N-Dia, Inc.
Country not established
- Devices
- 1
What N-Dia, Inc. makes
N-Dia, Inc. manufactures the AMNISURE Fetal Membranes Rupture Test (Model FMRT1), a diagnostic device used to determine whether a pregnant patient’s amniotic membranes have ruptured.
The AMNISURE Fetal Membranes Rupture Test is classified as a Class I medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does N-Dia, Inc. have in the registry?
The registry currently lists 1 device for N-Dia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list N-Dia, Inc.'s devices?
Among its 1 most recently registered device, N-Dia, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do N-Dia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for N-Dia, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from N-Dia, Inc. in the registry?
The most recently registered devices listed for N-Dia, Inc. include AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1.