BRINOX INŽENIRING D.O.O.
Fabricant industriel et exportateur slovène
BRINOX INŽENIRING D.O.O. est référencée par Sloexport dans le secteur de l'usinage et du travail des métaux. Son profil d'annuaire décrit les opérations, notamment. Basé sur 40 ans de tradition, d'expérience, de connaissances et de technologie de pointe, nous réalisons notre mission de fabriquer des systèmes et des équipements de processus clé en main de haute technologie pour les industries biopharmaceutiques et pharmaceutiques. Brinox est toujours capable d'écouter, de rechercher et de réaliser des solutions de processus sur mesure selon les besoins les plus adéquats.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Medvode, Slovenia
- Website
- https://brinox.eu
- Categories
- Production pharmaceutique, Fournitures médicales et de santé, Machines industrielles
- Markets
- Slovénie, Autriche, Allemagne, Italie, Croatie
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