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The Non-automatic Weighing Instruments Regulations 2016

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You searched for provisions that are applicable to England. The matching provisions are highlighted below. Where no highlighting is shown the matching result may be contained within a footnote.

  1. Introductory TextNext Match

  2. PART 1 INTRODUCTORYPrevious MatchNext Match

    1. 1.Citation commencement and extentPrevious MatchNext Match

    2. 2.InterpretationPrevious MatchNext Match

    3. 2A.Designated standardPrevious MatchNext Match

    4. 3.Application of these RegulationsPrevious MatchNext Match

    5. 4.Revocations and transitional and consequential provisionsPrevious MatchNext Match

    6. 4A.Transitional provision in relation to EU ExitPrevious MatchNext Match

  3. PART 2 REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS – OBLIGATIONS OF ECONOMIC OPERATORSPrevious MatchNext Match

    1. CHAPTER 1 OBLIGATIONS OF MANUFACTURERS AND PERSONS TO BE TREATED AS MANUFACTURERSPrevious MatchNext Match

      1. 5.IntroductoryPrevious MatchNext Match

      2. 6.Manufacturers' responsibilities – design, conformity assessment and marking of regulated non-automatic weighing instrumentsPrevious MatchNext Match

      3. 7.Manufacturers' obligations in respect of recordsPrevious MatchNext Match

      4. 8.Manufacturers' obligations to ensure continuing conformity with the essential requirementsPrevious MatchNext Match

      5. 9.Manufacturers' obligations in relation to the marking of regulated non-automatic weighing instruments with serial numbers etc.Previous MatchNext Match

      6. 10.Manufacturers to mark contact details on regulated non-automatic weighing instrumentsPrevious MatchNext Match

      7. 11.Documentation to accompany regulated non-automatic weighing instrumentsPrevious MatchNext Match

      8. 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

      9. 13.Provision of information to the competent authorityPrevious MatchNext Match

      10. 14.Use of authorised representatives by manufacturersPrevious MatchNext Match

    2. CHAPTER 2 OBLIGATIONS OF IMPORTERSPrevious MatchNext Match

      1. 15.IntroductoryPrevious MatchNext Match

      2. 16.Ensuring compliance of regulated non-automatic weighing instrumentsPrevious MatchNext Match

      3. 17.Importers duty to notify manufacturer and market surveillance authorities of non-compliant regulated non-automatic weighing instruments that present a riskPrevious MatchNext Match

      4. 18.Requirements to mark importers' details on regulated non-automatic weighing instrumentsPrevious MatchNext Match

      5. 19.Importers' duty to ensure that regulated non-automatic weighing instruments are accompanied by relevant documentation.Previous MatchNext Match

      6. 20.Duty of importers to ensure proper conditions of storage and transportPrevious MatchNext Match

      7. 21.Duties of importers with regard to monitoring etc.Previous MatchNext Match

      8. 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

      9. 23.Requirement for importer to keep copy of EU declaration of conformityPrevious MatchNext Match

      10. 24.Provision of information to a competent authorityPrevious MatchNext Match

    3. CHAPTER 3 OBLIGATIONS OF DISTRIBUTORSPrevious MatchNext Match

      1. 25.IntroductoryPrevious MatchNext Match

      2. 26.Distributors – duty to act with due carePrevious MatchNext Match

      3. 27.Distributors – verification obligationsPrevious MatchNext Match

      4. 28.Distributors not to make non-conforming non-automatic weighing instruments available on the market etc.Previous MatchNext Match

      5. 29.Duty of distributors to ensure proper conditions of storage and transportPrevious MatchNext Match

      6. 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

      7. 31.Provision of information to the competent authorityPrevious MatchNext Match

    4. CHAPTER 4 IDENTIFICATION OF ECONOMIC OPERATORSPrevious MatchNext Match

      1. 32.(1) Economic operators must, on request, identify to the market...Previous MatchNext Match

