- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/01/2013)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Directive 2009/23/EC of the European Parliament and of the Council of 23 April 2009 on non-automatic weighing instruments (Codified version) (Text with EEA relevance) (repealed)
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THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION,
Having regard to the Treaty establishing the European Community, and in particular Article 95 thereof,
Having regard to the proposal from the Commission,
Having regard to the opinion of the European Economic and Social Committee(1),
Acting in accordance with the procedure laid down in Article 251 of the Treaty(2),
Whereas:
(1) Council Directive 90/384/EEC of 20 June 1990 on the harmonisation of the laws of the Member States relating to non-automatic weighing instruments(3) has been substantially amended(4). In the interests of clarity and rationality the said Directive should be codified.
(2) Member States have the responsibility of protecting the public against incorrect results of weighing operations by means of non-automatic weighing instruments when used for certain categories of applications.
(3) In each Member State, mandatory provisions fix in particular the necessary performance requirements of non-automatic weighing instruments by specifying metrological and technical requirements, together with inspection procedures before and after going into service. These mandatory provisions do not necessarily lead to different levels of protection from one Member State to another but do, by their disparity, impede trade within the Community.
(4) This Directive should set out mandatory and essential requirements as regards metrology and performance in relation to non-automatic weighing instruments. To facilitate proof of conformity with the essential requirements, it is necessary to have harmonised standards at European level, in particular as to the metrological, design and construction characteristics, so that instruments complying with those harmonised standards may be assumed to conform to the essential requirements. These standards, harmonised at European level, are drawn up by private bodies and must remain non-mandatory texts. For that purpose the European Committee for Standardisation (CEN), the European Committee for Electrotechnical Standardisation (Cenelec) and the European Telecommunications Standards Institute (ETSI) are recognised as the competent bodies for the adoption of harmonised standards in accordance with the general guidelines(5) for cooperation between the Commission, the European Free Trade Association (EFTA) and those three bodies, signed on 28 March 2003.
(5) A series of Directives designed to remove technical barriers to trade in accordance with the principles established in the Council Resolution of 7 May 1985 on a new approach to technical harmonisation and standards(6) has been adopted; each of those Directives provides for the affixing of the ‘CE’ conformity marking. In its communication of 15 June 1989(7) on a global approach to certification and testing, the Commission proposed that common rules be drawn up concerning a ‘CE’ conformity marking with a single design. In its Resolution of 21 December 1989 on a global approach to conformity assessment(8), the Council approved as a guiding principle the adoption of a consistent approach such as this with regard to the use of the ‘CE’ conformity marking. The two basic elements of the new approach which should be applied are the essential requirements and the conformity assessment procedures.
(6) Assessment of conformity with the relevant metrological and technical provisions is necessary to provide effective protection for users and third parties. The existing conformity assessment procedures differ from one Member State to another. To avoid multiple assessments of conformity, which are in effect barriers to the free movement of the instruments, arrangements should be made for the mutual recognition of conformity assessment procedures by the Member States. To facilitate the mutual recognition of conformity assessment procedures, Community procedures should be set up, together with criteria for the designation of the bodies responsible for carrying out tasks pertaining to the conformity assessment procedures.
(7) It is therefore essential to ensure that such designated bodies ensure a high level of quality throughout the Community.
(8) The presence on a non-automatic weighing instrument of the ‘CE’ conformity marking or of the sticker bearing the letter ‘M’ should indicate that there is a presumption that it satisfies the provisions of this Directive and therefore make it unnecessary to repeat the assessments of conformity already carried out.
(9) This Directive should be without prejudice to the obligations of the Member States relating to the time limits for transposition into national law and application of the Directives set out in Annex VII, Part B,
HAVE ADOPTED THIS DIRECTIVE:
1.This Directive shall apply to all non-automatic weighing instruments.
2.For the purposes of this Directive, the following categories of use of non-automatic weighing instruments shall be distinguished:
determination of mass for commercial transactions;
determination of mass for the calculation of a toll, tariff, tax, bonus, penalty, remuneration, indemnity or similar type of payment;
determination of mass for the application of laws or regulations or for an expert opinion given in court proceedings;
determination of mass in the practice of medicine for weighing patients for the purposes of monitoring, diagnosis and medical treatment;
determination of mass for making up medicines on prescription in a pharmacy and determination of mass in analyses carried out in medical and pharmaceutical laboratories;
determination of price on the basis of mass for the purposes of direct sales to the public and the making-up of prepackages;
(b)all applications other than those listed in point (a).
