Radiplast AB
Country not established
- Devices
- 1
What Radiplast AB makes
Radiplast AB manufactures the RADI-BIOPSY device, which is a medical instrument used for biopsy procedures.
The company is based in the US, and its product is regulated as a Class II medical device listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Radi-Biopsy Device Ref K850605
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radiplast AB have in the registry?
The registry currently lists 1 device for Radiplast AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radiplast AB's devices?
Among its 1 most recently registered device, Radiplast AB has devices listed in FDA 510(k) (1 device).
What risk classes do Radiplast AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Radiplast AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radiplast AB in the registry?
The most recently registered devices listed for Radiplast AB include RADI-BIOPSY DEVICE.