Part I: Details of dispatched consignment

Model RUM-A

COUNTRY

Veterinary certificate to EU

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.

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

I.12.

I.13. Place of loading

Address

Approval number

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)

I.20. Quantity

I.21.

I.22. Number of packages

I.23. Seal/Container No

I.24.

I.25. Commodities certified for:

Approved body

I.26.

I.27. For import or admission into EU

I.28. Identification of the commodities

Species

(scientific name)

Identification system

Identification number

Age

Sex

Part II: Certification

COUNTRY

Model RUM-A

II. Health information

II.a. Certificate reference number

II.b.

II.1. Animal health attestation

I, the undersigned official veterinarian responsible for the approved body, institute or centre/holding (1) of origin certify that the animals described in Part I meet the following requirements:

II.1.1. They come from the country, territory or part thereof described in Box I.7.:

(a) where the diseases referred to in this certificate are notifiable,

(b) which at the date of issuing this certificate has been free for the past 12 months from rinderpest.

II.1.2. They come from the body, institute or centre/holding (1) described in Box I.11;

(a) which is approved according to the requirements and conditions set out in Part 3 and 4 of Annex VI to Regulation (EU) No 206/2010;

(b) which is not subjected to any restrictions relating to a national programme for the control of infectious diseases to which the animals referred to in Box I.28. are susceptible;

(c) where there have been no clinical cases of the following diseases to which the animals referred to in Box I.28. are susceptible:

anthrax for the last 30 days;

foot-and-mouth disease, bluetongue, Rift valley fever, vesicular stomatitis, rabies, contagious bovine pleuropneumonia, lumpy skin disease, peste des petits ruminants, sheep pox, goat pox, contagious caprine pleuropneumonia for the past 6 months;

(d) where there have been no clinical or non-clinical cases of tuberculosis and brucellosis for the past 6 months;

(e) around which in an area of 10 km radius for the last 30 days, there has been no case of the following diseases to which the animals referred to in Box I.28. are susceptible: foot-and-mouth disease, vesicular stomatitis, contagious bovine pleuropneumonia, peste des petits ruminants, sheep pox, goat pox, contagious caprine pleuropneumonia;

(f) around which in an area of 150 km radius for the last 30 days, there has been no case of the following diseases to which the animals referred to in Box I.28. are susceptible: bluetongue, epizootic haemorrhagic disease, Rift valley fever, lumpy skin disease;

(g) in which they have remained since birth or for the past 6 months before dispatch to the Union.

II.1.3. They:

(a) have not come into contact with other animals not complying with at least the same health requirements as described in this certificate for the last 30 days and during their transportation from the approved body, institute or centre/holding (1) to the place of shipment;

(b) were examined by an official veterinarian within 24 hours of loading and showed no clinical sign of disease and are fit for the intended transport;

(c) are not animals to be killed under a national programme for the eradication of diseases.

II.1.4. Foot-and-Mouth Disease

either (1) [(a) They come from the country, territory or part thereof described in Box I.7 which has been free for the past 12 months from foot-and-mouth disease with or without vaccination, and]

or (1) [(a) They have been subjected to the following tests:

a serological test for evidence of foot-and-mouth disease virus infection carried out in accordance with one of the prescribed tests for international trade laid down in the OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (OIE Terrestrial Manual), with negative results, taken within 10 days prior to dispatch to the Union,

(1)(2)[a probang test for evidence of foot-and-mouth disease virus infection carried out in accordance with the procedures described in the OIE Terrestrial Manual with negative results, (1)(3)[taken 10 days prior to dispatch to the Union] (1)(4)[taken on two occasions 15 days apart, the second of which must have been taken 10 days prior to dispatch to the Union, and]

(1) [(b) they have not been vaccinated against foot-and-mouth disease.

COUNTRY

Model RUM-A

II. Health information

II.a. Certificate reference number

II.b.

