Ez-Blocker B.V.
Country not established
- Devices
- 1
What Ez-Blocker B.V. makes
Ez-Blocker B.V. manufactures the EZ-BLOCKER, a medical device designed for vascular occlusion, intended to prevent blood flow in specific vessels during surgical procedures.
The EZ-BLOCKER is classified as a Class II device under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Ez-Blocker Ref K121462
510(k) 510(k)
Frequently asked questions
How many devices does Ez-Blocker B.V. have in the registry?
The registry currently lists 1 device for Ez-Blocker B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ez-Blocker B.V.'s devices?
Among its 1 most recently registered device, Ez-Blocker B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Ez-Blocker B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ez-Blocker B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ez-Blocker B.V. in the registry?
The most recently registered devices listed for Ez-Blocker B.V. include EZ-BLOCKER.