Government Decree No. 426 / 2000 Coll.
Government Regulation laying down technical requirements for radio and telecommunications terminal equipment
Valid
Regulation
Effective from 01.05.2001
Zobrazeno prvních 200 z celkem 246 ustanovení tohoto předpisu.
Zobrazit celý předpis →
Pro stažení celého znění použijte tlačítko Stáhnout výše.
426
GOVERNMENT REGULATION
of 23 October 2000
laying down technical requirements for radio and telecommunications terminal equipment
The Government mandates pursuant to Section 22 of Act No. 22 / 1997 Coll., on the technical requirements for products and on the amendment and addition of certain laws, as amended by Act No. 71 / 2000 Coll., (hereinafter referred to as "the Act") to implement Sections 11 (1), 12 (1), (4) and 13 (2) and (4) of the Act:
(1) This Regulation shall apply:
(a) telecommunications terminal equipment for the product or an important part thereof enabling communication to be connected to the interfaces of public telecommunications networks, 1)
(b) radio equipment of a product or an important part thereof, enabling communication on the basis of radio wave2) using the frequency spectrum allocated to terrestrial or cosmic radio communications, 3)
(c) an apparatus which is:
1. a component or separate technical unit of a motor vehicle intended for use on the road, with or without bodywork, having at least four wheels and a maximum design speed exceeding 25 km.h-1, including trailers, with the exception of railway vehicles and agricultural or forestry tractors, and self-driving and working machinery carried; or
2. a component or separate technical unit of a two or three-wheel motor vehicle intended for use on the road and components or individual technical units of such vehicles, except:
2.1. Vehicles with a maximum design speed not exceeding 6 km.h-1,
2.2. Treadmill vehicles,
2.3. Vehicles intended for use by disabled persons;
2.4. Vehicles intended for use in road or off-road racing;
2.5. Vehicles in service before the entry into force of this Regulation;
2.6. Tractors and machinery used for agricultural or similar purposes,
2.7. Vehicles originally designed for off-road use in free time, having wheels arranged symmetrically with one wheel in front and two rear,
2.8. Parts or technical units of the said vehicles, other than those intended for use on two or three-wheel motor vehicles intended for use on the road,
3. a component or separate technical unit of four-wheel motor vehicles having the following characteristics:
3.1. the unladen weight is not more than 350 kg (in the case of electric vehicles, the mass of batteries shall not count to that weight), the maximum design speed shall not exceed 45 km.hoh-1 and the cylinder capacity shall not exceed 50 cc for spark ignition engines with spark plugs or the maximum net power shall not exceed 4kW for other engine types; or
3.2. the unladen mass is not more than 400 kg or 550 kg for vehicles intended for the transport of goods (in the case of electric vehicles with a maximum net engine power not exceeding 15 kW, the mass of batteries shall not be counted against that mass),
(hereinafter referred to as "instruments and equipment ').
(2) This Regulation further covers:
(a) unwanted interference by interference which threatens the function of the radio navigation service or other security services or which otherwise seriously deteriorates, thwarts or repeatedly interrupts the radio communications service operated in accordance with the applicable regulations;
(b) the specified products referred to in Article 12 (1) of the Act of apparatus and equipment referred to in paragraph 1;
(c) the class of equipment the class identifying the types of instruments and equipment and the interfaces for which the apparatus or equipment is intended. The classes of equipment are determined by the Czech Telecommunications Authority (hereinafter referred to as the Office) by means of measures. (8) Instruments and equipment may be included simultaneously or gradually in more than one class of equipment.
This Regulation lays down technical requirements for radio and telecommunications terminal equipment, in accordance with the law of the European Communities (3a) and the international contract (3b).
(1) This Regulation shall apply to apparatus and equipment, except those listed in Annex 1 to this Regulation.
(2) Where the apparatus contains as an integral part or as an accessory
(a) medical devices provided for by special legislation, 4)
(b) active implantable medical devices provided for by specific legislation, 5)
It shall be subject to this Government Regulation.
(3) The specified products must meet the following essential requirements:
(a) the protection of the health and safety of the user and of any other person, including the objectives laid down by specific legislation, (6) but without taking into account the value of the voltage;
(b) protection relating to electromagnetic compatibility provided for in specific legislation, 7)
(c) radio equipment shall be designed in such a way as to effectively exploit the frequency spectrum allocated to earth or cosmic radio communications and sources located on orbits and to prevent unwanted interference.
