S.I. No. 407/2008 - European Communities (Machinery) Regulations 2008

Type Statutory Instrument
Publication 2008-10-24
Last updated 2016-01-05
State In force superseded text
Text As published
articles 51

This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.

4 amending acts · 2016-01-05, S.I. No. 621/2015 - European Communities (Machinery) (Amendment) Regulations 2015

Reform history JSON API

ARRANGEMENT OF REGULATIONS

PART 1 Citation, Commencement and Interpretation

1.

1.

Citation.

2.

2.

Commencement.

3.

3.

Interpretation and application.

PART 2 Requirements for placing on the market and putting into service

4.

4.

General duties of manufacturer or authorised representative as regards products.

5.

5.

Duties of manufacturer or authorised representative as regards compliance with Regulation 10 relating to partly completed machinery.

6.

6.

Duties of manufacturer or authorised representative as regards compliance with Regulation 9 relating to essential health and safety requirements.

7.

7.

Duties of manufacturer or authorised representative as regards compliance with other Directives.

8.

8.

Duties of persons showing products at trade fairs etc.

9.

9.

Duties of manufacturer or authorised representative as regards certifying the conformity of products.

10.

10.

Duties of manufacturer or authorised representative as regards relevant technical documentation, assembly instructions and declaration of incorporation relating to partly completed machinery.

11.

11.

Duties of manufacturer or authorised representative as regards application of CE marking as regards products.

12.

12.

CE marking and declaration of conformity.

13.

13.

Products manufactured in conformity with a harmonised standard.

PART 3 Notified Bodies

14.

14.

Appointment of notified bodies and their duties.

15.

15.

Provision of information to the Commission, other Member States and the public on notified bodies.

16.

16.

Monitoring of notified bodies.

17.

17.

Suspension or withdrawal of certificates or approvals by notified bodies.

18.

18.

Provision of information by notified bodies to relevant competent authority.

PART 4 Competent Authorities

19.

19.

Competent authorities.

20.

20.

Functions of competent authorities.

21.

21.

Immunity.

22.

22.

Indemnification.

23.

23.

Restriction or prohibition.

24.

24.

Directions regarding CE marking affixed unduly to products.

25.

25.

Notifications to the Commission in respect of application of Regulations 23 and 24.

26.

26.

Publication of information on products non-compliant with essential health and safety requirements.

27.

27.

Publication of information on action taken regarding non-compliant products.

28.

28.

Sharing of information on application of the Directive.

29.

29.

Power to require information.

30.

30.

Provision of information in response to a notice requiring information.

31.

31.

Appeal against a notice requiring information.

32.

32.

Suspension of application of a notice requiring information.

33.

33.

Admissibility of certain documents in evidence.

PART 5 Authorised Officers

34.

34.

Appointment of authorised officers.

35.

35.

Warrants or certificates of appointment.

36.

36.

Powers of authorised officers.

PART 6 Improvement plans, contravention notices and prohibition notices

37.

37.

Directions for improvement plan.

38.

38.

Contravention notice.

39.

39.

Prohibition notice.

40.

40.

Contravention of prohibition notice — application to High Court.

41.

41.

Publication of information relating to contravention notices and prohibition notices.

PART 7 Supplemental Provisions

42.

42.

Restrictions on the disclosure of information.

43.

43.

Service of notices etc.

PART 8 Offences and Penalties

44.

44.

Offences.

45.

45.

Penalties.

46.

46.

Offences by bodies corporate.

47.

47.

Defence in proceedings.

48.

48.

Prosecution of offences.

PART 9 Miscellaneous

49.

49.

Appeal to Circuit Court from certain orders of District Court.

50.

50.

Notice or direction to be in writing.

51.

51.

Revocation.

SCHEDULE 1 Annex I to Directive 2006/42/EC — Essential health and safety requirements relating to the design and construction of machinery.

SCHEDULE 2 Annex II to Directive 2006/42/EC — Declarations (EC Declaration of conformity of machinery and Declaration of incorporation of partly completed machinery).

SCHEDULE 3 Annex III to Directive 2006/42/EC — CE marking.

SCHEDULE 4 Annex IV to Directive 2006/42/EC — Categories of machinery to which one of the procedures referred to in Article 12(3) and (4) must be applied.

