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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)

Failid

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
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