Advanced Search

Lifts And Their Safety Components In The Design, Manufacture And Installation Of Lifts And Conformity Assessment Regulations

Original Language Title: Liftu un to drošības sastāvdaļu projektēšanas, ražošanas un liftu uzstādīšanas un atbilstības novērtēšanas noteikumi

Subscribe to a Global-Regulation Premium Membership Today!

Key Benefits:

Subscribe Now for only USD$40 per month.
Cabinet of Ministers Regulations No. 206 in 2016 (April 5. No 16 5) lifts and their safety components in the design, manufacture and installation of lifts and conformity assessment regulations Issued in accordance with the law "on conformity assessment" article 7 of the first and the second part 1. General questions 1. down the elevator and elevator safety components of essential requirements and their compliance monitoring mechanisms, as well as the order in which to market surveillance. 2. The terms used in the following terms: 2.1 elevator-lifting equipment, which the transporter moves along rigid guides angle relative to the horizontal is greater than 15 degrees, or lifting equipment, moving along a fixed course even where they do not move along rigid guides; 2.2. stall – part of the lift, which supports the people and (or) load to be raised or lowered; 2.3. the model lift-with objective technical parameter descriptors defined in the elevator, a representative whose technical dossier shows the way in which the lift conforms with the representative that elevator and with identical safety components of the lift meet the essential health and safety requirements; 2.4. market-economic activities to supply the lift safety components or not for its distribution or use within the Union; 2.5. the placing on the market-the first to offer lift safety components on the market of the European Union, but with respect to elevators, through economic activities in return for payment or not,-the use of the lift to supply the European market; 2.6. the installer: the natural or legal person responsible for the lift design, manufacture, installation and placing on the market; 2.7. manufacturer: the natural or legal person who manufactures or installs the lift safety components designed or manufactured and traded them with their name or trade mark; 2.8. the authorized representative: the natural or legal person established in the European Union and has received the installer or manufacturer's written authority to act on his behalf in relation to specified tasks; 2.9. importer: the natural or legal person carrying out economic activities in the European Union and the European Union are placed on the market of a third country elevator safety components; 2.10. Distributor: the natural or legal person in the supply chain, other than the manufacturer or importer and which offers lift safety components on the market; 2.11. the persons involved – Installer, manufacturer, the authorised representative, the importer and the Distributor; 2.12. technical specification-a document that lays down the technical requirements which correspond to the lift or safety component of the lift; 2.13. the notified body – the national accreditation bodies accredited elevator and elevator safety component conformity assessment body has been notified to the European Commission in accordance with the laws and regulations on the procedures for the notification of the Commission creates, as well as the order in which the Commission takes a decision and shall notify the European Commission of conformity assessment bodies performing conformity assessment of regulated sphere, or other Member States of the European Union or the European economic area and lift it notified the security component of the conformity assessment body; 2.14. revocation, any measure aimed at achieving a dismantling of the lift and safe disposal, but with regard to lift safety components recall is any measure, the aim of which is to get back on the elevator's security component that has already been available in the installer or end-user; 2.15. the withdrawal, any measure aimed at preventing that the safety component of the supply chain is offered to the market; 2.16. the CE conformity marking-marking, by which the manufacturer indicates that the lift complies with the applicable requirements of specific laws and regulations that provide for the labelling of products with this mark. 3. the rules apply to lifts permanently serving buildings and constructions intended to move: 3.1 people; 3.2. people and freight; 3.3. If the freight elevator only goods moving man may enter it without difficulty, and inside, or in another location, you can reach inside the elevator man, is the control device. 4. the rules apply to the following lift safety components: 4.1 landing door delay devices; 4.2. devices to prevent the fall of the cab or uncontrolled movement; 4.3. speed limiters; 4.4. energy-accumulating shock absorbers: shock for 4.4.1. with non-linear effect; 4.4.2. the reverse motion damping; 4.5. energy-dissipating shock absorbers for impact; 4.6. safety devices fitted to the hydraulic contour lift to prevent falls; 4.7. the safety switches with electronic components. 5. the provisions do not apply to: 5.1 lift installations with speed not exceeding 0.15 m/s; 5.2. construction site hoists; 5.3. cableways, including funicular railways; 5.4. lifts specially designed and constructed for military or the law "on police" prescribed authorities; 5.5. lifting appliances from which work can be performed; 5.6. the mines used lifting equipment; 5.7. lifting appliances intended for lifting performers during; 5.8. lifting equipment fitted to vehicles; 5.9. lifting appliances connected to machinery and intended exclusively for getting jobs, including car maintenance and inspection points; 5.10. rack and pinion type elevators; 5.11. the escalators and mechanical walkways. 6. On the lifts, which safety requirements are set out in other laws, these provisions set out the safety requirements apply in so far as they are not contrary to the safety requirements laid down therein. 7. lift safety components covered by the market believes: 7.1. import safety component of the lift in Latvia, if the recipient is the manufacturer's authorised representative, who entrusted the ingredient before placing on the market, prepare according to the requirements of these regulations; 7.2. the introduction of the safety component or development in Latvia, to then take from Latvia; 7.3. the safety components in manufacture for export to other countries. 8. The placing on the market requirements of this regulation can only be relevant to the safety of lifts and components. If the applicable standards for the design and construction are respected, and this is confirmed by these rules set out the procedures for the attestation of conformity, it is considered that the provisions referred to in Chapter 3 requirements are met. 9. the requirements of this Regulation shall not apply to trade fairs, exhibitions or demonstrations showcasing lifts or safety components of the lift, if it does not comply with the information is clearly indicated, which also indicated that they will not be placed on the market or the market until it provided. During demonstrations must take appropriate security measures for the protection of people. 10. The installer of the Lift, designing, producing and installing lifts and safety components of the lift manufacturer, so designed and constructed that the lift safety components, in addition to the requirements of these provisions comply with the essential security and safety requirements laid down in the legislation on car safety. 11. Lift or elevator safety device that complies with the applicable standards (or parts thereof) to which reference is published in the official journal of the European Union (hereinafter referred to as the applicable standards), the appropriate rules referred to in Chapter 3, with the essential safety requirements covered by the applicable standards. 12. The national standardisation body shall publish in its tīmekļvietn the list of applicable standards, adapted to national standards. 13. in order to guarantee proper operation of the lift and secure it using the installer of the lift shall ensure the exchange of technical information with the person who is responsible for the construction of a building or a building where the elevator is to be mounted. 14. The market surveillance authorities, which shall carry out the lift and elevator safety components of market surveillance, the meaning of these provisions is the consumer rights protection centre. 2. responsibilities of the parties involved 15. market surveillance authorities Upon request of the person concerned shall provide information on the rules referred to in paragraph 4, the elevator's security components, including: 15.1. all parties that they have supplied the lift safety components; 15.2. all parties that they have supplied the security components of the lift. 16. the parties concerned shall ensure that the provisions referred to in paragraph 15 of the availability of information to the supervisory authority of the market 10 years after they delivered or they have supplied the security components of the lift. 2.1. responsibilities of the installer

17. The placing on the market of the lift installer shall ensure that it is designed and manufactured according to this rules Chapter 3 essential requirements listed in. 18. The installer shall prepare technical documentation and carry out the provisions mentioned in paragraph 110 of the relevant conformity assessment procedures or provide them. 19. Where the conformity assessment procedure has been proved that the lift meets the requirements of these provisions, the installer shall draw up a declaration of conformity, to ensure that it is connected to the elevator, elevator and marked with the CE marking of conformity. 20. The installer shall keep the technical documentation and Declaration of conformity, where necessary, compliance with the supporting documentation for 10 years after the lift has been placed on the market. 21. The installer will, if necessary, examine and record complaints and placed on the market provided the elevators, as well as investigate lift cases of non-compliance, noting that it provides consumer health and safety protection. 22. The installer will ensure that the mounted elevator is a type, batch or serial number or other identification element. 23. The installer of the lift to indicate their name or registered trade mark and the address where you can contact the installer. 24. The installer will ensure that the lift is attached to this provision in paragraph 109 of the manual in the language of the country. 25. If the installer considers or has reason to believe that the elevator, which it has been put on the market do not meet the requirements of this regulation, it shall immediately take the necessary corrective actions to ensure conformity of the lifts. If the lift presents a risk, the installer shall immediately inform the market protection, giving detailed information about the non-compliance and measures taken to prevent non-compliance. 26. the market surveillance authorities on request the installer will provide all the necessary information and documentation in the national language, to prove the conformity of the lift, and cooperate with the market surveillance authority to prevent the lift market risks. 2.2. The manufacturer's obligations within the meaning of these rules 27, importer and distributor shall be considered a manufacturer and it is the obligations laid down in this chapter, if it is placed on the market of the safety component of the lift under his name or trademark or modifies marketed safety components of the lift so that it can affect their compliance with these provisions in Chapter 3 of those essential requirements. 28. The placing on the market of the safety component of the lift, the manufacturer shall ensure that they are designed and manufactured according to this rules Chapter 3 essential requirements listed in. 29. the manufacturer of the safety components of the lift shall prepare technical documentation and carry out the rules concerned referred to in paragraph 110 of the conformity assessment procedures or ensuring that it is carried out. 30. where the conformity assessment procedure has been demonstrated that the safety components satisfy the requirements of this regulation, the manufacturer shall draw up a declaration of conformity and affix to the security components of the lift with the CE marking of conformity. 31. the manufacturer shall keep the technical documentation and Declaration of conformity, conformity, if necessary supporting documentation for 10 years after the lift safety components placed on the market. 32. If the lift safety components are manufactured in series, producer establish control procedures, to ensure compliance with the requirements of this regulation, and shall take into account the changes in the design of the lift safety components or characteristics, as well as the applicable standards or other technical specifications on the basis of which attests the conformity of the safety components of lifts to the requirements of this regulation. 33. where necessary to assess the lift safety components, the risks, the manufacturer of consumer health and safety protection tested and evaluated in the market of the safety component of the lift, register complaints and information about inappropriate and withdrawn from the market for safety components of lifts, as well as inform distributors of the operations. 34. The manufacturer shall ensure that the lift is placed on the market of the safety component label contains a type, batch or serial number, or have other identification element. If the size of the lift safety components or features, the manufacturer does not allow this information to point to the "CE" marking. 35. the manufacturer of the safety components for lifts, or, if this is not possible, to the "CE" marking shall indicate their name or registered trade mark and the address where you can contact the manufacturer. 36. The manufacturer shall ensure that the lift safety components added this provision in paragraph 108 of the installation and operating instructions, as well as the information in the national language. 37. the manufacturer who believes or has reason to believe that the safety components which are placed on the market, it does not meet the requirements of these regulations, shall immediately take the corrective action, to ensure compliance with the safety component of the lift to the requirements of this regulation or, where necessary, to withdraw or remove them from the market. If the lift safety components risk, manufacturers shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and of the corrective actions taken. 38. the market surveillance authorities on request the manufacturer to provide it with all necessary information and documentation in the national language to show the lift safety components, compliance with the requirements of this regulation. 39. the market surveillance authorities shall cooperate with the request of the manufacturer, the market surveillance authority to fix the elevator on the market of the safety component risks. 2.3. The authorised representative of the manufacturer with 40 written mandate can appoint an authorized agent. The mandate does not include this provision 17., 18., paragraphs 28 and 29. 41. The authorized representative shall take at least the following: 41.1.10 years after the lift or safety component on the market of the lift shall keep available to the market surveillance authorities of the Declaration of conformity of the decision of approval (s) that apply to the manufacturer or the installer of the approved quality system and technical documentation; 41.2. upon reasoned request, the market surveillance authorities shall provide all the information and documentation necessary to demonstrate the safety component of the lift or elevator; 41.3. the market surveillance authorities shall cooperate with the request of the market surveillance authority to prevent the lift or safety component of the lift risks, subject to the authorisation. 2.4. the importer's obligations

