COMMISSION IMPLEMENTING REGULATION (EU) 2015/419
of 12 March 2015
approving tolylfluanid as an active substance for use in biocidal products for product-type 21
(Text with EEA relevance)
Article 1
Article 2
ANNEX
Common Name |
IUPAC Name Identification Numbers |
Minimum degree of purity of the active substance(1) |
Date of approval |
Expiry date of approval |
Product type |
Specific conditions(2) |
||||||||||
Tolylfluanid |
IUPAC Name: N-(Dichlorofluoromethylthio)-N′,N′-dimethyl-N-p-tolylsulfamide EC No: 211-986-9 CAS No: 731-27-1 |
960 g/kg |
1 July 2016 |
31 December 2025 |
21 |
The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the Union level risk assessment of the active substance. In the event that products containing tolylfluanid are subsequently authorised for use by non-professional users, persons making products containing tolylfluanid available on the market for non-professional users shall ensure that the products are supplied with appropriate gloves. For biocidal products, authorisations are subject to the following conditions:
For treated articles, the following condition applies: where a treated article has been treated with or intentionally incorporates one or more biocidal products containing tolylfluanid, and where necessary due to the possibility of skin contact as well as the release of tolylfluanid under normal conditions of use of the treated article, the person responsible for placing the treated article on the market shall ensure that the label provides information on the risk of skin sensitisation, as well as the information referred to in the second subparagraph of Article 58(3) of Regulation (EU) No 528/2012. |