Convergenza AG
Country not established
- Devices
- 1
What Convergenza AG makes
Convergenza AG manufactures the Dynamic Bubble Trap (DBT), a device designed to filter and remove microbubbles from medical and laboratory fluids to improve system performance and safety.
The company’s portfolio is regulated under FDA’s Class II designation and is listed via the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Dbt, Dynamic Bubble Trap Ref K031323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Convergenza AG have in the registry?
The registry currently lists 1 device for Convergenza AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Convergenza AG's devices?
Among its 1 most recently registered device, Convergenza AG has devices listed in FDA 510(k) (1 device).
What risk classes do Convergenza AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Convergenza AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Convergenza AG in the registry?
The most recently registered devices listed for Convergenza AG include DBT, DYNAMIC BUBBLE TRAP.