BRINOX INŽENIRING D.O.O.
Slowenischer Industriehersteller und Exporteur
BRINOX INŽENIRING D.O.O. ist bei Sloexport im Bereich Zerspanung und Metallbearbeitung gelistet. Das Verzeichnisprofil beschreibt die Tätigkeiten unter anderem. Basierend auf 40-jähriger Tradition, Erfahrung, Wissen und modernster Technologie verwirklichen wir unsere Mission, schlüsselfertige High-Tech-Prozesssysteme und Ausrüstung für die biopharmazeutische und pharmazeutische Industrie herzustellen. Brinox ist immer in der Lage, zuzuhören, maßgeschneiderte Prozesslösungen zu suchen und umzusetzen, je nach Bedarf.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Medvode, Slovenia
- Website
- https://brinox.eu
- Categories
- Pharmazeutische Produktion, Medizin- & Gesundheitsbedarf, Industriemaschinen
- 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 2026-08-07 Mail server of the company domain
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-08-07 EU EORI validation (European Commission)
- sanctions-clear (green), checked 2026-08-07 OpenSanctions
- debarment-clear (green), checked 2026-08-07 OpenSanctions
- vat-valid (green), checked 2026-08-07 VIES
- 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)
Import rules for these goods
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- 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)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment