Cabinet of Ministers Regulations No. 348 in 2016 (7 June. No 28 4) pressure equipment and complex regulations Issued in accordance with the law "on conformity assessment" article 7 of the first and the second part 1. General questions 1. determines the pressure equipment and the complex design and manufacturing of essential requirements, the compliance monitoring mechanisms and procedures for monitoring the market. 2. the terms used in the rules: 2.1.-pressure equipment vessels, piping, safety accessories and pressure devices, including, if necessary, details that added to the pressure parts such as flanges, nozzles, couplings, supports, lifting lugs; 2.2. tank-tank designed and built to contain fluids under pressure including its direct attachments up to the point of connection with other equipment. The tank can consist of several cameras; 2.3. pipeline-the pipeline element for fluid transmission and, joined together, form a pressure system, including pipes or pipe systems, multiples, fittings, connections, extension hoses or, where appropriate, other elements subjected to pressure. Coolant air for cooling or heating, consisting of pipes, consider the pipelines; 2.4. safety devices – devices designed to protect pressure equipment against the allowable limits being exceeded, including devices for direct pressure limitation (such as safety valves, safety sheets (membrane) the safety devices, buckling rods, controlled safety pressure reduction system and limiting devices), which activates the adjustment features, or the exclusion or exclusion and lock, such as pressure switches or temperature switches or fluid level switches and safety related measurement control and regulation devices; 2.5. the pressure device – the device with the control function and the pressure housings; 2.6. complex-number of pressure equipment, which the manufacturer is assembled, to form a single operational equipment; 2.7. pressure – pressure relative to atmospheric pressure, i.e. the manometric pressure (vacuum pressure down with negative value); 2.8. the maximum allowable pressure (PS): the manufacturer's specified maximum pressure for which the equipment is designed. It determines the location specified by the manufacturer, – security and (or) restrictive devices or equipment instead of adding up, or at any point specified by the manufacturer; 2.9. the maximum/minimum allowable temperature (TS) – the manufacturer's specified maximum/minimum temperatures for which the equipment is designed; 2.10. the volume (V) – the camera's internal volume in litres, including the volume of nozzles to the first connection or weld and excluding the volume of permanent internal parts. 2.11. the nominal size (DN)-size numerical value that is common to all components in a piping system other than components indicated by outside diameters or by thread size in. Nominal size is designated by the letters DNA, followed by manufacturing dimensions loosely related whole number that is easy-to-use references; 2.12. fluids, gases, liquids and vapours in pure phase as well as mixtures thereof, that may contain suspended solid particles; 2.13. Permanent connections-connection that cannot be separated by non-destructive methods; 2.14. European approval for materials, a technical document which defines the characteristics of materials intended for repeated use in the manufacture of pressure equipment not covered by the applicable standards; 2.15. the market-economic activities to supply the pressure equipment or assemblies or not for its distribution or use within the Union; 2.16. the placing on the market – the first placing on the market of pressure equipment or assemblies; 2.17. commissioning – the first time the user uses the pressure equipment or assemblies; 2.18. the manufacturer – natural or legal person who manufactures pressure equipment or assemblies or with the task of pressure equipment and assemblies are designed or manufactured and placed on the market of pressure equipment and assemblies that it under his name or trademark; 2.19. the authorised representative established in the European Union – natural or legal person who has received a written mandate from a manufacturer to act on his behalf in relation to specified tasks; 2.20. the importer established in the European Union – natural or legal person who places on the market of pressure equipment and assemblies from third countries; 2.21. the dealer – natural or legal persons established in, which has a market of pressure equipment and assemblies, and not the manufacturer or the importer; 2.22. the persons involved – the manufacturer, the authorised representative, the importer and the Distributor; 2.23. technical specification-a document which lays down the technical requirements which must comply with the pressure equipment directive or their assemblies; 2.24. the notified body – the national accreditation bodies accredited for pressure equipment and assemblies the 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 their complex pressure equipment reported a conformity assessment body; 2.25. revocation, any measure aimed at achieving that are returned and the complex pressure equipment that has already been delivered to the end user; 2.26. the withdrawal, any measure aimed at preventing the existing supply chain pressure equipment and the placing on the market of the complex; 2.27. the CE marking of conformity – a sign, with which the manufacturer indicates that the pressure equipment and the assemblies complies with the applicable requirements set out in the relevant legislation, which provides for the imposition of this label. 3. These provisions shall not apply to: 3.1. pressure equipment directive and their assemblies with a maximum allowable pressure PS is 0.5 bar and less; 3.2. pipelines, consisting of pipes or pipe systems and is designed for any fluid or transmission of other substances to or from the object (on land and at sea) from the first to the last object in the confines of the as well as all auxiliary equipment, designed specifically for these pipelines. This exception does not apply to standard pressure equipment directive which can be fitted in the pressure reduction stations or compressor station; 3.3. water offtake supply, distribution and network, associated equipment and headraces (such as hydroelectric facilities, spiedtuneļ spiedvad, spiedstobr hydroelectric) and associated special devices; 3.4. equipment set out in laws and regulations relating to simple pressure vessels; 3.5. equipment set out in the laws of the essential requirements and the aerosol bottle labelling and classification; 3.6. equipment of vehicles shall be governed by the following legislation: 3.6.1 on mopeds, motor vehicles, their trailers and the assessment of conformity of constituents; 3.6.2. European Parliament and Council on 5 February 2013 Regulation (EU) No 167/2013 for agricultural and forestry vehicles approval and market surveillance; 3.6.3. European Parliament and Council of 15 January 2013 the Regulation (EU) No 168/13 on two wheels or three-wheel vehicles and quadricycles for the approval and surveillance of the market, including laws on statutory markings for two-or three-wheel motor vehicle conformity assessment; 3.7. equipment in accordance with these rules 10, 11 and 15 point cannot be classified as category I and higher shall be governed by the laws on: 3.7.1. machine safety; 3.7.2. lifts and their safety components in the design, manufacture and installation of lifts and conformity assessment; 3.7.3. electrical safety of equipment; 3.7.4. the registration of medical devices, conformity assessment, distribution, operation and technical supervision; 3.7.5. the installations that use gaseous fuels; 3.7.6. explosive atmospheres-use of equipment and protective systems; 3.8. the arms, munitions and military equipment; 3.9. equipment designed for use in a nuclear accident which may result in the release of radioactive materials; 3.10 shaft inspection facilities for pressure maintenance and (or) the control shaft (shaft control connection equipment, exhaust pipe, manifold retardants and all related equipment) and used in the petroleum, gas or geothermal extraction and exploration, as well as underground storage facilities; 3.11. equipment containing shell or mechanisms that the size, material and construction, to determine the sufficient strength, rigidity and stability requirements to withstand the load arising from the following operating, and that pressure is not the determining factor in the design (for example, engines, turbines and internal combustion engines also, steam engines, gas or steam turbines, turbine generator, compressors, pumps and actuating devices); 3.12. blast furnaces (also a gorgeous cooling system), the karstpūšam recoverers, dust Extractor, and blast-furnace exhaust-gas cleaners, direct reducing cupolas (including the furnace cooling), gas convectors and cups steel, iron and non-ferrous metals shall, de-gassing and casting; 3.13 built-in high-voltage electrical equipment (such as switchgear, control gear, transformers and rotating machines); 3.14. communication system with pipes, pressure (such as electric and telephone cables); 3.15. ships, rockets, aircraft and mobile (floating) natural resources mining platforms, as well as equipment, specially designed for connection with these platforms; 3.16. the pressure equipment directive, which consists of a flexible casing (e.g. tyres, air cushions, balls, inflatable boats and other similar pressure equipment directive); 3.17. the engine intake and exhaust silencer; 3.18. bottles or containers designed for carbonated drinks for direct; 3.19. the containers for the transport and distribution of drinks having a maximum allowable pressure PS does not exceed seven bars and a product of PS and V is not greater than 500 bar/litre; 3.20. the equipment laid down in laws and regulations on the transport of dangerous goods; 3.21. the equipment laid down in laws and regulations concerning the transportation of the pressure equipment directive; 3.22. the equipment laid down in international agreements on the transport of dangerous goods by international waters; 3.23. the facilities established by international agreements on civil aviation; 3.24. radiators and pipes in warm water heating systems; 3.25. vessels designed to contain the liquid in which gas pressure above the liquid level is not greater than 0.5 bar. 4. Pressure equipment and assemblies allowed it to offer the market and put into service if properly installed and maintained, as well as use as intended, to meet the requirements contained in these provisions. 5. the requirements of this Regulation shall not apply to trade fairs, shows, or play in the pressure equipment directive and in trade fairs it package, if it does not comply with the information is clearly indicated that they will not be placed on the market and put into service in until they conform to the rules provided. During demonstrations adequate safety precautions safety and protection. 6. the pressure equipment and the assemblies referred to in that provision in paragraph 8 and 9 and meet the applicable standards (or part) requirements, references to which have been published in the official journal of the European Union, considers appropriate the provisions referred to in Chapter 3, with the essential safety requirements covered by these standards (or parts thereof). 7. National standardisation body shall publish in its tīmekļvietn the list of applicable standards, adapted to national standards. 2. Pressure equipment and assemblies of pressure equipment classifications 8. classify the following: 8.1 the tank (except this rule 8.2. referred to): 8.1.1. gases, liquefied gases, the pressure affect dissolved gases, vapours and liquids having a vapour pressure of maximum allowable temperature TS is more than 0.5 bar above normal atmospheric pressure (1013 mbar) within the following limits: 8.1.1.1. shifting group I substances having a capacity greater than a liter and a product of PS and V greater than 25 bar pressure PS per litre or greater than 200 bar (annex 1); 8.1.1.2. shifting Group II substances having a capacity greater than a liter and a product of PS and V greater than 50 bar/litre or pressure PS greater than 1000 bar, and all portable or mobile fire extinguishers and cylinders for breathing apparatus (Figure 2 of annex 1); 8.1.2. liquids having a vapour pressure of maximum allowable temperature TS is not greater than 0.5 bar above normal atmospheric pressure (1013 mbar) within the following limits: 8.1.2.1. shifting group I substances having a capacity greater than a liter and a product of PS and V greater than 200 bar/litre or pressure PS greater than 500 bar regardless of the volume (Figure 3 of annex 1); 8.1.2.2. Group II substances, which the shifting pressure PS greater than 10 bar and a product of PS and V greater than 10 000 bar/litre or pressure PS greater than 1000 bar regardless of the volume (Figure 4 of annex 1); 8.2. fired or otherwise heated pressure equipment (which may risk overheating) steam or superheated water (if the temperature exceeds 110 ° C), with a capacity of greater than two litres, and all household pressure cookers (annex 5); 8.3. pipelines: 8.3.1. gases, liquefied gases, the pressure affect dissolved gases, vapours and liquids having a vapour pressure of maximum allowable temperature TS is more than 0.5 bar above normal atmospheric pressure (1013 mbar) within the following limits: 8.3.1.1. shifting group I substances whose DN greater than 25 (annex 6); 8.3.1.2. the shifting of the Group II substances whose DN is greater than 32 and a product of PS and DN greater than 1000 bar (Figure 7 of annex 1;) 8.3.2. liquids having a vapour pressure of maximum allowable temperature TS is not greater than 0.5 bar above normal atmospheric pressure (1013 mbar) within the following limits: 8.3.2.1. Group I substances whose shifting DN greater than 25 and a product of PS and DN greater than 2 000 bar (annex 8, Figure 1); 8.3.2.2. the shifting of the Group II substances, which pressure PS greater than 10 bar, a DN greater than 200 and a product of PS and DN greater than 5000 bar (Figure 9, annex 1); 8.4. safety and pressure device this rule 8.1., 8.2. and 8.3. referred to the pressure equipment directive, if this pressure equipment is built or designed for the building of the complex. 9. the complex pressure equipment shall be classified as follows: 9.1. assemblies intended for steam or superheated water (if the temperature exceeds 110 ° C) and contain at least one item of fired or otherwise heated pressure equipment for which the risk of overheating is possible; 9.2. assemblies intended for warm water (if the temperature does not exceed 110 ° C) if solid fuel supply is used in the handmade and the product of PS and V greater than 50 bar/litre, and which comply with that rule 41, 42, 43, 44, 45, 53, 54, 55, and 63.4 in 39.2. these essential safety requirements; 9.3. other complexes, which are not mentioned in these regulations and in paragraph 9.1 9.2 the manufacturer, his authorized representative or the importer intends to offer on the market and putting into use as complexes. 10. This provision of the pressure equipment referred to in paragraph 8 shall be classified into categories in accordance with the provisions of annex 1, according to a growing degree of risk. 11. to classify the pressure equipment, flowing substances are classified in two groups: Group I includes 11.1. substances or mixtures which are pressure equipment with maximum allowable temperature TS, which is higher than the flash point of the pressurized fluid, and the fluid substances that form the substances and mixtures defined by the European Parliament and of the Council of 16 December 2008, Regulation (EC) no 1272/2008 on classification, labelling and packaging of substances and mixtures, and amending and repealing directives 67/548/EEC and 1999/45/EC and Regulation ( No 1907/2006 of the EC), article 2, paragraph 7 and 8 and which are to be classified as dangerous for such hazard classes (physical hazard and danger to health) in accordance with Annex I part 2 and 3 of: 11.1.1 unstable explosive material or explosive materials, which include 1.1., 1.2., 1.3, 1.4 and 1.5. subgroup; 11.1.2.1 and 2, category of flammable gases; 11.1.3. category 1 oxidizing gas; 11.1.4.1 and 2, category of flammable liquids; 11.1.5. category 3 flammable liquids, if maximum temperatures above the flash point; 11.1.6.1 and 2, category flammable solids; 11.1.7. type A to F pašreaģējoš substances and mixtures; 11.1.8. pyrophoric liquids category 1; 11.1.9. category 1 pyrophoric solids; 11.1.10.1, 2, and 3. the categories of substances and mixtures which, in contact with water emit flammable gases; 11.1.11.1, 2, and 3. oxidizing liquids category; 11.1.12.1, 2, and 3. the categories of solid oxidizing substances; 11.1.13. A to type F organic peroxides; 11.1.14. category 1 and 2 substances and mixtures with acute oral toxicity; 11.1.15. category 1 and 2 substances and mixtures with acute dermal toxicity; 11.1.16.1, 2 and 3 substances and mixtures category with acute toxicity inhalatīv; 11.1.17. substances and mixtures with a one-time 1. exposure category-specific toxic effects to irradiation; 11.2. Group II includes other substances or mixtures other than those mentioned in point 11.1 of these rules. 12. Security devices include in category IV, except if the devices are made specifically for the equipment they protect. The safety devices allowed to include in the same category, in which the pressure equipment is protected. 13. the pressure devices are classified according to their maximum allowable pressure PS and the volume V or nominal size DN and the fluid contained in the group for which they are intended, with the corresponding tank or pipeline chart to determine the conformity assessment category. 14. If the pressure device is possible according to classify both by volume and pressure, on the basis of the classification select the size, after which the device is to be granted a higher category. 15. If the tank comprises several cameras, and each is classified in a different category, the tank top classified by categories. If the camera contains several fluids, classification of the substances on the basis of the choice of the substance which is the highest in the group. 16. Pressure equipment and assemblies which characteristics are identical to the rules 8 and 9 mentioned in paragraph or is lower than the ones designed and manufactured in accordance with good practices in technology (the industry's professional recommend use of production technologies), to ensure their safe use. Pressure equipment directive and the package adds the appropriate instructions for use. That pressure equipment and assemblies may not be labelled with the CE marking of conformity. 3. Pressure equipment directive or the package in certain essential safety requirements 3.1 General requirements 17. Obligations arising under this chapter, those with the essential safety requirements of the pressure equipment directive, also applies to the package if the hazard exists. 18. This section above the parties ' obligations are applicable to such pressure equipment directive that the hazard in question when it is used reasonably intended by the manufacturer. 19. the manufacturer shall analyse the risks to determine which of them are associated with the equipment, if it occurs, the pressure, and the pressure equipment so designed and constructed that, taking into account the above analysis. 20. The essential safety requirements are interpreted and applied so as to design and manufacture take account of technical progress and the current practices, as well as technical and economic considerations, which ensure a high level of safety and health protection. 21. the pressure equipment shall be designed, manufactured, tested and, if necessary, be fitted and installed so as to ensure their safety, their transfer to the service in accordance with the manufacturer's instructions, or in reasonably foreseeable conditions. 22. In choosing the most appropriate solutions, the manufacturer, in a particular order, the following principles shall apply: 22.1. eliminate or reduce hazards as far as is reasonably practicable; 22.2. to take appropriate protection measures against hazards which cannot be eliminated; 22.3. If necessary, inform users of residual hazards and indicate whether or not to take special measures to reduce the risk of installation and (or) during use. 23. If there is a possibility that the pressure equipment may be used incorrectly, or it can clearly predict, then, that equipment shall be designed so as to avoid the risk of incorrect use, or, if this is not possible, adequate warning that pressure equipment must not be used in this way. 3.2. the pressure equipment design 24. Pressure equipment shall be designed, taking into account all relevant factors, in order to ensure that the equipment will be safe for the intended operation. 25. the project shall include appropriate safety coefficients using general methods known to be sufficient safety margins against all relevant failure. 