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Decision of the EEA Joint Committee No 182/2018 of 21 September 2018 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2021/296]

Decision of the EEA Joint Committee No 182/2018 of 21 September 2018 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2021/296]

THE EEA JOINT COMMITTEE,

Having regard to the Agreement on the European Economic Area (‘the EEA Agreement’), and in particular Article 98 thereof,

Whereas:

  1. Commission Implementing Regulation (EU) 2018/613 of 20 April 2018 approving PHMB (1415; 4.7) as an existing active substance for use in biocidal products of product-types 2 and 4(1) is to be incorporated into the EEA Agreement.

  2. Commission Implementing Regulation (EU) 2018/614 of 20 April 2018 approving azoxystrobin as an active substance for use in biocidal products of product-types 7, 9 and 10(2) is to be incorporated into the EEA Agreement.

  3. Commission Implementing Decision (EU) 2018/619 of 20 April 2018 not approving PHMB (1415; 4.7) as an existing active substance for use in biocidal products of product-types 1, 5 and 6(3) is to be incorporated into the EEA Agreement.

  4. Annex II to the EEA Agreement should therefore be amended accordingly,

HAS ADOPTED THIS DECISION:

Article 1

The following points are inserted after point 12zzzzzi (Commission Implementing Decision (EU) 2018/622) of Chapter XV of Annex II to the EEA Agreement:

  • 32018 R 0613: Commission Implementing Regulation (EU) 2018/613 of 20 April 2018 approving PHMB (1415; 4.7) as an existing active substance for use in biocidal products of product-types 2 and 4 (OJ L 102, 23.4.2018, p. 1).

  • 32018 R 0614: Commission Implementing Regulation (EU) 2018/614 of 20 April 2018 approving azoxystrobin as an active substance for use in biocidal products of product-types 7, 9 and 10 (OJ L 102, 23.4.2018, p. 5).

  • 32018 D 0619: Commission Implementing Decision (EU) 2018/619 of 20 April 2018 not approving PHMB (1415; 4.7) as an existing active substance for use in biocidal products of product-types 1, 5 and 6 (OJ L 102, 23.4.2018, p. 21).’.

Article 2

The texts of Implementing Regulations (EU) 2018/613 and (EU) 2018/614 and Implementing Decision (EU) 2018/619 in the Icelandic and Norwegian languages, to be published in the EEA Supplement to the Official Journal of the European Union, shall be authentic.

Article 3

This Decision shall enter into force on 22 September 2018, provided that all the notifications under Article 103(1) of the EEA Agreement have been made(****).

Article 4

This Decision shall be published in the EEA Section of, and in the EEA Supplement to, the Official Journal of the European Union.