II.1.5. Bluetongue and Epizootic haemorrhagic disease (EHD)

either (1) [They come from the country, territory or part thereof described in Box I.7 which has been free for 24 months from bluetongue/EHD in accordance with the OIE Terrestrial Animal Health Code (OIE Terrestrial Code).]

or (1) [They were held in a vector-protected facility in the approved body, institute or centre/holding (1) for at least 30 days prior to shipment and were subjected to a serology test according to the OIE Terrestrial Manual, with negative results, carried out at least 28 days after introduction into the approved body, institute or centre.]

or (1) [They were held in a vector-protected facility in the approved body, institute or centre/holding (1) for at least 30 days prior to shipment and were subjected to a PCR test according to the OIE Terrestrial Manual, with negative results, carried out at least 14 days after introduction into the approved body, institute or centre.]

or (1) [They come from a seasonally free area and were subjected during that period to an serology test according to the OIE Terrestrial Manual, with negative results, carried out at least 28 days after introduction into the approved body, institute or centre/holding (1).]

or (1) [They come from a seasonally free area and were subjected during that period to a PCR test according to the OIE Terrestrial Manual, with negative results, carried out at least 14 days after introduction into the approved body, institute or centre/holding (1).]

II.1.6. Rift valley fever

either (1) [They come from the country, territory or part thereof described in Box I.7. which has been free for 48 months from Rift valley fever and have not been vaccinated against that disease.]

or (1) [They were held in a vector-protected facility in the approved body, institute or centre/holding (1) for at least 30 days prior to shipment during which the animals showed no clinical signs of Rift valley fever and were protected from vectors between the vector-protected facility and the place of shipment to the Union as well as at the place of shipment.]

or (1) [They have been subjected to a virus neutralisation test (9) with negative results for evidence of Rift valley fever, as laid down and prescribed for international trade by the OIE Terrestrial Manual, taken at the beginning of the isolation/quarantine period and at least 42 days later on, the second of which must have been taken within 10 days of dispatch to the Union.]

II.1.7. Brucellosis

either (1) [They come from a country, territory or part thereof described in Box I.7 which has been free for the past 12 months from brucellosis and which have not been vaccinated against that disease;]

or (1) [They have been subjected to a test as laid down and prescribed for international trade by the OIE Terrestrial Manual, in the 30 days prior to dispatch to the Union;]

or (1) [They are castrated males of any age].

II.1.8. Other vaccinations

(a) They have not been vaccinated against vesicular stomatitis,

(5) (b) They have been vaccinated against:

(1) [anthrax on the … (dd/mm/yyyy)(date(s)) with the following vaccine(s) … (name of vaccine(s) used)],

(1) [rabies on the … (dd/mm/yyyy)(date(s)) with the following vaccine(s) … (name of vaccine(s) used) and a blood test performed on … (dd/mm/yyyy)(date(s)) shows a protective immune response.].

II.1.9. Parasite treatment

They have been treated at least twice during the 40 days prior to dispatch to the Union against internal and external parasites with the following product(s) … Specify the active ingredients and the doses of the products used …

II.1.10. Loading on the means of transport

They have been loaded for dispatch to the Union on … (dd/mm/yyyy) (6) in the means of transport described in Box I.15. that were cleaned and disinfected before loading with an officially authorised disinfectant and so constructed that faeces, urine, litter or fodder could not flow or fall out of the vehicle or container during transportation.

COUNTRY

Model RUM-A

II. Health information

II.a. Certificate reference number

II.b.

Notes

This certificate is to be used for live animals listed in the note for Box I.28. coming from an approved body, institute or centre in a third country, territory ot part thereof, and destined to an approved body, institute or centre situated within a Member State. Use one certificate per species.

Part I:

Box reference I.15.: Registration number (railway wagons or container and lorries), flight number (aircraft) or name (ship) is to be provided. In case of unloading and reloading, the consignor shall inform the BIP of entry into the EU.

Box reference I.19.: Use appropriate HS code: 010613 or 010619.

Box reference I.28.: Identification system: Specify the identification system (tag, tattoos, brand, chip, transponder). The identifier shall include the ISO code of the exporting country and permit tracing of their premises of origin.

Age: months.

Sex (M = male, F = female, C = castrated).

