POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
Slowenischer Industriehersteller und Exporteur
POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry wird von Sloexport im Bereich Sonstiges verarbeitendes Gewerbe gelistet. Sein Verzeichnisprofil beschreibt Betriebe, darunter Polident ist ein Hersteller von medizinischen Geräten für die Zahnheilkunde. Seit 1958 tun wir bei Polident unser Bestes, um qualitativ hochwertige Dentalprodukte anzubieten, damit Sie Ihren Kunden die bestmögliche Behandlung und ästhetische Lösungen bieten können. Zu unserem 55-jährigen Jubiläum präsentieren wir Ihnen die neue Linie anatomischer Zähne 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
- Pharmazeutische Produktion, Medizin- & Gesundheitsbedarf, Dentalbedarf & -geräte
- Markets
- Slowenien, Österreich, Deutschland, Italien, Kroatien
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)