- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (26/02/2014)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Directive 2014/31/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to the making available on the market of non-automatic weighing instruments (recast) (Text with EEA relevance)
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EU Directives are published on this site to aid cross referencing from UK legislation. Since IP completion day (31 December 2020 11.00 p.m.) no amendments have been applied to this version.
The terminology used is that of the International Organisation of...
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. Module B: EU-type examination
1.1. EU-type examination is the part of a conformity assessment procedure...
1.2. EU-type examination may be carried out in any of the...
1.3. The manufacturer shall lodge an application for EU-type examination with...
1.5. The notified body shall draw up an evaluation report that...
1.6. Where the type meets the requirements of this Directive, that...
1.7. The notified body shall keep itself apprised of any changes...
1.8. Each notified body shall inform its notifying authority concerning the...
1.9. The manufacturer shall keep a copy of the EU-type examination...
1.10. The manufacturer’s authorised representative may lodge the application referred to...
2. Module D: Conformity to type based on quality assurance of...
2.1. Conformity to type based on quality assurance of the production...
2.3.1. The manufacturer shall lodge an application for assessment of his...
2.3.2. The quality system shall ensure that the instruments are in...
2.3.3. The notified body shall assess the quality system to determine...
2.3.4. The manufacturer shall undertake to fulfil the obligations arising out...
2.3.5. The manufacturer shall keep the notified body that has approved...
2.4. Surveillance under the responsibility of the notified body
2.6. The manufacturer shall, for a period ending 10 years after...
2.7. Each notified body shall inform its notifying authority of quality...
3. Module D1: Quality assurance of the production process
3.1. Quality assurance of the production process is the conformity assessment...
3.3. The manufacturer shall keep the technical documentation at the disposal...
3.5.1. The manufacturer shall lodge an application for assessment of his...
3.5.2. The quality system shall ensure compliance of the instruments with...
3.5.3. The notified body shall assess the quality system to determine...
3.5.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5.5. The manufacturer shall keep the notified body that has approved...
3.6. Surveillance under the responsibility of the notified body
3.8. The manufacturer shall, for a period ending 10 years after...
3.9. Each notified body shall inform its notifying authority of quality...
4. Module F: Conformity to type based on product verification
7.1. The conformity assessment according to Module D, D1, F, F1...
7.2. If the instrument’s performance is sensitive to gravity variations the...
7.2.1. Where a manufacturer has opted for execution in two stages...
7.2.2. The party which has carried out the first stage of...
7.2.4. The CE marking and the supplementary metrology marking shall be...
1. Instruments intended to be used for the applications listed in...
2. Instruments not intended to be used for the applications listed...
EU DECLARATION OF CONFORMITY (No XXXX)
1. Instrument model/Instrument (product, type, batch or serial number):
2. Name and address of the manufacturer and, where applicable, his...
3. This declaration of conformity is issued under the sole responsibility...
4. Object of the declaration (identification of instrument allowing traceability; it...
5. The object of the declaration described above is in conformity...
6. References to the relevant harmonised standards used or references to...
7. The notified body … (name, number) performed … (description of...
ATTACHMENTS
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