Species: Select the species amongst those listed below:

Order

Family

Genera/species

Artiodactyla

Antilocapridae

Antilocapra

Bovidae

Addax ssp., Aepyceros ssp., Alcelaphus ssp., Ammodorcas ssp., Ammotragus ssp., Antidorcas ssp., Antilope ssp., Bison ssp., Bos ssp. (including Bibos, Novibos, Poephagus), Boselaphus ssp., Bubalus ssp. (including anoa), Budorcas ssp., Capra ssp., Cephalophus ssp., Connochaetes ssp., Damaliscus ssp. (including Beatragus), Dorcatragus ssp., Gazella ssp., Hemitragus ssp., Hippotragus ssp., Kobus ssp., Litocranius ssp., Madoqua ssp., Naemorhedus ssp. (including Nemorhaedus and Capricornis), Neotragus ssp., Oreamnos ssp., Oreotragus ssp., Oryx ssp., Ourebia ssp., Ovibos ssp., Ovis ssp., Patholops ssp., Pelea ssp., Procapra ssp., Pseudois ssp., Pseudoryx ssp., Raphicerus ssp., Redunca ssp., Rupicapra ssp., Saiga ssp., Sigmoceros-Alecelaphus ssp., Sylvicapra ssp., Syncerus ssp., Taurotragus ssp., Tetracerus ssp., Tragelaphus ssp. (including Boocerus).

Camelidae

Camelus ssp., Lama ssp., Vicugna ssp.

Cervidae

Alces ssp., Axis-Hyelaphus ssp., Blastocerus ssp., Capreolus ssp., Cervus-Rucervus ssp., Dama ssp., Elaphurus ssp., Hippocamelus ssp., Hydropotes ssp., Mazama ssp., Megamuntiacus ssp., Muntiacus ssp., Odocoileus ssp., Ozotoceros ssp., Pudu ssp., Rangifer ssp.

Giraffidae

Giraffa ssp., Okapia ssp.

Moschidae

Moschus ssp.

Tragulidae

Hyemoschus ssp., Tragulus-Moschiola ssp.

Part II:

(1) Keep as appropriate.

(2) This attestation is only applicable to Bovidae and Cervidae.

(3) This attestation is only applicable to Bovidae and Cervidae other than African buffalo (Syncerus caffer).

(4) This attestation is only applicable to African buffalo (Syncerus caffer).

(5) Vaccination is not compulsory, but if the animals have been vaccinated, information on the vaccine(s) used and the time of vaccination shall be filled in.

(6) Date of loading. Imports of these animals shall not be allowed when the animals were loaded either prior to the date of authorisation for exportation to the Union of the third country,territory or part thereof described in Boxes I.7. and I.8., or during a period where restrictive measures have been adopted by the Union against imports of these animals from that country,territory or part thereof.

COUNTRY

Model RUM-A

II. Health information

II.a. Certificate reference number

II.b.

Official veterinarian

Name (in capital letters):

Qualification and title:

Date:

Signature:

Stamp:

Part I: Details of dispatched consignment

Model SUI-A

COUNTRY

Veterinary certificate to EU

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.

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

I.12.

I.13. Place of loading

Address

Approval number

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)

01.06.19

I.20. Quantity

I.21.

I.22. Number of packages

I.23. Seal/Container No

I.24.

I.25. Commodities certified for:

Approved body

I.26.

I.27. For import or admission into EU

I.28. Identification of the commodities

Species

(scientific name)

Identification system

Identification number

Age

Sex

Part II: Certification

COUNTRY

Model SUI-A

II. Health information

II.a. Certificate reference number

II.b.

II.1. Animal health attestation

I, the undersigned official veterinarian responsible for the approved body, institute or centre/holding (1) of origin certify that the animals described in Part I meet the following requirements:

II.1.1. They come from the country, territory or part thereof described in Box I.7.

(a) where the diseases referred to in this certificate are notifiable,

(b) which at the date of issuing this certificate has been free for the past 12 months from rinderpest.

II.1.2. They come from the body, institute or centre/holding (1) described in Box I.11.

(a) which is approved according to the requirements and conditions set out in Part 3 and 4 of Annex VI to Regulation (EU) No 206/2010;

(b) which is not subjected to any restrictions relating to a national programme for the control of infectious diseases to which the animals referred to in Box I.28. are susceptible;

(c) where there have been no clinical cases of the following diseases to which the animals referred to in Box I.28. are susceptible:

anthrax for the last 30 days;

foot-and-mouth disease, vesicular stomatitis, rabies, African swine fever, classical swine fever and swine vesicular disease for the past 6 months;

(d) where there have been no clinical or non-clinical cases of tuberculosis and brucellosis for the past 6 months;

(e) around which in an area of radius of 10 km for the last 12 months, there has been no case/outbreak of African swine fever, classical swine fever and swine vesicular disease;

(f) around which in an area of 10 km radius for the past 30 days, there has been no case/outbreak of foot-and-mouth disease or vesicular stomatitis,

(g) in which they have remained since birth or for the past 6 months before dispatch to the Union.

