Corsano Health B.V.
NetherlandsFDA applicant, unverified
- Devices
- 4
What Corsano Health B.V. makes
Corsano Health B.V. manufactures the Corsano CardioWatch 287-2 System, a medical device designed for continuous cardiac monitoring and arrhythmia detection.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. Corsano Health B.V. is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Corsano CardioWatch 287-2 System Ref K261367
Regimes: 510(k) Registry: 510(k)Corsano CardioWatch 287-2 System Ref K232548
Regimes: CE MDR 510(k) Registry: 510(k)
Company details
- DUNS number
- 493148003
Frequently asked questions
How many devices does Corsano Health B.V. have in the registry?
The registry currently lists 4 devices for Corsano Health B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corsano Health B.V.'s devices?
Among its 4 most recently registered devices, Corsano Health B.V. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Corsano Health B.V.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Corsano Health B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corsano Health B.V. in the registry?
The most recently registered devices listed for Corsano Health B.V. include Strap Silicon Blue, Charge Station 10 Sensors A and Corsano CardioWatch 287-2 System.