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Commission Implementing Regulation (EU) 2026/1127 of 8 May 2026 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

Type Implementing Regulation

Publication 2026-08-07

State In force

Text As published

Department European Commission, SANTE

Source EUR-Lex

articles 2

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.

Reform history JSON API

I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of [ovine] ⁽¹⁾ [caprine] ⁽¹⁾ animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of [ovine] ⁽¹⁾ [caprine] ⁽¹⁾ animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I, as regards classical scrapie, ⁽¹⁾ either [were collected from animals which have been kept continuously since birth on a holding or holdings recognised as having a negligible or a controlled risk of classical scrapie in accordance with Chapter A, Section A, point 1, of Annex VIII to Regulation (EC) No 999/2001 of the European Parliament and of the Council.] ⁽¹⁾ or [were collected from animals which have been kept continuously for the last 3 years before the collection on a holding or holdings which have complied for the last 3 years before collection with the requirements laid down in Chapter A, Section A, points 1.3(a) to (f), of Annex VIII to Regulation (EC) No 999/2001.] ⁽¹⁾ or [were collected from animals which have been kept continuously since birth in a Member State or zone of a Member State listed in Chapter A, Section A, point 2.3, of Annex VIII to Regulation (EC) No 999/2001 as having a negligible risk status for classical scrapie.] ⁽¹⁾ or [were collected from ovine animals carrying at least one ARR allele.] ^{(1) (3)} or [were collected from caprine animals carrying at least one of the K222, D146 or S146 alleles.] II.3. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor ovine and caprine animals laid down in Articles 15 to 17, Article 22, Articles 24 and 25, and in Part 3, Chapter II, and Part 5, Chapters I to III, of Annex II to Delegated Regulation (EU) 2020/686. (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (4)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting ovine and caprine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes or embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting ovine and caprine animals and established for … ⁽⁵⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁶⁾;]] ⁽¹⁾ [and, in particular, they are … ⁽⁷⁾;]] ^{(1) (8)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (9)} [II.4. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and storage, or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex X to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 3, Chapter I, and Part 5, Chapters II and III, of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (10)} [II.5. The following antibiotic or mixture of antibiotics ⁽¹¹⁾ has been added to the collection, processing, washing or storage media: …] 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 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Species”: Select amongst “Ovis aries” or “Capra hircus” as appropriate. “Identification number”: Indicate the identification number of each donor animal. “Identification mark”: Indicate the mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: Indicate the date on which the oocytes or embryos of the consignment were collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection or production team by which the the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate the number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b,) of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Alternative applicable from 14 April 2024. ⁽⁴⁾ Applicable for frozen oocytes or embryos. ⁽⁵⁾ Insert the name of the disease(s). ⁽⁶⁾ 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. ⁽⁷⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁸⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of ovine or caprine animals are placed and transported in one container. ⁽⁹⁾ Does not apply to oocytes. ⁽¹⁰⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹¹⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.


I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of [ovine] ⁽¹⁾ [caprine] ⁽¹⁾ animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of [ovine] ⁽¹⁾ [caprine] ⁽¹⁾ animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I, as regards classical scrapie, ⁽¹⁾ either [were collected from animals which have been kept continuously since birth on a holding or holdings recognised as having a negligible or a controlled risk of classical scrapie in accordance with Chapter A, Section A, point 1, of Annex VIII to Regulation (EC) No 999/2001 of the European Parliament and of the Council.] ⁽¹⁾ or [were collected from animals which have been kept continuously for the last 3 years before the collection on a holding or holdings which have complied for the last 3 years before collection with the requirements laid down in Chapter A, Section A, points 1.3(a) to (f), of Annex VIII to Regulation (EC) No 999/2001.] ⁽¹⁾ or [were collected from animals which have been kept continuously since birth in a Member State or zone of a Member State listed in Chapter A, Section A, point 2.3, of Annex VIII to Regulation (EC) No 999/2001 as having a negligible risk status for classical scrapie.] ⁽¹⁾ or [were collected from ovine animals carrying at least one ARR allele.] ^{(1) (3)} or [were collected from caprine animals carrying at least one of the K222, D146 or S146 alleles.] II.3. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor ovine and caprine animals laid down in Articles 15 to 17, Article 22, Articles 24 and 25, and in Part 3, Chapter II, and Part 5, Chapters I to III, of Annex II to Delegated Regulation (EU) 2020/686. (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (4)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting ovine and caprine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes or embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting ovine and caprine animals and established for … ⁽⁵⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁶⁾;]] ⁽¹⁾ [and, in particular, they are … ⁽⁷⁾;]] ^{(1) (8)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (9)} [II.4. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and storage, or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex X to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 3, Chapter I, and Part 5, Chapters II and III, of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (10)} [II.5. The following antibiotic or mixture of antibiotics ⁽¹¹⁾ has been added to the collection, processing, washing or storage media: …] 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 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Species”: Select amongst “Ovis aries” or “Capra hircus” as appropriate. “Identification number”: Indicate the identification number of each donor animal. “Identification mark”: Indicate the mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: Indicate the date on which the oocytes or embryos of the consignment were collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection or production team by which the the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate the number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b,) of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Alternative applicable from 14 April 2024. ⁽⁴⁾ Applicable for frozen oocytes or embryos. ⁽⁵⁾ Insert the name of the disease(s). ⁽⁶⁾ 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. ⁽⁷⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁸⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of ovine or caprine animals are placed and transported in one container. ⁽⁹⁾ Does not apply to oocytes. ⁽¹⁰⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹¹⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.

