PFEFFER PROTHESE DENTAIRE
This domain is available for sale. Check out price, information and more on Dovendi.com
This domain is available for sale. Check out price, information and more on Dovendi.com
- Type
- Manufacturer
- Location
- Dardilly, France
- Founded
- 1974
- Website
- https://pfeffer.fr
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- web-presence-since (green), checked 2026-08-19 Internet Archive (Wayback)
- insolvency-clear (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- domain-registered (green), checked 2026-08-19 Domain registry record
- bodacc-accounts-filed (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- registry-change-published (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- financials-published (green), checked 2020-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-active-global (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-manufacturer (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- directors-on-file (green), checked 2026-07-23 INSEE Sirene (annuaire-entreprises)
- export-registered (green), checked 2026-07-23 EU EORI validation (European Commission)
- vat-valid (green), checked 2026-07-31 VIES (European Commission)
- sanctions-clear (green), checked 2026-07-23 OpenSanctions
- debarment-clear (green), checked 2026-07-23 OpenSanctions
- registry-id-verified (green), checked 2026-07-22 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)