Cabinet of Ministers Regulations No. 84 in 2013 (5 February. 7. § 17) the rules on the use of certain chemical substances restrictions of electrical and electronic equipment in accordance with the Issued chemical law article 16 the second part and the law "on conformity assessment" 7. the first paragraph of article i. General questions 1. determines: 1.1. separate dangerous chemical limits to the use of electrical and electronic equipment (hereinafter equipment); 1.2. the obligations of the person who manufactured, imported or distributed; 1.3. the essential requirements of the equipment and the compliance monitoring mechanisms. 2. The terms used in the following terms: 2.1 equipment-equipment for proper operation is dependent on electric currents or electromagnetic fields (that is, electrical current or electromagnetic field necessary to plant one of the design), as well as the equipment of such power and the generation, transfer and measurement of the use of which the nominal voltage not exceeding 1000 Volts for alternating current and 1500 volt for direct current; 2.2. the large stationary industrial machinery-machinery, equipment or component assembly that oversized work together for a particular purpose and that particular place permanently installed and dismantled, as well as industrial manufacturing or research and development use and serving object; 2.3. large stationary device – several types of apparatus and, where other devices oversized connection for permanent use of the previously designated specific location and that assembling and installation, as well as thwarted; 2.4. cables, cables with rated voltage below 250 volts, used as connectors or an extension cord to connect the equipment to an electrical outlet, or connect two or more devices; 2.5. the manufacturer – natural or legal person who manufactures a machine or ask to design or produce equipment and distributes it under his name or trademark; 2.6. the authorized representative: the natural or legal person who carries out economic activities in the European Union and who has written authorization of the manufacturer to act on his behalf, performing specific tasks; 2.7. Distributor: the natural or legal person other than the manufacturer or importer of the equipment, but which offers the equipment on the market; 2.8. importer: the natural or legal person carrying out economic activities in the European Union and put the equipment on the market of the European Union from third countries; 2.9. the economic operator, the manufacturer, his authorised representative, the importer and the Distributor; 2.10. to offer market-supply equipment for distribution, consumption or use on the European market for payment or free of charge, through economic activities; 2.11. the placing on the market-the first to offer equipment market of the European Union; 2.12. the applicable standard – at the request of the European Commission the European Committee for standardisation, European Committee for Electrotechnical Standardization or the European Telecommunications Standards Institute developed and accepted standard; 2.13. technical specification-a document which lays down the technical requirements which a product, process or service must meet; 2.14. the CE conformity marking-marking, by which the manufacturer indicates that the product complies with European Union harmonisation legislation requirements; 2.15. the conformity assessment – the process demonstrating whether the requirements of this Regulation as regards the equipment; 2.16. market surveillance, market surveillance authorities the activities carried out and measures taken to ensure compliance with this provision of the equipment requirements and prevent equipment damage health, security or other public interests; 2.17. withdrawal – measures to get back the plant, which already offered to end users; 2.18. withdrawal – measures to prevent the equipment from the supply chain is offered in the market; 2.19. the homogeneous materials-exactly the same composition material or material that consists of material connection that cannot be separated or split into individual materials by using the mechanical actions as unscrewing, cutting, crushing, grinding and abrasive techniques; 2.20. the industrial monitoring and control instruments-monitoring and control tools designed exclusively for industrial or professional purposes; 2.21. the availability of substitution treatment – the ability to produce and deliver a reasonable substitution period, comparable to the period required to produce and deliver these rules referred to in annex 1; 2.22. substitution reliability – the likelihood that equipment used in substitution treatment, excellent will perform the desired function in certain circumstances and within a specified time period; 2.23. spare part-individual equipment component that can replace some equipment parts and without which the machine is unable to perform the functions provided for, but the machine functions are restored or improved if any parts are replaced by spare parts; 2.24. the mobile technique, not only roads and professional needs, the technique with a built-in drive, which provides mobility and continuous or semi-continuous movement between a fixed workplaces during working hours only to professional needs; 2.25. medical device-medical device according to the regulations on treatment, if it is a machine; 2.26. in vitro diagnostic medical devices, in vitro diagnostic medical device according to the regulations on the registration of medical devices, conformity assessment, distribution, operation and technical supervision; 2.27. active implantable medical devices, active implantable medical devices according to the regulations on the registration of medical devices, conformity assessment, distribution, operation and technical supervision. 3. the rules apply to equipment listed in annex 2 to these regulations.

4. the rules do not apply to: 4.1 equipment directly used in the national security interests and military purposes, including weapons, ammunition and military equipment; 4.2. equipment destined for space; 4.3. the equipment specially designed and installed as part of another type of equipment not covered by these regulations and which can perform its functions only as a part of these devices, and they may be replaced only with the same specially designed equipment; 4.4. large stationary industrial machinery; 4.5. the large stationary devices; 4.6. the passenger or freight vehicles, except in a non-approved type of electric vehicles with two wheels; 4.7. the mobile technique, not only roads and professional needs; 4.8. active implantable medical devices; 4.9. the solar photovoltaic panels, which are intended to be used in the system that is designed, assembled and installed by a professional in a predefined location permanently to get electricity from the Sun, public, commercial and industrial needs, as well as the needs of the population; 4.10. equipment specially designed for research and development purposes and is available only to economic operators.
II. restriction of use of substances in equipment 5. Market equipment, including cables and spare parts to repair, re-use, or for updating function capacity must not exceed the provisions mentioned in annex 1 of the chemicals the maximum concentration in homogeneous materials. 6. The provisions of paragraph 5 shall not apply to: 6.1. cable or spare parts for repair, reuse, or to update the function capacity: 6.1.1. equipment placed on the market before 1 July 2006; 6.1.2. medical devices placed on the market before 2014 July 22; 6.1.3. medical devices, in vitro diagnostics, placed on the market before July 22, 2016; 6.1.4. monitoring and control instruments placed on the market before 2014 July 22; 6.1.5. the industrial monitoring and control instruments placed on the market before July 22, 2017; 6.1.6. equipment covered by the regulations on the use of certain chemical substances restrictions exceptions and certain equipment which is placed on the market before it lapsed exceptions; 6.2. the reusable parts obtained from equipment placed on the market before 1 July 2006, and used equipment placed on the market before 1 July 2016, if the parts used in the audited again in a closed system and the reuse of it is notified to the consumer; 6.3. This provision is referred to in the annex to the 3 levels of lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers of the of use; 6.4. the rules referred to in annex 4 levels of lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers in the use of medical devices and control and monitoring instruments. 7. Equipment manufacturer, the manufacturer's authorised representative, or any economic operator in the supply chain can submit proposals to the European Commission to determine the rules in annex 3 and 4 above a limit value for lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers of the use of the use of the extension or cancellation not later than 18 months before the expiry of the permitted use. The proposal shall include at least the following information: 7.1 the applicant firm proposal, its legal address and contact information; 7.2. information on the material or component and the use of this substance in the material or component for which the requested derogation or exception waiver, as well as their exact characteristics; 7.3. test for the determination of the permitted usage or cancellation justification (including references), taking into account that: 7.3.1. lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers in the use of the equipment, materials and components in accordance with the provisions of annex 3 and 4 is permitted if it complies with the European Parliament and of the Council of 18 December 2006 in Regulation No 1907/2006 concerning the registration, evaluation, authorisation and restriction of chemicals (REACH) and establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC, the requirements for environmental and health requirements and at least one of the following conditions : 7.3.1.1. the termination of the use of chemical or its replacement is technically or scientifically impossible by making changes to the facility or project inputs or components which do not require any of the rules referred to in annex 1; 7.3.1.2. it is not possible to ensure the reliability of the substitution; 7.3.1.3. total negative impact to the environment, health and consumer safety caused a second, larger than the total benefits would use the second environment, health and consumer safety; 7.3.2. lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers in the use of the equipment, materials and components should be annulled, if it does not comply with the provisions of point 7.3.1. conditions; 7.4. possible alternative substances, material or design analysis, based on the life cycle, as well as adding information about independent studies, comparative professional assessments and the development of the applicant's activities, as well as the availability of such alternative solutions; 7.5. information on the possible preparation of waste for reuse or recycling, as well as the relevant provisions of the processing in accordance with the laws and regulations on the management of waste, and other appropriate information; 7.6. the measures proposed by the applicant of the proposal to establish, develop or require the application of the alternative options, and the time schedule for the implementation of the measures; 7.7. If necessary, information on the ownership by adding verifiable justification; 7.8. precise and explicit exception, if submitted a proposal for a new exception; 4.9. Summary of the proposal.