For the purposes of this Directive, the following definitions shall apply:
:
a measuring instrument serving to determine the mass of a body by using the action of gravity on that body. A weighing instrument may also serve to determine other mass-related magnitudes, quantities, parameters or characteristics;
:
a weighing instrument requiring the intervention of an operator during weighing;
:
a technical specification (European standard or harmonised document) adopted by the European Committee for Standardisation (CEN), the European Committee for Electrotechnical Standardisation (Cenelec), or the European Telecommunications Standards Institute (ETSI), or by two or three of those bodies, upon a remit from the Commission in accordance with Directive 98/34/EC of the European Parliament and of the Council of 22 June 1998 laying down a procedure for the provision of information in the field of technical standards and regulations(9) and the general guidelines for cooperation between the Commission, the European Free Trade Association (EFTA) and those three bodies, signed on 28 March 2003.
1.Member States shall take all steps to ensure that only instruments that meet the requirements of this Directive may be placed on the market.
2.Member States shall take all steps to ensure that instruments may not be brought into service for the uses referred to in point (a) of Article 1(2) unless they meet the requirements of this Directive and accordingly bear the ‘CE’ conformity marking provided for in Article 11.
Instruments used for the applications listed in point (a) of Article 1(2) must satisfy the essential requirements set out in Annex I.
In cases where the instrument includes, or is connected to, devices which are not used for the applications listed in point (a) of Article 1(2), such devices shall not be subject to those essential requirements.
1.Member States shall not impede the placing on the market of instruments which meet the requirements of this Directive.
2.Member States shall not impede the putting into service, for the uses referred to in point (a) of Article 1(2), of instruments which meet the requirements of this Directive.
1.Member States shall presume conformity with the essential requirements set out in Annex I in respect of instruments which comply with the relevant national standards implementing the harmonised standards that meet those requirements.
2.The Commission shall publish the references of the harmonised standards referred to in paragraph 1 in the Official Journal of the European Union.
Member States shall publish the references of the national standards referred to in paragraph 1.
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Textual Amendments
F1 Deleted by Regulation (EU) No 1025/2012 of the European Parliament and of the Council of 25 October 2012 on European standardisation, amending Council Directives 89/686/EEC and 93/15/EEC and Directives 94/9/EC, 94/25/EC, 95/16/EC, 97/23/EC, 98/34/EC, 2004/22/EC, 2007/23/EC, 2009/23/EC and 2009/105/EC of the European Parliament and of the Council and repealing Council Decision 87/95/EEC and Decision No 1673/2006/EC of the European Parliament and of the Council (Text with EEA relevance).
1.Where a Member State considers that instruments bearing the ‘CE’ conformity marking referred to in Annex II, points 2, 3 and 4, do not meet the requirements of this Directive when properly installed and used for the purposes for which they are intended, it shall take all appropriate measures to withdraw those instruments from the market or to prohibit or restrict their being put into service and/or placed on the market.
The Member State concerned shall immediately inform the Commission of any such measure, indicating the reasons for its decision, and in particular whether non-compliance is due to:
(a)failure to meet the essential requirements set out in Annex I, where instruments do not meet the harmonised standards referred to in Article 6(1);
(b)incorrect application of the harmonised standards referred to in Article 6(1);
(c)shortcomings in the harmonised standards referred to in Article 6(1) themselves.
2.The Commission shall enter into consultation with the parties concerned as soon as possible.
After such consultation the Commission shall immediately inform the Member State which took the action of the result. Should it find that the measure is justified it shall immediately inform the other Member States.
If the decision is attributed to shortcomings in the standards, the Commission, after consulting the parties concerned, shall bring the matter before the Committee within two months if the Member State which has taken the measures intends to maintain them, and shall subsequently initiate the procedures referred to in Article 7.
3.Where an instrument which does not comply bears the ‘CE’ conformity marking, the competent Member State shall take appropriate action against whomsoever has affixed the marking and shall inform the Commission and the other Member States thereof.
