VESTON DARIUSZ KAWALEC
PL-MF-000038627 · Poland · Koszalin
VESTON DARIUSZ KAWALEC is registered in the European database on medical devices as a manufacturer, with 64 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 64 |
|---|
Devices declared under this manufacturer
- Formówki sekcyjne
- Formówki sekcyjne tytanowe
- PUREsthetic Anatomical Matrix Band Type 22 - premolar right-sided
- PUREsthetic Anatomical Matrix Band Type 23 - molar left-sided
- PUREsthetic Anatomical Matrix Band Type 29 Molar on both sides
- PUREsthetic Matrix Bands Type 8 – premolars
- PUREsthetic Restoration Kit no.2 molar on left-sided
- PUREsthetic Restoration Kit no.6 premolar on both sides
- Paski metalowe Tofflemire
- Paski metalowe profilowane przedtrzonowe obustronne
- Paski metalowe profilowane trzonowe jednostronne
- Paski metalowe proste
Showing 12 of 64 declared devices.
Catalogue references include 5906124397390, 5906124397444, 5906124397468, Formówki sekcyjne gr. 0,038 mm, średnie, S-02, 50 szt., PS01022, PS03008.
European nomenclature codes declared: Q01010401, Q01010403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 64 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 64 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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. VESTON DARIUSZ KAWALEC was not found in either the U.S. or the Canadian register.