ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav
Fabricante y exportador industrial esloveno
ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav cotiza en Sloexport en el sector de mecanizado y metalurgia. El perfil de su directorio describe operaciones que incluyen Compañía para el desarrollo y fabricación de: equipos de refrigeración en la preparación y procesamiento de alimentos, refrigeradores de laboratorio y farmacéuticos, refrigeradores especiales.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Logatec, Slovenia
- Website
- https://alpfrigo.com
- Categories
- Fabricación farmacéutica, Suministros médicos y sanitarios, Maquinaria industrial
- Markets
- Eslovenia, Austria, Alemania, Italia, Croacia
Listed in a source registry
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 2026-08-04 Mail server of the company domain
- lei-active (green), checked 2026-08-04 GLEIF
- sanctions-clear (green), checked 2026-08-04 OpenSanctions
- debarment-clear (green), checked 2026-08-04 OpenSanctions
- domain-registered (green), checked 2026-08-04 Domain registry record
- export-registered (green), checked 2026-08-04 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-08-16 Seznam davčnih zavezancev (FURS, Finančna uprava RS)
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- vat-valid (green), checked 2026-08-04 VIES
Import rules for these goods
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- 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)
- 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