Medica USA, Inc.
Country not established
- Devices
- 1
What Medica USA, Inc. makes
Medica USA, Inc. manufactures the Purema H Hemoconcentrator for pediatric use, a device designed for blood processing to remove plasma while retaining red blood cells.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. Medica USA, Inc. is based in the United States.
Catalogue
Purema H Hemoconcentrator - Pediatric Ref K243920
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medica USA, Inc. have in the registry?
The registry currently lists 1 device for Medica USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medica USA, Inc.'s devices?
Among its 1 most recently registered device, Medica USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medica USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medica USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medica USA, Inc. in the registry?
The most recently registered devices listed for Medica USA, Inc. include Purema H Hemoconcentrator - Pediatric.