LegalizeCommission Implementing Regulation (EU) 2025/243 of 30 January 2025 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of certain categories of terrestrial animals and germinal products thereof
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.
EUROPEAN UNION EUROPEAN UNION Certificate model CER-INTRA-X Certificate model CER-INTRA-X Certificate model CER-INTRA-X Certificate model CER-INTRA-X II. Health information II.a Certificate reference II.b IMSOC reference
I, the undersigned official veterinarian, hereby certify that: II.1. The cervid animals (1) of the consignment described in Part I meet the following requirements: II.1.1. They are identified as provided for in Article 73 or Article 74 of Commission Delegated Regulation (EU) 2019/2035. II.1.2. They, for at least 30 days prior to the date of departure of the consignment, or since birth, if they are younger than 30 days of age: II.1.2.1. have been continuously resident in the establishment of origin; II.1.2.2. have not been in contact with kept cervid animals of a lower health status or subject to movement restrictions for animal health reasons; II.1.2.3. have not been in direct or indirect contact with kept animals that have entered the Union from a third country or territory during the last 30 days prior to the date of departure of the consignment. II.1.3. They have not shown clinical signs or symptoms of diseases listed for cervid animals during the clinical examination which was carried out, within the last 24 hours prior to the time of departure of the consignment, on … (insert date dd/mm/yyyy). II.2. According to official information, the animals described in Part I meet the following health requirements: II.2.1. (2) either [They come from establishments or zones not subject to movement restrictions affecting cervid animals and established for reasons of diseases listed for those species or diseases subject to emergency measures relevant for those species, and they have not been in contact with kept animals of a listed species of a lower health status for an adequate period.] (2) or [They come from establishments or zones subject to movement restrictions affecting cervid animals and established for … (3), but derogations from movement restrictions have been granted, and: (2) [they comply with the requirements set out in … (4);]] (2) [and in particular, they are … (5).]] II.2.2. They come from establishments in which infection with Brucella abortus, B. melitensis and B. suis in cervid animals has not been reported during the last 42 days prior to the date of departure of the consignment. II.2.3. They come from establishments in which surveillance for infection with Mycobacterium tuberculosis complex (M. bovis, M. caprae and M. tuberculosis) has been carried out on the cervid animals kept in the establishments during at least 12 months prior to the date of departure of the consignment, as referred to in Article 26(1), point (e), of Commission Delegated Regulation (EU) 2020/688. II.2.4. They come from establishments in which infection with rabies virus in kept terrestrial animals has not been reported during the last 30 days prior to the date of departure of the consignment. II.2.5. They come from establishments situated within an area of at least 150 km radius around those establishments in which infection with epizootic haemorrhagic disease virus: (2) either [has not been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment;] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure and the animals have been kept in a zone seasonally free from epizootic haemorrhagic disease in accordance with Parts 1 and 2 of Annex IX to Delegated Regulation (EU) 2020/688: (2) either [for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of entry of the animals into the seasonally disease-free area;]] (2) and/or [for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of entry of the animals into the seasonally disease-free area;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals have been protected against attacks by vectors during transportation to the place of destination and they have been kept protected against attacks by vectors in a vector protected establishment fulfilling the requirements provided for in Part 3 of Annex IX to Delegated Regulation (EU) 2020/688: (2) either [for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of commencement of the period of protection against attacks by vectors;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals have been vaccinated against infection with epizootic haemorrhagic disease virus and the animals are within the immunity period guaranteed in the specifications of the vaccine and: (2) either [they have been vaccinated at least 60 days prior to the date of departure of the consignment;]] (2) and/or [they have been vaccinated with an inactivated vaccine and have been subject to a PCR test, with negative results on samples collected at least 14 days after the onset of the immunity set in the specifications of the vaccine;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the Member State of destination has informed the Commission and the other Member States that such movement is authorised;] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals comply with specific risk-mitigating measures defined by the competent authority of the Member State of destination and the Member State of destination has informed the Commission and the other Member States that such movement is authorised;] (2) and [the requirements laid down in Article 26(1), third subparagraph, of Delegated Regulation (EU) 2020/688 are fulfilled.] II.2.6. They come from establishments in which anthrax in ungulates has not been reported during the last 15 days prior to the date of departure of the consignment. II.2.7. They come from establishments in which surra (Trypanosoma evansi) has not been reported during the last 30 days prior to the date of departure of the consignment, and (2) either [surra has not been reported in the establishments during the last 2 years prior to the date of departure of the consignment.] (2) or [surra has been reported during the last 2 years prior to the date of departure of the consignment, and following the date of the last outbreak, the affected establishments have remained under movement restrictions until the date on which the infected animals have been removed from the establishments, and the remaining animals in the establishments have been subjected to a test for surra with one of the diagnostic methods provided for in Part 3 of Annex I to