Medel S.p.A.
Country not established
- Devices
- 4
What Medel S.p.A. makes
Medel S.P.A. makes medical devices such as breast pumps, including the MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP, and other products like the AG-PLUS, AG-CLASSIC, and AG-EDGE models.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
AG-Plus, Model 91210 Ref K060404
Regimes: 510(k) Registry: 510(k)AG-Classic Ref K072494
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
AG-Edge, Model 91200 Ref K063103
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medel S.P.A. have in the registry?
The registry currently lists 4 devices for Medel S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medel S.P.A.'s devices?
Among its 4 most recently registered devices, Medel S.P.A. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medel S.P.A.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medel S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medel S.P.A. in the registry?
The most recently registered devices listed for Medel S.P.A. include AG-PLUS, MODEL 91210, AG-CLASSIC, MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP and AG-EDGE, MODEL 91200.