Bipress, Inc.
Country not established
- Devices
- 1
What Bipress, Inc. makes
Bipress, Inc. manufactures the REDINOV Perfusion Set, a medical device designed for intravenous fluid administration and perfusion applications in clinical settings.
The REDINOV Perfusion Set is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Redinov Perfusion Set Ref K924010
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bipress, Inc. have in the registry?
The registry currently lists 1 device for Bipress, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bipress, Inc.'s devices?
Among its 1 most recently registered device, Bipress, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bipress, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bipress, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bipress, Inc. in the registry?
The most recently registered devices listed for Bipress, Inc. include REDINOV PERFUSION SET.