Delegated Regulation (EU) 2020/688, carried out, with negative results, on samples taken at least 6 months following the date on which the infected animals have been removed from the establishments.] (2) either [II.2.8. They originate from a Member State or a zone thereof free from infection with bluetongue virus (serotypes 1-24), where no case of infection with bluetongue virus (serotypes 1-24) has been confirmed in the targeted animal population during the last 24 months prior to the date of departure of the consignment and have not been vaccinated with a live vaccine against infection with bluetongue virus (serotypes 1-24) in the last 60 days prior to the date of departure of the consignment and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled.] (2) and/or [II.2.8. They originate from a Member State or a zone thereof covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled, and: (2) either [II.2.8.1. have been kept in a Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24) in accordance with Article 40(3) of Commission Delegated Regulation (EU) 2020/689: (2) either [II.2.8.1.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.1.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the entry of the animals into the Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24);]] (2) and/or [II.2.8.1.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of the entry of the animals into the Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24);]]] (2) and/or [II.2.8.2. have been protected against attacks by vectors during transportation to the place of destination and have been kept protected against attacks by vectors in a vector protected establishment: (2) either [II.2.8.2.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.2.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [II.2.8.2.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of the commencement of the period of protection against attacks by vectors;]]] (2) and/or [II.2.8.3. have been vaccinated against all serotypes 1-24 of infection with bluetongue virus which were reported during the last 2 years prior to the date of departure of the consignment in that Member State or zone thereof and are within the immunity period guaranteed in the specifications of the vaccine and: (2) either [II.2.8.3.1. have been vaccinated more than 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.3.2. have been vaccinated with an inactivated vaccine and subjected to a PCR test, with negative results on samples collected at least 14 days after the date of the onset of the immunity set in the specifications of the vaccine;]]] (2) and/or [II.2.8.4. have been subjected with positive results to a serological test able to detect specific antibodies against all serotypes 1-24 of infection with bluetongue virus reported during the last 2 years prior to the date of departure of the consignment in that Member State or zone thereof, and: (2) either [II.2.8.4.1. the serological test has been carried out on samples collected at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.4.2. the serological test has been carried out on samples collected at least 30 days prior to the date of the departure of the consignment and the animals have been subjected to a PCR test, with negative results, carried out on samples collected not earlier than 14 days prior to the date of departure of the consignment;]]] (2) and/or [II.2.8. They originate from a Member State or a zone thereof neither free from infection with bluetongue virus (serotypes 1-24) nor covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled, and: (2) either [II.2.8.1. have been protected against attacks by vectors during transportation to the place of destination and have been kept protected against attacks by vectors in a vector protected establishment: (2) either [II.2.8.1.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.1.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [II.2.8.1.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of the commencement of the period of protection against attacks by vectors;]]] (2) and/or [II.2.8.2. have been kept for the last 60 days prior to the date of departure of the consignment in an establishment situated in a Member State or within an area of at least 150 km radius centred on the establishment, where surveillance in compliance with the requirements set out in Part II, Chapter 1, Sections 1 and 2, of Annex V to Delegated Regulation (EU) 2020/689 has been carried out during that period, and: (2) either [II.2.8.2.1. the animals have been vaccinated against all serotypes 1-24 of infection with bluetongue virus which were reported during the last 2 years prior to the date of departure of the consignment within an area of at least 150 km radius centred on the place where the animals were kept and are within the immunity period guaranteed in the specifications of the vaccine and: (2) either [II.2.8.2.1.1. have been vaccinated more than 60 days prior to the date of departure of the consignment;]]] (2) and/or [II.2.8.2.1.2. have been vaccinated with an inactivated vaccine and subjected to a PCR test, with negative results, carried out on samples collected at least 14 days after the date of the onset of the immunity set in the specifications of the vaccine;]]]] (2) and/or [II.2.8.2.2. the animals have been immunised against all serotypes 1-24 of infection with bluetongue virus which were reported during the last 2 years prior to the date of departure of the consignment within an area of at least 150 km radius centred on the place where the animals were kept, and: (2) either [II.2.8.2.2.1. the animals have been subjected with positive results to a serological test carried out on samples collected at least 60 days prior to the date of departure of the consignment.]]] (2) and/or [II.2.8.2.2.2. the animals have been subjected with positive results to a serological test carried out on samples collected at least 30 days prior to the date of departure of the consignment and to a PCR test, with negative results, carried out on samples collected not earlier than 14 days prior to the date of departure of the consignment.]]]] (2) and/or [II.2.8. They do not fulfil the requirements laid down in Part II, Chapter 2, Section 1, points 1 to 3, of Annex V to Delegated Regulation (EU) 2020/689 and the competent authority of the Member State of origin authorised movement of those animals to another Member State or zone thereof: (2) either [II.2.8.1. with the status free from infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised subject