14.10.2019 |
EN |
Official Journal of the European Union |
L 261/1 |
COMMISSION IMPLEMENTING REGULATION (EU) 2019/1714
of 30 September 2019
amending Regulations (EC) No 136/2004 and (EC) No 282/2004 as regards the model of common veterinary entry document for products and animals and amending Regulation (EC) No 669/2009 as regards the model of common entry document for certain feed and food of non-animal origin
(Text with EEA relevance)
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union,
Having regard to Council Directive 91/496/EEC of 15 July 1991 laying down the principles governing the organisation of veterinary checks on animals entering the Community from third countries and amending Directives 89/662/EEC, 90/425/EEC and 90/675/EEC (1), and in particular Articles 3(2) and 7(2) thereof,
Having regard to Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries (2), and in particular Articles 3(5), 4(5) and 5(4) thereof,
Having regard to Regulation (EC) No 882/2004 of the European Parliament and of the Council of 29 April 2004 on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules (3), and in particular Article 15(5) thereof,
Having regard to Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (4), and in particular Article 53(1) thereof,
Whereas:
(1) |
Commission Regulation (EC) No 136/2004 (5) lays down the procedures for veterinary checks at border inspection posts on products entering the Union from third countries in accordance with Directive 97/78/EC. Annex III to that Regulation sets out the model for the common veterinary entry document (CVED) to be completed and transmitted by the person responsible for the load to notify the arrival of products to the veterinary staff of the border inspection post, and to be completed under the responsibility of the official veterinarian at the border inspection post, confirming the completion of veterinary checks. |
(2) |
Commission Regulation (EC) No 282/2004 (6) lays down rules on the procedures for the declaration of, and veterinary checks at border inspection posts on animals entering the Union from third countries in accordance with Directive 91/496/EEC. Annex I to that Regulation sets out the model for the common veterinary entry document (CVED animals) to be completed and transmitted by the person responsible for the load to notify the arrival of animals to the inspection staff of the border inspection post, and to be completed under the responsibility of the official veterinarian at the border inspection post, confirming the completion of veterinary checks. |
(3) |
Commission Regulation (EC) No 669/2009 (7) lays down rules on the increased level of official controls to be carried out at designated points of entry into the Union on imports of certain feed and food of non-animal origin from certain third countries in accordance with Regulation (EC) No 882/2004. Annex II to Regulation (EC) No 669/2009 sets out the model for the common entry document (CED) to be completed and transmitted by feed and food business operators to notify the arrival of consignments to the competent authority at the designated point of entry (DPE) or at the designated point of import (DPI) for certain feed and food referred to in Commission Implementing Regulation (EU) No 884/2014 (8), and to be completed by the authority confirming the completion of official controls. |
(4) |
The web-based system TRACES was established by Commission Decision 2004/292/EC (9) to streamline the work of operators and competent authorities and to enable automated exchange of information between customs and veterinary authorities. Decision 2004/292/EC also requires Member States to use TRACES to complete and transmit the CVEDs for products and animals. Since 2011, TRACES also enables the completion and transmission of the CED by the operators and the competent authorities and is used for that purpose by Member States on a voluntary basis. |
(5) |
Regulation (EU) 2017/625 of the European Parliament and of the Council (10) requires the Commission, in collaboration with the Member States, to set up and manage a computerised information management system for official controls (IMSOC) to manage, handle and automatically exchange data, information and documents in relation to official controls. The IMSOC is aimed to integrate and upgrade as necessary the information systems managed by the Commission, amongst them TRACES, and provide appropriate links between those systems and the existing national systems of the Member States. That Regulation repeals and replaces Directives 91/496/EEC and 97/78/EC and Regulation (EC) No 882/2004 with effect from 14 December 2019. |
(6) |
Regulation (EU) 2017/625 provides that for each consignment of the categories of animals and goods referred to in Article 47(1) of that Regulation a common health entry document (CHED) is to be used by the operators responsible for the consignment, in order to notify the authorities at the border control post in advance of the arrival of the consignment and by the authorities at the border control post, in order to record the outcome of official controls and any decision taken on that basis. The CHEDs will thus replace CVEDs and CEDs as of 14 December 2019. |
(7) |
Regulation (EU) 2017/625 also provides that the IMSOC is to allow for the production, handling and transmission of the CHED and it empowers the Commission to lay down rules on the format of the CHED and the instructions for its presentation and use, taking account of international standards, as well as the rules for the use of electronic signatures. |
(8) |
