NORDNES DENTAL AS
Medical & Healthcare Supplies, Norway
NORDNES DENTAL AS is a medical & healthcare supplies company based in Eidsvåg I Åsane, Norway. Listed in a public business registry.
- Type
- brand seeking distribution
- Location
- Eidsvåg I Åsane, Norway
- Founded
- 1987
- Website
- https://nordnesdental.no
- Categories
- اللوازم الطبية والرعاية الصحية
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 هنا يحمل الفوز بالعقد فحصًا أجراه طرف آخر أيضًا: في الاتحاد الأوروبي والمنطقة الاقتصادية الأوروبية يجب على المشتري العام استبعاد مقدّمي العروض المدانين بالاحتيال أو الفساد أو غسل الأموال، ومن ثبتت عليهم بقرار نهائي متأخرات ضريبية أو اشتراكات اجتماعية. 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)