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= 125mm, 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= 125 mm, Angled surgical handpiece 1:1, FG shank ø 2.35 mm, L= 70 mm, Angled surgical handpiece 1:1, FG shank ø 2.35 mm, L= 95 mm.
Among these devices, 5 are declared sterile, 39 reusable, 22 active.
Authorised representative in the Union: Nouvag Dental- und Medizintechnik GmbH.
Devices declared under this manufacturer
- Blades for Dermatome
- Dermatome 100 mm
- Dispenser DP 30 LipoPlus Set
- Dispenser DP 30 Set
- Duraguard pedriatic
- Foot pedal On/Off
- Foot pedal Vario
- HighSurg 30
- Irrigation nozzle
- MOS 5000
- Reduction support base
- Surgical handpiece 1:1
Showing 12 of 73 declared devices.
Catalogue references include 1513nou, 1906nou, 1936spi, 1960nou, 19871, 3360.
European nomenclature codes declared: Z12019080, Z12149080, Z12019080,Z12110180,Z12149080, L0103, Z12030301, Z12100980.
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 |
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | NOUVAG AG |
North American profile: Both markets. NOUVAG AG is registered in both the United States and Canada.