SCHEDULE 5 Annex V to Directive 2006/42/EC — Indicative list of the safety components referred to in Article 2(c).

SCHEDULE 6 Annex VI to Directive 2006/42/EC — Assembly instructions for partly completed machinery.

SCHEDULE 7 Annex VII to Directive 2006/42/EC — Part A, Technical file for machinery and Part B, Relevant technical documentation for partly completed machinery.

SCHEDULE 8 Annex VIII to Directive 2006/42/EC — Assessment of conformity with internal checks on the manufacture of machinery.

SCHEDULE 9 Annex IX to Directive 2006/42/EC — EC type-examination.

SCHEDULE 10 Annex X to Directive 2006/42/EC — Full quality assurance.

SCHEDULE 11 Annex XI to Directive 2006/42/EC — Minimum criteria to be taken into account by Member States for the notification of bodies.

SCHEDULE 12 Article 1(2) of Directive 2006/42/EC — Equipment excluded from application of these Regulations.

S.I. No. 407 of 2008

EUROPEAN COMMUNITIES (MACHINERY) REGULATIONS 2008

Notice of the making of this Statutory Instrument was published in

“Iris Oifigiúil” of 24th October, 2008.

I, MARY COUGHLAN, Minister for Enterprise, Trade and Employment, in exercise of the powers conferred on me by section 3 of the European Communities Act 1972 (No. 27 of 1972), and for the purpose of giving effect to Directive 2006/42/EC of the European Parliament and of the Council 1 on machinery, and amending Directive 95/16/EC (recast), hereby make the following regulations:

PART 1 Citation, Commencement and Interpretation

Citation

1.

These Regulations may be cited as the European Communities (Machinery) Regulations 2008.

Commencement

2.

(1) Subject to paragraph (2), these Regulations come into operation on 29 December 2009.

Interpretation and application

3.

(1) In these Regulations, subject to paragraph (3), and unless the context otherwise requires—

“Annex” means an Annex to the Directive;

“Article” means an Article of the Directive;

“authorised representative” means any natural or legal person established in the Community who has received a written mandate from a manufacturer to perform on his or her behalf all or part of the obligations and formalities connected with the Directive and these Regulations;

“Authority” means the Health and Safety Authority;

“CE marking” means the conformity marking referred to in Article 16 and in Regulation 11, details and requirements in respect of which are set out in Annex III, the text of which Annex (including the illustration of the mark) is, for ease of reference, set out in Schedule 3;

“chains, ropes and webbing” means chains, ropes and webbing designed and constructed for lifting purposes as part of lifting machinery or lifting accessories;

“Commission” means the Commission of the European Communities;

“Community” means the European Community;

“competent authority” means, as the context requires, one or other of the bodies specified in Regulation 19;

“declaration of conformity” means the EC declaration of conformity, appropriate to the product in question, referred to in Article 5, and details and requirements in respect of which are set out in part 1, Section A of Annex II, the text of which Annex is, for ease of reference, set out in Schedule 2;

“Directive” means Directive 2006/42/EC of the European Parliament and of the Council of 17 May 2006 1 on machinery, and amending Directive 95/16/EC (recast);

“EC type-examination certificate” means the certificate referred to in paragraph 4 of Annex IX, the text of which Annex is, for ease of reference, set out in Schedule 9;

“essential health and safety requirements” means the essential health and safety requirements of the Directive, relating to the design and construction of a product, set out in Annex I, the text of which Annex is, for ease of reference, set out in Schedule 1;

“harmonised standard” means a non-binding technical specification adopted by a standardisation body, namely the European Committee for Standardisation (CEN), the European Committee for Electrotechnical Standardisation (CENELEC) or the European Telecommunications Standards Institute (ETSI), on the basis of a remit issued by the Commission in accordance with the procedures laid down in Directive 98/34/EC of the European Parliament and of the Council of 22 June 1998 2 laying down a procedure for the provision of information in the field of technical standards and regulations and of rules on Information Society services, as last amended by the 2003 Act of Accession;

“interchangeable equipment” means a device which, after the putting into service of machinery or of a tractor, is assembled with that machinery or tractor by the operator himself or herself in order to change its function or attribute a new function, in so far as this equipment is not a tool;

