Miegmbh
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ancoris Ref K201807
Regimes: 510(k) Registry: 510(k)Mie Scintron Gamma Camera Systems Ref K101768
Regimes: 510(k) Registry: 510(k)Ecat Scintron Pet Ref K130269
Regimes: 510(k) Registry: 510(k)Modification To Scintron Iv Ref K101013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Miegmbh have in the registry?
The registry currently lists 4 devices for Miegmbh. Devices recorded under merged duplicate company entries are counted once.
Which registries list Miegmbh's devices?
Among its 4 most recently registered devices, Miegmbh has devices listed in FDA 510(k) (4 devices).
What risk classes do Miegmbh's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Miegmbh's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Miegmbh in the registry?
The most recently registered devices listed for Miegmbh include ANCORIS, MIE SCINTRON GAMMA CAMERA SYSTEMS, ECAT SCINTRON PET and MODIFICATION TO SCINTRON IV.