(4) Instruments and apparatus in certain classes or appliances of certain types must be published by the Office in the Telecommunications Bulletin by means of a communication which must comply with the relevant international contract, (8) and such instruments and equipment must be so constructed that:
(a) cooperate through a public telecommunications network with other equipment and equipment and to connect them to the interface of the public telecommunications network in the Czech Republic and the territory of a Member State of the European Union;
(b) it has not adversely affected the public telecommunications network, has not caused an unacceptable deterioration in the quality of the services or has not abused the capacity and possibilities of the public telecommunications network in its operation;
(c) contain security features ensuring the protection of personal data and the privacy of users and participants;
(d) promote fraud prevention functions;
(e) promote functions enabling access to emergency services;
(f) promote functions facilitating their use to disabled users.
(5) Where apparatus and equipment are covered by other government regulations laying down technical requirements for products, the apparatus and equipment shall also comply with those laid down in those Regulations.
(6) Where the requirements for apparatus and equipment are specified by harmonised standards under Article 4a (1) of the Act or by foreign technical standards transposing a harmonised European standard and the characteristics of the apparatus and equipment are consistent with them, those essential requirements shall be deemed to be met under paragraph 3.
(1) Before placing equipment and apparatus on the market, the manufacturer or his authorised representative established in a Member State of the European Union, or the person responsible for placing the apparatus and equipment on the market, shall carry out a conformity assessment in accordance with Article 12 (4) of the Act with the essential requirements of his choice by any of the following procedures:
(a) telecommunications terminal equipment which does not use frequencies or frequency bands allocated to terrestrial or cosmic radio communications and the receiving parts of radio equipment shall be subjected to one of the procedures described in Annex 2, Annex 4 or Annex 5;
(b) where harmonised standards have been applied, radio equipment not covered by point (a) shall be subjected to one of the procedures described in Annex 3, Annex 4 or Annex 5;
(c) if the harmonised standards have not been applied or only part of them has been used, radio equipment not covered by paragraph (a) shall be subjected to one of the procedures described in Annex 4 or Annex 5 at the choice of the manufacturer.
(2) In addition to the procedures laid down in paragraph 1, the conformity of instruments and equipment with the essential requirements referred to in Article 2 (3) may be demonstrated by means of procedures laid down by specific legislation, (6), (7) where the instruments and equipment concerned are subject to such specific legislation.
(3) The records and correspondence relating to the conformity assessment procedures referred to in paragraph 1 shall be kept in the official language of the Member State of the European Union in which the conformity assessment procedure takes place or in a language agreed by the notified person concerned pursuant to paragraphs 11 and 11a of the Act.
(4) The manufacturer or his authorised representative, having its registered office in a Member State of the European Union, or the person responsible for placing the apparatus on the market, shall issue a declaration of conformity to the essential requirements applicable to it and shall place on it a CE marking in accordance with Annex 7, in addition to which he shall indicate the year in which the conformity has been assessed. The manufacturer shall use the type number, serial number or serial number and the name of the manufacturer or the person responsible for placing the apparatus on the market to identify the apparatus or apparatus. Where the procedures laid down in Annex 3, Annex 4 or Annex 5 are applied, this marking shall be accompanied by the identification number of the notified person as set out in Annex 6. In addition, for radio equipment, the identification mark of the device class in Annex 7 shall be provided. Any other marking may be affixed to the device provided that this does not reduce the visibility and legibility of the CE marking. No instrument or device, whether or not it meets the relevant essential requirements, shall bear any other marking which may mislead third parties as regards the meaning or shape of the CE marking as set out in Annex 7.
(5) The manufacturer or his authorised representative established in a Member State of the European Union, or the person responsible for placing the apparatus and equipment on the market, shall provide users with information on the intended method of use, together with a declaration of conformity with the essential requirements laid down in this Regulation which apply to him. In the case of radio equipment, sufficient information shall be provided on the packaging and in the instructions for the use of the apparatus concerning the method and conditions of use of the apparatus and the marking on the apparatus referred to in point 5 of Annex No 7 shall indicate to the user any restrictions or authorisations to use radio equipment. For telecommunications terminal equipment, this information shall include sufficient data to identify the interfaces of the public telecommunications networks to which the equipment is to be connected. For all instruments, this information must be clearly stated.