To further facilitate and accelerate the administrative procedures for operators and competent authorities, the Commission has developed a new version of the TRACES system enabling the entire process of the CHED production to be performed electronically as of 14 December 2019. It uses international standards for paperless trade facilities, standards set out in Regulation (EU) No 910/2014 of the European Parliament and of the Council (11) for qualified electronic signature, seal and time stamp and the technical specifications laid down in the Annex to Commission Implementing Decision (EU) 2015/1506 (12) for advanced electronic signature and seal. |
(9) |
The current version of the TRACES system used to complete and transmit the CVEDs and CEDs will be phased out as of 14 December 2019 and from that date, operators and competent authorities will have to complete and submit the CHEDs using the new version of the TRACES system. |
(10) |
In order to allow for a smooth transition towards the use of the new version of the TRACES system, the possibility to use either the current or the new version of the TRACES system to complete and transmit the CVED and CED should be offered to operators and competent authorities until 13 December 2019. To this end, this Regulation should lay down a model of CVED for animals and products and a model of CED for certain feed and food of non-animal origin that are compatible with the new version of the TRACES system. |
(11) |
Regulations (EC) No 136/2004 and (EC) No 282/2004 provide that the production, use, transmission and storage of CVEDs may be done by electronic means at the discretion of the competent authority. Moreover, Regulation (EC) No 882/2004 provides that the Commission may adopt requirements concerning the principles to be respected to ensure reliable certification, including electronic certification. In order to streamline the completion and transmission of the models of CVEDs and CED in the new version of the TRACES system, this Regulation should establish the security requirements to be met with regard to the use of electronic CVEDs and CEDs in that system. |
(12) |
It is therefore appropriate to amend the provisions on the notification of arrival of products and animals to allow the use of two different models of CVED and to lay down requirements for the completion of an electronic CVED in Regulations (EC) No 136/2004 and (EC) No 282/2004. Furthermore, an Annex to those Regulations setting out the model of CVED for products and animals for use in the new version of the TRACES system should be added. |
(13) |
Similarly, it is appropriate to adapt the definition of the CED in Regulation (EC) No 669/2009 to allow the use of two different models of CED, to lay down requirements for the completion of an electronic CED and to add an Annex to that Regulation setting out the model of CED to be used in the new version of the TRACES system. |
(14) |
For the sake of consistency, the date until which this Regulation should apply should correspond to the date on which Directives 91/496/EEC and 97/78/EC and Regulation (EC) No 882/2004 cease to apply. |
(15) |
Regulations (EC) No 136/2004, (EC) No 282/2004 and (EC) No 669/2009 should therefore be amended accordingly. |
(16) |
The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed, |
HAS ADOPTED THIS REGULATION:
Article 1
Amendments to Regulation (EC) No 136/2004
Regulation (EC) No 136/2004 is amended as follows:
(1) |
in Article 2, paragraph 1 is replaced by the following: ‘1. Before the physical arrival of the consignment on Community territory the person responsible for the load shall notify the arrival of the products to the veterinary staff of the border inspection post to which the products are to be submitted, using a document drawn up in accordance with either of the models of common veterinary entry document (CVED) set out in Annex III and in Part 2 of Annex VI.’; |
(2) |
the following Article 10a is inserted: ‘Article 10a Requirements for completing an electronic CVED 1. Where an electronic CVED is used, it shall be completed in the TRACES system and meet all of the following requirements:
2. Each of the operations referred to in paragraph 1 shall be timestamped with a qualified electronic time stamp.’; |
(3) |
a new Annex VI is added, the text of which is set out in Annex I to this Regulation. |
Article 2
Amendments to Regulation (EC) No 282/2004
Regulation (EC) No 282/2004 is amended as follows:
(1) |
in Article 1, paragraph 1 is replaced by the following: ‘1. Where any animal referred to in Directive 91/496/EEC enters the Community from a third country, the person responsible for the load within the meaning of Article 2(2)(e) of Directive 97/78/EC shall give notice of such entry at least one working day before the expected arrival of the animal(s) on Community territory. Such notification shall be made to the inspection staff of the border inspection post using a document drawn up in accordance with either of the models of common veterinary entry document (CVED) set out in Annex I and Part 2 of Annex III.’; |
(2) |
the following Article 7a is inserted: ‘Article 7a Requirements for completing an electronic CVED 1. Where an electronic CVED is used, it shall be completed in the TRACES system and meet all of the following requirements:
2. Each of the operations referred to in paragraph 1 shall be timestamped with a qualified electronic time stamp.’; |
(3) |
a new Annex III is added, the text of which is set out in Annex II to this Regulation. |
Article 3
Amendments to Regulation (EC) No 669/2009
Regulation (EC) No 669/2009 is amended as follows:
(1) |
in Article 3, point (a) is replaced by the following:
|
(2) |
the following Article 7a is inserted: ‘Article 7a Requirements for completing an electronic CVED 1. Where an electronic CED is used, it shall be completed in the TRACES system and meet all of the following requirements:
2. Each of the operations referred to in paragraph 1 shall be timestamped with a qualified electronic time stamp.’; |
(3) |
a new Annex III is added, the text of which is set out in Annex III to this Regulation. |
Article 4
Entry into force and application
This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union.
