Data / Medical devices / Italy / Ascom Ums SRL
Ascom Ums SRL: FDA-registered device maker in Scandicci Firenze, Italy, 1 510(k) clearance
Ascom Ums SRL is registered with the FDA (registration 3015173634) in Scandicci Firenze, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 23, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015173634
- Address
- Via Amilcare Ponchielli 29, Scandicci Firenze, Italy, 50018
- Owner or operator
- Ascom UMS srl (10059298)
- Roles
- Manufacturer
- First device listed
- December 19, 2018
- Registered through
- 2026
- Brand names listed
- Digistat Smart Central
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Network And Communication, Physiological Monitors | MSX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 23, 2018 | K180430 | Digistat Smart Central | MSX | Substantially Equivalent | Ascom Ums Srl Unipersonale | accessdata.fda.gov |
Compare with other makers
Updated November 23, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.