Unisensor AG
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Unisensor AG is a medical device manufacturer, with 341 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 341
Registry facts
- Registries
- FDA GUDID 339
- EUDAMED 32
- FDA 510(k) 2
- Device classes
- FDA Class II 341
- Identifiers
- DUNS 483298907
Catalogue
Search and filter all 341 devicesShowing 1-50 of 341
Company details
- DUNS number
- 483298907
- qm@unisensor.ch
- Phone
- +1(603)570-2675
Frequently asked questions
How many devices does Unisensor AG have in the registry?
The registry currently lists 341 devices for Unisensor AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unisensor AG's devices?
Among its 50 most recently registered devices, Unisensor AG has devices listed in EUDAMED (4 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Unisensor AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Unisensor AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Unisensor AG in the registry?
The most recently registered devices listed for Unisensor AG include UniTip High Resolution Catheter K122359-L5-1716-D, UniTip High Resolution Catheter K101259-EL-1703-D, UniTip Catheter K8481-00-0476-D and UniTip High Resolution Catheter K10404-00-1720-D.