42. The importer places on the market according to the requirements of these regulations for safety components of lifts. 43. before the lift safety components placed on the market, importers shall ensure that the manufacturer has made this provision concerned referred to in paragraph 110 of the conformity assessment procedure, prepared by the appropriate technical documentation, labelled the lift safety components with the CE marking of conformity, added the Declaration of conformity and the required documentation, as well as 33 of these regulations are met and referred to in paragraph 34. 44. importers who consider or have reason to believe that the safety components do not meet the essential requirements are not placed on the market until it has been reached. If the lift safety components presents a risk, the importer shall inform the manufacturer and the market surveillance authorities. 45. The importer to lift safety components indicate their name or registered trade mark and the address where you can contact the importer. If that information is not likely to add to the security components of the lift, it shall be indicated on the packaging or attached to the safety component of the lift in the document. 46. The importer shall ensure that the safety components are added to the instructions for use of the national language. 47. Importers shall ensure that, while it is responsible for the safety of the lift components, storage or transport conditions do not adversely affect their compliance with these provisions in Chapter 3 of those essential requirements. 48. where necessary to assess the lift safety components, the risks, the importer of consumer health and safety protection tested and evaluated the market of safety components of lifts samples, register complaints and information about inappropriate and withdrawn from the market for safety components of lifts, as well as inform installers and distributors of the operations. 49. importers who consider or have reason to believe that the safety components which are placed on the market, it does not meet the requirements of these regulations, shall immediately take the corrective action to ensure compliance with the requirements of this regulation or, where necessary, to withdraw or remove them from the market. If the lift safety components risk, importers shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and corrective actions taken. 50. The importer, 10 years after the lift safety components placed on the market, keep market supervisors available a copy of the Declaration of conformity and, if necessary, the approval decision (s), as well as the market surveillance authority shall ensure the availability of technical documentation. 51. the market surveillance authorities on request, the importer shall provide it with all necessary information and documentation in the national language to show the lift safety components, compliance with the requirements of this regulation. 52. the market surveillance authorities shall cooperate with the request of the importer, the market surveillance authority to fix the elevator on the market of the safety component risks. 2.5. obligations of Distributors offering 53. lift safety components on the market, distributors shall act with due diligence to comply with the requirements of this regulation. 54. before the lift safety components on the market, distributors shall ensure that they are marked with the CE marking, accompanied by the Declaration of conformity and the required documentation, the package leaflet and the information in the national language, as well as the manufacturer has noticed that rule 34 and 35 of the requirements, while the importer is subject to the rule in paragraph 45. 55. distributors who consider or have reason to believe that the safety components do not conform to the requirements of this regulation, does not offer them on the market until it has been reached. If the lift safety components pose a risk, the distributor shall inform the manufacturer or the importer and the market surveillance authorities. 56. The distributor shall ensure that, while it is responsible for the safety of the lift components, storage or transport conditions do not adversely affect their compliance with these provisions in Chapter 3 of those essential requirements. 57. distributors who consider or have reason to believe that the safety component, which it has offered on the market do not meet the requirements of this regulation, ensure that the necessary remedial action to ensure compliance with the safety component of the lift to the requirements of this regulation or, where necessary, to withdraw or remove them from the market. If the lift safety components risk, distributors shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and corrective actions taken. 58. the market surveillance authorities on request, the distributor shall provide all the necessary information and documentation in the national language to show the lift safety components, compliance with the requirements of this regulation. 59. the market surveillance authorities on request, the distributor shall cooperate with the market surveillance authority to prevent lift marketed safety components, the risks. 3. The essential requirements for lifts and lift safety components 3.1. Design and construction of 60. Each transporter shall be fitted with a cab. The elevator car to be designed and constructed according to the maximum expected number of people move and lift the nominal load capacity, which is determined by the installer of the lift. 61. If the lift is intended for the movement of people and the size of the movement, the disabled allows the elevator cab designed to facilitate disabled access to the elevator car and the use of the lift. 62. The CAB suspension and (or) suspension features, their mounting and intermediate parts, taking into account the conditions of use of the lift, the materials used and the conditions of manufacture, selected and designed so as to ensure an adequate level of overall security and reduce the risk of the car falling. 63. If the cab suspension used for ropes or chains, used at least two independent cables or chains. Each system requires its own anchorage. 64. the suspension system of ropes and chains must not be connected or warp, except where it is necessary for the suspension ropes or chains or loops. 65. The elevator designed, produced and installed to prevent the initiation of movement, if the rated load is exceeded. 66. the Lift shall be fitted with speed limiters. 67. The provisions referred to in paragraph 66 of the requirement does not apply to lifts in which the movement system is designed to prevent speeding. 68. High-speed elevators equipped with speed control and containment device. 69. The elevator cab, which is moved to the dzenskriemeļ, designed to provide a towing cable (wire) cables on pulleys. 70. All passenger lifts need individual elevator drive mechanism. 71. The provisions referred to in paragraph 69 of the requirement does not apply to continuous operation of lift trucks has been replaced with another cab. 72. The installer of the Lift shall ensure that the lift machinery and the associated lift devices are available only for maintenance as well as emergencies. 73. Disabled people unaccompanied in lifts according to design and deploy the control device. 74. the functions of the controls indicate clearly and unambiguously. 75. the Group dialing devices control should be United or interconnected. 76. The electrical equipment set up and add it to: 76.1. they should not be confused with circuits which do not relate directly to the elevator; 76.2. energy supply is likely to turn on only when the elevator is loaded; 76.3. elevator movement is dependent on electrical safety devices, which is a separate electrical safety circuit; 76.4. damage the electrical circuit does not cause dangerous situations. 3.2. Risk Prevention outside the cab 77. the Lift shall be so designed and constructed that the room in which the cab travels should be available only for lift maintenance or emergency. 78. before the staff was getting into this provision in paragraph 77 room is provided the lift normal termination. 79. the Lift shall be so designed and constructed as to prevent the risk of crushing the cab when it is located in one of the movement's extreme conditions. 80. in order to prevent the stall induced people to the risk of crushing the movement end positions creates free space or a cover. If this requirement is not technically feasible to meet (especially into existing buildings), the installer of the lift after coordination with other institutions reported measures to avoid that risk. 81. the doorways in the elevator shaft, intended for the elevator and the entrance to the exit from the required conditions of use according to the Hardy doors. 82. Locking device prevents the movement of the carrier: 82.1. (whatever the case may be) as the elevator shaft doors are closed and sealed; 82.2. elevator shaft door opening while the car is moving and yet not in the stop position. 83. If the motion speed of the stop is controlled by the elevator door opening the stop motion is allowed. 3.3. Risk Prevention booth

84. The elevator car from floor to ceiling must be enclosed with walls, with the exception of ventilation apertures, and the cockpit door, which must be the full height of the cab. 85. The elevator car doors designed and built in such a way that the cab would not move when the doors are open, except for this provision, paragraph 82. 86. the cab should immediately stop when the door is opened. 87. If there is no elevator shaft, or if people might fall between the elevator car and shaft, the cockpit door must be closed and sealed when the elevator stops between floors. 88. the Lift provided by the devices for power transmission or failure of components in the case of fix cab free fall or uncontrolled movement. 89. devices that limit the fall of the cab, is independent from the cab suspension (suspension). When the elevator reaches the maximum lift speed if the cab is loaded according to the rated load capacities, the equipment to ensure the elevator cabs stopping.
90.89. These provisions in the case referred to in paragraph elevator cabs stop shall not harm the passengers irrespective of cabin occupancy. 91. Between the floor of the elevator shaft and the floor of the required buffer that the maximum compressed position provides this rule 80, paragraph free space. 92. in paragraph 91 of these rules in a particular requirement does not apply to lifts in which the cab can not get into this rule 80, paragraph spare room movement system design. 93. the Lift shall be so designed and constructed that its operation would not be possible if the rules referred to in paragraph 88 of the devices are not in working order. 3.4. other security requirements 94. Lift landing doors and car doors or the two doors if they are automated, shall be fitted with a device which prevents the risk of crushing them on the move. 95. the Lift landing doors (including those that are components of the glass) is sufficiently resistant to open flames and maintain integrity and insulation properties, as well as being resistant to thermal radiation. 96. The elevator shaft may not be in the piping, wiring or other structures, except those that are necessary for the operation and safety of the lift. 97. Counterweight fitted so as to avoid any risk of colliding with it or drop on the on it. 98. the Lift shall be equipped with means by which in exceptional cases it is possible to release people and evacuate them from the elevator. 99. The elevator car to be fitted with two-way means of communication that provides existing cab people constantly communicate with the assisting personnel. 100. the Lift shall be so designed and constructed that when the lift engine temperature exceeds the set temperature by the installer of the lift, the lift cabin can finish the movement, but did not start the next until you fix the damage. 101. The elevator cab designed and manufactured so as to ensure sufficient ventilation for passengers, the elevator continued standing. 102. The elevator cab is lit during its movement, and when the door is open. 103. the elevator's emergency lighting. 104. The provisions referred to in paragraph 99 of the means in these rules referred to in paragraph 103. emergency lighting devices shall be designed and constructed so that they work even if the power supply is not normal. Their duration must be sufficient to ensure the release and evacuation of passengers in an emergency. 105. The fire elevator control circuits that can be used in the event of fire, designed and made in such a way as to be able to provide the fire elevator cabs stopping at specific floors. Priority shall be given to those control circuits for the operation of the rescue services. 3.5. the legend 106. Elevator visibly placed sign clearly indicating the following information: 106.1. the lift installer's name and address; 106.2. the series or type designation; 106.3. the serial number (if any); year of installation of the lift 106.4.; 106.5. nominal load capacity in kilograms; 106.6. the maximum number of passengers; 106.7. the CE marking. 107. If the lift is designed for emergency prevention of people escaping from the cockpit without outside help, the instructions placed in a visible place in the booth, and they must be clear and unambiguous. 3.6. Usage instructions 108. Lift safety components are required for the installation and usage instructions. The instructions include safety components, installation, adjustment, and maintenance requirements under these rules. 109. Each elevator shall have at least the following documentation in the national language: 109.1. Manual (manual) with drawings and descriptions, which are necessary for normal use, Elevator maintenance, inspection, repair and periodic inspection, as well as the people and the release of the emergency evacuation; 109.2. log with notches for elevator repairs and periodic inspection. 4. Conformity assessment

