
Article 1 
Annexes VII, X and XI to Regulation (EC) No 1774/2002 are amended in accordance with the Annex to this Regulation.
Article 2 
Consignments of milk and milk products not intended for human consumption accompanied by a health certificate completed and signed in accordance with the appropriate model set out in Chapter 2 of Annex X to Regulation (EC) No 1774/2002 before the date of entry into force of this Regulation shall continue to be accepted for importation into the Union until 30 September 2010, where those certificates were completed and signed before 31 August 2010.
Article 3 
This Regulation shall enter into force on the 20th day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 7 September 2010.
For the Commission
The President
José Manuel BARROSO
ANNEX

Annexes VII, X and XI to Regulation (EC) No 1774/2002 are amended as follows:

1.. in Annex VII, Chapter V is amended as follows:

((a)) the heading is replaced by the following:
'
CHAPTER V'
((b)) Part A is amended as follows:

((i)) paragraph 3 is replaced by the following:
'
3. 

((a)) either be collected at least 16 hours following milk clotting and its pH must be recorded as below 6,0 before transport to animal holdings; or
((b)) have been produced at least 21 days before shipping and during that period no case of foot-and-mouth disease has been detected in the Member State of origin.
';
((ii)) the following paragraph 6 is added:
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6. 

6.1. be obtained from bovine animals kept on a holding on which all bovine herds are recognised as officially tuberculosis-free, officially brucellosis-free and officially enzootic-bovine-leukosis-free as defined in Article 2(2)(d), (f) and (j) of Directive 64/432/EEC;
6.2. have been produced at least 21 days before shipping and during that period no case of foot-and-mouth disease has been detected in the Member State of origin;
6.3. have undergone a single HTST treatment;
6.4. comply with the requirements set out in paragraph 4.
'
((c)) Part B is amended as follows:

((i)) paragraph 1.1 is replaced by the following:
'
1.1. they come from third countries appearing on the list in Part I(A) of Annex XI;
';
((ii)) paragraph 2 is replaced by the following:
'
2. 

((a)) have not been shipped before a period of at least 21 days has elapsed after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country; or
((b)) have been presented at an EU border inspection post at least 21 days after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country.
';
((iii)) the following paragraph 2a is inserted:
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2a. 

2a.1. they come from a third country appearing on the list in Part I(B) of Annex XI;
2a.2. they comply with the conditions set out in paragraphs 1.2 and 1.3;
2a.3. they have undergone a single HTST treatment and:

((a)) have not been shipped before a period of at least 21 days has elapsed after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country; or
((b)) have been presented at an EU border inspection post at least 21 days after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country;
2a.4. they have been obtained from bovine animals subject to regular veterinary inspections to ensure that animals come from holdings on which all bovine herds are:

((a)) either recognised as officially tuberculosis free and officially brucellosis free as defined in Article 2(2)(d) and (f) of Directive 64/432/EEC or not restricted under the national legislation of the third country of origin of the colostrum regarding eradication of tuberculosis and brucellosis; and
((b)) either recognised as official enzootic-bovine-leukosis-free as defined in Article 2(2)(j) of Directive 64/432/EEC or included in an official system for the control of enzootic-bovine-leukosis and there has been no evidence as a result of clinical and laboratory testing of this disease in the herd during the past two years;
2a.5. after completion of the processing, every precaution has been taken to prevent contamination of the colostrum or colostrum products;
2a.6. the final product has been labelled so as to indicate that it contains Category 3 material and is not intended for human consumption, and that it has been:

((a)) packed in new containers; or
((b)) transported in bulk in containers or other means of transport that before use were thoroughly cleansed and disinfected using a disinfectant approved for the purpose by the competent authority.
';
2.. in Annex X, Chapter 2 is replaced by the following:
'
CHAPTER 2  Health certificate 

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3.. Annex XI is amended as follows:

((a)) Part I is replaced by the following:
'
PART I 

A.. Milk and milk products:
Third countries listed as authorised in any of the columns of Annex I to Decision 2004/438/EC.
B.. Colostrum and colostrum products:
Third countries listed as authorised in column “A” of Annex I to Decision 2004/438/EC.
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((b)) Part XII is replaced by the following:
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PART XII 
Third countries listed in part 1 of Annex II to Regulation (EU) No 206/2010, and the following country:


— “(CM) Cameroon” 
'.
