Membrana
Country not established
- Devices
- 1
What Membrana makes
Membrana manufactures a hemodialysis transducer protector, designed to safeguard pressure monitoring systems during hemodialysis procedures.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Hemodialysis Transducer Protector Ref K812162
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Membrana have in the registry?
The registry currently lists 1 device for Membrana. Devices recorded under merged duplicate company entries are counted once.
Which registries list Membrana's devices?
Among its 1 most recently registered device, Membrana has devices listed in FDA 510(k) (1 device).
What risk classes do Membrana's devices fall under?
Among its 1 most recently registered device, the classes recorded for Membrana's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Membrana in the registry?
The most recently registered devices listed for Membrana include HEMODIALYSIS TRANSDUCER PROTECTOR.