BRINOX INŽENIRING D.O.O.
Produsen dan eksportir industri Slovenia
BRINOX INŽENIRING D.O.O. terdaftar oleh Sloexport di sektor permesinan dan pengerjaan logam. Profil direktorinya menggambarkan operasi termasuk Berdasarkan tradisi, pengalaman, pengetahuan, dan teknologi mutakhir selama 40 tahun, kami mewujudkan misi kami dalam memproduksi sistem dan peralatan proses siap pakai berteknologi tinggi untuk industri biofarmasi dan farmasi. Brinox selalu mampu mendengarkan, mencari dan mewujudkan solusi proses yang dipesan lebih dahulu.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Medvode, Slovenia
- Website
- https://brinox.eu
- Categories
- Manufaktur Farmasi, Perlengkapan Medis & Kesehatan, Mesin Industri
- Markets
- Slovenia, Austria, Jerman, Italia, Kroasia
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