(6) In the case of radio equipment using frequency bands the use of which is not harmonised in one of the Member States of the European Union, the manufacturer or his authorised representative established in the European Community or the person responsible for marketing the equipment shall notify the authority responsible for managing the frequency spectrum in the Czech Republic, (10) the intention to place such equipment on the market of the Czech Republic. This notification shall be made no later than 4 weeks before the equipment is placed on the market and shall include information on the radio characteristics of the equipment, in particular frequency bands, channel spacing, type of modulation and high frequency power, and the notified person's identification number in the Member State of the European Union as set out in Annex 4 or 5.
(7) Where instruments and equipment are covered by Directives of the European Communities other than those relating to radio equipment and terminal telecommunications equipment and the mutual recognition of their conformity, which include other aspects and also provide for the means of marking the CE conformity mark, that marking shall indicate that the apparatus and equipment also comply with the provisions of those other Directives. In this case, the documents, reports or instructions required by these Directives and attached to the products concerned shall contain a reference to those Directives in accordance with their publication in the Official Journal of the European Communities.
(1) Instruments and equipment which do not comply with the requirements laid down in this Regulation may not be placed on the market.
(2) In the case of radio equipment, including types of radio equipment that cause undesirable interference, including interference with existing or planned services on nationally assigned frequency bands, or for which these effects can reasonably be assumed, the supervisory authorities shall, in cooperation with the Authority, take all appropriate measures under the special legislature11) to prohibit or restrict their placing on the market or to ensure that they are withdrawn from the market.
(3) Against a person who has affixed a sign not complying with the provisions of § 3 (4) or § 4 (4) or Annex No 7, the supervisory authorities shall take measures under specific legislation. 11) If the person who affixed the marking cannot be identified, appropriate measures shall be taken against the person carrying the apparatus and equipment at the time when the non-conformity was first discovered.
(4) Instruments and equipment which do not comply with the requirements laid down in this Regulation may be made publicly available at trade fairs, exhibitions, demonstrations and similar events only on condition that they are visibly marked with a warning that they cannot be placed on the market and operated before their compliance with the requirements laid down in this Regulation is ensured.
Where a protective measure has been imposed on instruments and equipment under the special legislation11a) as a result of non-compliance with the requirements of this Regulation, the notification provided for in Article 7 (8) of the Act shall state whether the reason for the imposition of the protective measure was caused by:
(a) incorrect application of harmonised standards;
(b) shortcomings in harmonised standards;
(c) failure to comply with the requirements laid down in Article 2 (3) where instruments and equipment do not comply with harmonised standards.
(1) The provisions of the Government Regulation laying down technical requirements for products with regard to their electromagnetic compatibility, (7) shall not apply to apparatus and equipment covered by this Regulation, with the exception of the protection requirements laid down in paragraphs 1 and 3 of Section 3, Sections 4 (1) and (2), (5), (6), (7) and the Annexes to the Government Regulation laying down technical requirements for products with regard to their electromagnetic compatibility. 7)
(2) The provisions of the Government Regulation laying down technical requirements for low voltage electrical equipment, (6) shall not apply to apparatus and equipment covered by this Regulation, with the exception of the objectives relating to the safety requirements set out in Sections 3 (1), 4 (5) and Annex 2 to the Government Regulation laying down technical requirements for low voltage electrical equipment. 6)
Evidence of the method of assessment of conformity used pursuant to Paragraph 13 (4) of the Act shall include:
(a) the technical documentation set out in each of the Annexes to this Regulation;
(b) documents and findings issued in conformity assessment by an authorised person.
Only legal persons who fulfil the minimum conditions set out in Annex 6 may be authorised to assess the conformity of instruments and equipment under Section 11 of the Act.
(1) Instruments and apparatus approved until 30 June 2000 under the Decree of the Ministry of Economic Affairs No. 26 / 1996 Coll., on the method, conditions and procedure for verifying and approving telecommunications terminal equipment may be placed on the market by 30 June 2002 at the latest.
(2) Tasks of the authorized person shall be carried out by the date of entry into force of the Treaty of Accession of the Czech Republic to the European Union, Office 12)
(1) This Regulation shall enter into force on 1 May 2001, with the exception of Article 4, which shall take effect on the date of the entry into force of the Treaty of Accession of the Czech Republic to the European Union.
(2) The date of entry into force of the Treaty of Accession of the Czech Republic to the European Union Articles 3 and 9 shall cease to apply.
Prime Minister:
Ing. Zeman v. r.
Minister for Transport and Communications:
Ing. Schling v. r.
Příloha č. 1
Annex No. 1 to Government Decree No. 426 / 2000 Coll.
