Covidien Iic
Country not established
- Devices
- 1
What Covidien Iic makes
Covidien LLC manufactures the BARRX FLEX Radiofrequency Ablation (RFA) Energy Generator, a device used for tissue ablation procedures, including the treatment of liver tumors and other targeted lesions.
The BARRX FLEX RFA Energy Generator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Barrx Flex Rfa Energy Generator Ref K141357
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien Iic have in the registry?
The registry currently lists 1 device for Covidien Iic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien Iic's devices?
Among its 1 most recently registered device, Covidien Iic has devices listed in FDA 510(k) (1 device).
What risk classes do Covidien Iic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Covidien Iic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien Iic in the registry?
The most recently registered devices listed for Covidien Iic include BARRX FLEX RFA ENERGY GENERATOR.