to the conditions referred to in Article 43(2), points (a), (b) and (c), of Delegated Regulation (EU) 2020/689, and: (2) either [II.2.8.1.1. Part II, Chapter 2, Section 1, point 5, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.1.2. Part II, Chapter 2, Section 1, point 6, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.1.3. Part II, Chapter 2, Section 1, point 7, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.1.4. Part II, Chapter 2, Section 1, point 8, of Annex V to that Delegated Regulation, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled;]]] (2) and/or [II.2.8.2. with an approved eradication program for infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised subject to the conditions referred to in Article 43(2), points (a), (b) and (c), of Delegated Regulation (EU) 2020/689 and: (2) either [II.2.8.2.1. Part II, Chapter 2, Section 1, point 5, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.2. Part II, Chapter 2, Section 1, point 6, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.3. Part II, Chapter 2, Section 1, point 7, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.4. Part II, Chapter 2, Section 1, point 8, of Annex V to that Delegated Regulation, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled;]]] (2) and/or [II.2.8.3. neither free from infection with bluetongue virus (serotypes 1-24) nor covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised: (2) either [II.2.8.3.1. without any conditions, and: (2) and/or [II.2.8.3.2. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 5, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.3. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 6, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.4. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 7, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.5. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 8, of Annex V to Delegated Regulation (EU) 2020/689, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled.]]] II.2.9. With regard to chronic wasting disease (CWD), they (2) either [II.2.9.1. are moved from a Member State other than a Member State listed in Chapter A, Section C, point 1.1, of Annex VIII to Regulation (EC) 999/2001 of the European Parliament and of the Council.] (2) or [II.2.9.2. are semi-domesticated reindeer moved from Norway to an area in Finland listed in Chapter A, Section C, point 1.2(a), of Annex VIII to Regulation (EC) 999/2001 for seasonal grazing in Finland.] (2) or [II.2.9.3. are semi-domesticated reindeer moved from Norway to an area in Sweden listed in Chapter A, Section C, point 1.2(b), of Annex VIII to Regulation (EC) 999/2001 after seasonal grazing in Norway, or after having taken part in sporting or cultural events in Norway, or for seasonal grazing in Sweden, or for sporting or cultural events in Sweden, and the competent authority of Sweden has given its prior written consent to such movement.] (2) or [II.2.9.4. are semi-domesticated reindeer which have grazed in Norway in the area located between the Norwegian-Finnish border, and the Norwegian-Finnish Reindeer Fence and are returning to Finland.] (2) or [II.2.9.5. are moved from an area in Norway to another area in Norway with a transit through Sweden or Finland, and the competent authority of Sweden or Finland has given its prior written consent to such transit.] (2) or [II.2.9.6. are moved from an area in Sweden listed in Chapter A, Section C, point 1.2(b), of Annex VIII to Regulation (EC) 999/2001 to Norway, and the competent authority of Norway has given its prior written consent to such movement.] (2) or [II.2.9.7. are forest reindeer moved from an area in Sweden listed in Chapter A, Section C, point 1.2(b), of Annex VIII to Regulation (EC) 999/2001 to Finland, and the competent authority of Finland has given its prior written consent to such movement.] (2) or [II.2.9.8. are moved from an area in a Member State listed in Chapter A, Section C, point 1.1, of Annex VIII to Regulation (EC) 999/2001, other than an area listed in Chapter A, Section C, point 1.2, of Annex VIII to that Regulation, to another Member State listed in Chapter A, Section C, point 1.1, of Annex VIII to that Regulation, or to Norway, and the competent authority of destination has given its prior written consent to such movement.] (2) or [II.2.9.9. are moved from a confined establishment, as defined in Article 4, point (48), of Regulation (EU) 2016/429 of the European Parliament and of the Council, in a Member State listed in Chapter A, Section C, point 1.1, of Annex VIII to Regulation (EC) 999/2001, to a confined establishment in another Member State, and the competent authority of the Member State of destination has given its prior written consent to such movement.] (2) [II.2.10. They are moved to a Member State or zone thereof with the status free from infectious bovine rhinotracheitis/infectious pustular vulvovaginitis or with an approved eradication programme for infectious bovine rhinotracheitis/infectious pustular vulvovaginitis in bovine animals and they come from an establishment in which infectious bovine rhinotracheitis/infectious pustular vulvovaginitis in cervid animals has not been reported during the last 30 days prior to the date of departure of the consignment.] II.3. To the best of my knowledge and as declared by the operator, the animals come from establishments where there were no abnormal mortalities with an undetermined cause. II.4. Arrangements are made to transport the consignment in accordance with Article 4 of Delegated Regulation (EU) 2020/688. II.5. This animal health certificate is valid for 10 days from the date of issuing. In the case of transport by waterway/sea of animals, the period of validity of the certificate may be extended by the duration of the journey by waterway/sea. (2) (6) [II.6. Since the date of departure from their establishments of origin and prior to the date of arrival to this establishment approved for assembly operations, none of the animals of the consignment has undergone more than two assembly operations, and (2) either [they come from their establishments of origin.]] (2) or [at least one of the animals of the consignment has undergone one assembly operation in an approved establishment.]] (2) or [at least one of the animals of the consignment has undergone two assembly operations in the approved establishments.]] Animal welfare attestation At the time of inspection, the animals covered by this animal health certificate were fit to be transported in accordance with the provisions of Council