Kabi Diagnostica
Country not established
- Devices
- 2
What Kabi Diagnostica makes
Kabi Diagnostica makes chromogenic assays for measuring antithrombin and low molecular weight heparin or heparin activity in blood samples.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Coacute Antithrombin Chromogenic Assay Ref K902393
Regimes: 510(k) Registry: 510(k)Coatest Lmw Heparin/Heparin Chromogenic Assay Ref K901874
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kabi Diagnostica have in the registry?
The registry currently lists 2 devices for Kabi Diagnostica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kabi Diagnostica's devices?
Among its 2 most recently registered devices, Kabi Diagnostica has devices listed in FDA 510(k) (2 devices).
What risk classes do Kabi Diagnostica's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kabi Diagnostica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kabi Diagnostica in the registry?
The most recently registered devices listed for Kabi Diagnostica include COACUTE ANTITHROMBIN CHROMOGENIC ASSAY and COATEST LMW HEPARIN/HEPARIN CHROMOGENIC ASSAY.