Vupiesse SRL
Country not established
- Devices
- 1
What Vupiesse SRL makes
VuPiesse Srl manufactures transcutaneous neuromuscular electrical stimulation (TENS/NMES) systems designed for physical therapy applications. Their product line includes the Tua device, which delivers targeted electrical stimulation to promote muscle activation and rehabilitation.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. VuPiesse Srl operates from the United States, adhering to applicable U.S. medical device regulations.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 434514607
Frequently asked questions
How many devices does VUPIESSE SRL have in the registry?
The registry currently lists 1 device for VUPIESSE SRL. Devices recorded under merged duplicate company entries are counted once.
Which registries list VUPIESSE SRL's devices?
Among its 1 most recently registered device, VUPIESSE SRL has devices listed in FDA GUDID (1 device).
What risk classes do VUPIESSE SRL's devices fall under?
Among its 1 most recently registered device, the classes recorded for VUPIESSE SRL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VUPIESSE SRL in the registry?
The most recently registered devices listed for VUPIESSE SRL include Tua Face Fitness.