III. Evaluation of conformity and the CE marking of conformity 8. to demonstrate that the equipment complies with the provisions of paragraph 5 of the said requirements before placing on the market, the manufacturer shall carry out conformity evaluation procedure: internal production control, which include the following: 8.1 the equipment technical documentation development in accordance with the provisions of paragraph 10; 8.2. all manufactured equipment in the production process of ensuring compliance with the rules referred to in paragraph 10 of the technical documentation and with the requirements of this regulation; 8.3. installation the model Declaration of conformity with the European Union (hereinafter referred to as the Declaration), with which the manufacturer certifies that is shown to comply with the requirements of this regulation; 8.4. the marking of the equipment with the CE marking of conformity. 9. the manufacturer of the equipment with the provisions of paragraph 5 of these requirements can be shown also by performing a conformity assessment procedure in accordance with other legislation on conformity assessment, if they are defined as strict as the requirements in these regulations, and to develop common technical dossier. 10. Technical documentation contains all of the data or instructions about the features that are used by the manufacturer to enable the equipment conformity with the requirements of this regulation, including: 10.1. detailed equipment design and manufacturing schedule, information about equipment, ingredients and materials used, as well as the safety data sheets on chemicals used, received from chemical suppliers; 10.2. design sketches, production drawings, parts, Assembly, power circuits and other necessary schemes; 10.3. the descriptions and explanations necessary for the said drawings, diagrams and an understanding of the equipment; 10.4. the use of conformity assessment procedures; 10.5 applicable standards, parts (if standards are applied to the part) or the technical specifications to which reference is published in the official journal of the European Union; 10.6. the adopted solution description used to ensure equipment compliance with the requirements of this regulation, if the equipment is not used in the manufacture of these rules mentioned in paragraph 10.5. applicable standards or technical specifications; 10.7. a test report and a description of the features that the manufacturer has provided equipment for compliance with the applicable standards; 10.8. the design calculations made, examinations carried out, results and reports. 11. the Declaration affirms that the installations comply with the provisions in this paragraph 5. In preparing the Declaration, the manufacturer assumes responsibility for the equipment with the requirements of these regulations. The manufacturer or his authorised representative for each model of equipment produced prepares a written statement pursuant to the provisions of annex 5, and shall ensure that: 11.1. updating of the Declaration, except the Declaration of equipment is placed on the market before the entry into force of these regulations; 11.2. the Declaration of the State of the translation language. 12. The CE conformity marking applies general principles, the European Parliament and of the Council of 9 July 2008. Regulation 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, article 30. 13. The manufacturer shall ensure that before release onto the market of the equipment shall be marked with clearly legible and indelible marking of CE in the completed installations or equipment data plate. If the characteristics of the equipment that is not possible, with the "CE" marking shall be marked equipment packages and accompanying documents. 14. If the equipment is marked with the CE conformity marking, they are presumed to be in conformity with the requirements of this regulation, in the absence of evidence to the contrary. 15. materials, components and equipment comply with the requirements of this regulation, if satisfied one of the following: 15.1. they have undergone the tests and measurements, showing compliance with this provision in paragraph 5 above; 15.2. it complies with the applicable requirements of the standards to which reference has been published in the official journal of the European Union. 16. equipment that complies with the applicable standards or parts thereof, for which the requirements published in the reference Edition of the official journal of the European Union, shall be deemed to conform to those requirements in these rules covering these standards. The protection of the environment and regional development Ministry in cooperation with the society with limited liability "the standardization, accreditation and Metrology Centre" standardisation Office (hereinafter referred to as the standardisation Office) develop a list of the standards applicable to these rules and shall publish them in the internet homepage of standardisation Office (URwww.lvs.lv).
