Brivant Limited (Lake Region Medical)
IrelandFDA applicant, unverified
- Devices
- 1
What Brivant Limited (Lake Region Medical) makes
Brivant Limited produces coronary guidewires, including the Hi-Torque Vektor line in .014-inch diameter and lengths of 195 cm and 300 cm, available with straight or J-tip configurations.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Brivant Limited (Lake Region Medical) have in the registry?
The registry currently lists 1 device for Brivant Limited (Lake Region Medical). Devices recorded under merged duplicate company entries are counted once.
Which registries list Brivant Limited (Lake Region Medical)'s devices?
Among its 1 most recently registered device, Brivant Limited (Lake Region Medical) has devices listed in FDA 510(k) (1 device).
What risk classes do Brivant Limited (Lake Region Medical)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Brivant Limited (Lake Region Medical)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brivant Limited (Lake Region Medical) in the registry?
The most recently registered devices listed for Brivant Limited (Lake Region Medical) include Hi-Torque Vektor, .014, 195cm, Str, Hi-Torque Vektor, .014, 195cm, J, Hi-Torque Vektor, .014, 300cm, Str, Hi-Torque Vektor, .014, 300cm, J.