26. the pressure equipment designed for loadings appropriate to their intended use and other reasonably foreseeable operating conditions, taking particular account of the following factors: 26.1. internal and external pressure; 26.2. the ambient and operating temperature; 26.3. static pressure and mass of contents in operating pressure equipment and test conditions; 26.4. transportation, wind, earthquake load; 26.5. the reaction forces and moments which result from the supports, for example, auxiliary equipment, pipelines; 16.5. corrosion and erosion, fatigue, etc.; 16.6. unstable the fluid contained in the partition. 27. the calculation of the load, take into account the different loads, which could occur at the same time, taking into account such incidence. 28. In order to ensure sufficient strength, the design uses one of the following methods: 28.1. conventional calculation method in accordance with the provisions of paragraph 29, which, if necessary, supplemented with the provisions referred to in paragraph 30 of the experimental design method; 28.2. the experimental design method without calculation in accordance with the provisions of paragraph 30, where the product of PS and V is less than 6000 bar/litre and a product of PS and DN less than 3000 bars. 29. The normal calculation method takes into account that the pressure equipment must withstand: 29.1. pressure and other loads acting on the pressure equipment during its operation. The levels of pressure equipment voltage limits, taking into account the operating conditions, the reasonably foreseeable disturbance. For this purpose, the safety factors applied to completely eliminate all the confusion caused by the manufacture, actual operating conditions, voltage, calculated way, material properties and behavior. Calculating the resistance, use one of the methods which ensure sufficient safety thresholds, which correspond to the provisions of section 3.7 requirements, if necessary, supplementing or in combination with any of the following methods: 29.1.1. Design, using a formula. 29.1.2. Design based on analysis; 29.1.3. designing based on disruptive mechanics; 29.2. pressure equipment must have sufficient resistance ability: design pressure is not 29.2.1. less than the maximum pressure, account has been taken of the excess static, dynamic fluid pressures and the decomposition of the fluid. If the tank is split into individual pressure-containing Chambers, the separating wall strength is calculated on the basis of the highest possible chamber pressure relative to the lowest pressure of adjacent cells; 29.2.2. used in the calculation of the temperature, which ensures sufficient safety of limit values; 29.2.3. designing followed all possible combinations of temperature and pressure, which can occur in foreseeable operating conditions the equipment; 29.2.4. voltage and voltage maximum concentration values are safe; 29.2.5. spiedienizturīb is used in the calculation of the values that correspond to the characteristics of materials, the documented data, having regard to the provisions of section 3.4 above requirements and appropriate safety coefficients. Where relevant, comply with the following characteristics: the material yield strength-29.2.5.1.0.2% or 1.0% of checks the strength calculation temperature; 29.2.5.2. tensile strength; 29.2.5.3. laikatkarīg strength, i.e. creep strength; 29.2.5.4. fatigue; 29.2.5.5. Jung module (the module of elasticity); 29.2.5.6. the relevant size of plastic deformation; 29.2.5.7. the wrecking job leave; 29.2.5.8. lūzumizturīb; 29.2.6. use relevant material connection coefficients, for example, depending on the type of non-destructive testing, the materials joined and the operating conditions envisaged; 29.2.7. project provides the strength of graujošo all possible factors (e.g. corrosion, creep, fatigue) that matches the intended use of the equipment. 53. These provisions, 54, and 55 in the instructions referred to in paragraph indicate specific design features, of which depend on the duration of the operation of an installation, for example: 29.2.7.1. creep-design life in certain temperatures; 29.2.7.2. fatigue-design number of cycles at specified stress levels; 29.2.7.3. corrosion-corrosion design tolerance; 3. If the calculated thickness does not provide adequate stability of the structure, take the necessary measures to ensure the stability of the pressure equipment to prevent accident hazards during transport or handling. 30. Experimental design method is based on testing the program: one is made 18.7. copies or pressure equipment pressure equipment group; 30.2. clearly reflect the testing programme, approved by the notified body, which shall carry out the assessment of conformity of the project; 30.3. define test conditions and acceptance or rejection criteria. Before the test, the size of the actual key size and determine the characteristics of the materials from which created the test equipment; 18.9. the test run time provides the opportunity to assess critical areas of pressure equipment with suitable instruments for determining deformation and voltage; 5. include the following tests: 30.5.1. strength test with pressure to see if the pressure does not cause significant leaks or deformation exceeding a determined threshold (subject to safety margin in relation to the maximum pressure). The test pressure shall be determined on the basis of the testing conditions for differences between the geometric dimensions and characteristics of the material values and the values that are in the project. Observe the differences between the test and design temperatures; 30.5.2. If the risk of creep or fatigue exists, appropriate tests for the conditions of use of the equipment (for instance hold time at specified temperatures, number of cycles at specified stress levels); 30.5.3. If needed, additional tests other rules referred to in paragraph 26 of the factors (such as corrosion, external damage). 31. the pressure equipment for operational method is one in which all the equipment in action prevent reasonably foreseeable risks, taking into account in particular the following factors: 31.1. seals and vents; 31.2. dangerous the pressure in the exhaust from the overpressure valves; 31.3. devices that prevent physical access to the machine, if there is an increased pressure or vacuum; 19.5. surface temperature taking into consideration the intended use; 31.5. unstable fluid degradation of the substances. 32. the pressure equipment with the access door shall be fitted with a special automatic or manually operated device that lets the user easily to ascertain that the opening will not risk. In addition, where the opening may be quick, pressure equipment shall be equipped with a device to prevent the opening when the fluid pressure or temperature of the substance poses a risk. 33. the pressure equipment shall be designed and constructed so as to be able to perform all the necessary checks and make sure of its safety. 34. If necessary to ensure the safety of the equipment, construction of permanent provides funds of determining the internal condition of the equipment (for example, the access openings), allowing physical access to the inside of the pressure equipment concerned, checks are carried out safely and ergonomically. 35. where the pressure equipment is too small to be physically accessed from inside, or if opening the pressure equipment would adversely affect the inside, or if it is shown that the substance is not contained hazardous material from which the pressure equipment is made, and not reasonably foreseeable internal strength in other disruptive factors, you can use other means to ensure the safe condition of the pressure equipment. 36. Ensure appropriate means of drainage and ventilation of the pressure equipment so that, if necessary: 36.1. avoid harmful consequences (such as hydraulic shocks, vacuum collapse, corrosion caused by uncontrolled chemical reactions). Look at all the stages of the operational and testing, particularly pressure testing; 36.2. the cleaning, inspection and maintenance can be carried out safely. 37. If necessary, provide sufficient clearance or corrosion, protection against corrosion or other chemical damage, taking account of the intended and reasonably foreseeable use. 38. If the use of pressure equipment may result in serious erosion or abrasion: 38.1. take adequate measures to reduce their effects (such as increased material thickness or using inlays or coatings); 38.2. the possibility to exchange the most defective parts; 23.8. these rules 53, 54 and 55. paragraph instructions include the requirements for the safe use of pressure equipment. 39. The package shall be so designed that: 39.1. incompatible ingredients meet requirements and are safe to use; 39.2. all the ingredients combine properly and assembled in an appropriate manner. 40. If necessary, pressure equipment shall be designed and fitted with accessories or provide for the possibility of adding it to ensure safe filling and discharge, in particular, to the following risks: 24.9.-transfusion over the filling, exposure to too much pressure (especially considering the filling ratio and to vapour pressure at the reference temperature) and instability of the pressure equipment; 40.2., pressure emptying the uncontrolled release of the pressurized fluid; the filling or emptying of 40.3. — unsafe connection and disconnection. 41. where reasonably foreseeable conditions allowable limits could be exceeded, the pressure equipment shall be fitted with suitable safety devices or provide for the possibility of accession, unless the equipment protected by other complex security devices. 42. Protection devices or combinations of such devices is selected based on characteristics of pressure equipment or assemblies. Pressure equipment needed: 42.1. safety devices; 26.2. sufficient control devices (such as light and (or) the alarm) that, if necessary, automatically or manually allows you to take appropriate steps to keep the pressure equipment within the allowable. 43. security devices are: 43.1. designed and constructed to meet the requirements of the prescribed safe use and compliance with the maintenance and testing requirements; 43.2. independent of other functions, unless these other functions do not affect the safety function; 43.3. the appropriate design principles in order to achieve adequate and secure protection (including fail-safe mode, back up, diversity and self-diagnosis). 44. Pressure limiting devices shall be so designed that the pressure will not permanently exceed the maximum allowable pressure PS. If necessary, short-term pressure increase under this provision in paragraph 65 of those specifications. 45. Temperature control devices reliability is enough reaction time, which corresponds to be measured. 46. If necessary, pressure equipment shall be designed and fitted with accessories or, if necessary, provide for the possibility of adding it to the equipment, taking into account its intended use, comply with the requirements limiting the damage an external flame. 3.3. Pressure equipment manufacture 47. Producer, using appropriate methods of work and procedures, ensure the design stage with the rules, especially given that: 29.3. preparation of the component parts (such as the building and chamfering) must not present defects, cracks or mechanical properties changes that could reduce the safety of pressure equipment; 47.2. the connections that can be disassembled with destructive methods (permanent connection), and the connection zone (surface) is not external or internal defects that may impair the safety of pressure equipment; 47.3. permanent connection to compatible materials provides minimum requirements if the calculations are not subject to special requirements; 47.4. pressure equipment, which is in direct pressure, and ingredients that they directly attached permanent connection is carried out by qualified personnel in accordance with the appropriate procedures. Category II, III and IV of the pressure equipment directive these operating procedures, as well as the qualifications of the personnel concerned, the notified body or approved notified body, whose activities are concerned only with the operating procedures and staff approval (approval must be carried out before the issue of the applicable standards prescribed verifications and tests or equivalent examinations and tests); 29.5. pressure equipment connections not sagraujošo tests are performed according to the qualifications of the staff. Category III and IV pressure equipment directive these tests take staff qualifications approved by the notified body, whose activities are concerned only with the approval of the personnel; 29.6. the relevant production stages require a suitable heat treatment, if the manufacturing process material properties may vary to the extent that you can reduce the pressure equipment safety; 29.6. the materials that will be exposed to pressure, represents the (identify) and stores at every stage of manufacture to the final assessment of the pressure equipment produced. 48. to make the final assessment of the pressure equipment – the final test, strength test and assessment of the safety devices: 29.9. final inspection of pressure equipment evaluated visually examine the technical documentation and assess its compliance with the requirements of this regulation, also be taken into account at the time of making the performance of the tests. If necessary, the final examination in the course of the manufacture of pressure equipment shall be carried out for each part of the inside and outside (for example, when closing the checks during the control no longer possible); 48.2. the strength of the machine with the hydraulic pressure test of not less than that referred to in paragraph 69 of the rules. If the hydraulic is dangerous or not useful, you can take other equivalent examination (before equivalent checks made mandatory connection not sagraujošo tests or equivalent tests in accordance with the applicable standards). Pressure equipment directive category I, which are produced in series, strength inspection can be performed by using statistical methods; 48.3. the safety devices evaluated by checking their compliance with these rules, and 43 41 42. the requirements referred to in paragraph. 49. in addition to these provisions in Chapter 9 that the CE conformity marking to all pressure equipment directive specifies the following information: 30.5. name and address of the manufacturer or other identification of the manufacturer, and (if possible) the authorized representative of the manufacturer in Latvia; 30.6. the importer's name and address or other identification data of the importer; 30.6. year of manufacture; 49. the identification data of the pressure equipment according to its nature (for example, type, product ID, number); 30.8. main and (or) minimum maximum permissible limiting values. Maximum allowable pressure PS manufacturer indicates where you add aizsargietais and (or) restrictive devices or equipment at the top, or, if those sites are not appropriate in any other appropriate place. 50. Depending on the type of pressure equipment shall bear the following information, which requires the type of pressure equipment for safe installation, use, maintenance and periodic inspection of pressure equipment: 50.1. V (liters); 50.2. piping nominal size DN; 50.3. strength test pressure PT (bars) and date; 50.4. the safety devices set pressure (in bars); 50.5. pressure equipment in the outgoing power (kW); 50.6. electric power network voltage (V); 50.7. the purpose of the intended use; 50.8. filling degree (in kg/l); 50.9. maximum fill weight (kg); 50.10. tare weight (kg); 50.11. flowing substance group (according to this provision, paragraph 11). 51. If necessary, to pressure equipment shall be placed, also clearly legible pictograms and warning signs to ensure the correct use of pressure equipment. 52. The CE marking of conformity and the 49 and 50 of these provisions the information referred to in paragraph patterned directly on the pressure equipment or on pressure equipment firmly attached to the plate, except in the following cases: 52.1. to avoid marking of pressure equipment if they intended to combine complex, the information in the technical dossier; 52.2. the pressure equipment or equipment if the size is not large, this provision of the information referred to in paragraph 50 shall be indicated on the label attached to that pressure equipment which. 53. If the pressure equipment on the market, it is necessary to use the language of the country of the instruction, which contains the necessary information for safety: 53.1. Assembly, including individual pressure equipment items; 53.2. commencement of the use; 53.3.; 53.4. maintenance and monitoring, including the user checks to be carried out. 54. the package leaflet shall contain the information specified for pressure equipment in accordance with the provisions of paragraph 49 and 50 (with the exception of the series), as well as add technical documentation, drawings, charts and calculations, if it helps to understand the instructions for use. 55. The instructions warn about the threat of accidents which may occur when pressure equipment is used incorrectly (23 of these rules), and specify the particular features of the design (this provision 29.2.7.). 3.4. requirements for pressure equipment in the easy-to-use 56. Pressure equipment materials made of materials that are suitable for the respective functions of all intended use until their replacement. 57. Materials intended for use in pressurized surfaces must be: 57.1. with appropriate characteristics under all foreseeable conditions of use and inspection; 57.2. sufficiently flexible, tough, and, where necessary, steel characteristics must comply with the rules in paragraph 70. If specific reasons brittle material is used, take appropriate measures to prevent this tearing the material; 57.3. enough with the chemical pressure equipment in the existing substances. The chemical and physical properties of the preparation necessary for the safe use of pressure equipment, the foreseeable use of the pressure equipment may not change significantly; 57.4. enough with the aging; 57.5. suitable for the intended processing procedures; 57.6. so as to avoid unwanted effects, which can arise by connecting different materials. 58. the pressure equipment manufacturer: 58.1. in question qualifies this provision referred to in paragraph 29 of the design calculation of the required size and this provision in paragraph 57 of that most basic of materials and their processing; 58.2. provides technical documentation elements relating to compliance with these rules, the following material specifications, in one of the following ways: 58.2.1. by using materials which comply with the applicable standards; 58.2.2. using the materials in accordance with the provisions of Chapter 6 is included in the European material approval for pressure equipment materials; 58.2.3. with special material; 58.2.4. using materials that specific evaluation categories III and IV pressure equipment directive notified body that carried out the pressure equipment conformity assessment procedures. 59. The materials that are used in welding or other connecting elements, only apply this rule 58.1. the requirements referred to in point. 60. the manufacturer of pressure equipment shall take appropriate measures to ensure the compliance of the materials used in the manufacture of the requirements of the project. All materials needed for the materials prepared by the manufacturer of the documents that contain the material in compliance with the requirements of the project. Materials that are used in the manufacture of pressure parts II, III and IV in the categories of pressure equipment, you need a certificate of compliance with this provision of the materials. 61. If the manufacturer of the material is of a quality system that is certified by the competent conformity assessment bodies, and materials are subjected to special tests, then the certificate that is issued by the manufacturer, shall be sufficient proof of this provision that the requirements in paragraph 60. 3.5. Additional requirements with an open flame or otherwise heated pressure equipment directive, for which the risk of overheating may 62. With an open flame or otherwise heated pressure equipment with a risk of overheating may have: 62.1. This provision mentioned in paragraph 8.2. steam and hot water or liquid tanks (e.g. flame-heated steam and hot water or liquid boilers, steam and ekonomaizer, Super-heaters heating boiler emissions, emissions combustion boilers , elektroteņ or electrode type boilers, household pressure cookers, together with their devices and systems in water and fuel supply); 62.2. sildiekārt, which is not used for steam and hot water production, but its operational characteristics, refer to the rules referred to in point 8.1 pressure equipment directive (for example, chemical and similar processes generate heat heater and food production machines, which is the pressure). 