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’


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’

(8) Chapter 38 is replaced by the following:

‘CHAPTER 38

MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF CONSIGNMENTS OF SEMEN OF PORCINE 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 “POR-SEM-A-INTRA”)

Part I: Description of consignment

EUROPEAN UNION INTRA


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.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 ☐ Ambient ☐ Chilled ☐ Frozen

I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number

Container No Container No Seal No Seal No


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	☐ Ambient	☐ Chilled	☐ Frozen
I.19	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number
	Container No	Container No	Seal No	Seal No

I.20 Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for

☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Confined establishment ☐ Germinal products ☐ Germinal products

☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Exhibition ☐ Event or activity near borders ☐ Event or activity near borders

☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Ornamental aquaculture establishment

☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Technical use ☐ Quarantine or similar establishment ☐ Quarantine or similar establishment

☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Live aquatic animals for human consumption ☐ Other ☐ Other

I.21 ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country

Third country Third country ISO country code ISO country code ISO country code ISO country code

Exit point Exit point BCP code BCP code BCP code BCP code

Entry point Entry point BCP code BCP code BCP code BCP code

I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export ☐ For export

Member State ISO country code Third country ISO country code ISO country code

Member State ISO country code Exit point BCP code BCP code

Member State ISO country code

I.24 Estimated journey time Estimated journey time I.25 Journey log ☐ yes ☐ no

I.26 Total number of packages Total number of packages I.27 Total quantity Total quantity Total quantity

I.28 Total net weight/gross weight (kg) 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.20	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for
☐ Further keeping	☐ Further keeping	☐ Slaughter	☐ Confined establishment	☐ Confined establishment	☐ Germinal products	☐ Germinal products
☐ Registered equine animal	☐ Registered equine animal	☐ Travelling circus/animal act	☐ Exhibition	☐ Exhibition	☐ Event or activity near borders	☐ Event or activity near borders
☐ Release into the wild	☐ Release into the wild	☐ Dispatch centre	☐ Relaying area/purification centre	☐ Relaying area/purification centre	☐ Ornamental aquaculture establishment	☐ Ornamental aquaculture establishment
☐ Further processing	☐ Further processing	☐ Organic fertilizers and soil improvers	☐ Technical use	☐ Technical use	☐ Quarantine or similar establishment	☐ Quarantine or similar establishment
☐ Products for human consumption	☐ Products for human consumption	☐ Pollination	☐ Live aquatic animals for human consumption	☐ Live aquatic animals for human consumption	☐ Other	☐ Other
I.21	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country
	Third country	Third country	ISO country code	ISO country code	ISO country code	ISO country code
	Exit point	Exit point	BCP code	BCP code	BCP code	BCP code
	Entry point	Entry point	BCP code	BCP code	BCP code	BCP code
I.22	☐ For transit through Member State(s)	☐ For transit through Member State(s)	I.23	☐ For export	☐ For export	☐ For export
	Member State	ISO country code		Third country	ISO country code	ISO country code
	Member State	ISO country code		Exit point	BCP code	BCP code
	Member State	ISO country code
I.24	Estimated journey time	Estimated journey time	I.25	Journey log	☐ yes	☐ no
I.26	Total number of packages	Total number of packages	I.27	Total quantity	Total quantity	Total quantity
I.28	Total net weight/gross weight (kg)	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

CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity

Type

Region of origin Cold store Identification mark Type of packaging Net weight

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 POR-SEM-A-INTRA Certificate model POR-SEM-A-INTRA Certificate model POR-SEM-A-INTRA Certificate model POR-SEM-A-INTRA

II. Health information II.a Certificate reference II.b IMSOC reference

EUROPEAN UNION	EUROPEAN UNION	Certificate model POR-SEM-A-INTRA	Certificate model POR-SEM-A-INTRA	Certificate model POR-SEM-A-INTRA	Certificate model POR-SEM-A-INTRA
	II. Health information	II.a	Certificate reference	II.b	IMSOC reference

I, the undersigned official veterinarian, hereby certify that: II.1. The semen of porcine animals described in Part I: (a) has been collected, processed and stored, and dispatched from the semen collection centre ⁽¹⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for semen collection centres set out in Part 1 of Annex I to Commission Delegated Regulation (EU) 2020/686; ⁽²⁾ either [(b) is dispatched from the semen collection centre or a zone not subject to movement restrictions affecting porcine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to this semen because it was collected before the restrictions were established, and the semen has not been in contact with other semen of a lower health status for an adequate period;] ⁽²⁾ or [(b) is dispatched from the semen collection centre or a zone subject to movement restrictions affecting porcine animals and established for … ⁽³⁾, but derogations from movement restrictions have been granted, and ⁽²⁾ [it complies with the requirements set out in … ⁽⁴⁾;]] ⁽²⁾ [and in particular, it is … ⁽⁵⁾;]] (c) is intended for artificial reproduction and was obtained from donor animals which comply with the requirements for donor porcine animals laid down in Articles 15 to 19, Article 21, Articles 24 and 25, and Part 2, Chapter I, and in Part 5, Chapters I and IV, of Annex II to Delegated Regulation (EU) 2020/686; (d) has been collected, processed and stored in accordance with the requirements set out in Part 1, points 1 and 2, of Annex III to Delegated Regulation (EU) 2020/686; (e) is placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (f) is transported in a container which: (i) was sealed and numbered prior to the date of dispatch from the semen collection centre under the responsibility of the centre veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or a is single-use container; ^{(2) (6)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products.] ⁽²⁾ [II.2. Where an antibiotic or a mixture of antibiotics was added to the semen described in Part I: (a) the following antibiotic or mixture of antibiotics has been added to the semen after final dilution, or is contained in the used semen diluents: … ⁽⁷⁾; (b) immediately after the addition of the antibiotic(s), and before any possible freezing, the diluted semen was kept at a temperature of at least 15°C for not less than 45 minutes, or under a time-temperature regime with a documented equivalent bactericidal activity.] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 according to 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 the unique approval number and the name and address of the semen collection centre of dispatch of the consignment of semen. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of semen. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Semen. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the semen of the consignment is placed. “Date of collection/production”: Indicate the date on which the semen of the consignment was collected. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the semen collection centre where the semen of the consignment was collected. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Only semen collection centres approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁶⁾ Applicable for frozen semen. ⁽⁷⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration or the commercial name of the semen diluent containing antibiotic(s).


I, the undersigned official veterinarian, hereby certify that: II.1. The semen of porcine animals described in Part I: (a) has been collected, processed and stored, and dispatched from the semen collection centre ⁽¹⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for semen collection centres set out in Part 1 of Annex I to Commission Delegated Regulation (EU) 2020/686; ⁽²⁾ either [(b) is dispatched from the semen collection centre or a zone not subject to movement restrictions affecting porcine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to this semen because it was collected before the restrictions were established, and the semen has not been in contact with other semen of a lower health status for an adequate period;] ⁽²⁾ or [(b) is dispatched from the semen collection centre or a zone subject to movement restrictions affecting porcine animals and established for … ⁽³⁾, but derogations from movement restrictions have been granted, and ⁽²⁾ [it complies with the requirements set out in … ⁽⁴⁾;]] ⁽²⁾ [and in particular, it is … ⁽⁵⁾;]] (c) is intended for artificial reproduction and was obtained from donor animals which comply with the requirements for donor porcine animals laid down in Articles 15 to 19, Article 21, Articles 24 and 25, and Part 2, Chapter I, and in Part 5, Chapters I and IV, of Annex II to Delegated Regulation (EU) 2020/686; (d) has been collected, processed and stored in accordance with the requirements set out in Part 1, points 1 and 2, of Annex III to Delegated Regulation (EU) 2020/686; (e) is placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (f) is transported in a container which: (i) was sealed and numbered prior to the date of dispatch from the semen collection centre under the responsibility of the centre veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or a is single-use container; ^{(2) (6)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products.] ⁽²⁾ [II.2. Where an antibiotic or a mixture of antibiotics was added to the semen described in Part I: (a) the following antibiotic or mixture of antibiotics has been added to the semen after final dilution, or is contained in the used semen diluents: … ⁽⁷⁾; (b) immediately after the addition of the antibiotic(s), and before any possible freezing, the diluted semen was kept at a temperature of at least 15°C for not less than 45 minutes, or under a time-temperature regime with a documented equivalent bactericidal activity.] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 according to 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 the unique approval number and the name and address of the semen collection centre of dispatch of the consignment of semen. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of semen. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Semen. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the semen of the consignment is placed. “Date of collection/production”: Indicate the date on which the semen of the consignment was collected. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the semen collection centre where the semen of the consignment was collected. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Only semen collection centres approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁶⁾ Applicable for frozen semen. ⁽⁷⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration or the commercial name of the semen diluent containing antibiotic(s).

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’


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’

(9) Chapter 40 is replaced by the following:

‘CHAPTER 40

MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF CONSIGNMENTS OF OOCYTES AND EMBRYOS OF PORCINE ANIMALS COLLECTED OR PRODUCED, 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 BY THE EMBRYO COLLECTION OR PRODUCTION TEAM BY WHICH THE OOCYTES OR EMBRYOS WERE COLLECTED OR PRODUCED

(MODEL “POR-OOCYTES-EMB-A-INTRA”)

Part I: Description of consignment

EUROPEAN UNION INTRA


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.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 ☐ Ambient ☐ Chilled ☐ Frozen

I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number

Container No Container No Seal No Seal No


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	☐ Ambient	☐ Chilled	☐ Frozen
I.19	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number
	Container No	Container No	Seal No	Seal No

I.20 Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for

☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Confined establishment ☐ Germinal products ☐ Germinal products

☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Exhibition ☐ Event or activity near borders ☐ Event or activity near borders

☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Ornamental aquaculture establishment

☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Technical use ☐ Quarantine or similar establishment ☐ Quarantine or similar establishment

☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Live aquatic animals for human consumption ☐ Other ☐ Other

I.21 ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country

Third country Third country ISO country code ISO country code ISO country code ISO country code

Exit point Exit point BCP code BCP code BCP code BCP code

Entry point Entry point BCP code BCP code BCP code BCP code

I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export ☐ For export

Member State ISO country code Third country ISO country code ISO country code

Member State ISO country code Exit point BCP code BCP code

Member State ISO country code

I.24 Estimated journey time Estimated journey time I.25 Journey log ☐ yes ☐ no

I.26 Total number of packages Total number of packages I.27 Total quantity Total quantity Total quantity

