NORDNES DENTAL AS
Fournitures médicales et de santé, Norvège
NORDNES DENTAL AS est une entreprise de Fournitures médicales et de santé basée à Eidsvåg I Åsane, Norvège. Inscrite dans un registre public des entreprises.
- Type
- brand seeking distribution
- Location
- Eidsvåg I Åsane, Norway
- Founded
- 1987
- Website
- https://nordnesdental.no
- Categories
- Fournitures médicales et de santé
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- domain-registered (green), checked 2026-08-14 Domain registry record
- workforce-on-record (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- public-contract-awarded (green), checked 2024-06-13 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)
- facility-registered (green), checked 2026-08-14 Google Maps place record
- registry-activity (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- registry-active-global (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- registry-id-verified (green), checked 2026-07-11 Bronnoysund Register Centre, Central Coordinating Register of Legal Entities (Enhetsregisteret)
- annual-accounts-filed (green), checked 2026-08-14 Regnskapsregisteret (Brønnøysund)
- leadership-on-record (green), checked 2026-08-14 Brønnøysund (roller)
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)