IV. Market surveillance

17. market surveillance measures are carried out in accordance with the European Parliament and of the Council of 9 July 2008. Regulation 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, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28 and 29. 18. Market surveillance shall be carried out under the supervision and control authority, if its competence is laid down any equipment market surveillance and control (hereinafter referred to as the market supervisory authority). Carrying out market surveillance, market surveillance authorities officials are entitled: 18.1. to control and monitor equipment put on the market in compliance with the requirements of these rules, visit the trade, storage and production sites, as well as sample checks of the equipment (priekštestēšan), including opening the packaging and testing of samples; 18.2. to request and receive free of charge information (including technical documentation, test reports of declarations) required to carry out supervision according to the requirements in these rules; 18.3. to require the manufacturer or importer to ensure that the relevant parts of the technical documentation translation into national languages, giving reasons for the necessity of translation; 18.4. to request and receive, free of charge, samples of the equipment and expertise to organize it, to determine the compliance of the equipment with the requirements of these regulations. 19. The costs of inspection of equipment covered under the legislation on the safety of goods and services. 20. where the market surveillance authorities find that the facilities are not prepared or are not properly prepared for the EU Declaration of conformity, not available or not complete technical documentation or equipment is marked with the CE marking of conformity, not subject to the requirements of this regulation or not marked at all, the market surveillance authority of the producer concerned, the authorized representative or the importer instructs the specified period to prevent found. 21. If the rules referred to in paragraph 20 of the non-compliance with the deadline does not clear, the market surveillance authority may adopt a decision in accordance with the laws and regulations on the safety of goods and services, by prohibiting the placing on the market and offering and asking to remove the equipment from the market or to recall it. 22. where the market surveillance authorities find that the equipment does not meet the requirements contained in these provisions (except paragraph 20 of these rules), so, in view of the risk of the equipment, ensure that the reasonable time for corrective action to ensure equipment compliance requirements, its withdrawal from the market or recall.
23. market surveillance authorities shall be entitled to propose the manufacturer, his authorised representative, the importer or the Distributor to make the voluntary corrective actions for the prevention of non-compliance of the equipment. 24. If the manufacturer, the authorised representative, the importer or the distributor within a reasonable time does not take appropriate corrective action voluntarily, the market surveillance authority may adopt a decision according to the legislation on the safety of goods and services.
V. manufacturers, authorised representatives, importers and distributors ' obligations

25. when placing the machine on the market, manufacturers shall ensure that they are designed and produced according to the provisions in paragraph 5. 26. Manufacturer: 26.1. develop technical documentation, and carry out conformity assessment – internal production control according to point 8 of these rules; 26.2. the Declaration shall be prepared pursuant to paragraph 10 of these regulations and shall be marked with the CE mark according to the provisions of paragraph 13 if, conformity assessment has found that the equipment meets the requirements of these regulations; 26.3. save the technical documentation and Declaration of the 10 years following the placing on the market; 26.4. develop and apply procedures to series production equipment to ensure continued compliance with the requirements of these provisions, as well as take into account the design characteristics of equipment or changes, changes in applicable standards or technical specifications under which the declared equipment; 26.5. take appropriate facilities and equipment records withdrawn (the registering equipment type, batch or serial number or other reference that supports the identification of the equipment), as well as inform on those distributors; 16.5. ensure that equipment is a type, batch or serial number or other reference that supports their identification, or, where the size or nature of the equipment does not allow it, ensure that this information is provided on the packaging or in a document accompanying the equipment; 16.6. points to the equipment or, where that is not possible, on the packaging of the equipment or the documents attached to your name (company), registered trade name or registered trade mark and the address. Specifies the contact address that you may contact the manufacturer. If the legislation for the registration of medical devices, conformity assessment, distribution, operation and technical monitoring procedures are at least as strict conditions for the manufacturer's name and address, apply those laws and regulations; 26.8. If the manufacturer considers or has reason to believe that the equipment that it placed on the market do not meet the requirements of these regulations, shall immediately take the necessary corrective actions to ensure conformity of the equipment or, if necessary, to recall or withdraw them from the market, and to immediately inform the market surveillance authorities of the EU Member States where the equipment is available, giving detailed information about the non-compliance and of any measures taken to prevent non-compliance; 26.9. after market supervisory authority a reasoned request shall provide it with all necessary information and technical documentation in the national language, to demonstrate compliance with this provision of the equipment; 26.10. the market surveillance authorities shall cooperate with the request of the various activities to ensure the equipment placed on the market conform to the requirements of the rules. 