Fresenius AG
Country not established
- Devices
- 2
What Fresenius AG makes
Fresenius AG makes medical devices such as the C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM and associated sets like the AT1 AUTOTRANSFUSION SET and PSQ SET. These products are related to autotransfusion, which involves the collection and reinfusion of a patient's own blood.
The company's portfolio is regulated under Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
C.A.T.S. Continuous Autotransfusion System Ref K960006
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fresenius AG have in the registry?
The registry currently lists 2 devices for Fresenius AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fresenius AG's devices?
Among its 2 most recently registered devices, Fresenius AG has devices listed in FDA 510(k) (2 devices).
What risk classes do Fresenius AG's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fresenius AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fresenius AG in the registry?
The most recently registered devices listed for Fresenius AG include C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM, AT1 AUTOTRANSFUSION SET, PSQ SET and C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM.