POLE PARAMEDICAL DU PIED
Товары медицинского назначения и здравоохранения, Франция
POLE PARAMEDICAL DU PIED , компания, занимающаяся поставками медицинского оборудования и товаров медицинского назначения, расположенная в Шатенуа-Ле-Руаяль, Франция. Внесен в государственный реестр предприятий.
- Type
- brand seeking distribution
- Location
- Chatenoy-Le-Royal, France
- Founded
- 2013
- Website
- https://pole-pdp.fr
- Categories
- Медицинские товары и расходники
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)