Indena

What is established and what is not

No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.

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
• 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), effective since 2007-07-07 EEA Industrial Emissions Portal (IED), EU-wide permit register
• vat-valid (green), checked 2026-08-08 VIES
• registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record

Claimed certifications, not confirmed by us

• Good Manufacturing Practice
• ISO 9001, Quality Management IAF CertSearch

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)

Check independently

• Sanctions and watchlists (OpenSanctions)
• VAT number check (EU VIES)