Sedat
Country not established
- Devices
- 3
What Sedat makes
Sedat manufactures medical devices including the MYSHELL LITE, a portable shell for patient monitoring, and the NAUTIFLUX, a device for non-invasive fluid monitoring. The company also produces the FLAMINGO, a system designed for patient positioning and stabilization in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Sedat operates from the United States.
Catalogue
Sedat Myshell Lite Ref K080472
Regimes: 510(k) Registry: 510(k)Nautiflux Ref K060010
Regimes: 510(k) Registry: 510(k)Sedat Flamingo Ref K082755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sedat have in the registry?
The registry currently lists 3 devices for Sedat. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sedat's devices?
Among its 3 most recently registered devices, Sedat has devices listed in FDA 510(k) (3 devices).
What risk classes do Sedat's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sedat's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sedat in the registry?
The most recently registered devices listed for Sedat include SEDAT MYSHELL LITE, NAUTIFLUX and SEDAT FLAMINGO.