MEDIDEV - SENTECH FRANCE
FR-MF-000008021 · France · LYON
MEDIDEV - SENTECH FRANCE is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Among these devices, 3 are declared active.
Devices declared under this manufacturer
- SENTRY C1200C014550
- SENTRY HIC4550
- SENTRY HIPUPA
- SENTRY HIPUPA120200
- SENTRY HIPUPAXR
- SENTRY M1200MR02
- SENTRY MD98000120
- SENTRY SAC1200MR01B
- SENTRY SAC1200MR01R
- SENTRY SHI1200MR
- SENTRY SYS1200C014550
- SENTRY SYS1200MR02
Showing 12 of 13 declared devices.
Catalogue references include HIPUPA, HIPUPA120200, M1200MR02, MD98000120, SAC1200MR01R, SHI1200MR.
European nomenclature codes declared: T030502, V080701, T0399, V08030101, Z12030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. MEDIDEV - SENTECH FRANCE was not found in either the U.S. or the Canadian register.