CRIOSERVICE SRL
IT-MF-000029026 · Italy · Leverano
CRIOSERVICE SRL is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 7 |
|---|---|
| Class IIa | 2 |
Most frequent device types declared: Impianti Distribuzione Vuoto, Impianti Evacuazione Gas Anestetici, Impianto Distribuzione Gas Medicinali/Medicali.
Among these devices, 9 are declared active.
Devices declared under this manufacturer
- Impianto di Evacuazione Gas Anestetici Sistema Venturi
- Impianto di Evacuazione Gas Anestetici Sistema a Soffianti
- Impianto di distribuzione Anidride Carbonica medicinale
- Impianto di distribuzione Aria medicinale
- Impianto di distribuzione Ossigeno Medicinale
- Impianto di distribuzione aria per strumenti chirurgici
- Impianto di distribuzione azoto per alimentare strumenti chirurgici
- Impianto di distribuzione del vuoto
- Impianto di distribuzione protossido di azoto medicinale
Catalogue references include ASP, DGM Anidride Carbonica, DGM Aria Medicinale, DGM Azoto strumenti Chirurgici, DGM Ossigeno, DGM Protossido di azoto.
European nomenclature codes declared: Z120309, Z1203019099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. CRIOSERVICE SRL was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
55375 | issued | 2027-08-31 |
55374 | issued | 2027-08-31 |