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Pymetrozine Not Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
01/87/EC
, Reg. (EU) 2018/917 , Reg. (EU) No 540/2011 , Reg. (Eu) 2018/1501 |
Old Legislation |
2010/77/EU
, Reg. (EU) 2015/1885 , Reg. (EU) 2016/549 , Reg. (EU) 2017/841 |
|---|---|---|---|
| RMS
Co-RMS |
DE
BE |
Risk Assessment | Commission |
| Category | IN | Review Report |
Final Renewal Report 2018
List of studies relied upon (AIR 2) Inclusion 2002 |
| Remarks |
Non-renewal of approval: Reg. (EU) 2018/1501 Withdrawal of authorisations by 30 April 2019 Max period of grace: 30 January 2020 |
||
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, UK | BG, SK |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| Carc. 2 - H351 | Aquatic Chronic 3 - H412 |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.03 | Reg. (Eu) 2018/1501 | |
| ARfD | 0.1 | Reg. (Eu) 2018/1501 | |
| AOEL | 0.03 | Reg. (Eu) 2018/1501 | |
| Other | |||
| AAOEL: 0.1 mg/kg bw | |||
- Legend
-
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level