BioMerieux
Dispositifs médicaux, fournitures de soins de santé et produits cliniques.
BioMérieux fabrique des dispositifs médicaux, des fournitures de santé et des produits cliniques à partir de ses opérations de Marcy-l'Étoile. La société fournit des acheteurs d'hôpitaux, des distributeurs cliniques, des systèmes de santé ou des clients exportateurs sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Marcy-lEtoile, France
- Founded
- 1963
- Website
- biomerieux.com
- Categories
- Fournitures médicales et de santé, Fournitures industrielles
- Markets
- France, États-Unis, Allemagne, Chine
Verified facts
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- operating-permit (green), checked 2026-06-30 Georisques, French register of classified installations (ICPE)
- facility-inspected (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- workforce-on-record (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- fda-registered (green), checked 2026-08-26 FDA
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- industrial-site-registered (green), checked 2024-12-31 IREP, French register of pollutant releases and waste (declared by the operator)
- facility-activity-described (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- domain-registered (green), checked 2026-08-26 Domain registry record
- media-mention (green), checked 2026-07-18 Yahoo Finance
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- 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)