Dokumendiregister | Terviseamet |
Viit | 10.2-7/24/6672-1 |
Registreeritud | 25.06.2024 |
Sünkroonitud | 26.06.2024 |
Liik | Sissetulev dokument |
Funktsioon | 10.2 Toodete terviseohutusega seotud toimingud |
Sari | 10.2-7 Tubakatooted |
Toimik | 10.2-7/2024 |
Juurdepääsupiirang | Avalik |
Juurdepääsupiirang | |
Adressaat | 王超 |
Saabumis/saatmisviis | 王超 |
Vastutaja | Mikaela Pakosta (TA, Peadirektori asetäitja (1) vastutusvaldkond, Kemikaaliohutuse osakond) |
Originaal | Ava uues aknas |
Dear Sir/Madam,
In the EU TPD or in your national implementation act, we find the phrase: "Manufacturers and(not or) importers of electronic cigarettes and refill containers shall submit a notification to the competent authorities of the Member States of any such products which they intend to place on the market??.
From the materials or documents to be reported, is there any need for dual notifications? More specifically, do we need to report the same product as both a manufacturer and an importer?
What we are particularly interested in is the specific requirements of your country's competent authorities for the current notifier.
Thank you!
Tähelepanu! Tegemist on väljastpoolt asutust saabunud kirjaga. Tundmatu saatja korral palume linke ja faile mitte avada.