EUROPEAN UNION

Intra trade certificate

Part I: Details of consignment presented

I.1. Consignor

Name

Address

Postal code

I.2. Certificate reference No

I.2.a. Local reference No

I.3. Central competent authority

I.4. Local competent authority

I.5. Consignee

Name

Address

Postal code

I.6.

I.7.

I.8. Country of origin

ISO code

I.9. Region of origin

Code

I.10. Country of destination

ISO code

I.11. Region of destination

Code

I.12. Place of origin

Embryo team

Name Approval number

Address

Postal code

I.13. Place of destination

Holding Embryo team

Name Approval number

Address

Postal code

I.14.

I.15.

I.16. Means of transport

Aeroplane Ship Railway wagon

Road vehicle Other

Identification

I.17.

I.18. Description of commodity

I.19. Commodity code (CN code)

05 11 99 85

I.20. Quantity

I.21. Temperature of products

Ambient Chilled Frozen

I.22. Number of packages

I.23. Seal/Container No

I.24. Type of packaging

I.25. Commodities certified for:

Artificial reproduction

I.26. Transit through third country

Third country ISO code

Exit point Code

Entry point BIP No

I.27. Transit through Member States

Member State ISO code

Member State ISO code

Member State ISO code

I.28. Export

Third country ISO code

Exit point Code

I.29.

I.30.

I.31. Identification of the commodities

Species Category Donor identity Date of collection Approval number of the team Quantity

(Scientific name)

EUROPEAN UNION

Ovine and caprine ova/embryos — Part A

II. Health information

II.a. Certificate reference number

II.b.

I, the undersigned official veterinarian, hereby certify that:

(1) either [II.1. the in vivo derived embryos (1)/in vivo derived ova (1) described above were collected, processed and stored by an embryo collection team (2) approved and supervised in accordance with Chapter I(III)(1) of Annex D to Directive 92/65/EEC;]

(1) or [II.1. the in vitro produced embryos (1)/micromanipulated embryos (1) described above were produced, processed and stored by an embryo production team (2) approved and supervised in accordance with Chapter I(III)(1) and (2) of Annex D to Directive 92/65/EEC;]

(1) either [II.2. the in vivo derived embryos described above meet the requirements of Chapter III(II)(1) of Annex D to Directive 92/65/EEC;]

(1) or [II.2. the in vivo derived ova described above meet the requirements of Chapter III(II)(2) of Annex D to Directive 92/65/EEC;]

(1) or [II.2. the in vitro produced embryos described above meet the requirements of Chapter III(II)(3) of Annex D to Directive 92/65/EEC;]

(1) or [II.2. the micromanipulated embryos described above meet the requirements of Chapter III(II)(4) of Annex D to Directive 92/65/EEC;]

(1) [II.3. the consignment consists of embryos of the ovine or caprine species which:

(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 point 1 of Section A of Chapter A of Annex VIII to Regulation (EC) No 999/2001;]]

(1) or [were collected from animals which have been kept continuously for the last three years before the collection on a holding or holdings which have complied for the last three years before collection with the requirements laid down in points (a) to (f) of point 1.3. of Section A of Chapter A 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 with a negligible risk status for classical scrapie approved in accordance with the first subparagraph of point 2.2. of Section A of Chapter A of Annex VIII to Regulation (EC) No 999/2001;]]

(1) or [were collected from ovine animals and

(1) either [are of the ARR/ARR prion protein genotype;]]

(1) or [carry at least one ARR allele and were collected after the date of 1 January 2015;]]

II.4. the ova or embryos described above come from female donors of the ovine (1)/caprine species (1) which meet the requirements of Chapter IV(3) of Annex D to Directive 92/65/EEC;

(1) either [II.5. the embryos described above were conceived as a result of artificial insemination of the donor females with semen which was collected, processed, stored and transported under conditions which comply with the requirements of Chapters I(I), II(I) and III(I) of Annex D to Directive 92/65/EEC;]

(1) or [II.5. the embryos described above were conceived as a result of in vitro fertilisation of ova complying with the conditions in Chapter III(II)(2) of Annex D to Directive 92/65/EEC with semen which was collected, processed, stored and transported under conditions which comply with the requirements of Chapters I(I), II(I) and III(I) of Annex D to Directive 92/65/EEC;]

(1) or [II.5. the ova have not been in contact with semen of the ovine and caprine species;]

II.6. the ova or embryos described above were sent to the place of loading in a sealed container in accordance with point 6 of Chapter III(II) of Annex D to Directive 92/65/EEC and bearing the number detailed in Box I.23.

Notes

Part I:

Box I.12: Place of origin shall correspond to the embryo collection team or embryo production team of embryos collection/production.

Box I.13: Place of destination shall correspond to the embryo collection team, embryo production team or to the holding of ova/embryos destination.

