Ekuberg Pharma
IT-MF-000010732 · Italy · Carpignano Salentino
Ekuberg Pharma is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: ACCQ00510, BRLX00110, BRLX00210, BRLX00310, EKHP00310.
Devices declared under this manufacturer
- Concquer spray
- Dermoxen Bactor vaginal ovules
- Dermoxen Florexil vaginal douche
- Dermoxen Hydra
- Hemopran
- Lecoxen
- Saugella Poligyn 50+
Catalogue references include ACCQ00510, BRLX00210, BRLX00310, EKDX00110, EKDX01610, EKDX02010.
European nomenclature codes declared: U0803, M04041503, M9002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 1 |
|---|---|
| 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. Ekuberg Pharma was not found in either the U.S. or the Canadian register.