110. the security component of compliance with this provision in Chapter 3 with the essential safety requirements, certified by one of the following conformity assessment procedures: 110.1. Module B (subchapter 5.1) and C2 module (5.4. subchapter); 110.2. Module B (subchapter 5.1) and module E (5.2. subchapter); 110.3. Module H (subchapter 5.3). 111. the compliance with this provision in Chapter 3 with the essential safety requirements, certified by one of the following conformity assessment procedures: 111.1. If the lift is designed and manufactured in accordance with a model lift having made a declaration of conformity in accordance with module B (subchapter 6.1), use one of the following conformity assessment procedures: 111.1.1. final inspection of the lift (subchapter 6.2); 111.1.2. (E) module (subchapter 6.3); 111.1.3. (D) module (6.4. subchapter); 111.2. If the lift is designed and manufactured according to the quality system, which was approved by the module H1 (subchapter 6.5, except the design of the test), use one of the following conformity assessment procedures: 111.2.1. final inspection of the lift (subchapter 6.2); 111.2.2. (E) module (subchapter 6.3); 111.2.3. (D) module (6.4. subchapter); 111.3 G module (6.6. subchapter); 111.4. module H1 (6.5. subchapter). 112. These rules 111.1 and 111.2. in the cases referred to in paragraph a person who is responsible for the design and manufacture of the lift, and the person responsible for the lift installation and testing are one and the same person. On the elevator and the person in charge of production provides for the installation and testing of the lift to the person in charge of all the necessary documents and information to enable it to ensure correct and safe installation and testing of the lift. 113. any permissible differences (the maximum and minimum values) between the sample and the elevator lifts, which are created according to the lift, are clearly specified in the technical documentation. 114. on the basis of the calculations and (or) to design plans, allowed to prove the safety of lifts and lift components range in similarity, to comply with the essential safety requirements referred to in section 3 of these rules. 5. Lift the safety component conformity assessment procedures 5.1. EU type examination (module B) 115. EU type examination is the part of a conformity assessment procedure, the notified body which checked the elevator safety components, as well as the technical project examined and assessed, or lift safety components the technical design meets the provisions referred to in Chapter 3, with the essential requirements and ensure that the lift in which the component is correctly installed, meets these requirements. 116. the EU type-examination must be lodged by the manufacturer or his authorized representative to a single notified body of his choice. The application shall include: 116.1. authorised representative of the manufacturer and, if the application, name and address, as well as the lift safety components, the place of production; 116.2. a written declaration that the same application has not been lodged with any other notified body; 116.3. technical documentation. The technical documentation provides the opportunity to assess the safety of the lift components in compliance with the applicable requirements and include appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the evaluation, it covers the lift safety components of the design, manufacture and operation. The technical documentation shall, if necessary, include: 116.3.1. Description of the safety component, including its area of use (in particular possible speed, payload and power) and conditions (in particular explosive environments and weather conditions); 116.3.2. Design and manufacturing drawings and diagrams; 116.3.3. explanations required of the said drawings and diagrams and the operation of the lift safety components of understanding; 116.3.4. the full or partial list of the standards applied, the references to which have been published in the official journal of the European Union, and, if the standards have not been applied, the solutions adopted, to ensure that the safety component meet the requirements of these regulations, as well as other relevant technical specifications list. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 116.3.5. any manufacturer or on his behalf make design calculations; 116.3.6. test reports; 116.3.7. the lift safety components, the instructions copies; 116.3.8. the measures to be taken at the manufacturing stage to ensure that series-produced lift safety components conform to the safety component examined the elevator; 116.4. lift safety components representative sample or information on the site, which can be verified. The notified body may require new specimens if needed for carrying out the test programme; 116.5. certificates confirming compliance of the technical design solution. Receipts for all documents used, including other relevant technical specifications, in particular where not completely appropriate applicable standards. If necessary, also include the results of tests carried out in accordance with other relevant technical specifications has taken to the manufacturer's laboratory or other testing laboratories in the name of the manufacturer and to a producer responsibility. 117. The notified body shall carry out EU type examination in the following order: 117.1. examine the technical documentation and evidence to evaluate lift safety components in the project technical compliance; 117.2. agree with the applicant the location where the examinations and tests carried out; 117.3. make sure that the sample (s) is (are) produced in accordance with the technical documentation and identify the components designed in accordance with the applicable requirements of the standards, as well as items produced under other relevant technical specifications; 117.4. make appropriate inspections or tests or ensure to check that the manufacturer applied the standards provided for in relevant applicable specifications and whether they are correctly applied. 118. the notified body shall draw up an assessment report indicating the measures taken in accordance with paragraph 117 of these rules, and the results of such measures. Without prejudice to its obligations against the notifying authorities, the notified body only with the consent of the manufacturer fully or partially disclosed that the contents of the message. 119. If the lift safety components type meets the requirements of these provisions, the notified body shall issue a manufacturer the EU type-examination certificate including the name and address of the manufacturer, the conclusions of the EU type-examination, the conditions for validity of the certificate and for identification of the approved type the data you want. 120. the EU type-examination certificate can have one or more annexes containing all relevant information allowing an evaluation to be made of the conformity of the lift safety components to the type of test and inspection during use. 121. If the lift safety components type does not meet the requirements of these provisions, the notified body shall not be issued in the EU type-examination certificate and shall inform the applicant accordingly, indicating the reasons for such refusal. 122. The notified body shall keep the EU type-examination certificate, its annexes and additions, as well as the technical file and a copy of the assessment report for 15 years from the date of issue of the certificate. 123. the notified body shall identify the common standard changes, which indicate that the approved type may no longer comply with the requirements of this regulation, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the manufacturer. 124. The manufacturer shall inform the notified body that holds the technical documentation concerning the EU type-examination certificate of all modifications to the approved type that may affect the conformity of the lift safety components with the requirements of these regulations or of the EU type-examination certificate validity conditions. 125. the notified body shall examine the amendments and shall inform the applicant whether the EU type-examination certificate remains valid or need additional verification, verification or testing. Where applicable, the notified body shall issue a supplement to the original EU type-examination certificate or ask to submit a new application in the EU type-examination. 126. the Notified institution every six months or, upon request, inform the Ministry of the economy of the EU type-examination certificate and (or) any additions which it has issued or withdrawn, and shall submit the certificate and (or) additions to the list of certificates rejected or certificates which have been abolished or otherwise limited.

127. The notified body shall inform the other notified bodies of the EU type-examination certificate and (or) additions, which this body has refused, withdrawn, suspended or otherwise restricted, and, upon request, also for certificates and (or) additions, which it has issued. 128. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get the EU type-examination certificate and (or) the copy of the Appendix. 129. at the request of the European Commission and the Member States may receive technical documentation and notified body checks, verification and copies of the test results. 130. the manufacturer shall keep available for the national authorities in the EU type-examination certificate, its annexes and additions with copies of the technical documentation for 10 years after the lift safety components placed on the market. 131. The manufacturer's authorised representative may lodge the rules of application referred to in paragraph 116 and meet this provision in paragraph 124 and 130 obligations, if they are specified in the mandate. 5.2. safety components of the Lift conformity to type based on product quality assurance (module E) 132. Conformity to type based on quality assurance of the products the lift safety components is the part of a conformity assessment procedure in which the notified body shall assess the quality system of the manufacturer to ensure that the safety components are manufactured and controlled according to the EU type-examination certificate and comply with the type described in these provisions in Chapter 3. 133. the manufacturer of the product by an approved quality assurance system for elevator safety components, the final inspection and testing, and is subject to monitoring. 134. the manufacturer of the notified body of their choice shall submit an application for assessment of his quality system with the safety components of lifts. The application includes the: 134.1. the authorised representative of the manufacturer and, if the application, name and address; 134.2. a written declaration that the same application has not been lodged with any other notified body; 134.3. the space address where the lift safety components, the final inspection and testing; 134.4. all relevant information on safety components of lifts that are intended to produce; 134.5. documentation relating to the quality system; 134.6. approved lift safety components, the technical documentation and the EU type-examination certificate. 135. the manufacturer, in accordance with the quality system and the applicable standards each security component being examined and the appropriate tests or equivalent tests are carried out to ensure that it meets the requirements of this regulation. All material elements, requirements, and conditions the manufacturer systematically and adequately documented in writing, specifying the measures taken and the procedures adopted. 136. the quality system documentation shall ensure a common understanding of the quality programmes, plans, manuals and records. The quality system documentation describes: 136.1. quality objectives; 136.2. governing body structure, responsibilities and powers with regard to product quality; 136.3. the examinations and tests that will be carried out after manufacture; 136.4. techniques to monitor the effective operation of the quality system; 136.5. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 137. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 136. The notified body shall presume that these requirements meet these quality system elements that correspond to the standard applicable to the respective specifications. 138. One member of the inspection team in addition to experience in quality management systems must have experience in the technical evaluation of the lift and the knowledge of the safety requirements laid down in Chapter 3 of these rules. 139. the audit also includes the assessment of the plant. The audit team examined the rules of 134.6. referred to in the technical documentation to verify the manufacturer's ability to identify the relevant requirements of these regulations and to carry out the necessary checks to ensure the lift safety components satisfy the requirements. 140. The notified body the manufacturer shall notify the Court of a decision which shall contain the conclusions of the audit and the assessment of justification. 141. The manufacturer shall undertake to take all the measures arising out of the approved quality system, as well as to ensure the adequate and efficient work. 142. Of any intended change of the quality system, the manufacturer or his authorised representative shall inform the notified body that has approved the quality assurance system. 143. the notified body shall evaluate the proposed changes and decide whether the following amendments to the product quality assurance system still satisfies this rule 136. the requirements referred to in paragraph 1 or make a reassessment. 144. The notified body shall notify the manufacturer of its decision, which shall include the conclusions of the examination and assessment. 145. for the purposes of the evaluation the manufacturer provides the notified body access to the premises where the final inspection, testing and storage, and shall provide it with all necessary information, in particular: 145.1. the quality system documentation; 145.2. technical documentation; 145.3. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 146. The notified body shall periodically carry out audits to make sure that the manufacturer maintains and applies the quality system and shall provide an audit report to the manufacturer. The notified body may pay unexpected visits to the manufacturer's premises, the security component of the lift final inspection and test. During the visits, the notified body may, if necessary, carry out tests or have them carried out in order to verify that the product quality assurance system is functioning properly. The notified body must provide the manufacturer with a visit report and, if a test has been carried out, with a test report. 147. for each of the safety components for lifts which meet the EU type-examination certificate and to the type as described in the requirements of this regulation, the manufacturer shall impose those rules for the CE marking of conformity, as well as to the provisions referred to in paragraph 134 of the notified body responsible for the label adds its identification number. 148. the manufacturer shall draw up a written each lift safety components of the Declaration of conformity and ensure its availability market supervisory authority for 10 years after the lift safety components placed on the market. In the Declaration of conformity shall identify the safety components of lifts it up. 149. the manufacturer for at least 10 years after the lift safety components placed on the market market supervision authorities keep: 149.1. This provision is 134.6. the technical documentation referred to in point a; 149.2. This provision 134.5. referred to documentation; 149.3. information relating to this provision in paragraph 142 above changes; 149.4. notified body decisions and reports referred to in this provision in paragraph 144 and 146. 150. the Notified institution every six months or, upon request, inform the Ministry of economy issued and withdrawn on the quality assurance system approval decision and submit it to the approval decision list of rejected the decision and decisions, which have been suspended or otherwise restricted. 151. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, or where it is suspended. Upon request, the notified body shall also inform those decisions which it has issued. 152. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get a quality assurance system approval decision. 153. The manufacturer's authorised representative can perform this rule 134, 142, 147, 148, and referred to in paragraph 149 of the producer duties and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.3. Conformity based on full quality assurance for safety components of lifts (module H)

