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Active substance factsheet - Last updated: 28/06/2024

Active substance

EC number:

-

CAS number:

-

IUPAC name:

2,3,5,6-tetrafluoro-4-(methoxymethyl) benzyl (EZ)-(1RS,3RS;1SR,3SR)- 2,2-dimethyl-3-prop-1-eny lcyclopropanecarboxylate

BAS number:

45

Product-type:

PT18

Candidate for substitution:

Under assessment

Regulatory categorisation:

Substance not in Review Programme

Approval/Assessment status:

Approved - Renewal in progress
Opinion development by BPC

Related authorised biocidal products

2 related products

-

SUMIONE LIQUID VAPORISER

SUMIONE® LIQUID VAPORISER

SUMIONE® szúnyogirtó folyadék

SumiOne® Liquid Vapouriser

Sumione LV

Austria

Belgium

France

Germany

Greece

Hungary

Ireland

Italy

Netherlands

Poland

Spain

Sweden

Switzerland

United Kingdom

National authorisation Link to the factsheet

Insecticida en papel ReLeVi para uso durante todo el día

ReLeVi Full-Day Paper Insecticide

Spain

United Kingdom

National authorisation Link to the factsheet
Approval data details
Administrative identifiers

Evaluating competent authority:

Ireland

R4BP asset number:

EU-0005389-0000

Approval identifiers
Validity of approval

Start date:

01/05/2011

End date:

31/10/2024

Documents
Assessment Reports

Assessment Report

N/A

Study summaries (Document III-A)

Study summary

N/A

N/A

N/A

Other documents
Renewal of active substance
Assessment information

Evaluating competent authority:

Ireland

Assessment outcome:

In progress

Conclusion date:

Validity of approval

Start date:

End date:

Legal act:

Documents
Assessment Reports
Study summaries (Document III-A)
Other documents
Amendment of active substance - Conclusion Date: 07/09/2023   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

07/09/2023

Validity of approval

Start date:

01/05/2011

End date:

31/10/2024

Documents
Assessment Reports

Assessment Report

N/A

Study summaries (Document III-A)

Study summary

N/A

N/A

N/A

Other documents
Amendment of active substance - Conclusion Date: 23/03/2021   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

23/03/2021

Validity of approval

Start date:

01/05/2011

End date:

31/10/2023

Documents
Assessment Reports

Assessment Report

N/A

Study summaries (Document III-A)

Study summary

N/A

N/A

N/A

Other documents
Approval of active substance - Conclusion Date: 04/11/2010  
Assessment information

Evaluating competent authority:

United Kingdom

Assessment outcome:

Successful

Conclusion date:

04/11/2010

Validity of approval

Start date:

01/05/2011

End date:

30/04/2021

Documents
Assessment Reports

Assessment Report

N/A

Study summaries (Document III-A)

Study summary

N/A

N/A

N/A

Other documents