- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (a wnaed Fel)
There are currently no known outstanding effects for The Non-automatic Weighing Instruments Regulations 2016.
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PART 2 REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS – OBLIGATIONS OF ECONOMIC OPERATORSPrevious MatchNext Match
CHAPTER 1 OBLIGATIONS OF MANUFACTURERS AND PERSONS TO BE TREATED AS MANUFACTURERSPrevious MatchNext Match
6.Manufacturers' responsibilities – design, conformity assessment and marking of regulated non-automatic weighing instrumentsPrevious MatchNext Match
7.Manufacturers' obligations in respect of recordsPrevious MatchNext Match
8.Manufacturers' obligations to ensure continuing conformity with the essential requirementsPrevious MatchNext Match
9.Manufacturers' obligations in relation to the marking of regulated non-automatic weighing instruments with serial numbers etc.Previous MatchNext Match
10.Manufacturers to mark contact details on regulated non-automatic weighing instrumentsPrevious MatchNext Match
11.Documentation to accompany regulated non-automatic weighing instrumentsPrevious MatchNext Match
12.Action to be taken where regulated non-automatic weighing instruments placed on the market are not in conformity with the essential requirementsPrevious MatchNext Match
13.Provision of information to the competent authorityPrevious MatchNext Match
14.Use of authorised representatives by manufacturersPrevious MatchNext Match
CHAPTER 2 OBLIGATIONS OF IMPORTERSPrevious MatchNext Match
16.Ensuring compliance of regulated non-automatic weighing instrumentsPrevious MatchNext Match
17.Importers duty to notify manufacturer and market surveillance authorities of non-compliant regulated non-automatic weighing instruments that present a riskPrevious MatchNext Match
18.Requirements to mark importers' details on regulated non-automatic weighing instrumentsPrevious MatchNext Match
19.Importers' duty to ensure that regulated non-automatic weighing instruments are accompanied by relevant documentation.Previous MatchNext Match
20.Duty of importers to ensure proper conditions of storage and transportPrevious MatchNext Match
21.Duties of importers with regard to monitoring etc.Previous MatchNext Match
22.Action to be taken by importers where regulated non-automatic weighing instruments placed on the market by them are not in conformity with essential requirementsPrevious MatchNext Match
23.Requirement for importer to keep copy of EU declaration of conformityPrevious MatchNext Match
24.Provision of information to a competent authorityPrevious MatchNext Match
CHAPTER 3 OBLIGATIONS OF DISTRIBUTORSPrevious MatchNext Match
26.Distributors – duty to act with due carePrevious MatchNext Match
27.Distributors – verification obligationsPrevious MatchNext Match
28.Distributors not to make non-conforming non-automatic weighing instruments available on the market etc.Previous MatchNext Match
29.Duty of distributors to ensure proper conditions of storage and transportPrevious MatchNext Match
30.Action to be taken by distributors where regulated non-automatic weighing instruments placed on the market by them are not in conformity with essential requirementsPrevious MatchNext Match
31.Provision of information to the competent authorityPrevious MatchNext Match
CHAPTER 4 IDENTIFICATION OF ECONOMIC OPERATORSPrevious MatchNext Match
32.(1) Economic operators must, on request, identify to the market...Previous MatchNext Match
32A.Obligations which are met by complying with obligations in the DirectivePrevious MatchNext Match
32B.Conformity assessment procedure obligations that are met by complying with the DirectivePrevious MatchNext Match
32D.Qualifying Northern Ireland GoodsPrevious MatchNext Match
PART 3 CONFORMITY OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match
CHAPTER 1 ESTABLISHING COMPLIANCE WITH THE ESSENTIAL REQUIREMENTSPrevious MatchNext Match
CHAPTER 2 REQUIREMENTS RELATING TO EU DECLARATIONS OF CONFORMITYPrevious MatchNext Match
CHAPTER 3 CONFORMITY MARKINGPrevious MatchNext Match
43.Conformity with ... requirements to be indicated by the UK markingPrevious MatchNext Match
44.Prohibition on improper use of UK marking and the M markingPrevious MatchNext Match
45.Rules and conditions for affixing the UK marking and the M marking etc.Previous MatchNext Match
45B.Register of notified bodies established in the United Kingdom
PART 4 REQUIREMENTS FOR NON-REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match
PART 5 APPROVAL OF CONFORMITY ASSESSMENT BODIESPrevious MatchNext Match
PART 6 PUTTING INTO SERVICE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS FOR THE PURPOSES LISTED IN REGULATION 3(2)Previous MatchNext Match
PART 7 USE FOR TRADE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS IN GREAT BRITAINPrevious MatchNext Match
