Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS code)

05 11 99 85

I.20. Quantity

I.21. Temperature of product

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 a 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

(scientific name)

Breed

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Equine semen — Part A

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

II.1. The semen collection centre (2), in which the semen described above was collected, processed and stored for trade is approved and supervised by the competent authority in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC;

II.1.1. during the period commencing 30 days prior to the date of first collection of the semen described above until the date the fresh or chilled semen was dispatched or until the 30 days storage period for frozen semen elapsed, the semen collection centre;

II.1.1.1. was situated on the territory or in the case of regionalisation in a part of the territory (1) of a Member State which was not considered to be infected with African horse sickness in accordance with Article 5(2)(a) and (b) of Directive 2009/156/EC (3);

II.1.1.2. fulfilled the conditions for a holding laid down in Article 4(5) of Directive 2009/156/EC;

II.1.1.3. contained only equidae which were free of clinical signs of equine viral arteritis and contagious equine metritis.

II.2. Only equidae satisfying the conditions laid down in Articles 4 and 5 or Articles 12 to 16 of Directive 2009/156/EC have been admitted into the centre.

II.3. The semen described above was collected from donor stallions, which:

II.3.1. have not shown any clinical sign of an infectious or contagious disease at the time of admission into the centre and on the day the semen was collected;

II.3.2. have been kept for 30 days prior to the date of semen collection in holdings where no equine has shown any clinical sign of equine viral arteritis or contagious equine metritis during that period;

II.3.3. have not been used for natural mating during at least 30 days prior to the date of first semen collection and from the dates of the first sample referred to in points II.3.5.1, II.3.5.2 or II.3.5.3 until the end of the collection period;

II.3.4. have undergone the following tests, which meet at least the requirements of the relevant chapter of the Manual of Diagnostic Tests and Vaccines for Terrestrial Animals of the OIE, carried out on samples taken in accordance with one of the programmes specified in point II.3.5 in a laboratory recognised by the competent authority:

(1) either [II.3.4.1. an agar-gel immuno-diffusion test (Coggins test) for equine infectious anaemia (EIA) with negative result;]

(1) or [II.3.4.1. an ELISA for equine infectious anaemia (EIA) with negative result;]

and (1) either [II.3.4.2. a serum neutralisation test for equine viral arteritis (EVA) with negative result at a serum dilution of one in four;]

(1) or [II.3.4.2. a virus isolation test for equine viral arteritis (EVA) carried out with negative result on an aliquot of the entire semen of the donor stallion;]

and [II.3.4.3. an agent identification test for contagious equine metritis (CEM) carried out on two occasions on samples taken with an interval of seven days by isolation of Taylorella equigenitalis after a cultivation of 7 to 14 days from pre-ejaculatory fluid or a semen sample and from genital swabs taken at least from the penile sheath, urethra and urethral fossa with negative result in each case;

II.3.5. have been subjected with the results specified in II.3.4 in each case to at least one of the test programmes (4) detailed in points II.3.5.1, II.3.5.2 and II.3.5.3 as follows:

II.3.5.1. the donor stallion was continuously resident on the semen collection centre for at least 30 days prior to the date of the first collection and during the period of collection of the semen described above and no equidae on the semen collection centre came into direct contact with equidae of lower health status than the donor stallion;

the tests described in point II.3.4 have been carried out on samples taken (5) prior to the first semen collection and at least 14 days following the date of the commencement of the residence period of at least 30 days;

EUROPEAN UNION

Equine semen — Part A

II. Health information

II.a. Certificate reference No

II.b.

II.3.5.2. the donor stallion was resident on the semen collection centre for at least 30 days prior to the date of the first collection and during the period of collection of the semen described above, but has left the centre under the responsibility of the centre veterinarian for a continuous period of less than 14 days, and/or other equidae on the collection centre came into direct contact with equidae of lower health status;

the tests described in point II.3.4 have been carried out on samples taken (5) prior to the first semen collection of the breeding season or collection period in the year the semen described above was collected and at least 14 days following the date of the commencement of the residence period of at least 30 days;

and the test described in point II.3.4.1 for equine infectious anaemia was last carried out on a sample of blood taken (5) not more than 90 days before the semen described above was collected;

and (1) either [one of the tests described in point II.3.4.2 for equine viral arteritis was last carried out on a sample taken (5) not more than 30 days before the semen described above was collected;]

(1) or [a virus isolation test for equine viral arteritis was carried out with negative result on an aliquot of the entire semen of the donor stallion taken (5) not more than six months before the semen described above was collected and a blood sample taken on the same date (5) reacted positive in a serum neutralisation test for equine viral arteritis at a serum dilution of more than one in four;]

and the test described in point II.3.4.3 for contagious equine metritis was last carried out on samples taken (5) not more than 60 days before the semen described above was collected.

