DentaLab OÜ
Vous cherchiez peut-être autre chose, mais c'est tout ce que nous pouvons vous proposer pour l'instant. Selon toute vraisemblance, la page qui se trouvait auparavant ici a été déplacée ou supprimée.
- Type
- Manufacturer
- Location
- Kristiine linnaosa, Estonia
- Founded
- 2016
- Website
- dentalab.ee
- Categories
- Fournitures médicales et de santé
Listed in a source registry
Verified facts
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2016-08-02 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2026-07-27 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- public-contract-awarded (green), checked 2025-06-02 TED (Tenders Electronic Daily), EU public procurement award notices Ici l'attribution porte aussi un contrôle fait par d'autres: dans l'UE et l'EEE, l'acheteur public doit exclure les candidats condamnés pour fraude, corruption ou blanchiment, ainsi que ceux dont une décision définitive a établi des dettes fiscales ou sociales. Directive 2014/24/EU, Article 57 (exclusion grounds)
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- 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
- media-mention (green), checked 2016-09-09 kuulutaja.ee
- registry-id-verified (green), checked 2026-07-27 e-Business Register (e-Ariregister), Centre of Registers and Information Systems (RIK)
- workforce-on-record (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
- tax-filing-active (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)