Aguiflai Iberica S.L.
SpainFDA applicant, unverified
- Devices
- 1
What Aguiflai Iberica S.L. makes
Aguiflai Iberica S.L. manufactures the Multifunction Keito, a medical device designed for specific vascular or interventional procedures, including catheter-based applications.
The device is classified as Class II under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Multifunction Keito Ref K103058
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aguiflai Iberica S.L. have in the registry?
The registry currently lists 1 device for Aguiflai Iberica S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aguiflai Iberica S.L.'s devices?
Among its 1 most recently registered device, Aguiflai Iberica S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Aguiflai Iberica S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aguiflai Iberica S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aguiflai Iberica S.L. in the registry?
The most recently registered devices listed for Aguiflai Iberica S.L. include MULTIFUNCTION KEITO.