INDUSTRIAL FARMACEUTICA CANTABRIA S.A.
- Type
- Manufacturer
- Location
- Cantabria, Spain
- Website
- https://ifc.es
- Categories
- 의료 및 건강 관리 용품
- Markets
- 스페인
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-22 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-22 OpenSanctions
- debarment-clear (green), checked 2026-08-22 OpenSanctions
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- lei-active (green), checked 2026-08-22 GLEIF
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
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)