“lifting accessory” means a component or equipment not attached to the lifting machinery, allowing the load to be held, which is placed between the lifting machinery and the load or on the load itself, or which is intended to constitute an integral part of the load and which is independently placed on the market; slings and their components are also regarded as lifting accessories;

“machinery” (save in the Schedules) means machinery to which the Directive applies, being any or all of the following:

“manufacturer” means any natural or legal person who designs or manufactures a product or partly completed machinery and is responsible for the conformity of that product or partly completed machinery with the Directive with a view to its being placed on the market, under his, her or its own name or trademark, or for his, her or its own use. In the absence of a manufacturer as thus defined, any natural or legal person who places on the market or puts into service such product or partly completed machinery shall be considered a manufacturer;

“Minister” means Minister for Enterprise, Trade and Employment;

“notified body” means (except in Schedules 2, 3, 9, 10 and 11, where it also includes a person or body notified by another Member State) a person or body appointed by the Minister under Regulation 14 to be a notified body in the State;

“partly completed machinery” means partly completed machinery to which the Directive applies, being an assembly which is almost machinery but which cannot in itself perform a specific application. A drive system is partly completed machinery. Partly completed machinery is only intended to be incorporated into or assembled with other machinery or other partly completed machinery or equipment, thereby forming machinery;

“place on the market” means making a product or partly completed machinery available for the first time in the Community, with a view to distribution or use, whether by one or more of the following means, or otherwise:

“prescribed” means prescribed by regulations made by the Minister;

“product” means a product to which the Directive applies, being any or all of the following:

“putting into service” means the first use, for its intended purpose, in the Community, of a product;

“quality assurance system” means the system thus described and referred to in Annex X, the text of which Annex is, for ease of reference, set out in Schedule 10;

“record” includes any memorandum, book, report, statement, register, plan, chart, map, drawing, specification, diagram, pictorial or graphic work or other document, any photograph, film or recording (whether of sound or images or both), any form in which data (within the meaning of the Data Protection Acts 1988 and 2003) are held, any form (including machine-readable form) or thing in which information is held or stored manually, mechanically or electronically, and anything that is a part or copy, in any form, of any of, or any combination of, the foregoing;

“removable mechanical transmission device” means a removable mechanical transmission device to which the Directive applies, being a removable component for transmitting power between self-propelled machinery or a tractor and another item of machinery by joining them at the first fixed bearing. When it is placed on the market with the guard it shall be regarded as one piece of equipment;

“safety component” means a safety component to which the Directive applies, being a component—

an indicative list of safety components is set out in Annex V, the text of which Annex is, for ease of reference, set out in Schedule 5, which list may be updated in accordance with Article 8(1)(a);

“technical file” means the technical file referred to in part A of Annex VII, the text of which Annex is, for ease of reference, set out in Schedule 7.

PART 2 Requirements for placing on the market and putting into service

General duties of manufacturer or authorised representative as regards products

4.

A manufacturer or authorised representative shall ensure that before placing a product on the market or putting it into use that, in respect of same—

Duties of manufacturer or authorised representative as regards compliance with Regulation 10 relating to partly completed machinery

5.

A manufacturer or authorised representative shall ensure that before placing partly completed machinery on the market that the requirements in Regulation 10 are complied with.

Duties of manufacturer or authorised representative as regards compliance with Regulation 9 relating to essential health and safety requirements

6.

For the purposes of the procedures referred to in Regulation 9, a manufacturer or authorised representative shall have, or shall have access to, the necessary means of ensuring that the product concerned satisfies the essential health and safety requirements set out in Annex I.

Duties of manufacturer or authorised representative as regards compliance with other Directives

7.

Where a product is also the subject of a Directive other than the Directive, relating to other aspects and providing for the affixing of the CE marking, the manufacturer or authorised representative shall ensure that the product concerned also conforms to the provisions of such other Directive.

Duties of persons showing products or partly completed machinery at trade fairs etc

8.

A person showing a product or partly completed machinery which does not conform to the Directive at trade fairs, exhibitions, demonstrations and similar events shall—

Duties of manufacturer or authorised representative as regards certifying the conformity of products

9.

