Ghg Medizin-Elektronik AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Ghg Medizin-Elektronik AG makes
Ghg Medizin-Elektronik AG manufactures the TUBA TM, a transit-time ultrasonic breath analyzer used for measuring respiratory parameters such as minute ventilation and gas exchange.
The TUBA TM is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ghg Medizin-Elektronik AG have in the registry?
The registry currently lists 1 device for Ghg Medizin-Elektronik AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ghg Medizin-Elektronik AG's devices?
Among its 1 most recently registered device, Ghg Medizin-Elektronik AG has devices listed in FDA 510(k) (1 device).
What risk classes do Ghg Medizin-Elektronik AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ghg Medizin-Elektronik AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ghg Medizin-Elektronik AG in the registry?
The most recently registered devices listed for Ghg Medizin-Elektronik AG include TUBA TM (TRANSIT-TIME ULTRASONIC BREATH ANALYZER).