AL.MA. S.r.l. Packing and Packaging Machinery
AL.MA. srl sản xuất thuật ngữ, vỉ, máy thuật ngữ, thuật ngữ tự động, confezionatrici sottovuoto e automa
AL.MA. srl sản xuất thuật ngữ định dạng, vỉ, thuật ngữ máy, định dạng thuật ngữ tự động, confezionatrici sottovuoto e autohe, ad atmosfera modificata. Sản xuất confezionatrici per prodotti medi, alimentari e per mì ống tươi
- Type
- brand seeking distribution
- Location
- Cadorago (CO), Italy
- Founded
- 1979
- Website
- almapackaging.com
- Categories
- Vật tư y tế và chăm sóc sức khỏe, Đóng gói và vật tư in ấn
Listed in a source registry
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
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