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Directive 2014/32/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 measuring 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.
CHAPTER 3 CONFORMITY OF MEASURING INSTRUMENTS
Article 14.Presumption of conformity of measuring instruments
Article 15.Publication of the references of normative documents
Article 16.Withdrawal of the references of normative documents
Article 21.General principles of the CE marking and of the supplementary metrology marking
Article 22.Rules and conditions for affixing the CE marking and the supplementary metrology marking
7.1. A measuring instrument shall have no feature likely to facilitate...
7.2. A measuring instrument shall be suitable for its intended use...
7.3. The errors of a utility measuring instrument at flows or...
7.4. Where a measuring instrument is designed for the measurement of...
7.5. A measuring instrument shall be robust and its materials of...
7.6. A measuring instrument shall be designed so as to allow...
8. Protection against corruption
8.1. The metrological characteristics of a measuring instrument shall not be...
8.2. A hardware component that is critical for metrological characteristics shall...
8.3. Software that is critical for metrological characteristics shall be identified...
8.4. Measurement data, software that is critical for measurement characteristics and...
8.5. For utility measuring instruments the display of the total quantity...
9. Information to be borne by and to accompany the instrument...
9.1. A measuring instrument shall bear the following inscriptions:
9.2. An instrument of dimensions too small or of too sensitive...
9.3. The instrument shall be accompanied by information on its operation,...
9.4. Groups of identical measuring instruments used in the same location...
9.5. Unless specified otherwise in an instrument-specific annex, the scale interval...
9.6. A material measure shall be marked with a nominal value...
9.7. The units of measurement used and their symbols shall be...
9.8. All marks and inscriptions required under any requirement shall be...
11. Further processing of data to conclude the trading transaction
MODULE A2: INTERNAL PRODUCTION CONTROL PLUS SUPERVISED INSTRUMENT CHECKS AT RANDOM INTERVALS...
MODULE B: EU- TYPE EXAMINATION
1. ‘EU-type examination’ is the part of a conformity assessment procedure...
2. EU-type examination may be carried out in either of the...
3. The manufacturer shall lodge an application for EU-type examination with...
5. The notified body shall draw up an evaluation report that...
6. Where the type meets the requirements of this Directive, the...
7. The notified body shall keep itself apprised of any changes...
8. The manufacturer shall inform the notified body that holds the...
9. Each notified body shall inform its notifying authority concerning the...
10. The manufacturer shall keep a copy of the EU-type examination...
11. The manufacturer’s authorised representative may lodge the application referred to...
MODULE C: CONFORMITY TO TYPE BASED ON INTERNAL PRODUCTION CONTROL
MODULE C2: CONFORMITY TO TYPE BASED ON INTERNAL PRODUCTION CONTROL PLUS SUPERVISED...
MODULE D: CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTION...
1. Conformity to type based on quality assurance of the production...
3.1. The manufacturer shall lodge an application for assessment of his...
3.2. The quality system shall ensure that the measuring instruments are...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
4. Surveillance under the responsibility of the notified body
6. The manufacturer shall, for a period ending 10 years after...
7. Each notified body shall inform its notifying authority of quality...
MODULE D1: QUALITY ASSURANCE OF THE PRODUCTION PROCESS
1. Quality assurance of the production process is the conformity assessment...
3. The manufacturer shall keep the technical documentation at the disposal...
5.1. The manufacturer shall lodge an application for assessment of his...
5.2. The quality system shall ensure compliance of the measuring instruments...
5.3. The notified body shall assess the quality system to determine...
5.4. The manufacturer shall undertake to fulfil the obligations arising out...
5.5. The manufacturer shall keep the notified body that has approved...
6. Surveillance under the responsibility of the notified body
8. The manufacturer shall, for a period ending 10 years after...
9. Each notified body shall inform its notifying authority of quality...
MODULE E: CONFORMITY TO TYPE BASED ON INSTRUMENT QUALITY ASSURANCE
1. Conformity to type based on instrument quality assurance is that...
3.1. The manufacturer shall lodge an application for assessment of his...
3.2. The quality system shall ensure compliance of the measuring instruments...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
