AL.MA. S.r.l. Packing and Packaging Machinery

Listed in a source registry

interpack 2026 official exhibitor directory

Verified facts

• corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
• domain-registered (green), checked 2026-08-04 Domain registry record
• web-presence-since (green), checked 2026-08-02 Internet Archive (Wayback)
• sanctions-clear (green), checked 2026-08-04 OpenSanctions
• debarment-clear (green), checked 2026-08-04 OpenSanctions
• state-aid-sector (green), checked 2025-06-09 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
• export-registered (green), checked 2026-08-04 EU EORI validation (European Commission)
• vat-valid (green), checked 2026-08-01 VIES (European Commission)

Profiles

• linkedin

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)
• If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
• No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment

Check independently

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