154. the conformity based on full quality assurance lift safety components is the conformity assessment procedure whereby a notified body shall assess the quality system of the manufacturer to determine whether the elevator's security components are designed, manufactured, inspected, and tested according to the provisions referred to in Chapter 3, with the essential requirements and to ensure that the lift in which the component is correctly installed, meets these requirements. 155. the manufacturer shall use the approved quality assurance system for elevator safety components in the design, manufacture, final inspection and testing, and is subject to monitoring. 156. the manufacturer of the notified body of their choice shall submit an application for assessment of his quality assurance system. The application shall include: 156.1. manufacturer or authorized representative if the application, name and address; 156.2. the space address that the elevator safety components are designed, manufactured, inspected and tested; 156.3. all relevant information about the security components of the lift is intended to be manufactured; 156.4. the technical documentation referred to in paragraph 116.3. these provisions, one sample in each lift for the manufacture of the safety component category; 156.5. the quality assurance system documentation; 156.6. a written declaration that the same application has not been lodged with any other notified body. 157. the quality system shall ensure compliance of the safety components of lifts to the requirements of this regulation. All of the elements adopted by the manufacturer, the requirements and the conditions for systematic and adequately documented in writing, indicating the measures, procedures and instructions. 158. the quality assurance system documentation describes: for quality, 158.1. Management organisational structure, tasks and powers with regard to design and product quality; 158.2. design specifications, including the standards applicable and, if those standards are not applied or are applied in part, used techniques and other technical specifications, which will ensure compliance with these provisions; 158.3. the design control and inspection techniques, processes and systematic actions that you use when designing the safety components of the lift; 158.4. manufacturing, quality control and quality assurance techniques, processes and systematic actions; 158.5. the examinations and tests that will be carried out before the process, during and after its completion, as well as the frequency of the conduct; 158.6. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned; 158.7. monitoring processes to ensure appropriate design and adequate quality, as well as the effective operation of the quality system. 159. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 158 above requirements. The notified body shall presume that these requirements meet these quality system elements that correspond to the standard applicable to the respective specifications. 160. One member of the inspection team in addition to experience in quality management systems must have experience in the technical evaluation of the lift and the knowledge of the safety requirements laid down in Chapter 3 of these rules. 161. the audit also includes the assessment of the plant. The audit team examined the rules of 156.4. referred to in the technical documentation to verify the manufacturer's ability to identify the relevant requirements of these regulations and to carry out the necessary checks to ensure the safety of the lift components in compliance with these requirements. 162. The notified body audits the decision is notified to the manufacturer. The decision shall contain the conclusions of the audit and the assessment of the justification of the decision. 163. The manufacturer shall undertake to take all the measures arising out of the approved quality system, as well as to ensure the adequate and effective work. 164. If the intended change of the quality system, the manufacturer or his authorized representative shall inform the notified body that has approved the quality assurance system. 165. the notified body shall evaluate the proposed changes and decide whether the following amendments to the quality system still meets the rules in paragraph 158 above requirements or re-evaluation should be performed. 166. the notified body shall communicate its decision to the manufacturer. The notification shall contain the conclusions of the examination and assessment of the justification of the decision. 167. the purpose of the evaluation the manufacturer provides the notified body access to the premises where the final inspection, testing and storage, and shall provide it with all necessary information, in particular: 167.1. comprehensive quality system documentation; 167.2. the quality records provided for part of the quality system relating to design, such as results of analyses, calculations, tests results; 167.3. lift safety components, the technical documentation as regards manufactured elevators; 167.4. the quality records provided for in the comprehensive quality assurance part of the system, which applies to the manufacture, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 168. The notified body shall periodically carry out audits to make sure that the manufacturer maintains and applies the quality system and shall provide an audit report to the manufacturer. Notified body representatives without prior notice, you can visit the shop floor space in which to take the elevator to the final inspection of the safety components and testing. During the visits, the notified body may, if necessary, carry out tests or have them carried out in order to verify that the product quality assurance system is functioning properly. The notified body must provide the manufacturer with a visit report and, if a test has been carried out, with a test report. 169. Each lift safety components which comply with the requirements of this regulation, the manufacturer shall impose those rules for the CE marking of conformity, as well as to the provisions referred to in paragraph 157 of the notified body responsible for the label adds its identification number. 170. the manufacturer shall draw up a written each lift safety components of the Declaration of conformity and ensure its availability market supervisory authority for 10 years after the lift safety components placed on the market. In the Declaration of conformity shall identify the safety components of lifts it up. 171. the manufacturer for at least 10 years after the lift safety components placed on the market market supervision authorities keep: 171.1. This provision 156.5. the documentation referred to in point; 171.2. This provision 156.4. the technical documentation referred to in point a; 171.3. information relating to this provision in paragraph 164 above changes; 171.4. notified body decisions and reports referred to in these regulations and in paragraph 162.168. 172. the Notified institution every six months or, upon request, inform the Ministry of economy issued and withdrawn on the quality assurance system approval decision and submit it to the approval decision list of rejected the decision and decisions, which have been suspended or otherwise restricted. 173. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, or where it is suspended. Upon request, the notified body shall also inform those decisions which it has issued. 174. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get a quality assurance system approval decision. 175. The notified body shall keep the approval decision, its annexes and additions, as well as a copy of the technical documentation for a period of 15 years from the date of issue. 176. The manufacturer's authorised representative may meet this provision, 164.156, 169.170.171 points, and mentioned in the manufacturer's obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.4. the safety components of the Lift conformity to type based on random checks (C2 module)

177. Conformity to type based on random checks are part of a conformity assessment procedure, the notified body which carried out the safety components of lifts check to determine whether the lift safety components conform to the EU type-examination certificate to the approved type and this provision in Chapter 3 requirements and ensure that the lift in which the component is correctly installed, meets these requirements. 178. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure that the elevator safety components manufactured in conformity with the requirements of these provisions. 179. the manufacturer one notified body of his choice, submit random verification. The application shall include: 179.1. the manufacturer and authorized representative, if the application, name and address; 179.2. a written declaration that the same application has not been lodged with any other notified body; 179.3. all relevant information for the safety components manufactured in the elevator; the address of the premises 179.4. where you can take the lift safety components. 180. The notified body chosen by the manufacturer, periodically, but not less frequently than once a year in the establishment of random checks the lift produced safety components in accordance with the applicable standards or with equivalent methods to assess the conformity of the safety components and requirements of these provisions. 181. the requirements, which are evaluated for safety components of lifts, the notified body shall determine, subject to the security of the main characteristics of the components. 182. If the lift satisfies the security component of the notified body, the notified body shall issue a certificate of conformity for the type according to the examinations and tests. 183. If the lift safety components do not conform the notified body of the requirements, the notified body shall take appropriate measures to prevent further lift safety components marking the CE conformity marking, and immediately notify the market surveillance authority, as well as other notified bodies. 184. the European Commission, Member States and the other notified bodies the notified institution making the request, you can receive a copy of the certificate of conformity of type. 185. Each lift safety components which comply with the requirements of this regulation, the manufacturer shall impose those rules for the CE marking of conformity, as well as to the provisions referred to in paragraph 179 of the notified body responsible for the label adds its identification number. 186. the manufacturer shall draw up a written each lift safety components of the Declaration of conformity and ensure its availability market supervisory authority for 10 years after the lift safety components placed on the market. In the Declaration of conformity shall identify the safety components of lifts. 187. The manufacturer's authorised representative may fulfil the obligations of the manufacturer the manufacturer's task and responsibility, if they are specified in the mandate, with the exception of those rules specified in paragraph 178. 6. the conformity assessment procedures

