Aisoftw@Re Medical, S.p.A.
Country not established
- Devices
- 1
What Aisoftw@Re Medical, S.p.A. makes
Aisoftw@Re Medical, S.P.A. makes medical devices, including modifications to Medstation.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510k registry, with the company based in the US.
Catalogue
Modification To Medstation Ref K021934
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aisoftw@Re Medical, S.P.A. have in the registry?
The registry currently lists 1 device for Aisoftw@Re Medical, S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aisoftw@Re Medical, S.P.A.'s devices?
Among its 1 most recently registered device, Aisoftw@Re Medical, S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Aisoftw@Re Medical, S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aisoftw@Re Medical, S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aisoftw@Re Medical, S.P.A. in the registry?
The most recently registered devices listed for Aisoftw@Re Medical, S.P.A. include MODIFICATION TO MEDSTATION.