Telovital GmbH Telemedizin
Country not established
- Devices
- 2
What Telovital GmbH Telemedizin makes
Telovital GmbH Telemedizin manufactures CLUE Medical and CLUE Medical Basic, which appear to be medical devices designed for remote patient monitoring or telemedicine applications, likely focused on physiological data collection and analysis.
These devices are classified as Class II under FDA regulations and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Clue Medical And Clue Medical Basic Ref K083630
Regimes: 510(k) Registry: 510(k)Clue Medical And Clue Medical Basic Ref K082013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telovital GmbH Telemedizin have in the registry?
The registry currently lists 2 devices for Telovital GmbH Telemedizin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telovital GmbH Telemedizin's devices?
Among its 2 most recently registered devices, Telovital GmbH Telemedizin has devices listed in FDA 510(k) (2 devices).
What risk classes do Telovital GmbH Telemedizin's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Telovital GmbH Telemedizin's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telovital GmbH Telemedizin in the registry?
The most recently registered devices listed for Telovital GmbH Telemedizin include CLUE MEDICAL AND CLUE MEDICAL BASIC.