Cabinet of Ministers Regulations No. 115 in 2012 (21 February. No 10 3) amendments to the Cabinet of Ministers of 20 June 2006 regulations No. 483 "regulations on electromagnetic compatibility of equipment" Issued in accordance with the law "on conformity assessment" article 7 to make a Cabinet of 20 June 2006 regulations No. 483 "regulations on electromagnetic compatibility of equipment" (Latvian journal, 2006, 97. nr.) the following amendments: 1. Replace the words in paragraph 5.1 "terminal equipment" with the words "network Terminal". 2. Express 6, 7, 8 and 9 in paragraph by the following: "6. the equipment shall be designed and manufactured such that, in the light of scientific and technical developments, to ensure that they comply with the following essential requirements: 6.1 the electromagnetic disturbance generated does not exceed the level above which radio equipment, electronic equipment or other equipment could no longer work as intended by the manufacturer; 6.2. the resistance to electromagnetic interference, which is to be expected when using the equipment in the form provided, is sufficient to allow them to operate without unacceptable deterioration. 7. Ministry of the economy shall inform the standardisation Office of the official journal of the European Union published by the applicable standards electromagnetic compatibility of equipment. Society with limited liability "the standardization, accreditation and Metrology Centre ' shall be published in the internet home page of the Office for Standardization (www.lvs.lv) the national status of the standards adapted a list of the standards (applicable standards), you can apply this provision requirements. 8. If the equipment produced according to the requirements of the applicable standards, references to which have been published in the official journal of the European Union, considered that the equipment complies with the provisions in paragraph 6 and 32 requirements covering these standards. 9. Authorised for the placing on the market and to offer, as well as putting to use only equipment, installed or used according to intended, to meet the requirements of this regulation. " 3. Express points 11 and 12 as follows: "11. market surveillance functions take the consumer protection Centre (hereinafter referred to as the market supervisory authority). Electronic statutory body responsible for the clearance and the source of radio interference suppression, make decisions about prevention of the disturbance (hereinafter supervisory authority), the watch stationary complexes, which may cause harmful interference to radio communications. 12. equipment electromagnetic compatibility compliance can appreciate the society with limited liability "the standardization, accreditation and Metrology Centre" Latvian National Accreditation Bureau accredited conformity assessment bodies, on which the Ministry of Economic Affairs has announced the European Commission (hereinafter referred to as the notified body), or other Member States of the European Union or the European economic area countries notified body equipment electromagnetic compatibility. " 4. Supplement with 8.5., 8.6. and 13.9. subparagraph by the following:

"8.5. it participates in or supports the delegated representative membership of national standardization bodies in the relevant technical Committee for Standardization; 13.8. it shall inform the Ministry of economy on: 13.8.1. the market surveillance authorities and the supervisory authorities the requested information related to conformity assessment activities; 13.8.2. conformity assessment activities, carried out in accordance with these rules, and at the request of the Ministry of Economy – also for other activities; 13.9. the other notified bodies provide carrying out electromagnetic compatibility of equipment conformity assessment, information about the negative and, on request, positive conformity assessment results. " 5. Express 15 and 16 points as follows: "15. Apparatus complies with this provision set out in point 6 essential requirements. Compliance with this provision apparatus 6 essential requirements set out in the certifying, making this provision referred to in subsection 2.1. conformity assessment procedures (internal production control) or by manufacturer or its authorised representative shall also check-this provision set out in subsection 2.2. conformity assessment procedure. 16. each machine type, batch, serial number or any other information that allows the machines to be identified. The apparatus shall be accompanied by information about the name and address of the manufacturer or, where the manufacturer is not established in the European Union, its authorised representative or the person's name and address, which released an apparatus on the market of the European Union. " 6. Supplement with 16.1 and 16.2 of the following paragraph: "16.1 manufacturer shall provide information on any specific precautions that must be followed, mounted, installed and using AIDS or carrying out maintenance, to ensure the apparatus at the time of application for compliance with the rules set out in point 6 essential requirements. Instructions for use of the apparatus shall include the information required to ensure the use of the apparatus, according to the intended purpose. 