ENIKAM d.o.o.
SI-MF-000012876 · Slovenia · Ljubljana
ENIKAM d.o.o. is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: SKINOXID.
Devices declared under this manufacturer
- Skinoxid - Gel za kožo 30ml
- Skinoxid - Gel za kožo 50ml
- Skinoxid - Pršilo za kožo 100ml
- Skinoxid - Pršilo za kožo 200ml
- Skinoxid - Pršilo za kožo 50ml
- Skinoxid - raztopina za kožo 250ml
- Skinoxid - raztopina za kožo 500ml
Catalogue references include 600, 601, 602, 650, 651, 700.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| Country of registration | Slovenia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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. ENIKAM d.o.o. was not found in either the U.S. or the Canadian register.