I.28 Total net weight/gross weight (kg) 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.20	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for
☐ Further keeping	☐ Further keeping	☐ Slaughter	☐ Confined establishment	☐ Confined establishment	☐ Germinal products	☐ Germinal products
☐ Registered equine animal	☐ Registered equine animal	☐ Travelling circus/animal act	☐ Exhibition	☐ Exhibition	☐ Event or activity near borders	☐ Event or activity near borders
☐ Release into the wild	☐ Release into the wild	☐ Dispatch centre	☐ Relaying area/purification centre	☐ Relaying area/purification centre	☐ Ornamental aquaculture establishment	☐ Ornamental aquaculture establishment
☐ Further processing	☐ Further processing	☐ Organic fertilizers and soil improvers	☐ Technical use	☐ Technical use	☐ Quarantine or similar establishment	☐ Quarantine or similar establishment
☐ Products for human consumption	☐ Products for human consumption	☐ Pollination	☐ Live aquatic animals for human consumption	☐ Live aquatic animals for human consumption	☐ Other	☐ Other
I.21	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country
	Third country	Third country	ISO country code	ISO country code	ISO country code	ISO country code
	Exit point	Exit point	BCP code	BCP code	BCP code	BCP code
	Entry point	Entry point	BCP code	BCP code	BCP code	BCP code
I.22	☐ For transit through Member State(s)	☐ For transit through Member State(s)	I.23	☐ For export	☐ For export	☐ For export
	Member State	ISO country code		Third country	ISO country code	ISO country code
	Member State	ISO country code		Exit point	BCP code	BCP code
	Member State	ISO country code
I.24	Estimated journey time	Estimated journey time	I.25	Journey log	☐ yes	☐ no
I.26	Total number of packages	Total number of packages	I.27	Total quantity	Total quantity	Total quantity
I.28	Total net weight/gross weight (kg)	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

CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity

Type

Region of origin Cold store Identification mark Type of packaging Net weight

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 POR-OOCYTES-EMB-A-INTRA Certificate model POR-OOCYTES-EMB-A-INTRA Certificate model POR-OOCYTES-EMB-A-INTRA Certificate model POR-OOCYTES-EMB-A-INTRA

II. Health information II.a Certificate reference II.b IMSOC reference

EUROPEAN UNION	EUROPEAN UNION	Certificate model POR-OOCYTES-EMB-A-INTRA	Certificate model POR-OOCYTES-EMB-A-INTRA	Certificate model POR-OOCYTES-EMB-A-INTRA	Certificate model POR-OOCYTES-EMB-A-INTRA
	II. Health information	II.a	Certificate reference	II.b	IMSOC reference

I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of porcine animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of porcine animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor porcine animals laid down in Articles 15 to 17, Article 21, Articles 24 and 25, and in Part 2, Chapter II, and Part 5, Chapters I and IV, of Annex II to Delegated Regulation (EU) 2020/686; (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (3)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting porcine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes and embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting porcine animals and established for … ⁽⁴⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁵⁾;]] ⁽¹⁾ [and in particular, they are … ⁽⁶⁾;]] ^{(1) (7)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (8)} [II.3. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and/or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex XI to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 2, Chapter I, of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (9)} [II.4. The following antibiotic or mixture of antibiotics ⁽¹⁰⁾ has been added to the collection, processing, washing or storage media: …] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: Indicate the date on which the oocytes or embryos of the consignment were collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection team or the embryo production team by which the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Applicable for frozen oocytes or embryos. ⁽⁴⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of porcine animals are placed and transported in one container. ⁽⁵⁾ Insert the name of the disease(s). ⁽⁶⁾ 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. ⁽⁷⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁸⁾ Does not apply to oocytes. ⁽⁹⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹⁰⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.


I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of porcine animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of porcine animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor porcine animals laid down in Articles 15 to 17, Article 21, Articles 24 and 25, and in Part 2, Chapter II, and Part 5, Chapters I and IV, of Annex II to Delegated Regulation (EU) 2020/686; (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (3)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting porcine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes and embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting porcine animals and established for … ⁽⁴⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁵⁾;]] ⁽¹⁾ [and in particular, they are … ⁽⁶⁾;]] ^{(1) (7)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (8)} [II.3. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and/or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex XI to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 2, Chapter I, of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (9)} [II.4. The following antibiotic or mixture of antibiotics ⁽¹⁰⁾ has been added to the collection, processing, washing or storage media: …] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: Indicate the date on which the oocytes or embryos of the consignment were collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection team or the embryo production team by which the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Applicable for frozen oocytes or embryos. ⁽⁴⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of porcine animals are placed and transported in one container. ⁽⁵⁾ Insert the name of the disease(s). ⁽⁶⁾ 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. ⁽⁷⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁸⁾ Does not apply to oocytes. ⁽⁹⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹⁰⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.