It shall apply until 13 December 2019.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 30 September 2019.
For the Commission
The President
Jean-Claude JUNCKER
(1) OJ L 268, 24.9.1991, p. 56.
(3) OJ L 165, 30.4.2004, p. 1.
(5) Commission Regulation (EC) No 136/2004 of 22 January 2004 laying down procedures for veterinary checks at Community border inspection posts on products imported from third countries (OJ L 21, 28.1.2004, p. 11).
(6) Commission Regulation (EC) No 282/2004 of 18 February 2004 introducing a document for the declaration of, and veterinary checks on, animals from third countries entering the Community (OJ L 49, 19.2.2004, p. 11).
(7) Commission Regulation (EC) No 669/2009 of 24 July 2009 implementing Regulation (EC) No 882/2004 of the European Parliament and of the Council as regards the increased level of official controls on imports of certain feed and food of non-animal origin and amending Decision 2006/504/EC (OJ L 194, 25.7.2009, p. 11).
(8) Commission Implementing Regulation (EU) No 884/2014 of 13 August 2014 imposing special conditions governing the import of certain feed and food from certain third countries due to contamination risk by aflatoxins and repealing Regulation (EC) No 1152/2009 (OJ L 242, 14.8.2014, p. 4).
(9) Commission Decision 2004/292/EC of 30 March 2004 on the introduction of the Traces system and amending Decision 92/486/EEC (OJ L 94, 31.3.2004, p. 63).
(10) Regulation (EU) 2017/625 of the European Parliament and of the Council of 15 March 2017 on official controls and other official activities performed to ensure the application of food and feed law, rules on animal health and welfare, plant health and plant protection products, amending Regulations (EC) No 999/2001, (EC) No 396/2005, (EC) No 1069/2009, (EC) No 1107/2009, (EU) No 1151/2012, (EU) No 652/2014, (EU) 2016/429 and (EU) 2016/2031 of the European Parliament and of the Council, Council Regulations (EC) No 1/2005 and (EC) No 1099/2009 and Council Directives 98/58/EC, 1999/74/EC, 2007/43/EC, 2008/119/EC and 2008/120/EC, and repealing Regulations (EC) No 854/2004 and (EC) No 882/2004 of the European Parliament and of the Council, Council Directives 89/608/EEC, 89/662/EEC, 90/425/EEC, 91/496/EEC, 96/23/EC, 96/93/EC and 97/78/EC and Council Decision 92/438/EEC (OJ L 95, 7.4.2017, p. 1).
(11) Regulation (EU) No 910/2014 of the European Parliament and of the Council of 23 July 2014 on electronic identification and trust services for electronic transactions in the internal market and repealing Directive 1999/93/EC (OJ L 257, 28.8.2014, p. 73).
(12) Commission Implementing Decision (EU) 2015/1506 of 8 September 2015 laying down specifications relating to formats of advanced electronic signatures and advanced seals to be recognised by public sector bodies pursuant to Articles 27(5) and 37(5) of Regulation (EU) No 910/2014 of the European Parliament and of the Council on electronic identification and trust services for electronic transactions in the internal market (OJ L 235, 9.9.2015, p. 37).
