TERUMO EUROPE
Tıbbi ve Sağlık Malzemeleri, Belçika
TERUMO EUROPE, Leuven, Belçika merkezli bir tıbbi ve sağlık malzemeleri şirketidir. Kamu ticaret sicilinde listelenmiştir.
- Type
- brand seeking distribution
- Location
- Leuven, Belgium
- Categories
- Tıbbi ve Sağlık Malzemeleri
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 Burada ihalenin kazanılması başkasının yaptığı bir denetimi de taşır: AB ve AEA'da kamu alıcısı, dolandırıcılık, yolsuzluk veya kara para aklamadan hüküm giymiş istekliler ile kesinleşmiş kararla vergi veya sosyal güvenlik borcu saptananları elemek zorundadır. 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)