Regulation (EC) No 1/2005 on the intended journey due to start on … (insert date). Notes: In accordance with the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union and the European Atomic Energy Community, and in particular Article 5(4) of the Windsor Framework (see Joint Declaration No 1/2023 of the Union and the United Kingdom in the Joint Committee established by the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union and the European Atomic Energy Community of 24 March 2023, OJ L 102, 17.4.2023, p. 87) in conjunction with Annex 2 to that Framework, references to the Union in this animal health certificate include the United Kingdom in respect of Northern Ireland. This animal health certificate shall be completed in accordance with the notes for the completion of certificates provided for in Chapter 2 of Annex I to Commission Implementing Regulation (EU) 2020/2235. Part I: Box reference I.11 : “Place of dispatch”: Indicate an establishment of the origin of the animals in the consignment or an establishment approved for assembly operations in accordance with Articles 97 and 99 of Regulation (EU) 2016/429. Box reference I.12 : “Place of destination”: Indicate an establishment of the final destination of the consignment or an establishment approved for assembly operations in accordance with Articles 97 and 99 of Regulation (EU) 2016/429. Box reference I.17 : “Accompanying documents”: In case the animals are dispatched from an establishment approved for assembly operations in the Member State of origin, the reference number(s) of the official document(s), based on which the animal health certificate for this consignment is issued in this establishment approved for assembly operations, may be indicated. In case the animals are dispatched from an establishment approved for assembly operations in the Member State of passage, the reference number(s) of the certificate(s), based on which the animal health certificate for this consignment is issued in this establishment approved for assembly operations, shall be indicated. Box reference I.30 : “Identification number”: Indicate identification codes of the animals in the consignment identified in accordance with Article 73 or 74 of Delegated Regulation (EU) 2019/2035. Part II: (1) There may be one or more animals in the consignment. (2) Delete if not applicable. (3) Insert the name of the disease(s). (4) Insert the specific reference to the article(s), title, and number of the relevant legal act(s) adopted by the Commission providing for those requirements. (5) Insert the specific attestation(s) provided for in and required by the relevant legal act(s) adopted by the Commission, as referred to in Article 126(1), points (b)(ii) and (iii), of Regulation (EU) 2016/429. (6) Applicable in case the consignment is dispatched from the establishment approved for assembly operations.
Official veterinarian Official veterinarian Official veterinarian Official veterinarian Name (in capital letters) Qualification and title Local Control Unit name Local Control Unit code Date Stamp Signature’
;
- (5) Chapter 13 is replaced by the following:
‘CHAPTER 13
MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF KEPT UNGULATES OTHER THAN BOVINE, OVINE, CAPRINE, PORCINE, EQUINE, CAMELID AND CERVID ANIMALS NOT INTENDED FOR SLAUGHTER (MODEL “OTHER-UNGULATES-INTRA-X”)
Part I: Description of consignment
EUROPEAN UNION INTRA
I.1 Consignor I.2 IMSOC reference Name I.2a Local reference Address I.3 Central Competent Authority QR CODE Address I.3 Central Competent Authority Country ISO country code I.4 Local Competent Authority I.5 Consignee I.6 Operator conducting assembly operations independently of an establishment Operator conducting assembly operations independently of an establishment Operator conducting assembly operations independently of an establishment Name Name Name Registration No Address Address Address Country ISO country code Country Country ISO country code I.7 Country of origin ISO country code I.9 Country of destination Country of destination ISO country code I.8 Region of origin Code I.10 Region of destination Region of destination Code I.11 Place of dispatch I.12 Place of destination Place of destination Name Registration/Approval No Name Name Registration/Approval No Address Address Address Country ISO country code Country Country ISO country code I.13 Place of loading Place of loading I.14 Date and time of departure Date and time of departure Date and time of departure
I.15 Means of transport I.16 Transporter Transporter ☐ Vessel ☐ Aircraft Name Registration/Authorisation No ☐ Vessel ☐ Aircraft Address ☐ Railway ☐ Road vehicle Country ISO country code ☐ Railway ☐ Road vehicle I.17 Accompanying documents Accompanying documents Identification ☐ Other Type Code Document Document Country ISO country code Document Document Commercial document reference
I.18 Transport conditions ☐ Ambient ☐ Chilled ☐ Frozen I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container No Container No Seal No
I.20 Certified as or for Certified as or for Certified as or for Certified as or for ☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Germinal products ☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Event or activity near borders ☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Quarantine or similar establishment ☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Other
I.21 ☐ For transit through a third country ☐ For transit through a third country Third country ISO country code Exit point BCP code Entry point BCP code
I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export Member State ISO country code Third country ISO country code Member State ISO country code Exit point BCP code Member State ISO country code
I.24 Estimated journey time I.25 Journey log ☐ yes ☐ no I.26 Total number of packages I.27 Total quantity Total quantity Total quantity I.28 Total net weight/gross weight (kg) I.29 Total space foreseen for the consignment Total space foreseen for the consignment Total space foreseen for the consignment
I.30 Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment CN code CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity Type Region of origin Region of origin Cold store Identification mark Type of packaging Net weight Slaughterhouse Slaughterhouse Treatment type Nature of commodity Number of packages Batch No Date of collection/production Manufacturing plant Approval or registration number of plant/establishment/centre Test
Part II: Certification
EUROPEAN UNION EUROPEAN UNION Certificate model OTHER-UNGULATES-INTRA-X Certificate model OTHER-UNGULATES-INTRA-X Certificate model OTHER-UNGULATES-INTRA-X Certificate model OTHER-UNGULATES-INTRA-X II. Health information II.a Certificate reference II.b IMSOC reference
I, the undersigned official veterinarian, hereby certify that: II.1. The animals (1) of the consignment described in Part I are kept ungulates other than bovine, ovine, caprine, porcine, equine, camelid and cervid animals and meet the following requirements: II.1.1. They are identified as provided for in Article 117 of Regulation (EU) 2016/429 of the European Parliament and of the Council. II.1.2. They, for at least 30 days prior to the date of departure of the consignment, or since birth, if they are younger than 30 days of age: II.1.2.1. have been continuously resident in the establishment of origin; II.1.2.2. have not been in contact with other kept ungulates of a lower health status or subject to movement restrictions for animal health reasons; II.1.2.3. have not been in direct or indirect contact with kept animals that have entered the Union from a third country or territory during the last 30 days prior to the date of departure of the consignment. II.1.3. They have not shown clinical signs or symptoms of diseases listed for ungulates of the species concerned during the clinical examination which was carried out, within 24 hours prior to the time of departure of the consignment, on … (insert date dd/mm/yyyy). II.2. According to official information, the animals described in Part I meet the following health requirements: II.2.1. (2) either [They come from establishments or zones not subject to movement restrictions affecting the species of animals to be moved and established for reasons of diseases listed for those species or diseases subject to emergency measures relevant for those species, and they have not been in contact with kept animals of a listed species of a lower health status for an adequate period.] (2) or [They come from establishments or zones subject to movement restrictions affecting the species of animals to be moved and established for … (3), but derogations from movement restrictions have been granted, and: (2) [they comply with the requirements set out in … (4);]] (2) [and in particular. they are … (5).]] II.2.2. They come from establishments in which anthrax in ungulates has not been reported during the last 15 days prior to the date of departure of the consignment. (2) [II.2.3. They come from establishments in which infection with Brucella abortus, B. melitensis and B. suis in kept animals of listed species has not been reported during the last 42 days prior to the date of departure of the consignment.] (2) [II.2.4. They come from establishments in which infection with Mycobacterium tuberculosis complex (M. bovis, M. caprae and M. tuberculosis) in kept animals of listed species has not been reported during the last 42 days prior to the date of departure of the consignment.] (2) [II.2.5. They come from establishments in which infection with rabies virus in kept terrestrial animals has not been reported during the last 30 days prior to the date of departure of the consignment.] (2) [II.2.6. They come from establishments situated within an area of at least 150 km radius around those establishments in which infection with epizootic haemorrhagic disease virus: (2) either [has not been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment;] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals have been kept in a zone seasonally free from epizootic haemorrhagic disease in accordance with Parts 1 and 2 of Annex IX to Commission Delegated Regulation (EU) 2020/688: (2) either [for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of entry of the animals into the seasonally disease-free area;]] (2) and/or [for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of entry of the animals into the seasonally disease-free area;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals have been protected against attacks by vectors during transportation to the place of destination and they have been kept protected against attacks by vectors in a vector protected establishment fulfilling the requirements provided for in Part 3 of Annex IX to Delegated Regulation (EU) 2020/688: (2) either [for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of commencement of the period of protection against attacks by vectors;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals have been vaccinated against infection with epizootic haemorrhagic disease virus and the animals are within the immunity period guaranteed in the specifications of the vaccine and: (2) either [they have been vaccinated at least 60 days prior to the date of departure of the consignment;]] (2) and/or [they have been vaccinated with an inactivated vaccine and have been subject to a PCR test, with negative results on samples collected at least 14 days after the onset of the immunity set in the specifications of the vaccine;]] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the Member State of destination has informed the Commission and the other Member States that such movement is authorised;] (2) and/or [has been reported in kept animals of listed species for that disease during the last 2 years prior to the date of departure of the consignment and the animals comply with specific risk-mitigating measures defined by the competent authority of the Member State of destination and the Member State of destination has informed the Commission and the other Member States that such movement is authorised;] (2) and [the requirements laid down in Article 29(1), third subparagraph, of Delegated Regulation (EU) 2020/688 are fulfilled.] (2) [II.2.7. They come from establishments in which surra (Trypanosoma evansi) has not been reported during the last 30 days prior to the date of departure of the consignment, and (2) either [surra has not been reported in the establishments during the last 2 years prior to the date of departure of the consignment.]] (2) or [surra has been reported during the last 2 years prior to departure of the consignment, and following the date of the last outbreak, the affected establishments have remained under movement restrictions until the date on which the infected animals have been removed from the establishments, and the remaining animals in the establishments have been subjected to a test for surra with one of the diagnostic methods provided for in Part 3 of Annex I to Delegated Regulation (EU) 2020/688, carried out, with negative results, on samples taken