Commission Directive 2010/71/EU of 4 November 2010 amending Directive 98/8/EC of the European Parliament and of the Council to include metofluthrin as an active substance in Annex I thereto (Text with EEA relevance) (repealed)
Print Options
PrintThe Whole
Directive
PrintThe
Annexes
only
Status:
This is the original version (as it was originally adopted).
ANNEX
In Annex I to Directive 98/8/EC, the following entry for the substance metofluthrin is added:
|
No | Common Name | IUPAC NameIdentification Numbers | Minimum purity of the active substance in the biocidal product as placed on the market | Date of inclusion | Deadline for compliance with Article 16(3) (except for products containing more than one active substance, for which the deadline to comply with Article 16(3) shall be the one set out in the last of the inclusion decisions relating to its active substances) | Expiry date of inclusion | Product type | Specific provisions |
---|
‘36 | Metofluthrin | RTZ isomer:
2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl-(1R,3R)-2,2-dimethyl-3-(Z)-(prop-1-enyl)cyclopropanecarboxylate
EC No: n.a.
CAS No: 240494-71-7
Sum of all isomers:
2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl (EZ)-(1RS,3RS;1SR,3SR)-2,2-dimethyl-3-prop-1-enylcyclopropanecarboxylate
EC No: n.a.
CAS No: 240494-70-6
| The active substance shall comply with both the following minimum purities:
RTZ isomer:
754 g/kg
Sum of all isomers:
930 g/kg
| 1 May 2011 | Not applicable | 30 April 2021 | 18 | When assessing the application for authorisation of a product in accordance with Article 5 and Annex VI, Member States shall assess, when relevant for the particular product, those uses or exposure scenarios and those risks to compartments and populations that have not been representatively addressed in the European level risk assessment.’ |
Back to top