POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
Produsen dan eksportir industri Slovenia
POLIDENT d.o.o. Industrija dentalnih proizvodov, Industri Produk Gigi terdaftar oleh Sloexport di sektor manufaktur lainnya. Profil direktorinya menjelaskan operasi termasuk Polident yang merupakan produsen peralatan medis untuk kedokteran gigi. Sejak tahun 1958 kami di Polident telah melakukan yang terbaik untuk menawarkan produk gigi berkualitas tinggi untuk membantu Anda menawarkan perawatan dan solusi estetika terbaik kepada klien Anda. Untuk ulang tahun kami yang ke 55, kami mempersembahkan jajaran gigi anatomi baru REF-LINE secara maksimal.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- Manufaktur Farmasi, Perlengkapan Medis & Kesehatan, Perlengkapan & Peralatan Gigi
- Markets
- Slovenia, Austria, Jerman, Italia, Kroasia
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)