II.3.5.3. The tests described in point II.3.4 have been carried out on samples taken (5) prior to the first semen collection of the breeding season or collection period in the year the semen described above was collected,

and the tests described in point II.3.4 were last carried out on samples taken (5) not less than 14 days and not more than 90 days after the collection of the semen described above.

II.3.6. Have undergone the testing provided for in point II.3.5 on samples taken on the following dates:

Identification of semen

Test programme

Start date (5)

Date of sampling for health tests (5)

Donor residence

Semen collection

EIA II.3.4.1

EVA II.3.4.2

CEM II.3.4.3

Blood sample

Semen sample

1. sample

2. sample

(1) either [II.4 No antibiotics were added to the semen;]

(1) or [II.4 The following antibiotic or combination of antibiotics was added to produce a concentration in the final diluted semen of not less than (6): …

…;]

II.5. The semen described above was:

II.5.1. collected, processed, stored and transported under conditions which comply with the requirements of Chapters II(I)(1) and III(I) of Annex D to Directive 92/65/EEC;

II.5.2. sent to the place of loading in a sealed container in accordance with point 1.4 of Chapter III(I) of Annex D to Directive 92/65/EEC and bearing the number indicated in Box I.23.

EUROPEAN UNION

Equine semen — Part A

II. Health information

II.a. Certificate reference No

II.b.

Notes

Part I:

Box I.12: place of origin shall correspond to the semen collection centre of origin of the semen.

Box I.13: place of destination shall correspond to the semen collection or storage centre or to the holding of semen destination.

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

Box I.31: 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 centre shall correspond to the approval number of the semen centre indicated in Box I.12 where the semen was collected.

Part II:

Guidance for the completion of Table in II.3.6:

Abbreviations:

EIA-1 Equine infectious anaemia (EIA) testing first occasion

EIA-2 EIA testing second occasion

EVA-B1 Equine viral arteritis (EVA) testing on blood sample first occasion

EVA-B2 EVA testing on blood sample second occasion

EVA-S1 EVA testing on semen sample first occasion

EVA-S2 EVA testing on semen sample second occasion

CEM-11 Contagious equine metritis (CEM) testing first occasion first sample

CEM-12 CEM testing first occasion second sample taken 7 days after CEM-11

CEM-21 CEM testing second occasion first sample

CEM-22 CEM testing second occasion second sample taken 7 days after CEM-21

Instructions:

For each semen identification in column A in the example below, the test programme (II.3.5.1, II.3.5.2 and/or II.3.5.3) must be described in column B and columns C and D must be completed with the dates required.

The dates when samples where taken for laboratory testing prior to the first collection of the semen described above as required in II.3.5.1, II.3.5.2 and II.3.5.3, are entered in the upper line of columns 5 to 9 of the table, this being the boxes marked with EIA-1, EVA-B1 or EVA-S1 and CEM-11 and CEM-12 in the example below.

The dates when samples were taken for repeat laboratory testing as required in accordance with II.3.5.2 or II.3.5.3 are entered in the lower line of columns 5 to 9 in table, this being the boxes EIA-2, EVA-B2 or EVA-S2 and CEM-21 and CEM-22 in the example below.

EUROPEAN UNION

Equine semen — Part A

II. Health information

II.a. Certificate reference No

II.b.

Identification of semen

Test programme

Start date (5)

Date of sampling for health tests (5)

Donor residence

Semen collection

EIA II.3.4.1

EVA II.3.4.2

CEM II.3.4.3

Blood sample

Semen sample

1. sample

2. sample

A

B

C

D

EIA-1

EVA-B1

EVA-S1

CEM-11

CEM-12

EIA-2

EVA-B2

EVA-S2

CEM-21

CEM-22

(1) Delete as appropriate.

(2) Only approved semen collection centres listed in accordance with Article 11(4) of Council Directive 92/65/EEC on the Commission website:

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

(3) OJ L 192, 23.7.2010, p. 1.

(4) Cross out the programme(s) that do(es) not apply to the consignment.

(5) Insert date in table in point II.3.6 (follow guidance in part II of the Notes).

(6) Insert names and concentrations.

