Midian Intl.
Country not established
- Devices
- 1
What Midian Intl. makes
Midian Intl. manufactures the AGATHA-A-H2010, a Class I medical device designed for a specific diagnostic or monitoring purpose (exact function not specified).
The device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Agatha-A-H2010 Ref K983374
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midian Intl. have in the registry?
The registry currently lists 1 device for Midian Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midian Intl.'s devices?
Among its 1 most recently registered device, Midian Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Midian Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Midian Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Midian Intl. in the registry?
The most recently registered devices listed for Midian Intl. include AGATHA-A-H2010.