63. the pressure equipment referred to in this section shall be designed and constructed so as to reduce the risk of overheating, and take appropriate measures to avoid flammable, combustible substances and air mixture accumulation or flame, as well as its rebound provides: 39.2. appropriate remedies, which restricts the use of parameters (such as heat input, heat discharge and the fluid level), to prevent local or General overheating; 39.3. fluids sampling points, to determining the properties of these substances, avoid risks related to deposits and/or corrosion; 63.3. appropriate means, which reduces the risk of sediment; 63.4. appropriate means that after the machine off safely into the remaining heat. 3.6. Additional requirements for pipelines that rule 64.8.3. referred to in and construction of the pipeline project: 64.1. voltage control of the pipelines by appropriate means (for example, by supporting, forcing, anchor, and previously regulated the pretension), if the voltage of any permissive play or manufacturing process (residual voltage, such as coupling, or hose connections); 64.2. appropriate means for cleaning and removal of deposits from low areas to avoid damage that may cause hydraulic shock or corrosion, if is possible the emergence of a gaseous condensate from flowing substances inside of pipelines; 64.3. with due regard to the potential damages caused by turbulent flow; 64.4. due attention to material fatigue, the pipeline caused by vibration; 64.5. useful features that help to disconnect the drain pipe if the pipe contains a fluid substance in Group I and it can lead to an accident; 64.6. to deploy the pipeline clear indication of emptying area and the products that contain the pipeline to reduce risks that can lead to rough; emptying of the pipeline 64.7. include technical documentation for underground pipeline system housings and direction, to facilitate pipeline system maintenance, inspection or repair. 3.7. Specific quantitative requirements of pressure equipment directive 65. Permissible voltage labels are as follows: 65.1. Re/t – tensile limit calculation temperature: 65.1.1., the upper yield point, the value of materials which are of lower and upper yield stress; 65.1.2.1.0% checks the value of strength of austenitic steel and non-alloyed aluminium; 0.2% strength 65.1.3. value of other test materials; 65.2. Rm/20-strength limits the minimum value of 20 ° C; 65.3. Rm/t-strength limit calculation temperature. 66. the permissible voltage pamatapvalk of pressure equipment that provides resistance to static loads, outside temperature range in which creep may not be exceeded (depending on material) the smaller of the following values: 66.1. ferrite steel (including normalized (normalized rolled) steel) excluding fine-grained steel and hot-processed steel, 2/3 of Re/t and 5/12 of Rm/20; 66.2. austenitic steel, if its elongation after bursting exceeds 30%,-2/3 of Re/t; 66.3. austenitic steel, if the extension exceeds 35%, after bursting – 5/6 of Re/t and of Rm/t 1/3; 66.4. non-alloy or low steel castings – 10/19 of Re/t and 1/3 of Rm/20; 41.3. aluminium – 2/3 of Re/t; 66.6. aluminum alloy, except sediment precipitation hardening alloys, 2/3 of Re/t and 5/12 of Rm/20.67. Welded joints connecting factor must not exceed the following values (respecting the type and connection voltage the mechanical and technological characteristics): 67.1. equipment which connections are made disruptive and non-destructive testing, certifying that all the connection sequence has no significant defects,-1; 67.2. equipment which connections are made of random non-destructive testing: 0.85; 67.3. equipment connections No non-destructive testing, but only for Visual inspection,-0.7.68. Pressure limiting devices in the pressure equipment must withstand this provision, paragraph 44 temporary increase pressure within 10% of the maximum allowable pressure. 69. This rule 48.2. referred to a hydraulic test pressure of the pressure equipment directive must not be less than the higher of the following values: 69.1. maximum load of pressure equipment during operation, taking into account its maximum allowable pressure PS, multiplied by the coefficient 1.25, and maximum temperature; EB 69.2. maximum allowable pressure PS, multiplied by the coefficient 1.43.70. If the steel material is not defined more specific criteria, it is assumed that the steel meets this rule 57.2. the requirements referred to in subparagraph, if the extension of the standard tensile test procedure after the bursting of not less than 14% and its wrecking job put at ISO V test sample shall not be less than 27 J, at a temperature of no higher than 20 ° C, as well as does not exceed the lowest operating temperature. 4. responsibilities of the parties involved 71. Parties concerned by the market surveillance authorities to request information on the pressure equipment directive and their complexes, including: 71.1. all parties which they supplied pressure equipment or assemblies; 71.2. all parties, which they supplied pressure equipment or assemblies. 72. the parties concerned shall ensure that the provisions referred to in paragraph 71 of the accessibility of information to the supervisory authority of the market 10 years after they delivered the pressure equipment or assemblies or the supplied pressure equipment or assemblies. 4.1. The manufacturer's obligations 73. This provision within the meaning of the importer and the distributor shall be considered a manufacturer and has the responsibilities referred to in this subsection, if it is placed on the market of pressure equipment and assemblies under his name or trademark or modifies the pressure equipment placed on the market and their complexes that may affect the conformity of the pressure equipment and the assemblies of these provisions referred to in Chapter 3, with the essential safety requirements. 74. The placing on the market of these rules 8 and 9 of the pressure equipment referred to in paragraph 1 and their complex or using them for their own use, the manufacturer shall ensure that they are designed and manufactured in accordance with the provisions referred to in Chapter 3 of the essential safety requirements. 75. The placing on the market of these provisions referred to in paragraph 16 of the pressure equipment or assemblies, or using them for their own purposes, the manufacturer provides to be designed and constructed in accordance with good engineering practices (industry professional organizations proposed the use of technology in production). 76. This provision in paragraph 8 and 9 of those pressure equipment directive or the package manufacturer prepares this provision as referred to in Chapter 5 of the technical documentation and carry out the appropriate provisions of Chapter 5 of the mentioned conformity assessment procedure or provide them. 77. If this provision in paragraph 76 that procedure have shown that these rules 8 and 9 of the pressure equipment referred to in paragraph 2 or the package complies with the applicable requirements, the manufacturer shall draw up a declaration of conformity and affix the CE conformity marking. 78. the manufacturer shall keep the technical documentation and Declaration of conformity for 10 years from the pressure equipment or assemblies on the market. 79. where the pressure equipment or assemblies are produced in series, the producers provide a control procedure to ensure the pressure equipment or assemblies the conformity with the requirements of this regulation, and taking into account changes in the pressure equipment or assemblies or design characteristics, as well as the applicable standards or other technical specifications, which attests conformity of the pressure equipment or assemblies the requirements of this regulation. 80. If the pressure equipment to be evaluated, or the complex risks, manufacturers test and assess the market pressure equipment or assemblies, keep complaining, and recall from the market of pressure equipment or assemblies which it registers as well as inform distributors of the operations. 81. The manufacturer shall ensure that on the market of pressure equipment or assemblies is a type, batch or serial number or other item, after which they can be identified, or, if the pressure equipment or assemblies the size or nature of the do not allow, that the required information is indicated on the packaging or on the pressure equipment or an Assembly in the attached document. 82. the manufacturer of pressure equipment or assemblies to, or, where that is not possible, on the packaging or attached to the pressure equipment or an assembly language in the document shall indicate their name or registered trade mark and the address at which you can contact the manufacturer. 83. the manufacturer shall ensure that the provisions of paragraph 8 and 9 listed in the pressure equipment directive or the package in accordance with this provision, 53, 54 and 55 above. has added to the instructions and safety information in the national language. Instructions for use and safety information, as well as to the pressure equipment directive or other complex specified information is clear and understandable. 84. the manufacturer shall ensure that the provisions referred to in paragraph 16 of the pressure equipment or assemblies are added to the operating instructions and safety information in the national language. Instructions for use and safety information, as well as to the pressure equipment directive or other complex specified information is clear and understandable. 85. If the manufacturer believes that the pressure equipment or assemblies which it has placed on the market do not meet the requirements of this regulation, it shall immediately take the corrective action to ensure that the pressure equipment or assemblies the conformity with the requirements of this regulation or, if necessary, revoke or withdraw it from the market. If the pressure equipment or assemblies of risk, manufacturers shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and of the corrective actions taken. 86. the market surveillance authorities on request the manufacturer to provide it with all necessary information and documentation in the national language, to demonstrate compliance with the pressure equipment or assemblies the requirements of these provisions. 87. the market surveillance authorities shall cooperate with the request of the manufacturer, the market surveillance authority, on any action to avoid the pressure equipment placed on the market or the complex risks. 4.2. obligations of the authorised representative, 88. Producer with written mandate can appoint an authorized agent. The mandate does not include this provision, 74, 76 and 77.75. the obligations referred to in paragraph 1. 89. The authorized representative shall carry out at least the following obligations: 89.1.10 years after complex pressure equipment or stores on the market the market available to the supervisory authority of the Declaration of conformity and the technical documentation; 89.2. upon reasoned request, the market surveillance authorities shall provide all the information and documentation necessary to demonstrate the conformity of the pressure equipment or assemblies; 89.3. subject to authorisation by the market surveillance authorities to cooperate with their request, on any action taken to eliminate the pressure equipment or assemblies which risks posed them. 4.3. responsibilities of the importer. Importers are placed on the market in accordance with the provisions of the pressure equipment and the assemblies. 91. before these rules 8 and 9 of the pressure equipment referred to in paragraph 1 or a combination of the placing on the market importers shall ensure that the manufacturer, in accordance with the provisions of Chapter 5 is done properly the conformity assessment procedure, prepared by the appropriate technical documentation, or complex pressure equipment labelled with the CE marking of conformity, added instruction manual and the safety information in accordance with this provision, 53, 54 and 55., as well as these provisions have fulfilled and 82 81. obligations listed in paragraph. 92. before paragraph 16 of these rules in the pressure equipment or assemblies referred to on the market importers shall ensure that the manufacturer has drawn up the relevant technical documentation, add the appropriate operating instructions, as well as these provisions have fulfilled and 82 81. obligations listed in paragraph. 93. If the importer believes that the pressure equipment or assemblies do not satisfy the essential safety requirements of the pressure equipment or assemblies that are not placed on the market until such time as the person involved was not made to compliance with this provision with the essential safety requirements. If the pressure equipment or assemblies presents a risk, the importer shall inform the manufacturer and the market surveillance authorities. 94. the pressure equipment or assemblies in the importer's country shall indicate their name or registered trade mark and the address where you can contact the importer. If this information is needed to specify the pressure equipment or assemblies in the package is opened, it shall be indicated on the packaging or on the pressure equipment or an Assembly in the attached document. 95. The importer shall ensure that the pressure equipment or assemblies referred to in articles 8 and 9 of these regulations, in accordance with this provision, 53, 54 and 55 above. has added to the instructions and safety information in the national language. 96. The importer shall ensure that the pressure equipment or assemblies referred to in paragraph 16 of these rules are added to the operating instructions and safety information in the national language. 97. importers shall ensure that, at a time when it is responsible for the pressure equipment directive or a combination of these provisions in paragraphs 8 and 9, the storage or transport conditions do not adversely affect their compliance with the provisions referred to in Chapter 3, with the essential safety requirements. 98. Where appropriate, the importer, taking into account the pressure equipment or assemblies the risks posed, take the pressure equipment on the market or their complex sample testing and examination, the complainant maintained the non-compliance and recall from the market of pressure equipment or assemblies, as well as the register shall inform distributors of the operations. 99. If the importer believes that the pressure equipment or assemblies which it has placed on the market do not meet the requirements of this regulation, it shall immediately take the corrective action to ensure that the pressure equipment or assemblies the conformity with the requirements of this regulation or, if necessary, revoke or withdraw it from the market. If the pressure equipment or assemblies of risk, importers shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and corrective actions taken. 100. The importer, 10 years after the pressure equipment or assemblies stored in the placing on the market of the market available to the supervisory authority a copy of the Declaration of conformity, as well as the market surveillance authority shall ensure the availability of technical documentation. 101. the market surveillance authorities on request, the importer shall provide it with all necessary information and documentation in the national language, to prove the conformity of the pressure equipment or Assembly requirements of these provisions. 102. the market surveillance authorities shall cooperate with the request of the importer, the market surveillance authority, on any action to avoid the pressure equipment placed on the market or the complex risks. 4.4. obligations of Distributors offering 103. pressure equipment on the market or their complexes, with the appropriate distributor diligence to comply with the requirements of this regulation. 104. before these rules 8 and 9 of the pressure equipment referred to in paragraph 1 or a combination of the market, the dealer will make sure that the pressure equipment or assemblies are marked with the CE marking, in accordance with this provision, 53, 54 and 55 above. has been added to the documentation, instructions for use and safety information in the language of the country and that the manufacturer has noticed this provision and paragraph 81.82. the requirements referred to in but these provisions, the importer-94. the requirements referred to in paragraph 1. 105. If the dealer believes that the pressure equipment or assemblies do not comply with the provisions referred to in Chapter 3, with the essential safety requirements, it does not offer the market pressure equipment or assemblies until the person involved was not made to compliance with this provision with the essential safety requirements. If the pressure equipment or assemblies of risk, the distributor shall inform the manufacturer or the importer and the market surveillance authorities. 106. before the provisions referred to in paragraph 16 or complex pressure equipment on the market, distributors shall ensure that pressure equipment or an Assembly is added to the corresponding instructions for use and the manufacturer is subject to the rule in paragraph 82 and 81. those requirements, but the importer-this provision, paragraph 94. 107. The distributor shall ensure that, while it is responsible for this provision in paragraph 8 and 9 of those pressure equipment directive or their complexes, storage or transport conditions do not adversely affect their compliance with the provisions referred to in Chapter 3, with the essential safety requirements. 108. If the dealer believes that the pressure equipment or assemblies which that is offered on the market do not meet the requirements of this regulation, it shall ensure that the necessary remedial action to ensure compliance of the pressure equipment or assemblies of these rules or, if necessary, revoke or withdraw it from the market. If the pressure equipment or assemblies of risk, distributors shall immediately inform the market surveillance authority, giving details, in particular, of the non-compliance and corrective actions taken. 109. the market surveillance authorities on request, the distributor shall provide it with all necessary information and documentation in the national language, to prove the conformity of the pressure equipment or Assembly requirements of these provisions. 110. the market surveillance authorities on request, the distributor shall cooperate with the market surveillance authority, on any action to avoid the pressure equipment on the market or the complex risks. 5. Conformity assessment procedure 111. Chapter 5 of these regulations of such requirements apply to the pressure equipment directive pressure equipment complex. 5.1. General requirements 112. The conformity assessment procedures applicable for pressure equipment shall be determined according to the category to which the equipment is classified. The applicable conformity assessment procedures: 112.1. (I) category: 112.1.1. Module A; 112.2. Category II: 112.2.1. A2 module; 112.2.2. Module D1; 112.2.3. E1 module; 112.3. Category III: 112.3.1. B (project type) module + module D; 112.3.2. B (project type) module + module F; 112.3.3. B (product type) module + module E; 112.3.4. B (product type) module + C2 module; 112.3.5. (H) module; 112.4. Category IV: 112.4.1. (B) (product type) module + module D; 112.4.2. B (product type) module + module F; 112.4.3 G module; 112.4.4. Module H1. 113. the pressure equipment directive may be chosen by the manufacturer shall be subjected to one of the conformity assessment procedures laid down in the relevant category in which it is classified. The manufacturer may also choose to apply one of the procedures that apply to the higher category, if available. 114. the pressure equipment in categories III and IV referred to in that provision, and 8.1.1 8.1.2.1. in paragraph 8.2., quality assurance procedures, the notified body carries out within the framework of the visit, without warning, take a sample of equipment from the manufacturing or storage premises in order to make a final assessment or provide them out according to this provision, paragraph 48. The manufacturer shall inform the notified body of the intended production schedule. The first production year the notified body shall carry out at least two visits. The frequency of subsequent visits, the notified body shall determine, on the basis of the criteria laid down in the D, E, H and H1 modules. 115. If category III of each tank and pressure equipment referred to in paragraph 8.2 of these provisions, the separately produced pursuant to a procedure, module H, the notified body shall carry out the final evaluation of each unit under paragraph 48 of these rules. The manufacturer shall inform the notified body of the intended production schedule. 116. This provision of the pressure equipment referred to in point 9 of the general assemblies the conformity assessment procedure, which shall include such assessment: 116.1. assessment for each of the provisions referred to in point 8 of the pressure equipment within the complex, if it has not been subject to conformity assessment procedures, and is not marked with the CE marking of conformity. The evaluation procedure shall be determined for each category of pressure equipment; 116.2. assessment of how various ingredients creates this rule 31, 39 and 40, paragraph evaluation of complex, according to the highest category of the equipment, the differing categories of security devices; assessment of pressure equipment of 116.3. complex for protection against this provision in paragraph 41 and 48.3. the permissible actions referred to above, the limits of the evaluation carried out by the highest category applicable to any of the ingredients of the protected equipment. 