Official veterinarian (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

(*) The colour of the stamp and signature must be different from that of the other particulars on the certificate.

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS code)

05 11 99 85

I.20. Quantity

I.21. Temperature of product

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 a 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

(scientific name)

Breed

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Equine semen — Part B

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

II.1. The semen collection centre (2), in which the semen described above was collected, processed and stored for trade:

II.1.1. is approved and supervised by the competent authority according to the conditions of Chapter I of Annex D to Directive 92/65/EEC;

II.1.2. is situated on the territory or in the case of regionalisation in a part of the territory (1) of a Member State which was on the day semen was collected until the date the semen was dispatched as fresh/chilled (1) semen or until the 30 days mandatory storage period for frozen semen elapsed (1) not considered to be infected with African horse sickness in accordance with Article 5(2)(a) and (b) of Directive 2009/156/EC (3);

II.1.3. fulfilled during the period commencing 30 days prior to the date of semen collection until the date the semen was dispatched as fresh/chilled (1) semen or until the 30 days mandatory storage period for frozen semen elapsed (1), the conditions of Article 4 of Directive 2009/156/EC;

II.1.4. contained during the period commencing 30 days prior to the date of semen collection until the date the semen was dispatched as fresh/chilled (1) semen or until the 30 days mandatory storage period for frozen semen elapsed (1) only equidae which were free of clinical signs of equine viral arteritis and contagious equine metritis;

II.2. All equidae have been admitted into the centre under the provisions of Article 4 and 5 of Directive 2009/156/EC.

II.3. The semen described above was collected from donor stallions, which:

II.3.1. on the day the semen was collected have not shown clinical signs of an infectious or contagious disease;

II.3.2. during at least 30 days prior to collection of the semen have not been used for natural service;

II.3.3. during the last 30 days prior to collection of the semen have been kept on holdings where no equidae showed clinical signs of equine viral arteritis;

II.3.4. during the last 60 days prior to collection of the semen have been kept on holdings where no equidae showed clinical signs of contagious equine metritis;

II.3.5. to the best of my knowledge and as far as I could ascertain, have not been in contact with equidae suffering from an infectious or contagious disease during 15 days immediately preceding collection of the semen;

II.3.6. have undergone the following animal health tests, carried out in a laboratory recognised by the competent authority, in accordance with a test programme as specified in point II.3.7;

[II.3.6.1. an agar gel immunodiffusion test (Coggins test) for equine infectious anaemia with negative result;]

and (1) either [II.3.6.2. a serum neutralisation test for equine viral arteritis with negative result at a serum dilution of one in four; and]

(1) or [II.3.6.2. a virus isolation test for equine viral arteritis carried out with negative result on an aliquot of the entire semen of the donor stallion;]

and II.3.6.3. an agent identification test for contagious equine metritis carried out on two occasions on samples collected from the donor stallion with an interval of seven days by isolation of Taylorella equigenitalis from pre-ejaculatory fluid or a semen sample and from genital swabs taken at least from the penile sheath, urethra and urethral fossa with negative result in each case;

II.3.7. have been subject to the one of the following test programmes (4):

II.3.7.1. the donor stallion was continuously resident in the collection centre for at least 30 days prior to the semen collection, and during the collection period, and no equidae in the collection centre came during that time into direct contact with equidae of lower health status than the donor stallions;

the tests described in point II.3.6 have been carried out on samples taken on … (5) and in the case of contagious equine metritis on a second sample taken on … (5), being at least 14 days after the commencement of the above residence period and at least at the beginning of the breeding season;

EUROPEAN UNION

Equine semen — Part B

II. Health information

II.a. Certificate reference No

II.b.

II.3.7.2. the donor stallion was not continuously resident in the collection centre or other equidae in the collection centre came into contact with equidae of lower health status than the donor stallion;

the tests described in point II.3.6 have been carried out on samples taken on … (5) and in the case of contagious equine metritis on a second sample taken on … (5), being within the 14 days period before the first semen collection and at least at the beginning of the breeding season;

and the test described in point II.3.6.1 for equine infectious anaemia was last carried out on a sample of blood taken on … (5), being not more than 120 days before the semen described above was collected;

and (1) either [one of the tests described in point II.3.6.2 for equine viral arteritis was last carried out on a sample collected on … (5), being not more than 30 days before the semen described above was collected;]

(1) or [the non-shedder state of the seropositive stallion for equine viral arteritis was confirmed by a virus isolation test which was carried out on an aliquot of the entire semen of the donor stallion collected on … (5), being not more than one year before the semen described above was collected;]

II.3.7.3. The tests described in point II.3.6 have been carried out during the 30 days mandatory storage period of frozen semen and not less than 14 days after the collection of the semen on samples taken on … (5) and in the case of contagious equine metritis on a second sample taken on … (5).

