TERUMO EUROPE
Fournitures médicales et de santé, Belgique
TERUMO EUROPE est une entreprise de fournitures médicales et de soins de santé basée à Louvain, en Belgique. Inscrite au registre public des entreprises.
- Type
- brand seeking distribution
- Location
- Leuven, Belgium
- Categories
- Fournitures médicales et de santé
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-24 OpenSanctions
- sanctions-clear (green), checked 2026-08-24 OpenSanctions
- ownership-on-record (green), checked 2026-08-13 GLEIF global LEI index
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- public-contract-awarded (green), checked 2026-08-10 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)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- directors-on-file (green), checked 2026-08-20 Crossroads Bank for Enterprises (KBO/BCE) public search, Belgium
- registered-address (green), checked 2026-08-20 Crossroads Bank for Enterprises (KBO/BCE) public search, Belgium
- registered-since (green), checked 1971-05-05 Crossroads Bank for Enterprises (KBO/BCE) public search, Belgium
- workforce-on-record (green), checked 2026-08-20 Crossroads Bank for Enterprises (KBO/BCE) public search, Belgium
- fda-registered (green), checked 2026-08-24 FDA
Claimed certifications
- FDA Registered FDA Establishment Registration
- AEO, Authorised Economic Operator EU AEO database
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)