Sissetulev kiriAvalik
Küsimused
Ravimiamet · 2. jaanuar 2026
- Viit
- MSO-2/7-1
- Registreeritud
- 2. jaanuar 2026
- Dokumendi liik
- Sissetulev kiri
- Adressaat
- ADAS3D MEDICAL, S.L.
- Saabumis/saatmisviis
- e-post
- Funktsioon
- MSO Meditsiiniseadmed
- Sari
- MSO-2 Eesti turule lastavate/kasutusele võetavate/levitatavate seadmete teavitused ning EC sertifikaadid
- Toimik
- MSO-2/2026
- Vastutaja
- Karl Kalev Türk (RA, Meditsiiniseadmete osakond)
Sisu (failidest)
Saatja: Génesis Fuentes <[email protected]>
Saaja: RA MSO, Quality&Regulatory
Teema: Registration of medical devices in Estonia
Tähelepanu! Tegemist on väljastpoolt asutust saabunud kirjaga. Tundmatu saatja korral palume linke ja faile mitte avada.
Hi team
Nice to greet you
We have a question about the registration of products to be marketed in Estonia
We are a Spanish manufacturer that wants to market a class IIa product in Estonia and we understand that to comply with the regulatory requirements we must communicate the product from the Medical devices department however, we cannot find the link to register, nor the information on which documents attach.
thanks in advance for your help
I wait for your comments
Génesis Fuentes Casella
Quality & Regulatory Affairs Technician
Rambla Catalunya 53, 4-H, 08007 Barcelona