Duogenic Stemcells Corporation
TaiwanFDA 510(k) applicant, unverified
- Devices
- 1
What Duogenic Stemcells Corporation makes
Duogenic Stemcells Corporation manufactures the MoFi Cell Culture Basal Medium, a basal medium designed for culturing stem cells in laboratory settings.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
“MoFi” Cell Culture Basal Medium Ref K240247
510(k) 510(k)
Frequently asked questions
How many devices does Duogenic Stemcells Corporation have in the registry?
The registry currently lists 1 device for Duogenic Stemcells Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Duogenic Stemcells Corporation's devices?
Among its 1 most recently registered device, Duogenic Stemcells Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Duogenic Stemcells Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Duogenic Stemcells Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Duogenic Stemcells Corporation in the registry?
The most recently registered devices listed for Duogenic Stemcells Corporation include “MoFi” Cell Culture Basal Medium.