EUROTEKNIKA
FR-MF-000004032 · France · Sallanches
EUROTEKNIKA is registered in the European database on medical devices as a manufacturer, with 420 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 420 |
|---|
Most frequent device types declared: TL, CGC TG, BL.
Among these devices, 37 are declared sterile, 191 reusable.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | EUROTEKNIKA (FR) · FDA 3007521935 |
| Devices in EUDAMED | 420 |
| Country of registration | France |