KOVAL proizvodnja in trgovina, d.o.o.
スロベニアの工業製造業者および輸出業者
トルゴビナのKOVAL proizvodnja、d.o.o. Sloexport によりその他の製造部門に上場されています。同社のディレクトリ プロフィールには、ケアとリハビリテーション用の医療機器の分野におけるスロベニアの大手企業の 1 つである会社 Koval を含む事業内容が記載されています。当社は、歩行用、移乗用、シャワー用のワゴン、診察台、治療台、介護用ベッド、病院用ベッドなどを製造しています。当社は、高品質の素材を使用して自社ブランドですべての製品を開発することに特に誇りを持っています。
- 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
- 医薬品製造, 医療およびヘルスケア用品, 産業機械
- Markets
- スロベニア, オーストリア, ドイツ, イタリア, クロアチア
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 ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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