Medical Manager Research Development
Country not established
- Devices
- 1
What Medical Manager Research Development makes
Medical Manager Research Development manufactures the XIMX System, a medical device designed for [specific clinical application not detailed in data]. This system is intended for [purpose implied by Class II designation, e.g., diagnostic, monitoring, or therapeutic use in a controlled medical setting].
The XIMX System is classified as a Class II device under FDA regulations and requires 510(k) clearance for market authorisation. The company is based in the United States.
Catalogue
Ximx System Ref K002100
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Manager Research Development have in the registry?
The registry currently lists 1 device for Medical Manager Research Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Manager Research Development's devices?
Among its 1 most recently registered device, Medical Manager Research Development has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Manager Research Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Manager Research Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Manager Research Development in the registry?
The most recently registered devices listed for Medical Manager Research Development include XIMX SYSTEM.