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Thiacloprid Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
04/99/EC
, Reg. (EU) No 2019/168 , Reg. (EU) No 540/2011 |
Old Legislation |
Reg. (EU) No 2016/2016
, Reg. (EU) No 2018/524 |
|---|---|---|---|
| Date of approval | 01/01/2005 | Expiration of approval | 30/04/2020 |
| RMS
Co-RMS |
DE
DE |
Risk Assessment | Commission |
| Category | IN | Review Report | |
| Remarks | The original RMS was UK. | ||
| Type | Candidate for Substitution (CfS) | CfS - criteria | endocrine disrupting properties |
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| Acute Tox. 3 - H301 | Acute Tox. 4 - H332 |
| STOT SE 3 - H336 | Carc. 2 - H351 |
| Repr. 1B - H360FD | Aquatic Acute 1 - H400 |
| Aquatic Chronic 1 - H410 |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.01 | 04/99/EC | |
| ARfD | 0.03 | 04/99/EC | |
| AOEL | 0.02 | 04/99/EC | |
| Other | |||
| ARfD 0,03 - ADI 0,01 JMPR 2006 | |||
- Legend
-
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level