INSTRUMENTS AND EQUIPMENT TO WHICH THIS REGULATION IS NOT INCLUDED
1. Radio equipment used by radio amateurs pursuant to Article 1, definition 53 of the Regulations on Radio Communications of the International Telecommunications Union (ITU), where such equipment is not commercially available. Parts for the assembly of radio amateurs and commercial equipment modified by radio amateurs for their use are not considered commercially available.
2. Equipment falling under the gear when
2.1. Equipment means objects which must be placed on a vessel for use in order to comply with international regulations or are freely placed on a vessel for use for which approval is required under international regulations by the State Administration of the State where the vessel is registered (flag law),
2.2. Radio communication equipment means equipment referred to in Chapter IV. International Convention on the Safety of Life at Sea (SOLAS 1974, as amended by successive Regulations),
2.3. These are devices intended for use in:
(a) a new vessel registered in a Member State of the European Union, irrespective of whether it is present at the time of construction or not on the territory of a Member State of the European Union;
(b) existing vessels registered in a Member State of the European Union;
- if such equipment has not previously been placed on board, or
- if the equipment previously placed on board is replaced, except where an international agreement authorises the vessel to act differently, whether or not the vessel is located on the territory of a Member State of the European Union at the time the equipment is placed on board.
3. Cable and wire.
4. Radio equipment intended exclusively for the reception of radio and television broadcasting.
5. Products, equipment and components in the field of civil aviation:
(a) products (civil aircraft, engines, propulsion or equipment);
(b) equipment (tools, equipment, mechanisms, instruments or accessories used or intended to be used to control an aircraft in flight which is installed or intended to be installed or attached to a civil aircraft but does not form part of a dragon, engine or propulsion),
(c) components [materials, components or sub-components not mentioned in (a) or (b) intended for use in civil aircraft, their engines, propulsion or equipment].
6. Air traffic control equipment and systems, in particular:
- connection systems,
- aircraft tracking systems,
- systems providing automatic air traffic control support,
- navigation systems.
7. Apparatus exclusively used for:
(a) intelligence tasks, 13)
(b) tasks of the Police of the Czech Republic in the field of security, 14); or
(c) customs search services, 15)
(d) the tasks of the armed forces of the Czech Republic. 16)
Příloha č. 2
Annex No 2 to Decree No 426 / 2000 Coll.
CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 3 (1) (a) OR 4 (1) (a)
(Internal production control)
1. This conformity assessment procedure shall apply in cases where the manufacturer or importer, in accordance with Article 3, or the manufacturer or his authorised representative, in accordance with Articles 3 (8) and 4, fulfilling the obligations set out in point 2, ensures and issues a declaration that the products concerned comply with the requirements of this Regulation which apply to them. The manufacturer or importer shall affix the CE marking to each device and issue a written declaration of conformity with the essential requirements in accordance with the procedure referred to in Article 3 (8) and Article 4.
2. The manufacturer shall draw up the technical documentation referred to in point 4. The manufacturer or importer shall keep this documentation for at least 10 years after the production of the last product, or the manufacturer or his authorised representative, in accordance with the procedure referred to in Articles 3 (8) and 4, in order to be available to the supervisory authorities for inspection.
3. If the manufacturer does not have its registered office in the Czech Republic in the procedure provided for in § 3 or the manufacturer or his authorised representative in the procedure provided for in § 3 (8) and § 4, the obligation to keep the technical documentation in the available condition shall be for the person who places the products on the market of the Czech Republic.
4. The technical documentation shall allow the conformity assessment of the product with the essential requirements. It shall include the design, manufacture and function of the product, in particular:
- a general description of the product,
- drawing documentation of design and production drawings and diagrams of components, sub-assemblies, circuits, etc.,
- descriptions and explanations necessary to understand the drawings and diagrams and the function of the product,
- the list of technical standards referred to in Article 2 (6) which have been applied in full or in part. Descriptions and explanations of the solutions adopted to meet the essential requirements of this Regulation where the standards referred to in Article 2 (6) have not been applied or do not exist,
- results of design calculations, tests, etc.,
- test reports.
5. The manufacturer or importer shall keep, together with the technical documentation, a copy of the certificate of conformity, if issued, in accordance with the procedure referred to in Article 3 (8) or with the manufacturer or his authorised representative.
6. The manufacturer shall take all necessary measures to ensure that the production process ensures compliance of the manufactured products with the technical documentation referred to in point 2 and with the requirements of this Regulation applicable to them.
