Taiwan Unison Biotech, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Taiwan Unison Biotech, Inc. makes
Taiwan Unison Biotech, Inc. makes the UNISCAN -DOA System, a device used for drug of abuse testing.
The UNISCAN -DOA System is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Uniscan -Doa System Ref K080347
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taiwan Unison Biotech, Inc. have in the registry?
The registry currently lists 1 device for Taiwan Unison Biotech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taiwan Unison Biotech, Inc.'s devices?
Among its 1 most recently registered device, Taiwan Unison Biotech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Taiwan Unison Biotech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Taiwan Unison Biotech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Taiwan Unison Biotech, Inc. in the registry?
The most recently registered devices listed for Taiwan Unison Biotech, Inc. include UNISCAN -DOA SYSTEM.