B. Braun Vena-Tech
Country not established
- Devices
- 2
What B. Braun Vena-Tech makes
B. Braun Vena-Tech manufactures percutaneous introducers for vena cava filter systems and modification kits for vena cava filter systems.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. B. Braun Vena-Tech is based in the US.
Catalogue
- 510(k) 510(k)
Vena Cava Filter Systems, Modification Ref K925679
510(k) 510(k)
Frequently asked questions
How many devices does B. Braun Vena-Tech have in the registry?
The registry currently lists 2 devices for B. Braun Vena-Tech. Devices recorded under merged duplicate company entries are counted once.
Which registries list B. Braun Vena-Tech's devices?
Among its 2 most recently registered devices, B. Braun Vena-Tech has devices listed in FDA 510(k) (2 devices).
What risk classes do B. Braun Vena-Tech's devices fall under?
Among its 2 most recently registered devices, the classes recorded for B. Braun Vena-Tech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B. Braun Vena-Tech in the registry?
The most recently registered devices listed for B. Braun Vena-Tech include PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST and VENA CAVA FILTER SYSTEMS, MODIFICATION.