Päring
| Dokumendiregister | Terviseamet |
| Viit | 10.1-1/24/40-1 |
| Registreeritud | 19.06.2024 |
| Sünkroonitud | 20.06.2024 |
| Liik | Sissetulev dokument |
| Funktsioon | 10.1 Kemikaaliohutusega seotud toimingud |
| Sari | 10.1-1 REACH ja CLP kasutajatoe kirjavahetus, info- ja muud dokumendid |
| Toimik | 10.1-1/2024 |
| Juurdepääsupiirang | Avalik |
| Juurdepääsupiirang | |
| Adressaat | Nufarm Polska Sp. z o. o. |
| Saabumis/saatmisviis | Nufarm Polska Sp. z o. o. |
| Vastutaja | Aigi Lahe (TA, Peadirektori asetäitja (1) vastutusvaldkond, Kemikaaliohutuse osakond) |
| Originaal | Ava uues aknas |
Failid
|
Tähelepanu! Tegemist on väljastpoolt asutust saabunud kirjaga. Tundmatu saatja korral palume linke ja faile mitte avada. |
Dear Sir/Madam,
With the end of this year the transitional period for putting UFI codes on the labels is ending. Our company has started the process some time ago, so we’ve been able to place on the market all products classified as hazardous (fiz-chem or/and tox) with UFI code.
However as some products have for example 3 years of shelf life, it might happen that in distribution channel or in end professional users there will be still product on stocks without UFI label.
I have a question if in such situation does your country regulations require relabelling or can product be on the market as it is till end of shelf life? What is your approach?
Thank you in advance for reply. In case of any questions don’t hesitate to contact me.
Best regards / Pozdrawiam,
–––––––––––––––––––––––––––––––––––––––
Natalia Gackoska
Country Registration Manager Baltics
M +48 663 260 290
Nufarm Polska Sp. z o. o.
ul. Grójecka 1/3
02-019 Warszawa, Polska
nufarm.com
–––––––––––––––––––––––––––––––––––––
