gbo Medizintechnik AG
DE-MF-000018065 · Germany · Rimbach
gbo Medizintechnik AG 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: Pelvicenter with Oxygen without light, Pelvicenter without Oxygen with light, Pelvicenter without Oxygen without light, Sonostat touch 133, Stereodynator.
Among these devices, 20 are declared active.
Devices declared under this manufacturer
- Duodynator
- HiToP 1touch
- HiToP 2touch
- HiToP 4touch
- HiToP PNP
- MicroPro
- PelviCenter
- PelviPower
- Radiotherm
- Sonostat
- Sonostat touch 133
- Stereodynator
Showing 12 of 20 declared devices.
Catalogue references include 017-0-0191, 022-0-5000, 025-0-1000, 027-0-0040, 032-0-2000, 032-0-3100.
European nomenclature codes declared: Z120601, Z120606, Z120610, Z120608, Z120609, Z12062899.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | GBO MEDIZINTECHNIK AG (DE) · FDA 3005095860 |
| Devices in EUDAMED | 20 |
| Country of registration | Germany |
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 | GBO MEDIZINTECHNIK AG |
North American profile: Both markets. gbo Medizintechnik AG is registered in both the United States and Canada.