ANNEX I
‘ ANNEX VI
PART 1
Notes for guidance for the common veterinary entry document for products — model 2 (CVED-P2)
GENERAL
Part I is for completion by the declarant or person responsible for the load as defined in Article 2(2)(e) of Directive 97/78/EC.
Parts II and III is for completion by the official veterinarian or designated official agent (as in Decision 93/352/EEC).
The entries specified in this Part constitute the data dictionaries for the electronic version of the CVED-P2.
Paper copies of an electronic CVED-P2 must bear a unique machine-readable optical label which hyperlinks to the electronic version.
You must select one box from boxes I.20 to I.25 and boxes II.9 to II.16; for each box, you must select one option.
Where a box allows you to select one or more options, only the option(s) you select will be displayed in the electronic version of the CVED-P2.
Where a box is not compulsory, its contents will appear as strike-through text.
The sequences of boxes in the model of CVED-P2, the size and shape of those boxes are indicative.
Where a stamp is required, its electronic equivalent is an electronic seal.
PART I – DESCRIPTION OF CONSIGNMENT |
|
Box |
Description |
I.1. |
Consignor/Exporter |
|
Indicate the commercial organisation dispatching the consignment (in the third country). |
I.2 |
CVED reference |
|
This is the unique alpha-numeric code assigned by TRACES (repeated in boxes II.2 and III.2). |
I.3 |
Local reference |
|
Indicate the unique alpha-numeric code assigned by the competent authority. |
I.4 |
Border inspection post |
|
Select the name of the Border Inspection Post (BIP). In the case of a subsequent CVED for a non-conforming consignment, indicate the name of the TRACES unit in charge of supervising the free zone, free warehouse or customs warehouse where the consignment will be delivered and stored. |
I.5 |
Border inspection post code |
|
This is the unique alpha-numeric code assigned by TRACES to the BIP. |
I.6 |
Consignee/Importer |
|
Indicate the address of the person or commercial organisation given on the third-country certificate. If this not present on the certificate, the consignee in the relevant commercial documents may be used. |
I.7 |
Place of destination |
|
Indicate the delivery address in the Union. This applies to both conforming and non-conforming goods (see box I.19). |
I.8 |
Operator responsible for the load |
|
This is the person defined in Article 2(2)(e) of Directive 97/78/EC (also agent or declarant), who is in charge of the consignment when presented to the border inspection post and makes the necessary declarations to the competent authorities on behalf of the importer: give the name and address. |
I.9 |
Accompanying documents |
|
Veterinary certificate/document: Date of issue: The date on which the certificate/document was signed by the official veterinarian or the competent authority. Number: Give the unique official number of the certificate. For products from an approved or registered establishment or vessel, indicate the name and approval/registration number where appropriate. For embryos, ova or semen straws give an identity number of the approved collection team. Commercial document reference: the airway bill number, the bill of lading number or the commercial number of the train or road vehicle. |
I.10 |
Prior notification |
|
Give the estimated date and time on which the consignment is expected to arrive at the BIP. |
I.11 |
Country of origin |
|
This refers to where the final product was produced, manufactured or packaged. |
I.12 |
Not applicable |
I.13 |
Means of transport |
|
Give full details of the means of arrival transport: for aircraft the flight number, for vessels the ship name, for road vehicles the registration number plate with trailer number if appropriate, for railways the train identity and wagon number. |
I.14 |
Country of dispatch |
|
This refers to the third country where the consignment was placed aboard the means of final transport for the journey to the Union. |
I.15 |
Establishment of origin |
|
This box may be used to indicate the name and address (street, city and region/province/state, as appropriate), country and ISO country code of the establishment(s) of origin. Where applicable, indicate the registration or approval number. |
I.16 |
Transport conditions |
|
Select the appropriate transport temperature. |
I.17 |
Container number/Seal number |
|
Give all seal and container identification numbers where relevant. For official seal, indicate the official seal number as indicated in the official certificate and tick ‘official seal’ or indicate any other seal as mentioned in the accompanying documents. |
I.18 |
Certified as or for |
|
Tick the category for which the consignment is being presented: human consumption, feedstuff, pharmaceutical use, technical use or other. |
I.19 |
Conformity of the goods |
|
Tick ‘conforming’ for all products that will be presented for free circulation in the internal market including those that are acceptable but will be subjected to a channeling procedure and those that after receiving veterinary clearance as acceptable for free circulation, may be stored under customs control, and receive customs clearance at a later stage, either at the customs office on which the border inspection post is geographically dependent, or at another location. Tick ‘non-conforming’ for those products not meeting EU requirements and that are for free zones, free warehouses, customs warehouses, ship chandlers or ships or transit to a third country (see boxes 22 and 24). |
I.20 |
For transhipment to |
|
Tick this box where a consignment is not to be imported at this BIP but is to travel onward in another vessel or aircraft either for importation into the EU at a second and subsequent BIP in the EU/EEA, or for a third country destination. Indicate the name of the second and subsequent BIP and its unique alpha-numeric code assigned by TRACES or the name of the destination third country and ISO country code. |
I.21 |
Not applicable |
I.22 |
For transit to |
|
Tick this box for consignments that do not conform to EU requirements and are destined for a third country by movement across the relevant EU/EEA State by road, rail or waterway transport. Indicate the name of the BIP where the products are to leave the EU (exit BIP) and its unique alpha-numeric code assigned by TRACES. Indicate the name of the destination third country and ISO country code. |
I.23 |
For internal market |
|
Tick this box for consignments that are being presented for distribution in the single market. This also applies to those consignments that after receiving veterinary clearance as acceptable for free circulation, may be stored under customs control, and receive customs clearance at a later stage, either at the customs office on which the border inspection post is geographically dependent, or at another location. |
I.24 |
For non-conforming goods |
|
Select the type of destinations where the consignment will be delivered and stored under veterinary control: a free zone, a free warehouse, a customs warehouse or a ship supplier (chandler). |
I.25 |
For re-entry |
|
This refers to consignments of EU origin that have been refused acceptance or entry to a third country, and are being returned to the establishment of origin in the EU. |
I.26 |
Not applicable |
I.27 |
Means of transport after BIP |
|
Select the appropriate means of transport for goods subject to transhipment or re-entry and for non-conforming goods in transit (see guidance note in box I.13). |
I.28 |
Not applicable |
|
Not applicable. |
I.29 |
Not applicable |
|
Not applicable. |
I.30 |
Not applicable |
I.31 |
Description of consignment |
|
Indicate the species of animal, the treatment undergone by the products and the number and type of packages that comprise the load, e.g. 50 boxes of 2 kg, or the number of containers. Give as a minimum the first four digits of the relevant Combined Nomenclature (CN) code established pursuant to Council Regulation (EEC) No 2658/87 as last amended. These codes are also listed in Commission Decision 2007/275/EC (and are equivalent to the HS headings). In the case of fishery products only, where there is one certificate with one consignment having contents with more than one commodity code, the additional codes may be annotated onto the CVED as appropriate. |
I.32 |
Total number of packages |
|
Indicate the total number of packages in the consignment, where appropriate. |
I.33 |
Total quantity |
|
Indicate the total number of straws for semen, ova and embryos, where appropriate. |
I.34 |
Total net weight/total gross weight (kg) |
|
Net weight: weight of actual product in kg, excluding packaging. This is defined as the mass of the products themselves without immediate containers or any packaging. Gross weight: overall weight in kg. This is defined as the aggregate mass of the products and of the immediate containers and all their packaging, but excluding transport containers and other transport equipment. |
I.35 |
Declaration |
|
The declaration must be signed by the natural person responsible for the consignment: I, the undersigned person responsible for the load detailed above, certify that to the best of my knowledge and belief the statements made in Part I of this document are true and complete, and I agree to comply with the requirements of Directive 97/78/EC, including payment for veterinary checks, for repossession of any consignment rejected after transit across the EU to a third country [Article 11(1)(c)] or costs of destruction if necessary. |
PART II – CONTROLS |
|
Box |
Description |
II.1. |
Previous CVED |
|
This is the unique alpha-numeric code assigned by TRACES for the CVED used before transhipment. |
II.2 |
CVED reference |
|
This is the unique alpha-numeric code indicated in box I.2. |
II.3 |
Documentary check |
|
To be completed for all consignments. |
II.4 |
Identity check |
|
Tick ‘seal check’ where containers are not opened and the seal is only checked according to Article 4(4)(a)(i) of Directive 97/78/EC. Tick ‘no’ where goods are transhipped from one BIP to another BIP. |
II.5 |
Physical check |
|
‘Reduced checks’ refers to the regime laid down in Commission Decision 94/360/EEC where the consignment has not been selected for a physical check but is considered checked satisfactorily with documentary and identity check only. ‘Other’ refers to reimport procedure, channeled goods, transhipment, transit or Article 12 and 13 procedures. These destinations can be deduced from other boxes. |
