Vepro - Computersysteme GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Vepro - Computersysteme GmbH makes
Vepro - Computersysteme GmbH develops MEDIMAGE, a medical imaging software system designed for diagnostic and analytical purposes in clinical environments.
The company’s portfolio is regulated under Class II medical devices in the US, with MEDIMAGE listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Medimage Ref K972215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vepro - Computersysteme GmbH have in the registry?
The registry currently lists 1 device for Vepro - Computersysteme GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vepro - Computersysteme GmbH's devices?
Among its 1 most recently registered device, Vepro - Computersysteme GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Vepro - Computersysteme GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vepro - Computersysteme GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vepro - Computersysteme GmbH in the registry?
The most recently registered devices listed for Vepro - Computersysteme GmbH include MEDIMAGE.