4. Surveillance under the responsibility of the notified body
6. The manufacturer shall, for a period ending 10 years after...
7. Each notified body shall inform its notifying authority of quality...
MODULE E1: QUALITY ASSURANCE OF FINAL INSTRUMENT INSPECTION AND TESTING
1. Quality assurance of final instrument inspection and testing is the...
3. The manufacturer shall keep the technical documentation at the disposal...
5.1. The manufacturer shall lodge an application for assessment of his...
5.2. The quality system shall ensure compliance of the measuring instruments...
5.3. The notified body shall assess the quality system to determine...
5.4. The manufacturer shall undertake to fulfil the obligations arising out...
5.5. The manufacturer shall keep the notified body that has approved...
6. Surveillance under the responsibility of the notified body
8. The manufacturer shall, for a period ending 10 years after...
9. Each notified body shall inform its notifying authority of quality...
MODULE F: CONFORMITY TO TYPE BASED ON PRODUCT VERIFICATION
1. Conformity to type based on product verification is the part...
4. Verification of conformity by examination and testing of every instrument...
7. If the notified body agrees and under its responsibility, the...
MODULE F1: CONFORMITY BASED ON PRODUCT VERIFICATION
1. Conformity based on product verification is the conformity assessment procedure...
5. Verification of conformity by examination and testing of every instrument...
6. Statistical verification of conformity
6.1. The manufacturer shall take all measures necessary so that the...
6.2. A random sample shall be taken from each lot according...
6.3. All measuring instruments in the sample shall be individually examined...
6.4. The statistical procedure shall meet the following requirements:
6.5. If a lot is accepted, all measuring instruments of the...
8. If the notified body agrees and under its responsibility, the...
MODULE H: CONFORMITY BASED ON FULL QUALITY ASSURANCE
1. Conformity based on full quality assurance is the conformity assessment...
3.1. The manufacturer shall lodge an application for assessment of his...
3.2. The quality system shall ensure compliance of the measuring instruments...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
4. Surveillance under the responsibility of the notified body
6. The manufacturer shall, for a period ending 10 years after...
7. Each notified body shall inform its notifying authority of quality...
MODULE H1: CONFORMITY BASED ON FULL QUALITY ASSURANCE PLUS DESIGN EXAMINATION
1. Conformity based on full quality assurance plus design examination is...
3.1. The manufacturer shall lodge an application for assessment of the...
3.2. The quality system shall ensure compliance of the measuring instruments...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
3.6. Each notified body shall inform its notifying authority of quality...
4.1. The manufacturer shall lodge an application for examination of the...
4.2. The application shall make it possible to understand the design,...
4.3. The notified body shall examine the application, and where the...
4.4. The notified body shall keep itself apprised of any changes...
4.5. Each notified body shall inform its notifying authority of the...
5. Surveillance under the responsibility of the notified body
7. The manufacturer shall, for a period ending 10 years after...
MEASURING SYSTEMS FOR THE CONTINUOUS AND DYNAMIC MEASUREMENT OF QUANTITIES...
2. Accuracy classification and maximum permissible errors (MPEs)
2.1. For quantities equal to or greater than 2 litres the...
2.2. For quantities less than two litres the MPE on indications...
2.3. However, no matter what the measured quantity may be, the...
2.4.1. For minimum measured quantities greater than or equal to 2...
2.4.2. For minimum measured quantities of less than two litres, the...
2.7. The requirement (a) in point 2.6 applies to any calculation,...
2.8. The measuring system shall not exploit the MPEs or systematically...
CHAPTER I Requirements common to all types of automatic weighing instruments
2. Permissible effect of disturbances — Electromagnetic environment
3.1. Means shall be provided to limit the effects of tilt,...
3.2. Adequate material handling facilities shall be provided to enable the...
3.3. Any operator control interface shall be clear and effective.
3.4. The integrity of the display (where present) shall be verifiable...
3.5. Adequate zero setting capability shall be provided to enable the...
3.6. Any result outside the measurement range shall be identified as...
1. The taximeter shall be designed to calculate the distance and...
2. The taximeter shall be designed to calculate and display the...
3. A taximeter shall be able to apply the normal calculation...
4. A taximeter shall be able to supply the following data...
5. If relevant, it shall be possible to adjust a taximeter...
10. The conditions for the compatibility between the taximeter and the...
11. If there is a supplement charge for an extra service,...
12. If the fare is calculated according to calculation mode D...
13. All values displayed for the passenger shall be suitably identified....
14.2. The securing possibilities available in a taximeter shall be such...
15.1. A taximeter shall be fitted with non-resettable totalisers for all...
15.2. If disconnected from power, a taximeter shall allow the totalised...
15.3. Adequate measures shall be taken to prevent the display of...
17. If properties of the taxi are important for the correctness...
18. For the purpose of testing after installation, the taximeter shall...
19. A taximeter and its installation instructions specified by the manufacturer...
20. The general essential requirement dealing with fraudulent use shall be...
22. The taximeter shall be equipped with a real-timeclock by means...
23. The values of distance travelled and time elapsed, when displayed...
7. The standard deviation of 20 measurements shall not be greater...
8. For measuring CO, CO2 and HC, the instrument, including the...
9. The components in the exhaust gas, other than the components...
10. An exhaust gas analyser shall have an adjustment facility that...
11. For automatic or semi-automatic adjustment facilities, the instrument shall be...
12. An exhaust gas analyser shall detect hydrocarbon residues in the...
13. An exhaust gas analyser shall have a device for automatically...
14. If the exhaust gas analyser is capable to operate with...
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 or normative documents used...
7. Where applicable, the notified body … (name, number) performed …...
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