his authorised representative established within the Community ensures and declares that the safety components are in conformity with the type as described in the EC type-examination certificate ; comply with the relevant requirements of the Directive and that the safety components will give the lift on which they are properly installed, to comply with the essential health and safety requirements of the directive.

The manufacturer of the safety components or its authorised representative established within the Community shall affix the CE marking to each of the security component and draw up a declaration of EC declaration of conformity.

2. The manufacturer of the safety components shall take all necessary measures to ensure that the manufacturing process ensures that the safety components provided are in accordance with the type as described in the EC type-examination certificate and with the relevant ; requirements of the Directive.

3. The manufacturer of the safety components or its representative must keep a copy of the EC declaration of conformity for a period of 10 years from the date of manufacture of the safety component.

Where neither the manufacturer of the safety components or his authorised representative is established in the Community, the obligation to present the technical documentation shall be the responsibility of the person responsible for the placing on the market of the safety components in the Community.

4. A notified body of the choice of the safety component manufacturer shall, or may, carry out checks on the safety components with rotating spaces. The notified body shall, on the spot, replace an appropriate sample for checking the completed safety components and carry out tests as referred to in the appropriate standards referred to in, cf. Whereas Article 5 of the Directive or equivalent tests to verify that production meets the requirements of the Directive comply with the requirements of the Directive, which does not meet the requirements of one or more safety components, the notified body shall take the necessary measures.

The elements to be taken into consideration for the supervision of the safety components shall be determined by common agreement between all the notified bodies responsible for carrying out this procedure, taking into account the essential elements of safety components ; Characteristics referred to in Annex IV.

During the manufacturing process, the manufacturer must, under the responsibility of the notified body, be responsible for the identification number of the safety component.

5. Case files and correspondence relating to the procedures for random checks referred to in point 4 shall be drawn up in an official language of the Member State in which the notified body is established or in a language approved by it.

ANNEX XII

QUALITY ASSURANCE OF THE LIFT PRODUCTS

(module E)

1. Quality assurance of the products is the procedure whereby the installer of the lift satisfies the provisions of point 2, ensures and declares that the elevators installed are in accordance with the type as described in the EC type-examination certificate and meets the relevant requirements of the Directive.

The installer of the lift shall affix the CE marking to each lift and draw up a declaration of EC declaration of conformity. The CE marking must be accompanied by the identification number used by the notified body responsible for the checks referred to in paragraph 4.

2. The installer of the lift shall use an approved quality assurance system for the final checks of the lift and testing as described in point 3 and shall be subject to the checks referred to in Section 4.

3. Quality management system

3.1. The installer of an installer shall submit an application for assessment of the quality assurance system for the lifts for a notified body of his choice.

The application shall include :

-WHAT? all relevant information on the elevators envisaged,

-WHAT? the documentation concerning the quality system,

-WHAT? the technical documentation relating to the approved lift operators and a copy of the EC type-examination certificate.

3.2. Under the quality system, each lift shall be examined and the tests referred to in the relevant standards shall be carried out in accordance with the quality system. Article 5 or equivalent tests to ensure that the product meets the relevant requirements of the Directive.

All the conditions, requirements and provisions to which the installer of the lift has been taken into account shall be documented in a systematic and manageable manner in a written review of measures, procedures and instructions. This quality assurance system documentation must ensure that quality programmes, plans, manuals and records are interpreted in a similar way.

In particular, the statement shall contain an adequate description of :

a) quality objectives,

b) the organizational structure and responsibilities and powers of the management with regard to the quality of the lifts ;

c) the examinations and tests that will be carried out prior to the placing on the market, including at least the tests referred to in Annex VI (4) (b) ;

d) the means of verification of the effective operation of the quality system,

(e) the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

3.3. The notified body must assess the quality assurance system to determine whether it satisfies the requirements of point 3.2. The organism must assume that these requirements are met if the quality assurance systems are applying the relevant harmonized standard ; (22)

The assessment team shall include at least one member with experience of assessing the level of the lift in question. The assessment procedure must include a visit to the installer of the lift installer and a visit to a construction site.

The decision must be notified to the lift installer. The notification shall contain the results of the examination and the reasoned assessment decision.

3.4. The installer of the lift shall undertake to fulfil its obligations under the quality assurance system as approved and to ensure that it remains appropriate and effective.

The installer of the installer shall inform the notified body which has approved the quality assurance system informed of any intended change.

The notified body must assess the proposed changes and decide whether the modified quality system still complies with the requirements referred to in 3.2 or whether a re-evaluation is necessary.

It shall inform the installer of the installer of his decision. The communication shall contain the results of the checks and the reasoned assessment decision.

4. Monitoring under the responsibility of the notified body

4.1. The purpose of the verification is to ensure that the installer of the lift is properly fulfilled in accordance with the approved quality assurance system.

