TERUMO EUROPE

Listed in a source registry

Belgium Crossroads Bank for Enterprises (KBO/BCE)

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 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)
• 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)

Check independently

• Sanctions and watchlists (OpenSanctions)