      2. 32A.Obligations which are met by complying with obligations in the DirectivePrevious MatchNext Match

      3. 32B.Conformity assessment procedure obligations that are met by complying with the DirectivePrevious MatchNext Match

      4. 32C.Further use of UK markingPrevious MatchNext Match

      5. 32D.Qualifying Northern Ireland GoodsPrevious MatchNext Match

  4. PART 3 CONFORMITY OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match

    1. CHAPTER 1 ESTABLISHING COMPLIANCE WITH THE ESSENTIAL REQUIREMENTSPrevious MatchNext Match

      1. 33.IntroductoryPrevious MatchNext Match

      2. 34.Methods of establishing conformity with the essential requirementsPrevious MatchNext Match

      3. 35.Presumptions of conformity of regulated non-automatic weighing instrumentsPrevious MatchNext Match

      4. 36.Conformity assessment proceduresPrevious MatchNext Match

      5. 37.Subsidiaries and contractorsPrevious MatchNext Match

      6. 38.FeesPrevious MatchNext Match

    2. CHAPTER 2 REQUIREMENTS RELATING TO EU DECLARATIONS OF CONFORMITYPrevious MatchNext Match

      1. 39.Application of ChapterPrevious MatchNext Match

      2. 40.Form and contents of ... declaration of conformity etc.Previous MatchNext Match

      3. 41.Regulated instruments that require more than one declaration of conformityPrevious MatchNext Match

      4. 42.Responsibility of manufacturer that draws up declaration of conformityPrevious MatchNext Match

    3. CHAPTER 3 CONFORMITY MARKINGPrevious MatchNext Match

      1. 43.Conformity with ... requirements to be indicated by the UK markingPrevious MatchNext Match

      2. 44.Prohibition on improper use of UK marking and the M markingPrevious MatchNext Match

      3. 45.Rules and conditions for affixing the UK marking and the M marking etc.Previous MatchNext Match

      4. 45A.UK(NI) indication

      5. 45B.Register of notified bodies established in the United Kingdom

  5. PART 4 REQUIREMENTS FOR NON-REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match

    1. 46.(1) This regulation applies to a non-automatic weighing instrument which...Previous MatchNext Match

  6. PART 5 APPROVAL OF CONFORMITY ASSESSMENT BODIESPrevious MatchNext Match

    1. 47.Approved bodiesPrevious MatchNext Match

    2. 48.Approval of conformity assessment bodiesPrevious MatchNext Match

    3. 49.Presumption of conformity of approved bodiesPrevious MatchNext Match

    4. 50.MonitoringPrevious MatchNext Match

    5. 51.Restriction, suspension or withdrawal of approvalPrevious MatchNext Match

    6. 52.Subsidiaries and contractorsPrevious MatchNext Match

    7. 53.Register of approved bodiesPrevious MatchNext Match

    8. 54.UK national accreditation bodyPrevious MatchNext Match

  7. PART 6 PUTTING INTO SERVICE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS FOR THE PURPOSES LISTED IN REGULATION 3(2)Previous MatchNext Match

    1. 55.No person shall put into service a regulated non-automatic weighing...Previous MatchNext Match

  8. PART 7 USE FOR TRADE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS IN GREAT BRITAINPrevious MatchNext Match

    1. 56.Schedule 4 applies to the use for trade of regulated...Previous MatchNext Match

  9. PART 8 MARKET SURVEILLANCE AND ENFORCEMENTPrevious MatchNext Match

    1. CHAPTER 1 MARKET SURVEILLANCEPrevious MatchNext Match

      1. 57.The market surveillance authorityPrevious MatchNext Match

      2. 58.Regulated non-automatic weighing instruments presenting a riskPrevious MatchNext Match

      3. 59.EU safeguard procedurePrevious MatchNext Match

      4. 60.Compliant regulated non-automatic weighing instruments which present a riskPrevious MatchNext Match

