Menarini

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 2026-08-09 Mail server of the company domain
• domain-registered (green), checked 2026-08-09 Domain registry record
• debarment-clear (green), checked 2026-08-09 OpenSanctions
• lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
• sanctions-clear (green), checked 2026-08-09 OpenSanctions
• registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
• public-subsidy-received (green), checked 2026-08-25 OpenCoesione (opencoesione.gov.it), open data on project subjects

Claimed certifications, not confirmed by us

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

Import rules for these goods

• Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
• 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)