Příloha č. 3
Annex No. 3 to Government Decree No. 426 / 2000 Coll.
CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 3 (1) (b) OR IN ARTICLE 4 (1) (b)
(Internal production control and specific instrument testing)
For this procedure, Annex 2 and the following additional requirements apply:
1. For each type of apparatus and equipment, the manufacturer shall carry out or have carried out a series of all basic radio tests. An authorised person (a notified person in a Member State of the European Union, hereinafter referred to as "the notified person ') chosen by the manufacturer shall be responsible for determining the series of tests which are considered to be essential, unless those series are laid down in harmonised standards. The authorised person (notified person) shall take due account of previous decisions taken jointly by the authorised person (s).
2. The manufacturer or importer, in accordance with § 3 or the manufacturer or his authorised representative, in accordance with § 3 (8) and § 4, or the person responsible for placing the apparatus on the market, shall declare that these tests have been carried out and that the apparatus and equipment comply with all the essential requirements and shall, during the production process, attach to it the identification number of the authorised person (notified person).
3. The obligations referred to in points 1 and 2 in respect of the persons notified shall be fulfilled only on the date of entry into force of the Treaty of Accession of the Czech Republic to the European Union.
Příloha č. 4
Annex No 4 to Decree No 426 / 2000 Coll.
CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 3 (1) (a) TO (c) OR IN ARTICLE 4 (1) (a) TO (c)
(Technical structural file)
For this procedure, Annex 3 and the following additional requirements apply:
1. The technical documentation referred to in point 4 of Annex 2 together with the declaration of conformity relating to the specific series of radiological tests referred to in Annex 3 shall consist of a set of technical constructional documents.
2. The manufacturer or importer, in accordance with § 3 or the manufacturer or his authorised representative, in accordance with § 3 (8) and § 4, or the person responsible for placing the apparatus and equipment on the market, shall submit this set of documents to one or more authorised persons (one or more notified persons), each of whom shall be informed of the others receiving the file.
(3) The authorised person (the notified person) shall examine the file and, if it concludes that the requirements of this Directive have not been duly established, may notify its opinion to the manufacturer or importer in accordance with the procedure laid down in Article 3 (3) or to the manufacturer or his authorised representative in the procedure referred to in Article 3 (8) and (4), or to the person responsible for placing the apparatus and equipment on the market, and shall report to the other authorised persons (notified persons) who have received the file. The opinion shall be delivered within 4 weeks of the transmission of the file to the authorised person (notified person). On receipt of this opinion or at the end of a period of 4 weeks, the apparatus or equipment may be placed on the market without prejudice to the provisions of Sections 3 (6) and 5 (1).
4. The manufacturer or importer, in accordance with § 3 or the manufacturer or his authorised representative, in accordance with § 3 (8) and § 4, or the person responsible for placing the apparatus or equipment on the market shall keep a set of supporting documents for at least 10 years after the manufacture of the last product so that it is available to the supervisory authorities for inspection purposes.
5. The obligations referred to in points 2 and 3 in respect of notified persons shall be fulfilled only on the date of entry into force of the Treaty of Accession of the Czech Republic to the European Union.
Příloha č. 5
Annex No. 5 to Government Decree No. 426 / 2000 Coll.
CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 3 (1) (a) TO (c) OR § 4 (1) (a) TO (c)
(Complex quality assurance)
1. Comprehensive quality assurance is a procedure whereby a manufacturer who fulfils the obligations referred to in point 2 ensures and issues a declaration that the products concerned comply with the requirements of this Regulation which apply to them. The manufacturer shall affix to each product the marking referred to in Article 3 (4) in the procedure referred to in Article 3 or place on the product the CE marking in the procedure referred to in Articles 3 (8) and 3 (4) and issue a written declaration of conformity.
2. The manufacturer shall apply an approved quality system for design, production and final inspection and testing of the products referred to in point 3 and shall be subject to the supervision referred to in point 4.
3. Quality system
3.1. The manufacturer shall submit an application to the authorised person (notified person) for an assessment of his quality system.
The application shall contain:
(a) any relevant information on the products envisaged;
(b) documentation relating to the quality system.
3.2. The quality system shall ensure that the products comply with the requirements of this Regulation applicable to them. All basic principles, requirements and measures adopted by the manufacturer shall be systematically and properly documented in the form of written concepts, procedures and instructions. This quality system documentation shall ensure a uniform interpretation of quality assurance concepts and procedures such as quality programmes, quality plans, quality manuals and quality records.
