Directive 1999/5/EC of the European Parliament and of the Council (repealed)Dangos y teitl llawn

1. Introductory Text

2. CHAPTER I GENERAL ASPECTS

   1. Article 1. Scope and aim

   2. Article 2. Definitions

   3. Article 3. Essential requirements

   4. Article 4. Notification and publication of interface specifications

   5. Article 5. Harmonised standards

   6. Article 6. Placing on the market

   7. Article 7. Putting into service and right to connect

   8. Article 8. Free movement of apparatus

   9. Article 9. Safeguards

3. CHAPTER II CONFORMITY ASSESSMENT

   1. Article 10. Conformity assessment procedures

   2. Article 11. Notified bodies and surveillance authorities

4. CHAPTER III CE CONFORMITY MARKING AND INSCRIPTIONS

   1. Article 12. CE marking

5. CHAPTER IV THE COMMITTEE

   1. Article 13. Constitution of the Committee

   2. Article 14. Advisory committee procedure

   3. Article 15. Regulatory committee procedure

   4. Article 15a. Regulatory procedure with scrutiny

6. CHAPTER V FINAL AND TRANSITIONAL PROVISIONS

   1. Article 16. Third countries

   2. Article 17. Review and reporting

   3. Article 18. Transitional provisions

   4. Article 19. Transposition

   5. Article 20. Repeal

   6. Article 21. Entry into force

   7. Article 22. Addressees

7. 1. ANNEX I

      EQUIPMENT NOT COVERED BY THIS DIRECTIVE AS REFERRED TO IN ARTICLE 1(4)

      1. Radio equipment used by radio amateurs within Article 1, definition...

   2. ANNEX II

      CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 10(3)

      1. 1. This module describes the procedure whereby the manufacturer or his...

      2. 2. The manufacturer must establish the technical documentation described in point...

      3. 3. Where neither the manufacturer nor his authorised representative is established...

      4. 4. The technical documentation must enable the conformity of the product...

      5. 5. The manufacturer or his authorised representative must keep a copy...

      6. 6. The manufacturer must take all measures necessary in order that...

   3. ANNEX III

      CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 10(4)

      1. This Annex consists of Annex II, plus the following supplementary...

      2. For each type of apparatus, all essential radio test suites...

   4. ANNEX IV

      CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 10(5)

      1. This Annex consists of Annex III plus the following supplementary...

      2. The technical documentation described in point 4 of Annex II...

   5. ANNEX V

      CONFORMITY ASSESSMENT PROCEDURE REFERRED TO IN ARTICLE 10

      1. 1. Full quality assurance is the procedure whereby the manufacturer who...

      2. 2. The manufacturer must operate an approved quality system for design,...

      3. 3. Quality system

         1. 3.1. The manufacturer must lodge an application for assessment of his...

         2. 3.2. The quality system must ensure compliance of the products with...

         3. 3.3. The notified body must assess the quality system to determine...

         4. 3.4. The manufacturer must undertake to fulfil the obligations arising out...

      4. 4. EC surveillance under the responsibility of the notified body

         1. 4.1. The purpose of surveillance is to make sure that the...

         2. 4.2. The manufacturer must allow the notified body access for inspection...

         3. 4.3. The notified body must carry out audits at reasonable intervals...

         4. 4.4. Additionally, the notified body may pay unexpected visits to the...

      5. 5. The manufacturer must, for a period ending at least 10...

      6. 6. Each notified body must make available to the other notified...

   6. ANNEX VI

      MINIMUM CRITERIA TO BE TAKEN INTO ACCOUNT BY MEMBER STATES WHEN DESIGNATING NOTIFIED BODIES IN ACCORDANCE WITH ARTICLE 11(1)

      1. 1. The notified body, its director and the staff responsible for...

      2. 2. The notified body and its staff must carry out the...

      3. 3. The notified body must have at its disposal the necessary...

      4. 4. The staff responsible for inspections must have:

      5. 5. The impartiality of inspection staff must be guaranteed. Their remuneration...

      6. 6. The notified body must take out liability insurance unless its...

      7. 7. The staff of the notified body is bound to observe...

   7. ANNEX VII

      MARKING OF EQUIPMENT REFERRED TO IN ARTICLE 12(1)

      1. 1. The CE conformity marking must consist of the initials ‘CE’...

      2. 2. The CE marking must have a height of at least...

      3. 3. The CE marking must be affixed to the product or...

      4. 4. The CE marking must be affixed visibly, legibly and indelibly....

      5. 5. The equipment class identifier must take a form to be...