Search Legislation

Commission Implementing Regulation (EU) 2018/659Show full title

Commission Implementing Regulation (EU) 2018/659 of 12 April 2018 on the conditions for the entry into the Union of live equidae and of semen, ova and embryos of equidae (Text with EEA relevance)

 Help about what version

What Version

 Help about advanced features

Advanced Features

 Help about UK-EU Regulation

Legislation originating from the EU

When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.

Close

This item of legislation originated from the EU

Legislation.gov.uk publishes the UK version. EUR-Lex publishes the EU version. The EU Exit Web Archive holds a snapshot of EUR-Lex’s version from IP completion day (31 December 2020 11.00 p.m.).

Status:

Point in time view as at 31/01/2020.

Changes to legislation:

There are currently no known outstanding effects for the Commission Implementing Regulation (EU) 2018/659, Introductory Text. Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

Commission Implementing Regulation (EU) 2018/659

of 12 April 2018

on the conditions for the entry into the Union of live equidae and of semen, ova and embryos of equidae

(Text with EEA relevance)

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Council Directive 91/496/EEC of 15 July 1991 laying down the principles governing the organisation of veterinary checks on animals entering the Community from third countries and amending Directives 89/662/EEC, 90/425/EEC and 90/675/EEC(1), and in particular Article 3(2) and Article 9(1)(c) thereof,

Having regard to Council Directive 92/65/EEC of 13 July 1992 laying down animal health requirements governing trade in and imports into the Community of animals, semen, ova and embryos not subject to animal health requirements laid down in specific Community rules referred to in Annex A(I) to Directive 90/425/EEC(2), and in particular Article 17(3) thereof,

Having regard to Council Directive 2009/156/EC of 30 November 2009 on animal health conditions governing the movement and importation from third countries of equidae(3), and in particular Article 2(i), Article 12(1), (4) and (5), Article 13(2), Articles 15, 16, 17 and 19 thereof,

Whereas:

(1) Directive 2009/156/EC lays down the animal health requirements governing imports into the Union of equidae. It provides that only equidae that come from a third country or part of a third country on a list of third countries drawn up in accordance with that Directive, and accompanied by a health certificate corresponding to a model also drawn up in accordance with that Directive, may be imported into the Union. The health certificate must attest that the equidae comply with the health conditions set out in accordance with that Directive in the corresponding health certificate.

(2) The list of third countries from which Member States authorise imports of live equidae and semen, ova and embryos of the equine species and the regionalisation of certain of those third countries should be established on the basis of the animal health status of those third countries and be based on the list of third countries and parts of the territory of third countries set out in Commission Decision 2004/211/EC(4).

(3) In accordance with Article 12(2)(a) of Directive 2009/156/EC, the animal health requirements laid down in this Regulation should be based on a risk assessment. The principle of grouping countries in health zones, as provided for in Article 12(4) of Directive 2009/156/EC, according to common risks has proven to be effective. However, as the word ‘zones’ suggests certain contiguity and certain risks of the same kind may prevail in distant areas, countries should be assigned to specific ‘sanitary groups’.

(4) Directive 92/65/EEC lays down the animal health requirements governing imports into the Union of semen, ova and embryos of the equine species. It provides that only commodities that come from a third country or part of a third country on a list of third countries drawn up in accordance with that Directive, and accompanied by a health certificate corresponding to a model also drawn up in accordance with that Directive, may be imported into the Union. The health certificate must attest that the commodities come from approved collection and storage centres or collection and production teams offering guarantees at least equivalent to those established in Annex D(I) to that Directive.

(5) Directive 92/65/EEC, as amended by Council Directive 2008/73/EC(5), introduced a simplified procedure for the listing of semen collection and storage centres and embryo collection and production teams in third countries, approved for imports of the commodities into the Union. The lists are available at the Commission website(6).

(6) Annex D to Directive 92/65/EEC sets out certain requirements for semen, ova and embryos of equidae and provides for rules for the approval, supervision and operation of semen collection and storage centres and embryo collection and production teams and detailed conditions for the health status of the donor animals. Accordingly, it is necessary to establish model health certificates for imports into the Union of semen, ova and embryos of equidae.

(7) In addition, provision should be made for imports into the Union of existing stocks of commodities that comply with the provisions of Directive 92/65/EEC established prior to the entry into force of the amendments introduced by Commission Regulation (EU) No 176/2010(7). Accordingly, it is necessary to set out separate model health certificates for imports of consignments of semen, ova and embryos of equidae collected or produced, processed and stored in accordance with Annex D to Directive 92/65/EEC prior to 1 September 2010.

(8) The long lasting stocking capabilities for such commodities make it impossible at present to fix a date for the exhaustion of the existing stocks. Therefore, it is not possible to fix a date for the termination of the use of those model health certificates for the existing stocks.

(9) In order to ensure full traceability of the commodities, model health certificates should be set out in this Regulation for imports into the Union of semen of equidae collected in approved semen collection centres and dispatched from an approved semen storage centre, whether or not the latter constitutes part of a semen collection centre approved under a different approval number.

(10) In addition, it is appropriate that consignments of the commodities imported into the Union from Switzerland are accompanied by the health certificates drawn up in accordance with the models used for trade within the Union in semen, ova and embryos of animals of the equine species and set out in Commission Decision 2010/470/EU(8), with the adaptations set out in points 8 and 9 of Chapter IX(B) of Appendix 2 of Annex 11 to the Agreement between the European Community and the Swiss Confederation on trade in Agricultural Products, as approved by Decision 2002/309/EC, Euratom of the Council and of the Commission(9).

(11) Semen, ova and embryos of animals of the equine species consigned from Canada to the Union may be accompanied by health certificates laid down in accordance with the Agreement between the European Community and the Government of Canada on sanitary measures to protect public and animal health in respect of trade in live animals and animal products(10), as approved by Council Decision 1999/201/EC(11).

(12) Semen, ova and embryos of animals of the equine species consigned from New Zealand to the Union may be accompanied by health certificates laid down in accordance with the Agreement between the European Community and New Zealand on sanitary measures applicable to trade in live animals and animal products(12), as approved by Council Decision 97/132/EC(13).

(13) With the view to simplifying Union legislation, it is appropriate to group together in a single Regulation the animal health and certification requirements applicable for the entry into the Union of consignments of equidae and of semen, ova and embryos of equidae, including the list of third countries and parts of the territory of third countries from which Member States are to authorise the introduction into the Union of such consignments.

(14) In order to preserve the certified health status of equidae during their movement from the exporting third country to the Union, it is necessary to lay down animal health requirements concerning the transport of equidae.

(15) Provisions should be made for the quality of health testing and the recording of vaccinations. Provisions should also be made for the confirmation of test results by the European Union reference laboratory for equine diseases other than African horse sickness, designated in accordance with Commission Regulation (EC) No 180/2008(14) where risk based sampling of equidae, in accordance with Commission Decision 97/794/EC(15), produced results different to those certified by the dispatching third country.

(16) The tests used for the diagnosis of equine viral arteritis and the categories of male equidae to which the test requirements for equine viral arteritis apply should be defined based on the recommendations of the Scientific Veterinary Committee(16), which are contained in Commission Decision 95/329/EC(17), and the latest recommendations in Chapter 12.9. of the Terrestrial Animal Health Code of the World Organisation for Animal Health (OIE), 2016 Edition(18).

(17) A specific model health certificate should be laid down for transit through the Union of live equidae from one third country, or part of the territory of a third country, to another third country or to another part of the territory of the same third country.

(18) For the controls necessary to ensure a uniform implementation by Member States of the provisions on temporary admission of registered horses, the re-entry of registered horses after temporary export, the transit of equidae and the conversion of temporary admission of registered horses into permanent entry, it is necessary to lay down specific and additional provisions on the use of the integrated computerised veterinary system ‘TRACES’ provided for in Commission Decisions 2003/24/EC(19) and 2004/292/EC(20) from the veterinary border inspection post of entry, approved in accordance with Commission Decision 2009/821/EC(21) till the exit point from the Union.

(19) In the interests of consistency and simplification of Union legislation, the format of the model health certificates for entry into the Union of equidae and of semen, ova and embryos of the equidae should be based on the standard models for veterinary certificates set out in Annex I to Commission Decision 2007/240/EC(22).

(20) Provisions should be made to determine, in accordance with Article 19(c) of Directive 2009/156/EEC, the conditions for converting temporary entry into permanent entry, including provisions on the necessary information in TRACES and the exchange of the Common Veterinary Entry Document (CVED) set out in Annex I to Commission Regulation (EC) No 282/2004(23).

(21) Specific animal health conditions should be laid down for the re-entry of registered horses after temporary export to third countries in order to participate in races, competitions and cultural events, and the corresponding model certificates should be set out in an Annex to this Regulation.

