SARL ETABL BOUCHARENC (BOUCHARENC PODO-ORTHESISTES BOUCHARENC ORTHOPROTHESISTES BOUCHARENC FORMATION)
Товары медицинского назначения и здравоохранения, Франция
SARL ETABL BOUCHARENC (BOUCHARENC PODO-ORTHESISTES BOUCHARENC ORTHOPROTHESISTES BOUCHARENC FORMATION) , компания, занимающаяся поставками медицинских товаров и товаров для здоровья, базирующаяся в Сен-Шели-Д'Апшер, Франция. Внесен в государственный реестр предприятий.
- Type
- brand seeking distribution
- Location
- Saint-Chely-D'Apcher, France
- Founded
- 1988
- Website
- https://boucharenc.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
- 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)
- domain-registered (green), checked 2026-07-28 Domain registry record
- 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
- 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)
- vat-valid (green), checked 2026-07-31 VIES (European Commission)
- 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)