Omnimed B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Omnimed B.V. makes
Omnimed B.V. manufactures the Model 617 Cardiac Output Computer, a device used to measure and display cardiac output parameters during patient monitoring.
The Model 617 is classified as a Class II medical device and is listed in the FDA 510(k) registry. Omnimed B.V. is based in the United States.
Catalogue
Model 617 Cardiac Output Computer Ref K870375
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omnimed B.V. have in the registry?
The registry currently lists 1 device for Omnimed B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omnimed B.V.'s devices?
Among its 1 most recently registered device, Omnimed B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Omnimed B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omnimed B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omnimed B.V. in the registry?
The most recently registered devices listed for Omnimed B.V. include MODEL 617 CARDIAC OUTPUT COMPUTER.