CHAPTER 1 SCOPE, PLACING ON THE MARKET AND FREE MOVEMENT
Article 1.(1) This Directive shall apply to all non-automatic weighing instruments....
Article 2.For the purposes of this Directive, the following definitions shall...
Article 3.(1) Member States shall take all steps to ensure that...
Article 4.Instruments used for the applications listed in point (a) of...
Article 5.(1) Member States shall not impede the placing on the...
Article 6.(1) Member States shall presume conformity with the essential requirements...
Article 8.(1) Where a Member State considers that instruments bearing the...
Article 14.Member States shall take all steps to ensure that instruments...
Article 15.Any decision taken pursuant to this Directive and resulting in...
Article 16.Member States shall communicate to the Commission the texts of...
Article 17.Directive 90/384/EEC, as amended by the Directive listed in Annex...
Article 18.This Directive shall enter into force on the twentieth day...
Article 19.This Directive is addressed to the Member States.
5. Weighing results of an instrument shall be repeatable, and shall...
6. The instrument shall react to small variations in the load....
7. Influence quantities and time
7.1. Instruments of classes II, III and IIII, liable to be...
7.2. The instruments shall meet the metrological requirements within the temperature...
7.3. Instruments operated from a mains power supply shall meet the...
7.4. Electronic instruments, except those in class I and in class...
7.6. Under other conditions the instruments shall either continue to function...
8.1. Design and construction of the instruments shall be such that...
8.2. When exposed to disturbances, electronic instruments shall not display the...
8.4. When external equipment is connected to an electronic instrument through...
8.5. The instruments shall have no characteristics likely to facilitate fraudulent...
8.6. Instruments shall be designed to permit ready execution of the...
14. Instruments for direct sales to the public, with a maximum...
CONFORMITY ASSESSMENT PROCEDURES
1.1. EC type-examination is the procedure whereby a notified body verifies...
1.2. The application for EC type-examination shall be lodged with a...
1.3.1. examine the design documentation and verify that the type has...
1.3.2. agree with the applicant on the location where the examinations...
1.3.3. perform or have performed the appropriate examinations and/or tests to...
1.3.4. perform or have performed the appropriate examinations and/or tests to...
1.4. Where the type complies with the provisions of this Directive,...
1.5. Each notified body shall periodically make available to all Member...
1.7. The applicant shall keep the notified body that has issued...
2. EC declaration of type conformity (guarantee of production quality)
2.1. The EC declaration of type conformity (guarantee of production quality)...
2.2. The manufacturer shall have adequately implemented a quality system as...
2.3.1. The manufacturer shall lodge an application for approval of his...
2.3.2. The quality system shall ensure conformity of the instruments with...
2.3.3. The notified body shall examine and evaluate the quality system...
2.3.4. The manufacturer or his authorised representative shall keep the notified...
2.3.5. Any notified body that withdraws approval of a quality system...
3.1. EC verification is the procedure whereby the manufacturer or his...
3.2. The manufacturer shall take all necessary measures in order that...
3.3. The notified body shall carry out the appropriate examinations and...
3.4. For instruments not subject to EC type-approval, the documents relating...
3.5. Verification by checking and testing of each instrument
1. The bodies shall have at their disposal the necessary personnel,...
2. The personnel of the bodies shall have technical competence and...
3. The bodies shall work independently of all circles, groups or...
4. The personnel of the bodies shall respect professional confidentiality.
5. The bodies shall take out a civil liability insurance if...