Taugagreining HF
Country not established
- Devices
- 1
What Taugagreining HF makes
Taugagreining HF manufactures the Nervus Monitor, a device designed for real-time monitoring of nerve function during surgical procedures, particularly in orthopedic and spinal surgeries. It provides electrical stimulation and response analysis to assess nerve integrity and prevent intraoperative nerve damage.
The company’s portfolio is regulated under Class II devices in the United States, with the Nervus Monitor authorised through the FDA’s 510(k) clearance process. The company is based in the US.
Catalogue
Nervus Monitor Ref K021185
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taugagreining HF have in the registry?
The registry currently lists 1 device for Taugagreining HF. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taugagreining HF's devices?
Among its 1 most recently registered device, Taugagreining HF has devices listed in FDA 510(k) (1 device).
What risk classes do Taugagreining HF's devices fall under?
Among its 1 most recently registered device, the classes recorded for Taugagreining HF's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Taugagreining HF in the registry?
The most recently registered devices listed for Taugagreining HF include NERVUS MONITOR.