Part II: Certification

EUROPEAN UNION

Ovine and caprine ova/embryos — Part A

II. Health information

II.a. Certificate reference number

II.b.

Box I.23: Identification of container and seal number shall be indicated.

Box I.31: Category: specify if: in vivo derived embryos, in vivo derived ova, in vitro produced embryos or micromanipulated embryos.

Donor identity shall correspond to the official identification of the animal.

Date of collection shall be indicated in the following format: dd/mm/yyyy.

Approval number of the team shall correspond to the embryo collection team or embryo production team of ova/embryos collection/production.

Part II:

(1) Delete as appropriate.

(2) Only approved embryo collection or production teams listed in accordance with Article 11(4) of Directive 92/65/EEC on the Commission website:

http://ec.europa.eu/food/animal/approved_establishments/establishments_vet_field_en.htm.

— The colour of the stamp and signature must be different from that of the other particulars in the certificate.

Official veterinarian or official inspector

Name (in capital letters): Qualification and title:

Local veterinary unit: LVU No:

Date: Signature:

Stamp:

COUNTRY:

Veterinary certificate to EU

Part I: Details of dispatched consignment

I.1. Consignor

Name

Address

Tel.

I.2. Certificate reference No

I.2.a.

I.3. Central competent authority

I.4. Local competent authority

I.5. Consignee

Name

Address

Postal code

Tel.

I.6. Person responsible for the load in EU

Name

Address

Postal code

Tel.

I.7. Country of origin

ISO code

I.8. Region of origin

Code

I.9. Country of destination

ISO code

I.10. Region of destination

Code

I.11. Place of origin

Name Approval number

Address

Name Approval number

Address

Name Approval number

Address

I.12. Place of destination

Name

Address

Postal code

I.13. Place of loading

I.14. Date of departure

I.15. Means of transport

Aeroplane Ship Railway wagon

Road vehicle Other

Identification

Documentary references

I.16. Entry BIP in EU

I.17.

I.18. Description of commodity

I.19. Commodity code (HS code)

05 11 99 85

I.20. Quantity

I.21.

I.22. Number of packages

I.23. Seal/Container No

I.24.

I.25. Commodities certified for:

Artificial reproduction

I.26. For transit through EU to third country

Third country ISO code

I.27. For import or admission into EU

I.28. Identification of the commodities

Species Category Donor identity Date of collection Date of freezing Approval number of the team Quantity

(Scientific name)

COUNTRY

Ovine and caprine ova/embryos

II. Health information

II.a. Certificate reference number

II.b.

I, the undersigned, official veterinarian, hereby certify that:

II.1. The exporting country

(name of exporting country) (2)

II.1.1. has been free from rinderpest, peste des petits ruminants, sheep and goat pox, contagious caprine pleuropneumonia, and Rift Valley fever during the 12 months immediately prior to collection of the ova (1)/embryos (1) to be exported and until their date of dispatch to the Union and no vaccination against these diseases took place during that period;

(1) either [II.1.2. has been free from foot-and-mouth disease during the 12 months immediately prior to collection of the ova (1)/embryos (1) and did not carry out vaccination against foot-and-mouth disease during that period;]

(1) or [II.1.2. has not been free from foot-and-mouth disease during the 12 months immediately prior to collection of the ova (1)/embryos (1) and/or carried out vaccination against foot-and-mouth disease during that period and the donor females come from holdings on which no animal was vaccinated against foot-and-mouth disease during 30 days prior to collection and no animal of susceptible species showed clinical signs of foot-and-mouth disease during the 30 days prior to, and at least 30 days after, the ova (1)/embryos (1) were collected and the ova (1)/embryos (1) were not subjected to penetration of zona pellucida;]

II.2. The ova (1)/embryos (1) to be exported:

II.2.1. were collected (1)/produced (1) and processed on premises within a 10-km radius of which there was no incidence of foot-and-mouth disease, vesicular stomatitis, Rift Valley fever in the 30 days immediately prior to their collection;

II.2.2. were stored at all times on approved premises within a 10-km radius of which there was no incidence of foot-and-mouth disease, vesicular stomatitis or Rift Valley fever from the time of their collection until 30 days thereafter;

II.2.3. were collected (1)/produced (1) by the team described in Box I.11., which has been approved and supervised in accordance with the conditions for the approval and supervision of embryo collection teams and embryo production teams laid down in Chapter I(III) of Annex D to Directive 92/65/EEC;

II.2.4. meet the conditions for ova and embryos laid down in Chapter III(II) of Annex D to Directive 92/65/EEC;

II.2.5. come from the donor females of ovine (1)/caprine (1) species which:

(1) either [II.2.5.1. were kept in a bluetongue virus-free country or zone for at least 60 days prior to, and during collection of the ova (1)/embryos (1);]