In particular, they shall be described in an appropriate manner:
(a) quality objectives and the organisational structure, responsibilities and powers of management as regards the quality of design and production;
(b) the technical specifications, including harmonised standards and technical regulations, as well as the relevant test specifications to be applied and, if the standards referred to in Article 2 (6) are not fully applied, the means by which to ensure compliance with the essential requirements of this Regulation applicable to the products;
(c) methods of managing the work on the design and verification thereof, as well as procedures and systematic measures to be applied when designing products belonging to the category concerned;
(d) the corresponding production, quality management and quality assurance methods, procedures and systematic measures to be applied;
(e) the checks and tests to be carried out before, during and after manufacture, indicating the frequency to be carried out, including, where appropriate, the results of the tests carried out before manufacture,
(f) means to ensure that test and control equipment complies with the relevant requirements for carrying out the necessary tests;
(g) quality records such as inspection reports, test results, calibration data, qualification records of relevant personnel, etc.,
(h) means to monitor the achievement of the required quality of design and products as well as the effective functioning of the quality system.
3.3. The authorised person (notified person) shall assess the quality system in order to determine whether he meets the requirements of point 3.2. It envisages compliance with these requirements for quality systems applying the relevant harmonised standards.
In particular, the authorised person (notified person) shall assess whether the quality management system ensures conformity of the products with the requirements of this Regulation with regard to the relevant documentation submitted in accordance with points 3.1 and 3.2, including, where appropriate, the results of the tests submitted by the manufacturer.
At least one member of the group of assessors shall have experience in evaluating the technology of the product concerned. The evaluation procedure shall also include a visit to the manufacturer of the equipment.
The decision shall be notified to the manufacturer. The notification shall contain the conclusions of the assessment and a reasoned decision on its outcome.
3.4. The manufacturer shall undertake to fulfil the obligations arising from the quality system in the form in which it was approved and to maintain it in such a way that it remains effective and proportionate to its mission.
The manufacturer or his authorised representative in the Czech Republic shall inform the authorised person (the notified person) who approved the quality system of any intended update.
The authorised person (notified person) shall assess the proposed changes and decide whether the changed quality system still complies with the requirements of point 3.2 or whether a new assessment is necessary.
They shall notify the manufacturer of their decision. The notification shall contain the conclusions of the assessment and a reasoned assessment decision.
4. Supervision of the European Community under the responsibility of an authorised person (notified persons)
4.1. The purpose of supervision is to ensure that the manufacturer correctly fulfils the obligations arising from the approved quality system.
4.2. The manufacturer shall allow the authorised person (notified person) for inspection access to the premises where the design of the product is carried out, its production, inspection and testing, and to the warehouses and shall provide it with all necessary information, in particular:
(a) documentation of the quality system;
(b) the quality records foreseen in the part of the quality system relating to the design, such as the results of analyses, calculations, tests, etc.,
(c) the quality records foreseen in the production section of the quality system, such as inspection reports, test results, calibration data, qualification records of the relevant personnel, etc.
4.3. The authorised person (the notified person) shall carry out, at appropriate intervals, checks to ensure that the manufacturer maintains and applies the quality system and shall report to the manufacturer.
4.4. In addition, the authorised person (notified person) may make unexpected visits to the manufacturer. In such visits, the authorised person (the notified person) may, if necessary, carry out tests or have them carried out to verify the proper functioning of the quality system. The authorised person (notified person) shall provide the manufacturer with a visit report and, if the test is carried out, a test report.
5. The manufacturer shall keep for at least 10 years after manufacture of the last product:
(a) the documentation referred to in point 3.1 (b);
(b) the update data referred to in the second paragraph of point 3.4;
(c) decisions and reports of the authorised person (s) referred to in the last paragraph of point 3.4 and points 4.3 and 4.4 to be made available to the supervisory authorities.
6. Each authorised person (notified person) shall make available to other authorised persons (notified persons) relevant information on the quality system approvals issued or withdrawn, with reference to the product (s) concerned.
Sign in for notes, favorites and notifications
Regulation Information
| Citation | Government Regulation No. 426 / 2000 Coll., laying down technical requirements for radio and telecommunications terminal equipment |
|---|---|
| Regulation Type | Regulation |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 13.12.2000 |
|---|---|
| Effective from | 01.05.2001 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
Comments 0