POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
斯洛文尼亚工业制造商和出口商
POLIDENT d.o.o. Industrija denialnih proizvodov，牙科产品行业被 Sloexport 列为其他制造业。其目录简介描述了包括 Polident 在内的业务，Polident 是一家牙科医疗设备生产商。自 1958 年以来，Polident 一直竭尽全力提供高品质的牙科产品，帮助您为客户提供最佳的治疗和美容解决方案。为庆祝成立 55 周年，我们隆重推出全新解剖牙齿系列 REF-LINE。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- 药品制造, 医疗保健用品, 牙科用品和设备
- Markets
- 斯洛文尼亚, 奥地利, 德国, 意大利, 克罗地亚
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)