(22) Commission Decision 93/444/EEC(24) defines the ‘exit point’ and requires, inter alia, that animals destined for export to a third country are, on their way to the exit point, to be accompanied by a health certificate applicable at least to trade in animals for slaughter of the species concerned. It also requires the competent authority at the place of dispatch to notify the exit point of the intended movement. It is necessary to clarify that in order to ensure traceability the ‘exit point’ should be a border inspection post and that the health certificate referred to in Article 2(1) of Decision 93/444/EEC should be the health certificate set out in Annex III to Directive 2009/156/EC also in the case of registered horses intended for temporary export.

(23) For reasons of legal certainty, Commission Decisions 92/260/EEC(25), 93/195/EEC(26), 93/196/EEC(27), 93/197/EEC(28), 94/699/EC(29), 95/329/EC, 2003/13/EC(30), 2004/177/EC(31), 2004/211/EC, 2010/57/EU(32) and 2010/471/EU(33) should be repealed.

(24) In order to enable economic operators to adapt to the new rules laid down in this Regulation, it is appropriate to provide for a transitional period during which Member States are to authorise the entry into the Union of equidae and semen, ova and embryos of equidae which comply with the conditions set out in the model health certificates applicable before the date of application of this Regulation.

(25) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,

HAS ADOPTED THIS REGULATION:

(4)

Commission Decision 2004/211/EC of 6 January 2004 establishing the list of third countries and parts of territory thereof from which Member States authorise imports of live equidae and semen, ova and embryos of the equine species, and amending Decisions 93/195/EEC and 94/63/EC (OJ L 73, 11.3.2004, p. 1).

(5)

Council Directive 2008/73/EC of 15 July 2008 simplifying procedures of listing and publishing information in the veterinary and zootechnical fields and amending Directives 64/432/EEC, 77/504/EEC, 88/407/EEC, 88/661/EEC, 89/361/EEC, 89/556/EEC, 90/426/EEC, 90/427/EEC, 90/428/EEC, 90/429/EEC, 90/539/EEC, 91/68/EEC, 91/496/EEC, 92/35/EEC, 92/65/EEC, 92/66/EEC, 92/119/EEC, 94/28/EC, 2000/75/EC, Decision 2000/258/EC and Directives 2001/89/EC, 2002/60/EC and 2005/94/EC (OJ L 219, 14.8.2008, p. 40).

(6)

http://ec.europa.eu/food/animals/semen/equine_en

(7)

Commission Regulation (EU) No 176/2010 of 2 March 2010 amending Annex D to Council Directive 92/65/EEC as regards semen collection and storage centres, embryo collection and production teams, and conditions for donor animals of the equine, ovine and caprine species and for handling semen, ova and embryos of those species (OJ L 52, 3.3.2010, p. 14).

(8)

Commission Decision 2010/470/EU of 26 August 2010 laying down model health certificates for trade within the Union in semen, ova and embryos of animals of the equine, ovine and caprine species and in ova and embryos of animals of the porcine species (OJ L 228, 31.8.2010, p. 15).

(9)

Decision 2002/309/EC, Euratom of the Council, and of the Commission as regards the Agreement on Scientific and Technological Cooperation of 4 April 2002 on the conclusion of seven Agreements with the Swiss Confederation (OJ L 114, 30.4.2002, p. 1).

(11)

Council Decision 1999/201/EC of 14 December 1998 on the conclusion of the Agreement between the European Community and the Government of Canada on sanitary measures to protect public and animal health in respect of trade in live animals and animal products (OJ L 71, 18.3.1999, p. 1).

(13)

Council Decision 97/132/EC of 17 December 1996 on the conclusion of the Agreement between the European Community and New Zealand on sanitary measures applicable to trade in live animals and animal products (OJ L 57, 26.2.1997, p. 4).

(14)

Commission Regulation (EC) No 180/2008 of 28 February 2008 concerning the Community reference laboratory for equine diseases other than African horse sickness and amending Annex VII to Regulation (EC) No 882/2004 of the European Parliament and of the Council (OJ L 56, 29.2.2008, p. 4).

(15)

Commission Decision 97/794/EC of 12 November 1997 laying down certain detailed rules for the application of Council Directive 91/496/EEC as regards veterinary checks on live animals to be imported from third countries (OJ L 323, 26.11.1997, p. 31).

(16)

Report of the Scientific Veterinary Committee on Equine Viral Arteritis, 12 December 1994, VI/4994/94 — Rev. 4.

(17)

Commission Decision 95/329/EC of 25 July 1995 defining the categories of male equidae to which the requirement regarding viral arteritis laid down in Article 15 (b) (ii) of Council Directive 90/426/EEC applies (OJ L 191, 12.8.1995, p. 36).