      5. 61.Provisions as to directions under regulations 58 and 60Previous MatchNext Match

    2. CHAPTER 2 ENFORCEMENT PROCEDURESPrevious MatchNext Match

      1. 62.Competent authorities and enforcement proceedingsPrevious MatchNext Match

      2. 63.Compliance notice procedurePrevious MatchNext Match

      3. 64.Enforcement notice procedurePrevious MatchNext Match

      4. 65.Review of decisions of a competent authoritiesPrevious MatchNext Match

      5. 66.Offence of failing to comply with an enforcement noticePrevious MatchNext Match

      6. 67.DisqualificationPrevious MatchNext Match

      7. 68.Re-qualificationPrevious MatchNext Match

      8. 69.Testing of regulated non-automatic weighing instrumentsPrevious MatchNext Match

      9. 70.Unsuitable use of regulated non-automatic weighing instrumentsPrevious MatchNext Match

  10. PART 9 OFFENCESPrevious MatchNext Match

    1. 71.Unauthorised application of authorised marksPrevious MatchNext Match

    2. 72.Offences by economic operators etc.Previous MatchNext Match

    3. 73.Penalties for offencesPrevious MatchNext Match

    4. 74.Defence of due diligencePrevious MatchNext Match

    5. 75.Liability of persons other than the principal offenderPrevious MatchNext Match

  11. PART 10 MISCELLANEOUS AND SUPPLEMENTALPrevious MatchNext Match

    1. 76.Service of documents etc.Previous MatchNext Match

    2. 77.ReviewPrevious MatchNext Match

  12. SignaturePrevious MatchNext Match

    1. SCHEDULE A1Previous MatchNext Match

      Disqualification and re-qualification marksPrevious MatchNext Match

      1. 1.Disqualification markPrevious MatchNext Match

      2. 2.Re-qualification markPrevious MatchNext Match

    2. SCHEDULE 1Previous MatchNext Match

      INFORMATION TO BE MARKED ON REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTSPrevious MatchNext Match

      1. 1.The number of the EU-type examination certificate, where appropriate. Previous MatchNext Match

      2. 2.The manufacturer's name, registered trade name or registered trade mark....Previous MatchNext Match

      3. 3.The accuracy class, enclosed in an oval or in two...Previous MatchNext Match

      4. 4.Maximum capacity, in the form “Max …..”. Previous MatchNext Match

      5. 5.Minimum capacity, in the form “Min …..”. Previous MatchNext Match

      6. 6.Verification scale interval in the form “e =…..” Previous MatchNext Match

      7. 7.Type, batch and serial number Previous MatchNext Match

      8. 8.When applicable the following: (a) for instruments consisting of separate...Previous MatchNext Match

      9. 9.The requirements of points 1.2 to 1.5 of Schedule 8...Previous MatchNext Match

    3. SCHEDULE 2Previous MatchNext Match

      OPERATIONAL OBLIGATIONS OF APPROVED BODIESPrevious MatchNext Match

      1. 1.Conformity assessment must be carried out in a proportionate manner,...Previous MatchNext Match

      2. 2.Conformity assessment bodies must perform their activities taking due account...Previous MatchNext Match

      3. 3.Where an approved body finds that the essential requirements have...Previous MatchNext Match

      4. 4.Where in the course of the monitoring of conformity following...Previous MatchNext Match

      5. 5.Where corrective measured are not taken or do not have...Previous MatchNext Match

      6. 6.Where a person is aggrieved at a decision taken by...Previous MatchNext Match

      7. 7.Approved bodies must inform the Secretary of State of the...Previous MatchNext Match

      8. 8.Approved bodies must provide other bodies approved under these Regulations...Previous MatchNext Match

      9. 9.Notified bodies must— (a) when requested by the Secretary of...Previous MatchNext Match

