Xmed-MF
IT-MF-000027241 · Italy · Mirandola,MO
Xmed-MF is registered in the European database on medical devices as a manufacturer, with 145 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 145 |
|---|
Among these devices, 145 are declared sterile.
Devices declared under this manufacturer
- ENDOJACK
- ENDOSHAFT-COVER®
- ENDOSHAFT-COVER® PLUS
- ENDOSHAFT-COVER® – UDK FLEX
- TRACHEO SET
- UROTOP® CISTOPRO
Showing 12 of 145 declared devices.
Catalogue references include 300/30067*, 300/30097A, 500/9080E, 600/60075CP, 600/60075LP, 600/60085CP.
European nomenclature codes declared: T030203, R010699, K01020103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 145 |
| 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 | 145 |
|---|---|
| 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. Xmed-MF was not found in either the U.S. or the Canadian register.