Errecieffe srl
IT-MF-000017627 · Italy · Ponte San Pietro
Errecieffe srl is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 14 |
|---|---|
| Class IIa | 16 |
Among these devices, 4 are declared sterile, 14 implantable, 8 reusable.
Catalogue references include 011, EWB-ACC, MAS-33, MG-MPI, MUC45, SCAN-MPI.
European nomenclature codes declared: P01020180, P01020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 30 |
| 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 | 30 |
|---|---|
| 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. Errecieffe srl was not found in either the U.S. or the Canadian register.