16.2 If the machine match point 6 of these rules laid down in the essential requirements is not ensured in residential areas, the apparatus and, if possible, its packaging shall be accompanied by a clear indication of the limits of use. " 7. Replace paragraph 17, the number and the words "6. requirements set out in point" with a number and the words "set out in point 6 essential requirements". 8. Express 18 as follows: "6. the electromagnetic compatibility assessment of the apparatus, shall take into account all the circumstances of the action envisaged. If the machine can be used in different configurations, the electromagnetic compatibility assessment of the apparatus, shall certify compliance with this provision set out in point 6 the essential requirements for all its configurations. " 9. Express section 20.2 by the following: "manufacturer's proof of 20.2 AIDS compliance with applicable standards and their enumeration, if the manufacturer has applied them in whole or in part;". 10. Replace the words "in paragraph 20.4. certificate" with the word "opinion". 11. Supplement with 20.1 points as follows: "20.1 the manufacturer shall ensure that apparatus is made according to the rules referred to in point 19 of the technical documentation and with the requirements laid down in these rules." 12. Express 22.1, 22.2 and 22.3... subparagraph by the following: "22.1. the reference to the European Parliament and of the Council of 15 December 2004, Directive 2004/108/EC on the approximation of the laws of the Member States relating to electromagnetic compatibility and repealing Directive 89/336/EEC; 22.2. the identification of the apparatus in accordance with paragraph 16 of these terms; 22.3. the name and address of the manufacturer, as well as the manufacturer's authorised representative, if applicable, name and address; ". 13. Express 24, 25, 26 and 27 the following: 24. If the manufacturer or his authorised representative, before placing the apparatus on the market wants to take the assessment of conformity of the apparatus in the notified body, the manufacturer or his authorised representative shall pass at the disposal of the notified body, the technical documentation of the apparatus. To check the machine's electromagnetic compatibility, specifies the rules referred to in point 6 of the essential requirements aspects of the notified body must evaluate. 25. the notified body shall examine the instrument and assess the technical documentation, or technical documentation sufficient to show compliance of the apparatus that rule 6 of the essential requirements referred to in the aspects that are rated. 26. After the machine conformity assessment issued by the notified body the manufacturer or his authorised representative opinion attesting to the conformity of the apparatus, those that rule 6, paragraph aspects of the essential requirements by the notified body treatment. 27. If the notified body shall take a decision not to issue the rules referred to in paragraph 26 of the opinion, it shall give a reasoned refusal of the manufacturer or his authorised representative. " 14. Make the paragraph 29 by the following: "29. If the unit must also comply with other laws and regulations, which provide for the affixing of the CE marking, the apparatus may be marked only if it also meets these requirements. The CE marking shall indicate conformity with those laws and regulations under which the extinguisher is manufactured. " 15. Express 31 the following: "31. the apparatus, its packaging or the instructions for use must not deploy such a mark is likely to mislead as to the meaning and form of the CE marking. Other signs may be affixed to the apparatus, packaging or instruction for use only if the CE marking is reduced visibility and readability. " 16. Make the paragraph 32 as follows: "32. Stationary complexes set up by using the good inženierpraks (document) and accurately following the manufacturer's instructions and the information provided on the part of the complex (and devices) intended use to ensure compliance of the fixed installation this provision set out in point 6 essential requirements." 17. Make the following introductory paragraph 34: "34. If the apparatus, intended for fixed installation in question include, not otherwise commercially available, for these machines allowed not to apply the requirements of this regulation. In such cases, the documentation accompanying the machine indicates the particular hospital complex and its electromagnetic compatibility parameters as well: ". 18. Express 21.3. subparagraph by the following: "manufacturer or producer 34.2. authorized representative's name (or a name) and address;". 19. Delete the 35, 36 and 37. 20. Express 38 as follows:

"38. The Person who is in possession of fixed installation (hereinafter possessor): 38.1. keep that paragraph 32 of the provisions referred to in the documentation as long as operating stationary complex, and presented it to the market supervisory authority or supervisory body by market surveillance authorities or supervisory authority. If the documentation is not presented, believe that the stationary package does not meet the requirements of this regulation; 38.2. cooperate with the market surveillance authorities and supervisory bodies and, if requested, shall take remedial action with respect to the possession of the existing hospital complex. " 21. To complement the chapter 4 with 38.1 points as follows: "If the possessor without 38.1 mounted stationary, fixed installation package installer provides the possessor of this provision, the documentation referred to in paragraph 32. 22. Express 39, 40, 41 and 42 as follows: "39. in carrying out market surveillance, market surveillance authorities officials are entitled: 24.3. to control and monitor the compliance of the apparatus on the market to offer this rule requirements by visiting the machine of marketing, storage and production sites, as well as checking the samples (through priekštestēšan), including opening the packaging and testing of samples; 24.4. request and receive free of charge information (including EC declaration of conformity of the notified body opinion, test reports) required to carry out supervision of the market according to the requirements of this regulation; 39.3. to request and receive a free sample of the apparatus and to organize its expertise to determine the compliance of the apparatus requirements of these provisions. 40. The costs of inspection of equipment covered under the legislation on the safety of goods and services. 41. where the market surveillance authority finds that the machine unjustly labeled with the CE marking without complying with the requirements of this regulation, the market surveillance authority shall instruct the manufacturer or his authorised representative to prevent specified period found. 42. If the rules referred to in paragraph 41 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 restricting the placing and placing the apparatus on the market, asking to withdraw the apparatus from the market or to recall it. '; 23. To supplement the rules with 42.1 42.2 42.3, 42.4,, and 26.5 26.4 points, as follows: ' 42.1 market supervisory authority, subject to 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, laid down in article 21, the principle of proportionality, may ask the manufacturer, his authorised representative importer or distributor to take corrective action to prevent the non-compliance of the apparatus. 26.2 the manufacturer, the authorised representative, the importer and the Distributor is obliged to take appropriate corrective action for AIDS, which it has now offered to the market and to ensure that it meets the requirements of this regulation. 26.3 If the manufacturer, his authorised representative, the importer or the distributor does not take adequate corrective actions, the market surveillance authority may adopt a decision in accordance with the laws and regulations on the safety of goods and services by restricting the placing of the apparatus or the placing on the market and asking to withdraw the apparatus from the market or to recall it. 26.3 the manufacturer, its authorised representative, the importer or the distributor shall cooperate with the market surveillance authorities. 26.4 If the market surveillance authority shall prohibit the placing of the apparatus or the placing on the market, because the apparatus does not comply with the rules set out in point 6 of the essential requirements, the market surveillance authority shall report to the Ministry of Economy of the non-compliant apparatus for detection of and the measures taken, specifying the reasons for the decision, as well as inform, or non-compliance is due to machine non-compliance with the applicable standards, the standards applicable to defective or incorrect application of these standards, if it is applied by the manufacturer. 26.5 the Ministry of economy to the European Commission of the non-compliant apparatus for detection of and the market surveillance authorities of the measures taken. " 24. Make 43 as follows: "43. market surveillance authority or supervisory authorities may require the holder of a fixed installation is evidence of the compliance of the fixed installation and, if necessary, ask the hospital complex to provide means of conformity assessment in the notified body, if the fixed installation of signs suggest that it does not meet the requirements of these regulations or if there are complaints about the hospital complex disorders." 25. replace paragraph 44 number and the words "6. requirements set out in point" with a number and the words "set out in point 6 essential requirements". 26. To complement Chapter 5 of 44.1 and 44.2 point as follows: "44.1 the supervisory organ may require the holder of a fixed installation is evidence of the compliance of the fixed installation rules referred to in point 6.1 the essential requirements if the residential complex is the source of radio interference. 44.2 If the supervisory organ finds that a stationary complex radio-interference, so according to the laws and regulations in the field of radio communications may require the holder to take measures to ensure the compliance of the fixed installation rules referred to in point 6.1. essential requirements. " Prime Minister v. dombrovsky Minister d. Pavļut Economy in the