Commission Implementing Decision (EU) 2016/107 of 27 January 2016 not approving cybutryne as an existing active substance for use in biocidal products for product-type 21 (Text with EEA relevance)

What Commission Implementing Decision (EU) 2016/107 of 27 January 2016 not approving cybutryne as an existing active substance for use in biocidal products for product-type 21 (Text with EEA relevance) requires

The European Commission has decided not to approve cybutryne as an active substance for use in biocidal products for product-type 21, which includes antifouling products. This decision is based on the evaluation conducted by the Netherlands as the designated competent authority, which concluded that biocidal products containing cybutryne do not meet the requirements laid down in Article 5 of Directive 98/8/EC. The environmental risk assessment identified unacceptable risks, leading to the conclusion that cybutryne should not be approved for use in these products. The decision is in accordance with the opinion of the Standing Committee on Biocidal Products and enters into force twenty days after its publication in the Official Journal of the European Union.

Pillar: Legal & IP Sovereignty · Authority: European Commission · Version: 1.0.0 · Last updated: 2016-01-27

Primary source: https://eur-lex.europa.eu/legal-content/EN/TXT/HTML/?uri=CELEX:32016D0107

SHA-256 integrity: a9502aa5a2593869b6917fb4fcc253e886bb39b22243026f14b86257d30e348a

Primary Citations — 8 traced to source

• Article 1: Cybutryne (EC No 248-872-3, CAS No 28159-98-0) is not approved as an active substance for use in biocidal products for product-type 21.
• Article 2: This Decision shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.

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