FISIOTECH srl
IT-MF-000028185 · Italy · Cimavilla di Codognè (TV)
FISIOTECH srl is registered in the European database on medical devices as a manufacturer, with 110 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 110 |
|---|
Most frequent device types declared: GINNASTICA PROPRIOCETTIVA, PULEGGIO TERAPIA, RIABILITAZIONE ARTI, SERIE BOBATH, SERIE NEW PROFESSIONAL.
Among these devices, 71 are declared active.
Devices declared under this manufacturer
- LETTINO ADE 2
- LETTINO ELETTRA 3
- LETTINO FEBO 6 PLUS
- LETTINO FEBO 8
- LETTINO GEA
- LETTINO GIOVE 3
- LETTINO MARTE 5
- LETTINO MONTELEONE
- LETTINO POSEIDONE
- LETTINO TITAN 1
- LETTINO TITAN 2
- LETTINO ZEFIRO 4
Showing 12 of 110 declared devices.
Catalogue references include 1112C, 1113E, 1113S, 1117A, 1118C, 1121D.
European nomenclature codes declared: Z12069099, Y0504, Z120602, Y0580.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 110 |
| 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 | 110 |
|---|---|
| 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. FISIOTECH srl was not found in either the U.S. or the Canadian register.