KOVAL proizvodnja in trgovina, d.o.o.
Fabricante e exportador industrial esloveno
KOVAL proizvodnja in trgovina, d.o.o. é listada pela Sloexport no outro setor manufatureiro. O perfil do seu diretório descreve operações, incluindo a Empresa Koval, uma das empresas eslovenas líderes na área de equipamentos médicos para cuidados e reabilitação. Fabricamos carrinhos de caminhada, de transferência e de banho, mesas de exames - tratamentos, camas assistenciais e hospitalares. Estamos particularmente orgulhosos de desenvolver todos os produtos sob nossa própria marca a partir de materiais de alta qualidade.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Loka Pri Žusmu, Slovenia
- Website
- https://koval.si
- Categories
- Fabricação farmacêutica, Suprimentos médicos e de saúde, Maquinário industrial
- Markets
- Eslovênia, Áustria, Alemanha, Itália, Croácia
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 2026-08-09 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
- public-contract-awarded (green), effective since 2025-07-30 TED (Tenders Electronic Daily), EU public procurement award notices Aqui a adjudicação traz também uma verificação feita por outros: na UE e no EEE o comprador público tem de excluir concorrentes condenados por fraude, corrupção ou branqueamento, e aqueles com dívidas fiscais ou contributivas fixadas por decisão definitiva. Directive 2014/24/EU, Article 57 (exclusion grounds)
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- 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)
- vat-valid (green), checked 2026-08-09 VIES
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)
- 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