B. Braun Melsugen AG
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What B. Braun Melsugen AG makes
B. Braun Melsungen AG manufactures the SpaceStation MRI, a specialized magnetic resonance imaging system designed for use in space environments to support medical diagnostics during long-duration missions.
The SpaceStation MRI is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
SpaceStation MRI Ref K191910
510(k) 510(k)
Frequently asked questions
How many devices does B. Braun Melsugen AG have in the registry?
The registry currently lists 1 device for B. Braun Melsugen AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list B. Braun Melsugen AG's devices?
Among its 1 most recently registered device, B. Braun Melsugen AG has devices listed in FDA 510(k) (1 device).
What risk classes do B. Braun Melsugen AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for B. Braun Melsugen AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B. Braun Melsugen AG in the registry?
The most recently registered devices listed for B. Braun Melsugen AG include SpaceStation MRI.