(18)

http://www.oie.int/index.php?id=169&L=0&htmfile=chapitre_eav.htm

(19)

Commission Decision 2003/24/EC of 30 December 2002 concerning the development of an integrated computerised veterinary system (OJ L 8, 14.1.2003, p. 44).

(20)

Commission Decision 2004/292/EC of 30 March 2004 on the introduction of the Traces system and amending Decision 92/486/EEC (OJ L 94, 31.3.2004, p. 63).

(21)

Commission Decision 2009/821/EC of 28 September 2009 drawing up a list of approved border inspection posts, laying down certain rules on the inspections carried out by Commission veterinary experts and laying down the veterinary units in Traces (OJ L 296, 12.11.2009, p. 1).

(22)

Commission Decision 2007/240/EC of 16 April 2007 laying down new veterinary certificates for importing live animals, semen, embryos, ova and products of animal origin into the Community pursuant to Decisions 79/542/EEC, 92/260/EEC, 93/195/EEC, 93/196/EEC, 93/197/EEC, 95/328/EC, 96/333/EC, 96/539/EC, 96/540/EC, 2000/572/EC, 2000/585/EC, 2000/666/EC, 2002/613/EC, 2003/56/EC, 2003/779/EC, 2003/804/EC, 2003/858/EC, 2003/863/EC, 2003/881/EC, 2004/407/EC, 2004/438/EC, 2004/595/EC, 2004/639/EC and 2006/168/EC (OJ L 104, 21.4.2007, p. 37).

(23)

Commission Regulation (EC) No 282/2004 of 18 February 2004 introducing a document for the declaration of, and veterinary checks on, animals from third countries entering the Community (OJ L 49, 19.2.2004, p. 11).

(24)

Commission Decision 93/444/EEC of 2 July 1993 on detailed rules governing intra-Community trade in certain live animals and products intended for exportation to third countries (OJ L 208, 19.8.1993, p. 34).

(25)

Commission Decision 92/260/EEC of 10 April 1992 on animal health conditions and veterinary certification for temporary admission of registered horses (OJ L 130, 15.5.1992, p. 67).

(26)

Commission Decision 93/195/EEC of 2 February 1993 on animal health conditions and veterinary certification for the re-entry of registered horses for racing, competition and cultural events after temporary export (OJ L 86, 6.4.1993, p. 1).

(27)

Commission Decision 93/196/EEC of 5 February 1993 on animal health conditions and veterinary certification for imports of equidae for slaughter (OJ L 86, 6.4.1993, p. 7).

(28)

Commission Decision 93/197/EEC of 5 February 1993 on animal health conditions and veterinary certification for imports of registered equidae and equidae for breeding and production (OJ L 86, 6.4.1993, p. 16).

(29)

Commission Decision 94/699/EC of 19 October 1994 providing for less frequent identity and physical checks on the temporary admission of certain equidae from Sweden, Norway and Finland and repealing Decision 93/321/EEC (OJ L 280, 29.10.1994, p. 88).

(30)

Commission Decision 2003/13/EC of 10 January 2003 on the temporary admission of horses participating in the pre-Olympic test event in Greece in 2003 (OJ L 7, 11.1.2003, p. 86).

(31)

Commission Decision 2004/177/EC of 20 February 2004 on the temporary introduction of registered horses participating in the Olympic Games or the Paralympic Games in Greece in 2004 (OJ L 55, 24.2.2004, p. 64).

(32)

Commission Decision 2010/57/EU of 3 February 2010 laying down health guarantees for the transit of equidae being transported through the territories listed in Annex I to Council Directive 97/78/EC (OJ L 32, 4.2.2010, p. 9).

(33)

Commission Decision 2010/471/EU of 26 August 2010 on imports into the Union of semen, ova and embryos of animals of the equine species as regards lists of semen collection and storage centres and embryo collection and production teams and certification requirements (OJ L 228, 31.8.2010, p. 52).

Back to top

Options/Help

Print Options

Close

Legislation is available in different versions:

Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.

Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.

Point in Time: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.

Close

See additional information alongside the content

Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.

Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the EU Official Journal
  • lists of changes made by and/or affecting this legislation item
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

Timeline of Changes

This timeline shows the different versions taken from EUR-Lex before exit day and during the implementation period as well as any subsequent versions created after the implementation period as a result of changes made by UK legislation.

The dates for the EU versions are taken from the document dates on EUR-Lex and may not always coincide with when the changes came into force for the document.

For any versions created after the implementation period as a result of changes made by UK legislation the date 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. For further information see our guide to revised legislation on Understanding Legislation.

Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources