Medecell US, Inc.
Country not established
- Devices
- 1
What Medecell US, Inc. makes
Medecell Us, Inc. manufactures the TANYX, a medical device designed for vascular access or infusion therapy applications.
The TANYX is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Tanyx Ref K123866
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medecell Us, Inc. have in the registry?
The registry currently lists 1 device for Medecell Us, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medecell Us, Inc.'s devices?
Among its 1 most recently registered device, Medecell Us, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medecell Us, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medecell Us, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medecell Us, Inc. in the registry?
The most recently registered devices listed for Medecell Us, Inc. include TANYX.