KOVAL proizvodnja in trgovina, d.o.o.
Produsen dan eksportir industri Slovenia
KOVAL proizvodnja di trgovina, d.o.o. terdaftar oleh Sloexport di sektor manufaktur lainnya. Profil direktorinya menjelaskan operasi termasuk Perusahaan Koval adalah salah satu perusahaan Slovenia terkemuka di bidang peralatan medis untuk perawatan dan rehabilitasi. Kami membuat troli berjalan, transfer dan mandi, meja pemeriksaan - perawatan, perawatan dan tempat tidur rumah sakit. Kami sangat bangga mengembangkan semua produk dengan merek kami sendiri dari bahan berkualitas tinggi.
- 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
- 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 2026-08-09 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 Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. 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