Mesi d.o.o.; Mesi, Development of Medical Devices, Ltd.
SloveniaFDA applicant, unverified
- Devices
- 2
What Mesi d.o.o.; Mesi, Development of Medical Devices, Ltd. makes
Mesi D.O.O. makes automated ankle brachial pressure index measuring devices, including the MESI mTABLET system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based 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 D.O.O.; Mesi, Development of Medical Devices, Ltd. have in the registry?
The registry currently lists 2 devices for Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.'s devices?
Among its 2 most recently registered devices, Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. in the registry?
The most recently registered devices listed for Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. include Automated ankle brachial pressure index measuring device and Automated ankle brachial pressure index measuring device, MESI mTABLET system.