Mijnhardt B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Mijnhardt B.V. makes
Mijnhardt B.V. manufactures the OXYCON-ALPHA device.
The OXYCON-ALPHA is classified as a Class II medical 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
Oxycon-Alpha Ref K942230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mijnhardt B.V. have in the registry?
The registry currently lists 1 device for Mijnhardt B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mijnhardt B.V.'s devices?
Among its 1 most recently registered device, Mijnhardt B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Mijnhardt B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mijnhardt B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mijnhardt B.V. in the registry?
The most recently registered devices listed for Mijnhardt B.V. include OXYCON-ALPHA.