Problade Srl
IT-MF-000044499 · Italy · Vicenza
Problade Srl is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|
Among these devices, 34 are declared sterile.
Devices declared under this manufacturer
- LAMA SGORBIA MISURA 1 EDGE CUT
- LAMA SGORBIA MISURA 1 RUCK
- LAMA SGORBIA MISURA 10 EDGE CUT
- LAMA SGORBIA MISURA 2 EDGE CUT
- LAMA SGORBIA MISURA 3
- LAMA SGORBIA MISURA 3 RUCK
- LAMA SGORBIA MISURA 4
- LAMA SGORBIA MISURA 4 EDGE CUT
- LAMA SGORBIA MISURA 5
- LAMA SGORBIA MISURA 5 EDGE CUT
- LAMA SGORBIA MISURA 5 RUCK
- LAMA SGORBIA MISURA 8
Showing 12 of 34 declared devices.
Catalogue references include 2015003, 2015008, 385301, 385304, 385305, PB03SGM.
European nomenclature codes declared: V010301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| 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 | 34 |
|---|---|
| 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. Problade Srl was not found in either the U.S. or the Canadian register.