II.6 |
Laboratory test |
|
Select the category of substance or pathogen for which an investigation procedure is undertaken. ‘Random’ indicates sampling where the consignment is not detained pending a result, in which case the competent authority of destination must be notified in TRACES (see Article 8 of Directive 97/78/EC). ‘Suspicion’ includes cases where the consignment has been detained pending a favourable result, or tested because of a previous notification from the rapid alert system for food and feed (RASFF), or tested because of a safeguard measure in operation. |
II.7 |
Not applicable |
II.8 |
Not applicable |
II.9 |
Acceptable for transshipment |
|
Tick this box where a consignment is not to be imported at this border inspection post but is to travel onward in another vessel or aircraft either for importation into the EU at a second and subsequent BIP in the EU/EEA, or for a third-country destination (See Article 9 of Directive 97/78/EC and Commission Implementing Decision 2011/215/EU) (1). |
II.10 |
Not applicable |
II.11 |
Acceptable for transit |
|
Tick this box when it is acceptable to send consignments that do not conform to EU requirements to a third country across the relevant EU/EEA State by road, rail or waterway transport. This must be carried out under veterinary control in accordance with the requirements of Article 11 of Directive 97/78/EC and Decision 2000/208/EC. |
II.12 |
Acceptable for internal market |
|
This box is to be used for all consignments approved for free circulation within the single market. It should also be used for consignments that meet EU requirements but for financial reasons are not being customs cleared immediately at the border inspection post, but are being stored under customs control in a customs warehouse or will be customs cleared later and/or at a geographically separate destination. |
II.13 |
Acceptable for monitoring |
|
For use where consignments are accepted but must be channeled to a specific destination laid down in Articles 8 or 15 of Directive 97/78/EC. |
II.14 |
Acceptable as non-conforming goods |
|
Use for all non-conforming consignments destined to be moved to or stored in warehouses approved in accordance with Article 12(4) or to operators authorised pursuant to Article 13 of Directive 97/78/EC. |
II.15 |
Not applicable |
II.16 |
Not acceptable |
|
Indicate clearly, when import is refused, the subsequent process to be carried out. Give the date for completion of the action proposed. The address of the establishment of destination should be entered in box II.18. |
II.17 |
Reason for refusal |
|
Tick the appropriate box. |
II.18 |
Details of controlled destinations |
|
Give, as appropriate, approval number and address (or ship name and port) for all destinations where further veterinary control of the consignment is required. |
II.19 |
Consignment resealed |
|
Use this box when the original seal recorded on a consignment is destroyed on opening the container. A consolidated list of all seals that have been used for this purpose must be kept. |
II.20 |
Identification of BIP |
|
Apply the official stamp of the BIP or the competent authority in the case of non-conforming consignments. |
II.21 |
Certifying officer |
|
Signature of the veterinarian or in case of ports handling fish only, of the designated official agent as laid down in Decision 93/352/EEC: I the undersigned official veterinarian, or designated official agent, certify that the veterinary checks on this consignment have been carried out in accordance with EU requirements. |
II.22 |
Inspection fees |
|
For internal purposes. |
II.23 |
Customs document reference |
|
For use by customs services if necessary. |
II.24 |
Subsequent CVED |
|
Indicate the unique alphanumeric code assigned by TRACES for the CVED used to document the checks after transhipment. |
PART III – FOLLOW-UP |
|
Box |
Description |
III.1 |
Previous CVED |
This is the unique alpha-numeric code indicated in box II.1. |
|
III.2 |
CVED reference |
This is the unique alpha-numeric code indicated in box I.2. |
|
III.3 |
Subsequent CVED |
Indicate the alphanumeric code of one or more CVEDs indicated in box II.24. |
|
III.4 |
Details on re-dispatch |
Indicate the means of transport used, its identification details, the name of the BIP of exit, the country of destination and the date of re- dispatch, as soon as they are known. |
|
III.5 |
Follow-up by |
Indicate, as appropriate, the authority in charge of certifying the reception and compliance of the consignment covered by the CVED. |
|
III.6 |
Certifying officer |
This refers to the signature of the responsible official in the case of re-dispatch and follow-up of the consignments. |
PART 2
Model for the CVED-P2
(1) Commission Implementing Decision of 4 April 2011 implementing Council Directive 97/78/EC as regards transhipment at the border inspection post of introduction of consignments of products intended for import into the Union or for third countries (OJ L 90, 6.4.2011, p. 50).
