POLE PARAMEDICAL DU PIED

Listed in a source registry

France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)

Verified facts

• domain-registered (green), checked 2026-07-28 Domain registry record
• web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
• 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)
• sanctions-clear (green), checked 2026-08-16 OpenSanctions
• debarment-clear (green), checked 2026-08-16 OpenSanctions
• vat-valid (green), checked 2026-08-25 VIES (European Commission)
• financials-published (green), checked 2022-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
• registry-activity (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
• directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
• registry-active-global (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
• registry-id-verified (green), checked 2026-07-04 Annuaire des Entreprises (INSEE / INPI)
• workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)

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)
• VAT number check (EU VIES)