27. the manufacturer with the written mandate can appoint an authorized agent. Not be included in the mandate of the rules referred to in paragraph 25 of the manufacturer's responsibility to ensure that the equipment is designed and produced according to the provisions in paragraph 5 of these requirements, and the development of technical documentation. 28. the authorised representative shall perform the tasks specified in the mandate of the manufacturer. Authorised representative the manufacturer shall carry out at least the following obligations under the mandate: 28.1. retains the technical documentation and Declaration of the 10 years following the placing on the market, so it would be available to the market surveillance authority; 28.2. the market surveillance authorities a reasoned request shall provide it with all necessary information and documentation in the national language, to demonstrate compliance with this provision of the equipment; 28.3. the market surveillance authorities shall cooperate with the request of the various activities to ensure the mandate issued by the conformity of the equipment referred to in this regulation. 29. it is the responsibility of the importer to be placed on the market according to the requirements of this regulation. 30. The importer: 30.1. ensure that, prior to the placing on the market, the manufacturer has carried out the conformity assessment procedure of internal production control according to point 8 of these rules; 30.2. ensure that, prior to the placing on the market, the manufacturer has developed technical documentation according to point 10 of these regulations, labelled with the CE mark according to paragraph 13 of these regulations, as well as added the necessary documents and completed the rule 26.5 and 16.5. the requirements referred to in subparagraph; 30.3. where an importer considers or has reason to believe that the equipment does not comply with the provisions of paragraph 5 of the above requirements, this equipment should not be placed on the market, pending a equipment with, and shall inform the manufacturer and the market surveillance authority; 18.9. points to the equipment or, where that is not possible, on the packaging of the equipment or the documents attached to your name (company), registered trade name or registered trade mark and the address. Specifies the contact address that you may contact the importer. If the legislation for the registration of medical devices, conformity assessment, distribution, operation and technical monitoring procedures are at least as strict conditions for the importer's name and address, apply those laws and regulations;

5. take the appropriate facilities and equipment withdrawn records (recording equipment type, batch or serial number or other reference that supports the identification of the equipment), as well as inform on those distributors; 19.0. where an importer considers or has reason to believe that the equipment, which it placed on the market do not meet the requirements of these regulations, shall immediately take the necessary corrective actions to ensure conformity of the equipment or, if necessary, to recall or withdraw them from the market, and to immediately inform the market surveillance authorities of the EU Member States where the equipment is placed on the market, giving detailed information about the non-compliance and of any measures taken to prevent non-compliance; 19.1. in the 10 years following the placing on the market of the equipment in the EU kept a copy of the Declaration of conformity, available to the market surveillance authority, and by market surveillance authorities request technical documentation available to it; 19.1. the market surveillance authorities a reasoned request shall provide it with all necessary information and technical documentation in the national language, to prove the market equipment with the requirements of these regulations; 19.2. the market surveillance authorities shall cooperate with the request of the various activities to ensure the equipment placed on the market conform to the requirements of the rules. 31. Providing equipment on the market, distributors shall act with due care to ensure compliance with this provision of the equipment requirements. 32. Distributor: 32.1. before placing on the market of the equipment make sure that they are marked with the CE mark according to the provisions of paragraph 13 and are accompanied by the necessary documents in the language of the country, as well as the manufacturer has noticed this rules 26.5 and 16.5. the requirements referred to in point, but the importer of these regulations – 19.5. the requirements referred to in subparagraph; 32.2. If a distributor considers or has reason to believe that the equipment is not in conformity with this provision in paragraph 5 of these requirements, it does not offer the equipment on the market, pending compliance of equipment, and shall inform the manufacturer or the importer and market supervisory authority; 32.3. If a distributor considers or has reason to believe that the equipment, which it has offered on the market do not meet the requirements of this regulation, ensure that corrective action is taken to achieve conformity of the equipment or, if necessary, to recall or withdraw them from the market, and to immediately inform the market surveillance authorities of the EU Member States where the equipment is placed on the market, giving detailed information about the non-compliance and of any measures taken to prevent non-compliance; 32.4. the market surveillance authorities a reasoned request shall provide it with all necessary information and documentation in the national language, to prove the market equipment with the requirements of these regulations; 32.5. the market surveillance authorities shall cooperate with the request of the various activities to ensure the equipment placed on the market conform to the requirements of the rules. 33. under the terms of The importer or distributor shall be considered a manufacturer, and it is these rules 26 and 27. the manufacturer's obligations referred to in paragraph 1, if that equipment placed on the market under his name or trademark or modifies equipment placed on the market in a way that may affect the conformity of the equipment to the requirements of this regulation. 34. the market surveillance authorities on request operating operator for 10 years after the placing on the market provide information indicating any economic operator who has supplied it equipment, and any economic operator who has supplied it equipment.