6.1. the EU type-examination (module B) 188. Lifts EU type examination is the part of a conformity assessment procedure, the notified body which checked the model lift or elevator, which are not designed for extensions or variants, as well as the technical project, examine and evaluate whether the model lift and the technical design meets the provisions of this section 3. 189. the EU type examination shall include a representative sample of completed elevator check. 190. the EU type examination application installer or his authorized representative to a single notified body of his choice. The application shall include: 190.1. Installer and authorized representative, if the application, name and address; 190.2. the written declaration that the same application has not been lodged with any other notified body; 190.3. technical documentation that allows assessment of the conformity of the lift with the requirements of this regulation. The technical documentation shall, if necessary, include: 190.3.1. Description of the lift, clearly indicating all the permissible difference of lift; 190.3.2. Design and manufacturing drawings and diagrams and explanations necessary for the said drawings and diagrams and the operation of the understanding of the lift; 190.3.3. list of the essential requirements to be taken into account; 190.3.4. the full or partial list of the standards applied, the references to which have been published in the official journal of the European Union, and, if the standards have not been applied, the solutions adopted in the descriptions to ensure that elevator shall meet the requirements of these provisions, as well as other relevant technical specifications list. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 190.3.5. the lift elevator safety components, the copies of the Declaration of conformity; 190.3.6. any installer or it made the task of design calculations; 190.3.7. test reports; 190.3.8.109. these provisions referred to a copy of the instruction manual; 190.3.9. the measures to be taken in the installation stage to ensure that series-produced lift conforms to the provisions of Chapter 3 of the mentioned essential requirements; 190.4. information as to the place where the model lift can be verified. The model lift submitted for examination requires intermediate parts and should be able to get at least three levels (top, middle and bottom); 190.5. certificates confirming compliance of the technical design solution. Receipts for all documents used, including other relevant technical specifications, in particular, if not fully appropriate applicable standards. Supporting receipts for, if necessary, include the results of the tests in accordance with other relevant technical specifications has made the installer's laboratory or other test laboratory on behalf of the manufacturer and to a producer responsibility. 191. The notified body shall carry out EU type examination in the following order: 191.1. examine the technical documentation and receipts attached, to assess whether the model lift, or that a lift for which there is no down extension or variant, satisfies the technical project; 191.2. agree with the location where the lift will be checked and tests; 191.3. check lift, to ensure that it is in conformity with the technical documentation referred to, and find out which components have been designed in accordance with the relevant applicable standards and that, in accordance with the other technical specifications; 191.4. make appropriate inspections or tests or ensure to check whether the manufacturer applied standards provided for in relevant applicable specifications and whether they are correctly applied; 191.5. carry out the appropriate examinations and tests, or ensure to check whether, where the relevant applicable are not appropriate standards for specifications, Installer solutions, the application of other relevant technical specifications, meeting the requirements of this regulation. 192. the notified body shall draw up an assessment report indicating the measures taken in accordance with the provisions of paragraph 191, and the results of such measures. 193. Without prejudice to their obligations toward the notifying authorities, the rules referred to in paragraph 190 of the notified body only with the manufacturer's agreement to disclose all or part of the contents of that report. 194. If the lift type meets the requirements of these provisions, the notified body shall issue the installer in the EU type-examination certificate including the name and address of the manufacturer, the conclusions of the EU type-examination, the conditions for validity of the certificate and for identification of the approved type the data you want. 195. the EU type-examination certificate can have one or more annexes containing all relevant information allowing to assess the final inspection of the lift conform to the approved type. 196. If a type does not match the rule referred to in Chapter 3, with the essential requirements, the notified body shall not be issued in the EU type-examination certificate and shall inform the applicant accordingly, indicating the reasons for such refusal. 197. The notified body shall keep the EU type-examination certificate, its annexes and additions, as well as the technical file and a copy of the assessment report for 15 years from the date of issue of the certificate. 198. the notified body shall identify the common standard changes, which indicate that the approved type may no longer comply with the requirements of this regulation, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the manufacturer. 199. The installer shall inform the notified body of any modifications to the approved type, including the differences that are not specified in the original technical dossier and which may affect the conformity of the lift with the requirements of this regulation in the EU type examination or the conditions for validity of the certificate. 200. the notified body shall examine the changes and inform the installer, or EU type examination certificate is valid or whether further testing is needed, the verification or test. Where applicable, the notified body shall issue a supplement to the original EU type-examination certificate or ask to submit a new application in the EU type-examination. 201. the Notified institution every six months or, upon request, inform the Ministry of the economy of the EU type-examination certificate and (or) any additions which it has issued or withdrawn, and shall submit the certificate and (or) additions to the list of certificates rejected or certificates which have been abolished or otherwise limited. 202. The notified body shall inform the other notified bodies of the EU type-examination certificate and (or) additions, which this body has refused, withdrawn, suspended or otherwise restricted, and, upon request, also for certificates and (or) additions, which it has issued. 203. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get the EU type-examination certificate and (or) the copy of the Appendix. 204. at the request of the European Commission and the Member States of the European Union can get the technical documentation and the inspections carried out by the notified bodies, verification and copies of the test results. 205. The installer shall keep available for the national authorities in the EU type-examination certificate, its annexes and additions with copies of the technical documentation for 10 years after the lift has been placed on the market. 206. the installer's authorized representative may submit to this provision the application referred to in paragraph 191, and fulfill this rule 205.199. and the obligations referred to in paragraph 1, if they are specified in the mandate. 6.2. final inspection of the Lift

207. Final inspection is part of a conformity assessment procedure in which a notified body checks and certifies that the elevator, covered by the EU type-examination certificate, or which is designed and manufactured according to the approved quality system, meeting the requirements of this regulation. 208. The installer shall take all necessary measures to ensure that the lift which is mounted, complies with the provisions of Chapter 3 essential requirements listed in, as well as one of the following is met: 208.1. it is in the EU type-examination certificate described and approved type of lift; 208.2. the elevator is designed and manufactured according to the quality system according to the provisions of this subchapter 6.5 and the EU project inspection certificate if the project does not exactly conform to the applicable requirements of the standards. 209. The notified body chosen by the installer, the market made a final inspection of the lift in order to check the conformity of the lift with the requirements of this regulation. 210. The installer for a single notified body of his choice on application and the following documents: the plan of the complete lift 210.1.; 210.2. final inspection plans and diagrams, in particular control circuit diagrams; 210.3.109. these provisions referred to a copy of the instruction manual; 210.4. a written declaration that the same application has not been lodged with any other notified body. 211. the notified body shall require only the relevant information for the lifts, in so far as this is necessary for the fulfilment of the essential requirements. 212. the notified body shall carry out the appropriate examinations and tests laid down in the relevant applicable standards, or equivalent tests, to check the conformity of the lift with the requirements of this regulation. 213. The notified body shall carry out at least one of the following procedures: 213.1. This provision, paragraph 210 of document examination to check that the lift conforms with the approved type as described in the EU type-examination certificate under the EU type-examination of lifts; 213.2. This provision, paragraph 210 of document check to verify that the elevator is designed and manufactured according to the quality system according to the rules in this subchapter 6.5 requirements and, if the project does not exactly meet the requirements of the applicable standards, compliance with EU project examination certificate. 214. The notified body lift tests shall include at least the following checks: 214.1. empty and maximum load the lift check to ensure that the safety devices (end stops, locking devices, etc.) the proper installation and operation; 214.2. empty and maximum load the lift check to ensure proper safety devices in the event of disruption of power transmission; 214.3. static test with a load capacity of 1.25 times the rated load capacity. 215. in paragraph 214 of these rules After the tests referred to in the notified body checks that are not due to damage that adversely affects the use of the lift. 216. If after the checks listed in this subdivision the lift meets the requirements of these provisions, the notified body affixes its identification number or the number on the CE conformity marking and shall draw up a final inspection certificate which mentions the checks and tests. 217. The notified body shall fill out the relevant page that rule 109.2. log referred to in subparagraph. 218. If a notified body does not issue a certificate of final inspection, it explains in detail the reasons for the refusal and indicate the corrective measures taken. If the installer repeatedly submits an application for final inspection, it draws the same notified body. 219. The elevator cab, which comply with the requirements of these provisions, the installer shall affix the CE marking of conformity and the rules referred to in paragraph 210. notified body identification number of the notified body under the responsibility of the. 220. The installer of the lift shall draw up a written declaration of conformity and keep a copy of the final inspection certificate and 10 years after the lift has been placed on the market. A copy of the Declaration of conformity is available on request to the market surveillance authorities. 221. at the request of the European Commission and the Member States may obtain a copy of the final inspection certificate. 222. the installer's authorized representative may submit these rules 210. information referred to in paragraph 1 and 219 and 220 of these rules. the obligations referred to in paragraph, if they are specified in the mandate. 6.3. Conformity to type based on product quality assurance for lifts (module E) 223. Conformity to type based on product quality assurance for lifts, is the part of a conformity assessment procedure in which the notified body must assess the quality assurance system to ensure that the elevators to conform to the approved type as described in the EU type-examination certificate, or meet an elevator designed and manufactured under the full quality assurance system, approved in accordance with the provisions of subchapter 6.5 and meeting the requirements of this regulation. 224. The installer will use the approved quality assurance system for final inspection of the lift and testing, and is subject to supervision under this subchapter. 225. The installer for a single notified body of his choice for the elevator application for assessment of his quality assurance system. The application includes: Installer and 225.1. authorized representative if the application, name and address; 225.2. all relevant information for the lifts installation; 225.3. the quality assurance system documentation; 225.4. the on-site elevator technical documentation; 225.5. a written declaration that the same application has not been lodged with any other notified body. 226. Under the quality system, each elevator inspection and testing, as specified in the applicable standards, or equivalent tests, to ensure its conformity with the requirements of this regulation. All material elements, requirements, and conditions the manufacturer systematically and adequately documented in writing, specifying the measures taken and the procedures adopted. 227. the quality system documentation shall ensure a common understanding of the quality programmes, plans, manuals and records. The quality system documentation describes: 227.1. quality objectives; 227.2. the organizational structure of management, responsibilities and powers with regard to product quality; 227.3. the examinations and tests that will be carried out before placing on the market (at least the tests laid down in this provision, paragraph 214); 227.4. techniques to monitor the effective operation of the quality system; 227.5. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 228. The notified body shall assess the quality system to determine whether it meets this provision and paragraph 226.227.

229. The notified body shall accept that this provision in paragraph 226 and 227. these requirements conform to those elements of the quality system that comply with the relevant applicable standard specifications. 230. One member of the inspection team in addition to experience in quality management systems must have experience in the technical evaluation of the lift and the knowledge of the safety requirements laid down in Chapter 3 of these rules. The audit includes assessment of the premises and the lift installation site. 231. the decision shall be notified to the installer. The notification shall contain the conclusions of the examination and the reasoned assessment decision. 232. the manufacturer shall undertake to fulfil all measures arising from the quality system as approved and to ensure that it remains adequate and efficient. 233. The installer shall inform the notified body that has approved the quality system informed of any intended change of the quality system. 234. The notified body shall evaluate the proposed changes and decide whether the amended quality system will still meet the requirements referred to in these regulations and in paragraph 226.227, or need a revaluation. 235. The notified body shall notify the decision to the installer and, if appropriate, his authorised representative. The notification shall contain the conclusions of the evaluation and assessment of decision reasoned. 236. the notified body shall affix or cause to put its identification number adjacent to the CE marking of conformity. 237. the purpose of the evaluation the installer provides the notified body access to the premises where the installation, inspection and testing, and shall provide it with all necessary information, in particular: 237.1. the quality assurance system documentation; 237.2. technical documentation; 237.3. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 238. The notified body shall periodically carry out audits to make sure that the manufacturer maintains and applies the quality system and shall provide an audit report to the manufacturer. The notified body may pay unexpected visits to the installation site. During the visits, the notified body may, if necessary, carry out tests or have them carried out in order to verify that the quality system is working properly. The notified body must provide the manufacturer with a visit report and, if a test has been carried out, with a test report. 239. The elevator cab, which comply with the requirements of these provisions, the installer shall affix the CE marking of conformity and the next 225 these rules referred to the notified body identification number to that institution under the responsibility of the. 240. The installer of the lift shall draw up a written declaration of conformity and, upon request, made available to the supervisory authority of the market 10 years after the lift has been placed on the market. 241. The installer for at least 10 years after the last lift has been placed on the market market supervision authorities keep: 225.3. these provisions 241.1. referred to the quality system documentation; 225.4. these rules in 241.2. documentation referred to in subparagraph a; 241.3. This provision, the information referred to in paragraph 233; 235. these provisions 241.4. and 238. the notified body referred to in point decisions and reports. 242. the Notified institution every six months or, upon request, inform the Ministry of economy issued and withdrawn on the quality assurance system approval decision and submit it to the approval decision list of rejected the decision and decisions, which have been suspended or otherwise restricted. 243. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, or where it is suspended. Upon request, the notified body shall also inform those decisions which it has issued. 244. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get a quality assurance system approval decision. 245. the installer of the authorised representative can perform these rules 224.233, 239, 240 and 241, referred to in paragraph Installer responsibilities and tasks under the responsibility of the installer, if they are specified in the mandate. 6.4. Conformity to type based on quality assurance of production of lifts (module D)

246. Conformity to type based on quality assurance of the production of elevators, is part of a conformity assessment procedure in which the notified body shall assess the quality of production of the lift system to ensure that the lifts are installed in accordance with the approved type as described in the EU type-examination certificate, or according to the elevator, which designed and manufactured according to the quality assurance system, approved in accordance with the provisions of subchapter 6.5 and meeting the requirements of this regulation. 247. The installer will use the approved quality assurance system for elevator manufacture, construction, installation, final inspection and testing, and is subject to supervision under this subchapter. 248. The installer for a single notified body of his choice shall submit an application for assessment of his quality assurance system. The application includes: Installer and 248.1. authorized representative if the application, name and address; 248.2. all relevant information for the lifts installation; 248.3. the quality assurance system documentation; on-site elevator 248.4. technical documentation; 248.5. a written declaration that the same application has not been lodged with any other notified body. 249. The quality system shall ensure compliance of the lifts with the requirements of this regulation. All the principles adopted by the lift requirements and regulations in a systematic and orderly manner in the form of written measures, procedures and instructions, describing: the intended quality of 249.1. as well as the management of organisational structure, tasks and powers with regard to product quality; 249.2. used in the manufacturing, quality control and quality assurance techniques, processes and systematic actions; 249.3. the examinations and tests that will be carried out before installation, during installation and after it; 249.4. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned; 249.5. system of monitoring the efficient operation of the funds necessary for the attainment of quality and product quality. 250. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 249. 251. The notified body shall accept that this provision in paragraph 249 above requirements meet these quality system elements to meet the applicable standard in the relevant specifications. 252. One member of the inspection team in addition to experience in quality management systems must have experience in the technical evaluation of the lift and the knowledge of the safety requirements laid down in Chapter 3 of these rules. 253. the audit includes assessment of the premises and the lift installation site visit. 254. the respective decision shall be notified to the installer. The notification shall contain the conclusions of the audit and the reasoned assessment decision. 255. The installer will undertake all measures arising from the quality system as approved and to ensure that it remains adequate and efficient. 256. The installer shall inform the notified body that has approved the quality system informed of any intended change in the system. 257. The notified body shall evaluate the proposed changes and decide whether the amended quality system will still meet this provision in paragraph 249 above requirements or appreciable revaluation is necessary. 258. The notified body shall notify the decision to the installer and, if appropriate, his authorised representative. The notification shall contain the conclusions of the assessment and the assessment of the reasonable decision. 259. the notified body shall affix or cause to put its identification number adjacent to the CE marking of conformity. 260. the purpose of the evaluation the installer provides the notified body access to the premises where the manufacture, Assembly, installation, inspection, testing and storage premises and shall provide it with all necessary information, in particular: 260.1. the quality assurance system documentation; 260.2. technical documentation; 260.3. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 261. The notified body shall periodically carry out audits to make sure that the installer maintains and applies the quality system and shall provide an audit report to the manufacturer. The notified body may pay unexpected visits to the installation site. During the visits, the notified body may, if necessary, carry out tests or have them carried out in order to verify that the quality system is working properly. The notified body shall provide the installer with a visit report and, if a test has been carried out, with a test report. 262. The installer at least 10 years after the lift has been placed on the market market supervision authorities keep: 262.1. This provision referred 248.3. quality system documentation; 262.2. This provision 248.4. referred to in the technical documentation of the lift; 262.3. information on this provision in paragraph 255 above changes; 262.4. This provision. 257 and 261. notified body referred to in point decisions and reports. 263. The elevator cab, which comply with the requirements of these provisions, the installer shall affix the CE marking of conformity and the next 248. these provisions of the notified body referred to in paragraph 1 for the identification number of the body under the responsibility of the. 264. The installer of the lift shall draw up a written declaration of conformity and, upon request, made available to the supervisory authority of the market 10 years after the lift has been placed on the market. 265. the Notified institution every six months or, upon request, inform the Ministry of economy issued and withdrawn on the quality assurance system approval decision and submit it to the approval decision list of rejected the decision and decisions, which have been suspended or otherwise restricted. 266. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, or where it is suspended. Upon request, the notified body shall also inform those decisions which it has issued. 267. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get a quality assurance system approval decision. 268. the installer of the authorised representative can perform this provision 248., 256, 262, 263 and 264... Installer referred to duties and responsibilities on behalf of the installer, if they are specified in the mandate. 6.5. the conformity based on full quality assurance and verification project lifts (module H1)

269. the conformity based on quality assurance and test of elevators, the project is the conformity assessment procedure whereby a notified body assesses the installer the full quality assurance system, and, if necessary, the elevator project, to ensure that the lift meet the requirements of this regulation. 270. The installer will use the approved quality assurance system for the elevator in the design, manufacture, Assembly, installation, final inspection and testing, and is subject to supervision under this subchapter. The technical eligibility of the project the lift installer shall be checked in accordance with the procedure laid down in this section. 271. The installer for a single notified body of his choice shall submit an application for assessment of his quality assurance system. The application shall include: 271.1. Installer and authorized representative, if the application, name and address; 271.2. all the relevant information about the installation of the lifts, in particular information which makes for an understanding of the relationship between the design and operation of the lift; 271.3. the quality assurance system documentation; 271.4. technical documentation laid down in those provisions 190.3; 271.5. written declaration that the same application has not been lodged with any other notified body. 272. The quality system shall ensure compliance of the lifts with the requirements of this regulation. All the principles adopted by the lift requirements and regulations in a systematic and orderly manner in the form of written measures, procedures and instructions, describing: 290.2. quality, as well as the envisaged management organisational structure, tasks and powers with regard to product quality; 272.2. design specifications, including the standards applicable and, if applicable the standard will not apply in full, other appropriate means, including technical specifications that will be used to ensure compliance with these provisions; 272.3. the design control and design verification techniques, processes and systematic actions that will be used when designing the lifts; 272.4. the examinations and tests that will be carried out after the materials, components and sub-assemblies delivery; 272.5. relevant techniques, processes and systematic actions that will be used for installation, Assembly, quality control and quality assurance; 272.6. the examinations and tests that will be carried out before installation (installation conditions: shaft, check the position of the mechanism, etc.) during Setup and after Setup (including at least the tests referred to in paragraph 214 of these provisions); 272.7. the quality records, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned; 272.8. system of monitoring the efficient operation of the funds necessary for the attainment of quality and product quality. 273. If a project does not fully meet the requirements of the applicable standards, the notified body shall verify that the project complies with the provisions of Chapter 3 requirements listed in, and meets the issue if the EU project for the installer checks the certificate by setting the conditions for validity of the certificate and the listing of all the information necessary for identification of the approved project. 274. If a project does not meet the requirements of these provisions, the notified body shall issue the EU project not examination certificate and shall inform the installer, specifying the reasons for such refusal. 275. the notified body shall identify the common standard changes, which indicate that the approved type may no longer comply with the requirements of this regulation, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the installer. 276. The installer shall inform the notified body that has issued the EU design-examination certificate of all modifications to the approved design, which may affect the conformity with the requirements of this regulation or the conditions for validity of the certificate. Such modifications require additional approval (issued by the notified body has issued certificate of EU project), which are added as a supplement to the original EU draft examination certificate. 277. the Notified institution every six months or, upon request, inform the Ministry of the economy of the EU issued and withdrawn design-examination certificates and additions issued and (or) submitted to the EU project certificate and (or) additions to the list of certificates rejected or certificates which have been abolished or otherwise limited.

278. The notified body shall inform the other notified bodies of the EU project examination certificates and (or) additions, which it has refused, withdrawn, suspended or otherwise restricted, and, upon request, also for those certificates and (or) additions, which it has issued. 279. the European Commission, Member States and the other notified bodies the notified institution making the request, you can get EU project certificate and (or) the copy of the Appendix. On request, the European Commission and the Member States may receive technical documentation and reported the results of the inspections carried out by the institution. 280. The installer will keep the EU project examination certificate, its annexes and additions with the technical documentation a copy of and ensure the availability of a market supervisory authority 10 years after the lift has been placed on the market. 281. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 272 above requirements. The notified body shall presume that these requirements meet these quality system elements to meet the applicable standard in the relevant specifications. 282. One examination team must have experience in the technical evaluation of the lift and the knowledge of the safety requirements laid down in Chapter 3 of these rules. 283. the audit includes assessment of the premises and the lift installation site visit. 284. the audit team examined this provision 271.4. referred to in the technical documentation to verify the installer's ability to identify the applicable rules in this chapter 3 essential requirements mentioned and to carry out the necessary checks to ensure compliance with these requirements of the lift. 285. the decision shall be notified to the installer. The notification shall contain the conclusions of the audit and the reasoned assessment decision. 286. The installer will undertake all measures arising from the quality system as approved and to ensure that it remains adequate and efficient. 287. The installer shall inform the notified body that has approved the quality system informed of any intended change in the system. 288. The notified body shall evaluate the proposed changes and decide whether the amended quality system will still meet this provision of paragraph 271 or revaluation is necessary. 289. The notified body shall notify the decision to the installer and, if appropriate, his authorised representative. The notification shall contain the conclusions of the assessment and the assessment of the reasonable decision. 290. the notified body shall affix or cause to put its identification number adjacent to the CE marking of conformity. 291. The notified body shall periodically carry out audits to make sure that the installer duly fulfils the obligations arising out of the approved quality system. 292. the purpose of the evaluation the installer provides the notified body access to the design, manufacture, Assembly, installation, inspection, testing and storage premises and shall provide it with all necessary information, in particular: 292.1. the quality assurance system documentation; 292.2. the quality records provided for part of the quality system relating to design, such as results of analyses, calculations, tests results; 292.3. the quality records provided for part of the quality system on the supply and installation of acceptance, such as inspection reports and test data, calibration data, qualification reports of the personnel concerned. 293. The notified body shall periodically carry out audits to make sure that the installer maintains and applies the quality system and shall provide an audit report to the installer. The notified body may pay unexpected visits to the installation site. During the visits, the notified body may, if necessary, carry out tests or have them carried out in order to verify that the quality system is working properly. The notified body shall provide the installer with a visit report and, if a test has been carried out, with a test report. 294. The installer at least 10 years after the lift has been placed on the market market supervision authorities keep: this provision 271.3.294.1. referred to the quality system documentation; 294.2. This provision 271.4. the technical documentation referred to in point a; 294.3. This provision, the information referred to in paragraph 287; 289. these provisions 294.4. and 293. notified body referred to in point decisions and reports. 295. The notified body shall keep the approval decision, the annex and the Appendix and a copy of the technical documentation for a period of 15 years from the date of issue. 296. the Notified institution every six months or, upon request, inform the Ministry of Economic Affairs issued and withdrawn through all the full quality assurance system approvals the approval decision and shall submit to it a list of rejected the decision and decisions, which have been suspended or otherwise restricted. 297. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, suspended or withdrawn, and, upon request, on approval of the decisions which it has issued. 298. on request, the notified body shall submit to the European Commission and the Member States issued quality system approval decision. 299. The elevator cab, which comply with the requirements of these provisions, the installer shall affix the CE marking of conformity and the next point 271. these provisions in the notified body's identification number to that institution under the responsibility of the. 300. The installer of the lift shall draw up a written declaration of conformity and ensure its availability market supervisory authority 10 years after the lift has been placed on the market. 301. the installer of the authorised representative can perform this rule 271., 276, 280, 294.., 299. and referred to in paragraph 300 of the lift installer shall exercise the duties and responsibilities if they are specified in the mandate. 6.6. the conformity based on unit verification of lifts (module G)