II.4. The semen described above was collected, processed, stored and transported under conditions which comply with the requirements of Chapters II and III of Annex D to Directive 92/65/EEC.

Notes

Part I:

Box I.12: place of origin shall correspond to the semen collection centre of origin of the semen.

Box I.13: place of destination shall correspond to the semen collection or storage centre or to the holding of semen destination.

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

Box I.31: 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 centre shall correspond to the approval number of the semen centre indicated in Box I.12 where the semen was collected.

Part II:

(1) Delete as appropriate.

(2) Only approved semen collection centres listed in accordance with Article 11(4) of Council Directive 92/65/EEC on the Commission website:

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

(3) OJ L 192, 23.7.2010, p. 1.

(4) Cross out the programme(s) that do(es) not apply to the consignment.

(5) Insert date.

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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. No(s) of related original certificates

No(s) of accompanying documents

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS code)

05 11 99 85

I.20. Quantity

I.21. Temperature of product

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 a 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

(scientific name)

Breed

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Equine semen — Part C

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that the semen described above

(1) either [II.1. was collected, processed and stored for a minimum period of 30 days immediately following collection in an approved semen collection centre (2) situated in the Member State of origin of the semen and operated and supervised in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC, and from where the semen was moved to the semen storage centre detailed in Box I.12 situated in the same Member State of origin of the semen under animal health and veterinary certification conditions at least as strict as those provided for in;

(1) either [Part A of Annex I to Decision 2010/470/EU;]

(1) or [Part B of Annex I to Decision 2010/470/EU;]

(1) or [Decision 95/307/EC;]

(1) or [II.1. was collected, processed and stored for a minimum period of 30 days immediately following collection in an approved semen collection centre (2) situated in the European Union and operated and supervised in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC, and was moved to the semen storage centre detailed in Box I.12 in accordance with:

(1) either [Part A of Annex I to Decision 2010/470/EU;]

(1) or [Part B of Annex I to Decision 2010/470/EU;]

(1) or [Part C of Annex I to Decision 2010/470/EU;]

(1) or [Decision 95/307/EC;]

(1) or [II.1. was collected, processed and stored in an approved semen collection centre (2) situated in a third country or part(s) thereof listed in columns 2 and 4 of Annex I to Commission Decision 2004/211/EC which is operated and supervised in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC, and was imported into the European Union under the conditions of Article 4 of Decision 2004/211/EC in accordance with:

(1) either [Part A of Annex I to Decision 2010/471/EU;]

(1) or [Part B of Annex I to Decision 2010/471/EU;]

(1) or [Part C of Annex I to Decision 2010/471/EU;]

(1) or [Decision 96/539/EC;]]

II.2. was stored in the approved semen storage centre (2) indicated in Box I.12, which is operated and supervised in accordance with Chapter I(I)(2) and Chapter I(II)(2) of Annex D to Directive 92/65/EEC;

II.3. was sent to the place of loading in a sealed container in accordance with point 1.4 of Chapter III(I) of Annex D to Directive 92/65/EEC and bearing the number indicated in Box I.23.

Notes

Part I:

Box I.6: shall correspond to the serial number of the individual official document(s) or health certificate(s) [either INTRA or CVED] that accompanied the semen described above from the approved semen collection centre of its origin to the described above semen storage centre. The original(s) of this/these document(s) or certificate(s) or the officially endorsed copy/copies thereof must be attached to this certificate.

Box I.12: place of origin shall correspond to the semen storage centre of dispatch of the semen.

EUROPEAN UNION

Equine semen — Part C

II. Health information

II.a. Certificate reference No

II.b.

Box I.13: place of destination shall correspond to the semen collection or storage centre or to the holding of destination of the semen.

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

Box I.31: 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 centre shall correspond to the approval number of the semen collection centre of origin of the semen.

Part II:

(1) Delete as appropriate.

