Sino Canada Health Engineering Research Institute (Hefei)
ChinaFDA applicant, unverified
- Devices
- 1
What Sino Canada Health Engineering Research Institute (Hefei) makes
The company manufactures the MOBINEURO Alita Intraoperative MRI System, a device designed for real-time imaging during surgical procedures to enhance precision and reduce complications.
This device is classified as Class II under regulatory frameworks and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
MOBINEURO Alita Intraoperative MRI System Ref K223875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sino Canada Health Engineering Research Institute (Hefei) have in the registry?
The registry currently lists 1 device for Sino Canada Health Engineering Research Institute (Hefei). Devices recorded under merged duplicate company entries are counted once.
Which registries list Sino Canada Health Engineering Research Institute (Hefei)'s devices?
Among its 1 most recently registered device, Sino Canada Health Engineering Research Institute (Hefei) has devices listed in FDA 510(k) (1 device).
What risk classes do Sino Canada Health Engineering Research Institute (Hefei)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sino Canada Health Engineering Research Institute (Hefei)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sino Canada Health Engineering Research Institute (Hefei) in the registry?
The most recently registered devices listed for Sino Canada Health Engineering Research Institute (Hefei) include MOBINEURO Alita Intraoperative MRI System.