302. the conformity based on unit verification is the conformity assessment procedure whereby a notified body assesses whether the lift satisfies the provisions of this section 3. 303. The installer shall take all measures necessary in order that the manufacturing process and its monitoring ensure conformity of the lift requirements of these provisions. 304. The installer for a single notified body of his choice on application and the following documents: 304.1. Installer and authorized representative, if the application, name and address; 304.2. the installation site of the lift; 304.3. written declaration that the same application has not been lodged with any other notified body; 304.4. technical documentation that includes at least the following elements: 304.4.1. Description of the lift; 304.4.2. Design and manufacturing drawings and diagrams; 304.4.3. explanations required of the said drawings and diagrams and the operation of the understanding of the lift; 304.4.4. list of directives on health and safety requirements; 304.4.5. the full or partial list of the standards applied, the references to which have been published in the official journal of the European Union, and, if the standards have not been applied, the solutions adopted in the descriptions to ensure that elevator shall meet the requirements of these provisions, as well as other relevant technical specifications list. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 304.4.6. built-in lift elevator safety components in the EU type-examination certificate; 304.4.7. any installer or it made the task of design calculations; 304.4.8. test reports; 304.4.9. This provision in paragraph 109 above a copy of the instruction manual. 305. the notified body chosen by the installer checks the technical documentation and the elevator, as well as the appropriate tests laid down in the relevant applicable standards, or equivalent tests, to check the conformity of the lift with the requirements of this regulation. Tests include at least those tests referred to in paragraph 213 of these rules. 306. If the lift meets the requirements of these provisions, the notified body shall issue a certificate of conformity relating to the tests carried out. 307. The notified body shall fill out this rule 109.2. log in the referred to the relevant page. 308. If a notified body does not issue a certificate of conformity, it shall explain in detail the reasons for the refusal and indicate the corrective measures taken. If the installer repeatedly submits an application for final inspection, it draws the same notified body. 309. The elevator cab, which comply with the requirements of these provisions, the installer shall affix the CE marking of conformity and the rules referred to in paragraph 304. notified body identification number attached to the CE conformity marking, the notified body under the responsibility of the. 310. The installer of the lift shall draw up a written declaration of conformity and keep a copy of the final inspection certificate and 10 years after the lift has been placed on the market. The installer will, upon request, provide a copy of the Declaration of conformity with the accessibility of the market surveillance authorities. 311. Of the lift shall keep with the technical documentation copies of the certificate of conformity market surveillance authorities for a period of 10 years from the date on which the lift is placed on the market. 312. at the request of the European Commission and the Member States may obtain a copy of the final certificate of conformity. 313. the installer of the authorised representative can perform this provision and paragraph 304.311 Installer responsibilities listed in the task and responsibility of the installer, if they are specified in the mandate. 7. the notified body

314. The notified body shall meet the following requirements: 314.1. the institution has legal personality, and it acts as a third party that is independent of the economic operator (associations), which lifts or safety components of the lift it evaluated; 314.2. the institution has demonstrated independence and absence of conflict of interest, if it is a member of the Association or Foundation (member), associated with the lift or elevator to be evaluated for safety components in the design, manufacture, supply, installation, use or maintenance; the management of the institution and 314.3. employee responsible for conformity assessment shall not lift the lift or safety component designer, manufacturer, supplier, Installer, purchaser, owner, user or attendant or their authorized representatives. This does not prevent them from using the elevator or lift weights for safety components in the operation of a conformity assessment body or to use them for personal purposes; the management of the institution and 314.4. employee responsible for conformity assessment, is not directly related to the elevator or lift safety components, design, manufacture or construction, the marketing, installation, use, or service and do not represent the parties engaged in these activities; 314.5. institutions managers and employees do not engage in any activity (particularly in consulting), which may conflict with their independence and fairness of the decision in relation to the institution for evaluation activities; 314.6. the institution shall ensure that its affiliates and subcontractors do not affect the operation of conformity assessment confidentiality, objectivity and impartiality; 314.7 institution and its employees. conformity assessment shall be carried out in good faith and is a professional, technically competent. The staff in decision making and in the assessment of conformity are free from any influences (especially financial) and from persons or groups of persons with an interest in the impact of this activity; 314.8. institution is able to carry out all the conformity assessment tasks for which it has laid down these rules in Chapter 5 and 6 and for which it has been notified, whether these tasks are carried out by the same body or are made on its behalf, under the responsibility of the authority; the institution according to the activities 314.9. conformity assessment procedures for which it has been notified, and each elevator and lift safety components, type and category are: 314.9.1. necessary personnel with technical knowledge and relevant experience, to perform the necessary conformity assessment activities; 314.9.2. Description of the procedures, in accordance with which conformity assessment carried out, ensuring the transparency and the ability to repeat this procedure. The institution is designed according to the policies and procedures to the tasks it carries out as a notified body is separated from the other activities; 314.9.3. developed the procedures take account of the economic operator, the industry in which it operates, its structure, the elevator and the elevator safety components, the manufacturing technology complexity and the mass or serial nature of the production process; 314.10. institution has the necessary means to enable it to perform properly the technical and administrative tasks connected with conformity assessment activities, and have access to all the necessary equipment and facilities; 314.11. conformity assessment activities the staff responsible are: 314.11.1. provide technical and professional training for the relevant conformity assessment activities; 314.11.2. knowledge and permission, to comply with the requirements relating to the activities of conformity assessment activities; 314.11.3. knowledge and understanding of the provisions referred to in Chapter 3, with the essential requirements, applicable standards, relevant legislation and the legislation laying down harmonised conditions for the marketing of goods; 314.11.4. skills needed to prepare certificates, records and reports to the conformity assessment; 314.12. institutions is ensured by its management and employees, making the impartiality of the conformity assessment activities; the management of the institution and 314.13. officers carrying out conformity assessment activities, the remuneration shall not depend on the number of assessments carried out or on the results; the institution is to 314.14. insure civil liability in respect of the activities that it is entitled to make; staff 314.15. institutions respect professional confidentiality with regard to all information gained in carrying out the conformity assessment activities, with the exception of information that is provided to the market surveillance authorities; the institution participates in standardization 314.16. activities organized by the European Commission and notified bodies in the working groups on the elevators or ensure that information on these activities is available to its employees. The institution in its activities as guidelines used by the notified body working groups prepare for decisions and documents. 315. If a notified body certifies its compliance with the criteria laid down in the relevant applicable standards or parts thereof, the references to which have been published in the official journal of the European Union, it is deemed appropriate that provision in paragraph 314 above requirements, to the extent applicable standards cover those requirements. 316. If a notified body shall conclude a contract with the subcontractor on the specific conformity assessment tasks or pass this task to a branch, it shall ensure that the subcontractor and the branch meets this provision in paragraph 314 above requirements and shall inform the Commission of the notification that is created in accordance with the laws and regulations on the procedures for the notification of the Commission creates, as well as the order in which the Commission takes a decision and shall notify the European Commission of conformity assessment bodies carrying out the assessment of conformity with the regulated sphere. The notified body shall assume full responsibility for the subcontractors and affiliates activity.
317. The notified body shall transfer a specific conformity assessment activity or branch subcontractors only with the consent of the customer. 318. The notified body shall keep the documents for subcontractors and affiliates and their competence evaluation carried out the conformity assessment activities and the availability of this document provides notification to the Commission. 319. The notified body shall carry out conformity assessments in accordance with the provisions of Chapter 5 and 6 mentioned in the conformity assessment procedures. 320. the notified body in the conformity assessment shall be carried out in a proportionate, avoiding unnecessary burdens for the persons concerned, taking account of the sector in which it operates, the organisational structure, the elevator or lift safety components, the complexity of technology and mass production process or the nature of the series, however, have a toughness and level of protection required for lifts and safety components of the lift meet the requirements of this regulation. 321. If a notified body finds that the manufacturer has not adhered to the essential requirements, applicable standards or other technical specifications referred to the essential requirements, it shall require the manufacturer to take appropriate measures to remedy the non-compliance, and issue a certificate. 322. where monitoring of lifts and safety components of the lift conformity to the requirements of these regulations upon issuance of the certificate, a notified body finds that lifts and safety components of the lift no longer meets the requirements of this regulation, it shall require the manufacturer to take appropriate measures to remedy the non-compliance, and if there is a risk to the health and safety of consumers, suspend or revoke the certificate. 323. If corrective action is not taken or it does not produce the desired results, the notified body accordingly, limit, suspend or revoke the certificate. 324. The notified body shall inform the Ministry of economy on: each certificate withdrawal 324.1., limitation, suspension or revocation; 324.2. any circumstances affecting the scope of the notice and conditions; 324.3. any market surveillance authorities requesting information regarding conformity assessment activities; 324.4. carried out conformity assessment activities notify sphere and other transactions, including cross-border activities and subcontracting (upon request). 325. The notified body shall provide the relevant information concerning the negative and, on request, also on positive conformity assessment results reported by other bodies carrying out similar conformity assessment activities covering the same lifts or safety components of the lift. 8. labelling

