laboratorios salvat , s a

Listed in a source registry

CPHI exhibitor directory

Verified facts

• places-goods-on-market (green), checked 2026-08-07 Finnish Medicines Agency (Fimea), basic register of medicinal products
• lei-active (green), checked 2026-08-09 GLEIF
• corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
• debarment-clear (green), checked 2026-08-09 OpenSanctions
• domain-registered (green), checked 2026-08-09 Domain registry record
• sanctions-clear (green), checked 2026-08-09 OpenSanctions
• gmp-certified (green), checked 2026-04-13 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)
• Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)

Check independently

• Sanctions and watchlists (OpenSanctions)