Indena
Фармацевтические составы, дженерики и товары медицинского назначения.
Indena производит фармацевтические препараты, дженерики и товары медицинского назначения на своих предприятиях в Милане. Компания поставляет продукцию аптекам, покупателям больниц, дистрибьюторам медицинских услуг или экспортным клиентам на перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Milan, Italy
- Founded
- 1921
- Website
- indena.com
- Categories
- Медицинские товары и расходники, БАДы и товары для здоровья
- Markets
- Италия, Соединенные Штаты, Германия, Франция
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- vat-valid (green), checked 2026-08-08 VIES
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- export-registered (green), checked 2026-08-08 EU EORI validation (European Commission)
- operating-permit (green), checked 2007-07-07 EEA Industrial Emissions Portal (IED), EU-wide permit register
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- AEO, Authorised Economic Operator EU AEO database
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)