
Article 1 
The complement fixation test, the buffered Brucella antigen test (rose Bengal test (RBT)), the ELISA tests and the fluorescence polarisation assay (FPA) carried out in accordance with Annex C to Directive 64/432/EEC are hereby approved for certification purposes.
Article 2 
Where, for the purposes referred to in Article 6(2)(b) of Directive 64/432/EEC, a test referred to in Article 1 of this Decision is used, the test shall be specified in the column ‘Test’ of the tables in point 3, second indent, and in point 5 of Section A in Annex F, Model 1 (health certificate) to Directive 64/432/EEC.
Article 3 
Decision 2000/330/EC is repealed.
References to the repealed Decision shall be construed as references to this Decision and shall be read in accordance with the correlation table in Annex II.
Article 4 
This Decision is addressed to the Member States.
ANNEX I
Commission Decision 2000/330/EC (OJ L 114, 13.5.2000, p. 37)
Commission Regulation (EC) No 535/2002 (Article 2 only) (OJ L 80, 23.3.2002, p. 22)
ANNEX II
Decision 2000/330/EC This Decision
Articles 1 and 2 Articles 1 and 2
— Article 3
Article 3 Article 4
— Annex I
— Annex II