ITM d.o.o.
スロベニアの工業製造業者および輸出業者
ITM ドゥーオーSloexport により機械加工および金属加工部門に上場されています。そのディレクトリ プロファイルには、当社が医療機器やコンピューター機器のサービスに従事していることなどの業務が記載されています。弊社は医療機器メーカー日本光電株式会社の販売・サービス代理店です。製品の詳細については、Web サイトをご覧ください。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana, Slovenia
- Website
- https://itm.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 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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
- 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