326. For the elevator or lift safety components, compliance with the requirements of this regulation indicates the CE conformity marking. 327. The CE conformity marking applies general principles, the European Parliament and of the Council of 9 July 2008. Regulation (EC) no 765/2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 (hereinafter Regulation No 765/2008), article 30. 328. the CE conformity marking on each lift and elevator components of each security or, if that is not possible, on the information plate clearly visible, legible and indelible manner. 329. the Lift or safety component of the lift shall be marked with the CE marking of conformity before placing on the market. 330. the CE conformity marking placed its identification number of the notified body, which shall participate in the following conformity assessment procedures: 330.1. final inspection of the lift; 330.2. unit verification (module G); 330.3. quality system assurance (module E, module H1, module D). 331. the safety components for Lifts CE marking placed behind the identification number of the notified body, which shall participate in the following conformity assessment procedures: 331.1. product quality assurance (module E); 331.2. full quality assurance (module H1); 331.3. lift safety component conformity to type based on random checks (C2 module). 332. the CE conformity marking and the identification number of the notified body can be deployed to other labels for specific risks or other use-related information. 333. The notified body identification number imposed itself upon the institution or its instructions, the manufacturer or its authorised representative or the installer or his authorized representative. 9. Declaration of conformity declaration of conformity 334. States that have proven to lift and elevator components of security compliance Chapter 3 of these rules the essential requirements listed in. 335. The Declaration of conformity shall be drawn up according to the rules in paragraph 338 and 339. those requirements and complemented with the necessary information, derived from the relevant conformity assessment procedures, and regularly updated. Declaration of conformity the Member State of the European Union language (or languages) in which the lifts or safety components of the lift is placed or offered on the market. 336. If to the elevator or lift safety components subject to several laws requiring the Declaration of conformity, prepares one for the Declaration of conformity with all the applicable legislation laying down harmonised conditions for the marketing of goods. Declaration of conformity indicates the relevant law and references to their publications. 337. in drawing up a declaration of conformity, the manufacturer shall assume responsibility for the compliance of the safety components of lifts, but the installer of the lift, the compliance with the requirements contained in these provisions. 338. the Declaration of conformity for safety components shall contain the following information: 338.1. name and address of the manufacturer; 338.2. If necessary, the authorised representative, his name and address; 338.3. the description of the safety component, details of type or series and serial number (if any), if necessary, to identify the products may include security components of the lift; 338.4. function of the safety component, if not obvious by description; 338.5. lift safety components production year; 338.6. all relevant provisions to which the lift conforms to security; 338.7. indication that the safety component complies with the relevant legislation; 338.8. If necessary, references to the applicable standards; 338.9. If necessary, the notified body name, address and identification number, which made these rules 5.1 and 5.2 sub-chapter of the EU type-examination of safety components of lifts, and a reference to the EU type-examination certificate issued by the notified body; 338.10. If necessary, the notified body name, address and identification number, which made the C2 module conformity assessment procedure; 338.11. If necessary, the notified body name, address and identification number, which approved the regulations 5.2 and 5.3 of the sub-chapter quality system; 338.12. name of the person, name and position, which is empowered to sign the Declaration for the manufacturer or his authorised representative; location and signing 338.13. date; 338.14. signature. 339. the Declaration of conformity shall be drawn up in the language of the country and include the following information: 339.1. name and address of the installer; 339.2. If necessary, the authorised representative, his name and address; description of the lift, 339.3. detailed information on the type or series, serial number and the address where the lift is installed; year of installation of the lift 339.4.; 339.5. all relevant provisions to which the lift conforms; 339.6. indication that the lift conforms with relevant legislation; 339.7. If necessary, references to the applicable standards; 339.8. If necessary, the notified body name, address and identification number, which made the EU type-examination of lifts, and a reference to the EU type-examination certificate issued by it; 339.9. If necessary, the notified body name, address and identification number, which made this rule 6.6. sub-chapter of the conformity assessment procedures; 339.10. If necessary, the notified body name, address and identification number, which carried out the final inspection of the lift; 339.11. If necessary, the notified body name, address and identification number, which approved the Installer used by quality assurance system in accordance with this provision, and 6.5 6.4 6.3. sub-chapter of the conformity assessment procedures; 339.12. persons or its authorised representative, the name and position, which is empowered to sign the Declaration on behalf of the installer; location and signing 339.13. date; 339.14. signature. 10. Market surveillance

340. the Lift and elevator components of security market supervision over the provision referred to in paragraph 14. 341. The elevator and lift safety components, the market surveillance applicable Regulation No 765/2008 of the third paragraph of article 15 and in article 16-29. 342. The installer, manufacturer and importer by market surveillance authorities request the technical documentation or a translation of the portion of the national language. The market surveillance authority, requiring the submission of technical documentation, as well as part of the translation determines the time-limit of 30 days, unless it is necessary to set a shorter deadline for finding a serious and immediate risk. 343. The notified body by the market surveillance authority shall provide information on the certificates which it has granted, refused or withdrawn, including providing test reports and technical documentation. 344. the interested party concerned have the responsibility of market surveillance authorities within the time limits which are commensurate with the risks of non-compliance and prevent non-compliance, if the market surveillance authority finds that any of the following administrative irregularities: 344.1. CE conformity marking does not comply with the provisions referred to in Chapter 8; 344.2. The CE conformity marking has not been affixed; not imposed or 344.3. has not imposed these rules 22, 23, 34 and 35, paragraph markings; not imposed 344.4. notified body identification number, which was involved in the lift or safety component of the lift production of conformity assessment procedures, or that are not subject to this provision in the chapter 8; not prepared or 344.5 is prepared Declaration of conformity; 344.6. technical documentation is not available or it is incomplete; 344.7. is specified, the specified incorrect or incomplete 45 34. these provisions and the information referred to in paragraph; 344.8. not satisfied any other this provision 2.1., 2.2 and 2.4 in the sub-chapter administrative requirement. 345. where the market surveillance authorities find that the elevator or lift safety components, the risks to the public, it shall take the elevator or lift safety components of the evaluation, taking into account the said risks and to all the requirements laid down in these provisions. Involved parties have an obligation to cooperate with the market surveillance authorities in that assessment. 346. the person Involved by the market surveillance authorities and the prescribed time limit, which is proportionate to the risks of non-compliance, are obliged to take all the necessary corrective actions to ensure the elevator or lift safety components of the compliance with the requirements of this regulation or, if necessary, revoke or withdraw it from the market, as well as to inform the relevant authorities notified, if this provision in paragraph 345 rating the market surveillance authority finds one of the following situations: 346.1. elevator or lift the safety device does not meet the requirements laid down in these provisions; 346.2. elevator or lift the safety component complies with the requirements laid down in these rules, but still pose a risk to the public. 347. If the person involved in the market surveillance authorities do not resolve this within the time limit set in paragraph 346 of the rules of the irrelevance or 346. these provisions the obligations referred to in paragraph 1, the market surveillance authority shall take a decision in accordance with the legislation on the safety of goods and services to prohibit the lift or safety component of the lift or the placing on the placing on the market or, if necessary, revoke or withdraw them from the market. 11. cooperation with the European Commission and the Member States of the European Union lifts and lift 11.1 safety components which do not satisfy the requirements of this regulation 348. Where the market surveillance authority has reason to believe that the lift or safety component of the lift, which made this provision, paragraph 345 assessment and found that it does not meet the requirements of this regulation, are also offered in other Member States of the European Union, the market surveillance authority after obtaining all necessary information shall immediately inform the European Commission and the other Member States of the European Union on the results of the assessment, and market surveillance authorities laid down measures to be taken by specifying all the necessary details, including: lift or elevator 348.1. Security components to identify the required information; 348.2. details of lifts or safety components of the lift; 348.3. nature and non-compliance risks; 348.4. information about the specific nature of the measures to be taken and the duration, as well as relevant stakeholders explanations and arguments; 348.5. information on whether the lift or safety component of the lift complies with the essential requirements or is the lack of applicable standards. 349. If, within three months after this paragraph 348 of the provisions providing the information referred to in any Member State of the European Union or the European Commission has not objected to the market surveillance authorities for specific measures to be taken, it is considered reasonable. 350. If the European Commission decides that market surveillance authorities the measures are unjustified, they are irrevocable. 351. where the market surveillance authority receives this provision the information referred to in paragraph 347 of the other Member State of the European Union, it shall immediately inform the European Commission and the other Member States of the European Union on the measures taken and give the information about the elevator or lift safety components, as well as inform on their objections, if it does not agree with the other European Union market surveillance authorities laid down measures to be taken. 11.2. the requirements of this regulation according to the lifts and safety components of the lift, which creates the risk of 352. Where the market surveillance authority has reason to believe that the lift or safety component of the lift, which made this provision, paragraph 345 assessment and determined that they meet the requirements of these provisions, the risk to the public, the market surveillance authority after obtaining all necessary information shall immediately inform the European Commission and the other Member States of the European Union, indicating all available information including: lift or elevator 352.1. Security components to identify the required information; 352.2. details of lifts or safety components of the lift; 352.3. information on risks; 352.4. information on market surveillance authorities to identify the nature of the measures to be taken and duration. 353. The European Commission, the rules get the information referred to in paragraph 352, adopt a decision that the market surveillance authorities the measures are unjustified, they are irrevocable. 12. concluding issues. 354 to declare unenforceable in the Cabinet of Ministers of 25 April 2000, the provisions of no. 157 "rules about lifts and their safety components in the design, manufacture and installation of the lift conformity assessment" (Latvian journal, 2000, 151-153; 2002, nr. 97. No; 2004, nr. 68.145., no; 2008; 2010.12. no). 355. the elevator lifts and safety components which are placed on the market by 2016 April 20, may be placed on the market unless they comply with the Cabinet of Ministers of 25 April 2000, the provisions of no. 157 "rules about lifts and their safety components in the design, manufacture and conformity assessment of installation of the lift," the requirements. 356. the certificate and the decisions taken by the notified bodies have issued up to the date of entry into force of the provisions under the Cabinet of Ministers of 25 April 2000, the provisions of no. 157 "rules about lifts and their safety components in the design, manufacture and installation of the lift conformity assessment" is valid until the expiry of the period specified therein. 357. the rules shall enter into force on 20 April 2016. Informative reference to European Union directives, the provisions included in the law arising from the European Parliament and of the Council of 26 February 2014 2014/33 of the directive/EU on the harmonization of the laws of the Member States relating to lifts and safety components of the lift. Prime Minister Māris kučinskis Deputy Prime Minister, Minister of economy of Ašeraden of Arvil