(2) Only approved semen collection or storage centres listed in accordance with Article 11(4) or Article 17(3)(b) of Council 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/equine/index_en.htm

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Equine ova and embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

(1) either [II.1. the in vivo derived embryos/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/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;]

II.3. the ova or embryos described above come from donor mares which:

II.3.1. coming from holdings fulfilling the conditions laid down in Article 4(5) of Directive 2009/156/EC (4) onto which only equidae satisfying the conditions laid down in Articles 4 and 5 or Articles 12 to 16 of Directive 2009/156/EC have been admitted;

II.3.2. meet the additional requirements of Chapter IV(4) of Annex D to Directive 92/65/EEC;

II.3.3. have not been used for natural breeding during at least 30 days prior to the date of collection of ova or embryos and between the date of the first sample referred to in points II.3.4 and II.3.5 and the date of the collection of ova and embryos;

II.3.4. have been subjected with negative result to an agar-gel immuno-diffusion test (Coggins test) or an ELISA for equine infectious anaemia carried out on a blood samples taken on … (3), being during the past 30 days prior to the date of the first collection of ova or embryos and the last test was carried out on a sample of blood taken on … (3); being not more than 90 days before the ova and embryos were collected;

II.3.5. have been subjected to an agent identification test for contagious equine metritis by isolation of Taylorella equigenitalis after a cultivation of 7 to 14 days carried out with negative results in each case on samples taken during the past 30 days prior to the date of the first collection of ova or embryos from mucosal surfaces of the clitoral fossa and clitoral sinuses on two consecutives oestrus periods on … (3) and on … (3), and on an additional culture specimen taken during one of the oestrus periods from the endometrial cervix on … (3);

(1) either [II.4. the embryos described above were conceived as a result of artificial insemination of the donor mares 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.4. the embryos described above were conceived as a result of in vitro fertilisation of ova complying with the conditions in point 2 of Chapter III(II) 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.4. the ova have not been in contact with semen of the equine species;]

II.5. 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 ova/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.

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

EUROPEAN UNION

Equine ova and embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

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 Council Directive 92/65/EEC on the Commission website:

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

(3) Insert date.

(4) OJ L 192, 23.7.2010, p. 1.

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Equine ova and embryos — Part B

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

II.1. Ova/embryos (1) described above were collected by a collection team (2) approved by the competent authority and processed in an appropriate laboratory;

II.2. Ova/embryos (1) were collected from donor mares which:

II.2.1. on the day of collection have been located in premises situated on the territory or in the case of regionalisation in a part of the territory of a Member State which is not considered to be infected with African horse sickness in accordance with Article 5(2)(a) and (b) of Directive 2009/156/EC (3);

II.2.2. have been located in holdings under veterinary supervision which on the day of collection fulfilled the conditions of Article 4 of Directive 2009/156/EC;

II.2.3. have been kept prior to the collection in holdings free from clinical signs of contagious equine metritis for 60 days;

II.2.4. have not been used for natural breeding during the period of 30 days prior to the collection of ova/embryos (1);

II.2.5. to the best of my knowledge and as fare as I could ascertain, have not been in contact with equidae suffering from an infectious or contagious disease during the 15 days immediately preceding the collection of ova/embryos (1);

II.2.6. have on the day of collection not shown clinical signs of an infectious or contagious disease;

II.3. Ova/embryos (1) were collected, processed, stored and transported under conditions which comply with the requirements of Annex D of Directive 92/65/EEC;

II.4. The semen used for the artificial insemination of the donor mares complies with the requirements of Directive 92/65/EEC (4) (1);

II.5. The ova used for the in vivo production of embryos comply with the requirements of Directive 92/65/EEC (1).

Notes

Part I:

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

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

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 of ova/embryos collection.

Part II:

(1) Delete as appropriate.

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

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

(3) OJ L 192, 23.7.2010, p. 1.

(4) Does not apply to ova.

EUROPEAN UNION

Equine ova and embryos — Part B

II. Health information

II.a. Certificate reference No

II.b.

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS 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

(Scientific name)

Breed

Donor identity

Date of collection

Approval number of the centre

Quantity

Part II: Certification

EUROPEAN UNION

Ovine and caprine semen — Part A

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

II.1. the semen described above:

II.1.1. was collected, processed and stored in a semen collection centre (2) approved and supervised by the competent authority in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC;

II.1.2. comes from the donor animals which meet the requirements of Chapter II(II) of Annex D to Directive 92/65/EEC;

II.1.3. was collected, processed, stored and transported under conditions which comply with the requirements of Chapters II(II) and III(I) of Annex D to Directive 92/65/EEC;

(1) either [II.1.4. meets the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001;]

(1) or [II.1.4. meets the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and is destined for a Member State which benefits, for all or part of its territory, from the provisions laid down in point (b) or (c) of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and the donor animals comply regarding scrapie with the guarantees provided for by the programmes referred to in that point and with the guarantees (3) requested by the Member State of destination;]

II.1.5. was sent to the place of loading in a sealed container in accordance with point 1.4 of Chapter III(I) of Annex D to Directive 92/65/EEC and bearing the number detailed in Box I.23;

(1) either [II.2. no antibiotics or no mixture of antibiotics were added to the semen;]

(1) or [II.2. the following antibiotic or combination of antibiotics was added to produce a concentration in the final diluted semen of not less than (4): …]

Notes

Part I:

Box I.12: Place of origin shall correspond to the semen collection centre of origin of the semen.

