OTTOBOCK RESEAU ORTHOPEDIE & SERVICES
Suministros médicos y sanitarios, Francia
OTTOBOCK RESEAU ORTHOPEDIE & SERVICES es una empresa de suministros médicos y sanitarios con sede en Les Ulis, Francia. Inscrita en un registro público de empresas.
- Type
- brand seeking distribution
- Location
- Les Ulis, France
- Founded
- 2021
- Website
- https://amputation-avant-pied.fr
- Categories
- Suministros médicos y sanitarios
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- domain-registered (green), checked 2026-08-07 Domain registry record
- 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)
- public-contract-awarded (green), checked 2026-04-20 TED (Tenders Electronic Daily), EU public procurement award notices Aquí la adjudicación lleva además una comprobación ajena: en la UE y el EEE el comprador público debe excluir a los licitadores condenados por fraude, corrupción o blanqueo, y a aquellos con deudas tributarias o de cotizaciones establecidas por resolución firme. Directive 2014/24/EU, Article 57 (exclusion grounds)
- financials-published (green), checked 2024-12-31 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)
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)