4.The Commission shall ensure that the Member States are kept informed of the progress and outcome of this procedure.
1.The conformity of instruments to the essential requirements set out in Annex I may be certified by either of the following procedures as selected by the applicant:
(a)EC type examination as referred to in Annex II, point 1, followed either by the EC declaration of type conformity (guarantee of production quality) as referred to in Annex II, point 2, or by the EC verification as referred to in Annex II, point 3.
However, EC type examination shall not be compulsory for instruments which do not use electronic devices and the load-measuring device of which does not use a spring to balance the load;
(b)EC unit verification as referred to in Annex II, point 4.
2.The documents and correspondence relating to the procedures referred to in paragraph 1 shall be drafted in an official language of the Member State where the said procedures are carried out, or in a language accepted by the body notified in accordance with Article 10(1).
3.Where the instruments are subject to other Directives covering other aspects and which also provide for the affixing of the ‘CE’ conformity marking, that marking shall indicate that the instruments in question are also presumed to conform to the provisions of those other Directives.
However, where one or more of the Directives which apply to the instruments allow the manufacturer, during a transitional period, to choose which arrangements to apply, the ‘CE’ conformity marking shall indicate conformity only to the Directives applied by the manufacturer. In this case, particulars of publication in the Official Journal of the European Union of the Directives applied must be given in the documents, notices or instructions required by the Directives and accompanying such instruments.
1.Member States shall notify the Commission and the other Member States of the bodies which they have appointed to carry out the procedures referred to in Article 9 together with the specific tasks which these bodies have been appointed to carry out and the identification numbers assigned to them beforehand by the Commission.
The Commission shall publish in the Official Journal of the European Union a list of the notified bodies and their identification numbers and the tasks for which they have been notified. The Commission shall ensure that this list is kept up to date.
2.Member States shall apply the minimum criteria set out in Annex V for the designation of bodies. Bodies which satisfy the criteria fixed by the relevant harmonised standards shall be presumed to satisfy the criteria set out in that Annex.
3.A Member State which has designated a body shall cancel the designation if the body no longer meets the criteria for designation referred to in paragraph 2. It shall immediately inform the other Member States and the Commission thereof and withdraw the notification.
1.The ‘CE’ conformity marking and the required supplementary data as described in Annex IV, point 1, shall be affixed in a clearly visible, easily legible and indelible form to instruments for which EC conformity has been established.
2.The inscriptions referred to in Annex IV, point 2, shall be affixed in a clearly visible, easily legible and indelible form to all other instruments.
3.The affixing on the instruments of markings which are likely to deceive third parties as to the meaning and form of the ‘CE’ conformity marking shall be prohibited. Any other marking may be affixed to the instruments provided that the visibility and legibility of the ‘CE’ conformity marking is not thereby reduced.
Without prejudice to Article 8:
where a Member State establishes that the ‘CE’ conformity marking has been affixed unduly, the manufacturer or his authorised representative established within the Community shall be obliged to make the instrument conform as regards the provisions concerning the ‘CE’ conformity marking and to end the infringement under the conditions imposed by the Member State;
where non-conformity continues, the Member State must take all appropriate measures to restrict or prohibit the placing on the market of the instrument in question or to ensure that it is withdrawn from the market in accordance with the procedures laid down in Article 8.
Where an instrument which is used for any of the applications referred to in point (a) of Article 1(2) includes, or is connected to, devices that have not been subject to conformity assessment as referred to in Article 9, each of those devices shall bear the symbol restricting its use as defined by Annex IV, point 3. That symbol shall be affixed to the devices in a clearly visible and indelible form.
Member States shall take all steps to ensure that instruments bearing the ‘CE’ conformity marking attesting conformity with the requirements of this Directive continue to conform to those requirements.
Any decision taken pursuant to this Directive and resulting in restrictions on the putting into service of an instrument shall state the exact grounds on which it is based.
Such a decision shall be notified without delay to the party concerned, who shall at the same time be informed of the judicial remedies available to him under the laws in force in the Member State in question and of the time limits to which such remedies are subject.
Member States shall communicate to the Commission the texts of the main provisions of internal law which they adopt in the field covered by this Directive.
Directive 90/384/EEC, as amended by the Directive listed in Annex VII, Part A, is repealed, without prejudice to the obligations of the Member States relating to the time limits for transposition into national law and application of the Directives set out in Annex VII, Part B.
References to the repealed Directive shall be construed as references to this Directive and shall be read in accordance with the correlation table in Annex VIII.
This Directive shall enter into force on the twentieth day following its publication in the Official Journal of the European Union.
This Directive is addressed to the Member States.
The terminology used is that of the International Organisation of Legal Metrology.
Where an instrument includes, or is connected to, more than one indicating or printing device used for the applications listed in point (a) of Article 1(2), those devices which repeat the results of the weighing operation and which cannot influence the correct functioning of the instrument shall not be subject to the essential requirements if the weighing results are printed or recorded correctly and indelibly by a part of the instrument which meets the essential requirements and the results are accessible to both parties concerned by the measurement. However, in the case of instruments used for direct sales to the public, display and printing devices for the vendor and the customer must fulfil the essential requirements.
The units of mass used shall be the legal units within the meaning of Council Directive 80/181/EEC of 20 December 1979 on the approximation of the laws of the Member States relating to units of measurement(10).
Subject to compliance with this condition, the following units are permitted:
SI units: kilogram, microgram, milligram, gram, tonne,
imperial unit: troy ounce, if weighing precious metals,
other non-SI unit: metric carat, if weighing precious stones.
For instruments that make use of the imperial unit of mass referred to above, the relevant essential requirements specified below shall be converted to that unit, using simple interpolation.
special
high
medium
ordinary
The specifications of these classes are given in Table 1.
Accuracy classes
The minimum capacity is reduced to 5 e for instruments in classes II and III for determining a conveying tariff.
1 × 10k, 2 × 10k, or 5 × 10k mass units,
k being any integer or zero.
d = e.
e = 1 × 10k g,
d < e ≤ 10 d,
except for instruments of class I with d < 10–4 g, for which e = 10–3 g.
Instruments equipped with an auxiliary indicating device shall belong to class I or class II. For these instruments the minimum capacity lower limits for these two classes are obtained from Table 1 by replacement in column 3 of the verification scale interval (e) by the actual scale interval (d).
If d < 10–4 g, the maximum capacity of class I may be less than 50 000 e.
Multiple weighing ranges are permitted, provided they are clearly indicated on the instrument. Each individual weighing range is classified according to point 3.1. If the weighing ranges fall into different accuracy classes the instrument shall comply with the severest of the requirements that apply for the accuracy classes in which the weighing ranges fall.
Multi-interval instruments shall not be equipped with an auxiliary indicating device.
where:
=
1, 2, … r,
=
partial weighing range number,
=
the total number of partial weighing ranges.
All capacities are capacities of net load, irrespective of the value of any tare used.
Multi-interval instruments
i = 1, 2, … r i = partial weighing range number r = total number of partial weighing ranges | |||||
a For i = r, the corresponding column of Table 1 applies, with e replaced by er. | |||||
Class | Verification scale interval (e) | Minimum capacity (Min) | Number of verification scale intervals | ||
---|---|---|---|---|---|
Minimum value | Minimum valuea | Maximum value | |||
I | 0,001 | g ≤ ei | 100 e1 | 50 000 | — |
II | 0,001 | g ≤ ei ≤ 0,05 g | 20 e1 | 5 000 | 100 000 |
0,1 | g ≤ ei | 50 e1 | 5 000 | 100 000 | |
III | 0,1 | g ≤ ei | 20 e1 | 500 | 10 000 |
IIII | 5 | g ≤ ei | 10 e1 | 50 | 1 000 |
The maximum permissible errors apply to the net value and tare value for all possible loads, excluding preset tare values.
Maximum permissible errors
Load | Maximum permissible error | |||
---|---|---|---|---|
Class I | Class II | Class III | Class IIII | |
0 ≤ m ≤ 50 000 e | 0 ≤ m ≤ 5 000 e | 0 ≤ m ≤ 500 e | 0 ≤ m ≤ 50 e | ± 0,5 e |
50 000 e < m ≤ 200 000 e | 5 000 e < m ≤ 20 000 e | 500 e < m ≤ 2 000 e | 50 e < m ≤ 200 e | ± 1,0 e |
200 000 e < m | 20 000 e < m ≤ 100 000 e | 2 000 e < m ≤ 10 000 e | 200 e < m ≤ 1 000 e | ± 1,5 e |
The weighing results shall be sufficiently insensitive to changes in the position of the load on the load receptor.