II.1.3. They:

(a) have not come into contact with other animals not complying with at least the same health requirements as described in this certificate since birth or for the last 30 days and during their transportation from the approved body, institute or centre/holding (1) to the place of shipment;

(b) were examined by an official veterinarian within 24 hours of loading and showed no clinical sign of disease and are fit for the intended transport;

(c) are not animals to be killed under a national programme for the eradication of diseases.

II.1.4. Foot-and-Mouth Disease

either (1) [(a) They come from the country, territory or part thereof described in Box I.7. which at the date of issuing this certificate has been free for the past 12 months from foot-and-mouth disease and;]

or (1) [(a) They have been subjected to a virological and serological test for evidence of foot-and-mouth disease virus infection carried out in accordance with one of the prescribed tests for international trade laid down in the OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (OIE Terrestrial Manual), with negative results, taken in the 10 days prior to dispatch to the Union; and]

(b) they have not been vaccinated against foot-and-mouth disease.

II.1.5. Brucellosis

(1) either [They come from the country, territory or part thereof described in Box I.7 which has been free for the past 12 months from brucellosis and have not been vaccinated against that disease]

(1)(3) or [They have been subjected, with negative results, to a buffered Brucella antigen test for porcine brucellosis taken in the 30 days prior to dispatch to the Union.]

COUNTRY

Model SUI-A

II. Health information

II.a. Certificate reference number

II.b.

II.1.6. Swine vesicular disease

(1) either [They come from the country, territory or part thereof described in box 1.7 which has been free for the past 12 months from swine vesicular disease.]

(1) or [They have been subjected, with negative results, to a virology and serology test for evidence of swine vesicular disease, as laid down and prescribed for international trade by the OIE Terrestrial Manual, taken in the 30 days prior to dispatch to the Union.]

II.1.7. Vesicular Stomatitis

(1) either [They come from the country, territory or part thereof described in Box I.7 which has been free for the last 6 months from vesicular stomatitis.]

(1) or [They have been subjected, with negative results, to a virology and serology test for evidence of vesicular stomatitis, as laid down and prescribed for international trade by the OIE Terrestrial Manual, taken in the 30 days prior to dispatch to the Union.]

II.1.8. Classical swine fever

(1) either [They come from the country, territory or part thereof described in Box I.7 which has been free for the past 12 months from classical swine fever.]

(1) or [They have been subjected to a virological and serological test for classical swine fever carried out in accordance with one of the prescribed tests for international trade laid down in the OIE Terrestrial Manual, with negative results, taken in the 30 days prior to dispatch to the Union.]

II.1.9. African swine fever

(1) either [They come from the country, territory or part thereof described in Box I.7 which has been free for the past 12 months from African swine fever.]

(1) or [They have been subjected, with negative results, to a virus and serology test for African swine fever, as laid down and prescribed for international trade in the OIE Terrestrial Manual, taken in the 30 days prior to dispatch to the Union.]

II.1.10. Aujeszky’s disease

According to official information, no clinical, pathological or serological evidence of Aujeszky’s disease has been recorded for the last 12 months in the approved body, institute or centre/holding (1) and in an area with a 5 km radius around the approved body, centre or institute, and

They have been subjected, with negative results, to a virology and serology test for evidence of Aujeszky's disease, as laid down and prescribed for international trade by the OIE Terrestrial Manual, taken in the 30 days prior to dispatch to the Union, and

They have not been vaccinated against Aujeszky’s disease and have not been in contact with vaccinated animals.

II.1.11. Other vaccinations

(a) They have not been vaccinated against rinderpest, vesicular stomatitis, classical swine fever or swine vesicular disease,

(2)(b) They have been vaccinated against:

(1) [anthrax on the … (dd/mm/yyyy) with the following vaccine(s) … (name of vaccine (s) used)],

(1) [rabies on the … (dd/mm/yyyy) with the following vaccine(s) … (name of vaccine (s) used)].

