ECOSYSTEM
- Type
- Manufacturer
- Location
- Paris, France
- Founded
- 1989
- Categories
- اللوازم الطبية والرعاية الصحية
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-manufacturer (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registry-id-verified (green), checked 2026-07-22 Annuaire des Entreprises (INSEE / INPI)
- places-goods-on-market (green), checked 2026-08-09 Registre national des producteurs (ADEME/SYDEREP), France
- vat-valid (green), checked 2026-07-25 VIES
- sanctions-clear (green), checked 2026-07-25 OpenSanctions
- directors-on-file (green), checked 2026-07-25 INSEE Sirene (annuaire-entreprises)
- debarment-clear (green), checked 2026-07-25 OpenSanctions
- export-registered (green), checked 2026-07-25 EU EORI validation (European Commission)
- media-mention (green), checked 2026-07-15 cbnews.fr
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)