5 °C for an instrument in class I,
15 °C for an instrument in class II,
30 °C for an instrument in class III or IIII.
In the absence of a manufacturer’s specification, the temperature range of – 10 °C to + 40 °C applies.
Instruments operated from battery power shall indicate whenever the voltage drops below the minimum required value and shall under those circumstances either continue to function correctly or be automatically put out of service.
Upon automatic detection of a significant fault, electronic instruments shall provide a visual or audible alarm that shall continue until the user takes corrective action or the fault disappears.
Digital electronic devices shall always exercise adequate control of the correct operation of the measuring process, of the indicating device, and of all data storage and data transfer.
Upon automatic detection of a significant durability error, electronic instruments shall provide a visual or audible alarm that shall continue until the user takes corrective action or the error disappears.
The indication of the weighing results and other weight values shall be accurate, unambiguous and non-misleading and the indicating device shall permit easy reading of the indication under normal conditions of use.
The names and symbols of the units referred to in point 1 of this Annex shall comply with the provisions of Directive 80/181/EEC with the addition of the symbol for the metric carat which shall be the symbol ‘ct’.
Indication shall be impossible above the maximum capacity (Max), increased by 9 e.
An auxiliary indicating device is permitted only to the right of the decimal mark. An extended indicating device may be used only temporarily, and printing shall be inhibited during its functioning.
Secondary indications may be shown, provided that they cannot be mistaken for primary indications.
Printed results shall be correct, suitably identified and unambiguous. The printing shall be clear, legible, non-erasable and durable.
When appropriate, instruments shall be fitted with a levelling device and a level indicator, sufficiently sensitive to allow proper installation.
Instruments may be equipped with zeroing devices. The operation of these devices shall result in accurate zeroing and shall not cause incorrect measuring results.
The instruments may have one or more tare devices and a preset tare device. The operation of the tare devices shall result in accurate zeroing and shall ensure correct net weighing. The operation of the preset tare device shall ensure correct determination of the calculated net value.
Instruments for direct sale to the public shall show all essential information about the weighing operation and, in the case of price-indicating instruments, shall clearly show the customer the price calculation of the product to be purchased.
The price to pay, if indicated, shall be accurate.
Price-computing instruments shall display the essential indications long enough for the customer to read them properly.
Price-computing instruments may perform functions other than per-article weighing and price computation only if all indications related to all transactions are printed clearly and unambiguously and are conveniently arranged on a ticket or label for the customer.
Instruments shall bear no characteristics that can cause, directly or indirectly, indications the interpretation of which is not easy or straightforward.
Instruments shall safeguard customers against incorrect sales transactions due to their malfunctioning.
Auxiliary indicating devices and extended indicating devices are not permitted.
Supplementary devices are permitted only if they cannot lead to fraudulent use.
Instruments similar to those normally used for direct sales to the public which do not satisfy the requirements of this Section must carry near to the display the indelible marking ‘Not to be used for direct sale to the public’.
Price labelling instruments shall meet the requirements of price indicating instruments for direct sale to the public, as far as applicable to the instrument in question. The printing of a price label shall be impossible below a minimum capacity.
The application shall include:
the name and address of the manufacturer and, if the application is lodged by the authorised representative, his name and address in addition,
a written declaration that the application has not been lodged with any other notified body,
the design documentation, as described in Annex III.
The applicant shall place at the disposal of the notified body an instrument, representative of the production envisaged, hereinafter the ‘type’.
The certificate shall have a validity period of 10 years from the date of its issue, and may be renewed for subsequent periods of 10 years each.
In the event of fundamental changes to the design of the instrument, e.g. as a result of the application of new techniques, the validity of the certificate may be limited to two years and extended by three years.
applications received for EC type-examination,
EC type-approval certificates issued,
applications for type-certificates refused,
additions and amendments relating to documents already issued.