117. If it is justified, the market surveillance authority may permit the placing on the market and put into service in the territory of Latvia individual components of pressure equipment and assemblies which do not fit in these rules referred to in paragraph 112 of the conformity assessment procedures and used for experimental purposes. 5.2. Internal production control (module A) 118. Internal production control is the conformity assessment procedure whereby the manufacturer fulfils the rule 119, 120, 121, 122, and 123. obligations listed in paragraph, as well as provides and declares on his sole responsibility that the pressure equipment concerned satisfy the requirements of this regulation. 119. the manufacturer shall prepare technical documentation that provides the ability to assess the conformity of the pressure equipment with the applicable requirements of this regulation, and includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 119.1. General description of the pressure equipment; 119.2. sketch project and production drawings, components, assemblies, power circuits and other schemes; 119.3. descriptions and explanations necessary for the drawings and diagrams and the operation of the pressure equipment understanding; 119.4. it applicable in full or in part a list of standards for which references have been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 119.5. project carried out calculations and of the inspections carried out and other results; 119.6. test report. 120. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure compliance of the pressure equipment manufactured in the rules referred to in paragraph 119. technical documentation and with the requirements of this regulation. 121. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of these regulations. 122. the manufacturer shall draw up a written pressure equipment of each declaration of conformity with the technical documentation, ensure availability of market surveillance authorities for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 123. The manufacturer's authorised representative may meet this provision and 121 122. producers referred to the obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.3. Internal production control and monitoring of pressure equipment inspections at random intervals (A2 module) 124. Internal production control and monitoring of pressure equipment checks at random intervals is the conformity assessment procedure whereby the manufacturer fulfils the rule 125, 126, 127, 128, 129 and 130.. the obligations referred to in paragraph 1, as well as ensures and declares on his sole responsibility that the pressure equipment concerned satisfy the requirements of this regulation. 125. the manufacturer shall prepare technical documentation that provides the ability to assess the conformity of the pressure equipment with the applicable requirements of this regulation, and includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment, covering design, manufacture and operation. Technical documentation, if applicable, includes at least the following elements: 125.1. General description of the pressure equipment; 125.2. sketch project and production drawings, components, assemblies, power circuits and other schemes; 125.3. descriptions and explanations necessary for the drawings and diagrams and the operation of the pressure equipment understanding; 125.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 125.5. the project's calculations and of the inspections carried out and other results; 125.6. test reports. 126. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure compliance of the pressure equipment manufactured in the rules referred to in paragraph 125. technical documentation and with the requirements of this regulation. 127. the manufacturer shall take the final assessment of the pressure equipment, and monitored the notified body chosen by the manufacturer, by going visits without warning. 128. The notified body after a certain random intervals carry out or Commission checks on pressure equipment internal inspections of the quality of the pressure equipment technology also complexity and volume of production. Go visit without notice, notified body: 128.1. check that the manufacturer actually performs final assessment in accordance with paragraph 48 of these rules; 128.2. take samples of pressure equipment manufacturing or storage premises in order to conduct checks. The notified body assesses the number of items of equipment to sample and whether it should be carried out (or ask to make a) full or partial pressure equipment samples of the final assessment. 129. The applicable sampling procedures aims to determine whether pressure equipment manufacturing process is within acceptable limits, in order to ensure compliance of the pressure equipment. If one of the pressure equipment or Assembly unit or several units are not adequate, the notified body shall take appropriate measures. 130. the manufacturer to the notified body in the production process of responsibility obliges the notified body identification number. 131. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of these regulations. 132. the manufacturer shall draw up a written pressure equipment of each declaration of conformity with the technical documentation, ensure availability of market surveillance authorities for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 133. The manufacturer's authorised representative may fulfil this provision. 132.131 and producers referred to the obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.4. the EU type-examination (module B) 5.4.1.134. EU type examination production type examination is the part of a conformity assessment procedure whereby a notified body examines the technical design of the pressure equipment, as well as ensure and certify that the pressure equipment in the technical design meets the requirements of this regulation. 135. the EU type examination carried out production as the pressure equipment technical project evaluation, examination of the rules referred to in paragraph 136 of the technical documentation and supporting evidence, as well as checking the pressure equipment samples ready, representative for the production envisaged. 136. the EU type-examination must be lodged by the manufacturer shall be filed in one of the notified body of his choice. The application shall contain the following information and documentation: 136.1. the name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 136.2. a written declaration that the application has not been lodged with any other notified body; 136.3. technical documentation. The technical documentation provides an opportunity to assess the conformity of the pressure equipment with the applicable requirements of these regulations, and it includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 136.3.1. General description of the pressure equipment; 136.3.2. contests and drawings, production of components, sub-assemblies, circuits and other power schemes. 136.3.3. the descriptions and explanations necessary drawings and schemes and the operation of the pressure equipment understanding; 136.3.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 136.3.5. project carried out calculations and of the inspections carried out and other results; 136.3.6. the test report; 136.3.7. information about the tests provided for in manufacture; 136.3.8. information concerning the qualifications or approvals required under this provision, 47.3, 47.2 and 47.5 47.4. section; 136.3.9. samples, representative for the production envisaged. The sample may refer to several types of pressure equipment provided that the differences between the type do not affect the level of safety; 136.4. additional samples requested by the notified body and, if needed, to perform the program of testing evidence confirming the compliance of the technical design solution. This supporting evidence indicates all used documents (especially if not fully appropriate applicable standards). Supporting evidence, if necessary, include the results of tests carried out in accordance with other relevant technical specifications the manufacturer's task and responsibility carried out by the appropriate laboratory of the manufacturer, or by another testing laboratory. 137. The notified body: 137.1. examine the technical documentation and supporting evidence to assess the technical pressure equipment design and manufacturing procedures. In addition, the notified body: 137.1.1., when the material does not meet the applicable standards, or to European pressure equipment materials, and check the certificate in accordance with the provisions of paragraphs 60 and 61 shall be issued by the materials manufacturer; 137.1.2. Approves the procedures by which is permanently connected to the pressure equipment parts, or check their prior approval in accordance with this provision, 47.3 and 47.4 47.2... ". 137.1.3. check that personnel conducting part of the permanent pressure equipment connect and tests sagraujošo is not qualified and approved in accordance with this provision, 47.3, 47.2 and 47.5 47.4. section; 137.2. make sure that the model is manufactured in accordance with the technical documentation and identify the elements which are designed in accordance with the relevant applicable to the relevant provisions of the standards as well as the elements which developed under other relevant technical specifications, without applying the applicable standards referred to the relevant provisions; 137.3. the appropriate examinations and necessary tests to check whether, where the manufacturer has chosen to apply the relevant standards applicable solutions, provided they are properly applied; 137.4. perform the appropriate examinations and necessary tests to check whether, in cases where there is no applied standards provided for in relevant applicable solutions, the solutions adopted by the manufacturer, the application of other relevant technical specifications, to meet this provision with the essential safety requirements; 137.5. agree with manufacturers on site, which will be checked and tested. 138. the notified body shall draw up an assessment report indicating the measures taken in accordance with the provisions of paragraph 8, and the results of such measures. Notified body only with the consent of the manufacturer, wholly or in part the content of that report gets (this requirement does not extend to the obligations of the notified body to the notifying authorities). 139. Where the type meets the requirements of these provisions, the notified body shall issue a manufacturer the EU type-examination certificate. The period of validity of the certificate is 10 years (with the exception of this rule 142. and in paragraph 143.), and it is renewable. It shall include the name and address of the manufacturer, conclusions of the examination, the conditions for validity of the certificate, if any, and for identification of the approved type the necessary information. 140. the certificate shall be accompanied by the necessary technical documentation a parts list, and one copy kept by the notified body. The certificate and its annexes shall contain all relevant information for assessing the conformity of the manufactured pressure equipment to the type checking and inspection during use. 141. If the type does not satisfy the applicable requirements of these regulations, the notified body shall refuse to issue an EU type-examination certificate and shall inform the applicant accordingly, indicating the reasons for such refusal. 142. the notified body shall identify the common standard changes that indicate that the approved type may no longer comply with the applicable requirements of these regulations, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the manufacturer. 143. 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 pressure equipment defined in these provisions with the essential safety requirements, or that the conditions for validity of the certificate. Such modifications require additional approval, added an addition to the original EU type-examination certificate. 144. 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 to the Ministry of the economy of such certificates and (or) additions to the list, which has been rejected, the transaction is aborted or otherwise limited. 145. 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. 146. 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. 147. at the request of the European Commission and the Member States may receive technical documentation and reported the results of the inspections carried out by the institution. The notified body shall keep the EU type-examination certificate, its annexes and additions, technical documentation (including documentation provided by the manufacturer) copy that the certificate had expired. 148. the manufacturer shall provide the EU type-examination certificate, its annexes and additions and a copy of the technical documentation available to the supervisory authority of the market 10 years after the equipment and protective systems on the market. 149. The manufacturer's authorised representative may lodge the rules of application referred to in paragraph 136, and fulfill this rule 142, 143 and 148. the obligations referred to in paragraph 1, provided that they are specified in the mandate. 5.4.2. test project type 150. EU project type examination is the part of a conformity assessment procedure whereby a notified body examines the technical design of the pressure equipment, as well as ensure and certify that the pressure equipment in the technical design meets the requirements of this regulation. 151. the EU project type test shall be carried out as the pressure equipment technical project evaluation, examination of the rules referred to in paragraph 152 of the technical documentation and supporting evidence, but does not check the sample. 30. These provisions referred to in paragraph 1, the experimental design method may not be used in connection with the module. 152. the EU type-examination must be lodged by the manufacturer shall be filed in one of the notified body of his choice. The application shall contain the following information and documentation: 152.1. name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 152.2. a written declaration that the application has not been lodged with any other notified body; 152.3. technical documentation. The technical documentation provides an opportunity to assess the conformity of the pressure equipment with the applicable requirements of these regulations, and it includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 152.3.1. General description of the pressure equipment; 152.3.2. contests and drawings, production of components, sub-assemblies, circuits and other power schemes. 152.3.3. the descriptions and explanations necessary drawings and schemes and the operation of the pressure equipment understanding; 152.3.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 152.3.5. project carried out calculations and of the inspections carried out and other results; 152.3.6. information concerning the qualifications or approvals required under this provision, 47.3, 47.2 and 47.5 47.4. section; 152.4. evidence confirming the compliance of the technical design solution. This supporting evidence indicates all used documents (especially if not fully appropriate applicable standards). Supporting evidence, if necessary, include the results of tests carried out in accordance with other relevant technical specifications made by the appropriate laboratory of the manufacturer, or by another testing laboratory on his behalf and responsibility. 153. The notified body: 153.1. examine the technical documentation and supporting evidence to assess the adequacy of the technical design of the product. The notified body shall assess the extra: materials, 153.1.1. If they do not meet the applicable standards, or to European pressure equipment materials; 153.1.2. Approves the procedures by which is permanently connected to the pressure equipment parts, or check their prior approval in accordance with this provision, 47.3 and 47.4 47.2... ". 153.2. carry out appropriate inspections to check whether, where the manufacturer has chosen to apply the relevant standards applicable solutions, provided they are properly applied; 153.3. carry out the appropriate checks to ensure that in cases where it is not applied in the relevant standards applicable to the proposed solutions, the solutions adopted by the manufacturer, the application of other relevant technical specifications, to meet this provision with the essential safety requirements. 154. the notified body shall draw up an assessment report indicating the measures taken in accordance with the provisions of paragraph 153, and the results of such measures. Notified body only with the consent of the manufacturer, wholly or in part the content of that report gets (this requirement does not extend to the obligations of the notified body to the notifying authorities). 155. where the design meets the requirements of these provisions, the notified body shall issue a manufacturer the EU type-examination certificate. The period of validity of the certificate is 10 years (with the exception of this rule 158. and in paragraph 160.), and it is renewable. It shall include the name and address of the manufacturer, conclusions of the examination, the conditions for validity of the certificate, if any, and for identification of the approved project the necessary information. 156. the certificate shall be accompanied by the necessary technical documentation a parts list, and one copy kept by the notified body. The certificate and its annexes shall contain all relevant information for assessing the conformity of the manufactured pressure equipment test project and inspection during use. 157. If the project does not meet the applicable requirements of these regulations, the notified body shall refuse to issue an EU type-examination certificate and shall inform the the applicant, specifying the reasons for such refusal. 158. the notified body shall identify the common standard for changes that indicate that the approved design may no longer comply with the applicable requirements of these regulations, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the manufacturer. 159. The manufacturer shall inform the notified body that holds the technical documentation concerning the EU type-examination certificate of all modifications to the approved design changes which may affect the conformity of the pressure equipment defined in these provisions with the essential safety requirements, or that the conditions for validity of the certificate. Such modifications require additional approval, added an addition to the original EU type-examination certificate. 160. 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 to the Ministry of the economy of such certificates and (or) additions to the list, which has been rejected or whose operation is suspended or otherwise restricted. 161. 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. 162. 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. 163. at the request of the European Commission and the Member States may receive technical documentation and reported the results of the inspections carried out by the institution. The notified body shall keep the EU type-examination certificate, its annexes and additions, technical documentation (including documentation provided by the manufacturer) copy that the certificate had expired. 164. the manufacturer shall provide the EU type-examination certificate, its annexes and additions and a copy of the technical documentation available to the supervisory authority of the market 10 years after the equipment and protective systems on the market. 165. The manufacturer's authorised representative may lodge the rules of application referred to in paragraph 152 and fulfill this rule 158.159.164., and the obligations referred to in paragraph 1, provided that they are specified in the mandate. 5.5. Conformity to type based on internal production control plus supervised inspections of pressure equipment at random intervals (module C2) 166. Conformity to type based on internal production control plus supervised product checks at random intervals is the part of a conformity assessment procedure whereby the manufacturer fulfils the obligations referred to in this chapter, as well as just on his own responsibility, and declares that the pressure equipment in question satisfies the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 167. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure conformity of the manufactured pressure equipment EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 168. a notified body chosen by the manufacturer, by its specific random intervals carry out or ask to perform product testing to ensure that the pressure equipment final evaluation and internal quality checks, bearing pressure equipment of technological complexity and the volume of production. 169. The notified body shall check whether the manufacturer actually performs final assessment in accordance with paragraph 48 of these rules. 