Quantel Derma GmbH
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
EXELO2, Model 4010 Ref K090639
Regimes: 510(k) Registry: 510(k)Leda Ref K090762
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Quantel Derma GmbH have in the registry?
The registry currently lists 2 devices for Quantel Derma GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quantel Derma GmbH's devices?
Among its 2 most recently registered devices, Quantel Derma GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Quantel Derma GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Quantel Derma GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quantel Derma GmbH in the registry?
The most recently registered devices listed for Quantel Derma GmbH include EXELO2, MODEL 4010 and LEDA.