at least 6 months following the date on which the infected animals have been removed from the establishments.]] (2) either [II.2.8. They originate from a Member State or a zone thereof free from infection with bluetongue virus (serotypes 1-24), where no case of infection with bluetongue virus (serotypes 1-24) has been confirmed in the targeted animal population during the last 24 months prior to the date of departure of the consignment and have not been vaccinated with a live vaccine against infection with bluetongue virus (serotypes 1-24) during the last 60 days prior to the date of departure of the consignment and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled.] (2) and/or [II.2.8. They originate from a Member State or a zone thereof covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled, and: (2) either [II.2.8.1. have been kept in a Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24) in accordance with Article 40(3) of Commission Delegated Regulation (EU) 2020/689: (2) either [II.2.8.1.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.1.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of entry of the animals into the Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24);]] (2) and/or [II.2.8.1.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of entry of the animals into the Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24);]]] (2) and/or [II.2.8.2. have been protected against attacks by vectors during transportation to the place of destination and have been kept protected against attacks by vectors in a vector protected establishment: (2) either [II.2.8.2.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.2.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [II.2.8.2.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of the commencement of the period of protection against attacks by vectors;]]] (2) and/or [II.2.8.3. have been vaccinated against all serotypes 1-24 of infection with bluetongue virus which were reported in that Member State or zone thereof during the last 2 years prior to the date of departure of the consignment and are within the immunity period guaranteed in the specifications of the vaccine, and: (2) either [II.2.8.3.1. have been vaccinated more than 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.3.2. have been vaccinated with an inactivated vaccine and subjected to a PCR test, with negative results, carried out on samples collected at least 14 days after the date of the onset of the immunity set in the specifications of the vaccine;]]] (2) and/or [II.2.8.4. have been subjected with positive results to a serological test able to detect specific antibodies against all serotypes 1-24 of infection with bluetongue virus reported in that Member State or zone thereof during the last 2 years prior to the date of departure of the consignment, and: (2) either [II.2.8.4.1. the serological test has been carried out on samples collected at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.4.2. the serological test has been carried out on samples collected at least 30 days prior to the date of the departure of the consignment and the animals have been subjected to a PCR test, with negative results, carried out on samples collected not earlier than 14 days prior to the date of departure of the consignment;]]] (2) and/or [II.2.8. They originate from a Member State or a zone thereof neither free from infection with bluetongue virus (serotypes 1-24) nor covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 are fulfilled, and they: (2) either [II.2.8.1. have been protected against attacks by vectors during transportation to the place of destination and have been kept protected against attacks by vectors in a vector protected establishment: (2) either [II.2.8.1.1. for at least 60 days prior to the date of departure of the consignment;]] (2) and/or [II.2.8.1.2. for at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]] (2) and/or [II.2.8.1.3. for at least 14 days prior to the date of departure of the consignment and have been subjected to a PCR test, with negative results, carried out on samples collected at least 14 days following the date of the commencement of the period of protection against attacks by vectors;]]] (2) and/or [II.2.8.2. have been kept for the last 60 days prior to the date of departure of the consignment in an establishment situated in a Member State or within an area of at least 150 km radius centred on the establishment, where surveillance in compliance with the requirements set out in Part II, Chapter 1, Sections 1 and 2, of Annex V to Delegated Regulation (EU) 2020/689 has been carried out during that period, and: (2) either [II.2.8.2.1. the animals have been vaccinated against all serotypes 1-24 of infection with bluetongue virus which were reported during the last 2 years prior to the date of departure of the consignment in an area of at least 150 km radius centred on the place where the animals were kept and are within the immunity period guaranteed in the specifications of the vaccine, and: (2) either [II.2.8.2.1.1. have been vaccinated more than 60 days prior to the date of departure of the consignment;]]] (2) and/or [II.2.8.2.1.2. have been vaccinated with an inactivated vaccine and subjected to a PCR test, with negative results, carried out on samples collected at least 14 days after the date of the onset of the immunity set in the specifications of the vaccine;]]]] (2) and/or [II.2.8.2.2. the animals have been immunised against all serotypes 1-24 of infection with bluetongue virus which were reported during the last 2 years prior to the date of departure of the consignment within an area of at least 150 km radius centred on the place where the animals were kept, and: (2) either [II.2.8.2.2.1. the animals have been subjected with positive results to a serological test carried out on samples collected at least 60 days prior to the date of departure of the consignment;]]] (2) and/or [II.2.8.2.2.2. the animals have been subjected with positive results to a serological test carried out on samples collected at least 30 days prior to the date of the movement and to a PCR test, with negative results, carried out on samples collected not earlier than 14 days prior to the date of departure of the consignment;]]]] (2) and/or [II.2.8. They do not fulfil the requirements laid down in Part II, Chapter 2, Section 1, points 1 to 3, of Annex V to Delegated Regulation (EU) 2020/689 and the competent authority of the Member State of origin authorised movement of those animals to another