MINIPLAST, proizvodnja plastične embalaže d.o.o.
Slowenischer Industriehersteller und Exporteur
MINIPLAST, proizvodnja plastične embalaže d.o.o. wird von Sloexport im Bereich Sonstiges verarbeitendes Gewerbe gelistet. Sein Verzeichnisprofil beschreibt Betriebe, darunter Miniplast ist ein zuverlässiger Subunternehmer für eine Vielzahl von produzierenden Unternehmen in den Bereichen Verpackung und Automobil-, Elektro-, Chemie-, Medizin- und Agrarindustrie oder -tätigkeiten. Ein kleines, flexibles und hochprofessionelles Unternehmen mit völlig neuen, hochmodernen CNC-Maschinen, einem hochprofessionellen Team und einem.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://miniplast.si
- Categories
- Pharmazeutische Produktion, Medizin- & Gesundheitsbedarf, Chemie & Kunststoffe
- 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 2026-08-09 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
- 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-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)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- vat-valid (green), checked 2026-08-09 VIES
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)