Gruppo Strola srl
IT-MF-000054807 · Italy · Torino
Gruppo Strola srl is registered in the European database on medical devices as a manufacturer, with 71 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: AP1000, AP1200, DFB1500, DFB1800, GS1000-B.
Catalogue references include AP1000-F-PS-S, AP1200-F-PB-S, DFB180-F-B, GS1200-7515-F-B, GS1200-9015-X-B, GS1500-11015-F-B.
European nomenclature codes declared: W0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 71 |
| 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 | 71 |
|---|---|
| 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. Gruppo Strola srl was not found in either the U.S. or the Canadian register.