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Dazomet Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
2011/53/EU
, Reg. (EU) No 2018/1266 , Reg. (EU) No 540/2011 |
||
|---|---|---|---|
| Date of approval | 01/06/2011 | Expiration of approval | 31/05/2023 |
| RMS
Co-RMS |
BG
NL |
Risk Assessment | EFSA |
| Category | NE, FU, HB, ST | Review Report |
Confirmatory data 2015
Inclusion 2011 |
| Remarks | Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008. | ||
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, BG, CZ, EL, ES, FR, HR, HU, IE, IT, LU, NL, PL, PT, RO, SI, SK, UK |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| Acute Tox. 4 - H302 | Eye Irrit. 2 - H319 |
| Aquatic Acute 1 - H400 | Aquatic Chronic 1 - H410 |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.01 | 11/53/EU | |
| ARfD | 0.03 | 11/53/EU | |
| AOEL | 0.015 | 11/53/EU | |
| Other | |||
| 0,0005 AUS 1996 | |||
- Legend
-
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level