FOLIJAPLAST d.o.o.
Slovenian industrial manufacturer and exporter
FOLIJAPLAST d.o.o. is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including From the very beginning, the first priority was to satisfy the needs and requirements of the pharmaceutical industry. Development investments are still aimed at satisfying the requirements of the pharmaceutical industry as much as possible.
- Type
- Manufacturer
- Location
- Žužemberk, Slovenia
- Founded
- 1970
- Website
- https://folijaplast.si
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- vat-valid (green), checked 2026-08-08 VIES
- export-registered (green), checked 2026-08-08 EU EORI validation (European Commission)
- 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)
- 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)