POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
Fabricant industriel et exportateur slovène
POLIDENT d.o.o. Industrija dentalnih proizvodov, Industrie des produits dentaires, est répertoriée par Sloexport dans le secteur autre fabrication. Son profil d'annuaire décrit les opérations dont Polident est un producteur de dispositifs médicaux pour la dentisterie. Depuis 1958, chez Polident, nous faisons de notre mieux pour offrir des produits dentaires de qualité supérieure afin de vous aider à offrir à vos clients le meilleur traitement et les meilleures solutions esthétiques possibles. Pour notre 55ème anniversaire, nous vous présentons la nouvelle gamme de dents anatomiques REF-LINE pour le plus.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- Production pharmaceutique, Fournitures médicales et de santé, Fournitures et équipements dentaires
- Markets
- Slovénie, Autriche, Allemagne, Italie, Croatie
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)