Carewill, Lda
PT-MF-000010054 · Portugal · Senhora da Hora
Carewill, Lda is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|
Most frequent device types declared: P011032, P011102, P011122, P012052, P012102.
Among these devices, 10 are declared sterile.
Devices declared under this manufacturer
- Bladeless Trocar System
- Bladless Trocar System
Catalogue references include P011032, P011052, P011122, P012052, P012102, P013032.
European nomenclature codes declared: K01010101, K01010103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Portugal |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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: Neither register. Carewill, Lda was not found in either the U.S. or the Canadian register.