Erakliinik Dentes Aktsiaselts
Dentesest on kolmekümne viie tegevusaasta jooksul saanud üks juhtivaid hambaproteeside tootjaid ja eksportijaid Eestis, rakendatud on
Dentesest on kolmekümne viie tegevusaasta jooksul saanud üks juhtivaid hambaproteeside tootjaid ja eksportijaid Eestis, rakendatud on kvaliteedijuhtimise ISO
- Type
- Manufacturer
- Location
- Tartu linn, Estonia
- Founded
- 1996
- Website
- http://www.dentes.ee
- Categories
- 医疗保健用品
Listed in a source registry
Verified facts
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 1996-07-24 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-manufacturer (green), checked 2026-08-06 e-Äriregister (teatatud tegevusalad)
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- registry-id-verified (green), checked 2026-07-27 e-Business Register (e-Ariregister), Centre of Registers and Information Systems (RIK)
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- tax-filing-active (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
- workforce-on-record (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)