MINIPLAST, proizvodnja plastične embalaže d.o.o.
슬로베니아 산업 제조업체 및 수출업체
MINIPLAST, proizvodnja plastične embalaže d.o.o. Sloexport에 의해 기타 제조 부문에 상장되어 있습니다. 디렉토리 프로필에는 Miniplast가 포장 및 자동차, 전기, 화학, 의료 및 농업 산업 분야 또는 활동 분야의 광범위한 제조 회사를 위한 신뢰할 수 있는 하청업체임을 포함하여 운영이 설명되어 있습니다. 완전히 새로운 최첨단 CNC 기계, 고도로 전문적인 팀 및 a.를 갖춘 소규모의 유연하며 고도로 전문적인 회사입니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://miniplast.si
- Categories
- 의약품 제조, 의료 및 건강 관리 용품, 화학제품 및 플라스틱
- Markets
- 슬로베니아, 오스트리아, 독일, 이탈리아, 크로아티아
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)