ITM d.o.o.
Словенский промышленный производитель и экспортер
ИТМ о.о.о. котируется Sloexport в секторе механической обработки и металлообработки. В его справочном профиле описаны операции, в том числе Мы занимаемся обслуживанием медицинского и компьютерного оборудования. Мы являемся агентом по продаже и обслуживанию медицинского оборудования производителя Nihon KOHDEN, Япония. Узнайте больше о продуктах, которые вы видите на их сайте.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana, Slovenia
- Website
- https://itm.si
- Categories
- Фармацевтическое производство, Медицинские товары и расходники, Промышленные станки и машины
- Markets
- Словения, Австрия, Германия, Италия, Хорватия
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