Mesi, Development of Medical Devices, Ltd.; Mesi d.o.o.
SloveniaFDA applicant, unverified
- Devices
- 2
What Mesi, Development of Medical Devices, Ltd.; Mesi d.o.o. makes
Mesi develops diagnostic systems for traumatic brain injury (TBI) and electrocardiogram (ECG) monitoring, including portable tablet-based platforms designed for point-of-care use.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. Mesi is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. have in the registry?
The registry currently lists 2 devices for Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.'s devices?
Among its 2 most recently registered devices, Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. in the registry?
The most recently registered devices listed for Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. include MESI mTABLET TBI diagnostic system, MESI mTABLET TBI and MESI mTablet ECG Diagnostic System, MESI mTablet ECG.