MILESTONE S.P.A.
IT-MF-000024414 · Italy · Sorisole
MILESTONE S.P.A. is registered in the European database on medical devices as a manufacturer, with 298 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: DecalMATE KIT, EGROSS PRO-X, FLASHFREEZE, FineFIX Module, HISTODREAM EW.
Devices declared under this manufacturer
- EGROSS
- FLASHFREEZE
- HISTODREAM DM
- HISTODREAM EW
- HISTODREAM SH
- HISTODREAM TM
- KOS HR16M R8SM
- Loading bay E
- MLD3426-5
- MLD3939 3333-5
- MLD4129 3324-7
- MLD5951-5
Showing 12 of 298 declared devices.
Catalogue references include 100606-A, 100692, 100700, 100780, 500002, 500101.
European nomenclature codes declared: W05030501, W02079080, W0202059010, W05030580, W02079099, W0202059004.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MILESTONE S.P.A. (IT) · FDA 1000391282 |
| Devices in EUDAMED | 298 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 298 |
|---|---|
| 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: United States only. MILESTONE S.P.A. is registered in the United States but was not found in the Canadian register.