170. the notified body shall examine the pressure equipment samples, of which it has taken the place of production before placing on the market, as well as take appropriate tests specified in the applicable standards in relevant parts, and (or) the equivalent tests pursuant to another specification, to check the conformity of the pressure equipment with the relevant requirements of these rules. 171. The notified body shall determine the number of items of equipment to sample and whether it should be carried out (or ask to make a) full or partial pressure equipment samples of the final assessment. 172. The applicable sampling procedures aims to determine whether pressure equipment manufacturing process is within acceptable limits, in order to ensure compliance of the pressure equipment. If the sample does not meet the acceptable quality level, the notified body shall take appropriate measures. 173. when checking out the notified body, the manufacturer, to the responsibility of the notified body the manufacturing process imposed on notified body identification number. 174. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 175. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability in the market surveillance authorities for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. A copy of the Declaration of conformity is available on request to the authorities. 176. The manufacturer's authorised representative may fulfil these rules 175.173. and producers referred to the obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.6. Conformity to type based on quality assurance of the production process (module D) 177. Conformity to type based on quality assurance of the production process is the part of a conformity assessment procedure whereby the manufacturer fulfils the rule 178., 194, 195, 196.. 197.198., and the responsibilities of paragraph, and only on his own responsibility, and declares that the pressure equipment or assemblies in question meet the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 178. the manufacturer shall use the approved quality assurance system for the manufacture of pressure equipment concerned, the final inspection and testing according to this provision, 179, 181, 182 180.183, 184, 185,..., 186, 187 and 188..., and he is the subject of this provision, 189, 190, 192, 193 191.194. and monitoring referred to in paragraph 1. 179. the manufacturer of the pressure equipment concerned to assess the application of the quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 179.1. the name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 179.2. a written declaration that the application has not been lodged with any other notified body; 179.3. all relevant information on the pressure equipment intended for type; 179.4. quality system documentation; 179.5. technical documentation relating to the approved type and the EU type-examination certificate. 180. the quality assurance system ensures that pressure equipment satisfies the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 181. All the elements adopted by the manufacturer, the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 181.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to the quality of the pressure equipment; 181.2. the manufacture, quality control and quality assurance techniques, processes and systematic actions to be used (including this provision, 47.3 and 47.4 47.2...) (approved procedure for permanent bonding of parts); 181.3. the examinations and tests which will be carried out before the process, during and after its completion, and the frequency in which they are carried out; 181.4. quality records, such as inspection reports and test data, calibration data, and reports on the qualifications of the staff (especially concerning the personnel carrying out permanent joining parts of pressure equipment and sagraujošo tests in accordance with this provision, 47.3, 47.2 and 47.5 47.4); 181.5. features the required product quality and the monitoring of achievement of quality assurance for the efficient operation of the system. 182. The notified body shall assess the quality system to determine whether it meets this provision 181.180. and requirements referred to in paragraph 1. These requirements match these elements of the quality system that comply with the relevant applicable standard specifications. 183. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge of the applicable requirements of these regulations. The audit includes a verification visit at the premises. 184. The Audit team examined this provision referred to 179.5. technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and carry out the necessary checks to ensure the product meets these requirements. 185. the decision shall be notified to the manufacturer. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 186. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 187. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 188. The notified body shall evaluate any proposed changes and decide whether the changed quality system will still meet the requirements referred to in that provision and paragraph 180.181, or need a revaluation. 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. 189. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 190. the purpose of the evaluation the manufacturer provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 190.1. the quality assurance system documentation; 190.2. the quality records (such as inspection reports and test data, calibration data, qualification reports of the personnel concerned). 191. 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. Periodic audits must be carried out regularly to every three years for complete revaluations. 192. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 192.1. category of pressure equipment; 192.2. results of previous monitoring visits; 192.3. need to monitor corrective actions; 192.4. where applicable, special conditions linked to the approval of the system; 192.5. significant changes in manufacturing organization, policies or methods. 193. The notified body additional visits, if necessary, may make the product tests or organize them in order to check that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 194. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the EU type-examination certificate and to the type as described in the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 179 of the notified body responsible for the label adds its identification number. 195. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 196. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: this provision 179 196.1. the documentation referred to in paragraph; 196.2. information relating to this provision in paragraph 187 and 188 of those changes approved; 196.3. notified body decisions and reports referred to in this provision, 182 183 184, 185, 186, 187, 188, 191, and 192 in.. 197. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 198. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 199. The manufacturer's authorised representative may meet this provision 179, 187, 188, 194, 195 and referred to in paragraph 196 of the manufacturer's obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.7. quality assurance of the production process (module D1) 200. Production quality assurance is the conformity assessment procedure whereby the manufacturer fulfils this provision 201.203.218., 219, and the obligations referred to in the paragraph, and only on his own responsibility, and declares that the pressure equipment concerned satisfy the requirements of these provisions, which apply to them. 201. the manufacturer shall prepare technical documentation that provides the ability to assess the conformity of the pressure equipment with the applicable requirements of this regulation, and includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 201.1. General description of the pressure equipment; 201.2. the sketch project and production drawings, components, assemblies, power circuits and other schemes; 201.3. descriptions and explanations necessary for the drawings and diagrams and the operation of the pressure equipment understanding; 201.4. it applicable in full or in part a list of standards for which references have been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; the project is 201.5. calculations and of the inspections carried out and other results; 201.6. test reports. 202. the manufacturer shall provide the technical documentation available to the supervisory authority of the market 10 years after the placing on the market of pressure equipment. 203. the manufacturer shall use the approved quality assurance system for the manufacture of pressure equipment concerned, the final inspection and testing under this rule 204.205, 206, 207, 208, 209,..., 210.211.212., and point, and he is the subject of this rule 213.214, 215, 216 and 217..., referred to in paragraph 1. 204. the manufacturer of the pressure equipment concerned to assess the application of the quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 204.1. name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 204.2. a written declaration that the application has not been lodged with any other notified body; 204.3. all relevant information on the pressure equipment intended for type; 204.4. quality system documentation; 204.5. the technical documentation referred to in paragraph 201 of these rules. 205. the quality system shall ensure that the pressure equipment satisfies the requirements of these regulations that apply to them. 206. All the elements adopted by the manufacturer, the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 206.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to the quality of the pressure equipment; concerned by 206.2. quality control and quality assurance techniques, processes and systematic actions to be used (including under this provision, 47.3 and 47.4 47.2...) (approved procedure for permanent bonding of parts); 206.3. the examinations and tests which will be carried out before the process, during and after its completion, and the frequency in which they are carried out; 206.4. quality records, such as inspection reports and test data, calibration data, and reports concerning the qualifications or approvals of the personnel concerned (in particular concerning the personnel carrying out permanent joining parts of pressure equipment and sagraujošo tests in accordance with this provision, 47.3, 47.2 and 47.5 47.4); 206.5. features the required product quality and the monitoring of achievement of quality assurance for the efficient operation of the system. 207. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 205 and 206. These requirements conform to those elements of the quality assurance system that complies with the applicable standard. 208. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge on the applicable requirements of these regulations. 209. Audit includes assessment visit to the manufacturer's premises. The audit team examined the rules referred to in paragraph 201 of the technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and make the necessary controls to ensure compliance of the pressure equipment with the requirements. The decision is notified to the manufacturer. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 210. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 211. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 212. The notified body shall evaluate any proposed changes and decide whether the changed quality system will still meet the requirements referred to in that provision and paragraph 205.206, or need a revaluation. 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. 213. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 214. the purpose of the evaluation the manufacturer provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 214.1. the quality assurance system documentation; 214.2. This provision 201. documentation referred to in point; 214.3. data on quality (such as inspection reports and test data, calibration data, qualification reports of the personnel concerned). 215. 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. Periodic audits must be carried out regularly to a full reassessment is carried out every three years. 216. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 216.1. category of pressure equipment; 216.2. results of previous monitoring visits; 216.3. need to monitor corrective actions; 216.4. where applicable, special conditions linked to the approval of the system; 216.5. significant changes in manufacturing organization, policies or methods. 217. The notified body additional visits, if necessary, may make the product tests or organize them in order to check that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out, the test report. 218. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of these regulations, as well as to the provisions referred to in paragraph 204 of the notified body responsible for the label adds its identification number. 219. the manufacturer shall draw up a written pressure equipment of each declaration of conformity with the technical documentation, ensure availability of market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. A copy of the Declaration of conformity is available on request to the authorities. 220. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: 220.1. This provision of the documentation referred to in paragraph 204; 220.2. information relating to this provision and 212.211. changes referred to in paragraph 1; 220.3. the notified body and the reports referred to in this provision, 211, 215, 216 212 and 217. in paragraph. 221. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 222. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 223. The manufacturer's authorised representative may meet this provision, 202, 204.211.212, 218, 219 and 220..., referred to the manufacturer's obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.8. Conformity to type based on quality assurance of pressure equipment (module E) 224. Conformity to type based on quality assurance of pressure equipment, is the part of a conformity assessment procedure whereby the manufacturer fulfils the rule 225.241.242, and the obligations referred to in paragraph and only on his own responsibility, and declares that the pressure equipment in question satisfies the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 225. the manufacturer shall use the approved quality assurance system for the final pressure equipment inspection and testing in accordance with the provisions of paragraph 226, and he is the subject of this provision, 236, 238, 239.237.240. and monitoring referred to in paragraph 1. 226. the manufacturer of the pressure equipment concerned to assess the application of the quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 226.1. name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 226.2. written confirmation that the application has not been lodged with any other notified body; 226.3. all relevant information on the pressure equipment intended for type; 226.4. quality system documentation; 226.5. technical documentation relating to the approved type and the EU type-examination certificate. 227. the quality system shall ensure compliance of the products in the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 228. All the elements adopted by the manufacturer, the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 228.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to product quality; 228.2. the examinations and tests that will be carried out after manufacture; 228.3. quality records, such as inspection reports and test data, calibration data, and reports concerning the qualifications or approvals of the personnel concerned (in particular concerning the personnel carrying out permanent joining parts of pressure equipment and sagraujošo tests in accordance with this provision, 47.3, 47.2 and 47.5 47.4); 228.4. means for the effective operation of the quality assurance system of supervision. 229. The notified body shall assess the quality system to determine whether it complies with this provision and in paragraph 227.228. These requirements match these elements of the quality system that comply with the relevant applicable standard specifications. 230. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge of the applicable requirements of these regulations. The audit includes assessment visit to the manufacturer's premises. 231. The Audit team examined this provision referred to 226.5. technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and to carry out the necessary checks to ensure the product meets these requirements. 232. the decision shall be notified to the manufacturer. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 233. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 234. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 235. The notified body shall evaluate any proposed changes and decide whether the changed quality system will still meet the requirements referred to in these regulations and in paragraph 227.228, or need a revaluation. 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. 236. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 237. the manufacturer shall for the purposes of the evaluation provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 237.1. the quality assurance system documentation; 237.2. technical documentation; 237.3. 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. Periodic audits must be carried out regularly to a full reassessment is carried out every three years. 239. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 239.1. category of pressure equipment; 239.2. previous monitoring visits; 239.3. need to monitor corrective actions; 239.4. where applicable, special conditions linked to the approval of the system; 239.5. significant changes in manufacturing organization, policies or methods. 240. The notified body additional visits, if necessary, may make the product tests or organize them in order to check that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 241. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the EU type-examination certificate and to the type as described in the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 226 of the notified body responsible for the label adds its identification number. 242. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 243. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: this provision 226 243.1. the documentation referred to in paragraph; 243.2. information concerning this provision. 235.234 and referred the approved changes; 243.3. notified body decisions and reports referred to in this provision 229.230.231.232, 234, 235, 238, 239, 240, and.. 244. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 245. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 246. The manufacturer's authorised representative may meet this provision, 226, 235, 234.241.242.243., and referred to the manufacturer's obligations and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.9. the final pressure equipment inspection and testing-quality assurance (module E1) 247. final pressure equipment inspection and testing, quality assurance is that part of a conformity assessment procedure whereby the manufacturer fulfils the provisions of 248, 250, 267.268 and obligations referred to in paragraph and only on his own responsibility, and declares that the pressure equipment concerned satisfy the requirements of these provisions, which apply to them. 248. the manufacturer shall prepare technical documentation that provides the ability to assess the conformity of the pressure equipment with the applicable requirements of this regulation, and includes the appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 248.1. General description of the pressure equipment; sketch project and 248.2. fabrication drawings, components, assemblies, power circuits and other schemes; 248.3. descriptions and explanations necessary for the drawings and diagrams and the operation of the pressure equipment understanding; 248.4. it applicable in full or in part a list of standards for which references have been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet the essential safety requirements of the rules. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 248.5. project carried out calculations and of the inspections carried out and other results; 248.6. test reports. 249. the manufacturer shall provide the technical documentation available to the supervisory authority of the market 10 years after the placing on the market of pressure equipment. 250. the manufacturer shall use the approved quality assurance system for the final pressure equipment inspection and testing under this rule 251., 252, 253, 254.., 255, 256, 257.., 258, 259, 260,..., and 261 points and he is the subject of this rule 262., 263, 264, 265..., and the supervision referred to in paragraph 266. 251. the manufacturer of the pressure equipment concerned an application for assessment of his quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 251.1. name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 251.2. written confirmation that the application has not been lodged with any other notified body; 251.3. all relevant information on the pressure equipment intended for type; 251.4. quality system documentation; 251.5. This provision referred to in paragraph 248 technical documentation. 