Iodp SA
Country not established
- Devices
- 1
What Iodp SA makes
Iodp SA manufactures the MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM, which is a Class II medical device.
The company is based in the US, and its device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Model I0-3DUIMS 3D Ultrasound Management System Ref K011095
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iodp SA have in the registry?
The registry currently lists 1 device for Iodp SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iodp SA's devices?
Among its 1 most recently registered device, Iodp SA has devices listed in FDA 510(k) (1 device).
What risk classes do Iodp SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iodp SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iodp SA in the registry?
The most recently registered devices listed for Iodp SA include MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM.