Vik Dental d.o.o.
HR-MF-000033824 · Croatia · Zagreb
Vik Dental d.o.o. is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 28 |
|---|
Most frequent device types declared: 10001, 10002, 10004, 10005, 10007.
Devices declared under this manufacturer
- DORA LATEX POWDER-FREE GLOVES L
- DORA LATEX POWDER-FREE GLOVES M
- DORA LATEX POWDERED GLOVES L
- DORA LATEX POWDERED GLOVES M
- DORA LATEX POWDERED GLOVES xs
- DORA NITRILE GLOVES BLACK L
- DORA NITRILE GLOVES BLACK M
- DORA NITRILE GLOVES BLACK XL
- DORA NITRILE GLOVES PINK L
- DORA NITRILE GLOVES PINK S
- DORA NITRILE GLOVES PINK XS
- DORA NITRILE GLOVES VIOLET L
Showing 12 of 28 declared devices.
Catalogue references include 10001, 10002, 10004, 10005, 10006, 10007.
European nomenclature codes declared: T01020204, T010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| Country of registration | Croatia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 28 |
|---|---|
| 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. Vik Dental d.o.o. was not found in either the U.S. or the Canadian register.