Each notified body shall moreover inform all the Member States forthwith of withdrawals of EC type-approval certificates.
Each Member State shall make this information available to the bodies which it has notified.
Modifications to the approved type must receive additional approval from the notified body that issued the EC type-approval certificate where such changes influence conformity with the essential requirements of this Directive or the prescribed conditions for use of the instrument. This additional approval is given in the form of an addition to the original EC type-approval certificate.
The manufacturer or his authorised representative established within the Community shall affix the ‘CE’ conformity marking to each instrument and the inscriptions provided for in Annex IV and shall draw up a written declaration of conformity.
The ‘CE’ conformity marking shall be accompanied by the identification number of the notified body responsible for the EC surveillance referred to in point 2.4.
The application shall include:
an undertaking to carry out the obligations arising from the approved quality system,
an undertaking to maintain the approved quality system to ensure its continuing suitability and effectiveness.
The manufacturer shall make available to the notified body all relevant information, in particular the quality system’s documentation and the design documentation of the instrument.
All the elements, requirements and provisions adopted by the manufacturer shall be documented in a systematic and orderly manner in the form of written rules, procedures and instructions. This quality system documentation shall ensure a proper understanding of the quality programmes, plans, manuals and records.
It shall contain in particular an adequate description of:
the quality objectives and the organisational structure, responsibilities and powers of the management with regard to product quality,
the manufacturing process, the quality control and assurance techniques and the systematic measures that will be used,
the examinations and tests that will be carried out before, during and after manufacture, and the frequency with which they will be carried out,
the means to monitor the achievement of the required product quality and the effective operation of the quality system.
It shall notify its decision to the manufacturer and inform the other notified bodies thereof. The notification to the manufacturer shall contain the conclusions of the examination and, in the event of refusal, the justification for the decision.
the quality system documentation,
the design documentation,
the quality records, e.g. the inspection reports and tests and calibration data, reports on the qualifications of the personnel concerned, etc.
The notified body shall periodically carry out audits in order to ensure that the manufacturer is maintaining and applying the quality system; it shall provide the manufacturer with an audit report.
In addition, the notified body may carry out unscheduled visits to the manufacturer. During such visits, the notified body may carry out full or partial audits. It shall provide the manufacturer with a report on the visit, and, where appropriate, an audit report.
The notified body shall affix, or cause to be affixed, its identification number to the instrument the conformity of which to requirements has been established, and shall draw up a written certificate of conformity concerning the tests carried out.
The party which carries out the second stage of the procedure shall carry out those examinations and tests that have not yet been carried out.
The manufacturer or his authorised representative shall ensure that he is able to supply the notified body’s certificates of conformity on request.
The technical documentation must render the design, manufacture and operation of the product intelligible and enable an assessment to be made of its conformity with the requirements of this Directive.
The documentation shall include in so far as relevant for assessment:
a general description of the type,
conceptual designs and manufacturing drawings and plans of components, sub-assemblies, circuits, etc.,
descriptions and explanations necessary for the understanding of the above, including the operation of the instrument,
a list of the harmonised standards referred to in Article 6(1), applied in full or in part, and descriptions of the solutions adopted to meet the essential requirements where the harmonised standards referred to in Article 6(1) have not been applied,
results of design calculations made and of examinations, etc.,
test reports,
the EC type-approval certificates and the results of relevant tests on instruments containing parts identical to those in the design.
the ‘CE’ conformity marking comprising the ‘CE’ symbol as described in Annex VI,
the identification number(s) of the notified body/bodies that has/have carried out the EC surveillance or the EC verification.
The abovementioned marking and inscriptions shall be affixed to the instrument and distinctly grouped together;
a green sticker at least 12,5 mm × 12,5 mm square bearing a capital letter ‘M’ printed in black;
the following inscriptions:
the number of the EC type-approval certificate, where appropriate,
the manufacturer’s mark or name,
the accuracy class, enclosed in an oval or in two horizontal lines joined by two half circles,
maximum capacity, in the form Max …,
minimum capacity, in the form Min …,
verification scale interval, in the form e = …,
the last two digits of the year in which the ‘CE’ conformity marking was affixed,
plus, when applicable:
serial number,
for instruments consisting of separate but associated units: identification mark on each unit,
scale interval if it is different from e, in the form d = …,
maximum additive tare effect, in the form T = + …,
maximum subtractive tare effect if it is different from Max, in the form T = – …,
tare interval if it is different from d, in the form dT = …,
maximum safe load if it is different from Max, in the form Lim …,
the special temperature limits, in the form … °C/… °C,
ratio between load receptor and load.