Box I.13: Place of destination shall correspond to the semen collection or storage centre or to the holding of semen destination.

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

Box I.31: 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 centre shall correspond to the approval number of the semen centre indicated in Box I.12 where the semen was collected.

Part II:

(1) Delete as appropriate.

(2) Only approved semen collection centres listed in accordance with Article 11(4) of Council Directive 92/65/EEC on the Commission website:

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

(3) Additional guarantees as laid down in Article 2 of Regulation (EC) No 546/2006 (OJ L 94, 1.4.2006, p. 28).

(4) Insert names and concentrations.

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS 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

(Scientific name)

Breed

Donor identity

Date of collection

Approval number of the centre

Quantity

Part II: Certification

EUROPEAN UNION

Ovine and caprine semen — Part B

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that the semen described above:

II.1. was collected, processed and stored in a semen collection centre (2) approved and supervised by the competent authority in accordance with Chapter I(I) and Chapter I(II) of Annex D to Directive 92/65/EEC;

II.2. comes from the donor animals which meet the requirements of Chapter II(II) of Annex D to Directive 92/65/EEC;

II.3. was collected, processed, stored and transported under conditions which comply with the requirements of Chapters II(II) and III of Annex D to Directive 92/65/EEC;

(1) either [II.4. meets the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001;]

(1) or [II.4. meets the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and is destined for a Member State which benefits, for all or part of its territory, from the provisions laid down in point (b) or (c) of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and the donor animals comply regarding scrapie with the guarantees provided for by the programmes referred to in that point and with the guarantees (3) requested by the Member State of destination.]

Notes

Part I:

Box I.12: Place of origin shall correspond to the semen collection centre of origin of the semen.

Box I.13: Place of destination shall correspond to the semen collection or storage centre or to the holding of semen destination.

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

Box I.31: 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 centre shall correspond to the approval number of the semen centre indicated in Box I.12 where the semen was collected.

Part II:

(1) Delete as appropriate.

(2) Only approved semen collection centres listed in accordance with Article 11(4) of Council Directive 92/65/EEC on the Commission website:

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

(3) Additional guarantees as laid down in Article 2 of Regulation (EC) No 546/2006 (OJ L 94, 1.4.2006, p. 28).

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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. No(s) of related original certificates

No(s) of accompanying documents

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

Semen centre

Name

Approval number

Address

Postal code

I.13. Place of destination

Semen centre

Holding

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 (HS 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

(Scientific name)

Breed

Donor identity

Date of collection

Approval number

of the centre

Quantity

Part II: Certification

EUROPEAN UNION

Ovine and caprine semen — Part C

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that the semen described above:

(1) either [II.1. was collected, processed and stored for a minimum period of 30 days immediately following collection in an approved semen collection centre (2) situated in the Member State of origin of the semen and operated and supervised in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC, and from where the semen was moved to the semen storage centre detailed in Part I.12 situated in the same Member State of origin of the semen under animal health and veterinary certification at least as strict as those provided for in:

(1) either [Part A of Annex III to Decision 2010/470/EU;]

(1) or [Part B of Annex III to Decision 2010/470/EU;]

(1) or [Decision 95/388/EC;]]

(1) or [II.1. was collected, processed and stored for a minimum period of 30 days immediately following collection in an approved semen collection centre (2) situated in the European Union and operated and supervised in accordance with Chapter I(I) and Chapter I(II) of Annex D to Directive 92/65/EEC and was moved to the semen storage centre detailed in Box I.12, in accordance with:

(1) either [Part A of Annex III to Decision 2010/470/EU;]

(1) or [Part B of Annex III to Decision 2010/470/EU;]

(1) or [Decision 95/388/EC;]]

