Eumedic Limited
Country not established
- Devices
- 1
What Eumedic Limited makes
Eumedic Limited manufactures the Fenzian Treatment System, a medical device designed for specific therapeutic applications in clinical settings.
The Fenzian Treatment System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Fenzian Treatment System Ref K041575
510(k) 510(k)
Frequently asked questions
How many devices does Eumedic Limited have in the registry?
The registry currently lists 1 device for Eumedic Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eumedic Limited's devices?
Among its 1 most recently registered device, Eumedic Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Eumedic Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eumedic Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eumedic Limited in the registry?
The most recently registered devices listed for Eumedic Limited include FENZIAN TREATMENT SYSTEM.