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Spirodiclofen Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
2010/25/EU
, Reg. (EU) No 540/2011 |
||
|---|---|---|---|
| Date of approval | 01/08/2010 | Expiration of approval | 31/07/2020 |
| RMS
Co-RMS |
AT
NL |
Risk Assessment | EFSA |
| Category | AC, IN | Review Report | |
| Remarks | Extension provisional authorisation (2009/579) | ||
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, BG, CY, DE, EE, EL, ES, FI, FR, HR, HU, IT, LT, LU, LV, NL, PL, PT, RO, SI, UK |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| No classification |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.015 | EFSA ´09 | |
| ARfD | Not applicable | EFSA ´09 | |
| AOEL | 0.009 | EFSA ´09 | |
| Other | |||
- Legend
-
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level