TERUMO EUROPE
医療およびヘルスケア用品、ベルギー
テルモ ヨーロッパは、ベルギーのルーヴェンに拠点を置く医療およびヘルスケア用品会社です。公的事業登録簿に登録されています。
- Type
- brand seeking distribution
- Location
- Leuven, Belgium
- Categories
- 医療およびヘルスケア用品
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 ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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)