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’


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’

(10) Chapter 45 is replaced by the following:

‘CHAPTER 45

MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF CONSIGNMENTS OF SEMEN OF EQUINE 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 “EQUI-SEM-A-INTRA”)

Part I: Description of consignment

EUROPEAN UNION INTRA


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.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 ☐ Ambient ☐ Chilled ☐ Frozen

I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number

Container No Container No Seal No Seal No


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	☐ Ambient	☐ Chilled	☐ Frozen
I.19	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number
	Container No	Container No	Seal No	Seal No

I.20 Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for

☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Confined establishment ☐ Germinal products ☐ Germinal products

☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Exhibition ☐ Event or activity near borders ☐ Event or activity near borders

☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Ornamental aquaculture establishment

☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Technical use ☐ Quarantine or similar establishment ☐ Quarantine or similar establishment

☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Live aquatic animals for human consumption ☐ Other ☐ Other

I.21 ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country

Third country Third country ISO country code ISO country code ISO country code ISO country code

Exit point Exit point BCP code BCP code BCP code BCP code

Entry point Entry point BCP code BCP code BCP code BCP code

I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export ☐ For export

Member State ISO country code Third country ISO country code ISO country code

Member State ISO country code Exit point BCP code BCP code

Member State ISO country code

I.24 Estimated journey time Estimated journey time I.25 Journey log ☐ yes ☐ no

I.26 Total number of packages Total number of packages I.27 Total quantity Total quantity Total quantity

I.28 Total net weight/gross weight (kg) 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.20	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for
☐ Further keeping	☐ Further keeping	☐ Slaughter	☐ Confined establishment	☐ Confined establishment	☐ Germinal products	☐ Germinal products
☐ Registered equine animal	☐ Registered equine animal	☐ Travelling circus/animal act	☐ Exhibition	☐ Exhibition	☐ Event or activity near borders	☐ Event or activity near borders
☐ Release into the wild	☐ Release into the wild	☐ Dispatch centre	☐ Relaying area/purification centre	☐ Relaying area/purification centre	☐ Ornamental aquaculture establishment	☐ Ornamental aquaculture establishment
☐ Further processing	☐ Further processing	☐ Organic fertilizers and soil improvers	☐ Technical use	☐ Technical use	☐ Quarantine or similar establishment	☐ Quarantine or similar establishment
☐ Products for human consumption	☐ Products for human consumption	☐ Pollination	☐ Live aquatic animals for human consumption	☐ Live aquatic animals for human consumption	☐ Other	☐ Other
I.21	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country
	Third country	Third country	ISO country code	ISO country code	ISO country code	ISO country code
	Exit point	Exit point	BCP code	BCP code	BCP code	BCP code
	Entry point	Entry point	BCP code	BCP code	BCP code	BCP code
I.22	☐ For transit through Member State(s)	☐ For transit through Member State(s)	I.23	☐ For export	☐ For export	☐ For export
	Member State	ISO country code		Third country	ISO country code	ISO country code
	Member State	ISO country code		Exit point	BCP code	BCP code
	Member State	ISO country code
I.24	Estimated journey time	Estimated journey time	I.25	Journey log	☐ yes	☐ no
I.26	Total number of packages	Total number of packages	I.27	Total quantity	Total quantity	Total quantity
I.28	Total net weight/gross weight (kg)	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

CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity

Type

Region of origin Cold store Identification mark Type of packaging Net weight

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 EQUI-SEM-A-INTRA Certificate model EQUI-SEM-A-INTRA Certificate model EQUI-SEM-A-INTRA Certificate model EQUI-SEM-A-INTRA

II. Health information II.a Certificate reference II.b IMSOC reference

EUROPEAN UNION	EUROPEAN UNION	Certificate model EQUI-SEM-A-INTRA	Certificate model EQUI-SEM-A-INTRA	Certificate model EQUI-SEM-A-INTRA	Certificate model EQUI-SEM-A-INTRA
	II. Health information	II.a	Certificate reference	II.b	IMSOC reference

I, the undersigned official veterinarian, hereby certify that: II.1. The semen of equine animals described in Part I: (a) has been collected, processed and stored, and dispatched from the semen collection centre ⁽¹⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for semen collection centres set out in Part 1 of Annex I to Commission Delegated Regulation (EU) 2020/686; ⁽²⁾ either [(b) is dispatched from a semen collection centre or a zone not subject to movement restrictions affecting equine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to this semen because it was collected before the restrictions were established, and the semen has not been in contact with other semen of a lower health status for an adequate period;] ⁽²⁾ or [(b) is dispatched from a semen collection centre or a zone subject to movement restrictions affecting equine animals and established for … ⁽³⁾, but derogations from movement restrictions have been granted, and ⁽²⁾ [it complies with the requirements set out in … ⁽⁴⁾;]] ⁽²⁾ [and in particular, it is … ⁽⁵⁾;]] (c) is intended for artificial reproduction and was obtained from donor animals which comply with the requirements for donor equine animals laid down in Articles 15 to 19, Articles 23 and 24, and in Part 4, Chapter I, of Annex II to Delegated Regulation (EU) 2020/686; (d) has been collected, processed and stored in accordance with the requirements set out in Part 1, points 1 and 2, of Annex III to Delegated Regulation (EU) 2020/686; (e) is placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (f) is transported in a container which: (i) was sealed and numbered prior to the date of dispatch from the semen collection centre under the responsibility of the centre veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(2) (6)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products.] ^{(2) (7)} [II.2. Where an antibiotic or a mixture of antibiotics was added to the semen: (a) the following antibiotic or mixture of antibiotics has been added to the semen after final dilution, or is contained in the used semen diluents: … ⁽⁸⁾; (b) immediately after the addition of the antibiotic(s), and before any possible freezing, the diluted semen was kept at a temperature of at least 5°C for not less than 45 minutes, or under a time-temperature regime with a documented equivalent bactericidal activity.] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the semen collection centre of dispatch of the consignment of semen. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of semen. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Indicate semen. “Identification number”: Indicate the identification number of each donor animal. “Identification mark”: Indicate the mark on the straw or other packages where the semen of the consignment is placed. “Date of collection/production”: Indicate the date on which the semen of the consignment was collected. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the semen collection centre where the semen of the consignment was collected. “Quantity”: Indicate the number of straws or other packages with the same mark. Part II: ⁽¹⁾ Only semen collection centres approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁶⁾ Applicable for frozen semen. ⁽⁷⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽⁸⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration or the commercial name of the semen diluent containing antibiotic(s).


