Hemaedics, Inc.
Country not established
- Devices
- 1
What Hemaedics, Inc. makes
Hemaedics, Inc. manufactures the DUOFLO DISPENSER, a device designed for the precise dispensing of blood components or intravenous fluids in clinical settings. This system is intended to improve workflow efficiency in transfusion medicine and patient care environments by automating the preparation and administration of blood products.
The DUOFLO DISPENSER is classified as a Class II medical device under FDA regulations and has been authorised through the 510(k) clearance process. The company is based in the United States and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Duoflo Dispenser Ref K872565
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemaedics, Inc. have in the registry?
The registry currently lists 1 device for Hemaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemaedics, Inc.'s devices?
Among its 1 most recently registered device, Hemaedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hemaedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemaedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemaedics, Inc. in the registry?
The most recently registered devices listed for Hemaedics, Inc. include DUOFLO DISPENSER.