(1) or [II.2.5.1. were kept during a bluetongue virus seasonally free period in a seasonally free zone;]

(1) or [II.2.5.1. were kept protected from the vector for at least 60 days prior to, and during the collection of the ova (1)/embryos (1);]

(1) or [II.2.5.1. underwent a serological test for the detection of antibody to the bluetongue virus serogroup, carried out in accordance with the Manual of Diagnostic Tests and Vaccines for Terrestrial Animals between 21 and 60 days after collection of the ova (1)/embryos (1) and giving negative results;]

(1) or [II.2.5.1. underwent an agent identification test for bluetongue virus, carried out in accordance with the Manual of Diagnostic Tests and Vaccines for Terrestrial Animals on a blood sample taken on the day of the ova (1)/embryos (1) collection or the day of slaughtering and giving negative results;]

II.2.5.2. to the best of my knowledge do not come from holdings and have not been in contact with animals of a holding, in which, based on the official notification system and according to the written declaration made by the owner, any of the following diseases has been clinically detected within the periods referred to in points (a) to (d) prior to collection of the ova (1)/embryos (1) to be exported:

(a) contagious agalactia of sheep or goats (Mycoplasma agalactiae, Mycoplasma capricolum, Mycoplasma mycoides var. mycoides ‘large colony’), within the last six months;

(b) paratuberculosis and caseous lymphadenitis, within the last 12 months;

Part II: Certification

COUNTRY

Ovine and caprine ova/embryos

II. Health information

II.a. Certificate reference number

II.b.

(c) pulmonary adenomatosis, within the last three years;

(1) either [(d) Maedi/Visna for sheep or caprine viral arthritis/encephalitis for goats, within the last three years;]

(1) or [(d) Maedi/Visna for sheep or caprine viral arthritis/encephalitis for goats, within the last 12 months, and all the infected animals were slaughtered and remaining animals subsequently reacted negatively to two tests carried out at least six months apart;]

II.2.5.3. showed no clinical signs of disease on the day of the ova (1)/embryos (1) collection;

(1)(4) either [II.2.5.4. originate from the region described in Box I.8., which has been recognised as officially brucellosis (B. melitensis)-free, and]

(1) or [II.2.5.4. have belonged to a holding which has obtained and maintained its officially brucellosis (B. melitensis)-free status in accordance with Directive 91/68/EEC, and]

(1) or [II.2.5.4. originate from a holding, where in respect of brucellosis (B. melitensis) all susceptible animals have been free from any clinical or any signs of this disease for the last 12 months, none of the ovine and caprine animals have been vaccinated against this disease, save those vaccinated with Rev. 1 vaccine more than two years ago, and all ovine and caprine animals over six months of age have been subjected to at least two tests (3), carried out with negative results on samples taken on (date) and on (date) at least six months apart, the latter being within 30 days prior to collection of the ova (1)/embryos (1),]

and have not been kept previously in a holding of a lower status;

(1) either [II.2.5.5. have remained in the exporting country for at least the past six months prior to collection of the ova (1)/embryos (1) to be exported;]

(1) or [II.2.5.5. during the past six months prior to collection of the ova (1)/embryos (1) they complied with the animal health conditions applying to donors of the ova/embryos(1) which are intended for export to the Union and they have been imported into the exporting country at least 30 days prior to collection of the ova (1)/embryos (1) from (2);]

II.2.5.6. have been kept continuously since birth in a country where the following conditions are fulfilled:

II.2.5.6.1. classical scrapie is compulsorily notifiable;

II.2.5.6.2. an awareness, surveillance and monitoring system is in place;

II.2.5.6.3. ovine and caprine animals affected with classical scrapie are killed and completely destroyed;

II.2.5.6.4. the feeding to ovine and caprine animals of meat-and-bone meal, or greaves of ruminant origin has been banned and effectively enforced in the whole country for a period of at least the last seven years;

(1) either [II.2.5.7. have been kept continuously for the last three years before the collection of the embryos to be exported in a holding or holdings which has/have been complying for the last three years before the collection of the embryos to be exported with the requirements laid down in points (a) to (f) of point 1.3. of Section A of Chapter A of Annex VIII to Regulation (EC) No 999/2001;]

(1) or [II.2.5.7. are ovine animals and the embryos

(1) either [are of the ARR/ARR prion protein genotype;]]

(1) or [carry at least one ARR allele and were collected after the date of 1 January 2015;]]

[II.2.6. were collected (1)/produced (1) in the exporting country,

(1) either [II.2.6.1. which according to official findings is free from epizootic haemorrhagic disease (EHD);]]

(1)(5) or [II.2.6.1. in which according to official findings the following serotypes of epizootic haemorrhagic disease (EHD) exist: and the donor females of ovine (1)/caprine (1) species were subjected with negative results in each case to the following tests carried out in an approved laboratory:

(1) either [a serological test (6) for the detection of antibody to the EHD virus serogroup, carried out on samples of blood taken on two occasions not more than 12 months apart prior to and not less than 21 days following collection for this consignment of ova (1)/embryos (1);]]

(1) or [a serological test (6) for the detection of antibody to the EHD virus serogroup, carried out on samples of blood taken at intervals of not more than 60 days throughout the collection period and between 21 and 60 days after the final collection for this consignment of ova (1)/embryos (1);]]

COUNTRY

Ovine and caprine ova/embryos

II. Health information

II.a. Certificate reference number

II.b.

