M Nobird, Inc.
Country not established
- Devices
- 1
What M Nobird, Inc. makes
M Nobird, Inc. manufactures a radioimmunoassay test system designed for diagnostic laboratory use, enabling precise measurement of specific antigens or antibodies in patient samples. This system supports quantitative analysis in clinical settings, aiding in the diagnosis of conditions requiring hormone or peptide level assessment.
The company’s radioimmunoassay test system is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The device is listed with the U.S. Food and Drug Administration, adhering to federal requirements for diagnostic in vitro tests.
Catalogue
Dig Radioimmunoassay Test System Ref K852343
510(k) 510(k)
Frequently asked questions
How many devices does M Nobird, Inc. have in the registry?
The registry currently lists 1 device for M Nobird, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M Nobird, Inc.'s devices?
Among its 1 most recently registered device, M Nobird, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do M Nobird, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for M Nobird, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from M Nobird, Inc. in the registry?
The most recently registered devices listed for M Nobird, Inc. include DIG RADIOIMMUNOASSAY TEST SYSTEM.