KOVAL proizvodnja in trgovina, d.o.o.
Slovenian industrial manufacturer and exporter
KOVAL proizvodnja in trgovina, d.o.o. is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including Company Koval is one of the leading Slovenian companies in the field of medical equipment for care and rehabilitation. We make walking, transfer and shower trolleys, examination - treatment tables, care and hospital beds. We are particularly proud to develop all products under our own brand from high-quality materials.
- Type
- Manufacturer
- Location
- Loka Pri Žusmu, Slovenia
- Website
- https://koval.si
- 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 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-09 GLEIF
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- vat-valid (green), checked 2026-08-09 VIES
- public-contract-awarded (green), checked 2025-07-30 TED (Tenders Electronic Daily), EU public procurement award notices Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- 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)