Veterinary Certificate To Eu (Page 3 of 4) in pdf

COUNTRY

Non-commercial movement of

five or less dogs, cats or ferrets

II.

Health information

II.a.

Certificate reference No

II.b.

Place and date:

Signature:

Notes

(a)

The original of each certificate shall consist of a single sheet of paper, or, where more text is required it must

be in such a form that all sheets of paper required are part of an integrated whole and indivisible.

(b)

The certificate shall be drawn up at least in the language of the Member State of entry and in English. It shall

be completed in block letters in the language of the Member State of entry or in English.

(c)

If additional sheets of paper or supporting documents are attached to the certificate, those sheets of paper or

document shall also be considered as forming part of the original of the certificate by the application of the

signature and stamp of the official veterinarian, on each of the pages.

(d)

When the certificate, including additional sheets referred to in (c), comprises more than one page, each page

shall be numbered, (page number) of (total number of pages), at the end of the page and shall bear the

certificate reference number that has been designated by the competent authority at the top of the pages.

(e)

The certificate is valid for 10 days from the date of issue by the official veterinarian until the date of the

checks at the EU travellers' point of entry and for the purpose of further movements within the Union, for a

total of 4 months from the date of issue of this certificate or until the date of expiry of the anti-rabies

vaccination, whichever date is earlier.

(f)

The competent authorities of the exporting third country or territory shall ensure that rules and principles of

certification equivalent to those laid down in Directive 96/93/EC are followed.

Part I:

Box I.11.:

Place of origin: name and address of the dispatch establishment. Indicate approval or registration

number

Box I.28.:

Identification system : Select of the following : microchip or tattoo

Date of application of the microchip or tattoo : The tattoo must be clearly readable and applied before

3 July 2011

Identification number : Indicate the microchip or tattoo number

Date of birth : Indicate only if known

Part II:

(1)

Any revaccination must be considered a primary vaccination if it was not carried out within the period of

validity of a previous vaccination.

(2)

A certified copy of the identification and vaccination details of the animals concerned shall be attached to the

certificate.

(3)

Keep as appropriate. Where the certificate states that certain statements shall be kept as appropriate,

statements which are not relevant may be crossed out and initialled and stamped by the official veterinarian, or

completely deleted from the certificate.

(4)

The rabies antibody test referred to in point II.3:

must be carried out on a sample collected by a veterinarian authorised by the competent authority, at least

30 days after the date of vaccination and three months before the date of import;

must measure a level of neutralising antibody to rabies virus in serum equal to or greater than 0.5 IU/ml;

must be performed by a laboratory approved in accordance with Article 3 of Council Decision

2000/258/EC designating a specific institute responsible for establishing criteria necessary for

standardising the serological tests to monitor the effectiveness of rabies vaccines (list of approved

laboratories available at );

needs not be renewed on an animal, which following that test with satisfactory results, has been

revaccinated against rabies within the period of validity of a previous vaccination.

(5)

A certified copy of the official report from the approved laboratory on the results of the rabies antibody tests

referred to in point II.3 shall be attached to the certificate.

(6)

The treatment against Echinococcus multilocularis referred to in point II.5 must:

be administered by a veterinarian within a period of not more than 120 hours and not less than 24 hours

before the time of the scheduled entry of the dogs into one of the Member States or parts thereof listed in

Annex I to Regulation (EU) No 1152/2011;

consist of an approved medicinal product which contains the appropriate dose of praziquantel or

pharmacologically active substances, which alone or in combination, have been proven to reduce the

burden of mature and immature intestinal forms of Echinococcus multilocularis in the host species

concerned.

Veterinary Certificate To Eu Page 3

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