Unetixs, Inc.
Country not established
- Devices
- 1
What Unetixs, Inc. makes
Unetixs, Inc. manufactures the MULTILAB 2000, a laboratory instrument designed for automated sample processing and analysis in clinical or research settings. This device is intended for handling multiple sample types, including blood, serum, or plasma, to streamline workflows in diagnostic testing environments.
The MULTILAB 2000 is classified as a Class II medical device under FDA regulations and has undergone the 510(k) clearance process. The product is listed in the FDA’s 510(k) database, reflecting its compliance with U.S. regulatory requirements. The company is headquartered in the United States.
Catalogue
Multilab 2000 Ref K904392
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unetixs, Inc. have in the registry?
The registry currently lists 1 device for Unetixs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unetixs, Inc.'s devices?
Among its 1 most recently registered device, Unetixs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Unetixs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unetixs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Unetixs, Inc. in the registry?
The most recently registered devices listed for Unetixs, Inc. include MULTILAB 2000.