PART 8 MARKET SURVEILLANCE AND ENFORCEMENTPrevious MatchNext Match
CHAPTER 1 MARKET SURVEILLANCEPrevious MatchNext Match
57.The market surveillance authorityPrevious MatchNext Match
58.Regulated non-automatic weighing instruments presenting a riskPrevious MatchNext Match
60.Compliant regulated non-automatic weighing instruments which present a riskPrevious MatchNext Match
61.Provisions as to directions under regulations 58 and 60Previous MatchNext Match
CHAPTER 2 ENFORCEMENT PROCEDURESPrevious MatchNext Match
62.Competent authorities and enforcement proceedingsPrevious MatchNext Match
65.Review of decisions of a competent authoritiesPrevious MatchNext Match
66.Offence of failing to comply with an enforcement noticePrevious MatchNext Match
69.Testing of regulated non-automatic weighing instrumentsPrevious MatchNext Match
70.Unsuitable use of regulated non-automatic weighing instrumentsPrevious MatchNext Match
PART 10 MISCELLANEOUS AND SUPPLEMENTALPrevious MatchNext Match
SCHEDULE A1Previous MatchNext Match
Disqualification and re-qualification marksPrevious MatchNext Match
SCHEDULE 1Previous MatchNext Match
INFORMATION TO BE MARKED ON REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match
1.The number of the EU-type examination certificate, where appropriate. Previous MatchNext Match
2.The manufacturer's name, registered trade name or registered trade mark....Previous MatchNext Match
3.The accuracy class, enclosed in an oval or in two...Previous MatchNext Match
4.Maximum capacity, in the form “Max …..”. Previous MatchNext Match
5.Minimum capacity, in the form “Min …..”. Previous MatchNext Match
6.Verification scale interval in the form “e =…..” Previous MatchNext Match
8.When applicable the following: (a) for instruments consisting of separate...Previous MatchNext Match
9.The requirements of points 1.2 to 1.5 of Schedule 8...Previous MatchNext Match
SCHEDULE 2Previous MatchNext Match
OPERATIONAL OBLIGATIONS OF APPROVED BODIESPrevious MatchNext Match
1.Conformity assessment must be carried out in a proportionate manner,...Previous MatchNext Match
2.Conformity assessment bodies must perform their activities taking due account...Previous MatchNext Match
3.Where an approved body finds that the essential requirements have...Previous MatchNext Match
4.Where in the course of the monitoring of conformity following...Previous MatchNext Match
5.Where corrective measured are not taken or do not have...Previous MatchNext Match
6.Where a person is aggrieved at a decision taken by...Previous MatchNext Match
7.Approved bodies must inform the Secretary of State of the...Previous MatchNext Match
8.Approved bodies must provide other bodies approved under these Regulations...Previous MatchNext Match
9.Notified bodies must— (a) when requested by the Secretary of...Previous MatchNext Match
SCHEDULE 3Previous MatchNext Match
APPROVED BODY REQUIREMENTSPrevious MatchNext Match
1.(1) A conformity assessment body must have legal personality and...Previous MatchNext Match
2.A conformity assessment body must be a third party body...Previous MatchNext Match
3.A body belonging to a business association or professional federation...Previous MatchNext Match
4.A conformity assessment body, its top level management and the...Previous MatchNext Match
5.A conformity assessment body, its top level management and the...Previous MatchNext Match
6.Conformity assessment bodies must ensure that the activities of their...Previous MatchNext Match
7.Conformity assessment bodies and their personnel must carry out the...Previous MatchNext Match
8.A conformity assessment body must be capable of carrying out...Previous MatchNext Match
9.At all times and for each conformity assessment procedure and...Previous MatchNext Match
10.A conformity assessment body must have the means necessary to...Previous MatchNext Match
11.The personnel responsible for carrying out conformity assessment tasks must...Previous MatchNext Match
12.Conformity assessment bodies, their top-level management and the personal responsible...Previous MatchNext Match
13.The remuneration of the top-level management and personnel responsible for...Previous MatchNext Match
14.A conformity assessment body must satisfy the Secretary of State...Previous MatchNext Match
15.The personnel of a conformity assessment body must observe professional...Previous MatchNext Match
16.Conformity assessment bodies must participate in, or ensure that their...Previous MatchNext Match
SCHEDULE 4Previous MatchNext Match
USE FOR TRADE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS IN GREAT BRITAINPrevious MatchNext Match
1.Restrictions on use of instruments for tradePrevious MatchNext Match
2.Manner of erection of regulated non-automatic weighing instrumentsPrevious MatchNext Match
3.Regulated non-automatic weighing instruments marked with temperature rangePrevious MatchNext Match