(1) or [II.1. was collected, processed and stored for a minimum period of 30 days immediately following collection in an approved semen collection centre (2) situated in a third country or part(s) thereof listed in Annex I to Decision 2010/472/EU which is operated and supervised in accordance with Chapter I(I)(1) and Chapter I(II)(1) of Annex D to Directive 92/65/EEC, and was imported into the European Union under the conditions of Article 17(2) of Directive 92/65/EEC in accordance with:

(1) either [Section A of Part 2 of Annex II to Decision 2010/472/EU;]

(1) or [Section B of Part 2 of Annex II to Decision 2010/472/EU;]

(1) or [Annex II to Decision 2008/635/EC;]

II.2. was stored in the approved semen storage centre (2) indicated in Box I.12 which is operated and supervised in accordance with Chapter I(I)(2) and Chapter I(II)(2) of Annex D to Directive 92/65/EEC;

II.3. was sent to the place of loading in a sealed container in accordance with point 1.4 of Chapter III(I) of Annex D to Directive 92/65/EEC and bearing the number indicated in Box I.23.

Notes

Part I:

Box I.6: Shall correspond to the serial number of the individual official document(s) or health certificate(s) (either INTRA or CVED) that accompanied the semen described above from the approved semen collection centre of its origin to the described above semen storage centre. The original of this/these document(s) or certificate(s), or the officially endorsed copy/copies thereof must be attached to this certificate.

Box I.12: Place of origin shall correspond to the semen storage centre of dispatch of the semen.

Box I.13: Place of destination shall correspond to the semen collection or storage centre or to the holding of destination of the semen.

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

Box I.31: 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 centre shall correspond to the approval number of the semen collection centre of the semen origin.

EUROPEAN UNION

Equine ova and embryos — Part C

II. Health information

II.a. Certificate reference No

II.b.

Part II:

(1) Delete as appropriate.

(2) Only approved semen collection or storage centres listed in accordance with Article 11(4) or Article 17(3)(b) of Council 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

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

1.14.

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Ovine and caprine ova/embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

(1) either [II.1. the in vivo derived embryos/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/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;]

II.3. the ova or embryos described above:

(1) either [II.3.1. meet the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001;]

(1) or [II.3.1. meet the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and are destined for a Member States which benefits, for all or part of its territory, from the provisions laid down in point (b) or (c) of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and the donor animals comply regarding scrapie with the guarantees provided for by the programmes referred to in that point and with the guarantees (3) requested by the Member States of destination;]

II.3.2. come from female donors of the ovine/caprine species (1) which meet the requirements of Chapter IV(3) of Annex D to Directive 92/65/EEC;

(1) either [II.4. the embryos described above were conceived as a result of artificial insemination of the donor females with semen which was collected, produced, 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.4. 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.4. the ova have not been in contact with semen of the ovine and caprine species;]

II.5. 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.

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.

EUROPEAN UNION

Ovine and caprine ova/embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

Part II:

(1) Delete as appropriate.

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

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

(3) Additional guarantees as laid down in Article 2 of Regulation (EC) No 546/2006 (OJ L 94, 1.4.2006, p. 28).

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

1.14.

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Ovine and caprine ova/embryos — Part B

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that the ova/embryos (1) described above:

II.1. were collected, processed and stored under conditions which meet the requirements of Directive 92/65/EEC;

II.2. come from female donors of the ovine/caprine species (1) which meet the requirements of Chapter IV of Annex D to Directive 92/65/EEC;

(1) either [II.3. meet the requirements of Chapter III of Annex D to Directive 92/65/EEC and of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001.]

(1) or [II.3. meet the requirements of Chapter III of Annex D to Directive 92/65/EEC and of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and are destined for a Member State which benefits, for all or part of its territory, from the provisions laid down in point (b) or (c) of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and the donor animals comply regarding scrapie with the guarantees provided for by the programmes referred to in that point and with the guarantees (2) requested by the Member State of destination.]

(1) either [II.4. in the case of embryos, the semen used for fertilisation meets the requirements of Directive 92/65/EEC and the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001.]

(1) or [II.4. in the case of embryos, the semen used for fertilisation meets the requirements of Directive 92/65/EEC and the requirements of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and is destined for a Member State which benefits, for all or part of its territory, from the provisions laid down in point (b) or (c) of Chapter A(I) of Annex VIII to Regulation (EC) No 999/2001 and the donor animals comply regarding scrapie with the guarantees provided for by the programmes referred to in that point and with the guarantees (2) requested by the Member State of destination.]

Notes

Part I:

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

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

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 of ova/embryos collection indicated in Box I.12.

Part II:

(1) Delete as appropriate.

