A more recent version of this regulatory record is available. This version is kept only as a historical record. Please see the Record history section for link to the most recent version.
List details
Basic info
Status | Intention |
---|---|
Submitter | Austria |
Regulatory programme |
|
Classification
Intention timeline
Date of intention | 2019-02-12 |
---|---|
Expected date of submission | 2019-12-31 |
Documents
Related substances
By adding any of the following substances to your watchlist, you would be monitoring this regulatory record and all possible new regulatory records related to that substance.
Related regulatory records
Record history
The following timeline shows when we detected changes of this regulatory record (the date might slightly differ from the date of the actual change). Additions between versions are hightlighted in green color, red color shows data removed between versions.
June 18, 2019
- Proposed harmonised classification by the dossier submitter: Germ cell mutagenicity
- Proposed harmonised classification by the dossier submitter: Reproductive toxicity
- Proposed harmonised classification by the dossier submitter: Skin sensitisation
- Proposed harmonised classification by the dossier submitter: Specific target organ toxicity - repeated exposure
Jan. 14, 2020
- Proposed harmonised classification by the dossier submitter: Germ cell mutagenicity → Acute Tox. 2, H330
- Proposed harmonised classification by the dossier submitter: Reproductive toxicity → Acute Tox. 4, H302
- Proposed harmonised classification by the dossier submitter: Skin sensitisation → Eye Dam. 1, H318
- Proposed harmonised classification by the dossier submitter: Specific target organ toxicity - repeated exposure → Muta. 2, H341
- Proposed harmonised classification by the dossier submitter: Repr. 1B, H360FD
- Proposed harmonised classification by the dossier submitter: STOT RE 1, H372
- Proposed harmonised classification by the dossier submitter: Skin Corr. 1, H314
- Proposed specific concentration limits by the dossier submitter: Oral: ATE = 510 mg/kg bw Inhalation: ATE = 0.317 mg/L
- Status: Intention → Submitted
- Submitted for accordance check: 2019-12-20
Nov. 30, 2020
- Annexes to the CLH Report: https://echa.europa.eu/documents/10162/56a42449-87f6-77ff-e4e9-c2e1ddf60c93
- CLH report: https://echa.europa.eu/documents/10162/7e6f3b83-664e-b13c-7f72-7c4f83b5db7c
- Deadline for commenting: 2021-01-29
- Final submission date: 2020-09-02
- Hazard classes open for commenting: Germ cell mutagenicity Reproductive toxicity Acute Toxicity - inhalation Acute Toxicity - dermal Acute Toxicity - oral Specific target organ toxicity – single exposure Specific target organ toxicity – repeated exposure Skin corrosion/irritation Serious eye damage/eye irritation Skin Sensitisation
- Legal deadline for opinion adoption: 2022-03-04
- Status: Submitted → Consultation
- Start of consultation: 2020-11-16
Feb. 17, 2021
- Comments received: https://echa.europa.eu/documents/10162/1451411a-93de-c6f0-d74e-3f4a6eb0ec92
- Status: Consultation → Opinion Development
Oct. 8, 2021
- Date of opinion: 2021-09-16
- Status: Opinion Development → Opinion Adopted
Jan. 6, 2022
- Background document: https://echa.europa.eu/documents/10162/648aa561-e803-32ff-58fb-63cd700dafac
- Comments received: https://echa.europa.eu/documents/10162/1451411a-93de-c6f0-d74e-3f4a6eb0ec92 → https://echa.europa.eu/documents/10162/46f99d83-8910-c3d9-5f18-c520a346b3b1
- RAC opinion: https://echa.europa.eu/documents/10162/23b00ab5-0072-6282-6a73-d103a3696f43
This version
Add the related substance to your watchlist to monitor this regulatory record.