4.Regulated non-automatic weighing instruments marked with manner of usePrevious MatchNext Match
5.Regulated non-automatic weighing instruments fitted with printing devicesPrevious MatchNext Match
7.Operation of regulated non-automatic weighing instrumentPrevious MatchNext Match
8.Regulated non-automatic weighing instruments to be set to zero or to be balanced before usePrevious MatchNext Match
SCHEDULE 6Previous MatchNext Match
(Annex I to the Directive)Previous MatchNext Match
ESSENTIAL REQUIREMENTSPrevious MatchNext Match
The terminology used is that of the International Organisation of Legal MetrologyPrevious MatchNext Match
Preliminary observation
Metrological requirementsPrevious MatchNext Match
1.Units of mass The units of mass used shall be...Previous MatchNext Match
2.1.The following accuracy classes have been defined— Previous MatchNext Match
2.2.1.The actual scale interval (d) and the verification scale interval...Previous MatchNext Match
2.2.2.For all instruments other than those with auxiliary indicating devices—...Previous MatchNext Match
2.2.3.For instruments with auxiliary indicating devices the following conditions apply—...Previous MatchNext Match
3.1.Instruments with one weighing range Instruments equipped with an auxiliary...Previous MatchNext Match
3.2.Instruments with multiple weighing ranges Multiple weighing ranges are permitted,...Previous MatchNext Match
3.3.1.Instruments with one weighing range may have several partial weighing...Previous MatchNext Match
3.3.2.Each partial weighing range i of multi-interval instruments is defined...Previous MatchNext Match
3.3.3.The partial weighing ranges are classified according to Table 2....Previous MatchNext Match
4.1.On implementation of the procedures laid down in regulation 36,...Previous MatchNext Match
4.2.The maximum permissible errors in service are twice the maximum...Previous MatchNext Match
5.Weighing results of an instrument shall be repeatable, and shall...Previous MatchNext Match
6.The instrument shall react to small variations in the load....Previous MatchNext Match
7.1.Instruments of classes II, III and IIII, liable to be...Previous MatchNext Match
7.2.The instruments shall meet the metrological requirements within the temperature...Previous MatchNext Match
7.3.Instruments operated from a mains power supply shall meet the...Previous MatchNext Match
7.4.Electronic instruments, except those in class I and in class...Previous MatchNext Match
7.5.Loading an instrument in class II, III or IIII for...Previous MatchNext Match
7.6.Under other conditions the instruments shall either continue to function...Previous MatchNext Match
Design and constructionPrevious MatchNext Match
8.1.Design and construction of the instruments shall be such that...Previous MatchNext Match
8.2.When exposed to disturbances, electronic instruments shall not display the...Previous MatchNext Match
8.3.The requirements of points 8.1 and 8.2 shall be met...Previous MatchNext Match
8.4.When external equipment is connected to an electronic instrument through...Previous MatchNext Match
8.5.The instruments shall have no characteristics likely to facilitate fraudulent...Previous MatchNext Match
8.6.Instruments shall be designed to permit ready execution of the...Previous MatchNext Match
9.Indication of weighing results and other weight values The indication...Previous MatchNext Match
10.Printing of weighing results and other weight values Printed results...Previous MatchNext Match
11.Levelling When appropriate, instruments shall be fitted with a levelling...Previous MatchNext Match
12.Zeroing Instruments may be equipped with zeroing devices. The operation...Previous MatchNext Match
13.Tare devices and preset tare devices The instruments may have...Previous MatchNext Match
14.Instruments for direct sales to the public, with a maximum...Previous MatchNext Match
15.Price labelling instruments Price labelling instruments shall meet the requirements...Previous MatchNext Match
SCHEDULE 7Previous MatchNext Match
(Annex II to the Directive)Previous MatchNext Match
CONFORMITY ASSESSMENT PROCEDURESPrevious MatchNext Match
1.1.type examination is the part of a conformity assessment procedure...Previous MatchNext Match
1.2.type examination may be carried out in any of the...Previous MatchNext Match
1.3.The manufacturer shall lodge an application for type examination with...Previous MatchNext Match
1.4.The approved body shall— For the instrument— Previous MatchNext Match
1.4.1.examine the technical documentation and supporting evidence to assess the...Previous MatchNext Match
1.4.2.verify that the specimen(s) have been manufactured in conformity with...Previous MatchNext Match
1.4.3.carry out appropriate examinations and tests, or have them carried...Previous MatchNext Match
1.4.4.carry out appropriate examinations and tests, or have them carried...Previous MatchNext Match
