Ascom Ums SRL Unipersonale
ItalyFDA applicant, unverified
- Devices
- 2
What Ascom Ums SRL Unipersonale makes
Ascom Ums Srl Unipersonale manufactures the Digistat Smart Central, a medical device designed for centralized monitoring and management of patient data in healthcare settings.
The Digistat Smart Central is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Digistat Care Ref K261287
Regimes: 510(k) Registry: 510(k)Digistat Smart Central Ref K180430
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ascom Ums Srl Unipersonale have in the registry?
The registry currently lists 2 devices for Ascom Ums Srl Unipersonale. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ascom Ums Srl Unipersonale's devices?
Among its 2 most recently registered devices, Ascom Ums Srl Unipersonale has devices listed in FDA 510(k) (2 devices).
What risk classes do Ascom Ums Srl Unipersonale's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ascom Ums Srl Unipersonale's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ascom Ums Srl Unipersonale in the registry?
The most recently registered devices listed for Ascom Ums Srl Unipersonale include Digistat Care and Digistat Smart Central.