II.1.12. Parasite treatment

They have been treated at least twice in the 40 days prior to dispatch to the Union against internal and external parasites with the following product(s) … Specify the active ingredients and the doses of the products used …

COUNTRY

Model SUI-A

II. Health information

II.a. Certificate reference number

II.b.

II.1.13. Loading on the means of transport

They have been loaded for dispatch to the Union on …(dd/mm/yyyy) (4) in the means of transport described in Box I.15. that were cleaned and disinfected before loading with an officially authorised disinfectant and so constructed that faeces, urine, litter or fodder could not flow or fall out of the vehicle or container during transportation.

Notes

This certificate is meant for animals of species listed in the note for Box I. 28. coming from an approved body, institute or centre in a third country, territory ot part thereof, and destined to an approved body, institute or centre located within a Member State.

Part I:

Box reference I.15.: Registration number (railway wagons or container and lorries), flight number (aircraft) or name (ship) is to be provided. In case of unloading and reloading, the consignor shall inform the BIP of entry into the EU.

Box reference I.28.: Identification system: Specify the identification system (tag, tattoos, brand, chip, transponder). The identifier shall include the ISO code of the exporting country and permit tracing of their premises of origin.

Age: months.

Sex (M = male, F = female, C = castrated).

Species Select the species amongst those listed below:

Order

Family

Genera/species

Artiodactyla

Suidae

Babyrousa ssp., Hylochoerus ssp., Phacochoerus ssp., Potamochoerus ssp., Sus ssp.

Tayassuidae

Catagonus ssp., Pecari-Tayassu ssp.

Hippopotamidae

Hexaprotodon-Choeropsis, Hippopotamus ssp.

Part II:

(1) Keep as appropriate.

(2) Vaccination is not compulsory, but if the animals have been vaccinated, information on the vaccine(s) used and the time of vaccination must be filled in.

(3) Tests carried out in accordance with the protocols that, for the disease concerned, are described in Part 6 of Annex I to Regulation (EU) No 206/2010.

(4) Date of loading. Imports of these animals shall not be allowed when the animals were loaded either prior to the date of authorisation for exportation to the Union of the country, territory or part thereof decribed in Boxes I.7. and I.8., or during a period where restrictive measures have been adopted by the Union against imports of these animals from that country,territory or part thereof.

Official veterinarian

Name (in capital letters):

Qualification and title:

Date:

Signature:

Stamp:

PartI : Details of dispatched consignment

Model TRE-A

COUNTRY

Veterinary certificate to EU

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.

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

I.12.

I.13. Place of loading

Address

Approval number

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)

01.06.19

I.20. Quantity

I.21.

I.22. Number of packages

I.23. Seal/Container No

I.24.

I.25. Commodities certified for:

Approved body

I.26.

I.27. For import or admission into EU

I.28. Identification of the commodities

Species

(scientific name)

Identification system

Identification number

Age

Sex

Part II: Certification

COUNTRY

Model TRE-A

II. Health information

II.a. Certificate reference number

II.b.

II.1. Animal health attestation

I, the undersigned official veterinarian responsible for the approved body, institute or centre/holding (1) of origin certify that the animals described in Part I meet the following requirements:

II.1.1. They come from the third country, territory or part thereof described in Box I.7.

(a) where the diseases referred to in this certificate are notifiable,

(b) which at the date of issuing this certificate has been free for the past 12 months from rinderpest.

II.1.2. They come from the body, institute or centre/holding (1) described in Box I.11.,

(a) which is approved according to the requirements and conditions set out in Part 3 and 4 of Annex VI to Regulation (EU) No 206/2010;

(b) which is not subjected to any restrictions relating to a national programme for the control of infectious diseases to which the animals referred to in Box I.28. are susceptible;

(c) where there have been no clinical cases of the following diseases to which the animals referred to in Box I.28. are susceptible:

anthrax for the last 30 days;

foot–and–mouth disease, rabies, (1)(2) [African horse sickness] for the past 6 months,

(d) where there have been no clinical or non-clinical cases of tuberculosis for the past 6 months;

(e) around which in an area of 10 km radius for the last 30 days, there has been no case/outbreak of foot–and–mouth disease,

(f) in which they have remained since birth or for the past 6 months before dispatch to the Union,

(1)(2) [(g) around which in an area of radius of 150 km for the last 60 days, there has been no case/outbreak of African horse sickness].