    4. SCHEDULE 3Previous MatchNext Match

      APPROVED BODY REQUIREMENTSPrevious MatchNext Match

      1. 1.(1) A conformity assessment body must have legal personality and...Previous MatchNext Match

      2. 2.A conformity assessment body must be a third party body...Previous MatchNext Match

      3. 3.A body belonging to a business association or professional federation...Previous MatchNext Match

      4. 4.A conformity assessment body, its top level management and the...Previous MatchNext Match

      5. 5.A conformity assessment body, its top level management and the...Previous MatchNext Match

      6. 6.Conformity assessment bodies must ensure that the activities of their...Previous MatchNext Match

      7. 7.Conformity assessment bodies and their personnel must carry out the...Previous MatchNext Match

      8. 8.A conformity assessment body must be capable of carrying out...Previous MatchNext Match

      9. 9.At all times and for each conformity assessment procedure and...Previous MatchNext Match

      10. 10.A conformity assessment body must have the means necessary to...Previous MatchNext Match

      11. 11.The personnel responsible for carrying out conformity assessment tasks must...Previous MatchNext Match

      12. 12.Conformity assessment bodies, their top-level management and the personal responsible...Previous MatchNext Match

      13. 13.The remuneration of the top-level management and personnel responsible for...Previous MatchNext Match

      14. 14.A conformity assessment body must satisfy the Secretary of State...Previous MatchNext Match

      15. 15.The personnel of a conformity assessment body must observe professional...Previous MatchNext Match

      16. 16.Conformity assessment bodies must participate in, or ensure that their...Previous MatchNext Match

    5. SCHEDULE 4Previous MatchNext Match

      USE FOR TRADE OF REGULATED NON-AUTOMATIC WEIGHING INSTRUMENTS IN GREAT BRITAINPrevious MatchNext Match

      1. 1.Restrictions on use of instruments for tradePrevious MatchNext Match

      2. 2.Manner of erection of regulated non-automatic weighing instrumentsPrevious MatchNext Match

      3. 3.Regulated non-automatic weighing instruments marked with temperature rangePrevious MatchNext Match

      4. 4.Regulated non-automatic weighing instruments marked with manner of usePrevious MatchNext Match

      5. 5.Regulated non-automatic weighing instruments fitted with printing devicesPrevious MatchNext Match

      6. 6.Load receptorsPrevious MatchNext Match

      7. 7.Operation of regulated non-automatic weighing instrumentPrevious MatchNext Match

      8. 8.Regulated non-automatic weighing instruments to be set to zero or to be balanced before usePrevious MatchNext Match

    6. SCHEDULE 5Previous MatchNext Match

      MONETARY PENALTIESPrevious MatchNext Match

      1. 1.IntroductionPrevious MatchNext Match

      2. 2.ProcedurePrevious MatchNext Match

      3. 3.AppealsPrevious MatchNext Match

      4. 4.Interest and recoveryPrevious MatchNext Match

    7. SCHEDULE 6Previous MatchNext Match

      (Annex I to the Directive)Previous MatchNext Match

      1. ESSENTIAL REQUIREMENTSPrevious MatchNext Match

        1. The terminology used is that of the International Organisation of Legal MetrologyPrevious MatchNext Match

          1. Preliminary observation

        2. Metrological requirementsPrevious MatchNext Match

          1. 1.Units of mass The units of mass used shall be...Previous MatchNext Match

          2. 2.Accuracy classes Previous MatchNext Match

          3. 2.1.The following accuracy classes have been defined— Previous MatchNext Match

          4. 2.2.Scale intervals Previous MatchNext Match

          5. 2.2.1.The actual scale interval (d) and the verification scale interval...Previous MatchNext Match

          6. 2.2.2.For all instruments other than those with auxiliary indicating devices—...Previous MatchNext Match

          7. 2.2.3.For instruments with auxiliary indicating devices the following conditions apply—...Previous MatchNext Match

          8. 3.Classification Previous MatchNext Match

          9. 3.1.Instruments with one weighing range Instruments equipped with an auxiliary...Previous MatchNext Match

          10. 3.2.Instruments with multiple weighing ranges Multiple weighing ranges are permitted,...Previous MatchNext Match

          11. 3.3.Multi-interval instruments Previous MatchNext Match

          12. 3.3.1.Instruments with one weighing range may have several partial weighing...Previous MatchNext Match

          13. 3.3.2.Each partial weighing range i of multi-interval instruments is defined...Previous MatchNext Match

          14. 3.3.3.The partial weighing ranges are classified according to Table 2....Previous MatchNext Match

          15. 4.Accuracy Previous MatchNext Match

          16. 4.1.On implementation of the procedures laid down in regulation 36,...Previous MatchNext Match

          17. 4.2.The maximum permissible errors in service are twice the maximum...Previous MatchNext Match

          18. 5.Weighing results of an instrument shall be repeatable, and shall...Previous MatchNext Match

          19. 6.The instrument shall react to small variations in the load....Previous MatchNext Match

          20. 7.Influence quantities and time Previous MatchNext Match

          21. 7.1.Instruments of classes II, III and IIII, liable to be...Previous MatchNext Match

          22. 7.2.The instruments shall meet the metrological requirements within the temperature...Previous MatchNext Match

          23. 7.3.Instruments operated from a mains power supply shall meet the...Previous MatchNext Match

          24. 7.4.Electronic instruments, except those in class I and in class...Previous MatchNext Match

          25. 7.5.Loading an instrument in class II, III or IIII for...Previous MatchNext Match

          26. 7.6.Under other conditions the instruments shall either continue to function...Previous MatchNext Match

        3. Design and constructionPrevious MatchNext Match

          1. 8.General requirements Previous MatchNext Match

          2. 8.1.Design and construction of the instruments shall be such that...Previous MatchNext Match

          3. 8.2.When exposed to disturbances, electronic instruments shall not display the...Previous MatchNext Match

          4. 8.3.The requirements of points 8.1 and 8.2 shall be met...Previous MatchNext Match

          5. 8.4.When external equipment is connected to an electronic instrument through...Previous MatchNext Match

          6. 8.5.The instruments shall have no characteristics likely to facilitate fraudulent...Previous MatchNext Match

          7. 8.6.Instruments shall be designed to permit ready execution of the...Previous MatchNext Match

          8. 9.Indication of weighing results and other weight values The indication...Previous MatchNext Match

          9. 10.Printing of weighing results and other weight values Printed results...Previous MatchNext Match

          10. 11.Levelling When appropriate, instruments shall be fitted with a levelling...Previous MatchNext Match

          11. 12.Zeroing Instruments may be equipped with zeroing devices. The operation...Previous MatchNext Match

          12. 13.Tare devices and preset tare devices The instruments may have...Previous MatchNext Match

          13. 14.Instruments for direct sales to the public, with a maximum...Previous MatchNext Match

          14. 15.Price labelling instruments Price labelling instruments shall meet the requirements...Previous MatchNext Match

    8. SCHEDULE 7Previous MatchNext Match

      (Annex II to the Directive)Previous MatchNext Match

      1. CONFORMITY ASSESSMENT PROCEDURESPrevious MatchNext Match

        1. 1.Module B: type examination Previous MatchNext Match

        2. 1.1.type examination is the part of a conformity assessment procedure...Previous MatchNext Match

        3. 1.2.type examination may be carried out in any of the...Previous MatchNext Match

        4. 1.3.The manufacturer shall lodge an application for type examination with...Previous MatchNext Match

        5. 1.4.The approved body shall— For the instrument— Previous MatchNext Match

        6. 1.4.1.examine the technical documentation and supporting evidence to assess the...Previous MatchNext Match

        7. 1.4.2.verify that the specimen(s) have been manufactured in conformity with...Previous MatchNext Match

