Beuro Technology
Country not established
- Devices
- 1
What Beuro Technology makes
Beuro Technology manufactures the DIGISTIM II, a medical device designed for electrical stimulation and nerve testing, commonly used in clinical settings to assess nerve function and muscle response.
The DIGISTIM II is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Digistim Ii Ref K822137
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beuro Technology have in the registry?
The registry currently lists 1 device for Beuro Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beuro Technology's devices?
Among its 1 most recently registered device, Beuro Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Beuro Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Beuro Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beuro Technology in the registry?
The most recently registered devices listed for Beuro Technology include DIGISTIM II.