4.2. The installer of the installer must allow the notified body access to check the inspection and testing facilities and provide it with all necessary information, including :

-WHAT? the documentation concerning the quality system,

-WHAT? technical documentation,

-WHAT? the quality records, such as inspection reports, test and calibration data, reports on the qualifications of the personnel concerned, etc.

4.3. The notified body must carry out periodic inspections to ensure that the installer of the installer maintains and applies the quality assurance system and must submit a control report to the installer of the lift.

4.4. In addition, the notified body may pay unannounced visits to sites where lift lifts are installed.

During such visits, the notified body may, if necessary, carry out or perform tests to check whether the quality system and the lift are working satisfactorily ; it shall issue a visit report and, where appropriate, a test report ; for the installer installer.

5. The installer of the installer must, for a period of 10 years from the date of the lift, be able to submit to the national authorities :

-WHAT? the documentation referred to in the third indent of the second subparagraph of 3.1,

-WHAT? the updating referred to in the second paragraph of point 3.4,

-WHAT? the decisions and reports from the notified body referred to in points 3.4, last paragraph, and points 4.3 and 4.4.

6. Each notified body must communicate to the other notified bodies the relevant information concerning the quality assurance system approvals issued or withdrawn.

ANNEX XIII

FULL QUALITY ASSURANCE OF ELEVATORS

(module H)

1. Full quality assurance is the procedure whereby the installer of the lift who satisfies the provisions of paragraph 2 ensures and declares that the lifts satisfy the relevant requirements of the Directive.

The installer of the lift shall affix the CE marking to each lift and draw up a declaration of EC declaration of conformity. The CE marking must be accompanied by the identification number used by the notified body responsible for the checks referred to in paragraph 4.

2. The installer of the lift must operate an approved quality assurance system for the design, manufacture, assembly, installation and final verification of the lifts and tests as described in point 3 and shall be subject to the checks referred to in Section 4.

3. Quality management system

3.1. The installer of an installer shall submit an application for assessment of the quality assurance system to a notified body of his choice.

The application shall include :

-WHAT? all relevant information concerning the lifts, in particular those making it possible to understand the consistency between the design and functioning of the lift, and to assess conformity with the requirements of the Directive ;

-WHAT? the documentation concerning the quality assurance system.

3.2. The quality assurance system must ensure that the lifts comply with the requirements of the Directive which apply to it.

All the conditions, requirements and provisions to which the installer of the lift has been taken into account shall be documented in a systematic and manageable manner in a written review of measures, procedures and instructions. The quality system documentation must ensure that the procedures, such as quality programmes, plans, manuals and registers, are interpreted in the same way.

In particular, the statement shall contain an adequate description of :

-WHAT? the quality objectives and the organizational structure, responsibilities and powers of the management with regard to the quality of design and the quality of the lifts ;

-WHAT? the technical design specifications, including standards that will be used, and, if the standards referred to in Article 5 of this Directive are not fully applied, how to ensure that the essential requirements of the Directive which apply to the lifts, will be met

-WHAT? the design control and verification techniques and processes and systematic actions that will be used in the commissioning of the lift design ;

-WHAT? the examinations and the tests to be carried out on the receipt of the supplies of materials, components and sub-assemmonds ;

-WHAT? the appropriate assembly, installation and quality control techniques, and the systematic practices and measures which will be used ;

-WHAT? the examinations and tests to be carried out before (check on installation conditions : shaft, placement of the lift system, etc.), during and after installation (including at least the tests referred to in Annex VI (4) (b)) ;

-WHAT? the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

-WHAT? the means of verification of the achievement of the required design and installation quality and the effective operation of the quality assurance system.

3.3. Construction Control

If the design is not entirely consistent with the harmonized standards, the notified body must examine whether the design meets the provisions of the Directive and, if so, shall issue a EC design-examination certificate to : the installer of the lift, specifying the validity of the certificate and the data necessary to identify the approved design.

3.4. Control of the quality assurance system

The notified body must assess the quality assurance system to determine whether it satisfies the requirements of point 3.2. The organism must assume that these requirements are met if the quality assurance systems are applying the relevant harmonized standard ; 23)

The assessment team shall include at least one member with experience of assessing the level of the lift in question. The assessment procedure must include a visit to the installer of the lift installer and a visit to a construction site.

The decision must be notified to the lift installer. The notification shall contain the results of the examination and the reasoned assessment decision.

3.5. The installer of the lift shall undertake to fulfil its obligations under the quality assurance system as approved and to ensure that it remains appropriate and effective.

The installer of the installer shall inform the notified body which has approved the quality assurance system informed of any intended change.

