BRINOX INŽENIRING D.O.O.
Slovenian industrial manufacturer and exporter
BRINOX INŽENIRING D.O.O. is listed by Sloexport in the machining and metalworking sector. Its directory profile describes operations including Based on 40-year tradition, experience, knowledge and cutting-edge technology, we realize our mission of manufacturing high-tech turnkey process systems and equipment for biopharmaceutical and pharmaceutical industries. Brinox is always able to listen, to seek and realize bespoke process solutions according to the most.
- Type
- Manufacturer
- Location
- Medvode, Slovenia
- Website
- https://brinox.eu
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Industrial Machinery
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
Listed in a source registry
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)
- vat-valid (green), checked 2026-08-07 VIES
- lei-active (green), checked 2026-08-23 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
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- registered-manufacturer (green), checked 2026-08-16 Seznam davčnih zavezancev (FURS, Finančna uprava RS)
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)
- 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)