1.4.5.agree with the manufacturer on a location where the examinations...Previous MatchNext Match
1.5.The approved body shall draw up an evaluation report that...Previous MatchNext Match
1.6.Where the type meets the requirements of these Regulations, that...Previous MatchNext Match
1.7.The approved body shall keep itself apprised of any changes...Previous MatchNext Match
1.8.Each approved body shall inform the Secretary of State concerning...Previous MatchNext Match
1.9.The manufacturer shall keep a copy of the type examination...Previous MatchNext Match
1.10.The manufacturer's authorised representative may lodge the application referred to...Previous MatchNext Match
2.Module D: Conformity to type based on quality assurance of...Previous MatchNext Match
2.1.Conformity to type based on quality assurance of the production...Previous MatchNext Match
2.2.Manufacturing The manufacturer shall operate an approved quality system for...Previous MatchNext Match
2.3.1.The manufacturer shall lodge an application for assessment of his...Previous MatchNext Match
2.3.2.The quality system shall ensure that the instruments are in...Previous MatchNext Match
2.3.3.The approved body shall assess the quality system to determine...Previous MatchNext Match
2.3.4.The manufacturer shall undertake to fulfil the obligations arising out...Previous MatchNext Match
2.3.5.The manufacturer shall keep the approved body that has approved...Previous MatchNext Match
2.4.Surveillance under the responsibility of the approved body Previous MatchNext Match
2.4.1.The purpose of surveillance is to make sure that the...Previous MatchNext Match
2.4.2.The manufacturer shall, for assessment purposes, allow the approved body...Previous MatchNext Match
2.4.3.The approved body shall carry out periodic audits to make...Previous MatchNext Match
2.4.4.In addition, the approved body may pay unexpected visits to...Previous MatchNext Match
2.5.Conformity marking and declaration of conformity Previous MatchNext Match
2.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match
2.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match
2.6.The manufacturer shall, for a period ending 10 years after...Previous MatchNext Match
2.7.Each approved body shall inform the Secretary of State of...Previous MatchNext Match
2.8.Authorised representative The manufacturer's obligations set out in points 2.3.1,...Previous MatchNext Match
3.Module D1: Quality assurance of the production process Previous MatchNext Match
3.1.Quality assurance of the production process is the conformity assessment...Previous MatchNext Match
3.2.Technical documentation The manufacturer shall establish the technical documentation. The...Previous MatchNext Match
3.3.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match
3.4.Manufacturing The manufacturer shall operate an approved quality system for...Previous MatchNext Match
3.5.1.The manufacturer shall lodge an application for assessment of his...Previous MatchNext Match
3.5.2.The quality system shall ensure compliance of the instruments with...Previous MatchNext Match
3.5.3.The approved body shall assess the quality system to determine...Previous MatchNext Match
3.5.4.The manufacturer shall undertake to fulfil the obligations arising out...Previous MatchNext Match
3.5.5.The manufacturer shall keep the approved body that has approved...Previous MatchNext Match
3.6.Surveillance under the responsibility of the approved body Previous MatchNext Match
3.6.1.The purpose of surveillance is to make sure that the...Previous MatchNext Match
3.6.2.The manufacturer shall, for assessment purposes, allow the approved body...Previous MatchNext Match
3.6.3.The approved body shall carry out periodic audits to make...Previous MatchNext Match
3.6.4.In addition, the approved body may pay unexpected visits to...Previous MatchNext Match
3.7.Conformity marking and declaration of conformity Previous MatchNext Match
3.7.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match
3.7.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match
3.8.The manufacturer shall, for a period ending 10 years after...Previous MatchNext Match
3.9.Each approved body shall inform the Secretary of State of...Previous MatchNext Match
3.10.Authorised representative The manufacturer's obligations set out in points 3.3,...Previous MatchNext Match
4.Module F: Conformity to type based on product verification Previous MatchNext Match
4.1.Conformity to type based on product verification is the part...Previous MatchNext Match
4.2.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match
4.3.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match
4.4.Verification of conformity by examination and testing of every instrument...Previous MatchNext Match
4.4.1.All instruments shall be individually examined and appropriate tests set...Previous MatchNext Match