The notified body must assess the proposed changes and decide whether the modified quality system still complies with the requirements referred to in 3.2 or whether a re-evaluation is necessary.

It shall inform the installer of the decision. The communication shall contain the results of the checks and the reasoned assessment decision.

4. Monitoring under the responsibility of the notified body

4.1. The purpose of the verification is to ensure that the installer of the lift is properly fulfilled in accordance with the approved quality assurance system.

4.2. The installer of the installer must allow the notified body access to verify the design, production, installation, inspection and testing, and storage facilities, and must provide it with all necessary information, including :

-WHAT? the documentation concerning the quality system,

-WHAT? the quality records in accordance with the design part of the quality system, such as results of analyses, calculations, tests, etc.

-WHAT? the quality records as provided for in the part of the quality system related to the receipt of supplies and installation, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

4.3. The notified body must carry out periodic inspections to ensure that the installer of the installer maintains and applies the quality assurance system and submit a control report to the installer of the lift.

4.4. In addition, the notified body may pay unannounced visits to the installer or in places where lift lifts are installed. During such visits, the notified body may, if necessary, carry out or perform tests to check whether the quality system functions satisfactorily.

It shall issue a visit report and, where appropriate, a test report to the installer of the lift.

5. The installer of the installer must for ten years from the date on which the lift was first placed on the market, could submit to the national authorities :

-WHAT? the documentation referred to in the second indent of the second subparagraph of 3.1,

-WHAT? the updating referred to in the second paragraph of the 3.5, second subparagraph,

-WHAT? the decisions and reports from the notified body referred to in 3.5, last paragraph and 4.3 and 4.4.

If the installer of the lift is not established in the Community, then it shall be the responsibility of the notified body.

6. Each notified body must communicate to the other notified bodies the relevant information concerning the quality assurance system approvals issued or withdrawn.

7. Case files and correspondence relating to the procedures for full quality assurance shall be made out in an official language of the Member State in which the notified body is established or in a language approved by it.

ANNEX XIV

QUALITY ASSURANCE OF PRODUCTION

(module D)

1. Production quality assurance is the procedure whereby the installer of the installer who satisfies the provisions of paragraph 2 ensures and declares that the elevators concerned meet the relevant requirements of the Directive. The installer of the lift shall affix the CE marking to each lift and draw up a written declaration of conformity. The CE marking must be accompanied by the identification number used by the notified body responsible for the checks referred to in paragraph 4.

2. The installer of the installer must use an approved quality assurance system for production, installation, final checking of the lifts and testing as described in point 3 and shall be subject to the checks referred to in Section 4.

3. Quality management system

3.1. The installer of an installer shall submit an application for assessment of the quality assurance system to a notified body of his choice.

The application shall include :

-WHAT? all relevant information concerning the lifts,

-WHAT? the documentation concerning the quality system,

-WHAT? where applicable, the technical documentation of the approved type and a copy of the EC type-examination certificate.

3.2. The quality assurance system must ensure that the lifts comply with the requirements of the Directive which apply to it.

All the conditions, requirements and provisions to which the installer of the lift has been taken into account shall be documented in a systematic and manageable manner in a written review of measures, procedures and instructions. This quality assurance system documentation must ensure that the quality programmes, plans, manuals and records are interpreted in a similar way.

In particular, the statement shall contain an adequate description of :

-WHAT? the quality objectives and the organizational structure, responsibilities and powers of the management with regard to the quality of the lifts ;

-WHAT? manufacturing processes, quality control and security techniques, and the systematic techniques and measures that will be used ;

-WHAT? the examinations and tests to be carried out before, during and after installation ; 24)

-WHAT? the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

-WHAT? the means of monitoring the achievement of the quality of the quality of the elevators and the effective operation of the quality system.

3.3. The notified body must assess the quality assurance system to determine whether it satisfies the requirements of point 3.2. The organism must assume that these requirements are met if the quality assurance systems use the harmonizing standard in the area ; 25)

The assessment team shall include at least one member with experience of assessing the level of the lift in question. The assessment procedure must include a visit to the installer of the lift installer.

The decision must be notified to the lift installer. The notification shall contain the results of the examination and the reasoned assessment decision.

3.4. The installer of the lift shall undertake to fulfil its obligations under the quality assurance system as approved and to ensure that it remains appropriate and effective.

The installer of the installer shall inform the notified body which has approved the quality assurance system informed of any intended change.

The notified body must assess the proposed changes and decide whether the modified quality system still complies with the requirements referred to in 3.2 or whether a re-evaluation is necessary.

It shall inform the installer of the decision. The communication shall contain the results of the checks and the reasoned assessment decision.

4. Monitoring under the responsibility of the notified body

4.1. The purpose of EC control is to ensure that the installer of the lift is properly fulfilled in accordance with the approved quality assurance system.

