POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
Fabricante y exportador industrial esloveno
POLIDENT d.o.o. Industrija dentalnih proizvodov, la industria de productos dentales figura en Sloexport en el otro sector manufacturero. Su perfil de directorio describe operaciones que incluyen Polident es un productor de dispositivos médicos para odontología. Desde 1958 en Polident hemos hecho todo lo posible para ofrecer productos dentales de primera calidad para ayudarle a ofrecer a sus clientes el mejor tratamiento y soluciones estéticas posibles. Por nuestro 55 aniversario, presentamos la nueva línea de dientes anatómicos REF-LINE para los más.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- Fabricación farmacéutica, Suministros médicos y sanitarios, Suministros y equipos dentales
- Markets
- Eslovenia, Austria, Alemania, Italia, Croacia
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)