Resmed Germany, Inc.
Country not established
- Devices
- 8
What Resmed Germany, Inc. makes
Resmed Germany, Inc. makes sleep apnea diagnostic devices, including the ApneaLink, ApneaLink Pro, ApneaLink Air, and ApneaLink Plus models.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Stellar 150 Ref K113640
Regimes: 510(k) Registry: 510(k)Stellar 150 Ref K103167
Regimes: 510(k) Registry: 510(k)Stellar 150 Ref K122715
Regimes: 510(k) Registry: 510(k)Apnealink Ref K070263
Regimes: 510(k) Registry: 510(k)Apnealink Pro Ref K131932
Regimes: 510(k) Registry: 510(k)ApneaLink Air Ref K143272
Regimes: 510(k) Registry: 510(k)Apnealink Plus, Model: 22328 Ref K083575
Regimes: 510(k) Registry: 510(k)Apnealink, Model 22302 Ref K061405
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Resmed Germany, Inc. have in the registry?
The registry currently lists 8 devices for Resmed Germany, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resmed Germany, Inc.'s devices?
Among its 8 most recently registered devices, Resmed Germany, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Resmed Germany, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Resmed Germany, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resmed Germany, Inc. in the registry?
The most recently registered devices listed for Resmed Germany, Inc. include STELLAR 150, APNEALINK, APNEALINK PRO and ApneaLink Air.