Servox Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mediport 2000 Mobile Ref K013585
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Servox Medizintechnik GmbH have in the registry?
The registry currently lists 1 device for Servox Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Servox Medizintechnik GmbH's devices?
Among its 1 most recently registered device, Servox Medizintechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Servox Medizintechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Servox Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Servox Medizintechnik GmbH in the registry?
The most recently registered devices listed for Servox Medizintechnik GmbH include MEDIPORT 2000 MOBILE.