NOUVAG AG
CH-MF-000018882 · Switzerland · Goldach
NOUVAG AG is registered in the European database on medical devices as a manufacturer, with 73 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 73 |
|---|
Most frequent device types declared: Angled High-Speed surgical handpiece 1:1 FG shank ø 2.35 mm, L= 70mm, Angled surgical handpiece 1:1, FG shank ø 2.35 mm, L= 70 mm, Surgical handpiece 1:1, FG shank Ø 2.35 mm, L=44 mm, Angled surgical handpiece 1:1, FG shank ø 2.35 mm, L= 125 mm, High-speed surgical handpiece 1:1, FG shank ø 2.35 mm, L= 70mm.
Among these devices, 5 are declared sterile, 39 reusable, 22 active.
Authorised representative in the Union: DE-AR-000005643.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NOUVAG AG (CH) · FDA 9680741 |
| Devices in EUDAMED | 73 |
| Country of registration | Switzerland |