POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
슬로베니아 산업 제조업체 및 수출업체
폴리덴트 d.o.o. Industrija dentalnih proizvodov, Dental Products Industry is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including Polident is a producer of medical devices for dentistry. 1958년부터 Polident는 귀하가 고객에게 가능한 최고의 치료 및 미용 솔루션을 제공할 수 있도록 최고 품질의 치과 제품을 제공하기 위해 최선을 다해 왔습니다. For our 55th anniversary, we present the new line of anatomical teeth REF-LINE for the most.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- 의약품 제조, 의료 및 건강 관리 용품, 치과용품 및 장비
- 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
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-09 - 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)
- 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)