Bladhs Plast AB
Country not established
- Devices
- 1
What Bladhs Plast AB makes
Bladhs Plast AB manufactures the BONETRAP, a Class I medical device.
The BONETRAP is regulated as a Class I device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bonetrap Ref K980049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bladhs Plast AB have in the registry?
The registry currently lists 1 device for Bladhs Plast AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bladhs Plast AB's devices?
Among its 1 most recently registered device, Bladhs Plast AB has devices listed in FDA 510(k) (1 device).
What risk classes do Bladhs Plast AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bladhs Plast AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bladhs Plast AB in the registry?
The most recently registered devices listed for Bladhs Plast AB include BONETRAP.