DURAND SA
Medizin- und Gesundheitsbedarf, Frankreich
DURAND SA ist ein Unternehmen für Medizin- und Gesundheitsbedarf mit Sitz in La Richardais, Frankreich. Eintragung in ein öffentliches Handelsregister.
- Type
- brand seeking distribution
- Location
- La Richardais, France
- Founded
- 1987
- Website
- https://durand-production.com
- Categories
- Medizin- & Gesundheitsbedarf
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
- insolvency-clear (green), checked 2026-08-21 BODACC (annuaire-entreprises)
- 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)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- vat-valid (green), checked 2026-07-31 VIES (European Commission)
- bodacc-accounts-filed (green), checked 2026-08-21 BODACC (annuaire-entreprises)
- registry-change-published (green), checked 2026-08-21 BODACC (annuaire-entreprises)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- financials-published (green), checked 2016-12-31 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)
- registry-activity (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- 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)