RI.MOS. SRL
IT-MF-000025629 · Italy · MIRANDOLA (MO)
RI.MOS. SRL is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 10 |
|---|
Most frequent device types declared: Multi-iniettori senza aghi.
Among these devices, 6 are declared sterile.
Devices declared under this manufacturer
- Multi-iniettore circolare senza aghi con 3 connessioni
- Multi-iniettore circolare senza aghi con 5 connessioni
- Multi-iniettore circolare senza aghi con 7 connessioni
- Multi-iniettore lineare senza aghi con 3 connessioni
- Multi-iniettore lineare senza aghi con 5 connessioni
- RAMCOVER
- VAGILUB
Catalogue references include 710101, 710103, 710104, 710105, 720132, 720132F.
European nomenclature codes declared: A018099, U0899, U100102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RI.MOS. SRL (IT) · FDA 9614868 |
| Devices in EUDAMED | 10 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. RI.MOS. SRL is registered in the United States but was not found in the Canadian register.