I, the undersigned official veterinarian, hereby certify that: II.1. The semen of equine animals described in Part I: (a) has been collected, processed and stored, and dispatched from the semen collection centre ⁽¹⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for semen collection centres set out in Part 1 of Annex I to Commission Delegated Regulation (EU) 2020/686; ⁽²⁾ either [(b) is dispatched from a semen collection centre or a zone not subject to movement restrictions affecting equine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species, or those restrictions do not apply to this semen because it was collected before the restrictions were established, and the semen has not been in contact with other semen of a lower health status for an adequate period;] ⁽²⁾ or [(b) is dispatched from a semen collection centre or a zone subject to movement restrictions affecting equine animals and established for … ⁽³⁾, but derogations from movement restrictions have been granted, and ⁽²⁾ [it complies with the requirements set out in … ⁽⁴⁾;]] ⁽²⁾ [and in particular, it is … ⁽⁵⁾;]] (c) is intended for artificial reproduction and was obtained from donor animals which comply with the requirements for donor equine animals laid down in Articles 15 to 19, Articles 23 and 24, and in Part 4, Chapter I, of Annex II to Delegated Regulation (EU) 2020/686; (d) has been collected, processed and stored in accordance with the requirements set out in Part 1, points 1 and 2, of Annex III to Delegated Regulation (EU) 2020/686; (e) is placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (f) is transported in a container which: (i) was sealed and numbered prior to the date of dispatch from the semen collection centre under the responsibility of the centre veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(2) (6)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products.] ^{(2) (7)} [II.2. Where an antibiotic or a mixture of antibiotics was added to the semen: (a) the following antibiotic or mixture of antibiotics has been added to the semen after final dilution, or is contained in the used semen diluents: … ⁽⁸⁾; (b) immediately after the addition of the antibiotic(s), and before any possible freezing, the diluted semen was kept at a temperature of at least 5°C for not less than 45 minutes, or under a time-temperature regime with a documented equivalent bactericidal activity.] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the semen collection centre of dispatch of the consignment of semen. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of semen. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Indicate semen. “Identification number”: Indicate the identification number of each donor animal. “Identification mark”: Indicate the mark on the straw or other packages where the semen of the consignment is placed. “Date of collection/production”: Indicate the date on which the semen of the consignment was collected. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the semen collection centre where the semen of the consignment was collected. “Quantity”: Indicate the number of straws or other packages with the same mark. Part II: ⁽¹⁾ Only semen collection centres approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁶⁾ Applicable for frozen semen. ⁽⁷⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽⁸⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration or the commercial name of the semen diluent containing antibiotic(s).

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’


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’

(11) Chapter 49 is replaced by the following:

‘CHAPTER 49

MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF CONSIGNMENTS OF OOCYTES AND EMBRYOS OF EQUINE ANIMALS COLLECTED OR PRODUCED, 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 BY THE EMBRYO COLLECTION OR PRODUCTION TEAM BY WHICH THE OOCYTES OR EMBRYOS WERE COLLECTED OR PRODUCED (MODEL “EQUI-OOCYTES-EMB-A-INTRA”)

Part I: Description of consignment

EUROPEAN UNION INTRA


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.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 ☐ Ambient ☐ Chilled ☐ Frozen

I.19 Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number Container number/Seal number

Container No Container No Seal No Seal No


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	☐ Ambient	☐ Chilled	☐ Frozen
I.19	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number	Container number/Seal number
	Container No	Container No	Seal No	Seal No

I.20 Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for Certified as or for

☐ Further keeping ☐ Further keeping ☐ Slaughter ☐ Confined establishment ☐ Confined establishment ☐ Germinal products ☐ Germinal products

☐ Registered equine animal ☐ Registered equine animal ☐ Travelling circus/animal act ☐ Exhibition ☐ Exhibition ☐ Event or activity near borders ☐ Event or activity near borders

☐ Release into the wild ☐ Release into the wild ☐ Dispatch centre ☐ Relaying area/purification centre ☐ Relaying area/purification centre ☐ Ornamental aquaculture establishment ☐ Ornamental aquaculture establishment

☐ Further processing ☐ Further processing ☐ Organic fertilizers and soil improvers ☐ Technical use ☐ Technical use ☐ Quarantine or similar establishment ☐ Quarantine or similar establishment

☐ Products for human consumption ☐ Products for human consumption ☐ Pollination ☐ Live aquatic animals for human consumption ☐ Live aquatic animals for human consumption ☐ Other ☐ Other

I.21 ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country ☐ For transit through a third country

Third country Third country ISO country code ISO country code ISO country code ISO country code

Exit point Exit point BCP code BCP code BCP code BCP code

Entry point Entry point BCP code BCP code BCP code BCP code

I.22 ☐ For transit through Member State(s) ☐ For transit through Member State(s) I.23 ☐ For export ☐ For export ☐ For export