4.4.2.The approved body shall issue a certificate of conformity in...Previous MatchNext Match
4.5.Conformity marking and declaration of conformity Previous MatchNext Match
4.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match
4.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match
4.6.If the approved body agrees and under its responsibility, the...Previous MatchNext Match
4.7.Authorised representative The manufacturer's obligations may be fulfilled by his...Previous MatchNext Match
5.Module F1: Conformity based on product verification Previous MatchNext Match
5.1.Conformity based on product verification is the conformity assessment procedure...Previous MatchNext Match
5.2.1.The manufacturer shall establish the technical documentation. The documentation shall...Previous MatchNext Match
5.2.2.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match
5.3.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match
5.4.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match
5.5.Verification of conformity by examination and testing of every instrument...Previous MatchNext Match
5.5.1.All instruments shall be individually examined and appropriate tests, set...Previous MatchNext Match
5.5.2.The approved body shall issue a certificate of conformity in...Previous MatchNext Match
5.6.Conformity marking and declaration of conformity Previous MatchNext Match
5.6.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match
5.6.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match
5.7.If the approved body agrees and under its responsibility, the...Previous MatchNext Match
5.8.Authorised representative The manufacturer's obligations may be fulfilled by his...Previous MatchNext Match
6.Module G: Conformity based on unit verification Previous MatchNext Match
6.1.Conformity based on unit verification is the conformity assessment procedure...Previous MatchNext Match
6.2.1.The manufacturer shall establish the technical documentation and make it...Previous MatchNext Match
6.2.2.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match
6.3.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match
6.4.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match
6.5.Conformity marking and declaration of conformity Previous MatchNext Match
6.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match
6.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match
6.6.Authorised representative The manufacturer's obligations set out in points 6.2.2...Previous MatchNext Match
7.1.The conformity assessment according to Module D, D1, F, F1...Previous MatchNext Match
7.2.If the instrument's performance is sensitive to gravity variations the...Previous MatchNext Match
7.2.1.Where a manufacturer has opted for execution in two stages...Previous MatchNext Match
7.2.2.The party which has carried out the first stage of...Previous MatchNext Match
7.2.3.A manufacturer who has opted for Module D or D1...Previous MatchNext Match
7.2.4.The UK marking and the M metrology marking shall be...Previous MatchNext Match
SCHEDULE 8Previous MatchNext Match
(Annex III to the Directive)Previous MatchNext Match
INSCRIPTIONSPrevious MatchNext Match
1.Instruments intended to be used for the applications listed in...Previous MatchNext Match
1.1.Those instruments shall bear visibly, legibly and indelibly the following...Previous MatchNext Match
1.2.Those instruments shall have adequate facilities for the affixing of...Previous MatchNext Match
1.3.Where a data plate is used it shall be possible...Previous MatchNext Match
1.4.The inscriptions Max, Min, e, and d, shall also be...Previous MatchNext Match
1.5.Each load measuring device which is connected or can be...Previous MatchNext Match
2.Instruments not intended to be used for the applications listed...Previous MatchNext Match
3.Restrictive use symbol referred to in regulation 9(3). The restrictive...Previous MatchNext Match
SCHEDULE 9Previous MatchNext Match
DECLARATION OF CONFORMITY (No XXXX) Previous MatchNext Match
1.Instrument model/Instrument (product, type, batch or serial number): Previous MatchNext Match
2.Name and address of the manufacturer and, where applicable, his...Previous MatchNext Match
3.This declaration of conformity is issued under the sole responsibility...Previous MatchNext Match
4.Object of the declaration (identification of instrument allowing traceability; it...Previous MatchNext Match
5.The object of the declaration described above is in conformity...Previous MatchNext Match
6.References to the relevant designated standards used or references to...Previous MatchNext Match
7.The approved body … (name, number) performed … (description of...Previous MatchNext Match
8.Additional information: — Signed for and on behalf of: —...Previous MatchNext Match
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