Aries srl
IT-MF-000029317 · Italy · Mirandola
Aries srl is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Among these devices, 1 are declared active, 1 with a measuring function.
Devices declared under this manufacturer
- Cannule per clismi
- Connessione di tubatismi di varie misure
- Pinze premifistola e Pinze Klemmer
- Sacche trasparenti per trasporto farmaci e sacche per la protezione di
- Sistema per il drenaggio e raccolta liquidi biologici da 2000 mL
- Supporto universale per rampe di rubinetti
Catalogue references include 11/0201., 498001310-001R1, CH000001, IN049010, IN062100, SP069000.
European nomenclature codes declared: V9099, A06030301, A0799, A070199, A0899, V0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 6 |
|---|---|
| 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. Aries srl was not found in either the U.S. or the Canadian register.