Kinetec SAS
FR-MF-000000364 · France · Tournes
Kinetec SAS is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Centura, Kinetec Optima S4.
Among these devices, 20 are declared active.
Devices declared under this manufacturer
- 6080 avec chaise
- Centura
- KINETEC SAS
- Kinetec 6080 avec module de coude
- Kinetec Centura B&W
- Kinetec Optima Kompanion - KINETEC SAS
- Kinetec SAS
- Kinevia - KINETEC SAS
- Optima Essential - KINETEC SAS
- Performa - Kinetec SAS
- Prima Advance - KINETEC SAS
- Spectra - KINETEC SAS
Showing 12 of 20 declared devices.
Catalogue references include 03760246246996, 46210018XX, 4621003102, 462100360X, 46210062X3, 46210062XX.
European nomenclature codes declared: Z120603, Z120616.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Kinetec SAS (FR) · FDA 8020836 |
| Devices in EUDAMED | 20 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | KINETEC SAS |
North American profile: Both markets. Kinetec SAS is registered in both the United States and Canada.