| Dokumendiregister | Ravimiamet |
| Viit | MSO-11/4803-6 |
| Registreeritud | 06.10.2025 |
| Sünkroonitud | 07.10.2025 |
| Liik | Sissetulev kiri |
| Funktsioon | MSO Meditsiiniseadmed |
| Sari | MSO-11 Seadmete vastavuse hindamisega seotud kirjavahetus |
| Toimik | MSO-11/2025 |
| Juurdepääsupiirang | AK |
| Juurdepääsupiirang | AvTS § 35 lg 1 p 17 teave, mille avalikustamine võib kahjustada ärisaladust |
| Adressaat | Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices |
| Saabumis/saatmisviis | Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices |
| Vastutaja | Kristina Kübar (RA, Meditsiiniseadmete osakond) |
| Originaal | Ava uues aknas |
| Nimi | K.p. | Δ | Viit | Tüüp | Org | Osapooled |
|---|---|---|---|---|---|---|
| Request concerning Straumann medical devices | 01.10.2025 | 1 | MSO-11/4803-4 🔒 | Sissetulev kiri | ra | botiss biomaterials GmbH |
| Request concerning Straumann medical devices | 01.10.2025 | 1 | MSO-11/4803-5 🔒 | Väljaminev kiri | ra | Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices, Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices, mdc medical device certification GmbH |
| Request concerning Straumann medical devices | 29.09.2025 | 1 | MSO-11/4803-3 🔒 | Sissetulev kiri | ra | botiss biomaterials GmbH |
| Request concerning Straumann medical devices | 29.09.2025 | 1 | MSO-11/4803-2 🔒 | Väljaminev kiri | ra | botiss biomaterials GmbH, botiss biomaterials GmbH |