Seastar Medical Incorporated
Country not established
- Devices
- 1
What Seastar Medical Incorporated makes
Seastar Medical Incorporated manufactures apheresis systems designed for selective leukocyte adsorption, including the Quelimmune device. These systems are intended for therapeutic blood filtration to remove leukocytes from plasma.
The company’s products fall under FDA Class III regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 100323889
Frequently asked questions
How many devices does SEASTAR MEDICAL INCORPORATED have in the registry?
The registry currently lists 1 device for SEASTAR MEDICAL INCORPORATED. Devices recorded under merged duplicate company entries are counted once.
Which registries list SEASTAR MEDICAL INCORPORATED's devices?
Among its 1 most recently registered device, SEASTAR MEDICAL INCORPORATED has devices listed in FDA GUDID (1 device).
What risk classes do SEASTAR MEDICAL INCORPORATED's devices fall under?
Among its 1 most recently registered device, the classes recorded for SEASTAR MEDICAL INCORPORATED's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from SEASTAR MEDICAL INCORPORATED in the registry?
The most recently registered devices listed for SEASTAR MEDICAL INCORPORATED include Quelimmune 02-1006-01.