ANNEX II
‘ ANNEX III
PART 1
Notes for guidance for the common veterinary entry document for animals — model 2 (CVED-A2)
GENERAL
The entries specified in Part I constitute the data dictionaries for the electronic version of the CVED-A2.
Paper copies of an electronic CVED-A2 must bear a unique machine-readable optical label which hyperlinks to the electronic version.
You must select one box from boxes I.20 to I.26 and boxes II.9 to II.16; for each box, you must select one option.
Where a box allows you to select one or more options, only the option(s) you select will be displayed in the electronic version of the CVED-A2.
Where a box is not compulsory, its contents will appear as strike-through text.
The sequences of boxes in the model of CVED-A2, the size and shape of those boxes are indicative.
Where a stamp is required, its electronic equivalent is an electronic seal.
PART I – DESCRIPTION OF CONSIGNMENT |
|
Box |
Description |
I.1. |
Consignor/Exporter |
|
Indicate the commercial organization dispatching the consignment (in the third country). |
I.2 |
CVED reference |
|
This is the unique alpha-numeric code assigned by TRACES (repeated in boxes II.2 and III.2). |
I.3 |
Local reference |
|
Indicate the unique alpha-numeric code assigned by the competent authority. |
I.4 |
Border inspection post |
|
Select the name of the Border Inspection Post (BIP). |
I.5 |
Border inspection post code |
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This is the unique alpha-numeric code assigned by TRACES to the BIP (published in the Official Journal). |
I.6 |
Consignee/Importer |
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Indicate the address of the person or commercial organisation given on the third-country certificate. All these details are compulsory. |
I.7 |
Place of destination |
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Place to where the animals are being taken for final unloading (not counting control posts) and kept in accordance with the current rules. Give the name, country, address and post code. The place of destination may be the same as the location of the consignee. |
I.8 |
Operator responsible for the load |
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This is the person (including agent or declarant) who is in charge of the consignment when presented to the border inspection post and who makes the necessary declarations to the competent authorities on behalf of the importer: give the name and address. This person is required to notify the BIP in accordance with Article 3(1)(a) of Directive 91/496/EEC. The person responsible for the load and the consignee may be the same person. |
I.9 |
Accompanying documents |
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Number: give the unique official number of the certificate. Date of issue: this is the date on which the certificate/document was signed by the official veterinarian or the competent authority. Accompanying documents: this mainly concerns certain types of horses (horse passport), zootechnical documents or CITES permits. Commercial document reference: the airway bill number, the bill of lading number or the commercial number of the train or road vehicle. |
I.10 |
Prior notification |
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Give the date and time when consignments are expected to arrive at the BIP. Importers or their representatives are required (pursuant to Article 3(1)(a) of Directive 91/496/EEC) to give one working day’s notice to the veterinary staff of the BIP where the animals are to be presented, specifying the number, nature and expected time of arrival of the animals. |
I.11 |
Country of origin |
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This means the country in which the animals spent the requisite period (three months in the case of cattle, pigs, sheep, goats and equidae intended for slaughter; breeding, store or registered equidae, and poultry; six months in the case of breeding and store cattle and pigs; sheep and goats for breeding, store or fattening). For horses re-entering, this means the country from which they were last consigned |
I.12 |
Region of origin |
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Region in which the animals spent the same period as specified for the country: this is a requirement only for those countries which are divided into regions and for which imports are authorised only from one or more parts of the country concerned. The regional codes are given in the relevant rules. |
I.13 |
Means of transport |
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Give details of the means of transport to the BIP: The mode of transport (air, maritime, rail, road). Identification of the means of transport: for transport by air, the flight number; for maritime transport, the name of the vessel; for rail transport, the number of the train and the wagon and for road transport, the registration number of the r |