Hill-Rom S.A.S.
FR-MF-000003176 · France · Pluvigner
Hill-Rom S.A.S. is registered in the European database on medical devices as a manufacturer, with 59 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 59 |
|---|
Among these devices, 23 are declared active, 7 with a measuring function.
Devices declared under this manufacturer
- Accella Therapy
- Ampera
- Anatome
- Baxter
- Centuris
- Hill-Rom 900
- Hill-Rom 900 Accella
- Hillrom Centuris Bed
- Syntheto
- Therapy2
Showing 12 of 59 declared devices.
Catalogue references include AC959A, AC962A, ASS007, ASS035, CS900B2, P006788A.
European nomenclature codes declared: V08068099, V080701, V080702, V08060101, V08060103, V080202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 59 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 59 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | HILL-ROM S.A.S. |
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 1 |
| First licensed | 2020-12-14 |
Licence types: Device Family (1).
Licensed under: ACCELLA THERAPY.
North American profile: Canada only. Hill-Rom S.A.S. holds a Canadian licence but was not found in the U.S. register.