        8. 1.4.3.carry out appropriate examinations and tests, or have them carried...Previous MatchNext Match

        9. 1.4.4.carry out appropriate examinations and tests, or have them carried...Previous MatchNext Match

        10. 1.4.5.agree with the manufacturer on a location where the examinations...Previous MatchNext Match

        11. 1.5.The approved body shall draw up an evaluation report that...Previous MatchNext Match

        12. 1.6.Where the type meets the requirements of these Regulations, that...Previous MatchNext Match

        13. 1.7.The approved body shall keep itself apprised of any changes...Previous MatchNext Match

        14. 1.8.Each approved body shall inform the Secretary of State concerning...Previous MatchNext Match

        15. 1.9.The manufacturer shall keep a copy of the type examination...Previous MatchNext Match

        16. 1.10.The manufacturer's authorised representative may lodge the application referred to...Previous MatchNext Match

        17. 2.Module D: Conformity to type based on quality assurance of...Previous MatchNext Match

        18. 2.1.Conformity to type based on quality assurance of the production...Previous MatchNext Match

        19. 2.2.Manufacturing The manufacturer shall operate an approved quality system for...Previous MatchNext Match

        20. 2.3.Quality system Previous MatchNext Match

        21. 2.3.1.The manufacturer shall lodge an application for assessment of his...Previous MatchNext Match

        22. 2.3.2.The quality system shall ensure that the instruments are in...Previous MatchNext Match

        23. 2.3.3.The approved body shall assess the quality system to determine...Previous MatchNext Match

        24. 2.3.4.The manufacturer shall undertake to fulfil the obligations arising out...Previous MatchNext Match

        25. 2.3.5.The manufacturer shall keep the approved body that has approved...Previous MatchNext Match

        26. 2.4.Surveillance under the responsibility of the approved body Previous MatchNext Match

        27. 2.4.1.The purpose of surveillance is to make sure that the...Previous MatchNext Match

        28. 2.4.2.The manufacturer shall, for assessment purposes, allow the approved body...Previous MatchNext Match

        29. 2.4.3.The approved body shall carry out periodic audits to make...Previous MatchNext Match

        30. 2.4.4.In addition, the approved body may pay unexpected visits to...Previous MatchNext Match

        31. 2.5.Conformity marking and declaration of conformity Previous MatchNext Match

        32. 2.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match

        33. 2.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match

        34. 2.6.The manufacturer shall, for a period ending 10 years after...Previous MatchNext Match

        35. 2.7.Each approved body shall inform the Secretary of State of...Previous MatchNext Match

        36. 2.8.Authorised representative The manufacturer's obligations set out in points 2.3.1,...Previous MatchNext Match

        37. 3.Module D1: Quality assurance of the production process Previous MatchNext Match

        38. 3.1.Quality assurance of the production process is the conformity assessment...Previous MatchNext Match

        39. 3.2.Technical documentation The manufacturer shall establish the technical documentation. The...Previous MatchNext Match

        40. 3.3.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match

        41. 3.4.Manufacturing The manufacturer shall operate an approved quality system for...Previous MatchNext Match

        42. 3.5.Quality system Previous MatchNext Match

        43. 3.5.1.The manufacturer shall lodge an application for assessment of his...Previous MatchNext Match

        44. 3.5.2.The quality system shall ensure compliance of the instruments with...Previous MatchNext Match

        45. 3.5.3.The approved body shall assess the quality system to determine...Previous MatchNext Match

        46. 3.5.4.The manufacturer shall undertake to fulfil the obligations arising out...Previous MatchNext Match

        47. 3.5.5.The manufacturer shall keep the approved body that has approved...Previous MatchNext Match

        48. 3.6.Surveillance under the responsibility of the approved body Previous MatchNext Match

        49. 3.6.1.The purpose of surveillance is to make sure that the...Previous MatchNext Match

