MINIPLAST, proizvodnja plastične embalaže d.o.o.
Словенский промышленный производитель и экспортер
МИНИПЛАСТ, производство пластиковых эмбалаже о.о.о. котируется Sloexport в другом производственном секторе. В его каталоге описаны операции, в том числе Miniplast является надежным субподрядчиком для широкого круга производственных компаний в области упаковки, автомобильной, электротехнической, химической, медицинской и сельскохозяйственной промышленности или деятельности. Небольшая, гибкая и высокопрофессиональная компания со всеми новыми современными станками с ЧПУ, высокопрофессиональной командой и.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://miniplast.si
- Categories
- Фармацевтическое производство, Медицинские товары и расходники, Химия и пластмассы
- Markets
- Словения, Австрия, Германия, Италия, Хорватия
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)