Bruker Belgium
Товары медицинского назначения и здравоохранения, Бельгия
Bruker Belgium , компания, занимающаяся поставками медицинского оборудования и товаров медицинского назначения, базирующаяся в Контиче, Бельгия. Внесен в государственный реестр предприятий.
- Type
- brand seeking distribution
- Location
- Kontich, Belgium
- Website
- https://bruker.com
- Categories
- Медицинские товары и расходники
Listed in a source registry
Verified facts
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- domain-registered (green), checked 2026-08-14 Domain registry record
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- public-contract-awarded (green), checked 2025-08-28 TED (Tenders Electronic Daily), EU public procurement award notices Здесь награда несёт ещё и чужую проверку: в ЕС и ЕЭЗ заказчик обязан отстранить участника, осуждённого за мошенничество, коррупцию или отмывание, и того, за кем окончательным решением признаны долги по налогам или социальным взносам. Directive 2014/24/EU, Article 57 (exclusion grounds)
- 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 1971-01-04 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
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)