Electromedicarin, S.A.
Country not established
- Devices
- 1
What Electromedicarin, S.A. makes
Electromedicarin, S.A. manufactures the Electromedicarin 900, a medical device designed for electrophysiological monitoring and analysis, likely used in cardiac or neurological diagnostics.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Electromedicarin 900 authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Electromedicarin 900 Ref K020478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electromedicarin, S.A. have in the registry?
The registry currently lists 1 device for Electromedicarin, S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electromedicarin, S.A.'s devices?
Among its 1 most recently registered device, Electromedicarin, S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Electromedicarin, S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Electromedicarin, S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electromedicarin, S.A. in the registry?
The most recently registered devices listed for Electromedicarin, S.A. include ELECTROMEDICARIN 900.