Member State ISO country code Third country ISO country code ISO country code

Member State ISO country code Exit point BCP code BCP code

Member State ISO country code

I.24 Estimated journey time Estimated journey time I.25 Journey log ☐ yes ☐ no

I.26 Total number of packages Total number of packages I.27 Total quantity Total quantity Total quantity

I.28 Total net weight/gross weight (kg) 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.20	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for	Certified as or for
☐ Further keeping	☐ Further keeping	☐ Slaughter	☐ Confined establishment	☐ Confined establishment	☐ Germinal products	☐ Germinal products
☐ Registered equine animal	☐ Registered equine animal	☐ Travelling circus/animal act	☐ Exhibition	☐ Exhibition	☐ Event or activity near borders	☐ Event or activity near borders
☐ Release into the wild	☐ Release into the wild	☐ Dispatch centre	☐ Relaying area/purification centre	☐ Relaying area/purification centre	☐ Ornamental aquaculture establishment	☐ Ornamental aquaculture establishment
☐ Further processing	☐ Further processing	☐ Organic fertilizers and soil improvers	☐ Technical use	☐ Technical use	☐ Quarantine or similar establishment	☐ Quarantine or similar establishment
☐ Products for human consumption	☐ Products for human consumption	☐ Pollination	☐ Live aquatic animals for human consumption	☐ Live aquatic animals for human consumption	☐ Other	☐ Other
I.21	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country	☐ For transit through a third country
	Third country	Third country	ISO country code	ISO country code	ISO country code	ISO country code
	Exit point	Exit point	BCP code	BCP code	BCP code	BCP code
	Entry point	Entry point	BCP code	BCP code	BCP code	BCP code
I.22	☐ For transit through Member State(s)	☐ For transit through Member State(s)	I.23	☐ For export	☐ For export	☐ For export
	Member State	ISO country code		Third country	ISO country code	ISO country code
	Member State	ISO country code		Exit point	BCP code	BCP code
	Member State	ISO country code
I.24	Estimated journey time	Estimated journey time	I.25	Journey log	☐ yes	☐ no
I.26	Total number of packages	Total number of packages	I.27	Total quantity	Total quantity	Total quantity
I.28	Total net weight/gross weight (kg)	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

CN code Species Subspecies/Category Sex Identification system Identification number Age Quantity

Type

Region of origin Cold store Identification mark Type of packaging Net weight

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 EQUI-OOCYTES-EMB-A-INTRA Certificate model EQUI-OOCYTES-EMB-A-INTRA Certificate model EQUI-OOCYTES-EMB-A-INTRA Certificate model EQUI-OOCYTES-EMB-A-INTRA

II. Health information II.a Certificate reference II.b IMSOC reference

EUROPEAN UNION	EUROPEAN UNION	Certificate model EQUI-OOCYTES-EMB-A-INTRA	Certificate model EQUI-OOCYTES-EMB-A-INTRA	Certificate model EQUI-OOCYTES-EMB-A-INTRA	Certificate model EQUI-OOCYTES-EMB-A-INTRA
	II. Health information	II.a	Certificate reference	II.b	IMSOC reference

I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of equine animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of equine animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor equine animals laid down in Articles 15 to 17, Articles 23 and 24, and in Part 4, Chapter II, of Annex II to Delegated Regulation (EU) 2020/686; (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (3)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting equine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes or embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting equine animals and established for … ⁽⁴⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁵⁾;]] ⁽¹⁾ [and in particular, they are … ⁽⁶⁾;]] ^{(1) (7)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (8)} [II.3. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and/or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex XII to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 4, Chapter I of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (9)} [II.4. The following antibiotic or mixture of antibiotics ⁽¹⁰⁾ has been added to the collection, processing, washing or storage media: …] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: indicate the date on which the oocytes or embryos of the consignment are collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection or production team by which the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Applicable for frozen oocytes or embryos. ⁽⁴⁾ Insert the name of the disease(s). ⁽⁵⁾ 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. ⁽⁶⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁷⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of equine animals are placed and transported in one container. ⁽⁸⁾ Does not apply to oocytes. ⁽⁹⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹⁰⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.


