Centrimed Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Centrimed Corp. makes
Centrimed Corp. manufactures centrifugal blood processing systems designed for medical procedures requiring controlled separation of blood components. These systems include base units with optional manual pump drives, battery-powered variants, and system adapters for compatibility with specific medical applications.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. These systems are intended for use in the United States, where regulatory compliance is required for market authorisation.
Catalogue
Centrimed System 1 Ref K842007
Regimes: 510(k) Registry: 510(k)Centrimed System 1 W/Manual Pump Drive Ref K851615
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Centrimed System 1 W/System 1 Adapter Ref K851613
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Centrimed Corp. have in the registry?
The registry currently lists 4 devices for Centrimed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centrimed Corp.'s devices?
Among its 4 most recently registered devices, Centrimed Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Centrimed Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Centrimed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centrimed Corp. in the registry?
The most recently registered devices listed for Centrimed Corp. include CENTRIMED SYSTEM 1, CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE, CENTRIMED SYSTEM 1 W/24 VOLT BATTERY POWER SUPPLY and CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTER.