KOVAL proizvodnja in trgovina, d.o.o.
슬로베니아 산업 제조업체 및 수출업체
trgovina의 KOVAL proizvodnja, d.o.o. Sloexport에 의해 기타 제조 부문에 상장되어 있습니다. 디렉토리 프로필에는 치료 및 재활용 의료 장비 분야의 슬로베니아 선도 기업 중 하나인 Koval 회사를 포함한 운영이 설명되어 있습니다. 우리는 걷기, 이동 및 샤워 카트, 검사-치료 테이블, 간병 및 병원 침대를 만듭니다. 우리는 특히 고품질 소재를 사용하여 자체 브랜드로 모든 제품을 개발하게 된 것을 자랑스럽게 생각합니다.
- 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
- 의약품 제조, 의료 및 건강 관리 용품, 산업기계
- Markets
- 슬로베니아, 오스트리아, 독일, 이탈리아, 크로아티아
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 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. EU와 EEA에서는 공공 발주자가 사기, 부패, 자금세탁으로 유죄가 확정된 입찰자와 최종 결정으로 세금 또는 사회보험료 체납이 확인된 입찰자를 반드시 배제해야 합니다. 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