        50. 3.6.2.The manufacturer shall, for assessment purposes, allow the approved body...Previous MatchNext Match

        51. 3.6.3.The approved body shall carry out periodic audits to make...Previous MatchNext Match

        52. 3.6.4.In addition, the approved body may pay unexpected visits to...Previous MatchNext Match

        53. 3.7.Conformity marking and declaration of conformity Previous MatchNext Match

        54. 3.7.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match

        55. 3.7.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match

        56. 3.8.The manufacturer shall, for a period ending 10 years after...Previous MatchNext Match

        57. 3.9.Each approved body shall inform the Secretary of State of...Previous MatchNext Match

        58. 3.10.Authorised representative The manufacturer's obligations set out in points 3.3,...Previous MatchNext Match

        59. 4.Module F: Conformity to type based on product verification Previous MatchNext Match

        60. 4.1.Conformity to type based on product verification is the part...Previous MatchNext Match

        61. 4.2.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match

        62. 4.3.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match

        63. 4.4.Verification of conformity by examination and testing of every instrument...Previous MatchNext Match

        64. 4.4.1.All instruments shall be individually examined and appropriate tests set...Previous MatchNext Match

        65. 4.4.2.The approved body shall issue a certificate of conformity in...Previous MatchNext Match

        66. 4.5.Conformity marking and declaration of conformity Previous MatchNext Match

        67. 4.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match

        68. 4.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match

        69. 4.6.If the approved body agrees and under its responsibility, the...Previous MatchNext Match

        70. 4.7.Authorised representative The manufacturer's obligations may be fulfilled by his...Previous MatchNext Match

        71. 5.Module F1: Conformity based on product verification Previous MatchNext Match

        72. 5.1.Conformity based on product verification is the conformity assessment procedure...Previous MatchNext Match

        73. 5.2.Technical documentation Previous MatchNext Match

        74. 5.2.1.The manufacturer shall establish the technical documentation. The documentation shall...Previous MatchNext Match

        75. 5.2.2.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match

        76. 5.3.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match

        77. 5.4.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match

        78. 5.5.Verification of conformity by examination and testing of every instrument...Previous MatchNext Match

        79. 5.5.1.All instruments shall be individually examined and appropriate tests, set...Previous MatchNext Match

        80. 5.5.2.The approved body shall issue a certificate of conformity in...Previous MatchNext Match

        81. 5.6.Conformity marking and declaration of conformity Previous MatchNext Match

        82. 5.6.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match

        83. 5.6.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match

        84. 5.7.If the approved body agrees and under its responsibility, the...Previous MatchNext Match

        85. 5.8.Authorised representative The manufacturer's obligations may be fulfilled by his...Previous MatchNext Match

        86. 6.Module G: Conformity based on unit verification Previous MatchNext Match

        87. 6.1.Conformity based on unit verification is the conformity assessment procedure...Previous MatchNext Match

        88. 6.2.Technical documentation Previous MatchNext Match

        89. 6.2.1.The manufacturer shall establish the technical documentation and make it...Previous MatchNext Match

        90. 6.2.2.The manufacturer shall keep the technical documentation at the disposal...Previous MatchNext Match

        91. 6.3.Manufacturing The manufacturer shall take all measures necessary so that...Previous MatchNext Match

        92. 6.4.Verification An approved body chosen by the manufacturer shall carry...Previous MatchNext Match

        93. 6.5.Conformity marking and declaration of conformity Previous MatchNext Match

        94. 6.5.1.The manufacturer shall affix the UK marking and the M...Previous MatchNext Match

        95. 6.5.2.The manufacturer shall draw up a written declaration of conformity...Previous MatchNext Match

        96. 6.6.Authorised representative The manufacturer's obligations set out in points 6.2.2...Previous MatchNext Match

        97. 7.Common provisions Previous MatchNext Match

        98. 7.1.The conformity assessment according to Module D, D1, F, F1...Previous MatchNext Match

        99. 7.2.If the instrument's performance is sensitive to gravity variations the...Previous MatchNext Match

        100. 7.2.1.Where a manufacturer has opted for execution in two stages...Previous MatchNext Match

        101. 7.2.2.The party which has carried out the first stage of...Previous MatchNext Match

        102. 7.2.3.A manufacturer who has opted for Module D or D1...Previous MatchNext Match

        103. 7.2.4.The UK marking and the M metrology marking shall be...Previous MatchNext Match

    9. SCHEDULE 8Previous MatchNext Match

      (Annex III to the Directive)Previous MatchNext Match

      1. INSCRIPTIONSPrevious MatchNext Match

        1. 1.Instruments intended to be used for the applications listed in...Previous MatchNext Match

        2. 1.1.Those instruments shall bear visibly, legibly and indelibly the following...Previous MatchNext Match

        3. 1.2.Those instruments shall have adequate facilities for the affixing of...Previous MatchNext Match

        4. 1.3.Where a data plate is used it shall be possible...Previous MatchNext Match

        5. 1.4.The inscriptions Max, Min, e, and d, shall also be...Previous MatchNext Match

        6. 1.5.Each load measuring device which is connected or can be...Previous MatchNext Match

        7. 2.Instruments not intended to be used for the applications listed...Previous MatchNext Match

        8. 3.Restrictive use symbol referred to in regulation 9(3). The restrictive...Previous MatchNext Match

    10. SCHEDULE 9Previous MatchNext Match

      DECLARATION OF CONFORMITY (No XXXX) Previous MatchNext Match

      1. 1.Instrument model/Instrument (product, type, batch or serial number): Previous MatchNext Match

      2. 2.Name and address of the manufacturer and, where applicable, his...Previous MatchNext Match

      3. 3.This declaration of conformity is issued under the sole responsibility...Previous MatchNext Match

      4. 4.Object of the declaration (identification of instrument allowing traceability; it...Previous MatchNext Match

      5. 5.The object of the declaration described above is in conformity...Previous MatchNext Match

      6. 6.References to the relevant designated standards used or references to...Previous MatchNext Match

      7. 7.The approved body … (name, number) performed … (description of...Previous MatchNext Match

      8. 8.Additional information: — Signed for and on behalf of: —...Previous MatchNext Match

  13. Explanatory NotePrevious Match

Yn ôl i’r brig

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Mae deddfwriaeth ar gael mewn fersiynau gwahanol:

Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.

Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.

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Dewisiadau Agor

Dewisiadau gwahanol i agor deddfwriaeth er mwyn gweld rhagor o gynnwys ar y sgrin ar yr un pryd

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Memorandwm Esboniadol

Mae Memoranda Esboniadol yn nodi datganiad byr o ddiben Offeryn Statudol ac yn rhoi gwybodaeth am ei amcan polisi a goblygiadau polisi. Maent yn ceisio gwneud yr Offeryn Statudol yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol, ac maent yn cyd-fynd ag unrhyw Offeryn Statudol neu Offeryn Statudol Drafft a gyflwynwyd ger bron y Senedd o Fehefin 2004 ymlaen.

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Rhagor o Adnoddau

Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:

  • y PDF print gwreiddiol y fel deddfwyd fersiwn a ddefnyddiwyd am y copi print
  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • slipiau cywiro
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill
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Asesiadau Effaith

Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:

  • Why the government is proposing to intervene;
  • The main options the government is considering, and which one is preferred;
  • How and to what extent new policies may impact on them; and,
  • The estimated costs and benefits of proposed measures.
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Llinell Amser Newidiadau

This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.

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Rhagor o Adnoddau

Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:

  • y PDF print gwreiddiol y fel gwnaed fersiwn a ddefnyddiwyd am y copi print
  • slipiau cywiro

liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys

  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill
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