252. the quality system shall ensure that the pressure equipment satisfies the requirements of these regulations that apply to them. 253. Under the quality system, each of the pressure equipment is examined and appropriate tests set out in these rules referred to in paragraph 6, the applicable standards, or equivalent tests, as well as a final assessment in accordance with paragraph 48 of these provisions to ensure compliance with the requirements of these provisions, which apply to it. 254. All the elements adopted by the manufacturer, the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 254.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to the quality of the pressure equipment; 254.2. under this provision, and 47.2 47.3 47.4...) (approved procedure for permanent bonding of parts; 254.3. the examinations and tests that will be carried out after manufacture; data on quality of 254.4., such as inspection reports and test data, calibration data, and reports concerning the qualifications or approvals of the personnel concerned (in particular concerning the personnel carrying out part of the permanent pressure equipment connect in accordance with this provision, and 47.2 47.3 47.4...); 254.5. means for the effective operation of the quality assurance system of supervision. 255. The notified body shall assess the quality system to determine whether it meets this provision 252.254.253, and the requirements contained in point. These requirements match these elements of the quality system that comply with the relevant applicable standard specifications. 256. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge of the applicable requirements of these regulations. The audit includes assessment visit to the manufacturer's premises. 257. The Audit team examined the provisions referred to in paragraph 248. technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and make the necessary controls to ensure compliance of the pressure equipment with the requirements. 258. the decision shall be notified to the manufacturer. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 259. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 260. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 261. The notified body shall evaluate any proposed changes and decide whether the changed quality assurance system still meets the requirements referred to in this provision, and 253.252.254. point or revaluation is necessary. 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. 262. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 263. the purpose of the evaluation the manufacturer provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 263.1. the quality assurance system documentation; 248. these provisions 263.2. documentation referred to in point; 263.3. quality records (such as inspection reports and test data, calibration data, qualification reports of the personnel concerned). 264. 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. Periodic audits must be carried out regularly to a full reassessment is carried out every three years. 265. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 265.1. installations category; 265.2. the results of previous surveillance visits; 265.3. the need to monitor corrective actions; 265.4. where applicable, special conditions linked to the approval of the system; 265.5. significant changes in manufacturing organization, policies or methods. 266. The notified body additional visits, if necessary, may make the product tests or organize them in order to check that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 267. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 251 of the notified body responsible for the label adds its identification number. 268. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 269. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: this rule 251.269.1. the documentation referred to in point; 269.2. information relating to this provision in paragraph 260 and 261 above changes; 269.3. notified body decisions and reports referred to in this provision, 256.255., 257, 258, 260.., 261, 264, 265.. and in paragraph 266. 270. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 271. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 272. The manufacturer's authorised representative may meet this provision, 249, 251, 260, 267, 268 261.. and the producers referred to in paragraph 269 of the duties and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.10. Conformity to type based on pressure equipment verification (module F) 273. Conformity to type based on pressure equipment-verification is the part of a conformity assessment procedure whereby the manufacturer fulfils the terms of article 274, 281, 282 and 283... the obligations referred to in paragraph 1 and only on his own responsibility, and declares that the pressure equipment concerned, subject to the provisions 275 and 276 of these. the requirements referred to in paragraph, comply with the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. 274. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure conformity of the manufactured pressure equipment EU type examination certificate the approved type as described in the applicable regulations and requirements. 275. the notified body chosen by the manufacturer shall carry out the necessary examinations and tests in order to verify the conformity of the pressure equipment EU type examination certificate the approved type as described in the applicable regulations and requirements. 276. The examinations and tests that allow to check the conformity of the pressure equipment with the relevant requirements shall examine and testing of every pressure equipment in accordance with this provision and paragraph 277.278. 277. individual checks each pressure equipment and carrying out the tests laid down in the relevant specified in applicable standards, or equivalent tests, to check the conformity with the EU type-examination certificate and to the type as described in the applicable requirements of this regulation. If there is no such standard, applicable to the notified body concerned shall decide on what tests should be performed. 278. The notified body: 278.1. check that personnel conducting part of the permanent pressure equipment connect and tests sagraujošo is not qualified and approved in accordance with this provision, 47.3, 47.2 and 47.5 47.4. section; 278.2. check the certificate under this rule 59, 60 and 61 of the material provided by the manufacturer; out or entrust 278.3. this rule 48.1. the conclusion referred to in those rules and 48.2. strength referred to check and, if necessary, check the safety devices. 279. the notified body shall, on the basis of the checks carried out and issue a certificate of conformity and affix its identification number to each approved pressure equipment or, on his own responsibility, to charge it. 280. the manufacturer shall ensure the availability of the certificate of conformity market surveillance authority 10 years after placing pressure equipment on the market. 281. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the EU type-examination certificate and to the type as described in the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 275 of the notified body responsible for the label adds its identification number. 282. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. 283. If these provisions 275. the notified body referred to in paragraph agrees and takes on the responsibility, the manufacturer may also pressure equipment directive notified body identification number. 284. If the notified body agrees and takes on the responsibility of the notified body, the manufacturer, the identification number of the pressure equipment directive may be imposed in the course of manufacture. 285. 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. Authorized representative can not fulfill the provisions referred to in paragraph 274 of the manufacturer. 5.11. Conformity based on unit verification (module G) 286. Conformity based on unit verification is the conformity assessment procedure whereby the manufacturer fulfils this provision 287, 288, 289.., 293 and 294. obligations listed in paragraph and only on his own responsibility, and declares that the pressure equipment concerned, subject to these rules, 291 and 292 290. the requirements referred to in paragraph shall comply with the requirements of these provisions, which apply to them. 287. the manufacturer shall establish the technical documentation and make it available to the notified body. Documentation provides the ability to assess the conformity of the pressure equipment with the relevant requirements, and shall include appropriate risk analysis and assessment. The technical documentation shall specify the applicable requirements and, so far as is necessary for the assessment of pressure equipment it covers the design, production and operation. Technical documentation, if applicable, includes at least the following elements: 287.1. General description of the pressure equipment; sketch project and 287.2. fabrication drawings, components, assemblies, power circuits and other schemes; 287.3. descriptions and explanations necessary for the drawings and diagrams and the operation of the pressure equipment understanding; 287.4. it applicable in full or in part a list of standards for which references have been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 287.5. the project carried out calculations and of the inspections carried out and other results; 287.6. test report; 287.7. relevant information on the manufacturing and testing procedures, approvals and information on the qualifications or approvals required under this provision, 47.3, 47.2 and 47.5 47.4. section. 288. the manufacturer shall provide the technical documentation available to the supervisory authority of the market 10 years after the placing on the market of pressure equipment. 289. the manufacturer shall take all measures necessary in order that the manufacturing process and its monitoring ensure conformity of the manufactured pressure equipment to the requirements of this regulation. 290. a notified body chosen by the manufacturer shall carry out or ask to perform the necessary examinations and tests defined in the relevant standards, applicable and (or) equivalent tests, to check the conformity of the pressure equipment requirements of these provisions. If there is no such standard, applicable to the notified body concerned shall decide on what tests should be carried out using other technical specifications. 291. The notified body: 291.1. examine the technical documentation, to assess technical design and manufacturing procedures compliance; 291.2. assess the materials used where these are not in conformity with the applicable standards or European approvals for materials for pressure equipment materials, and check the certificate in accordance with paragraph 48 of these regulations provided by the material manufacturer; 291.3. Approves the procedures by which is permanently connected to the pressure equipment parts, or check their prior approval in accordance with this provision, 47.3 and 47.4 47.2... ". checks the qualifications or 291.4. approvals required in accordance with this provision, 47.3, 47.2 and 47.5 47.4. section; carry out or entrust 291.5. this rule 48.1. the conclusion referred to in those rules and 48.2. strength referred to check and, if necessary, check the safety devices. 292. the notified body shall, on the basis of the checks carried out and issue a certificate of conformity and affix its identification number to each approved pressure equipment or, on his own responsibility, to charge it. The manufacturer shall ensure the availability of the certificate of conformity market surveillance authority for 10 years after the placing on the market of pressure equipment. 293. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 291 of the notified body responsible for the label adds its identification number. 294. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. A copy of the Declaration of conformity is available on request to the authorities. 295. The manufacturer's authorised representative may meet this provision 287.288, 293, and referred to in paragraph 294 of the producer duties and responsibilities on behalf of the manufacturer, if they are specified in the mandate. 5.12. Conformity based on full quality assurance (module H) 296. Conformity based on full quality assurance is the conformity assessment procedure whereby the manufacturer fulfils this provision 297, 313 and 312. paragraph and only on his own responsibility, and declares that the pressure equipment concerned satisfy the requirements of these provisions, which apply to them. 297. the manufacturer shall use the approved quality assurance system for production, final pressure equipment inspection and testing under this provision and paragraph 298.299, and he is the subject of this provision 307.308, 309, 310 and 311..., referred to in paragraph 1. 298. the manufacturer of the pressure equipment concerned to assess the application of the quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 298.1. the name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 298.2. technical documentation for one model of pressure equipment intended for the production of each type. Technical documentation, if applicable, includes at least the following elements: 298.2.1. General description of the pressure equipment; 298.2.2. contests and drawings, manufacturing of components, sub-assemblies, circuits and other power schemes. 298.2.3. the descriptions and explanations necessary drawings and schemes and the operation of the pressure equipment understanding; 298.2.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet the essential safety requirements of the rules. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 298.2.5. project carried out calculations and of the inspections carried out and other results; 298.2.6. the test report; 298.3. quality system documentation; 298.4. written confirmation that the application has not been lodged with any other notified body. 299. All the elements adopted by the manufacturer to the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 299.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to the quality of the pressure equipment; 299.2. technical design specifications, including standards that will be applied and, where the relevant applicable standards will not be applied in full, the means to be used which will ensure compliance with these provisions of the pressure equipment requirements that apply to it; 299.3. project control and design verification techniques, processes and systematic actions that will be used when designing the pressure equipment type in question (in particular with respect to the materials in accordance with the provisions of subsection 3.4); 299.4 of manufacture concerned, quality control and quality assurance techniques, processes and systematic actions to be used (including under this provision, 47.3 and 47.4 47.2...) (approved procedure for permanent bonding of parts); 299.5. the examinations and tests which will be carried out before the process, during and after its completion, and the frequency in which they are carried out; 299.6. about the quality of the data, such as inspection reports and test data, calibration data, and reports concerning the qualifications or approvals of the personnel concerned (in particular concerning the personnel carrying out permanent joining parts of pressure equipment and sagraujošo tests in accordance with this provision, 47.3, 47.2 and 47.5 47.4); 299.7. means of monitoring compliance with controls for project and the quality of the pressure equipment, as well as the effective operation of the quality system. 300. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 299. These requirements match these elements of the quality system that comply with the relevant applicable standard specifications. 301. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge of the applicable requirements of these regulations. The audit includes assessment visit to the manufacturer's premises. 302. The Audit team examined this provision referred 298.2. technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and make the necessary controls to ensure compliance of the pressure equipment with the requirements. 303. the decision shall be notified to the manufacturer. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 304. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 305. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 306. The notified body shall evaluate any proposed changes and decide whether the changed quality system will still meet the requirements referred to in paragraph 299 of these rules, or you need a revaluation. 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. 307. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 308. the purpose of the evaluation the manufacturer provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 308.1. the quality assurance system documentation; 308.2. data on quality (for example, results of analyses, calculations, tests, and other results in accordance with the part of the quality system relating to design); 308.3. quality records (such as inspection reports and test data, calibration data, qualification reports of the personnel concerned in accordance with the part of the quality system relating to manufacture). 309. 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. Periodic audits must be carried out regularly to a full reassessment is carried out every three years. 310. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 310.1. category of pressure equipment; 310.2. results of previous monitoring visits; 310.3. the need to monitor corrective actions; 310.4. where applicable, special conditions linked to the approval of the system; 310.5. significant changes in manufacturing organization, policies or methods. 311. The notified body additional visits, if necessary, may make the product tests or organize them in order to check that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 312. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 298 of the notified body responsible for the label adds its identification number. 313. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years after the placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it prepared. A copy of the Declaration of conformity is available on request to the authorities. 314. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: this provision 298 314.1. the documentation referred to in paragraph; 314.2. documentation on the rules referred to in paragraph 298 of the quality assurance system; 314.3. information relating to the provisions referred to in paragraph 304; 314.4. notified body decisions and reports referred to in this provision, 301, 302 300, 303, 304, 309, 310 and 311... point. 315. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 316. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 317. The manufacturer's authorised representative may meet this provision 298., 305, 306, 312.., 313 and 314.. referred to the obligations of the manufacturer the manufacturer's task and responsibility, if they are specified in the mandate. 5.13. Conformity based on full quality assurance plus design examination (module H1) 318. Conformity based on full quality assurance and verification of the project as well as the final evaluation special surveillance is the conformity assessment procedure whereby the manufacturer fulfils the rule 319., 349 and 350. obligations listed in paragraph and only on his own responsibility, and declares that the pressure equipment concerned satisfy the requirements of these provisions, which apply to them. 319. the manufacturer shall use the approved quality assurance system for production, final pressure equipment inspection and testing according to this provision, 320, 322, 323 321..., 324, 325, 326.327, 328, 329, 330,..., and 331, and he is the subject of this provision 343 344, 345, 346..., 347 and 348 referred. monitoring. Pressure equipment the conformity of the technical project in accordance with this provision, 333.332, 334, 335, 336.337, 338, 339, 340,..., 341 and 342, paragraph. those requirements. 320. the manufacturer of the pressure equipment concerned an application for assessment of his quality assurance system shall be submitted to the notified body that you choose. The application shall contain the following information and documentation: 320.1. the name and address of the manufacturer and, if the application is lodged by the authorized representative, its name and address; 320.2. technical documentation for one model of pressure equipment intended for the production of each type. Technical documentation, if applicable, includes at least the following elements: 320.2.1. General description of the pressure equipment; 320.2.2. contests and drawings, manufacturing of components, sub-assemblies, circuits and other power schemes. 320.2.3. the descriptions and explanations necessary drawings and schemes and the operation of the pressure equipment understanding; 320.2.