The manufacturer or authorised representative shall, in order to certify the conformity of a product with the provisions of the Directive, apply the appropriate procedure described below:

Duties of manufacturer or authorised representative as regards relevant technical documentation, assembly instructions and declaration of incorporation relating to partly completed machinery

10.

The manufacturer of partly completed machinery or an authorised representative shall, before placing same on the market ensure that, in respect of the partly completed machinery concerned—

Duties of manufacturer or authorised representative as regards application of CE marking as regards products

11.

A manufacturer or authorised representative shall ensure in respect of the application of the CE marking to a product that—

CE marking and declaration of conformity

12.

A product bearing the CE marking and accompanied by the appropriate declaration of conformity shall be regarded as complying with the provisions of these Regulations unless there are reasonable indications that the said product does not comply.

Products manufactured in conformity with a harmonised standard

13.

A product manufactured in conformity with a harmonised standard, the references to which have been published in the Official Journal of the European Union, shall be presumed to comply with the essential health and safety requirements covered by such a harmonised standard unless there are reasonable indications that the said product does not comply.

PART 3 Notified Bodies

Appointment of notified bodies and their duties

14.

(1) The Minister may appoint, in writing, such one or more persons or bodies as satisfy the minimum criteria set out in Annex XI, the text of which Annex is, for ease of reference, set out in Schedule 11, to be a notified body in the State, for a specified period of time, to carry out the assessment of conformity, with the Directive and these Regulations, of a product for placing on the market. Subject to paragraph (3), the duration of the appointment shall be at the discretion of the Minister who may renew or withdraw the appointment as appropriate.

Provision of information to the Commission, other Member States and the public on notified bodies

15.

(1) The Minister shall, without delay, inform the Commission and other Member States of the name and address of each notified body appointed to carry out the assessment of conformity in accordance with the Directive and these Regulations. The information will include the specific conformity assessment procedures and the categories of product for which the body concerned has been appointed and the identification number assigned to it beforehand by the Commission.

Monitoring of notified bodies

16.

(1) A notified body shall be monitored by or on behalf of the Minister as is necessary to ensure—

Suspension, withdrawal or restriction of certificates or approvals by notified bodies

17.

(1) If a notified body finds that relevant requirements of the Directive have not been met or are no longer being met by a manufacturer, or that an EC type-examination certificate or the approval of a quality assurance system should not have been issued, it shall, taking account of the principle of proportionality, suspend or withdraw the certificate or the approval issued, or place restrictions on it.

Provision of information by notified bodies to relevant competent authority

18.

(1) A notified body shall inform the relevant competent authority—

PART 4 Competent Authorities

Competent authorities

19.

(1) The Authority shall be the competent authority for a product or partly completed machinery, other than for any product or partly completed machinery that may be prescribed by the Minister under paragraph (2).

Functions of competent authorities

20.

(1) Without prejudice to such other functions or powers assigned to a competent authority by these Regulations, a competent authority shall—

the product or partly completed machinery concerned,

Immunity

21.

None of the following persons, that is to say, a competent authority, an authorised officer, or a member or a member of staff of a competent authority shall be liable in damages in respect of any act done or omitted to be done by it or him or her in the performance, or purported performance, of that person’s functions, unless the act or omission concerned was done in bad faith.

Indemnification

22.

A competent authority shall, subject to the provisions of any enactment or rule of law, indemnify an authorised officer appointed by that competent authority, or a member or member of staff of that competent authority, in respect of any act done or omitted to be done by him or her in the performance, or purported performance, of his or her functions as such authorised officer, member or member of staff, unless the act or omission concerned was done in bad faith.

Restriction or prohibition

23.

Where, in the opinion of a competent authority, a product, when correctly maintained and used for its intended purpose or under conditions which can be reasonably foreseen, is liable to endanger the health or safety of persons and, where appropriate, domestic animals or property, notwithstanding the fact that it bears the CE marking, the competent authority may restrict or prohibit the placing on the market or the use of the product in question or have it withdrawn from the market or from circulation.

Directions regarding CE marking affixed unduly to products

24.