I, the undersigned official veterinarian, hereby certify that: ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vivo derived embryos] ⁽¹⁾ of equine animals described in Part I have been collected, processed and stored, and dispatched by the embryo collection team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo collection teams set out in Part 2 of Annex I to Commission Delegated Regulation (EU) 2020/686.] ⁽¹⁾ [II.1. The [oocytes] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ of equine animals described in Part I have been collected or produced, processed and stored, and dispatched by the embryo production team ⁽²⁾ which is approved and kept in a register by the competent authority, and which complies with the requirements for embryo production teams set out in Parts 2 and 3 of Annex I to Delegated Regulation (EU) 2020/686.] II.2. The [oocytes] ⁽¹⁾ [embryos] ⁽¹⁾ described in Part I: (a) are intended for artificial reproduction and were obtained from donor animals which comply with the requirements for donor equine animals laid down in Articles 15 to 17, Articles 23 and 24, and in Part 4, Chapter II, of Annex II to Delegated Regulation (EU) 2020/686; (b) have been collected, processed and stored in accordance with the requirements set out in [Part 2] ⁽¹⁾ [Part 3] ⁽¹⁾ [Part 4] ⁽¹⁾ [Part 5] ⁽¹⁾ and Part 6 of Annex III to Delegated Regulation (EU) 2020/686; (c) are placed in straws or other packages which are marked in accordance with Article 10 of Delegated Regulation (EU) 2020/686, and that mark is indicated in box I.30; (d) are transported in a container which: (i) was sealed and numbered prior to the date of dispatch by the embryo collection or production team under the responsibility of the team veterinarian, or by an official veterinarian, and the seal bears the number indicated in box I.19; (ii) has been cleaned and either disinfected or sterilised before use, or is a single-use container; ^{(1) (3)} [(iii) has been filled in with a cryogenic agent which has not been previously used for other products;] (e) are dispatched by ⁽¹⁾ either [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone not subject to movement restrictions affecting equine animals and established for reasons of listed diseases relevant for those species or diseases subject to emergency measures relevant for those species or those restrictions do not apply to these oocytes or embryos because they were collected before the restrictions were established, and they have not been in contact with other oocytes or embryos of a lower health status for an adequate period;] ⁽¹⁾ or [an [embryo collection team] ⁽¹⁾ [embryo production team] ⁽¹⁾ or from a zone subject to movement restrictions affecting equine animals and established for … ⁽⁴⁾, but derogations from movement restrictions have been granted, and ⁽¹⁾ [they comply with the requirements set out in … ⁽⁵⁾;]] ⁽¹⁾ [and in particular, they are … ⁽⁶⁾;]] ^{(1) (7)} [(f) are placed in straws or other packages which are securely and hermetically sealed; (g) are transported in a container where the different types are separated from each other by physical compartments or by being placed in secondary protective bags.] ^{(1) (8)} [II.3. The [in vivo derived embryos] ⁽¹⁾ [in vitro produced embryos] ⁽¹⁾ [micromanipulated embryos] ⁽¹⁾ described in Part I were conceived by artificial insemination using semen coming from a semen collection centre, germinal product processing establishment or germinal product storage centre approved for the collection, processing and/or storage of semen by the competent authority of a Member State or by the competent authority of a third country or territory, or zone thereof listed in Annex XII to Commission Implementing Regulation (EU) 2021/404, and which was collected, processed and stored in accordance with the requirements of Part 4, Chapter I of Annex II, and of Part 1 of Annex III to Delegated Regulation (EU) 2020/686.] ^{(1) (9)} [II.4. The following antibiotic or mixture of antibiotics ⁽¹⁰⁾ has been added to the collection, processing, washing or storage media: …] 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 Protocol on Ireland/Northern Ireland in conjunction with Annex 2 to that Protocol, 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 the unique approval number and the name and address of the embryo collection or production team of dispatch of the consignment of oocytes or embryos. Box reference I.12 : “Place of destination”: Indicate the address and unique registration or approval number of the establishment of destination of the consignment of oocytes or embryos. Box reference I.19 : Seal number shall be indicated. Box reference I.26 : Total number of packages shall correspond to the number of containers. Box reference I.30 : “Type”: Specify if in vivo derived embryos, in vivo derived oocytes, in vitro produced embryos or micromanipulated embryos. “Identification number”: Indicate identification number of each donor animal. “Identification mark”: Indicate mark on the straw or other packages where the oocytes or embryos of the consignment are placed. “Date of collection/production”: indicate the date on which the oocytes or embryos of the consignment are collected or produced. “Approval or registration number of plant/establishment/centre”: Indicate the unique approval number of the embryo collection or production team by which the oocytes or embryos of the consignment were collected or produced. “Quantity”: Indicate number of straws or other packages with the same mark. Part II: ⁽¹⁾ Delete if not applicable. ⁽²⁾ Only embryo collection or production teams approved by the competent authority and included in the register referred to in Article 101(1), point (b), of Regulation (EU) 2016/429 of the European Parliament and of the Council and Article 7 of Delegated Regulation (EU) 2020/686. ⁽³⁾ Applicable for frozen oocytes or embryos. ⁽⁴⁾ Insert the name of the disease(s). ⁽⁵⁾ 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. ⁽⁶⁾ 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 159(2), points (a), (b) and (c), of Regulation (EU) 2016/429. ⁽⁷⁾ Applicable for consignments where oocytes, in vivo derived embryos, in vitro produced embryos and micromanipulated embryos of equine animals are placed and transported in one container. ⁽⁸⁾ Does not apply to oocytes. ⁽⁹⁾ Mandatory attestation in case antibiotic(s) was/were added. ⁽¹⁰⁾ Insert the name(s) of the antibiotic(s) added and its (their) concentration.

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’


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’

(12) Chapter 58 is replaced by the following:

‘CHAPTER 58

MODEL ANIMAL HEALTH CERTIFICATE FOR THE MOVEMENT BETWEEN MEMBER STATES OF TERRESTRIAL ANIMALS BETWEEN CONFINED ESTABLISHMENTS (MODEL “CONFINED-LIVE-INTRA”)

Part I: Description of consignment

EUROPEAN UNION INTRA


EUROPEAN UNION	INTRA

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I.30	Description of consignment	Description of consignment	Description of consignment	Description of consignment	Description of consignment	Description of consignment	Description of consignment
CN code	Species	Subspecies/Category	Sex	Identification system	Identification number	Age	Quantity
							Type
Region of origin		Cold store		Identification mark	Type of packaging		Net weight

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