II.1.3. They:

(a) have not come into contact with other animals not complying with at least the same health requirements as described in this certificate since birth or for the past 30 days and during their transportation from the approved body, institute or centre/holding (1) to the place of shipment;

(b) were examined by an official veterinarian within 24 hours of loading and showed no clinical sign of disease and are fit for the intended transport;

(c) are not animals to be killed under a national programme for the eradication of diseases.

(1)(3)[II.1.4. Foot–and-Mouth Disease

either (1) [(a) They come from the country, territory or part thereof described in Box I.7 which has been free for the past 12 months from foot-and-mouth disease with or without vaccination, and]

or (1) [(a) They have been subjected to the following tests:

a serological test for evidence of foot-and-mouth disease virus infection carried out in accordance with one of the prescribed tests for international trade laid down in the OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (OIE Terrestrial Manual), with negative results, taken in the 10 days prior to dispatch to the Union, and

[a probang test for evidence of foot-and-mouth disease virus infection carried out in accordance with the procedures described in the OIE Terrestrial Manual with negative results, taken 10 days prior to dispatch to the Union and ]

(b) have not been vaccinated against foot-and-mouth disease.

II.1.5. Other vaccinations

(a) They have not been vaccinated against rinderpest,

COUNTRY

Model TRE-A

II. Health information

II.a. Certificate reference number

II.b.

(4) (b) They have been vaccinated against:

(1) [anthrax on the … (dd/mm/yyyy)(date(s)) with the following vaccine(s) … (name of vaccine(s) used)],

(1) [rabies on the … (dd/mm/yyyy)(date(s)) with the following vaccine(s) … (name of vaccine (s) used)].

II.1.6. Parasite treatment

They have been treated at least twice in the 40 days prior to dispatch to the Union against internal and external parasites with the following product(s) … Specify the active ingredients and the doses of the products used …

II.1.7. Loading on the means of transport

They have been loaded for dispatch to the Union on … (dd/mm/yyyy) (5) in the means of transport described in Box I.15 that were cleaned and disinfected before loading with an officially authorised disinfectant and so constructed that faeces, urine, litter or fodder could not flow or fall out of the vehicle or container during transportation.

Notes

This certificate is meant for live animals as listed in the note for Box I.28. coming from an approved body, institute or centre in a third country, territory or part thereof, and destined for an approved body, institute or centre located within a Member State. Use one certificate per species.

Part I:

Box reference I.15.: Registration number (railway wagons or container and lorries), flight number (aircraft) or name (ship) is to be provided. In case of unloading and reloading, the consignor shall inform the BIP of entry into the EU.

Box reference I.28.: Identification system: Specify the identification system (tag, tattoos, brand, chip, transponder). The identifier shall include the ISO code of the exporting country and permit tracing of their premises of origin.

Age: months.

Sex (M = male, F = female, C = castrated).

Species: Select the species amongst those listed below:

Order

Family

Genera/species

Perissodactyla

Tapiridae

Tapirus ssp.

Rhinocerotidae

Ceratotherium ssp., Dicerorhinus ssp., Diceros ssp., Rhinoceros ssp

Proboscidea

Elephantidae

Elephas ssp., Loxodonta ssp.

Part II:

(1) Keep as appropriate.

(2) This attestation is only applicable to Rhinocerotidae.

(3) This attestation is only applicable to Elephas. ssp.

(4) Vaccination is not compulsory, but if the animals have been vaccinated, information on the vaccine(s) used and the time of vaccination must be filled in.

(5) Date of loading. Imports of these animals shall not be allowed when the animals were loaded either prior to the date of authorisation for exportation to the Union of the third country,territory or part thereof described in Boxes I.7. and I.8., or during a period where restrictive measures have been adopted by the Union against imports of these animals from that third country, territory or part thereof.

COUNTRY

Model TRE-A

II. Health information

II.a. Certificate reference number

II.b.

Official veterinarian

Name (in capital letters):

Qualification and title:

Date:

Signature:

Stamp: