Hospitex International S.r.l.
IT-MF-000041985 · Italy · Sesto Fiorentino
Hospitex International S.r.l. is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Alcol Etilico 70% DS, Alcol Etilico 96% DS, Alcol Etilico assoluto 99,9%, Alcol Etilico neutro 96%, BLOCKfast.
Devices declared under this manufacturer
- Alcol Etilico 70% DS - 1 lt
- Alcol Etilico 70% DS - 2,5 lt
- Alcol Etilico assoluto 99,9% - 1 lt
- Alcol Etilico neutro 96% - 5 lt
- BLOCKfast
- BLOCKfast - 10 confezioni
- BLOCKfast Clear
- Citocamera monouso 8 ml ad Innesto Rapido - 100 pz
- Portavetrino ad innesto rapido - 1 pz
- Saccomanno CYTOfast - Centrifuge Ready 9x20 ml
- Saccomanno CYTOfast 500 ml
- Soluzione CYTOfast - Blister flaconi 20x12/20 ml
Showing 12 of 54 declared devices.
Catalogue references include CYA000090, CYR000035, CYR000110, CYR000120, CYR000140, CYR00036.
European nomenclature codes declared: W0102090207, W01030705, W01030799, W0202059099, W02069004, W02029099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| 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 | 54 |
|---|---|
| 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. Hospitex International S.r.l. was not found in either the U.S. or the Canadian register.