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 320.2.5. project carried out calculations and of the inspections carried out and other results; 320.2.6. the test report; 320.3. quality system documentation; 320.4. a written declaration that the application has not been lodged with any other notified body. 321. the quality system shall ensure that the pressure equipment satisfies the requirements of these regulations that apply to them. 322. All the elements adopted by the manufacturer, the requirements and conditions for the systematic and proper documentation of written policies, procedures and instructions. The quality system documentation allows a consistent interpretation of the quality programmes, plans, manuals and documentation, and include appropriate to describe the following information: 322.1. quality objectives and the organisational structure, responsibilities and powers of the management with regard to the quality of the pressure equipment; 322.2. technical design specifications, including standards that will be applied and, where the relevant applicable standards will not be applied in full, the means to be used which will ensure compliance of the pressure equipment referred to in these provisions with the essential safety requirements that apply to it; 322.3. project control and design verification techniques, processes and systematic actions that will be used when designing the pressure equipment type in question (in particular with respect to the materials in accordance with the provisions of subsection 3.4); manufacture of 322.4. the relevant, quality control and quality assurance techniques, processes and systematic actions to be used (including under this provision, 47.3 and 47.4 47.2...) (approved procedure for permanent bonding of parts); 322.5. the examinations and tests which will be carried out before the process, during and after its completion, and the frequency in which they are carried out; data on quality of 322.6., such as inspection reports and test data, calibration data, and reports concerning the qualifications or approvals of the personnel concerned (in particular concerning the personnel carrying out permanent joining parts of pressure equipment and sagraujošo tests in accordance with this provision, 47.3, 47.2 and 47.5 47.4); 322.7. means of monitoring compliance with controls for project and the quality of the pressure equipment, as well as the effective operation of the quality system. 323. The notified body shall assess the quality system to determine whether it meets this provision in paragraph 321 and 322. These requirements match these elements of the quality system that comply with the relevant applicable standard specifications. 324. in addition to experience in quality assurance systems with at least one audit team has experience in the field of pressure equipment pressure equipment and for the evaluation of the technology and knowledge of the applicable requirements of these regulations. The audit includes assessment visit to the manufacturer's premises. 325. The Audit team examined this provision referred to 320.2. technical documentation and verify the manufacturer's ability to identify the relevant requirements of this regulation and make the necessary controls to ensure compliance of the pressure equipment with the requirements. 326. The decision shall be communicated to the manufacturer or his authorized representative. The notice shall contain the conclusions of the audit and the assessment of the justification of the decision. 327. The manufacturer shall undertake to fulfil the obligations arising from the quality system as approved and to uphold it so that it remains adequate and efficient. 328. the manufacturer shall keep the notified body that has approved the quality system informed of any intended change of the quality system. 329. The notified body shall evaluate any proposed changes and decide whether the changed quality system will still meet the requirements referred to in these regulations and in paragraph 321.322, or need a revaluation. 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. 330. the Notified institution every six months or, upon request, inform the Ministry of the economy of all issued or withdrawn approval of the quality system and shall provide the Ministry of the economy the quality system approval list that have been rejected, which has been suspended or otherwise restricted. 331. The notified body shall inform the other notified bodies on those quality assurance system approval decisions, which it has refused, withdrawn, suspended or otherwise restricted. Upon request, the notified body shall inform on the quality assurance system approval decision, those it has issued. 332. the manufacturer shall provide the notified body an application for examination of the project each pressure equipment that performs the above project. The application allows to understand the pressure equipment project, production, and operations, as well as to evaluate its compliance with the requirements of these provisions, which apply to it. The application shall contain the following information and documentation: 332.1. the name and address of the manufacturer; 332.2. a written declaration that the application has not been lodged with any other notified body; 332.3. technical documentation. Documentation provides the ability to assess the conformity of the pressure equipment with the relevant requirements, and shall 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 design and operation of the pressure equipment. Technical documentation, if applicable, includes at least the following elements: 332.3.1. General description of the pressure equipment; 332.3.2. contests and drawings, manufacturing of components, sub-assemblies, circuits and other power schemes. 332.3.3. the descriptions and explanations necessary drawings and schemes and the operation of the pressure equipment understanding; 332.3.4. the full or partial list of applicable standards, to which reference has been published in the official journal of the European Union, but, if the applicable standards referred to are not appropriate,-descriptions of the solutions adopted to meet this provision with the essential safety requirements, including other relevant technical specifications listing. If the applicable standards are appropriate, the technical documentation shall specify the parts of the standard; 332.3.5. project carried out calculations and of the inspections carried out and other results; 332.3.6. the test report; 332.4. evidence confirming the compliance of the technical design solution. This supporting evidence indicates all used documents (especially if not fully appropriate applicable standards) and, if necessary, include the results of tests carried out by the appropriate laboratory of the manufacturer, or by another testing laboratory on his behalf and responsibility. 333. the notified body shall examine the application and where the design meets the pressure equipment directive applicable requirements of this regulation, the manufacturer shall issue the inspection certificate of the EU project. The certificate shall contain the name and address of the manufacturer, conclusions of the examination, if necessary, the conditions for validity of the certificate and for identification of the approved project the necessary data. 334. the certificate and its annexes shall contain all relevant information allowing an evaluation to be made of the conformity of the pressure equipment inspected the project and, where appropriate, to carry out an inspection. 335. If a project does not meet the applicable requirements of these regulations, the notified body shall refuse to issue a design examination certificate and shall inform the applicant accordingly, indicating the reasons for such refusal. 336. the notified body shall identify the common standard for changes that indicate that the approved design may no longer comply with the applicable requirements of these regulations, and shall determine whether such changes require further investigations. If necessary, the notified body shall inform the manufacturer. 337. The manufacturer shall inform the notified body which issued the EU design-examination certificate of all modifications to the approved design changes which may affect the conformity with the requirements of these regulations with the essential safety requirements or the conditions for validity of the certificate. Such modifications require additional approval from the notified body which issued the design examination certificate in the EU, and this additional approval adds an addition to the original EU draft examination certificate. 338. the Notified institution every six months or, upon request, inform the Ministry of the economy of the EU project examination certificates and/or any additions which it has issued or withdrawn, and shall submit to the Ministry of the economy of such certificates and (or) additions to the list, which has been rejected or whose operation is suspended or otherwise restricted. 339. The notified body shall inform the other notified bodies of the EU project examination certificates and/or any additions thereto which it has refused, the institution has withdrawn, suspended or otherwise restricted, and, upon request, also for certificates and (or) additions, which it has issued. 340. 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. 341. The notified body shall keep the EU project examination certificate, its annexes and additions, as well as technical documentation (including documentation provided by the manufacturer) copy that the certificate had expired. 342. the manufacturer shall provide the EU design examination certificate, its annexes and additions and a copy of the technical documentation available to the supervisory authority of the market 10 years after the placing on the market of pressure equipment. 343. The notified body for the purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations arising out of the approved quality system. 344. the purpose of the evaluation the manufacturer provides the notified body access to the manufacture, inspection, testing and storage premises and shall provide it with all necessary information, including: 344.1. the quality assurance system documentation; 344.2. data on quality (such as results of analyses, calculations, tests, and other results in accordance with the part of the quality system relating to design); 344.3. quality records (such as inspection reports and test data, calibration data, qualification reports of the personnel concerned in accordance with the part of the quality system relating to manufacture). 345. 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. Periodic audits must be carried out regularly to a full reassessment is carried out every three years. 346. the notified body representatives may attend at the manufacturer without notice. The need for such additional visits and their frequency shall be determined on the basis of a visit control system operated by the notified body. In the visit control system shall take particular account of the following factors: 346.1. category of pressure equipment; 346.2. results of previous monitoring visits; .346.3 need to monitor corrective actions; 346.4. where applicable, special conditions linked to the approval of the system; 346.5. significant changes in manufacturing organization, policies or methods. 347. The notified body additional visits, if necessary, may make the product tests or to organize it, to verify that the quality system is functioning correctly. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 348. This provision, paragraph 48 final assessment attributable to increased surveillance and the notified body shall proceed by going visits without warning. During such visits, the notified body shall carry out inspections of pressure equipment representative. The notified body must provide the manufacturer with a visit report and, if tests have been carried out in the test report. 349. the manufacturer shall affix the CE marking to each individual pressure equipment that complies with the applicable requirements of this Regulation as well as to the provisions referred to in paragraph 320. the notified body responsible for the label adds its identification number. 350. the manufacturer shall draw up a written pressure equipment of each declaration of conformity and ensure its availability market supervisory authority for 10 years After placing on the market of pressure equipment. Declaration of conformity identifying the pressure equipment model that it set, and specify the number of the certificate of inspection of the project. A copy of the Declaration of conformity is available on request to the authorities. 351. the manufacturer for at least 10 years after the placing on the market of pressure equipment market surveillance authorities needs, keep: 351.1 documentation about this provision. 320. above the quality system; 351.2. information relating to this provision and paragraph 328.329 mentioned authorized changes; 351.3. notified body decisions and reports referred to in this provision 328., 329, 345 and 346... ". 352. The manufacturer's authorised representative the manufacturer's task and responsibility, you can submit these rules referred to in paragraph 332 application and fulfill this rule 320, 328.329, 337, 336.., 342, 349, 350 and 351.. the obligations referred to in paragraph provided that they are specified in the mandate. 6. European approval for materials 353. pressure equipment manufacturers By materials or request the notified body authorised to issue European material approval shall take the necessary tests and checks to ensure that the material from which the pressure equipment will be made in meeting the requirements of this regulation. European approval for materials not needed for those intended for the manufacture of pressure equipment materials for the bearing of applicable standards. 354. the notified body shall forward to the Commission information on the checks and tests carried out. If, within three months after the sending of the information they have received no objections from the European Commission, the notified body shall draw up the approval of European material and material or pressure equipment shall be issued to the manufacturer. A copy of the approval no later than one month shall be forwarded to the European Commission, and the other notified bodies. 355. If a notified body finds that European approval for materials wrongly granted or that the material is contained in applicable standards, it shall withdraw the approval of the European materials and shall inform the European Commission, as well as other notified bodies. 356. the pressure equipment or materials used for the manufacture of complex conforming with European approvals for materials, the references of which have been published in the official journal of the European Union, considers appropriate the provisions referred to in Chapter 3, with the essential safety requirements. 7. The notified body of the requirements and 357. The notified body shall be entitled to assess pressure equipment or assemblies, as well as the compliance of the materials and the welder or issue the pressure equipment used in the manufacture of European material approval if it has confirmed its compliance with this provision in paragraph 361. 358. The manufacturer's internal inspectorate is entitled to assess pressure equipment or assemblies, according to the rules referred to in section 5 of the conformity assessment procedures-A2, C2, (F) and (G) if the module manufacturer's internal Inspectorate has demonstrated compliance with this provision in paragraph 362 above requirements. In this case, you can not apply this provision in paragraph 357. 359. the pressure equipment or assemblies the conformity of which has been assessed by the manufacturer's internal inspectorate, only apply to organizations or groups of companies in their territories, which may be used for pressure equipment and running a group of companies, which is the manufacturer of the unit the internal inspectorate. Group of companies apply common security policies regarding technical specifications and their complex pressure equipment design, manufacturing, inspection, maintenance, and use. 360. the pressure equipment or assemblies the conformity of which has been assessed by the manufacturer's internal inspectorate, no CE marking. 361. The notified body shall meet the following requirements: 361.1. the institution has legal personality, and it acts as a third party that is independent of the economic operator (associations), pressure equipment or assemblies which it assessed; 361.2. 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 estimate or a complex pressure equipment design, manufacture, supply, installation, use or maintenance; the management of the institution and 361.3. employees who are responsible for the conformity assessment of pressure equipment not being valued or complex the designer, manufacturer, supplier, Installer, purchaser, owner, user, attendant or their authorised representatives. This does not prevent them from using the rated pressure equipment or assemblies in their business or personal purposes; the management of the institution and 361.4. employee responsible for conformity assessment, is not directly related to the pressure equipment or assemblies of design, manufacture or construction, the marketing, installation, use, or service and do not represent the parties engaged in these activities; the management of the institution and 361.5. staff shall not engage in activities (including counselling), which may conflict with their independence and fairness of the decision in relation to the institution for evaluation activities; 361.6. the institution shall ensure that its affiliates and subcontractors do not affect the operation of conformity assessment confidentiality, objectivity and impartiality; 361.7 institution and its employees. conformity assessment shall be carried out in good faith and is a professional, technically competent. The personnel are free from any influences (including financial), which might influence their judgement or the results of the conformity assessment, especially from persons or groups of persons with an interest in the result of this procedure; 361.8. the institution of is able to carry out all the conformity assessment tasks for which it has fixed this rule 47.4 47.5 in and or 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 361.9. conformity assessment procedures and categories of pressure equipment and for which it has been notified, is: 361.9.1. necessary personnel with technical knowledge and relevant experience, to perform the necessary conformity assessment activities; 361.9.2. 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; 361.9.3. operation procedures that take into account the economic size of the offender, the industry in which it operates, its structure, the degree of complexity of the technology in question and the mass or serial nature of the production process; 361.10. 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; 361.11. the staff responsible for carrying out conformity assessment activities are: 361.11.1. the technical and professional training for all relevant conformity assessment activities; 361.11.2. knowledge of the requirements for the activities to the conformity assessment activities and appropriate powers; 361.11.3. knowledge and understanding of the essential safety requirements, applicable standards and relevant legislation; 361.11.4. the necessary ability to draw up the certificates, records and reports to the conformity assessment; are institutions 361.12., its management and employees, making the impartiality of the conformity assessment activities; 361.13. wages received by the institution's management and employees carrying out conformity assessment activities, does not depend on the number of assessments carried out or on the results; 361.14. institution of civil liability is insured for the activities which it is empowered to make; 361.15. institutions employees observe professional confidentiality with regard to all information gained in carrying out conformity assessment activities (except for information that is provided to the market surveillance authorities); the institution participates in standardization 361.16. activities organized by the European Commission and notified bodies in the working groups on pressure equipment or assemblies, 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. 