(2) Additional guarantees as laid down in Article 2 of Regulation (EC) No 546/2006 (OJ L 94, 1.4.2006, p. 28).

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

1.14.

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Porcine ova/embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that the ova/embryos (1) described above:

II.1. were produced/collected (1), processed and stored by an embryo collection/production (1) team (2) approved and supervised in accordance with Chapter I(III) of Annex D to Directive 92/65/EEC;

II.2. meet the requirements of Chapter III(II) of Annex D to Directive 92/65/EEC;

II.3. come from donor females of the porcine species which meet the requirements of Chapter IV(2) of Annex D to Directive 92/65/EEC;

(1) either [II.4. are in vivo derived embryos which:

II.4.1. were conceived as a result of artificial insemination with semen meeting the requirements of Directive 90/429/EEC,

II.4.2. originate from a Member State or region thereof:

(1) either [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC;]

(1) or [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC and have been washed with trypsin;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex II to Decision 2008/185/EC;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I or II to Decision 2008/185/EC and have been washed with trypsin;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]]

(1) or [II.4. are in vitro produced/micromanipulated (1) embryos which:

II.4.1. were conceived as a result of in vitro fertilisation with semen meeting the requirements of Directive 90/429/EEC,

II.4.2. originate from a Member State or region thereof:

(1) either [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC;]

(1) or [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC and the donor females of the ova used for their production comply with the conditions of Article 1 of Decision 2008/185/EC;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex II to Decision 2008/185/EC;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I or II to Decision 2008/185/EC and the donor females of the ova used for their production comply with the conditions of Article 1 of Decision 2008/185/EC;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]]

EUROPEAN UNION

Porcine ova/embryos — Part A

II. Health information

II.a. Certificate reference No

II.b.

(1) or [II.4. are in vivo derived ova which originate from a Member State or region thereof:

(1) either [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC;]

(1) or [listed in Annex I to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I to Decision 2008/185/EC and which come from donor females complying with the conditions of Article 1 of Decision 2008/185/EC;]

(1) or [listed in Annex II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex II to Decision 2008/185/EC;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof listed in Annex I or II to Decision 2008/185/EC and which come from donor females complying with the conditions of Article 1 of Decision 2008/185/EC;]

(1) or [not listed in Annex I or II to Decision 2008/185/EC and are destined for a Member State or region thereof not listed in Annex I or II to Decision 2008/185/EC;]]

II.5. were sent to the place of loading in a sealed container under conditions complying 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 ova/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.

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 indicated in Box I.12.

Part II:

(1) Delete as appropriate.

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

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

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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

Part I: Details of consignment presented

EUROPEAN UNION

Intra trade certificate

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

1.14.

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 (HS 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

(Scientific name)

Breed

Category

Donor identity

Date of collection

Approval number of the team

Quantity

Part II: Certification

EUROPEAN UNION

Porcine ova/embryos — Part B

II. Health information

II.a. Certificate reference No

II.b.

I, the undersigned official veterinarian, hereby certify that:

II.1. The ova/embryos (1) described above:

II.1.1. were collected, processed and stored under conditions which meet the requirements of Directive 92/65/EEC;

II.1.2. come from donor female swine which meet the requirements of Chapter IV of Annex D to Directive 92/65/EEC;

II.1.3. meet the requirements of Chapter III of Annex D to Directive 92/65/EEC.

(1) either [II.2. In the case of embryos,

II.2.1. the semen used for fertilisation meets the requirements of Directive 90/429/EEC;

II.2.2. the embryos have been washed with trypsin (2).]

(1) or [II.2. In the case of ova, the ova comes from a donor female swine which meets the conditions of Article 1 of Decision 2008/185/EC (2).]

Notes

Part I:

Box I.12: place of origin shall correspond to the embryo collection team of ova/embryos collection.

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

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 of ova/embryos collection indicated in Box I.12.

Part II:

(1) Delete as appropriate.

(2) This condition applies only to ova and embryos which originate in the Member States or regions thereof not listed in Annexes I and II to Decision 2008/185/EC (OJ L 59, 4.3.2008, p. 19) and destined to the Member States or regions thereof so listed. It shall also apply to movements from Member States or regions thereof listed in Annex II of Decision 2008/185/EC to Member States or regions thereof listed in Annex I of Decision 2008/185/EC.

Official veterinarian or official inspector (*)

Name (in capital letters):

Qualification and title:

Local veterinary unit:

LVU No:

Date:

Signature:

Stamp:

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