BIOINDUSTRIA LABORATORIO ITALIANO MEDICINALI S.P.A. (SIGLABILE BIOINDUSTRIA L.I.M. S.P.A.)

Listed in a source registry

ANAC open data (Italy)

Verified facts

• lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
• vat-valid (green), checked 2026-08-05 VIES (European Commission)
• facility-registered (green), checked 2026-08-10 Ministero della Salute, stabilimenti riconosciuti (Reg. CE 853/2004)
• gmp-certified (green), checked 2025-07-25 EudraGMDP, EU register of GMP certificates (EMA)

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)