Vi. Closing questions 35. Be declared unenforceable in the Cabinet of Ministers of 17 august 2004, Regulation No 723 "rules on the restriction of use of chemical substances in electrical and electronic equipment" (Latvian journal, 2004, no. 131; 2006, 21, nr. 140; 2007, 2008 57 no; no 139; 2010, 101 no). 36. the equipment before the entry into force of these regulations shall not apply to laws on hazardous chemical substances restrictions and that the date of entry into force of the rules do not match the requirements of this regulation are allowed on the market until 2019. on 22 July. 37. paragraph 5 of these rules shall apply: 37.1. medical devices and monitoring and control instruments placed on the market from July 22, 2014; 37.2. in vitro diagnostic medical devices placed on the market from 22 July 2016; 37.3. industrial monitoring and control instruments placed on the market from July 22, 2017.
Informative reference to European Union directives, the regulations include provisions resulting from: 1) of the European Parliament and of the Council of 8 June 2011-2011/65/EU directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment; 2) of the European Commission in 2012 delegated 10 October 2012/50/EU directive, which, by adapting to scientific and technical progress, the European Parliament and the Council amending Directive 65/2011/EU Annex III in respect of applications containing lead; 3) 2012 the European Commission's delegation in 10 October 2012/51/EU directive, which, by adapting to scientific and technical progress, the European Parliament and the Council amending Directive 65/2011/EU Annex III in respect of applications containing cadmium. Prime Minister v. dombrovsky environmental protection and regional development Minister e. Sprūdž of annex 1 of the Cabinet of Ministers of 5 February 2013 regulations No 84 chemicals whose use equipment is limited, and their maximum permissible concentrations no PO box Chemicals and chemical groups of maximum concentrations of homogeneous material mass 1. Lead 0.1% 2. Mercury 0.1% 3. 0.01% cadmium 4. Hexavalent chromium 0.1% 5. Polybrominated biphenyls (PBB) 0.1% 6. Polybrominated diphenyl ethers (PBDE) 0.1% of environmental protection and regional development Minister e. Sprūdž in annex 2 of the Cabinet of Ministers of 5 February 2013 regulations No 84 categories of equipment covered by these rules

No PO box Category of equipment 1. Large household appliances 2. Small household appliances 3. Information technology and electronic communication equipment 4. Consumer equipment 5. Lighting equipment 6. Electrical and electronics tools 7. Toys, leisure and sports equipment 8. Medical devices 9. Monitoring and control instruments, including industrial monitoring and control instruments 10. Vending machines 11. Facilities that do not fit into any of these categories of environmental protection and regional development Minister e. Sprūdž in annex 3 of the Cabinet of Ministers of 5 February 2013 regulations No 84 levels of lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers in the use of the no PO box Usage scope and time limits 1. Mercury single (compact) fluorescent lamps (one light emitting): 1.1. for general lighting not more than 2.5 W < 30 mg 1.2. for general lighting > = 30 W 50 W maximum and < 3.5 mg 1.3. for general lighting ≥ 50 W and 150 W < not more than 5 mg 1.4. general lighting > = 150 W maximum 15 mg 1.5 for general lighting with the circle or square and tube diameter ≤ 17 mm, not more than 7 mg 1.6. special needs not more than 5 mg of Mercury 2 linear fluorescent lamps in double for general lighting (one lamp): 2.1 tri-band phosphor lining a lamp with a normal life and the tube diameter < 9 mm (e.g. T2) not more than 4 mg 2.2. tri-band phosphor lining a lamp with a normal life and the tube diameter ≥ 9 mm and ≤ 17 mm (e.g. T5) not more than 3 mg 2.3. tri-band phosphor lining bulbs with normal life and tube diameter > 17 mm and ≤ 28 mm (such as T8) not exceeding 3.5 mg 2.4. Tri-band phosphor lining a lamp with a normal life and the tube diameter > 28 mm (e.g. S8) not exceeding 3.5 mg 2.5. Tri-band phosphor lining a lamp with a long service life (> = 25000 h) not more than 5 mg 3. Mercury in other lamps fluorescent (one lamp): 3.1. for the non-linear halofosfāt lamp (all diameter) not more than 15 mg in effect until 2016 13 April 3.2. non linear tri-band phosphor lining a lamp with the tube diameter > 17 mm (such as T9) not more than 15 mg of 3.3. another type of lamp for general lighting and special needs (e.g. Induction lamp) not more than 15 mg 4. Mercury cold cathode fluorescent lamps (CCFL) and an external electrode fluorescent lamps (EEFL) special needs (one lamp): 4.1. light bulb with a length ≤ 500 mm up to 3.5 mg 4.2. light bulb with a length of 500 mm and ≤ 1500 mm > in not more than 5 mg of 4.3. bulb length of 1500 mm with > not more than 13 mg per 5. Mercury in other low pressure discharge lamp (single lamp) not more than 15 mg 6. Mercury high pressure sodium (vapour) lamp for general lighting with will improve color rendering index Ra > 60 (one light emitting): 6.1. 