Sanofi-Aventis Deutschland GmbH
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Company details
- DUNS number
- 313218430
Frequently asked questions
How many devices does Sanofi-Aventis Deutschland GmbH have in the registry?
The registry currently lists 2 devices for Sanofi-Aventis Deutschland GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanofi-Aventis Deutschland GmbH's devices?
Among its 2 most recently registered devices, Sanofi-Aventis Deutschland GmbH has devices listed in FDA GUDID (2 devices).
What risk classes do Sanofi-Aventis Deutschland GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sanofi-Aventis Deutschland GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanofi-Aventis Deutschland GmbH in the registry?
The most recently registered devices listed for Sanofi-Aventis Deutschland GmbH include My Dose Coach 2.x.x and My Dose Coach 1.x.x.