XENODERM S.R.L.
IT-MF-000031000 · Italy · scafati
XENODERM S.R.L. is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 2 |
|---|---|
| Class IIa | 16 |
Most frequent device types declared: GERM A, GERM B, GPX1001, GPX1010, GPX1201.
Among these devices, 4 are declared sterile.
Devices declared under this manufacturer
- DENSITY
- DENSITY PLATELET GEL
- GERM A
- GERM B
Showing 12 of 18 declared devices.
Catalogue references include DAA1002, DAP0035, DAP0050, DAP1001, DAP2500, DAS1001.
European nomenclature codes declared: D0799, B0501, D0901.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 16 |
|---|---|
| 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. XENODERM S.R.L. was not found in either the U.S. or the Canadian register.