155 W p ≤ 30 mg 6.2. 155 W < 405 P ≤ W, not more than 40 mg 6.3 P > 405 W not more than 40 mg 7. Mercury in other high pressure sodium (vapour) lamp for general lighting in (one light emitting): 7.1. P ≤ 155 W maximum 25 mg 7.2. 155 W < P ≤ 405 W not more than 30 mg 7.3 P > 405 W not more than 40 mg 8. Mercury high pressure mercury (vapour) lamp (HPMV) in force until 2015 April 13, 9. Mercury metal halide (MH) lamps 10. Mercury in other gas discharge lamps, which are not specifically mentioned in this annex 11. Lead in glass of cathode-ray 12. Lead glass, fluorescent lamps not exceeding 0.2% 13. Lead as an alloying element in steel tooling and galvanized steels containing up to 0.35% lead by weight 14. Lead as an alloying element in aluminum, which is up to 0.4% lead by weight 15. Copper alloy containing up to 4% lead by weight 16. Lead in solders with high melting temperature (i.e., lead alloys with a lead content of at least 85%)   17. Lead in solders for servers, storage and storage array systems, network infrastructure switching, signalling and transmission equipment as well as network management for telecommunications in the field of 18. Electric and electronic components in which the lead is glass or ceramics, ceramic dielectric capacitors are not, such as piezoelectric device, or a glass or ceramic matrix, 19. Lead ceramic dielectric capacitors rated voltage of at least 125 V AC 250 V DC or 20. Lead ceramic dielectric capacitors rated voltage of less than 125 V AC 250 V for direct current or allowed to use spare parts equipment placed on the market before January 1, 2013 21. Cadmium and its compounds the lump-sum termodrošinātājo is allowed to use spare parts equipment placed on the market before January 1, 2012, 22. Cadmium and its compounds in electrical contacts 23. Chromium (VI) as the carbon steel cooling system in absorption refrigerators anti-corrosion feature up to 0.75% cooling solution 24. Lead bearing ieliktņo and compressors with aukstumnesēj box in the heating, ventilation, air conditioning and refrigeration (HVACR) 25. Lead, used C-press kontaktsaderīg connector systems allowed to use spare parts equipment placed on the market before the 2010 24 September 26. Lead, used in the kontaktsaderīg connector systems that do not have C-press allowed to use spare parts equipment placed on the market before 1 January 2013 27. Lead as a coating material for the thermal conduction module C-ring is permitted to use the equipment, spare parts, which are placed on the market before September 24 2010 28. Lead white glasses, used in optics  

29. Cadmium and lead glass filters and glass used for refractive standards 30. Lead in solders containing more than two elements for the connection, and the connection mikropocesor packages that lead content is more than 80% and less than 85 allowed to use spare parts equipment placed on the market before 1 January 2011 to 31. Lead in solders for stable electrical connection between semiconductor chip and integrated media flip-chip packages, 32. Lead straight incandescent tubes with silicate coating in force until 1 September 2013 to 33. Lead halide as emitting high intensity discharge (HID) lamps used for professional reprography in 34. Lead as activator in the fluorescent powder (1% lead by weight not more than) gas discharge lamps when used as tanning lamps that have phosphor lining such as BSP (bass 2 O 5: Pb) 35. Lead and cadmium in color for enamel and glass (borosilicate glass and glass natronkaļķ) 36. Lead in finishes of fine pitch components other than connectors with a step at least 0.65 mm allowed use of spare parts, the EEE placed on the market before the year 2010 September 24, 37. Lead in solders that used hollow and flat disc matrix ceramic multilayer capacitors to 38. Lead oxide surface conductivity of electron emiter displays (SED) used in structural elements, particularly the soldering material stiklkeramik and the ring of the stiklkeramik 39. Lead crystal glass composition such as referred to in Council Directive 69/493/EEC [1] of annex I (1, 2, 3 and 4. category) 40. Cadmium alloys electric/mechanical solder joints to electrical drivers directly on the winding sound transducers used in high-powered loudspeakers with sound pressure levels of 100 dB (A) at