Schering Research
Country not established
- Devices
- 1
What Schering Research makes
Schering Research makes the GENTLEHALER(R) device.
The GENTLEHALER(R) is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Gentlehaler(R) Ref K892117
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schering Research have in the registry?
The registry currently lists 1 device for Schering Research. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schering Research's devices?
Among its 1 most recently registered device, Schering Research has devices listed in FDA 510(k) (1 device).
What risk classes do Schering Research's devices fall under?
Among its 1 most recently registered device, the classes recorded for Schering Research's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Schering Research in the registry?
The most recently registered devices listed for Schering Research include GENTLEHALER(R).