ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav
Sloveense industriële fabrikant en exporteur
ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav wordt door Sloexport vermeld in de sector verspaning en metaalbewerking. Het directoryprofiel beschrijft activiteiten van onder meer het bedrijf voor de ontwikkeling en productie van: koelapparatuur voor de bereiding en verwerking van voedsel, laboratorium- en farmaceutische koelkasten, speciale koelkasten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Logatec, Slovenia
- Website
- https://alpfrigo.com
- Categories
- Farmaceutische productie, Medische en gezondheidszorgbenodigdheden, Industriële machines
- Markets
- Slovenië, Oostenrijk, Duitsland, Italië, Kroatië
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