KENTAMED Ltd.
BG-MF-000022619 · Bulgaria · Plovdiv
KENTAMED Ltd. is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 5 |
|---|
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- KENTAMED ACTIS-150
- KENTAMED ACTIS-150a
- KENTAMED ACTIS-400
- KENTAMED RF-120
- KENTAMED RF-120a
Catalogue references include 10-11-01, 10-11-02, 10-11-03, 10-11-04, 10-11-05.
European nomenclature codes declared: Z12010902.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Bulgaria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| 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. KENTAMED Ltd. was not found in either the U.S. or the Canadian register.