MINIPLAST, proizvodnja plastične embalaže d.o.o.
Slovenian industrial manufacturer and exporter
MINIPLAST, proizvodnja plastične embalaže d.o.o. is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including Miniplast is a reliable subcontractor for a wide range of manufacturing companies in the field of packaging and automotive, electrical, chemical, medical and agricultural industries or activities. A small, flexible and highly professional company with all new cutting edge CNC machines, a highly professional team and a.
- Type
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://miniplast.si
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Chemicals & Plastics
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-09 Domain registry record
- vat-valid (green), checked 2026-08-09 VIES
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- 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)
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)
- 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)