Gruendler GmbH
Country not established
- Devices
- 1
What Gruendler GmbH makes
Gruendler GmbH manufactures the HUMICARE D900, a device designed for the controlled delivery of humidified medical gases, such as oxygen or air, to patients in clinical settings.
The HUMICARE D900 is classified as a Class II medical device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Humicare D900 Ref K133766
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gruendler GmbH have in the registry?
The registry currently lists 1 device for Gruendler GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gruendler GmbH's devices?
Among its 1 most recently registered device, Gruendler GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Gruendler GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gruendler GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gruendler GmbH in the registry?
The most recently registered devices listed for Gruendler GmbH include HUMICARE D900.