(1) or [an agent identification test (6), carried out on samples of blood collected at commencement and conclusion of, and at least every 7 days, if carried out as virus isolation test, or at least every 28 days, if carried out as polymerase chain reaction, during collection for this consignment of ova (1)/embryos (1);]]

II.2.7. were collected (1)/produced (1) after the date on which the embryo collection team was approved by the competent authority of the exporting country;

II.2.8. were processed and stored under approved conditions for at least 30 days immediately after their collection (1)/production (1) and transported under conditions for ova and embryos laid down in Chapter III(II) of Annex D to Directive 92/65/EEC;

II.2.9. were sent to the place of loading in a sealed container in accordance with the requirements for the transport of embryos laid down in point 6 of Chapter III(II) of Annex D to Directive 92/65/EEC and bearing the number detailed in Box I.23.

(1) [II.2.10. the consignment consists of embryos of the ovine or caprine species which were conceived by artificial insemination (1)/as a result of in vitro fertilisation (1) using semen coming from semen collection centres approved (7) in accordance with:

(1) either [II.2.10.1. Article 11(2) of Directive 92/65/EEC and located in a Member State of the European Union; and the semen complies with the requirements of Directive 92/65/EEC.]]

(1) or [II.2.10.1. Article 17(3)(b) of Directive 92/65/EEC and located in a third country or part thereof listed in Annex I to Decision 2010/472/EU, and the semen complies with the requirements set out in Part 2 of Annex II to that Decision.]]

Notes

Part I:

Box I.6: Person responsible for the load in EU: this box is to be filled in only if it is a certificate for transit commodity.

Box I.11: Place of origin shall correspond to the approved embryo collection team or embryo production team by which the ova/embryos were collected/produced, processed and stored; and listed in accordance with Article 17(3)(b) of Directive 92/65/EEC on the Commission website: http://ec.europa.eu/food/animal/semen_ova/ovine/index_en.htm.

Box I.22: Number of packages shall correspond to the number of containers.

Box I.23: Identification of container and seal number shall be indicated.

Box I.26: Fill in according to whether it is a transit or an import certificate.

Box I.27: Fill in according to whether it is a transit or an import certificate.

Box I.28: Species: select amongst ‘Ovis aries’ or ‘Capra hircus’ as appropriate.

Category: specify if in vivo derived embryos, in vivo derived ova, in vitro produced embryos or micromanipulated embryos.

Donor identity shall correspond to the official identification of the animal.

Date of collection shall be indicated for in vivo derived embryos and in the following format: dd.mm.yyyy.

Date of freezing shall be indicated in the following format: dd.mm.yyyy.

Approval number of the team: shall correspond to the approved embryo collection team or embryo production team by which the ova/embryos were collected/produced, processed and stored; and listed in accordance with Article 17(3)(b) of Directive 92/65/EEC on the Commission website: http://ec.europa.eu/food/animal/semen_ova/ovine/index_en.htm.

Part II:

(1) Delete as appropriate.

(2) Only third countries or parts thereof listed in Annex I to Decision 2010/472/EU.

COUNTRY

Ovine and caprine ova/embryos

II. Health information

II.a. Certificate reference number

II.b.

(3) Tests shall be carried out in accordance with Annex C to Directive 91/68/EEC.

(4) Only for the territory appearing with the entry ‘V’ in column 6 of Part 1 of Annex I to Commission Regulation (EU) No 206/2010 (OJ L 73, 20.3.2010, p. 1).

(5) See remarks for exporting country or part thereof concerned in Annex III to Decision 2010/472/EU.

(6) Standards for EHD virus diagnostic tests are described in Chapter 2.1.3. of the OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals.

(7) Only approved semen collection centres listed in accordance with Article 11(4) and Article 17(3)(b) of Directive 92/65/EEC on the Commission websites:

http://ec.europa.eu/food/animal/approved_establishments/establishments_vet_field_en.htm; http://ec.europa.eu/food/animal/semen_ova/ovine/index_en.htm.

— The signature and the stamp must be in a different colour to that of the printing.

Official veterinarian

Name (in capital letters): Qualification and title:

Date: Signature:

Stamp: