Mercury Produzione Srl
IT-MF-000030831 · Italy · Gualdo Tadino
Mercury Produzione 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 IIa | 9 |
|---|
Most frequent device types declared: Endoscopio Ultrasottile SF-10K1N, SF-10K2N, SF-17K1G, SF-17K2G, SF-30K, NS-3200, NS-3200U, NS-4422, VP-1000.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- NS-3200
- NS-3200U
- NS-4422
- SF-10K1N
- SF-10K2N
- SF-17K1G
- SF-17K2G
- SF-30K2S
- VP-1000
Catalogue references include 2802, 2803, 2816, 3181, 3182, 3184.
European nomenclature codes declared: Z12020903, Z12021006, Z12020406.
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. Mercury Produzione Srl was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
IT327042 | issued | 2028-11-15 |