Member State or zone thereof: (2) either [II.2.8.1. with the status free from infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised subject to the conditions referred to in Article 43(2), points (a), (b) and (c), of Delegated Regulation (EU) 2020/689, and: (2) either [II.2.8.1.1. Part II, Chapter 2, Section 1, point 5, of Annex V to that Regulation, and (2) and/or [II.2.8.1.2. Part II, Chapter 2, Section 1, point 6, of Annex V to that Regulation, and (2) and/or [II.2.8.1.3. Part II, Chapter 2, Section 1, point 7, of Annex V to that Regulation, and (2) and/or [II.2.8.1.4. Part II, Chapter 2, Section 1, point 8, of Annex V to that Regulation, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled;]]] (2) and/or [II.2.8.2. with an approved eradication programme for infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised subject to the conditions referred to in Article 43(2), points (a), (b) and (c), of Delegated Regulation (EU) 2020/689, and: (2) either [II.2.8.2.1. Part II, Chapter 2, Section 1, point 5, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.2. Part II, Chapter 2, Section 1, point 6, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.3. Part II, Chapter 2, Section 1, point 7, of Annex V to that Delegated Regulation, and (2) and/or [II.2.8.2.4. Part II, Chapter 2, Section 1, point 8, of Annex V to that Delegated Regulation, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled;]]] (2) and/or [II.2.8.3. neither free from infection with bluetongue virus (serotypes 1-24) nor covered by the eradication programme for infection with bluetongue virus (serotypes 1-24) and the Member State of destination has informed the Commission and the other Member States that such movement is authorised: (2) either [II.2.8.3.1. without any conditions, and (2) and/or [II.2.8.3.2. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 5, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.3. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 6, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.4. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 7, of Annex V to Delegated Regulation (EU) 2020/689, and (2) and/or [II.2.8.3.5. subject to the conditions referred to in Part II, Chapter 2, Section 1, point 8, of Annex V to Delegated Regulation (EU) 2020/689, and the requirements laid down in Article 32(1), point (a), (b) or (c), or Article 32(2) of Delegated Regulation (EU) 2020/688 and the requirements laid down in Article 33 of that Delegated Regulation are fulfilled.]]]] II.3. To the best of my knowledge and as declared by the operator, the animals come from establishments where there were no abnormal mortalities with an undetermined cause. II.4. Arrangements are made to transport the consignment in accordance with Article 4 of Delegated Regulation (EU) 2020/688. II.5. This animal health certificate is valid for 10 days from the date of issuing. In the case of transport by waterway/sea of animals, the period of validity of the certificate may be extended by the duration of the journey by waterway/sea. (2)(6) [II.6. Since the date of departure from their establishments of origin and prior to the date of arrival to this establishment approved for assembly operations, none of the animals of the consignment has undergone more than two assembly operations, and (2) either [they come from their establishments of origin.]] (2) or [at least one of the animals of the consignment has undergone one assembly operation in an approved establishment.]] (2) or [at least one of the animals of the consignment has undergone two assembly operations in the approved establishments.]] Animal welfare attestation At the time of inspection, the animals covered by this animal health certificate were fit to be transported in accordance with the provisions of Council Regulation (EC) No 1/2005 on the intended journey due to start on … (insert date). Notes In accordance with the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union and the European Atomic Energy Community, and in particular Article 5(4) of the Windsor Framework (see Joint Declaration No 1/2023 of the Union and the United Kingdom in the Joint Committee established by the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union and the European Atomic Energy Community of 24 March 2023, OJ L 102, 17.4.2023, p. 87) in conjunction with Annex 2 to that Framework, references to the Union in this animal health certificate include the United Kingdom in respect of Northern Ireland. This animal health certificate shall be completed in accordance with the notes for the completion of certificates provided for in Chapter 2 of Annex I to Commission Implementing Regulation (EU) 2020/2235. Part I: Box reference I.11 : “Place of dispatch”: Indicate an establishment of the origin of the animals in the consignment or an establishment approved for assembly operations in accordance with Articles 97 and 99 of Regulation (EU) 2016/429. Box reference I.12 : “Place of destination”: Indicate an establishment of the final destination of the consignment or an establishment approved for assembly operations in accordance with Articles 97 and 99 of Regulation (EU) 2016/429. Box reference I.17 : “Accompanying documents”: In case the animals are dispatched from an establishment approved for assembly operations in the Member State of origin, the reference number(s) of the official document(s), based on which the animal health certificate for this consignment is issued in this establishment approved for assembly operations, may be indicated. In case the animals are dispatched from an establishment approved for assembly operations in the Member State of passage, the reference number(s) of the certificate(s), based on which the animal health certificate for this consignment is issued in this establishment approved for assembly operations, shall be indicated. Box reference I.30 : “Identification number”: Indicate identification number of each animal. Part II: (1) There may be one or more animals in the consignment. (2) Delete if not applicable. (3) Insert the name of the disease(s). (4) Insert the specific reference to the article(s), title, and number of the relevant legal act(s) adopted by the Commission providing for those requirements. (5) Insert the specific attestation(s) provided for in and required by the relevant legal act(s) adopted by the Commission, as referred to in Article 126(1), points (b)(ii) and (iii), of Regulation (EU) 2016/429. (6) Applicable in case the consignment is dispatched from the establishment approved for assembly operations.
