ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav
Slowenischer Industriehersteller und Exporteur
ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav ist bei Sloexport im Bereich Zerspanung und Metallbearbeitung gelistet. Sein Verzeichnisprofil beschreibt Aktivitäten, einschließlich Unternehmen für die Entwicklung und Herstellung von: Kühlgeräten für die Zubereitung und Verarbeitung von Lebensmitteln, Labor- und Pharmakühlschränken, Spezialkühlschränken.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Logatec, Slovenia
- Website
- https://alpfrigo.com
- Categories
- Pharmazeutische Produktion, Medizin- & Gesundheitsbedarf, Industriemaschinen
- Markets
- Slowenien, Österreich, Deutschland, Italien, Kroatien
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