4.2. The installer of the installer must allow the notified body access to check the production, control, installation, testing and storage facilities, and provide it with all necessary information, including :

-WHAT? the documentation concerning the quality system,

-WHAT? the quality records, such as inspection reports, test and calibration data, reports on the qualifications of the personnel concerned, etc.

4.3. The notified body must carry out periodic inspections to ensure that the installer of the installer maintains and applies the quality assurance system ; it emits a control report to the installer of the lift.

4.4. In addition, the notified body may pay unannounced visits to the installer and to the installation site. During such visits, it may, if necessary, carry out or perform tests to check whether the quality assurance system functions satisfactorily. It shall issue a visit report and, where appropriate, a test report to the lift installer.

5. The installer of the installer must, for a period of 10 years from the date of the product ' s last manufacturing date, be able to submit to the national authorities

-WHAT? the documentation referred to in the second indent of the second subparagraph of 3.1,

-WHAT? the updating referred to in the second paragraph of point 3.4,

-WHAT? the decisions and reports from the notified body referred to in points 3.4, fourth subparagraph and 4.3 and 4.4.

6. Each notified body must communicate to the other notified bodies the relevant information concerning the quality assurance system approvals issued or withdrawn.

7. The dossiers and correspondence relating to the quality assurance procedures for production shall be made out in an official language of the Member State in which the notified body is established or in a language approved by it.

1) The commotion contains provisions implementing Directive 95 /16/EC of the European Parliament and of the Council of 29. In June 1995 on the approximation of the laws of the Member States relating to lifts, the EU ' s Official Journal, In 213, page 1, and parts of Directive 2006/42 of the European Parliament and of the Council of 17. May 2006 on machinery and amending Directive 95 /16/EC, EU-Official Journal 2006, nr. L157, page 24.

2) OJ No L C 62 of 11. 3. 1992, s. 4 and OJ No C C 180 of 2. 7. 1993, s. 11.

3) OJ No L C 287 of 4. 11. 1992, s. 2.

4) The European Parliament's opinion of 29 October 1992 (OJ No C C 305, 23.11.1992, p. 114), the Council common position of 16. June 1994 (OJ No No, C 232 of 20. 8. 1994, s. 1) and Decision of the European Parliament of 28. September 1994 (OJ No C, C 305 by 31. 10. 1994, s. 48).

5) OJ No L L 300 of 19. 11. 1984, s. 86. Directive as last amended by Directive 90 /486/EEC (OJ No N ° C), L 270 of 2. 10. 1990, s. 21).

6) OJ No L L 300 of 19. 11. 1984, s. 72. Directive as last amended by Directive 88 /665/EEC (OJ No 2, L 382 of 31. 12. 1988, s. FORTY-TWO.

7) OJ No L L 384 of 31. 12. 1986, s. 12.

8) OJ No L I was in 198 by 22. 7. 1991, s. 16.

9) No! L 134 of 20. 6. 1995, s. 37.

10) OJ No L I'm 220 of 30. 8. 1993, s. 23.

11) OJ No L I 109, 26. 4. 1983, s. 8. Directive as last amended by the European Parliament and Council Directive 94 /10/EC (OJ No C), L 100 of 19. 4. 1994, s. (30).

12) OJ No L L40 of 11. 2. 1989, s. 12.

13) Council Decision 1999 /468/EC of 28. The following June 1999 laying down the procedures for the exercise of implementing powers conferred on the Commission (OJ L 184, 17.7.1999, p. 23).

14) This declaration must be written on the machine or printed letters and be drawn up in the same language as the instructions provided for in Annex I, Section 6.1.

15) Company name and full address ; if it is a representative, the manufacturer must also specify the name and address of the safety components.

16) This declaration must be written on the machine or printed letters and be drawn up in the same language as the instructions provided for in Annex I, Section 6.2.

17) Company name and full address.

18) If the notified body considers it necessary, it may either issue a supplement to the original EC type-examination certificate or request that a new request be made.

(19) If the notified body considers it necessary, it may either issue a supplement to the original EC type-examination certificate or request that a new request be made.

20) This harmonised standard is EN 29003, where necessary, supplemented in order to take account of the specific characteristics of the safety components.

21) This harmonised standard is EN 29001, if necessary, in order to take account of the specific characteristics that apply to safety components.

(22) This harmonised standard is EN 29003, where necessary, supplemented in order to take account of the specific characteristics of the lifts.

23) This harmonised standard is EN 29001, if necessary, in order to take account of the specific characteristics that apply to the lifts.

24) These tests shall include at least the tests as referred to in Annex VI (4) (b).

25) This harmonising standard is EN 29002, if necessary, in order to take account of the specific characteristics that apply to the lifts.