Where a competent authority establishes that the CE marking has been affixed to a product unduly, it may direct the manufacturer or the authorised representative to ensure that the product concerned conforms with these Regulations, and where non-conformity persists, the competent authority may restrict or prohibit the placing on the market, transport or use of the product in question, or have it withdrawn from the market or from circulation.

Notifications to the Commission in respect of application of Regulations 23 and 24

25.

The competent authority concerned shall forthwith notify the Commission of any restriction, prohibition, requirement or direction made, imposed or given by it under Regulation 23 or Regulation 24.

Publication of information on products non-compliant with essential health and safety requirements

26.

Subject to Regulation 42, a competent authority may publish information on specific products in relation to failure to satisfy the essential health and safety requirements set out in Annex 1.

Publication of information on action taken regarding non-compliant products

27.

Subject to Regulation 42, a competent authority may publish information in respect of action taken by a Member State in respect of non-conformity of products with the requirements of the Directive, particularly where it relates to—

Sharing of information on application of the Directive

28.

A competent authority may provide information to any EU information network, the Commission or a competent authority of another Member State for the purpose of sharing information related to the application of the Directive.

Power to require information

29.

(1) A competent authority may, for the purpose of obtaining information which it requires for the discharge of functions under these Regulations, by a notice in writing (in these Regulations referred to as “a notice requiring information”) served on any person, require such person to furnish to the competent authority concerned within a period specified in the notice and in such form, if any, as may be specified in the notice, information about any matters to which these Regulations or the Directive relate specified in the notice.

Provision of information in response to a notice requiring information

30.

A person shall provide the information requested in a notice requiring information—

whichever is the later;

whichever is the later.

Appeal against a notice requiring information

31.

Where a person is aggrieved by a notice requiring information served on him or her, he or she may, within the period of 7 days beginning on the day on which the notice is so served, appeal to a judge of the District Court in the District Court District in which the notice is served against the notice and, in determining the appeal, the judge may—

Suspension of application of a notice requiring information

32.

(1) Where on the hearing of an appeal made under Regulation 31, a notice requiring information is confirmed, the judge by whom the appeal is heard may, on the application of the appellant, suspend the operation of the notice for such period as in the circumstances of the case he or she considers appropriate.

Admissibility of certain documents in evidence

33.

Where an opinion (whether one to which Regulation 23 relates, or otherwise), finding, statement or determination of a competent authority is contained in a document which—

such document shall be admissible in evidence and shall be evidence of any such opinion, finding, statement or determination in such proceedings without further proof.

PART 5 Authorised Officers

Appointment of authorised officers

34.

A competent authority may appoint such and so many persons as it thinks fit to be authorised officers for the purposes of these Regulations and any function conferred on a competent authority by these Regulations may be performed by an authorised officer.

Warrants or certificates of appointment

35.

A person appointed under Regulation 34 shall, on his or her appointment, be furnished by the competent authority concerned with a warrant or certificate of his or her appointment, and when exercising a power conferred by these Regulations shall, if requested by any person thereby affected, produce a copy of such warrant or certificate to that person for inspection, together with a form of personal identification.

Powers of authorised officers

36.

(1) An authorised officer shall, for the purposes of these Regulations, have power to do any one or more of the following:

to ascertain whether these Regulations have been or are being complied with and, for that purpose, take with him or her and use any equipment or materials he or she consider necessary;

the judge may issue a warrant authorising an authorised officer, accompanied by such other authorised officers or such other competent persons as may be appropriate or members of the Garda Síochána as may be necessary, at any time or times, within one month from the date of issue of the warrant, on production of the warrant if requested, to enter the place, if necessary by the use of reasonable force, and perform the functions conferred on an authorised officer by or under these Regulations.

“person in charge” means, in relation to a place—

“place” means a place at or in which the authorised officer concerned believes there is or may be a product, partly completed machinery, equipment or item connected to a matter to which these Regulations apply, or may apply.

PART 6 Improvement plans, contravention notices and prohibition notices

Directions for improvement plan

37.

(1) Where an authorised officer is of the opinion that there is occurring or likely to occur any situation or activity that involves or is likely to involve a risk to safety or health arising from or in connection with a product or partly completed machinery to which a duty under these Regulations applies, he or she may give a direction to the person (in these Regulations referred to as “the person in control”) who has, or whom the authorised officer reasonably presumes to have, control of the said product or partly completed machinery, requiring submission to the officer of a plan (in these Regulations referred to as an “improvement plan”) specifying the remedial action proposed to be taken to remove the risk.