least 41. Lead in solders for flat bezdzīvsudrab fluorescent lamps (used, for example, liquid crystal displays, design or industrial lighting) 42. Stiklkeramik soldering of lead oxide in materials used for argon and krypton laser light Assembly 43. Lead in solders for electrical transformer soldering copper wire with a diameter up to 100 mm 44. Lead elements of the maiņrezistor adjustable base cermets 45. Lead high-voltage diode coating layer on zinc Borate glass hull 46. Cadmium and cadmium oxide films biezslāņ post, covered on the oxide with aluminium link 47. Cadmium color Confluence led (LED) with Group II-VI Semiconductors (10 μg Cd/mm2 < light-emitting area), intended for use in solid-state lighting or display systems in force until 1 July 2014 to 48. Lead the dielectric ceramic material composition on lead zirconate titanate as (PZ) base designed for capacitors that are discrete semiconductor circuits or devices part valid until 2016 July 21, 49. Cadmium analogue of fotorezistoro of optoelektronisk joining devices used in professional audio effect 31 December 2013 for environmental protection and regional development Minister e. Sprūdž in annex 4 of the Cabinet of Ministers of 5 February 2013 regulations No 84 levels of lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls and polybrominated diphenyl ethers in the use of medical devices and control and monitoring instruments no PO box Permissible usage 1. Equipment used for determining 1.1 ionizing radiation. lead, cadmium and mercury in detectors of ionising radiation 1.2. lead bearings in x-ray tube-1.3. lead in electromagnetic radiation amplification devices: microchannel plate and the kapilārplat 1.4. lead glass frit of x-ray tube and image intensifiers and lead in glass frit Binder for Assembly of gas lasers and for connection to convert electromagnetic radiation electrons 1.5. lead in shielding against ionizing radiation 1.6. lead test objects that are used in the field of radiolucent 1.7. lead stearate crystals used in x-ray diffraction in 1.8. radioactive isotopes of cadmium source portable x-ray fluorescence spectrometers 2. Sensors, detectors and electrodes 2.1. lead and cadmium ion selective electrodes including glass in body pH electrodes 2.2. lead anodes in electrochemical oxygen sensoro 2.3. lead, cadmium and mercury in infrared detectors 2.4. Mercury in reference electrodes: low chloride mercury chloride, mercury sulphate content and mercuric oxide 3. Other 3.1. cadmium in helium-cadmium lāzero 3.2. lead and cadmium lamps used in the spectroscopic atomabsorbcij 3.3. lead alloys as the heat conveying of superconducting and magnetic resonance image acquisition device (MRI) 3.4. lead and cadmium in superconducting materials, which are metal mounts MRI and SQUID detectors 3.5. lead counterweights 3.6. single crystal piezoelectric materials of lead for ultrasonic transducers 3.7. lead in soldering materials used ultrasonic transducers 3.8. Mercury in very high precision capacitive resistance and loss ratio and high frequency RF switches and relays, which is monitoring and control instruments, the amount of mercury per switch or relay not exceeding 20 mg 3.9. lead in soldering, portable emergency defibrilatoro provided to 3.10. lead soldering in high resolution infrared image render modules to determine the radiation in the range of 8-14 μm 3.11. lead in liquid crystals used in displays of Silicon (LCoS ') 3.12. cadmium x-radiation measuring filters environmental protection and regional development Minister e. Sprūdž in annex 5 of the Cabinet of Ministers of 5 February 2013 regulations No 84 of the European Union Declaration of conformity 1. Equipment (s) unique identification number 2 of the manufacturer or of his authorised representative, the firm and the legal address
 

3. the manufacturer (or installers) shall assume full responsibility for the message specified in the Declaration. 4. equipment (equipment identification that ensure its traceability, if needed, including a clear colorful image of the installations) 5. Confirmation that the installation complies with the European Parliament and of the Council of 8 June 2011-2011/65/EU Directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment 6. references to applicable standards or technical specifications in relation to which conformity is declared 7. EU Declaration of conformity information prepared (title) (name first name, last name) (signature) (place) (date) Note. Document properties in the "signature" and "date" does not fill in, if the electronic document has been prepared according to the law on electronic document design. Environmental protection and regional development Minister Sprūdž in the E.