POLE PARAMEDICAL DU PIED
اللوازم الطبية والرعاية الصحية، فرنسا
POLE PARAMEDICAL DU PIED هي شركة متخصصة في الإمدادات الطبية والرعاية الصحية ومقرها في شاتينوي لو رويال، فرنسا. مُدرج في السجل التجاري العام.
- Type
- brand seeking distribution
- Location
- Chatenoy-Le-Royal, France
- Founded
- 2013
- Website
- https://pole-pdp.fr
- Categories
- اللوازم الطبية والرعاية الصحية
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)