Hi-D Imaging AG
SwitzerlandFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hi-D Imaging 4TAVR Ref K261535
Regimes: 510(k) Registry: 510(k)Hi-D Imaging 4TAVR Ref K241984
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hi-D Imaging AG have in the registry?
The registry currently lists 2 devices for Hi-D Imaging AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hi-D Imaging AG's devices?
Among its 2 most recently registered devices, Hi-D Imaging AG has devices listed in FDA 510(k) (2 devices).
What risk classes do Hi-D Imaging AG's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hi-D Imaging AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hi-D Imaging AG in the registry?
The most recently registered devices listed for Hi-D Imaging AG include Hi-D Imaging 4TAVR.