ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav
Slovenian industrial manufacturer and exporter
ALPFRIGO d.o.o., družba za razvoj, projektiranje in proizvodnjo hladilnih naprav is listed by Sloexport in the machining and metalworking sector. Its directory profile describes operations including Company for development and manufacture of : refrigeration equipment in the preparation and processing of food, lab and pharmaceutical refrigerators, special refrigerators.
- Type
- Manufacturer
- Location
- Logatec, Slovenia
- Website
- https://alpfrigo.com
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Industrial Machinery
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
Listed in a source registry
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
- vat-valid (green), checked 2026-08-04 VIES
- export-registered (green), checked 2026-08-04 EU EORI validation (European Commission)
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- registered-manufacturer (green), checked 2026-08-16 Seznam davčnih zavezancev (FURS, Finančna uprava RS)
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)
- 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)