The other instruments must bear:
the manufacturer’s mark or name,
maximum capacity, in the form Max ….
Those instruments may not bear the stickers provided for in point 1.1(b).
That symbol shall be constituted by a capital letter ‘M’ printed in black on a red background at least 25 mm × 25 mm square with two intersecting diagonals forming a cross.
The fulfilment of the conditions under points 1 and 2 shall be periodically verified by the Member States.
The ‘CE’ conformity marking shall consist of the initials ‘CE’ taking the following form:
If the ‘CE’ conformity marking is reduced or enlarged the proportions given in the above graduated drawing must be respected.
The various components of the ‘CE’ conformity marking must have substantially the same vertical dimension, which may not be less than 5 mm.
(referred to in Article 17)
Council Directive 90/384/EEC | |
Council Directive 93/68/EEC | Article 1, point 7, and Article 8 only |
(referred to in Article 17)
a In accordance with Article 15(3) of Directive 90/384/EEC Member States shall permit, during a period of 10 years from the date on which they apply the laws, regulations and administrative provisions adopted by the Member States in order to transpose that Directive into national law, the placing on the market and/or putting into service of instruments which conform to the rules in force before 1 January 1993. | ||
b In accordance with Article 14(2) of Directive 93/68/EEC: ‘Until 1 January 1997, Member States shall allow the placing on the market and the bringing into service of products which comply with the marking arrangements in force before 1 January 1995’. | ||
Directive | Time limit for transposition | Date of application |
---|---|---|
90/384/EEC | 30 June 1992 | 1 January 1993a |
93/68/EEC | 30 June 1994 | 1 January 1995b |
Directive 90/384/EEC | This Directive |
---|---|
Recital 5, last sentence | Article 2, point (3) |
Article 1(1), first subparagraph | Article 2, point (1) |
Article 1(1), second subparagraph | Article 2, point (2) |
Article 1(1), third subparagraph | Article 1(1) |
Article 1(2), introductory wording | Article 1(2), introductory wording |
Article 1(2), point (a)(1) | Article 1(2), point (a)(i) |
Article 1(2), point (a)(2) | Article 1(2), point (a)(ii) |
Article 1(2), point (a)(3) | Article 1(2), point (a)(iii) |
Article 1(2), point (a)(4) | Article 1(2), point (a)(iv) |
Article 1(2), point (a)(5) | Article 1(2), point (a)(v) |
Article 1(2), point (a)(6) | Article 1(2), point (a)(vi) |
Article 1(2), point (b) | Article 1(2), point (b) |
Article 2 | Article 3 |
Article 3 | Article 4 |
Article 4 | Article 5 |
Article 5 | Article 6 |
Article 6, first paragraph, first sentence | Article 7, first paragraph |
Article 6, first paragraph, second sentence | Article 7, second paragraph |
Article 6, second paragraph | Article 7, third paragraph |
Article 7 | Article 8 |
Article 8(1) and (2) | Article 9(1) and (2) |
Article 8(3), point (a) | Article 9(3), first subparagraph |
Article 8(3), point (b) | Article 9(3), second subparagraph |
Article 9 | Article 10 |
Article 10 | Article 11 |
Article 11 | Article 12 |
Article 12 | Article 13 |
Article 13 | Article 14 |
Article 14, first sentence | Article 15, first paragraph |
Article 14, second sentence | Article 15, second paragraph |
Article 15(1) to (3) | — |
Article 15(4) | Article 16 |
Article 15(5) | — |
— | Article 17 |
— | Article 18 |
Article 16 | Article 19 |
Annexes I to VI | Annexes I to VI |
— | Annex VII |
— | Annex VIII |
Opinion of the European Parliament of 11 December 2007 (OJ C 323 E, 18.12.2008, p. 57) and Council Decision of 23 March 2009.
See Annex VII, Part A.
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