Contravention notice

38.

(1) An authorised officer who is of the opinion that a person—

may serve a notice (in these Regulations referred to as a “contravention notice”) on the person in control.

Prohibition notice

39.

(1) Where an authorised officer is of the opinion that at any place there is occurring or is likely to occur any situation or activity relating to a product or partly completed machinery that involves or is likely to involve a serious risk to safety or health, or in relation to which product or partly completed machinery the CE marking is not affixed in circumstances in which it should have been affixed, or is affixed in circumstances in which it should not have been affixed, the authorised officer may serve a notice (in these Regulations referred to as a “prohibition notice”) on the person in control.

whichever occurs later.

shall at the same time notify the relevant competent authority of the appeal or the application, and the grounds for the appeal or application.

Contravention of prohibition notice — application to High Court

40.

(1) Where a person contravenes a prohibition notice, an authorised officer may apply ex parte to the High Court for an order prohibiting the continued contravention of the notice.

Publication of information relating to contravention notices and prohibition notices

41.

(1) A competent authority may, in the interest of the protection of safety or health and in consultation, where appropriate, with another competent authority, take such measures as it considers appropriate to bring to the attention of the public matters giving rise to any contravention notice or prohibition notice served under these Regulations.

PART 7 Supplemental Provisions

Restrictions on the disclosure of information

42.

A person in receipt of information as a result of the application of these Regulations shall treat same as confidential. In particular, business, professional and trade secrets shall be treated as confidential unless the divulging of such information is—

Service of notices etc

43.

(1) A notice or other document required or authorised to be served on, sent or given to a person under these Regulations shall, subject to paragraph (2), be addressed to the person concerned by name, and may be served on, sent or given to the person in one of the following ways:

PART 8 Offences and Penalties

Offences

44.

(1) A person who contravenes a provision or requirement of Regulation 4, 5, 6, 7, 8,9, 10 or 11, commits an offence.

commits an offence.

commits an offence.

Penalties

45.

(1) A person guilty of an offence under Regulation 44 shall be liable—

Offences by bodies corporate

46.

Where an offence under these Regulations has been committed by a body corporate and is proved to have been committed with the consent or connivance of, or to be attributable to any neglect on the part of, a person being a director, manager, secretary or other officer of the body corporate, or a person who was purporting to act in any such capacity, that person as well as the body corporate commits an offence and shall be liable to be proceeded against and punished as if he or she had committed the first-mentioned offence.

Defence in proceedings

47.

In any proceedings for an offence for a contravention of any of the provisions of these Regulations it shall be a defence for the person charged to prove that—

Prosecution of offences

48.

(1) Subject to paragraph (2), summary proceedings in relation to an offence under these Regulations may be brought and prosecuted by a competent authority.

PART 9 Miscellaneous

Appeal to Circuit Court from certain orders of District Court

49.

For the avoidance of doubt, an order of the District Court confirming, varying or cancelling a notice under Regulation 31, 38(6) or 39(6) is a decision of a judge of the District Court for the purposes of section 84 of the Courts of Justice Acts 1924.

Notice or direction to be in writing

50.

Any notice or direction under these Regulations shall be in writing.

Revocation

51.

The European Communities (Machinery) Regulations 2001 ( S.I. No. 518 of 2001 ) are revoked with effect from 29 December 2009.

Regulation 3(1)

SCHEDULE 1 Annex I to Directive 2006/42/EC

Essential health and safety requirements relating to the design and construction of machinery.

GENERAL PRINCIPLES

This document does not substitute the official text published in the Irish Statute Book. We accept no responsibility for any inaccuracies arising from the transcription of the original into this format.

This text is published under Irish Statute Book's own terms of reuse, not a Legalize or public-domain licence. Irish Statute Book
CC-BY 4.0 (Oireachtas Open Data PSI Licence)
Contains Irish Public Sector Information licensed under the Oireachtas (Houses of the Oireachtas) Open Data PSI Licence / Creative Commons Attribution 4.0 International, sourced from https://www.irishstatutebook.ie.