BRACCO SUISSE SA
CH-MF-000022733 · Switzerland · Cadempino
BRACCO SUISSE SA is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Authorised representative in the Union: ACIST Europe BV.
Devices declared under this manufacturer
- GI-Perfusion & Liver DVP version 8
- VueBox GI-Perfusion & Plaque version 7
- VueBox GI-Perfusion Version 8
- Vuebox GI-Perfusion & Liver DVP & Plaque version 7
- Vuebox GI-Perfusion & Liver DVP version 7
- Vuebox GI-Perfusion version 7
Catalogue references include 680029, 680032, 680033, 680034.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. BRACCO SUISSE SA was not found in either the U.S. or the Canadian register.