Geratherm AG
Country not established
- Devices
- 1
What Geratherm AG makes
Geratherm AG manufactures the BabyWatch temperature monitor, a device designed for continuous, non-invasive monitoring of neonatal body temperature to support clinical care and early intervention.
The BabyWatch temperature monitor is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Geratherm Babywatch Temperature Monitor Ref K001281
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geratherm AG have in the registry?
The registry currently lists 1 device for Geratherm AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geratherm AG's devices?
Among its 1 most recently registered device, Geratherm AG has devices listed in FDA 510(k) (1 device).
What risk classes do Geratherm AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Geratherm AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geratherm AG in the registry?
The most recently registered devices listed for Geratherm AG include GERATHERM BABYWATCH TEMPERATURE MONITOR.