Official veterinarian Official veterinarian Official veterinarian Official veterinarian Name (in capital letters) Qualification and title Local Control Unit name Local Control Unit code Date Stamp Signature’
;
- (6) Chapter 30 is replaced by the following:
‘CHAPTER 30
MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF CONSIGNMENTS OF SEMEN OF OVINE AND CAPRINE ANIMALS COLLECTED, PROCESSED AND STORED IN ACCORDANCE WITH REGULATION (EU) 2016/429 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL AND COMMISSION DELEGATED REGULATION (EU) 2020/686 AFTER 20 APRIL 2021, DISPATCHED FROM THE SEMEN COLLECTION CENTRE WHERE THE SEMEN WAS COLLECTED (MODEL “OV/CAP-SEM-A-INTRA”)
Part I: Description of consignment
EUROPEAN UNION INTRA
I.1 Consignor I.2 IMSOC reference Name I.2a Local reference Address I.3 Central Competent Authority QR CODE Address I.3 Central Competent Authority Country ISO country code I.4 Local Competent Authority I.5 Consignee I.6 Operator conducting assembly operations independently of an establishment Operator conducting assembly operations independently of an establishment Operator conducting assembly operations independently of an establishment Name Name Name Registration No Address Address Address Country ISO country code Country Country ISO country code I.7 Country of origin ISO country code I.9 Country of destination Country of destination ISO country code I.8 Region of origin Code I.10 Region of destination Region of destination Code I.11 Place of dispatch I.12 Place of destination Place of destination Name Registration/Approval No Name Name Registration/Approval No Address Address Address Country ISO country code Country Country ISO country code I.13 Place of loading Place of loading I.14 Date and time of departure Date and time of departure Date and time of departure
I.15 Means of transport I.16 Transporter Transporter ☐ Vessel ☐ Aircraft Name Registration/Authorisation No ☐ Vessel ☐ Aircraft Address ☐ Railway ☐ Road vehicle Country ISO country code ☐ Railway ☐ Road vehicle I.17 Accompanying documents Accompanying documents Identification ☐ Other Type Code Document Document Country ISO country code Document Document Commercial document reference
I.18 Transport conditions ☐ Ambient ☐ Chilled ☐ Frozen I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container No Container No Seal No
I.20 Certified as or for Certified as or for Certified as or for Certified as or for ☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Germinal products ☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Event or activity near borders ☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Quarantine or similar establishment ☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Other
I.21 ☐ For transit through a third country ☐ For transit through a third country Third country ISO country code Exit point BCP code Entry point BCP code
I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export Member State ISO country code Third country ISO country code Member State ISO country code Exit point BCP code Member State ISO country code
I.24 Estimated journey time I.25 Journey log ☐ yes ☐ no I.26 Total number of packages I.27 Total quantity Total quantity Total quantity I.28 Total net weight/gross weight (kg) I.29 Total space foreseen for the consignment Total space foreseen for the consignment Total space foreseen for the consignment
I.30 Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment Description of consignment CN code CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity Type Region of origin Region of origin Cold store Identification mark Type of packaging Net weight Slaughterhouse Slaughterhouse Treatment type Nature of commodity Number of packages Batch No Date of collection/production Manufacturing plant Approval or registration number of plant/establishment/centre Test
Part II: Certification
EUROPEAN UNION EUROPEAN UNION Certificate model OV/CAP-SEM-A-INTRA Certificate model OV/CAP-SEM-A-INTRA Certificate model OV/CAP-SEM-A-INTRA Certificate model OV/CAP-SEM-A-INTRA II. Health information II.a Certificate reference II.b IMSOC reference
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