BRINOX INŽENIRING D.O.O.
Sloven endüstriyel üretici ve ihracatçı
BRINOX INZENIRING D.O.O. Talaşlı imalat ve metal işleme sektöründe Sloexport tarafından listelenmiştir. Dizin profilinde aşağıdakiler yer almaktadır: 40 yıllık geleneğe, deneyime, bilgi birikimine ve en son teknolojiye dayanarak, biyofarmasötik ve ilaç endüstrileri için yüksek teknolojili anahtar teslim proses sistemleri ve ekipmanları üretme misyonumuzu gerçekleştiriyoruz. Brinox her zaman en iyi şekilde dinleyebilir, ısmarlama süreç çözümlerini arayabilir ve gerçekleştirebilir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Medvode, Slovenia
- Website
- https://brinox.eu
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri, Endüstriyel Makineler
- Markets
- Slovenya, Avusturya, Almanya, İtalya, Hırvatistan
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