POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
スロベニアの工業製造業者および輸出業者
ポリデント ドゥーオーIndustrija Dentalnih Proizvodov、歯科製品産業は、Sloexport のその他の製造部門にリストされています。そのディレクトリ プロファイルには、歯科用医療機器の製造会社である Polident などの事業内容が記載されています。 1958 年以来、私たちポリデントは、クライアントに最高の治療と審美的なソリューションを提供できるよう、最高品質の歯科製品を提供することに全力を尽くしてきました。創立55周年を記念して、解剖学的な歯の新しいライン「REF-LINE」を発表します。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- 医薬品製造, 医療およびヘルスケア用品, 歯科用品および歯科用機器
- 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
- 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)