INTERDENT proizvodnja in trgovina, d.o.o.
SI-MF-000004584 · Slovenia · Celje
INTERDENT proizvodnja in trgovina, d.o.o. is registered in the European database on medical devices as a manufacturer, with 592 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 592 |
|---|
Most frequent device types declared: ARTICULPAPER1, BASEPLATES1, CCDISKPMMA1, DENTALACRYLICS1, DENTALACRYLICS2A.
Devices declared under this manufacturer
- ACCESSORY FOR DENTAL PHOTOGRAPHY
- BASE PLATES
- CC DISK EASY CoCr
- CC DISK PEEK
- CC DISK PMMA
- CC DISK Ti5
- CC DISK Zr HT
- CC DISK Zr HT MULTILAYER
- CC DISK Zr SMILE MULTILAYER
- I-BOND LO
- INTERACRYL CAST
- INTERACRYL COLD
Showing 12 of 592 declared devices.
Catalogue references include REF 1894, REF 1912, REF 1931B3, REF 1932E1, REF 1934B3, REF 1943MLB2.
European nomenclature codes declared: Q010699, Q010601, Q01020199, Q01010401, Q010504, Q01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 592 |
| Country of registration | Slovenia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. INTERDENT proizvodnja in trgovina, d.o.o. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 1076832-1 | supplemented | 2028-05-09 |