362. The manufacturer's internal inspectorate shall meet the following requirements: 362.1. Inspectorate has legal personality and is the organisational distinction between. The group, which is part of the Inspectorate are laid down in the reporting methods that ensure and demonstrate its impartiality; 362.2. Inspectorate management and employee responsible for conformity assessment shall not be assessed or complex pressure equipment Designer, manufacturer, supplier, Installer, purchaser, owner, user, attendant or their authorised representatives. This does not prevent them from using the estimated pressure equipment or assemblies or in the operation of the Inspectorate for personal purposes; 362.3. Inspectorate management and employee responsible for conformity assessment, is not directly related to the pressure equipment or assemblies of design, manufacture or construction, the marketing, installation, use, or service and do not represent the parties engaged in these activities; 362.4. Inspectorate's management and employees do not engage in any activity (including counselling), which may conflict with their independence and fairness of the decision in relation to the evaluation activities provided to it; 362.5. Inspectorate and its personnel conformity assessment shall be carried out in good faith and is a professional, technically competent. The personnel are free from any influences (including financial), which might influence their judgement or the results of the conformity assessment, especially from persons or groups of persons with an interest in the result of this procedure; 362.6. Inspectorate is able to carry out all the conformity assessment tasks for which it has been notified, whether these tasks are carried out by the Inspectorate itself or they are made in the name of the Inspectorate's responsibility; According to the Inspectorate activities 362.7. conformity assessment procedures and categories of pressure equipment and for which it has been notified, is: 362.7.1. necessary personnel with technical knowledge and relevant experience, to perform the necessary conformity assessment activities; 362.7.2. Description of the procedures, in accordance with which conformity assessment carried out, ensuring the transparency and the ability to repeat this procedure. Inspectorate has developed appropriate policies and procedures to tasks that it performed as the Inspectorate, were separated from the other activities; 362.7.3. operation procedures that take into account the economic size of the offender, the industry in which it operates, its structure, the degree of complexity of the technology in question and the mass or serial nature of the production process; 362.8. Inspectorate has the necessary means to enable it to perform properly the technical and administrative tasks connected with conformity assessment activities, and has access to all the necessary equipment and facilities; 362.9. the staff responsible for carrying out conformity assessment activities are: 362.9.1. the technical and professional training for all relevant conformity assessment activities; 362.9.2. knowledge of the requirements for the activities to the conformity assessment activities and appropriate powers; 362.9.3. knowledge and understanding of the essential safety requirements, applicable standards and relevant legislation; 362.9.4. the necessary ability to draw up the certificates, records and reports to the conformity assessment; 362.10. Inspectorate is assured, its management and employees, making the impartiality of the conformity assessment activities. Inspectorate must not engage in any activities that may conflict with the independence and fairness of the decision in relation to the activities of the Inspectorate; 362.11. wages received by the Inspectorate management and employees carrying out conformity assessment activities, does not depend on the number of assessments carried out or on the results; Inspectorate has insured 362.12. civil liability regarding the actions that it is entitled to make (unless civil liability is to insure a group of companies, which is part of the Inspectorate); the staff of the Inspectorate 362.13. observe professional confidentiality with regard to all information gained in carrying out conformity assessment activities (except for information that is provided to the market surveillance authorities); 362.14. Inspectorate participates in standardization activities and in the European Commission notified bodies in the working groups on pressure equipment directive or the package or ensure that information on these activities is available to its employees. In its activities the Inspectorate as guidelines used by the notified body working groups prepare for decisions and documents. 363. where the conformity assessment body shall certify its conformity 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 361 or 362. those requirements in so far as applicable standards cover those requirements. 364. If a notified body or the manufacturer's internal inspectorate concluded 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 rule 361.362, paragraph or these requirements and shall inform the Ministry of the economy. The notified body and the manufacturer's internal inspectorate shall assume full responsibility for the subcontractors and affiliates activity. 365. The notified body or by the manufacturer's internal inspectorate specific conformity assessment activity or branch transfer subcontractors only with the consent of the customer. 366. The notified body or by the manufacturer's internal Inspectorate keeps the records of subcontractors and affiliates and their competence assessment activities, the conformity assessment activities for these documents to be available to the Ministry of the economy. 367. The notified body and the manufacturer's internal inspectorate 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 of the pressure equipment or assemblies, the degree of complexity of technology and mass production process or the nature of the series, however, have a toughness and the level of protection required for pressure equipment meets the requirements of this regulation. 368. If the notified body and the manufacturer's internal inspectorate finds that the manufacturer has not adhered to the essential requirements or the corresponding applicable standards or other technical specifications laid down in the essential requirements, it shall require the manufacturer to take appropriate measures to remedy the non-compliance, and issue a certificate. 369. when monitoring of pressure equipment and assemblies the conformity requirements of these regulations upon issuance of the certificate, the notified body or by the manufacturer's internal inspectorate finds that the pressure equipment or assemblies no longer meet the requirements of this regulation, it shall require the manufacturer to take appropriate measures to remedy the non-compliance, and, if necessary, suspend or revoke the certificate. 370. If corrective action is not taken or it does not produce the desired results, the notified body or the manufacturer's internal inspectorate accordingly, limit, suspend or revoke the certificate. 371. The notified body and the manufacturer's internal inspectorate shall inform the Ministry of economy on: 371.1. each certificate of refusal, restriction, suspension or withdrawal; 371.2. any circumstances affecting the scope of the notice and conditions; 371.3. any market surveillance authorities requesting information regarding conformity assessment activities; 371.4. carried out conformity assessment activities notify sphere and other transactions, including cross-border activities and subcontracting (upon request). 372. The notified body and the manufacturer's internal inspectorate shall provide appropriate information on the negative and, on request, also on positive conformity assessment results reported other institutions carrying out similar conformity assessment activities covering the same pressure equipment and assemblies. 8. Declaration of conformity the Declaration of conformity for 373. indicates that the pressure equipment or assemblies in question compliance with the provisions referred to in Chapter 3, with the essential safety requirements. 374. The Declaration of conformity shall be drawn up according to the rules referred to in annex 2, supplemented with necessary information, derived from the relevant conformity assessment procedures, and regularly updated. The Declaration of conformity shall be drawn up in the Member States of the European Union language (s) in which the pressure equipment or assemblies is placed or offered on the market. 375. the pressure equipment or assemblies to apply more than one piece of legislation that requires a declaration of conformity, prepare one declaration of conformity to all applicable laws. Declaration of conformity indicates the relevant law and references to their publications. 376. in drawing up a declaration of conformity, the manufacturer takes responsibility for the conformity of the pressure equipment or assemblies referred to in these provisions. 9.377. Marking On 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. 378. The CE conformity marking shall be visible, easily legible and indelible manner on each copy of the pressure equipment and the assemblies of pressure equipment or, where that is not possible, the information on the plate. If this is not possible for the pressure equipment or Assembly, of the nature of the The CE conformity marking on the packaging and accompanying documents. 379. the CE conformity marking must not be affixed to each copy of the pressure equipment constituting complex. If the individual pressure equipment, which already have the CE conformity marking, built into the complex, the "CE" marking is not removed from them. 380. The CE marking of conformity puts on the pressure equipment or Assembly before the placing on the market. 381. the CE conformity marking indicates the identification number of the notified body, if the notified body involved in the production control phase. Notified body identification number shall be the same institution or under its instructions to oblige the manufacturer or its authorised representative. 382. the CE conformity marking and the identification number of the notified body may specify other labels for specific risks or use. 10.383. Pressure equipment market surveillance and supervision of the complex market consumer protection centre, and that the meaning of these provisions constitute a market supervisory authority. 384. Pressure equipment and assemblies under the supervision of the market applicable to Regulation No 765/2008 article 15, paragraph 3, and article 16-29. 385. the manufacturer and importer to market surveillance authorities to request the technical documentation or a translation of the portion of the national language. Market surveillance authority requests the technical documentation or the submit portion of the translation determines within 30 days of the period (except in the case of serious and immediate risk detection is required due to the shorter term). 386. 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. 387. the interested party concerned is obliged to prevent inconsistency market surveillance authorities within the time limits which are commensurate with the risks of non-compliance, if the market surveillance authority finds that any of the following administrative irregularities: 387.1. CE conformity marking does not comply with the provisions referred to in Chapter 9; 387.2. The CE conformity marking has not been affixed; not imposed on its 387.3. notified body identification number, which was involved in the production of pressure equipment and assemblies the control phase, or it is imposed without regard to the provisions of Chapter 9 of such requirements; 387.4. the Declaration of conformity is made or it is ready; 387.5. technical documentation is not available or it is incomplete; 82. these provisions 387.6. and information referred to in paragraph 94 is not specified or it is faulty or incomplete; This is what 387.7. other 4.1. and 4.3 in sub-chapter administrative requirement. 388. where the market surveillance authorities find that the pressure equipment or complex presents a risk to the public interest, taking into account the pressure equipment or assemblies the risks, take the appropriate assessment of the pressure equipment or Assembly, including all relevant requirements in these rules. The person involved has an obligation to cooperate with the market surveillance authorities in that assessment. 389. 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 measures to ensure the conformity of the pressure equipment and assemblies the requirements of these regulations or, if necessary, withdraw, or withdraw it from the market, as well as to inform the concerned found the notified body, if the rules referred to in paragraph 387. pressure equipment and assemblies assessment the market surveillance authority finds one of the following situations: 389.1. pressure equipment or complex does not meet the requirements of these regulations; the pressure equipment or assemblies 389.2. complies with the requirements laid down in these rules, but the risks for the protection of the public interest. 390. If the person involved in market surveillance authorities within the time limits which are commensurate with the risks of non-compliance does not prevent this provision in paragraph 387 of the non-compliance with this rule or 389. the obligations referred to in paragraph 1, the market surveillance authority shall, in accordance with the legislation on the safety of goods and services is entitled to adopt a decision prohibiting the pressure equipment and assemblies the placing on the market or the placing on the market or, if need be , recall or withdraw it from the market. 11. cooperation with the European Commission and the Member States of the European Union and their complex pressure equipment 11.1, which does not comply with the requirements of this regulation 391. Where the market surveillance authority has reason to believe that the pressure equipment and assemblies which made this provision, paragraph 388 assessment and found that they do not meet the requirements of this regulation, are also offered in other Member States of the European Union, the market surveillance authority, obtaining all the necessary information, shall promptly inform the European Commission and the other Member States of the European Union about the results of the assessment carried out and the market surveillance authorities for specific measures to be taken by specifying all the necessary details, including: pressure equipment and assemblies 391.1. the identification of the necessary information; 391.2. details of pressure equipment and assemblies of origin; 391.3. nature and non-compliance risks; 391.4. information about the specific nature of the measures to be taken and the duration, as well as relevant stakeholders explanations and arguments; 391.5. information about the nature of non-compliance – pressure equipment and assemblies of non-compliance with the essential safety requirements or deficiencies in the applicable standards. 392. If, within three months after this provision in paragraph 391 of the information given 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. 393. The European Commission shall take a decision that the market surveillance authorities imposed the measures are unjustified, they are irrevocable. 394. where the market surveillance authority receives the rules referred to in paragraph 390. information from another Member State of the European Union, the market surveillance authority shall immediately inform the European Commission and the other Member States of the European Union on the measures taken and provide the information on the pressure equipment and the assemblies, as well as inform on their objections, if it does not agree with the other European Union market surveillance authorities for specific measures to be taken. 11.2. the requirements of this regulation in accordance with pressure equipment and assemblies, with risk of 395. Where the market surveillance authority has reason to believe that the pressure equipment and assemblies which made this provision, paragraph 388 assessment and determined that they meet the requirements of these provisions, but the risk to the health or safety of people or pets or property, the market surveillance authority shall inform the European Commission and the other Member States of the European Union, indicating all available information including: pressure equipment and assemblies 395.1. the identification of the necessary information; 395.2. details of pressure equipment and assemblies to the origin and the supply chain; 395.3. information on risks; 395.4. information on market surveillance authorities to identify the nature of the measures to be taken and duration. 396. The European Commission by this provision in paragraph 395 of receipt of the information referred to in the decision that the market surveillance authorities the measures are unjustified, they are irrevocable. 12. concluding issues 397. Be declared unenforceable on Cabinet 2 May 2000 by Regulation No 165 "provisions of the pressure equipment directive and their complexes" (Latvian journal, 2000, 161/163. No; 2002, 139. No; 2004, nr. 68.145., no; 2008; 2009, 204. no). 398. Pressure equipment and assemblies thereof placed on the market until the date of entry into force of the provisions, may be placed on the market and put into use if it meets the Cabinet 2 May 2000 by Regulation No 165 "provisions of the pressure equipment directive and their complexes". 399. the certificate and decisions issued up to the effective date of the rules under the Cabinet of Ministers of 2 May 2000 by Regulation No 165 "provisions of the pressure equipment directive and the package" specified therein shall be valid until the expiry date. 400. the rules shall enter into force on 19 July 2016. Informative reference to European Union directives, the provisions included in the law arising from the European Parliament and of the Council on 2014 15 may 2014/68/EU directive on the harmonisation of the laws of Member States relating to pressure equipment available on the market. Prime Minister, Minister of finance Dan Reizniec-Oak of the Deputy Prime Minister, Minister of economy of 1. Ašeraden Arvil annex Cabinet June 2016 7. Regulations No 348 of pressure equipment pressure equipment categories are divided into categories according to this annex 1., 2., 3., 4., 5., 6., 7., 8 and 9 are specified in conformity evaluation drawing charts. Line charts that specify each category of pressure equipment for the upper limit.
1. mark. 8.1.1.1. The provisions for vessels referred to in point breakdown categories note. Containers intended for unstable to contain gas and complies with category I or II, are to be classified in category III.
2. mark. Provision 8.1.1.2. the vessels referred to in point breakdown of categories note. Portable or transportable fire extinguishers and tanks of the tank breathing equipment be classified not lower than class III.
3. mark. 8.1.2.1. The provisions referred to in the breakdown of categories 4 tanks. sign. 8.1.2.2. The provisions referred to in the breakdown of categories tanks note. 9.2. The provisions referred to in subparagraph complex intended for the warm water production, respectively, subject either to the project type examination (module B) as to their conformity with the essential requirements referred to in rule 41, 42, 43, 44, 45, 53, 54, 55, and 63.4 in 39.2., or comprehensive quality assurance (module H).
5. mark. Rule 8.2. containers referred to in categories of note. Household pressure cookers for projects subject to a conformity assessment procedure equivalent to at least one of the terms referred to 112.3. Category III modules.
6. mark. 8.3.1.1. The provisions referred to in the pipeline Division categories note. Pipeline unstable gases according to this drawing correspond to category I or II, are to be classified in category III.
7. mark. 8.3.1.2. The provisions referred to in the pipeline Division categories note. All piping containing fluids with temperatures above 350 ° C and in accordance with this drawing correspond to category II, are to be classified in category III.
8. mark. 8.3.2.1. The provisions referred to in the category of pipeline breakdown 9. Fig. 8.3.2.2. The provisions referred to in the category of pipeline breakdown Deputy Prime Minister, Minister of economy of Ašeraden of Arvil annex 2 Cabinet 2016 7. Regulation No 348 June Declaration of conformity 1. pressure equipment pressure equipment or complex model (product type, batch or serial number). 2. the manufacturer and, where applicable, the authorized representative's name and address. 3. A statement that the Declaration of conformity is issued only to the manufacturer's responsibility. 4. Object of the Declaration (or complex pressure equipment pressure equipment identification to ensure traceability. If it is necessary for identification of the pressure equipment may be added or complex image): 4.1 description of the pressure equipment or assemblies; 4.2. carry out the conformity assessment procedure; 4.3. the pressure equipment – the complex description of the pressure equipment within the complex, and the conformity assessment procedures. 5. A statement that the pressure equipment or complex pressure equipment complies with relevant legislation. 6. References of applicable standards or other technical specifications in relation to which conformity is declared. 7. information on the notified body involved, name and number of institution, the institution of the conformity assessment activities and issued certificates (a reference to the EU type-examination certificate, the type of production, the EU type-examination certificate, project type, project the EU certificate of inspection or certificate of compliance). 8. additional information. 9. information on preparation of the Declaration of conformity: 9.1 the place and date of issue; 9.2. the establishment's name, position and signature. Deputy Prime Minister, Minister of economy of Ašeraden of Arvil